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You searched for subject:(G1). Showing records 1 – 30 of 62 total matches.

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1. Iwakura, Takamasa. A high ratio of G1 to G0 phase cells and an accumulation of G1 phase cells before S phase progression after injurious stimuli in the proximal tubule : 近位尿細管での高いG1/G0期細胞比率と傷害刺激後におけるS期進行前のG1期細胞蓄積.

Degree: 博士(医学), 2015, Hamamatsu University School of Medicine / 浜松医科大学

Proximal tubule (PT) cells can proliferate explosively after injurious stimuli. To investigate this proliferative capacity, we examined cell cycle status and the expression of cyclin-dependent… (more)

Subjects/Keywords: Cell cycle; G0-G1 transition; G1 arrest; proximal tubule.

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

APA (6th Edition):

Iwakura, T. (2015). A high ratio of G1 to G0 phase cells and an accumulation of G1 phase cells before S phase progression after injurious stimuli in the proximal tubule : 近位尿細管での高いG1/G0期細胞比率と傷害刺激後におけるS期進行前のG1期細胞蓄積. (Thesis). Hamamatsu University School of Medicine / 浜松医科大学. Retrieved from http://hdl.handle.net/10271/2907

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):

Iwakura, Takamasa. “A high ratio of G1 to G0 phase cells and an accumulation of G1 phase cells before S phase progression after injurious stimuli in the proximal tubule : 近位尿細管での高いG1/G0期細胞比率と傷害刺激後におけるS期進行前のG1期細胞蓄積.” 2015. Thesis, Hamamatsu University School of Medicine / 浜松医科大学. Accessed July 23, 2019. http://hdl.handle.net/10271/2907.

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

MLA Handbook (7th Edition):

Iwakura, Takamasa. “A high ratio of G1 to G0 phase cells and an accumulation of G1 phase cells before S phase progression after injurious stimuli in the proximal tubule : 近位尿細管での高いG1/G0期細胞比率と傷害刺激後におけるS期進行前のG1期細胞蓄積.” 2015. Web. 23 Jul 2019.

Vancouver:

Iwakura T. A high ratio of G1 to G0 phase cells and an accumulation of G1 phase cells before S phase progression after injurious stimuli in the proximal tubule : 近位尿細管での高いG1/G0期細胞比率と傷害刺激後におけるS期進行前のG1期細胞蓄積. [Internet] [Thesis]. Hamamatsu University School of Medicine / 浜松医科大学; 2015. [cited 2019 Jul 23]. Available from: http://hdl.handle.net/10271/2907.

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

Council of Science Editors:

Iwakura T. A high ratio of G1 to G0 phase cells and an accumulation of G1 phase cells before S phase progression after injurious stimuli in the proximal tubule : 近位尿細管での高いG1/G0期細胞比率と傷害刺激後におけるS期進行前のG1期細胞蓄積. [Thesis]. Hamamatsu University School of Medicine / 浜松医科大学; 2015. Available from: http://hdl.handle.net/10271/2907

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


McMaster University

2. Mahadeo, Crystal. INVESTIGATING THE MECHANISM OF ACTION OF GUANOSINE BY THE G1 RECEPTOR.

Degree: MSc, 2016, McMaster University

When released extracellularly, the purine nucleoside guanosine (Guo) can exert a wide range of physiological effects in vitro and in vivo. Guo can induce the… (more)

Subjects/Keywords: Guanosine; GPCR; G1 receptor; Binding Assay

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APA (6th Edition):

Mahadeo, C. (2016). INVESTIGATING THE MECHANISM OF ACTION OF GUANOSINE BY THE G1 RECEPTOR. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/20626

Chicago Manual of Style (16th Edition):

Mahadeo, Crystal. “INVESTIGATING THE MECHANISM OF ACTION OF GUANOSINE BY THE G1 RECEPTOR.” 2016. Masters Thesis, McMaster University. Accessed July 23, 2019. http://hdl.handle.net/11375/20626.

MLA Handbook (7th Edition):

Mahadeo, Crystal. “INVESTIGATING THE MECHANISM OF ACTION OF GUANOSINE BY THE G1 RECEPTOR.” 2016. Web. 23 Jul 2019.

Vancouver:

Mahadeo C. INVESTIGATING THE MECHANISM OF ACTION OF GUANOSINE BY THE G1 RECEPTOR. [Internet] [Masters thesis]. McMaster University; 2016. [cited 2019 Jul 23]. Available from: http://hdl.handle.net/11375/20626.

Council of Science Editors:

Mahadeo C. INVESTIGATING THE MECHANISM OF ACTION OF GUANOSINE BY THE G1 RECEPTOR. [Masters Thesis]. McMaster University; 2016. Available from: http://hdl.handle.net/11375/20626

3. Drougat, Ludivine. Etude de la dynamique de O-GlcNAcylation et identification de protéines différentiellement O-GlcNAcylées au cours de la transition G1/S du cycle cellulaire de cellules épithéliales humaines : Characterization of O-GlcNAc cycling and proteomic identification of differentially O-GlcNAcylated proteins during G1/S transition in human epithelial cells.

Degree: Docteur es, Sciences de la Vie et de la Santé, 2012, Université Lille I – Sciences et Technologies

La O-GlcNAcylation est une glycosylation dynamique et réversible sous le contrôle de la O-GlcNAc Transférase (OGT) qui transfère un résidu de GlcNAc sur les Ser/Thr… (more)

Subjects/Keywords: O-GlcNAcylation; Transition G1/S; 572.68

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APA (6th Edition):

Drougat, L. (2012). Etude de la dynamique de O-GlcNAcylation et identification de protéines différentiellement O-GlcNAcylées au cours de la transition G1/S du cycle cellulaire de cellules épithéliales humaines : Characterization of O-GlcNAc cycling and proteomic identification of differentially O-GlcNAcylated proteins during G1/S transition in human epithelial cells. (Doctoral Dissertation). Université Lille I – Sciences et Technologies. Retrieved from http://www.theses.fr/2012LIL10086

Chicago Manual of Style (16th Edition):

Drougat, Ludivine. “Etude de la dynamique de O-GlcNAcylation et identification de protéines différentiellement O-GlcNAcylées au cours de la transition G1/S du cycle cellulaire de cellules épithéliales humaines : Characterization of O-GlcNAc cycling and proteomic identification of differentially O-GlcNAcylated proteins during G1/S transition in human epithelial cells.” 2012. Doctoral Dissertation, Université Lille I – Sciences et Technologies. Accessed July 23, 2019. http://www.theses.fr/2012LIL10086.

MLA Handbook (7th Edition):

Drougat, Ludivine. “Etude de la dynamique de O-GlcNAcylation et identification de protéines différentiellement O-GlcNAcylées au cours de la transition G1/S du cycle cellulaire de cellules épithéliales humaines : Characterization of O-GlcNAc cycling and proteomic identification of differentially O-GlcNAcylated proteins during G1/S transition in human epithelial cells.” 2012. Web. 23 Jul 2019.

Vancouver:

Drougat L. Etude de la dynamique de O-GlcNAcylation et identification de protéines différentiellement O-GlcNAcylées au cours de la transition G1/S du cycle cellulaire de cellules épithéliales humaines : Characterization of O-GlcNAc cycling and proteomic identification of differentially O-GlcNAcylated proteins during G1/S transition in human epithelial cells. [Internet] [Doctoral dissertation]. Université Lille I – Sciences et Technologies; 2012. [cited 2019 Jul 23]. Available from: http://www.theses.fr/2012LIL10086.

Council of Science Editors:

Drougat L. Etude de la dynamique de O-GlcNAcylation et identification de protéines différentiellement O-GlcNAcylées au cours de la transition G1/S du cycle cellulaire de cellules épithéliales humaines : Characterization of O-GlcNAc cycling and proteomic identification of differentially O-GlcNAcylated proteins during G1/S transition in human epithelial cells. [Doctoral Dissertation]. Université Lille I – Sciences et Technologies; 2012. Available from: http://www.theses.fr/2012LIL10086


Boston College

4. Szatanek, Tomasz Artur. A Temperature Sensitive Mutation in Cactin Causes a G1 Phase Arrest in Toxoplasma gondii.

Degree: PhD, Biology, 2010, Boston College

 The length of the tachyzoite cell cycle, in particular G1, is an important virulence factor in Toxoplasma gondii. Cdk and Cyclin activities ultimately control the… (more)

Subjects/Keywords: Cactin; cell division; G1 phase; Toxoplasma gondii

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APA (6th Edition):

Szatanek, T. A. (2010). A Temperature Sensitive Mutation in Cactin Causes a G1 Phase Arrest in Toxoplasma gondii. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:101644

Chicago Manual of Style (16th Edition):

Szatanek, Tomasz Artur. “A Temperature Sensitive Mutation in Cactin Causes a G1 Phase Arrest in Toxoplasma gondii.” 2010. Doctoral Dissertation, Boston College. Accessed July 23, 2019. http://dlib.bc.edu/islandora/object/bc-ir:101644.

