Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for subject:(Cyclin dependent kinase Inhibitor p21). Showing records 1 – 30 of 7783 total matches.

[1] [2] [3] [4] [5] … [260]

Search Limiters

Last 2 Years | English Only

Degrees

Levels

Languages

Country

▼ Search Limiters

1. Santos, André Bandiera de Oliveira. Expressão imuno-histoquímica das proteínas p16, ciclina D1, CDK4, pRb, p53 e p21 em melanomas cutâneos de cabeça, pescoço e tronco e sua relação com prognóstico.

Degree: PhD, Clínica Cirúrgica, 2010, University of São Paulo

O melanoma cutâneo é a neoplasia de pele de maior mortalidade. A imprevisibilidade de sua evolução é uma de suas características principais, o tratamento do… (more)

Subjects/Keywords: Ciclina D1; Cyclin D1; Cyclin-dependent kinase 4; Cyclin-dependent kinase inhibitor p16; Cyclin-dependent kinase inhibitor p21; Immunohistochemistry; Imunoistoquímica; Inibidor de quinase dependente de ciclina p21; Inibidor p16 de quinase ciclina-dependente; Melanoma; Melanoma; Micro-array; Micro-array analysis; Prognosis; Prognóstico; Proteína do retinoblastoma; Proteína supressora de tumor p53; Quinase 4 dependente de ciclina; Retinoblastoma protein; Tumor suppressor protein p53

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Santos, A. B. d. O. (2010). Expressão imuno-histoquímica das proteínas p16, ciclina D1, CDK4, pRb, p53 e p21 em melanomas cutâneos de cabeça, pescoço e tronco e sua relação com prognóstico. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5132/tde-21062010-171113/ ;

Chicago Manual of Style (16th Edition):

Santos, André Bandiera de Oliveira. “Expressão imuno-histoquímica das proteínas p16, ciclina D1, CDK4, pRb, p53 e p21 em melanomas cutâneos de cabeça, pescoço e tronco e sua relação com prognóstico.” 2010. Doctoral Dissertation, University of São Paulo. Accessed December 05, 2020. http://www.teses.usp.br/teses/disponiveis/5/5132/tde-21062010-171113/ ;.

MLA Handbook (7th Edition):

Santos, André Bandiera de Oliveira. “Expressão imuno-histoquímica das proteínas p16, ciclina D1, CDK4, pRb, p53 e p21 em melanomas cutâneos de cabeça, pescoço e tronco e sua relação com prognóstico.” 2010. Web. 05 Dec 2020.

Vancouver:

Santos ABdO. Expressão imuno-histoquímica das proteínas p16, ciclina D1, CDK4, pRb, p53 e p21 em melanomas cutâneos de cabeça, pescoço e tronco e sua relação com prognóstico. [Internet] [Doctoral dissertation]. University of São Paulo; 2010. [cited 2020 Dec 05]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5132/tde-21062010-171113/ ;.

Council of Science Editors:

Santos ABdO. Expressão imuno-histoquímica das proteínas p16, ciclina D1, CDK4, pRb, p53 e p21 em melanomas cutâneos de cabeça, pescoço e tronco e sua relação com prognóstico. [Doctoral Dissertation]. University of São Paulo; 2010. Available from: http://www.teses.usp.br/teses/disponiveis/5/5132/tde-21062010-171113/ ;

2. Kfouri, Flavia. Papel do p21 e do estresse oxidativo na resistência renal isquêmica.

Degree: PhD, Nefrologia, 2007, University of São Paulo

A resistência tubular renal tem sido estudada a fim de se ampliar a compreensão da fisiopatologia da Insuficiência renal aguda (IRA). A isquemia renal induz… (more)

Subjects/Keywords: Cyclin-Dependent Kinase Inhibitor p21; Estresse oxidativo; Inibidor quinase dependente de ciclina p21; Ischemia/fisiopatologia; Ischemia/phisiopathology; Kidney tubules proximal; Oxidative stress; Ratos Wistar; Rats Wistar; Túbulos renais proximais

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Kfouri, F. (2007). Papel do p21 e do estresse oxidativo na resistência renal isquêmica. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5148/tde-11032008-151200/ ;

Chicago Manual of Style (16th Edition):

Kfouri, Flavia. “Papel do p21 e do estresse oxidativo na resistência renal isquêmica.” 2007. Doctoral Dissertation, University of São Paulo. Accessed December 05, 2020. http://www.teses.usp.br/teses/disponiveis/5/5148/tde-11032008-151200/ ;.

MLA Handbook (7th Edition):

Kfouri, Flavia. “Papel do p21 e do estresse oxidativo na resistência renal isquêmica.” 2007. Web. 05 Dec 2020.

Vancouver:

Kfouri F. Papel do p21 e do estresse oxidativo na resistência renal isquêmica. [Internet] [Doctoral dissertation]. University of São Paulo; 2007. [cited 2020 Dec 05]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5148/tde-11032008-151200/ ;.

Council of Science Editors:

Kfouri F. Papel do p21 e do estresse oxidativo na resistência renal isquêmica. [Doctoral Dissertation]. University of São Paulo; 2007. Available from: http://www.teses.usp.br/teses/disponiveis/5/5148/tde-11032008-151200/ ;


University of Texas Southwestern Medical Center

3. Todorova, Pavlina Krasimirova. Mechanistic Analysis of Radiation-Induced Gliomagenesis.

Degree: 2017, University of Texas Southwestern Medical Center

 Glioblastomas (GBM) are devastating brain tumors refractory to any available treatment. Exposure to ionizing radiation (IR) is the only known GBM risk factor. The link… (more)

Subjects/Keywords: Brain Neoplasms; Cyclin-Dependent Kinase Inhibitor p15; Cyclin-Dependent Kinase Inhibitor p16; Glioblastoma; Proto-Oncogene Proteins c-met

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Todorova, P. K. (2017). Mechanistic Analysis of Radiation-Induced Gliomagenesis. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/7205

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Todorova, Pavlina Krasimirova. “Mechanistic Analysis of Radiation-Induced Gliomagenesis.” 2017. Thesis, University of Texas Southwestern Medical Center. Accessed December 05, 2020. http://hdl.handle.net/2152.5/7205.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Todorova, Pavlina Krasimirova. “Mechanistic Analysis of Radiation-Induced Gliomagenesis.” 2017. Web. 05 Dec 2020.

Vancouver:

Todorova PK. Mechanistic Analysis of Radiation-Induced Gliomagenesis. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2017. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/2152.5/7205.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Todorova PK. Mechanistic Analysis of Radiation-Induced Gliomagenesis. [Thesis]. University of Texas Southwestern Medical Center; 2017. Available from: http://hdl.handle.net/2152.5/7205

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Texas Southwestern Medical Center

4. Sung, Caroline Yeh-Chien. Establishing a Dual-Reporter Mouse Model to Monitor INK4A/ARF Regulation in Vivo.

Degree: 2015, University of Texas Southwestern Medical Center

Note: The general metadata  – e.g., title, author, abstract, subject headings, etc.  – is publicly available, but access to the submitted files is restricted to… (more)

Subjects/Keywords: Cyclin-Dependent Kinase Inhibitor p16; Gene Silencing; Tumor Suppressor Protein p14ARF

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Sung, C. Y. (2015). Establishing a Dual-Reporter Mouse Model to Monitor INK4A/ARF Regulation in Vivo. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/7068

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Sung, Caroline Yeh-Chien. “Establishing a Dual-Reporter Mouse Model to Monitor INK4A/ARF Regulation in Vivo.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed December 05, 2020. http://hdl.handle.net/2152.5/7068.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Sung, Caroline Yeh-Chien. “Establishing a Dual-Reporter Mouse Model to Monitor INK4A/ARF Regulation in Vivo.” 2015. Web. 05 Dec 2020.