MLA Handbook (7th Edition):

Szatanek, Tomasz Artur. “A Temperature Sensitive Mutation in Cactin Causes a G1 Phase Arrest in Toxoplasma gondii.” 2010. Web. 23 Jul 2019.

Vancouver:

Szatanek TA. A Temperature Sensitive Mutation in Cactin Causes a G1 Phase Arrest in Toxoplasma gondii. [Internet] [Doctoral dissertation]. Boston College; 2010. [cited 2019 Jul 23]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101644.

Council of Science Editors:

Szatanek TA. A Temperature Sensitive Mutation in Cactin Causes a G1 Phase Arrest in Toxoplasma gondii. [Doctoral Dissertation]. Boston College; 2010. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101644


Universidade Nova

5. Salvador, Sílvia Filipa Alves Beato. Contributo para o estudo da caracterização genética de estirpes portuguesas de Echinococcus granulosus.

Degree: 2016, Universidade Nova

 A hidatidose/equinococose é uma zoonose causada pelo céstode Echinococcus granulosus, juntamente com as suas variantes específicas denominadas de genótipos. Estão descritos 11 genótipos diferentes sendo… (more)

Subjects/Keywords: Echinococcus granulosus; Portugal; Genótipos G1-G3;

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APA (6th Edition):

Salvador, S. F. A. B. (2016). Contributo para o estudo da caracterização genética de estirpes portuguesas de Echinococcus granulosus. (Thesis). Universidade Nova. Retrieved from http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/19019

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):

Salvador, Sílvia Filipa Alves Beato. “Contributo para o estudo da caracterização genética de estirpes portuguesas de Echinococcus granulosus.” 2016. Thesis, Universidade Nova. Accessed July 23, 2019. http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/19019.

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

MLA Handbook (7th Edition):

Salvador, Sílvia Filipa Alves Beato. “Contributo para o estudo da caracterização genética de estirpes portuguesas de Echinococcus granulosus.” 2016. Web. 23 Jul 2019.

Vancouver:

Salvador SFAB. Contributo para o estudo da caracterização genética de estirpes portuguesas de Echinococcus granulosus. [Internet] [Thesis]. Universidade Nova; 2016. [cited 2019 Jul 23]. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/19019.

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

Council of Science Editors:

Salvador SFAB. Contributo para o estudo da caracterização genética de estirpes portuguesas de Echinococcus granulosus. [Thesis]. Universidade Nova; 2016. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/19019

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

6. Fernanda Carraro Dal-Vitt. A NOTÍCIA NO WEBJORNALISMO PARTICIPATIVO: UMA ANÁLISE DO CANAL VC NO G1, DO PORTAL GLOBO.

Degree: 2009, UNIVERSIDADE TUIUTI DO PARANÁ

O objetivo desta pesquisa é refletir sobre a notícia no webjornalismo participativo, que possibilita envolver o público no seu processo de coleta, criação, análise e… (more)

Subjects/Keywords: comunicação; jornalismo digital; webjornalismo participativo; Vc no G1; COMUNICACAO; communication; digital jornalism; participative web journalism; Vc no G1

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APA (6th Edition):

Dal-Vitt, F. C. (2009). A NOTÍCIA NO WEBJORNALISMO PARTICIPATIVO: UMA ANÁLISE DO CANAL VC NO G1, DO PORTAL GLOBO. (Thesis). UNIVERSIDADE TUIUTI DO PARANÁ. Retrieved from http://tede.utp.br/tde_busca/arquivo.php?codArquivo=284 ; http://tede.utp.br/tde_busca/arquivo.php?codArquivo=285

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):

Dal-Vitt, Fernanda Carraro. “A NOTÍCIA NO WEBJORNALISMO PARTICIPATIVO: UMA ANÁLISE DO CANAL VC NO G1, DO PORTAL GLOBO.” 2009. Thesis, UNIVERSIDADE TUIUTI DO PARANÁ. Accessed July 23, 2019. http://tede.utp.br/tde_busca/arquivo.php?codArquivo=284 ; http://tede.utp.br/tde_busca/arquivo.php?codArquivo=285.

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

MLA Handbook (7th Edition):

Dal-Vitt, Fernanda Carraro. “A NOTÍCIA NO WEBJORNALISMO PARTICIPATIVO: UMA ANÁLISE DO CANAL VC NO G1, DO PORTAL GLOBO.” 2009. Web. 23 Jul 2019.

Vancouver:

Dal-Vitt FC. A NOTÍCIA NO WEBJORNALISMO PARTICIPATIVO: UMA ANÁLISE DO CANAL VC NO G1, DO PORTAL GLOBO. [Internet] [Thesis]. UNIVERSIDADE TUIUTI DO PARANÁ; 2009. [cited 2019 Jul 23]. Available from: http://tede.utp.br/tde_busca/arquivo.php?codArquivo=284 ; http://tede.utp.br/tde_busca/arquivo.php?codArquivo=285.

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

Council of Science Editors:

Dal-Vitt FC. A NOTÍCIA NO WEBJORNALISMO PARTICIPATIVO: UMA ANÁLISE DO CANAL VC NO G1, DO PORTAL GLOBO. [Thesis]. UNIVERSIDADE TUIUTI DO PARANÁ; 2009. Available from: http://tede.utp.br/tde_busca/arquivo.php?codArquivo=284 ; http://tede.utp.br/tde_busca/arquivo.php?codArquivo=285

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

7. Coronado, Diana. The brevity of G1 is an intrinsic determinant of naïve pluripotency : La brièveté de la phase G1 est une caractéristique fondamentale de l’état naïf de pluripotence.

Degree: Docteur es, Biologie moléculaire et cellulaire, 2011, Université Claude Bernard – Lyon I

Les cellules souches embryonnaires (cellules ES) sont capables de se multiplier de façon autonome en l’absence de facteurs de croissance et de cytokines, un état… (more)

Subjects/Keywords: Cellules souches embryonnaires; Phase G1; Pluripotence; Cycline E; Embryonic stem cells; G1 phase; Pluripotency; Cyclin E; 571.6

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APA (6th Edition):

Coronado, D. (2011). The brevity of G1 is an intrinsic determinant of naïve pluripotency : La brièveté de la phase G1 est une caractéristique fondamentale de l’état naïf de pluripotence. (Doctoral Dissertation). Université Claude Bernard – Lyon I. Retrieved from http://www.theses.fr/2011LYO10311

Chicago Manual of Style (16th Edition):

Coronado, Diana. “The brevity of G1 is an intrinsic determinant of naïve pluripotency : La brièveté de la phase G1 est une caractéristique fondamentale de l’état naïf de pluripotence.” 2011. Doctoral Dissertation, Université Claude Bernard – Lyon I. Accessed July 23, 2019. http://www.theses.fr/2011LYO10311.

MLA Handbook (7th Edition):

Coronado, Diana. “The brevity of G1 is an intrinsic determinant of naïve pluripotency : La brièveté de la phase G1 est une caractéristique fondamentale de l’état naïf de pluripotence.” 2011. Web. 23 Jul 2019.

Vancouver:

Coronado D. The brevity of G1 is an intrinsic determinant of naïve pluripotency : La brièveté de la phase G1 est une caractéristique fondamentale de l’état naïf de pluripotence. [Internet] [Doctoral dissertation]. Université Claude Bernard – Lyon I; 2011. [cited 2019 Jul 23]. Available from: http://www.theses.fr/2011LYO10311.

Council of Science Editors:

Coronado D. The brevity of G1 is an intrinsic determinant of naïve pluripotency : La brièveté de la phase G1 est une caractéristique fondamentale de l’état naïf de pluripotence. [Doctoral Dissertation]. Université Claude Bernard – Lyon I; 2011. Available from: http://www.theses.fr/2011LYO10311


Laurentian University

8. Albalawi, Ghadah. The effect of andrographis paniculata on the growth of malignant cancer cells .

Degree: 2016, Laurentian University

 There are a variety of plants that have been recognized and used in traditional medicine for their health benefits. Among these plants is Andrographis paniculata,… (more)

Subjects/Keywords: Andrographis paniculata; malignant cancer cells; Apoptosis; Caspase 3,; Sub-G1

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APA (6th Edition):

Albalawi, G. (2016). The effect of andrographis paniculata on the growth of malignant cancer cells . (Thesis). Laurentian University. Retrieved from https://zone.biblio.laurentian.ca/handle/10219/2674

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):

Albalawi, Ghadah. “The effect of andrographis paniculata on the growth of malignant cancer cells .” 2016. Thesis, Laurentian University. Accessed July 23, 2019. https://zone.biblio.laurentian.ca/handle/10219/2674.

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

MLA Handbook (7th Edition):

Albalawi, Ghadah. “The effect of andrographis paniculata on the growth of malignant cancer cells .” 2016. Web. 23 Jul 2019.

Vancouver:

Albalawi G. The effect of andrographis paniculata on the growth of malignant cancer cells . [Internet] [Thesis]. Laurentian University; 2016. [cited 2019 Jul 23]. Available from: https://zone.biblio.laurentian.ca/handle/10219/2674.

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

Council of Science Editors:

Albalawi G. The effect of andrographis paniculata on the growth of malignant cancer cells . [Thesis]. Laurentian University; 2016. Available from: https://zone.biblio.laurentian.ca/handle/10219/2674

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


University of Louisville

9. Muenyi, Clarisse S. Mitigating cisplatin resistance in ovarian cancer.

Degree: PhD, 2011, University of Louisville

 Epithelial Ovarian cancer (EOC) is the leading cause of gynecological cancer death in the USA. Recurrence rates are high after front-line platinum chemotherapy and most… (more)

Subjects/Keywords: Ovarian cancer; Hyperthermic; Cisplatin; HIPEC; Arsenic; Pseudo-G1

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APA (6th Edition):

Muenyi, C. S. (2011). Mitigating cisplatin resistance in ovarian cancer. (Doctoral Dissertation). University of Louisville. Retrieved from 10.18297/etd/1023 ; https://ir.library.louisville.edu/etd/1023

Chicago Manual of Style (16th Edition):

Muenyi, Clarisse S. “Mitigating cisplatin resistance in ovarian cancer.” 2011. Doctoral Dissertation, University of Louisville. Accessed July 23, 2019. 10.18297/etd/1023 ; https://ir.library.louisville.edu/etd/1023.

MLA Handbook (7th Edition):

Muenyi, Clarisse S. “Mitigating cisplatin resistance in ovarian cancer.” 2011. Web. 23 Jul 2019.

Vancouver:

Muenyi CS. Mitigating cisplatin resistance in ovarian cancer. [Internet] [Doctoral dissertation]. University of Louisville; 2011. [cited 2019 Jul 23]. Available from: 10.18297/etd/1023 ; https://ir.library.louisville.edu/etd/1023.

Council of Science Editors:

Muenyi CS. Mitigating cisplatin resistance in ovarian cancer. [Doctoral Dissertation]. University of Louisville; 2011. Available from: 10.18297/etd/1023 ; https://ir.library.louisville.edu/etd/1023

10. Oréal, Vincent. Rôles distincts des différentes formes de méthylation de H3K4 dans deux mécanismes de répression transcriptionnelle et mise en évidence d'une nouvelle voie de surveillance moléculaire liée à l'excès d'histones libres : Disctincts roles for different formes of H3K4 methylation in two transcriptional repression mechanisms and discovery of a new molecular surveillance pathway linked to an excess of free histones.

Degree: Docteur es, Bioinformatique, biochimie structurale et génomique, 2010, Aix-Marseille 2

Les relations entre les histones qui composent les nucléosomes et le processus de transcription des gènes codants, sont à la fois multiples et extrêmement complexes.… (more)

Subjects/Keywords: Histones; Set1; Transcription; Fact; ARN anti-sens; Histones libres; Checkpoint G1

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APA (6th Edition):

Oréal, V. (2010). Rôles distincts des différentes formes de méthylation de H3K4 dans deux mécanismes de répression transcriptionnelle et mise en évidence d'une nouvelle voie de surveillance moléculaire liée à l'excès d'histones libres : Disctincts roles for different formes of H3K4 methylation in two transcriptional repression mechanisms and discovery of a new molecular surveillance pathway linked to an excess of free histones. (Doctoral Dissertation). Aix-Marseille 2. Retrieved from http://www.theses.fr/2010AIX22051

Chicago Manual of Style (16th Edition):

Oréal, Vincent. “Rôles distincts des différentes formes de méthylation de H3K4 dans deux mécanismes de répression transcriptionnelle et mise en évidence d'une nouvelle voie de surveillance moléculaire liée à l'excès d'histones libres : Disctincts roles for different formes of H3K4 methylation in two transcriptional repression mechanisms and discovery of a new molecular surveillance pathway linked to an excess of free histones.” 2010. Doctoral Dissertation, Aix-Marseille 2. Accessed July 23, 2019. http://www.theses.fr/2010AIX22051.

MLA Handbook (7th Edition):

Oréal, Vincent. “Rôles distincts des différentes formes de méthylation de H3K4 dans deux mécanismes de répression transcriptionnelle et mise en évidence d'une nouvelle voie de surveillance moléculaire liée à l'excès d'histones libres : Disctincts roles for different formes of H3K4 methylation in two transcriptional repression mechanisms and discovery of a new molecular surveillance pathway linked to an excess of free histones.” 2010. Web. 23 Jul 2019.

Vancouver:

Oréal V. Rôles distincts des différentes formes de méthylation de H3K4 dans deux mécanismes de répression transcriptionnelle et mise en évidence d'une nouvelle voie de surveillance moléculaire liée à l'excès d'histones libres : Disctincts roles for different formes of H3K4 methylation in two transcriptional repression mechanisms and discovery of a new molecular surveillance pathway linked to an excess of free histones. [Internet] [Doctoral dissertation]. Aix-Marseille 2; 2010. [cited 2019 Jul 23]. Available from: http://www.theses.fr/2010AIX22051.

Council of Science Editors:

Oréal V. Rôles distincts des différentes formes de méthylation de H3K4 dans deux mécanismes de répression transcriptionnelle et mise en évidence d'une nouvelle voie de surveillance moléculaire liée à l'excès d'histones libres : Disctincts roles for different formes of H3K4 methylation in two transcriptional repression mechanisms and discovery of a new molecular surveillance pathway linked to an excess of free histones. [Doctoral Dissertation]. Aix-Marseille 2; 2010. Available from: http://www.theses.fr/2010AIX22051

11. Bállega Moreno, Elisabet. Caracterización cuantitativa de las ciclinas de la fase G1 del ciclo celular en Saccharomyces cerevisiae.

Degree: Departament de Ciències Bàsiques, 2017, Universitat Internacional de Catalunya

 Saccharomyces cerevisiae és un microorganisme unicel·lular eucariota que per presentar el seu genoma totalment seqüenciat, gran facilitat de manipulació en el treball de laboratori, ja… (more)

Subjects/Keywords: Ciclo celular; G1; Pho85; Ciclinas; Estrés; Cuantificación; Ciencias básicas; 577

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

APA (6th Edition):

Bállega Moreno, E. (2017). Caracterización cuantitativa de las ciclinas de la fase G1 del ciclo celular en Saccharomyces cerevisiae. (Thesis). Universitat Internacional de Catalunya. Retrieved from http://hdl.handle.net/10803/456049

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):

Bállega Moreno, Elisabet. “Caracterización cuantitativa de las ciclinas de la fase G1 del ciclo celular en Saccharomyces cerevisiae.” 2017. Thesis, Universitat Internacional de Catalunya. Accessed July 23, 2019. http://hdl.handle.net/10803/456049.

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

MLA Handbook (7th Edition):

Bállega Moreno, Elisabet. “Caracterización cuantitativa de las ciclinas de la fase G1 del ciclo celular en Saccharomyces cerevisiae.” 2017. Web. 23 Jul 2019.