Vancouver:

Sung CY. Establishing a Dual-Reporter Mouse Model to Monitor INK4A/ARF Regulation in Vivo. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/2152.5/7068.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Sung CY. Establishing a Dual-Reporter Mouse Model to Monitor INK4A/ARF Regulation in Vivo. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/7068

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

5. Viciana, Ana Carolina de Bragança. Estudo da deficiência de vitamina D no modelo de isquemia/reperfusão renal em ratos.

Degree: PhD, Nefrologia, 2014, University of São Paulo

A deficiência de vitamina D (dVD) aumenta o risco de morte em pacientes hospitalizados. A injúria de isquemia/reperfusão renal (Isq) ativa vias de necrose e/ou… (more)

Subjects/Keywords: Acute kidney injury; Cyclin-dependent kinase inhibitor p21; Deficiência de vitamina D; Inibidor de quinase dependente de ciclina p21; Lesão renal aguda; Ratos Wistar; Receptores de vitamina D; Vitamin D deficiency; Vitamin D receptors; Wistar rats

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Viciana, A. C. d. B. (2014). Estudo da deficiência de vitamina D no modelo de isquemia/reperfusão renal em ratos. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5148/tde-01122014-114531/ ;

Chicago Manual of Style (16th Edition):

Viciana, Ana Carolina de Bragança. “Estudo da deficiência de vitamina D no modelo de isquemia/reperfusão renal em ratos.” 2014. Doctoral Dissertation, University of São Paulo. Accessed December 05, 2020. http://www.teses.usp.br/teses/disponiveis/5/5148/tde-01122014-114531/ ;.

MLA Handbook (7th Edition):

Viciana, Ana Carolina de Bragança. “Estudo da deficiência de vitamina D no modelo de isquemia/reperfusão renal em ratos.” 2014. Web. 05 Dec 2020.

Vancouver:

Viciana ACdB. Estudo da deficiência de vitamina D no modelo de isquemia/reperfusão renal em ratos. [Internet] [Doctoral dissertation]. University of São Paulo; 2014. [cited 2020 Dec 05]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5148/tde-01122014-114531/ ;.

Council of Science Editors:

Viciana ACdB. Estudo da deficiência de vitamina D no modelo de isquemia/reperfusão renal em ratos. [Doctoral Dissertation]. University of São Paulo; 2014. Available from: http://www.teses.usp.br/teses/disponiveis/5/5148/tde-01122014-114531/ ;

6. Bastos, Ana Paula Almeida. A haploinsuficiência de Pkd1 aumenta a lesão renal e induz formação de microcistos após isquemia/reperfusão em camundongos.

Degree: PhD, Nefrologia, 2010, University of São Paulo

A maior parte dos casos de doença renal policística autossômica dominante (DRPAD) é causada por mutações no gene PKD1 (Polycystic Kidney Disease 1). O insulto… (more)

Subjects/Keywords: Autosomal dominant polycystic kidney disease; Cell proliferation; Cyclin-dependent kinase Inhibitor p21; Cystic kidney diseases; Doenças renais císticas; Inibidor de quinase dependente de ciclina p21; Ischemia; Isquemia; Mutação; Mutation; Proliferação de células; Reperfusion injury; Rim policístico autossômico dominante; Traumatismo por reperfusão

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Bastos, A. P. A. (2010). A haploinsuficiência de Pkd1 aumenta a lesão renal e induz formação de microcistos após isquemia/reperfusão em camundongos. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5148/tde-25082010-112042/ ;

Chicago Manual of Style (16th Edition):

Bastos, Ana Paula Almeida. “A haploinsuficiência de Pkd1 aumenta a lesão renal e induz formação de microcistos após isquemia/reperfusão em camundongos.” 2010. Doctoral Dissertation, University of São Paulo. Accessed December 05, 2020. http://www.teses.usp.br/teses/disponiveis/5/5148/tde-25082010-112042/ ;.

MLA Handbook (7th Edition):

Bastos, Ana Paula Almeida. “A haploinsuficiência de Pkd1 aumenta a lesão renal e induz formação de microcistos após isquemia/reperfusão em camundongos.” 2010. Web. 05 Dec 2020.

Vancouver:

Bastos APA. A haploinsuficiência de Pkd1 aumenta a lesão renal e induz formação de microcistos após isquemia/reperfusão em camundongos. [Internet] [Doctoral dissertation]. University of São Paulo; 2010. [cited 2020 Dec 05]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5148/tde-25082010-112042/ ;.

Council of Science Editors:

Bastos APA. A haploinsuficiência de Pkd1 aumenta a lesão renal e induz formação de microcistos após isquemia/reperfusão em camundongos. [Doctoral Dissertation]. University of São Paulo; 2010. Available from: http://www.teses.usp.br/teses/disponiveis/5/5148/tde-25082010-112042/ ;


NSYSU

7. Peng, Yu-Ting. Studies on the regulatory mechanisms of GTN-induced protein kinase inhibitors in hepatocellular carcinoma-derived cells.

Degree: Master, Institute of Biomedical Sciences, 2014, NSYSU

 The study was to investigate the regulatory mechanisms of goniothalamin (GTN)-induced protein kinase inhibitors, which means cyclin-dependent kinase inhibitors (CKIs), in two hepatocellular carcinoma (HCC)-derived… (more)

Subjects/Keywords: E3-ligase inhibitor; HDAC inhibitor; Goniothalamin (GTN); CDKN1B; Cyclin-dependent kinase inhibitors (CKIs); CDKN1C

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Peng, Y. (2014). Studies on the regulatory mechanisms of GTN-induced protein kinase inhibitors in hepatocellular carcinoma-derived cells. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0720114-004147

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Peng, Yu-Ting. “Studies on the regulatory mechanisms of GTN-induced protein kinase inhibitors in hepatocellular carcinoma-derived cells.” 2014. Thesis, NSYSU. Accessed December 05, 2020. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0720114-004147.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Peng, Yu-Ting. “Studies on the regulatory mechanisms of GTN-induced protein kinase inhibitors in hepatocellular carcinoma-derived cells.” 2014. Web. 05 Dec 2020.

Vancouver:

Peng Y. Studies on the regulatory mechanisms of GTN-induced protein kinase inhibitors in hepatocellular carcinoma-derived cells. [Internet] [Thesis]. NSYSU; 2014. [cited 2020 Dec 05]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0720114-004147.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Peng Y. Studies on the regulatory mechanisms of GTN-induced protein kinase inhibitors in hepatocellular carcinoma-derived cells. [Thesis]. NSYSU; 2014. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0720114-004147

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Universiteit Utrecht

8. Isik, G. Regulation of p16INK4A, The Cyclin Dependent Kinase Inhibitor & the Tumor Suppressor.

Degree: 2009, Universiteit Utrecht

 p16INK4A is a tumor suppressor protein which inhibits the activities of CDK4 and CDK6 thus leading cell cycle arrest in G1 phase. Therefore, regulation of… (more)

Subjects/Keywords: Geneeskunde; p16, INK4A, Regulation of p16INK4A, Cyclin Dependent Kinase Inhibitor, Tumor Suppressor

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Isik, G. (2009). Regulation of p16INK4A, The Cyclin Dependent Kinase Inhibitor & the Tumor Suppressor. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/35791

Chicago Manual of Style (16th Edition):

Isik, G. “Regulation of p16INK4A, The Cyclin Dependent Kinase Inhibitor & the Tumor Suppressor.” 2009. Masters Thesis, Universiteit Utrecht. Accessed December 05, 2020. http://dspace.library.uu.nl:8080/handle/1874/35791.