Vancouver:

Bállega Moreno E. Caracterización cuantitativa de las ciclinas de la fase G1 del ciclo celular en Saccharomyces cerevisiae. [Internet] [Thesis]. Universitat Internacional de Catalunya; 2017. [cited 2019 Jul 23]. Available from: http://hdl.handle.net/10803/456049.

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

Council of Science Editors:

Bállega Moreno E. Caracterización cuantitativa de las ciclinas de la fase G1 del ciclo celular en Saccharomyces cerevisiae. [Thesis]. Universitat Internacional de Catalunya; 2017. Available from: http://hdl.handle.net/10803/456049

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


University of the Western Cape

12. Mapolie, S. F. Metallodendrimers as catalysts for C-C coupling reactions .

Degree: 2011, University of the Western Cape

 In this work, we describe the synthesis of ferrocenylimine and G1 dendrimeric N,N′ ligands, and their palladium(II) complexes. The ligands L1 – L4 were synthesized… (more)

Subjects/Keywords: Synthesis of ferrocenylimine; G1 dendrimeric N; N′ ligands

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

APA (6th Edition):

Mapolie, S. F. (2011). Metallodendrimers as catalysts for C-C coupling reactions . (Thesis). University of the Western Cape. Retrieved from http://hdl.handle.net/11394/3567

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):

Mapolie, S F. “Metallodendrimers as catalysts for C-C coupling reactions .” 2011. Thesis, University of the Western Cape. Accessed July 23, 2019. http://hdl.handle.net/11394/3567.

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

MLA Handbook (7th Edition):

Mapolie, S F. “Metallodendrimers as catalysts for C-C coupling reactions .” 2011. Web. 23 Jul 2019.

Vancouver:

Mapolie SF. Metallodendrimers as catalysts for C-C coupling reactions . [Internet] [Thesis]. University of the Western Cape; 2011. [cited 2019 Jul 23]. Available from: http://hdl.handle.net/11394/3567.

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

Council of Science Editors:

Mapolie SF. Metallodendrimers as catalysts for C-C coupling reactions . [Thesis]. University of the Western Cape; 2011. Available from: http://hdl.handle.net/11394/3567

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

13. Feurer, Christian. A ship parametric model for isogeometric analysis.

Degree: 2013, National Technical University of Athens (NTUA); Εθνικό Μετσόβιο Πολυτεχνείο (ΕΜΠ)

This dissertation presents the development of a parametric model of a container ship hull for the particular requirements of isogeometric analysis. In the construction process… (more)

Subjects/Keywords: Εξομάλυνση; Ισογεωμετρική ανάλυση; Ισογεωμετρική ΜΣΣ; Παραμετρική μοντελοποίηση; Πλαίσιο; Συνέχεια G1; Σχεδίαση γάστρας πλοίου; CAD; CAGD; Frame; G1 continuity; Isogeometric analysis; Isogeometric BEM; Parametric modelling; Ship hull design; Smoothness

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

APA (6th Edition):

Feurer, C. (2013). A ship parametric model for isogeometric analysis. (Thesis). National Technical University of Athens (NTUA); Εθνικό Μετσόβιο Πολυτεχνείο (ΕΜΠ). Retrieved from http://hdl.handle.net/10442/hedi/35507

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):

Feurer, Christian. “A ship parametric model for isogeometric analysis.” 2013. Thesis, National Technical University of Athens (NTUA); Εθνικό Μετσόβιο Πολυτεχνείο (ΕΜΠ). Accessed July 23, 2019. http://hdl.handle.net/10442/hedi/35507.

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

MLA Handbook (7th Edition):

Feurer, Christian. “A ship parametric model for isogeometric analysis.” 2013. Web. 23 Jul 2019.

Vancouver:

Feurer C. A ship parametric model for isogeometric analysis. [Internet] [Thesis]. National Technical University of Athens (NTUA); Εθνικό Μετσόβιο Πολυτεχνείο (ΕΜΠ); 2013. [cited 2019 Jul 23]. Available from: http://hdl.handle.net/10442/hedi/35507.

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

Council of Science Editors:

Feurer C. A ship parametric model for isogeometric analysis. [Thesis]. National Technical University of Athens (NTUA); Εθνικό Μετσόβιο Πολυτεχνείο (ΕΜΠ); 2013. Available from: http://hdl.handle.net/10442/hedi/35507

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

14. Κύρκου, Αθηνά. Μοριακοί μηχανισμοί δράσης των μικρών GTPασών στις αγγειογενετικές αποκρίσεις των ενδοθηλιακών κυττάρων: ο ρόλος της RHOD στη ρύθμιση του κυτταρικού κύκλου.

Degree: 2009, University of Ioannina; Πανεπιστήμιο Ιωαννίνων

 The human Rho family of small GTPases represents a major branch of the Ras superfamily, best documented for the regulation of the actin cytoskeleton. In… (more)

Subjects/Keywords: Ενδοθηλιακά κύτταρα; Κυτταρικός πολλαπλασιασμός; Κυτταρικός κύκλος; Αγγειογενετικές αποκρίσεις; RhoD GTPase; Diaphanous 1; G1/S progression

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APA (6th Edition):

Κύρκου, . . (2009). Μοριακοί μηχανισμοί δράσης των μικρών GTPασών στις αγγειογενετικές αποκρίσεις των ενδοθηλιακών κυττάρων: ο ρόλος της RHOD στη ρύθμιση του κυτταρικού κύκλου. (Thesis). University of Ioannina; Πανεπιστήμιο Ιωαννίνων. Retrieved from http://hdl.handle.net/10442/hedi/27146

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):

Κύρκου, Αθηνά. “Μοριακοί μηχανισμοί δράσης των μικρών GTPασών στις αγγειογενετικές αποκρίσεις των ενδοθηλιακών κυττάρων: ο ρόλος της RHOD στη ρύθμιση του κυτταρικού κύκλου.” 2009. Thesis, University of Ioannina; Πανεπιστήμιο Ιωαννίνων. Accessed July 23, 2019. http://hdl.handle.net/10442/hedi/27146.

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

MLA Handbook (7th Edition):

Κύρκου, Αθηνά. “Μοριακοί μηχανισμοί δράσης των μικρών GTPασών στις αγγειογενετικές αποκρίσεις των ενδοθηλιακών κυττάρων: ο ρόλος της RHOD στη ρύθμιση του κυτταρικού κύκλου.” 2009. Web. 23 Jul 2019.

Vancouver:

Κύρκου . Μοριακοί μηχανισμοί δράσης των μικρών GTPασών στις αγγειογενετικές αποκρίσεις των ενδοθηλιακών κυττάρων: ο ρόλος της RHOD στη ρύθμιση του κυτταρικού κύκλου. [Internet] [Thesis]. University of Ioannina; Πανεπιστήμιο Ιωαννίνων; 2009. [cited 2019 Jul 23]. Available from: http://hdl.handle.net/10442/hedi/27146.

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

Council of Science Editors:

Κύρκου . Μοριακοί μηχανισμοί δράσης των μικρών GTPασών στις αγγειογενετικές αποκρίσεις των ενδοθηλιακών κυττάρων: ο ρόλος της RHOD στη ρύθμιση του κυτταρικού κύκλου. [Thesis]. University of Ioannina; Πανεπιστήμιο Ιωαννίνων; 2009. Available from: http://hdl.handle.net/10442/hedi/27146

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


Rockefeller University

15. Di, Talia, Stefano. Cell Size Control And Asymmetric Cell Fates In Start Of The Saccharomyces cerevisiae Cell Cycle.

Degree: 2009, Rockefeller University

 Understanding the molecular and biophysical mechanisms that couple the process of cell growth to cell division is one of the major challenges of modern cell… (more)

Subjects/Keywords: Saccharomyces cerevisiae; budding yeast cell cycle; G1 cyclins; CLN3; cell type specific regulation; Life Sciences

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APA (6th Edition):

Di, Talia, S. (2009). Cell Size Control And Asymmetric Cell Fates In Start Of The Saccharomyces cerevisiae Cell Cycle. (Masters Thesis). Rockefeller University. Retrieved from http://digitalcommons.rockefeller.edu/student_theses_and_dissertations/108

Chicago Manual of Style (16th Edition):

Di, Talia, Stefano. “Cell Size Control And Asymmetric Cell Fates In Start Of The Saccharomyces cerevisiae Cell Cycle.” 2009. Masters Thesis, Rockefeller University. Accessed July 23, 2019. http://digitalcommons.rockefeller.edu/student_theses_and_dissertations/108.

MLA Handbook (7th Edition):

Di, Talia, Stefano. “Cell Size Control And Asymmetric Cell Fates In Start Of The Saccharomyces cerevisiae Cell Cycle.” 2009. Web. 23 Jul 2019.

Vancouver:

Di, Talia S. Cell Size Control And Asymmetric Cell Fates In Start Of The Saccharomyces cerevisiae Cell Cycle. [Internet] [Masters thesis]. Rockefeller University; 2009. [cited 2019 Jul 23]. Available from: http://digitalcommons.rockefeller.edu/student_theses_and_dissertations/108.

Council of Science Editors:

Di, Talia S. Cell Size Control And Asymmetric Cell Fates In Start Of The Saccharomyces cerevisiae Cell Cycle. [Masters Thesis]. Rockefeller University; 2009. Available from: http://digitalcommons.rockefeller.edu/student_theses_and_dissertations/108


Université de Sherbrooke

16. Coulombe, Patrice. Étude de la fonction du variant d'histone H2A.Z dans la régulation des cyclines G1-S du cycle cellulaire et dans la réponse aux stress cellulaires chez saccharomyces cerevisiae .

Degree: 2013, Université de Sherbrooke

 La chromatine est l'assemblage du matériel génétique, l'ADN et de protéines appelées histones. En plus de leur fonction d'entreposage du génome, ces dernières régulent l'accessibilité… (more)

Subjects/Keywords: Chromatine; H2A.Z; Saccharomyces cerevisiae; Cycle cellulaire; START; Cyclines G1-S; Stress cellulaire; ChIP

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APA (6th Edition):

Coulombe, P. (2013). Étude de la fonction du variant d'histone H2A.Z dans la régulation des cyclines G1-S du cycle cellulaire et dans la réponse aux stress cellulaires chez saccharomyces cerevisiae . (Masters Thesis). Université de Sherbrooke. Retrieved from http://savoirs.usherbrooke.ca/handle/11143/55

Chicago Manual of Style (16th Edition):

Coulombe, Patrice. “Étude de la fonction du variant d'histone H2A.Z dans la régulation des cyclines G1-S du cycle cellulaire et dans la réponse aux stress cellulaires chez saccharomyces cerevisiae .” 2013. Masters Thesis, Université de Sherbrooke. Accessed July 23, 2019. http://savoirs.usherbrooke.ca/handle/11143/55.

MLA Handbook (7th Edition):

Coulombe, Patrice. “Étude de la fonction du variant d'histone H2A.Z dans la régulation des cyclines G1-S du cycle cellulaire et dans la réponse aux stress cellulaires chez saccharomyces cerevisiae .” 2013. Web. 23 Jul 2019.

Vancouver:

Coulombe P. Étude de la fonction du variant d'histone H2A.Z dans la régulation des cyclines G1-S du cycle cellulaire et dans la réponse aux stress cellulaires chez saccharomyces cerevisiae . [Internet] [Masters thesis]. Université de Sherbrooke; 2013. [cited 2019 Jul 23]. Available from: http://savoirs.usherbrooke.ca/handle/11143/55.

Council of Science Editors:

Coulombe P. Étude de la fonction du variant d'histone H2A.Z dans la régulation des cyclines G1-S du cycle cellulaire et dans la réponse aux stress cellulaires chez saccharomyces cerevisiae . [Masters Thesis]. Université de Sherbrooke; 2013. Available from: http://savoirs.usherbrooke.ca/handle/11143/55

17. Francisco Marques Sampaio. FunÃÃes discursivas do InfogrÃfico da webnotÃcia do G1.

Degree: Master, 2018, Universidade Federal do Ceará

Esta pesquisa qualitativa tem como objetivo geral analisar as funÃÃes discursivas do infogrÃfico da webnotÃcia do G1 â o Portal de NotÃcias da Globo. No… (more)

Subjects/Keywords: LINGUISTICA; FunÃÃes discursivas; InfogrÃfico; WebnotÃcia do G1; ComunicaÃÃo de massa e linguagem; FunÃÃes discursivas; G1 Portal de notÃcias - Analise linguÃstica InfogrÃfico - Analise linguÃstica; LinguÃstica aplicada; Noticias â GÃneros Discursivos â Analise linguÃstica; Discursive functions; Infographic; Webnews of the G1

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APA (6th Edition):

Sampaio, F. M. (2018). FunÃÃes discursivas do InfogrÃfico da webnotÃcia do G1. (Masters Thesis). Universidade Federal do Ceará. Retrieved from http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=20566 ;

Chicago Manual of Style (16th Edition):

Sampaio, Francisco Marques. “FunÃÃes discursivas do InfogrÃfico da webnotÃcia do G1.” 2018. Masters Thesis, Universidade Federal do Ceará. Accessed July 23, 2019. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=20566 ;.

MLA Handbook (7th Edition):

Sampaio, Francisco Marques. “FunÃÃes discursivas do InfogrÃfico da webnotÃcia do G1.” 2018. Web. 23 Jul 2019.

Vancouver:

Sampaio FM. FunÃÃes discursivas do InfogrÃfico da webnotÃcia do G1. [Internet] [Masters thesis]. Universidade Federal do Ceará 2018. [cited 2019 Jul 23]. Available from: http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=20566 ;.

Council of Science Editors:

Sampaio FM. FunÃÃes discursivas do InfogrÃfico da webnotÃcia do G1. [Masters Thesis]. Universidade Federal do Ceará 2018. Available from: http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=20566 ;


Addis Ababa University

18. YONAS, HAILESELASSIE. ASSESSMENT OF IMMUNOPATHOGENIC RISK MARKERS FOR HIV ASSOCIATED NEPHROPATHY (HIVAN) IN ETHIOPIA .

Degree: 2012, Addis Ababa University

 Background: HIV-1 infected patients are at risk of developing several types of chronic kidney disease, of which HIV-associated nephropathy (HIVAN) is the most prevalent. HIVAN… (more)

Subjects/Keywords: Proteinuria; Serum creatinine; APOL1 G1 and G2 risk Markers; MYH9 E-1 risk haplotype; ESRD; HIVAN

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APA (6th Edition):

YONAS, H. (2012). ASSESSMENT OF IMMUNOPATHOGENIC RISK MARKERS FOR HIV ASSOCIATED NEPHROPATHY (HIVAN) IN ETHIOPIA . (Thesis). Addis Ababa University. Retrieved from http://etd.aau.edu.et/dspace/handle/123456789/2915

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):

YONAS, HAILESELASSIE. “ASSESSMENT OF IMMUNOPATHOGENIC RISK MARKERS FOR HIV ASSOCIATED NEPHROPATHY (HIVAN) IN ETHIOPIA .” 2012. Thesis, Addis Ababa University. Accessed July 23, 2019. http://etd.aau.edu.et/dspace/handle/123456789/2915.

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

MLA Handbook (7th Edition):

YONAS, HAILESELASSIE. “ASSESSMENT OF IMMUNOPATHOGENIC RISK MARKERS FOR HIV ASSOCIATED NEPHROPATHY (HIVAN) IN ETHIOPIA .” 2012. Web. 23 Jul 2019.

Vancouver:

YONAS H. ASSESSMENT OF IMMUNOPATHOGENIC RISK MARKERS FOR HIV ASSOCIATED NEPHROPATHY (HIVAN) IN ETHIOPIA . [Internet] [Thesis]. Addis Ababa University; 2012. [cited 2019 Jul 23]. Available from: http://etd.aau.edu.et/dspace/handle/123456789/2915.