MLA Handbook (7th Edition):

Isik, G. “Regulation of p16INK4A, The Cyclin Dependent Kinase Inhibitor & the Tumor Suppressor.” 2009. Web. 05 Dec 2020.

Vancouver:

Isik G. Regulation of p16INK4A, The Cyclin Dependent Kinase Inhibitor & the Tumor Suppressor. [Internet] [Masters thesis]. Universiteit Utrecht; 2009. [cited 2020 Dec 05]. Available from: http://dspace.library.uu.nl:8080/handle/1874/35791.

Council of Science Editors:

Isik G. Regulation of p16INK4A, The Cyclin Dependent Kinase Inhibitor & the Tumor Suppressor. [Masters Thesis]. Universiteit Utrecht; 2009. Available from: http://dspace.library.uu.nl:8080/handle/1874/35791


Louisiana State University

9. Kumar, Narender. Functional Motifs in SIAMESE, a Plant Cyclin-Dependent Kinase Inhibitor.

Degree: PhD, 2015, Louisiana State University

 SIAMESE (SIM) and SIAMESE-RELATED-PROTEIN1 (SMR1), the founding members of the SIM/SMRs gene family, suppress mitosis and onset of endoreplication in the Arabidopsis’s trichome and sepal… (more)

Subjects/Keywords: SIAMESE RELATED PROTEINS (SMRs); SIAMESE (SIM); Cyclin-Dependent Kinase inhibitor; Endoreplication; Cell Cycle; Arabidopsis thaliana

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Kumar, N. (2015). Functional Motifs in SIAMESE, a Plant Cyclin-Dependent Kinase Inhibitor. (Doctoral Dissertation). Louisiana State University. Retrieved from etd-04092015-230646 ; https://digitalcommons.lsu.edu/gradschool_dissertations/2135

Chicago Manual of Style (16th Edition):

Kumar, Narender. “Functional Motifs in SIAMESE, a Plant Cyclin-Dependent Kinase Inhibitor.” 2015. Doctoral Dissertation, Louisiana State University. Accessed December 05, 2020. etd-04092015-230646 ; https://digitalcommons.lsu.edu/gradschool_dissertations/2135.

MLA Handbook (7th Edition):

Kumar, Narender. “Functional Motifs in SIAMESE, a Plant Cyclin-Dependent Kinase Inhibitor.” 2015. Web. 05 Dec 2020.

Vancouver:

Kumar N. Functional Motifs in SIAMESE, a Plant Cyclin-Dependent Kinase Inhibitor. [Internet] [Doctoral dissertation]. Louisiana State University; 2015. [cited 2020 Dec 05]. Available from: etd-04092015-230646 ; https://digitalcommons.lsu.edu/gradschool_dissertations/2135.

Council of Science Editors:

Kumar N. Functional Motifs in SIAMESE, a Plant Cyclin-Dependent Kinase Inhibitor. [Doctoral Dissertation]. Louisiana State University; 2015. Available from: etd-04092015-230646 ; https://digitalcommons.lsu.edu/gradschool_dissertations/2135


Duke University

10. Yong, Sheila T. A novel, non-apoptotic role for Scythe/BAT3: a functional switch between the pro- and anti-proliferative roles of p21 during the cell cycle.

Degree: 2012, Duke University

 Scythe/BAT3 is a member of the BAG protein family whose role in apoptosis, a form of programmed cell death, has been extensively studied. However, since… (more)

Subjects/Keywords: Apoptosis; Blotting, Western; Bone Neoplasms; Cell Cycle; Cell Proliferation; Cyclin-Dependent Kinase Inhibitor p21; DNA Replication; Flow Cytometry; Fluorescent Antibody Technique; Humans; Molecular Chaperones; Osteosarcoma; Phosphorylation; RNA, Small Interfering; Tumor Cells, Cultured

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Yong, S. T. (2012). A novel, non-apoptotic role for Scythe/BAT3: a functional switch between the pro- and anti-proliferative roles of p21 during the cell cycle. (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/4958

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Yong, Sheila T. “A novel, non-apoptotic role for Scythe/BAT3: a functional switch between the pro- and anti-proliferative roles of p21 during the cell cycle. ” 2012. Thesis, Duke University. Accessed December 05, 2020. http://hdl.handle.net/10161/4958.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Yong, Sheila T. “A novel, non-apoptotic role for Scythe/BAT3: a functional switch between the pro- and anti-proliferative roles of p21 during the cell cycle. ” 2012. Web. 05 Dec 2020.

Vancouver:

Yong ST. A novel, non-apoptotic role for Scythe/BAT3: a functional switch between the pro- and anti-proliferative roles of p21 during the cell cycle. [Internet] [Thesis]. Duke University; 2012. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/10161/4958.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Yong ST. A novel, non-apoptotic role for Scythe/BAT3: a functional switch between the pro- and anti-proliferative roles of p21 during the cell cycle. [Thesis]. Duke University; 2012. Available from: http://hdl.handle.net/10161/4958

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Freie Universität Berlin

11. Stövesand, Kirsten. Expression profile of the cyclin-dependent kinase inhibitors p21CIP1/WAF1 and p27KIP1 in spontaneous canine mammary tumors.

Degree: 2008, Freie Universität Berlin

 The cell cycle and its mechanisms of control play an important role concerning the carcinogenesis of epithelial neoplasia. The different regulators of the cell cycle… (more)

Subjects/Keywords: Dogs, dog diseases, mammary gland diseases; neoplasms, cell cycle, kinases, cyclin-dependent kinases (MeSH), enzyme inhibitors, Cyclin-Dependent Kinase Inhibitor p21 (MeSH), Cyclin-Dependent Kinase Inhibitor p27 (MeSH), immunohistochemistry, polymerase chain reaction; 600 Technik, Medizin, angewandte Wissenschaften::630 Landwirtschaft::630 Landwirtschaft und verwandte Bereiche

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Stövesand, K. (2008). Expression profile of the cyclin-dependent kinase inhibitors p21CIP1/WAF1 and p27KIP1 in spontaneous canine mammary tumors. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-10401

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Stövesand, Kirsten. “Expression profile of the cyclin-dependent kinase inhibitors p21CIP1/WAF1 and p27KIP1 in spontaneous canine mammary tumors.” 2008. Thesis, Freie Universität Berlin. Accessed December 05, 2020. http://dx.doi.org/10.17169/refubium-10401.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Stövesand, Kirsten. “Expression profile of the cyclin-dependent kinase inhibitors p21CIP1/WAF1 and p27KIP1 in spontaneous canine mammary tumors.” 2008. Web. 05 Dec 2020.

Vancouver:

Stövesand K. Expression profile of the cyclin-dependent kinase inhibitors p21CIP1/WAF1 and p27KIP1 in spontaneous canine mammary tumors. [Internet] [Thesis]. Freie Universität Berlin; 2008. [cited 2020 Dec 05]. Available from: http://dx.doi.org/10.17169/refubium-10401.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Stövesand K. Expression profile of the cyclin-dependent kinase inhibitors p21CIP1/WAF1 and p27KIP1 in spontaneous canine mammary tumors. [Thesis]. Freie Universität Berlin; 2008. Available from: http://dx.doi.org/10.17169/refubium-10401

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


The Ohio State University

12. Ni, Wenjun. Pharmacokinetic-Pharmacodynamic and Pharmacogenetic Studies of Flavopiridol and its Glucuronide Metabolite.