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

Council of Science Editors:

YONAS H. ASSESSMENT OF IMMUNOPATHOGENIC RISK MARKERS FOR HIV ASSOCIATED NEPHROPATHY (HIVAN) IN ETHIOPIA . [Thesis]. Addis Ababa University; 2012. Available from: http://etd.aau.edu.et/dspace/handle/123456789/2915

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


Universiteit Utrecht

19. Korzelius, J.P. Cell cycle entry in C. elegans development.

Degree: 2010, Universiteit Utrecht

 Cell division is controlled by a mechanism that uses Cyclins, in association with their Cyclin-dependent kinase partners (Cdk’s), to regulate the transitions in the cell… (more)

Subjects/Keywords: Biologie; Cell cycle; C. elegans; Cyclin; Cdk; DNA replication; terminal differentiation; MCM4; G1/S regulation; muscle

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APA (6th Edition):

Korzelius, J. P. (2010). Cell cycle entry in C. elegans development. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/39351

Chicago Manual of Style (16th Edition):

Korzelius, J P. “Cell cycle entry in C. elegans development.” 2010. Doctoral Dissertation, Universiteit Utrecht. Accessed July 23, 2019. http://dspace.library.uu.nl:8080/handle/1874/39351.

MLA Handbook (7th Edition):

Korzelius, J P. “Cell cycle entry in C. elegans development.” 2010. Web. 23 Jul 2019.

Vancouver:

Korzelius JP. Cell cycle entry in C. elegans development. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2010. [cited 2019 Jul 23]. Available from: http://dspace.library.uu.nl:8080/handle/1874/39351.

Council of Science Editors:

Korzelius JP. Cell cycle entry in C. elegans development. [Doctoral Dissertation]. Universiteit Utrecht; 2010. Available from: http://dspace.library.uu.nl:8080/handle/1874/39351

20. Pope, Patricia A. Investigation of Multiple Concerted Mechanisms Underlying Stimulus-induced G1 Arrest in Yeast: A Dissertation.

Degree: Interdisciplinary Graduate Program, Biochemistry and Molecular Pharmacology, 2013, U of Massachusetts : Med

  Progression through the cell cycle is tightly controlled, and the decision whether or not to enter a new cell cycle can be influenced by… (more)

Subjects/Keywords: G1 Phase Cell Cycle Checkpoints; Pheromones; Saccharomyces cerevisiae; Cell Biology; Cellular and Molecular Physiology; Molecular Biology

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APA (6th Edition):

Pope, P. A. (2013). Investigation of Multiple Concerted Mechanisms Underlying Stimulus-induced G1 Arrest in Yeast: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/680

Chicago Manual of Style (16th Edition):

Pope, Patricia A. “Investigation of Multiple Concerted Mechanisms Underlying Stimulus-induced G1 Arrest in Yeast: A Dissertation.” 2013. Doctoral Dissertation, U of Massachusetts : Med. Accessed July 23, 2019. http://escholarship.umassmed.edu/gsbs_diss/680.

MLA Handbook (7th Edition):

Pope, Patricia A. “Investigation of Multiple Concerted Mechanisms Underlying Stimulus-induced G1 Arrest in Yeast: A Dissertation.” 2013. Web. 23 Jul 2019.

Vancouver:

Pope PA. Investigation of Multiple Concerted Mechanisms Underlying Stimulus-induced G1 Arrest in Yeast: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2013. [cited 2019 Jul 23]. Available from: http://escholarship.umassmed.edu/gsbs_diss/680.

Council of Science Editors:

Pope PA. Investigation of Multiple Concerted Mechanisms Underlying Stimulus-induced G1 Arrest in Yeast: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2013. Available from: http://escholarship.umassmed.edu/gsbs_diss/680


University of Oslo

21. Anda, Silje. In vivo og in vitro karakterisering av humant NCU-G1.

Degree: 2007, University of Oslo

 Identifikasjonen av proteinet hNCU-G1 er basert på interaksjonen med hCRBP1-promoterens FP1-element (+66-+99), som ble gjort ved EMSA-studier. Videre studier avslørte at hNCU-G1 kunne fungere som… (more)

Subjects/Keywords: NCU-G1 transfeksjon transient ekspresjon PParbeta EMSA; VDP::476

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APA (6th Edition):

Anda, S. (2007). In vivo og in vitro karakterisering av humant NCU-G1. (Thesis). University of Oslo. Retrieved from http://urn.nb.no/URN:NBN:no-16405 ; https://www.duo.uio.no/handle/10852/11384 ; Fulltext https://www.duo.uio.no/bitstream/handle/10852/11384/1/masterriktig.pdf

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):

Anda, Silje. “In vivo og in vitro karakterisering av humant NCU-G1.” 2007. Thesis, University of Oslo. Accessed July 23, 2019. http://urn.nb.no/URN:NBN:no-16405 ; https://www.duo.uio.no/handle/10852/11384 ; Fulltext https://www.duo.uio.no/bitstream/handle/10852/11384/1/masterriktig.pdf.

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

MLA Handbook (7th Edition):

Anda, Silje. “In vivo og in vitro karakterisering av humant NCU-G1.” 2007. Web. 23 Jul 2019.

Vancouver:

Anda S. In vivo og in vitro karakterisering av humant NCU-G1. [Internet] [Thesis]. University of Oslo; 2007. [cited 2019 Jul 23]. Available from: http://urn.nb.no/URN:NBN:no-16405 ; https://www.duo.uio.no/handle/10852/11384 ; Fulltext https://www.duo.uio.no/bitstream/handle/10852/11384/1/masterriktig.pdf.

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

Council of Science Editors:

Anda S. In vivo og in vitro karakterisering av humant NCU-G1. [Thesis]. University of Oslo; 2007. Available from: http://urn.nb.no/URN:NBN:no-16405 ; https://www.duo.uio.no/handle/10852/11384 ; Fulltext https://www.duo.uio.no/bitstream/handle/10852/11384/1/masterriktig.pdf

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


McMaster University

22. Calder, Ashley. LENGTHENED G1 PHASE INDICATES DIFFERENTIATION STATUS IN HUMAN EMBRYONIC STEM CELLS.

Degree: MSc, 2011, McMaster University

Human embryonic stem cells (hESC) have potential applications as tools for drug screening to identify small molecule regulators of self-renewal or differentiation. Elucidating the… (more)

Subjects/Keywords: human embryonic stem cells; cell cycle; G1 length; differentiation; lineage committment; loss of pluripotency; Cell Biology; Cell Biology

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APA (6th Edition):

Calder, A. (2011). LENGTHENED G1 PHASE INDICATES DIFFERENTIATION STATUS IN HUMAN EMBRYONIC STEM CELLS. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/11176

Chicago Manual of Style (16th Edition):

Calder, Ashley. “LENGTHENED G1 PHASE INDICATES DIFFERENTIATION STATUS IN HUMAN EMBRYONIC STEM CELLS.” 2011. Masters Thesis, McMaster University. Accessed July 23, 2019. http://hdl.handle.net/11375/11176.

MLA Handbook (7th Edition):

Calder, Ashley. “LENGTHENED G1 PHASE INDICATES DIFFERENTIATION STATUS IN HUMAN EMBRYONIC STEM CELLS.” 2011. Web. 23 Jul 2019.

Vancouver:

Calder A. LENGTHENED G1 PHASE INDICATES DIFFERENTIATION STATUS IN HUMAN EMBRYONIC STEM CELLS. [Internet] [Masters thesis]. McMaster University; 2011. [cited 2019 Jul 23]. Available from: http://hdl.handle.net/11375/11176.

Council of Science Editors:

Calder A. LENGTHENED G1 PHASE INDICATES DIFFERENTIATION STATUS IN HUMAN EMBRYONIC STEM CELLS. [Masters Thesis]. McMaster University; 2011. Available from: http://hdl.handle.net/11375/11176


University of Notre Dame

23. Thomas M Durcan. Centrosome duplication in mammalian cells arrested prior to entry into S phase and the role of tektin 2 in centrosome duplication, mid body formation and cytokinesis</h1>.

Degree: PhD, Biological Sciences, 2007, University of Notre Dame

  Once every cell cycle, centrosomes duplicates precisely once. This facilitates the formation of a bipolar spindle, permitting equal segregation of chromosomes between both daughter… (more)

Subjects/Keywords: G1; centrosomes; CDK2; mid body; mimosine; duplication; tektins; cytokinesis

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APA (6th Edition):

Durcan, T. M. (2007). Centrosome duplication in mammalian cells arrested prior to entry into S phase and the role of tektin 2 in centrosome duplication, mid body formation and cytokinesis</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/xp68kd19z8m

Chicago Manual of Style (16th Edition):

Durcan, Thomas M. “Centrosome duplication in mammalian cells arrested prior to entry into S phase and the role of tektin 2 in centrosome duplication, mid body formation and cytokinesis</h1>.” 2007. Doctoral Dissertation, University of Notre Dame. Accessed July 23, 2019. https://curate.nd.edu/show/xp68kd19z8m.

MLA Handbook (7th Edition):

Durcan, Thomas M. “Centrosome duplication in mammalian cells arrested prior to entry into S phase and the role of tektin 2 in centrosome duplication, mid body formation and cytokinesis</h1>.” 2007. Web. 23 Jul 2019.

Vancouver:

Durcan TM. Centrosome duplication in mammalian cells arrested prior to entry into S phase and the role of tektin 2 in centrosome duplication, mid body formation and cytokinesis</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2007. [cited 2019 Jul 23]. Available from: https://curate.nd.edu/show/xp68kd19z8m.

Council of Science Editors:

Durcan TM. Centrosome duplication in mammalian cells arrested prior to entry into S phase and the role of tektin 2 in centrosome duplication, mid body formation and cytokinesis</h1>. [Doctoral Dissertation]. University of Notre Dame; 2007. Available from: https://curate.nd.edu/show/xp68kd19z8m

24. Rocha, Fabio Carlos da. Formulação do MEC considerando efeitos microestruturais e continuidade geométrica G1: tratamento de singularidade e análise de convergência.

Degree: PhD, Estruturas, 2015, University of São Paulo

 Neste trabalho, uma abordagem micromecânica com aproximação da geometria dada por funções de Bézier triangulares com continuidade geométrica G1 é inserida ao Método dos Elementos… (more)

Subjects/Keywords: Análise de convergência; Continuidade geométrica G1; Convergence analysis; Geometric continuity G1; Laurent series; Método dos Elementos de Contorno (MEC) micromecânico; Micromechanical BEM; Série de Laurent; Tratamento de singularidade; Treatment of singularity

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APA (6th Edition):

Rocha, F. C. d. (2015). Formulação do MEC considerando efeitos microestruturais e continuidade geométrica G1: tratamento de singularidade e análise de convergência. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/18/18134/tde-20052015-085721/ ;

Chicago Manual of Style (16th Edition):

Rocha, Fabio Carlos da. “Formulação do MEC considerando efeitos microestruturais e continuidade geométrica G1: tratamento de singularidade e análise de convergência.” 2015. Doctoral Dissertation, University of São Paulo. Accessed July 23, 2019. http://www.teses.usp.br/teses/disponiveis/18/18134/tde-20052015-085721/ ;.

MLA Handbook (7th Edition):

Rocha, Fabio Carlos da. “Formulação do MEC considerando efeitos microestruturais e continuidade geométrica G1: tratamento de singularidade e análise de convergência.” 2015. Web. 23 Jul 2019.

Vancouver:

Rocha FCd. Formulação do MEC considerando efeitos microestruturais e continuidade geométrica G1: tratamento de singularidade e análise de convergência. [Internet] [Doctoral dissertation]. University of São Paulo; 2015. [cited 2019 Jul 23]. Available from: http://www.teses.usp.br/teses/disponiveis/18/18134/tde-20052015-085721/ ;.

Council of Science Editors:

Rocha FCd. Formulação do MEC considerando efeitos microestruturais e continuidade geométrica G1: tratamento de singularidade e análise de convergência. [Doctoral Dissertation]. University of São Paulo; 2015. Available from: http://www.teses.usp.br/teses/disponiveis/18/18134/tde-20052015-085721/ ;

25. 脇本, 麗. Differential Anticancer Activity of Pterostilbene Against Three Subtypes of Human Breast Cancer Cells : Differential Anticancer Activity of Pterostilbene Against Three Subtypes of Human Breast Cancer Cells; サブタイプ別乳癌細胞に対するプテロスチルベンの抗腫痬効果の検討.

Degree: 博士, 2018, Nakamura Gakuen University / 中村学園大学

平成29年度

Subjects/Keywords: Breast cancer; G0/G1 arrest; apoptosis; cell cycle; pterostilbene; Breast cancer; G0/G1 arrest; apoptosis; cell cycle; pterostilbene

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APA (6th Edition):

脇本, . (2018). Differential Anticancer Activity of Pterostilbene Against Three Subtypes of Human Breast Cancer Cells : Differential Anticancer Activity of Pterostilbene Against Three Subtypes of Human Breast Cancer Cells; サブタイプ別乳癌細胞に対するプテロスチルベンの抗腫痬効果の検討. (Thesis). Nakamura Gakuen University / 中村学園大学. Retrieved from http://id.nii.ac.jp/1094/00002375/

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):

脇本, 麗. “Differential Anticancer Activity of Pterostilbene Against Three Subtypes of Human Breast Cancer Cells : Differential Anticancer Activity of Pterostilbene Against Three Subtypes of Human Breast Cancer Cells; サブタイプ別乳癌細胞に対するプテロスチルベンの抗腫痬効果の検討.” 2018. Thesis, Nakamura Gakuen University / 中村学園大学. Accessed July 23, 2019. http://id.nii.ac.jp/1094/00002375/.

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

MLA Handbook (7th Edition):

脇本, 麗. “Differential Anticancer Activity of Pterostilbene Against Three Subtypes of Human Breast Cancer Cells : Differential Anticancer Activity of Pterostilbene Against Three Subtypes of Human Breast Cancer Cells; サブタイプ別乳癌細胞に対するプテロスチルベンの抗腫痬効果の検討.” 2018. Web. 23 Jul 2019.

Vancouver:

脇本 . Differential Anticancer Activity of Pterostilbene Against Three Subtypes of Human Breast Cancer Cells : Differential Anticancer Activity of Pterostilbene Against Three Subtypes of Human Breast Cancer Cells; サブタイプ別乳癌細胞に対するプテロスチルベンの抗腫痬効果の検討. [Internet] [Thesis]. Nakamura Gakuen University / 中村学園大学; 2018. [cited 2019 Jul 23]. Available from: http://id.nii.ac.jp/1094/00002375/.

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

Council of Science Editors:

脇本 . Differential Anticancer Activity of Pterostilbene Against Three Subtypes of Human Breast Cancer Cells : Differential Anticancer Activity of Pterostilbene Against Three Subtypes of Human Breast Cancer Cells; サブタイプ別乳癌細胞に対するプテロスチルベンの抗腫痬効果の検討. [Thesis]. Nakamura Gakuen University / 中村学園大学; 2018. Available from: http://id.nii.ac.jp/1094/00002375/

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

26. ムコンデ, ガブリエル ヤコブ. Intracellular calcium dynamics and expression of P2Y and IP3 receptors in a cycling G1-phase cell : 細胞周期回転G1期細胞における細胞内カルシウム動態とP2YおよびIP3受容体の発現.

Degree: 医学博士, 2017, Iwate Medical University / 岩手医科大学

2016

Subjects/Keywords: G1-interphase cell; calcium signaling; receptor expression; cell cycle; G1-interphase cell; calcium signaling; receptor expression; cell cycle

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

APA (6th Edition):

ムコンデ, . (2017). Intracellular calcium dynamics and expression of P2Y and IP3 receptors in a cycling G1-phase cell : 細胞周期回転G1期細胞における細胞内カルシウム動態とP2YおよびIP3受容体の発現. (Thesis). Iwate Medical University / 岩手医科大学. Retrieved from http://id.nii.ac.jp/1181/00008776/

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):

ムコンデ, ガブリエル ヤコブ. “Intracellular calcium dynamics and expression of P2Y and IP3 receptors in a cycling G1-phase cell : 細胞周期回転G1期細胞における細胞内カルシウム動態とP2YおよびIP3受容体の発現.” 2017. Thesis, Iwate Medical University / 岩手医科大学. Accessed July 23, 2019. http://id.nii.ac.jp/1181/00008776/.

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

MLA Handbook (7th Edition):

ムコンデ, ガブリエル ヤコブ. “Intracellular calcium dynamics and expression of P2Y and IP3 receptors in a cycling G1-phase cell : 細胞周期回転G1期細胞における細胞内カルシウム動態とP2YおよびIP3受容体の発現.” 2017. Web. 23 Jul 2019.