Degree: PhD, Pharmacy, 2011, The Ohio State University

 Chronic lymphocytic leukemia (CLL) is the most common adult leukemia in Western world. Flavopiridol (Alvocidib, NSC 649890), as a pan cyclin-dependent kinases inhibitor (CDKI), initiates… (more)

Subjects/Keywords: Pharmaceuticals; Pharmacy Sciences; Chronic lymphocytic leukemia; cyclin-dependent kinase inhibitor; pharmacokinetics; pharmacodynamics; pharmacogenetics; drug transporters; OATP1B1; glutathionep

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Ni, W. (2011). Pharmacokinetic-Pharmacodynamic and Pharmacogenetic Studies of Flavopiridol and its Glucuronide Metabolite. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1299680524

Chicago Manual of Style (16th Edition):

Ni, Wenjun. “Pharmacokinetic-Pharmacodynamic and Pharmacogenetic Studies of Flavopiridol and its Glucuronide Metabolite.” 2011. Doctoral Dissertation, The Ohio State University. Accessed December 05, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1299680524.

MLA Handbook (7th Edition):

Ni, Wenjun. “Pharmacokinetic-Pharmacodynamic and Pharmacogenetic Studies of Flavopiridol and its Glucuronide Metabolite.” 2011. Web. 05 Dec 2020.

Vancouver:

Ni W. Pharmacokinetic-Pharmacodynamic and Pharmacogenetic Studies of Flavopiridol and its Glucuronide Metabolite. [Internet] [Doctoral dissertation]. The Ohio State University; 2011. [cited 2020 Dec 05]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1299680524.

Council of Science Editors:

Ni W. Pharmacokinetic-Pharmacodynamic and Pharmacogenetic Studies of Flavopiridol and its Glucuronide Metabolite. [Doctoral Dissertation]. The Ohio State University; 2011. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1299680524

13. Sasaki, Mina; Kajiya, Hiroshi; Ozeki, Satoru; Okabe, Koji. Reactive oxygen species promotes cellular senescence in normal human epidermal keratinocytes through epigenetic regulation of p16(INK4a.). : Reactive oxygen species promotes cellular senescence in normal human epidermal keratinocytes through epigenetic regulation of p16(INK4a.).

Degree: 博士(歯学), 2015, Fukuoka Dental College / 福岡歯科大学

Reactive oxygen species (ROS) can cause severe damage to DNA, proteins and lipids in normal cells, contributing to carcinogenesis and various pathological conditions. While cellular… (more)

Subjects/Keywords: Cellar senescence; Reactive oxygen species; Cyclin-dependent kinase inhibitors; Normal human epidermal keratinocyte; Biological Markers; Cell Aging; Cell Line, Tumor; Cyclin-Dependent Kinase 4; Cyclin-Dependent Kinase Inhibitor p16; DNA Methylation; Epidermis; Epigenesis, Genetic; G1 Phase Cell Cycle Checkpoints; Humans; Hydrogen Peroxide; Keratinocytes; Organ Specificity; Promoter Regions, Genetic; Reactive Oxygen Species; Retinoblastoma Protein; Signal Transduction; beta-Galactosidase

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Sasaki, Mina; Kajiya, Hiroshi; Ozeki, Satoru; Okabe, K. (2015). Reactive oxygen species promotes cellular senescence in normal human epidermal keratinocytes through epigenetic regulation of p16(INK4a.). : Reactive oxygen species promotes cellular senescence in normal human epidermal keratinocytes through epigenetic regulation of p16(INK4a.). (Thesis). Fukuoka Dental College / 福岡歯科大学. Retrieved from http://id.nii.ac.jp/1167/00000033/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Sasaki, Mina; Kajiya, Hiroshi; Ozeki, Satoru; Okabe, Koji. “Reactive oxygen species promotes cellular senescence in normal human epidermal keratinocytes through epigenetic regulation of p16(INK4a.). : Reactive oxygen species promotes cellular senescence in normal human epidermal keratinocytes through epigenetic regulation of p16(INK4a.).” 2015. Thesis, Fukuoka Dental College / 福岡歯科大学. Accessed December 05, 2020. http://id.nii.ac.jp/1167/00000033/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Sasaki, Mina; Kajiya, Hiroshi; Ozeki, Satoru; Okabe, Koji. “Reactive oxygen species promotes cellular senescence in normal human epidermal keratinocytes through epigenetic regulation of p16(INK4a.). : Reactive oxygen species promotes cellular senescence in normal human epidermal keratinocytes through epigenetic regulation of p16(INK4a.).” 2015. Web. 05 Dec 2020.

Vancouver:

Sasaki, Mina; Kajiya, Hiroshi; Ozeki, Satoru; Okabe K. Reactive oxygen species promotes cellular senescence in normal human epidermal keratinocytes through epigenetic regulation of p16(INK4a.). : Reactive oxygen species promotes cellular senescence in normal human epidermal keratinocytes through epigenetic regulation of p16(INK4a.). [Internet] [Thesis]. Fukuoka Dental College / 福岡歯科大学; 2015. [cited 2020 Dec 05]. Available from: http://id.nii.ac.jp/1167/00000033/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Sasaki, Mina; Kajiya, Hiroshi; Ozeki, Satoru; Okabe K. Reactive oxygen species promotes cellular senescence in normal human epidermal keratinocytes through epigenetic regulation of p16(INK4a.). : Reactive oxygen species promotes cellular senescence in normal human epidermal keratinocytes through epigenetic regulation of p16(INK4a.). [Thesis]. Fukuoka Dental College / 福岡歯科大学; 2015. Available from: http://id.nii.ac.jp/1167/00000033/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

14. Schorr, Anna L. Yeast Two Hybrid Screen of a Putative Toxoplasma gondii Cyclin, TGME49_266900.

Degree: Biological Sciences - Cell and Molecular: M.S., Biology, 2018, St. Cloud State University

  In this current research, protein-protein interactions with a putative Toxoplasma gondii cyclin, TGME49_266900 or "Cyc6," were discovered via a yeast two hybrid screen. Several… (more)

Subjects/Keywords: Toxoplasma gondii; cyclin; yeast two hybrid screen; cyclin dependent kinase

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Schorr, A. L. (2018). Yeast Two Hybrid Screen of a Putative Toxoplasma gondii Cyclin, TGME49_266900. (Masters Thesis). St. Cloud State University. Retrieved from https://repository.stcloudstate.edu/biol_etds/31

Chicago Manual of Style (16th Edition):

Schorr, Anna L. “Yeast Two Hybrid Screen of a Putative Toxoplasma gondii Cyclin, TGME49_266900.” 2018. Masters Thesis, St. Cloud State University. Accessed December 05, 2020. https://repository.stcloudstate.edu/biol_etds/31.

MLA Handbook (7th Edition):

Schorr, Anna L. “Yeast Two Hybrid Screen of a Putative Toxoplasma gondii Cyclin, TGME49_266900.” 2018. Web. 05 Dec 2020.

Vancouver:

Schorr AL. Yeast Two Hybrid Screen of a Putative Toxoplasma gondii Cyclin, TGME49_266900. [Internet] [Masters thesis]. St. Cloud State University; 2018. [cited 2020 Dec 05]. Available from: https://repository.stcloudstate.edu/biol_etds/31.

Council of Science Editors:

Schorr AL. Yeast Two Hybrid Screen of a Putative Toxoplasma gondii Cyclin, TGME49_266900. [Masters Thesis]. St. Cloud State University; 2018. Available from: https://repository.stcloudstate.edu/biol_etds/31


University of Texas Southwestern Medical Center

15. Franco, Jorge. Targeting Cyclin Dependent Kinases 4/6 Activity in Pancreatic Ductal Adenocarcinoma.

Degree: 2016, University of Texas Southwestern Medical Center

Pages vi-xiii are incorrectly numbered as pages v-xii.

Pancreatic ductal Adenocarcinoma (PDA) is an aggressive and lethal disease that lacks an adequate treatment. Given that… (more)

Subjects/Keywords: Carcinoma, Pancreatic Ductal; Cyclin-Dependent Kinase 4; Cyclin-Dependent Kinase 6; Pancreatic Neoplasms; Protein Kinase Inhibitors

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Franco, J. (2016). Targeting Cyclin Dependent Kinases 4/6 Activity in Pancreatic Ductal Adenocarcinoma. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/5728

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Franco, Jorge. “Targeting Cyclin Dependent Kinases 4/6 Activity in Pancreatic Ductal Adenocarcinoma.” 2016. Thesis, University of Texas Southwestern Medical Center. Accessed December 05, 2020. http://hdl.handle.net/2152.5/5728.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Franco, Jorge. “Targeting Cyclin Dependent Kinases 4/6 Activity in Pancreatic Ductal Adenocarcinoma.” 2016. Web. 05 Dec 2020.

Vancouver:

Franco J. Targeting Cyclin Dependent Kinases 4/6 Activity in Pancreatic Ductal Adenocarcinoma. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2016. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/2152.5/5728.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Franco J. Targeting Cyclin Dependent Kinases 4/6 Activity in Pancreatic Ductal Adenocarcinoma. [Thesis]. University of Texas Southwestern Medical Center; 2016. Available from: http://hdl.handle.net/2152.5/5728

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Louisiana State University

16. Churchman, Michelle Lynn. Isolation and characterization of the SIAMESE family: a novel class of cell cycle regulators in plants.

Degree: PhD, 2007, Louisiana State University

 Recessive mutations in the SIAMESE (SIM) gene of Arabidopsis result in multicellular trichomes harboring individual nuclei with a low ploidy level, a phenotype strikingly different… (more)

Subjects/Keywords: cyclin-dependent kinase inhibitor; endoreduplication; endoreplication; arabidopsis thaliana; cell cycle

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Churchman, M. L. (2007). Isolation and characterization of the SIAMESE family: a novel class of cell cycle regulators in plants. (Doctoral Dissertation). Louisiana State University. Retrieved from etd-06052007-093854 ; https://digitalcommons.lsu.edu/gradschool_dissertations/341

Chicago Manual of Style (16th Edition):

Churchman, Michelle Lynn. “Isolation and characterization of the SIAMESE family: a novel class of cell cycle regulators in plants.” 2007. Doctoral Dissertation, Louisiana State University. Accessed December 05, 2020. etd-06052007-093854 ; https://digitalcommons.lsu.edu/gradschool_dissertations/341.

MLA Handbook (7th Edition):

Churchman, Michelle Lynn. “Isolation and characterization of the SIAMESE family: a novel class of cell cycle regulators in plants.” 2007. Web. 05 Dec 2020.

Vancouver:

Churchman ML. Isolation and characterization of the SIAMESE family: a novel class of cell cycle regulators in plants. [Internet] [Doctoral dissertation]. Louisiana State University; 2007. [cited 2020 Dec 05]. Available from: etd-06052007-093854 ; https://digitalcommons.lsu.edu/gradschool_dissertations/341.

Council of Science Editors:

Churchman ML. Isolation and characterization of the SIAMESE family: a novel class of cell cycle regulators in plants. [Doctoral Dissertation]. Louisiana State University; 2007. Available from: etd-06052007-093854 ; https://digitalcommons.lsu.edu/gradschool_dissertations/341

17. Bendjeddou, Lyamin. Synthèse et évaluation biologique de nouveaux inhibiteurs de kinases : identification d‘inhibiteurs de kinases parasitaires : Synthesis and biological evaluation of new kinase inhibitors : identification of inhibitors of several parasite protein kinases.

Degree: Docteur es, Chimie thérapeutique, 2014, Université Paris Descartes – Paris V

La phosphorylation des protéines par les kinases est l’une plus importantes modification post-traductionnelle dans les processus cellulaires tels que la division, la différenciation, la prolifération… (more)

Subjects/Keywords: Inhibiteur de protéine kinase; Imidazo[1,2-b]pyridazine; Imidazo[4,5-b]pyridine; Kinase cycline-dépendante (CDKs); CDC-like kinase (CLKs); Dual specificity tyrosine-phosphorylation-regulated kinase (DYRKs); Parasite unicellulaire; Maladie d’Alzheimer; Trisomie 21; Kinase inhibitor; Imidazo[1,2-b]pyridazine; Imidazo[4,5-b]pyridine; Dual specificity tyrosine-phosphorylation-regulated kinase (DYRKs); Cyclin-dependent kinase (CDKs); Unicellular parasite; Alzheimer’s disease; Down syndrome; 615.19

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Bendjeddou, L. (2014). Synthèse et évaluation biologique de nouveaux inhibiteurs de kinases : identification d‘inhibiteurs de kinases parasitaires : Synthesis and biological evaluation of new kinase inhibitors : identification of inhibitors of several parasite protein kinases. (Doctoral Dissertation). Université Paris Descartes – Paris V. Retrieved from http://www.theses.fr/2014PA05P615

Chicago Manual of Style (16th Edition):

Bendjeddou, Lyamin. “Synthèse et évaluation biologique de nouveaux inhibiteurs de kinases : identification d‘inhibiteurs de kinases parasitaires : Synthesis and biological evaluation of new kinase inhibitors : identification of inhibitors of several parasite protein kinases.” 2014. Doctoral Dissertation, Université Paris Descartes – Paris V. Accessed December 05, 2020. http://www.theses.fr/2014PA05P615.

MLA Handbook (7th Edition):

Bendjeddou, Lyamin. “Synthèse et évaluation biologique de nouveaux inhibiteurs de kinases : identification d‘inhibiteurs de kinases parasitaires : Synthesis and biological evaluation of new kinase inhibitors : identification of inhibitors of several parasite protein kinases.” 2014. Web. 05 Dec 2020.

Vancouver:

Bendjeddou L. Synthèse et évaluation biologique de nouveaux inhibiteurs de kinases : identification d‘inhibiteurs de kinases parasitaires : Synthesis and biological evaluation of new kinase inhibitors : identification of inhibitors of several parasite protein kinases. [Internet] [Doctoral dissertation]. Université Paris Descartes – Paris V; 2014. [cited 2020 Dec 05]. Available from: http://www.theses.fr/2014PA05P615.

Council of Science Editors:

Bendjeddou L. Synthèse et évaluation biologique de nouveaux inhibiteurs de kinases : identification d‘inhibiteurs de kinases parasitaires : Synthesis and biological evaluation of new kinase inhibitors : identification of inhibitors of several parasite protein kinases. [Doctoral Dissertation]. Université Paris Descartes – Paris V; 2014. Available from: http://www.theses.fr/2014PA05P615

18. Nordberg, Joshua J. The Importance of the Centrosomal Localization Sequence of Cyclin E for Promoting Centrosome Duplication: A Dissertation.