Vancouver:

ムコンデ . Intracellular calcium dynamics and expression of P2Y and IP3 receptors in a cycling G1-phase cell : 細胞周期回転G1期細胞における細胞内カルシウム動態とP2YおよびIP3受容体の発現. [Internet] [Thesis]. Iwate Medical University / 岩手医科大学; 2017. [cited 2019 Jul 23]. Available from: http://id.nii.ac.jp/1181/00008776/.

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

Council of Science Editors:

ムコンデ . Intracellular calcium dynamics and expression of P2Y and IP3 receptors in a cycling G1-phase cell : 細胞周期回転G1期細胞における細胞内カルシウム動態とP2YおよびIP3受容体の発現. [Thesis]. Iwate Medical University / 岩手医科大学; 2017. Available from: http://id.nii.ac.jp/1181/00008776/

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


Brno University of Technology

27. Krivoklatský, Filip. Systém FLATcon – bytová ústředna s RF komunikací .

Degree: 2017, Brno University of Technology

 Táto bakalárska práca sa zaoberá riešeniami inteligentných domácností. Predstavuje niektoré dostupné riešenia na trhu a poukazuje na ich výhody a nevýhody. Primárne sa práca zameriava… (more)

Subjects/Keywords: FLATcon; bytová ústredňa; inteligentná domácnosť; RF bezdrôtová komunikácia; Li- Ion batéria; UPS; Raspberry Pi; RFM22B; TPS61230; MCP73834; bq27441-G1; Homebridge; FLATcon; smart home; RF wireless communication; Li-Ion battery; UPS; Raspberry Pi; RFM22B; TPS61230; MCP73834; bq27441-G1; Homebridge

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APA (6th Edition):

Krivoklatský, F. (2017). Systém FLATcon – bytová ústředna s RF komunikací . (Thesis). Brno University of Technology. Retrieved from http://hdl.handle.net/11012/66106

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):

Krivoklatský, Filip. “Systém FLATcon – bytová ústředna s RF komunikací .” 2017. Thesis, Brno University of Technology. Accessed July 23, 2019. http://hdl.handle.net/11012/66106.

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

MLA Handbook (7th Edition):

Krivoklatský, Filip. “Systém FLATcon – bytová ústředna s RF komunikací .” 2017. Web. 23 Jul 2019.

Vancouver:

Krivoklatský F. Systém FLATcon – bytová ústředna s RF komunikací . [Internet] [Thesis]. Brno University of Technology; 2017. [cited 2019 Jul 23]. Available from: http://hdl.handle.net/11012/66106.

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

Council of Science Editors:

Krivoklatský F. Systém FLATcon – bytová ústředna s RF komunikací . [Thesis]. Brno University of Technology; 2017. Available from: http://hdl.handle.net/11012/66106

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


The Ohio State University

28. Lucas, Jessica Regan. Microtubule arrays and cell divisions of stomatal development in Arabidopsis.

Degree: PhD, Plant Biology, 2007, The Ohio State University

 Little is known about how preprophase bands (PPBs) of microtubules mark division sites, or how phragmoplasts later grow towards these sites. To more clearly define… (more)

Subjects/Keywords: Arabidopsis; stomata; stoma; stomate; guard cell; patterning; microtubule; PPB; Preprophase Band; Phragmoplast; Cell division; Cytokinesis; too many mouths; tonneau2; M to G1 interface; cytokinesis-interphase transition

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APA (6th Edition):

Lucas, J. R. (2007). Microtubule arrays and cell divisions of stomatal development in Arabidopsis. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1181759887

Chicago Manual of Style (16th Edition):

Lucas, Jessica Regan. “Microtubule arrays and cell divisions of stomatal development in Arabidopsis.” 2007. Doctoral Dissertation, The Ohio State University. Accessed July 23, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1181759887.

MLA Handbook (7th Edition):

Lucas, Jessica Regan. “Microtubule arrays and cell divisions of stomatal development in Arabidopsis.” 2007. Web. 23 Jul 2019.

Vancouver:

Lucas JR. Microtubule arrays and cell divisions of stomatal development in Arabidopsis. [Internet] [Doctoral dissertation]. The Ohio State University; 2007. [cited 2019 Jul 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1181759887.

Council of Science Editors:

Lucas JR. Microtubule arrays and cell divisions of stomatal development in Arabidopsis. [Doctoral Dissertation]. The Ohio State University; 2007. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1181759887

29. Bhaduri, Samyabrata. Regulation of CDK1 Activity during the G1/S Transition in S. cerevisiae through Specific Cyclin-Substrate Docking: A Dissertation.

Degree: Interdisciplinary Graduate Program, Biochemistry and Molecular Pharmacology, 2014, U of Massachusetts : Med

  Several cell cycle events require specific forms of the cyclin-CDK complexes. It has been known for some time that cyclins not only contribute by… (more)

Subjects/Keywords: Cell Cycle; Cell Cycle Proteins; Saccharomyces cerevisiae Proteins; Cyclin B; Cyclin G1; Cyclins; Cyclin-Dependent Kinases; CDC2 Protein; Biochemistry; Cell Biology; Molecular Biology

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APA (6th Edition):

Bhaduri, S. (2014). Regulation of CDK1 Activity during the G1/S Transition in S. cerevisiae through Specific Cyclin-Substrate Docking: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/871

Chicago Manual of Style (16th Edition):

Bhaduri, Samyabrata. “Regulation of CDK1 Activity during the G1/S Transition in S. cerevisiae through Specific Cyclin-Substrate Docking: A Dissertation.” 2014. Doctoral Dissertation, U of Massachusetts : Med. Accessed July 23, 2019. http://escholarship.umassmed.edu/gsbs_diss/871.

MLA Handbook (7th Edition):

Bhaduri, Samyabrata. “Regulation of CDK1 Activity during the G1/S Transition in S. cerevisiae through Specific Cyclin-Substrate Docking: A Dissertation.” 2014. Web. 23 Jul 2019.

Vancouver:

Bhaduri S. Regulation of CDK1 Activity during the G1/S Transition in S. cerevisiae through Specific Cyclin-Substrate Docking: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2014. [cited 2019 Jul 23]. Available from: http://escholarship.umassmed.edu/gsbs_diss/871.

Council of Science Editors:

Bhaduri S. Regulation of CDK1 Activity during the G1/S Transition in S. cerevisiae through Specific Cyclin-Substrate Docking: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2014. Available from: http://escholarship.umassmed.edu/gsbs_diss/871


University of Oslo

30. Elvik, Solrun. Regulering av G1/S-overgangen i fisjonsgjær : dannelse av pre-replikasjonskomplekser.

Degree: 2004, University of Oslo

Subjects/Keywords: mikrobiologi fisjonsgjær cellesyklusG-1/S-overgang Schizosaccharomyces pombe Checkpoints G1; VDP::568

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APA (6th Edition):

Elvik, S. (2004). Regulering av G1/S-overgangen i fisjonsgjær : dannelse av pre-replikasjonskomplekser. (Thesis). University of Oslo. Retrieved from http://urn.nb.no/URN:NBN:no-11410 ; https://www.duo.uio.no/handle/10852/12071

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):

Elvik, Solrun. “Regulering av G1/S-overgangen i fisjonsgjær : dannelse av pre-replikasjonskomplekser.” 2004. Thesis, University of Oslo. Accessed July 23, 2019. http://urn.nb.no/URN:NBN:no-11410 ; https://www.duo.uio.no/handle/10852/12071.

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

MLA Handbook (7th Edition):

Elvik, Solrun. “Regulering av G1/S-overgangen i fisjonsgjær : dannelse av pre-replikasjonskomplekser.” 2004. Web. 23 Jul 2019.

Vancouver:

Elvik S. Regulering av G1/S-overgangen i fisjonsgjær : dannelse av pre-replikasjonskomplekser. [Internet] [Thesis]. University of Oslo; 2004. [cited 2019 Jul 23]. Available from: http://urn.nb.no/URN:NBN:no-11410 ; https://www.duo.uio.no/handle/10852/12071.

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

Council of Science Editors:

Elvik S. Regulering av G1/S-overgangen i fisjonsgjær : dannelse av pre-replikasjonskomplekser. [Thesis]. University of Oslo; 2004. Available from: http://urn.nb.no/URN:NBN:no-11410 ; https://www.duo.uio.no/handle/10852/12071

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

[1] [2] [3]

.