Degree: Interdisciplinary Graduate Program, Radiology, 2011, U of Massachusetts : Med

  This thesis comprises three separate studies that investigate the consequences of supernumary centrosomes, the effect of centrosome loss, and a control mechanism for regulating… (more)

Subjects/Keywords: Centrosome; Cell Cycle; Cyclin-Dependent Kinase 2; Cyclin E; Cell Biology; Cells; Enzymes and Coenzymes

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Nordberg, J. J. (2011). The Importance of the Centrosomal Localization Sequence of Cyclin E for Promoting Centrosome Duplication: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/547

Chicago Manual of Style (16th Edition):

Nordberg, Joshua J. “The Importance of the Centrosomal Localization Sequence of Cyclin E for Promoting Centrosome Duplication: A Dissertation.” 2011. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 05, 2020. https://escholarship.umassmed.edu/gsbs_diss/547.

MLA Handbook (7th Edition):

Nordberg, Joshua J. “The Importance of the Centrosomal Localization Sequence of Cyclin E for Promoting Centrosome Duplication: A Dissertation.” 2011. Web. 05 Dec 2020.

Vancouver:

Nordberg JJ. The Importance of the Centrosomal Localization Sequence of Cyclin E for Promoting Centrosome Duplication: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2011. [cited 2020 Dec 05]. Available from: https://escholarship.umassmed.edu/gsbs_diss/547.

Council of Science Editors:

Nordberg JJ. The Importance of the Centrosomal Localization Sequence of Cyclin E for Promoting Centrosome Duplication: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2011. Available from: https://escholarship.umassmed.edu/gsbs_diss/547


University of Alberta

19. Newman, Emma. The mechanism of inhibition of herpes simplex virus type 1 DNA replication by roscovitine.

Degree: MS, Department of Biochemistry, 2011, University of Alberta

 Transcription and DNA replication of herpes simplex virus type 1 (HSV-1) occur in nuclear domains adjacent to structures named ND10. The HSV-1 single-stranded DNA binding… (more)

Subjects/Keywords: Herpes simplex virus; roscovitine OR Seliciclib OR cyc202; cyclin dependent kinase

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Newman, E. (2011). The mechanism of inhibition of herpes simplex virus type 1 DNA replication by roscovitine. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/ww72bc61d

Chicago Manual of Style (16th Edition):

Newman, Emma. “The mechanism of inhibition of herpes simplex virus type 1 DNA replication by roscovitine.” 2011. Masters Thesis, University of Alberta. Accessed December 05, 2020. https://era.library.ualberta.ca/files/ww72bc61d.

MLA Handbook (7th Edition):

Newman, Emma. “The mechanism of inhibition of herpes simplex virus type 1 DNA replication by roscovitine.” 2011. Web. 05 Dec 2020.

Vancouver:

Newman E. The mechanism of inhibition of herpes simplex virus type 1 DNA replication by roscovitine. [Internet] [Masters thesis]. University of Alberta; 2011. [cited 2020 Dec 05]. Available from: https://era.library.ualberta.ca/files/ww72bc61d.

Council of Science Editors:

Newman E. The mechanism of inhibition of herpes simplex virus type 1 DNA replication by roscovitine. [Masters Thesis]. University of Alberta; 2011. Available from: https://era.library.ualberta.ca/files/ww72bc61d


Universitat Autònoma de Barcelona

20. Zeng, Fanli. Novel Modes of Regulation of Cyclin Dependent Kinase Cdk1.

Degree: Departament de Bioquímica i Biologia Molecular, 2014, Universitat Autònoma de Barcelona

Cyclin dependent kinases are drive cell division cycle progression in eukaryotic cells. In the model eukaryotic organism Saccharomyces cerevisiae (budding yeast) a single Cyclin Dependent(more)

Subjects/Keywords: Cyclin dependent kinase; Cell cycle; Rad53; Ciències de la Salut; 577

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Zeng, F. (2014). Novel Modes of Regulation of Cyclin Dependent Kinase Cdk1. (Thesis). Universitat Autònoma de Barcelona. Retrieved from http://hdl.handle.net/10803/133357

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Zeng, Fanli. “Novel Modes of Regulation of Cyclin Dependent Kinase Cdk1.” 2014. Thesis, Universitat Autònoma de Barcelona. Accessed December 05, 2020. http://hdl.handle.net/10803/133357.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Zeng, Fanli. “Novel Modes of Regulation of Cyclin Dependent Kinase Cdk1.” 2014. Web. 05 Dec 2020.

Vancouver:

Zeng F. Novel Modes of Regulation of Cyclin Dependent Kinase Cdk1. [Internet] [Thesis]. Universitat Autònoma de Barcelona; 2014. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/10803/133357.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Zeng F. Novel Modes of Regulation of Cyclin Dependent Kinase Cdk1. [Thesis]. Universitat Autònoma de Barcelona; 2014. Available from: http://hdl.handle.net/10803/133357

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Oxford

21. Hole, Alison Jennifer. The regulation and inhibition of P-TEFb.

Degree: PhD, 2011, University of Oxford

 Correct regulation of transcription is essential for maintaining a healthy cellular state. During transcription RNA polymerase II (Pol II) proceeds in a regulated manner through… (more)

Subjects/Keywords: 572.8; Molecular biophysics (biochemistry); Biochemistry; transcription; cyclin dependent kinase; phosphorylation

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Hole, A. J. (2011). The regulation and inhibition of P-TEFb. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:18ba1399-e3db-4ed6-bd9b-019bbd3c0b65 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.580884

Chicago Manual of Style (16th Edition):

Hole, Alison Jennifer. “The regulation and inhibition of P-TEFb.” 2011. Doctoral Dissertation, University of Oxford. Accessed December 05, 2020. http://ora.ox.ac.uk/objects/uuid:18ba1399-e3db-4ed6-bd9b-019bbd3c0b65 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.580884.

MLA Handbook (7th Edition):

Hole, Alison Jennifer. “The regulation and inhibition of P-TEFb.” 2011. Web. 05 Dec 2020.

Vancouver:

Hole AJ. The regulation and inhibition of P-TEFb. [Internet] [Doctoral dissertation]. University of Oxford; 2011. [cited 2020 Dec 05]. Available from: http://ora.ox.ac.uk/objects/uuid:18ba1399-e3db-4ed6-bd9b-019bbd3c0b65 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.580884.

Council of Science Editors:

Hole AJ. The regulation and inhibition of P-TEFb. [Doctoral Dissertation]. University of Oxford; 2011. Available from: http://ora.ox.ac.uk/objects/uuid:18ba1399-e3db-4ed6-bd9b-019bbd3c0b65 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.580884


University of Edinburgh

22. Gallogly, Susan. Promoting endothelialisation to reduce vascular injury following coronary angioplasty and stent implantation.

Degree: PhD, 2017, University of Edinburgh

 Rationale and Objectives: New therapeutic approaches that promote repair of the vasculature following injury are necessary to improve the clinical outcomes in patients undergoing angioplasty… (more)

Subjects/Keywords: novel cyclin-dependent kinase; coronary endothelial outgrowth cells

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Gallogly, S. (2017). Promoting endothelialisation to reduce vascular injury following coronary angioplasty and stent implantation. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/35575

Chicago Manual of Style (16th Edition):

Gallogly, Susan. “Promoting endothelialisation to reduce vascular injury following coronary angioplasty and stent implantation.” 2017. Doctoral Dissertation, University of Edinburgh. Accessed December 05, 2020. http://hdl.handle.net/1842/35575.

MLA Handbook (7th Edition):

Gallogly, Susan. “Promoting endothelialisation to reduce vascular injury following coronary angioplasty and stent implantation.” 2017. Web. 05 Dec 2020.

Vancouver:

Gallogly S. Promoting endothelialisation to reduce vascular injury following coronary angioplasty and stent implantation. [Internet] [Doctoral dissertation]. University of Edinburgh; 2017. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1842/35575.

Council of Science Editors:

Gallogly S. Promoting endothelialisation to reduce vascular injury following coronary angioplasty and stent implantation. [Doctoral Dissertation]. University of Edinburgh; 2017. Available from: http://hdl.handle.net/1842/35575


University of Edinburgh

23. Matrone, Gianfranco. Role of cyclin-dependent Kinase 9 in the zebrafish embryonic heart.

Degree: PhD, 2013, University of Edinburgh

 Cardiac hypertrophy leading to heart failure remains a leading cause of morbidity and mortality in the 21st century despite major therapeutic advances. Improved understanding of… (more)

Subjects/Keywords: 616.1; zebrafish; heart; cyclin-dependent kinase; cardiac hypertrophy

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Matrone, G. (2013). Role of cyclin-dependent Kinase 9 in the zebrafish embryonic heart. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/11820

Chicago Manual of Style (16th Edition):

Matrone, Gianfranco. “Role of cyclin-dependent Kinase 9 in the zebrafish embryonic heart.” 2013. Doctoral Dissertation, University of Edinburgh. Accessed December 05, 2020. http://hdl.handle.net/1842/11820.

MLA Handbook (7th Edition):

Matrone, Gianfranco. “Role of cyclin-dependent Kinase 9 in the zebrafish embryonic heart.” 2013. Web. 05 Dec 2020.

Vancouver:

Matrone G. Role of cyclin-dependent Kinase 9 in the zebrafish embryonic heart. [Internet] [Doctoral dissertation]. University of Edinburgh; 2013. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1842/11820.

Council of Science Editors:

Matrone G. Role of cyclin-dependent Kinase 9 in the zebrafish embryonic heart. [Doctoral Dissertation]. University of Edinburgh; 2013. Available from: http://hdl.handle.net/1842/11820


National University of Ireland – Galway

24. Kwenda Hardiman, Lucretia. Cell cycle regulation of centromere assembly in Drosophila male meiosis .

Degree: 2018, National University of Ireland – Galway

 Centromeres are chromosomal sites required for faithful chromosome segregation. CENP-A is the histone H3 variant that demarcates centromeres from bulk chromatin. Errors in centromere assembly… (more)

Subjects/Keywords: Meoisis; Centromere; CENP-A; Spermatogenesis; Cyclin dependent kinase; Natural sciences; Biochemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Kwenda Hardiman, L. (2018). Cell cycle regulation of centromere assembly in Drosophila male meiosis . (Thesis). National University of Ireland – Galway. Retrieved from http://hdl.handle.net/10379/7419

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Kwenda Hardiman, Lucretia. “Cell cycle regulation of centromere assembly in Drosophila male meiosis .” 2018. Thesis, National University of Ireland – Galway. Accessed December 05, 2020. http://hdl.handle.net/10379/7419.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Kwenda Hardiman, Lucretia. “Cell cycle regulation of centromere assembly in Drosophila male meiosis .” 2018. Web. 05 Dec 2020.

Vancouver:

Kwenda Hardiman L. Cell cycle regulation of centromere assembly in Drosophila male meiosis . [Internet] [Thesis]. National University of Ireland – Galway; 2018. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/10379/7419.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Kwenda Hardiman L. Cell cycle regulation of centromere assembly in Drosophila male meiosis . [Thesis]. National University of Ireland – Galway; 2018. Available from: http://hdl.handle.net/10379/7419

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Melbourne

25. binte Roesley, Siti Nur Ain. Roles of cyclin-dependent kinase substrates: cell cycle and beyond.

Degree: 2015, University of Melbourne

 The cyclin-dependent kinases (CDKs) are serine/threonine specific kinases that are key regulators of the cell cycle. However, several reports indicated their roles in other pathways.… (more)

Subjects/Keywords: Cyclin-Dependent Kinase; CDK; Drosophila; Brahma; phosphorylation; breast cancer; BRMS1; metastasis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

binte Roesley, S. N. A. (2015). Roles of cyclin-dependent kinase substrates: cell cycle and beyond. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/91519

Chicago Manual of Style (16th Edition):

binte Roesley, Siti Nur Ain. “Roles of cyclin-dependent kinase substrates: cell cycle and beyond.” 2015. Doctoral Dissertation, University of Melbourne. Accessed December 05, 2020. http://hdl.handle.net/11343/91519.

MLA Handbook (7th Edition):

binte Roesley, Siti Nur Ain. “Roles of cyclin-dependent kinase substrates: cell cycle and beyond.” 2015. Web. 05 Dec 2020.

Vancouver:

binte Roesley SNA. Roles of cyclin-dependent kinase substrates: cell cycle and beyond. [Internet] [Doctoral dissertation]. University of Melbourne; 2015. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/11343/91519.

Council of Science Editors:

binte Roesley SNA. Roles of cyclin-dependent kinase substrates: cell cycle and beyond. [Doctoral Dissertation]. University of Melbourne; 2015. Available from: http://hdl.handle.net/11343/91519


University of Southern California

26. Tao, Litao. Investigation of the molecular mechanisms of ototoxicity.

Degree: PhD, Genetic, Molecular and Cellular Biology, 2014, University of Southern California

 Sensory hair cells are essential for transforming the mechanical vibrations of sound into electric signals that our nervous system can interpret. However, sensory hair cells… (more)

Subjects/Keywords: aminoglycoside antibiotics; ototoxicity; cyclin-dependent kinase 2; c-Jun; RNA sequencing

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Tao, L. (2014). Investigation of the molecular mechanisms of ototoxicity. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/426847/rec/3651

Chicago Manual of Style (16th Edition):

Tao, Litao. “Investigation of the molecular mechanisms of ototoxicity.” 2014. Doctoral Dissertation, University of Southern California. Accessed December 05, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/426847/rec/3651.

MLA Handbook (7th Edition):

Tao, Litao. “Investigation of the molecular mechanisms of ototoxicity.” 2014. Web. 05 Dec 2020.

Vancouver:

Tao L. Investigation of the molecular mechanisms of ototoxicity. [Internet] [Doctoral dissertation]. University of Southern California; 2014. [cited 2020 Dec 05]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/426847/rec/3651.

Council of Science Editors:

Tao L. Investigation of the molecular mechanisms of ototoxicity. [Doctoral Dissertation]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/426847/rec/3651

27. KOSARAJU VAMSI KRISHNA. BIOINFORMATICS ANALYSIS OF CYCLIN-DEPENDENT KINASE 5: INSIGHTS TO DRUG DISCOVERY.

Degree: 2013, National University of Singapore

Subjects/Keywords: cyclin dependent kinase drug discovery

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

KRISHNA, K. V. (2013). BIOINFORMATICS ANALYSIS OF CYCLIN-DEPENDENT KINASE 5: INSIGHTS TO DRUG DISCOVERY. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/79599

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

KRISHNA, KOSARAJU VAMSI. “BIOINFORMATICS ANALYSIS OF CYCLIN-DEPENDENT KINASE 5: INSIGHTS TO DRUG DISCOVERY.” 2013. Thesis, National University of Singapore. Accessed December 05, 2020. http://scholarbank.nus.edu.sg/handle/10635/79599.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

KRISHNA, KOSARAJU VAMSI. “BIOINFORMATICS ANALYSIS OF CYCLIN-DEPENDENT KINASE 5: INSIGHTS TO DRUG DISCOVERY.” 2013. Web. 05 Dec 2020.

Vancouver:

KRISHNA KV. BIOINFORMATICS ANALYSIS OF CYCLIN-DEPENDENT KINASE 5: INSIGHTS TO DRUG DISCOVERY. [Internet] [Thesis]. National University of Singapore; 2013. [cited 2020 Dec 05]. Available from: http://scholarbank.nus.edu.sg/handle/10635/79599.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

KRISHNA KV. BIOINFORMATICS ANALYSIS OF CYCLIN-DEPENDENT KINASE 5: INSIGHTS TO DRUG DISCOVERY. [Thesis]. National University of Singapore; 2013. Available from: http://scholarbank.nus.edu.sg/handle/10635/79599

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Penn State University

28. Dick, Taryn Eve. A promising anti-cancer agent that functions as a dual target inhibitor of SphK1 and microtubule dynamics.

Degree: 2016, Penn State University

 An extensive amount of data points to sphingosine kinase 1 (SphK1) and aberrant regulation of sphingolipids as important components of tumorigenesis. We previously developed SKI-178… (more)

Subjects/Keywords: Sphingosine Kinase; Cyclin-dependent kinase 1; cell cycle arrest; mitotic arrest; mitotic cell death; microtubules

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Dick, T. E. (2016). A promising anti-cancer agent that functions as a dual target inhibitor of SphK1 and microtubule dynamics. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/29574

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Dick, Taryn Eve. “A promising anti-cancer agent that functions as a dual target inhibitor of SphK1 and microtubule dynamics.” 2016. Thesis, Penn State University. Accessed December 05, 2020. https://submit-etda.libraries.psu.edu/catalog/29574.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Dick, Taryn Eve. “A promising anti-cancer agent that functions as a dual target inhibitor of SphK1 and microtubule dynamics.” 2016. Web. 05 Dec 2020.

Vancouver:

Dick TE. A promising anti-cancer agent that functions as a dual target inhibitor of SphK1 and microtubule dynamics. [Internet] [Thesis]. Penn State University; 2016. [cited 2020 Dec 05]. Available from: https://submit-etda.libraries.psu.edu/catalog/29574.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Dick TE. A promising anti-cancer agent that functions as a dual target inhibitor of SphK1 and microtubule dynamics. [Thesis]. Penn State University; 2016. Available from: https://submit-etda.libraries.psu.edu/catalog/29574

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of South Carolina

29. Perkins, Tracy. A Novel Approach to the Design of Selective Inhibitors for Cell Cycle Cyclin Dependent Kinases.

Degree: MS, College of Pharmacy, 2013, University of South Carolina

  CDK2/cyclin A and CDK4/cyclin D1 are proven targets for cancer drug discovery. The development of novel CDK inhibitors, with high selectivity, are being investigated… (more)

Subjects/Keywords: Medicine and Health Sciences; Pharmacy and Pharmaceutical Sciences; CDK; Cyclin Binding Groove; Cyclin Dependent Kinases; Inhibitor; Non-ATP Competitive

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Perkins, T. (2013). A Novel Approach to the Design of Selective Inhibitors for Cell Cycle Cyclin Dependent Kinases. (Masters Thesis). University of South Carolina. Retrieved from https://scholarcommons.sc.edu/etd/2301

Chicago Manual of Style (16th Edition):

Perkins, Tracy. “A Novel Approach to the Design of Selective Inhibitors for Cell Cycle Cyclin Dependent Kinases.” 2013. Masters Thesis, University of South Carolina. Accessed December 05, 2020. https://scholarcommons.sc.edu/etd/2301.

MLA Handbook (7th Edition):

Perkins, Tracy. “A Novel Approach to the Design of Selective Inhibitors for Cell Cycle Cyclin Dependent Kinases.” 2013. Web. 05 Dec 2020.

Vancouver:

Perkins T. A Novel Approach to the Design of Selective Inhibitors for Cell Cycle Cyclin Dependent Kinases. [Internet] [Masters thesis]. University of South Carolina; 2013. [cited 2020 Dec 05]. Available from: https://scholarcommons.sc.edu/etd/2301.

Council of Science Editors:

Perkins T. A Novel Approach to the Design of Selective Inhibitors for Cell Cycle Cyclin Dependent Kinases. [Masters Thesis]. University of South Carolina; 2013. Available from: https://scholarcommons.sc.edu/etd/2301


Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ)

30. Τσόλκας, Γρηγόριος. Μελέτη της επίδρασης του ρετινοϊκού οξέος και αναστολέων των κυκλινοεξαρτώμενων κινασών στη διαφοροποίηση λευχαιμικών κυττάρων.

Degree: 2012, Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ)

Acute promyelocytic leukemia (APL) is characterized by chromosome translocations, which generate fusion oncogenic proteins that play critical roles in pathogenesis. Of these chromosomal translocations, the… (more)

Subjects/Keywords: Οξεία προμυελοκυτταρική λευχαιμία; Ολομουκίνη; Ροσκοβιτίνη; Διαφοροποίηση; Κυκλινοεξαρτώμενες κινάσες; Αναστολείς κυκλινοεξαρτωμένων κινασών; Κυκλίνη Α1; Acute promyelocytic leukemia; Olomoucine; Roscovitine; Differentiation therapy; Cyclin A1; Cyclin dependent kinases; Cyclin dependent kinase inhibitors

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Τσόλκας, . . (2012). Μελέτη της επίδρασης του ρετινοϊκού οξέος και αναστολέων των κυκλινοεξαρτώμενων κινασών στη διαφοροποίηση λευχαιμικών κυττάρων. (Thesis). Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ). Retrieved from http://hdl.handle.net/10442/hedi/28088

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Τσόλκας, Γρηγόριος. “Μελέτη της επίδρασης του ρετινοϊκού οξέος και αναστολέων των κυκλινοεξαρτώμενων κινασών στη διαφοροποίηση λευχαιμικών κυττάρων.” 2012. Thesis, Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ). Accessed December 05, 2020. http://hdl.handle.net/10442/hedi/28088.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Τσόλκας, Γρηγόριος. “Μελέτη της επίδρασης του ρετινοϊκού οξέος και αναστολέων των κυκλινοεξαρτώμενων κινασών στη διαφοροποίηση λευχαιμικών κυττάρων.” 2012. Web. 05 Dec 2020.

Vancouver:

Τσόλκας . Μελέτη της επίδρασης του ρετινοϊκού οξέος και αναστολέων των κυκλινοεξαρτώμενων κινασών στη διαφοροποίηση λευχαιμικών κυττάρων. [Internet] [Thesis]. Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ); 2012. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/10442/hedi/28088.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Τσόλκας . Μελέτη της επίδρασης του ρετινοϊκού οξέος και αναστολέων των κυκλινοεξαρτώμενων κινασών στη διαφοροποίηση λευχαιμικών κυττάρων. [Thesis]. Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ); 2012. Available from: http://hdl.handle.net/10442/hedi/28088

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

[1] [2] [3] [4] [5] … [260]

.