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You searched for subject:(chromatin remodeling). Showing records 1 – 30 of 112 total matches.

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University of Ottawa

1. Pépin, David. The Role of the ISWI Proteins SNF2H and SNF2L in Ovarian Folliculogenesis .

Degree: 2011, University of Ottawa

 Folliculogenesis is a complex process which describes the maturation of the ovarian follicle, from the primordial stage all the way to the ovulation of the… (more)

Subjects/Keywords: fulliculogenesis; endocrinology; chromatin remodeling; ISWI

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APA (6th Edition):

Pépin, D. (2011). The Role of the ISWI Proteins SNF2H and SNF2L in Ovarian Folliculogenesis . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/19840

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):

Pépin, David. “The Role of the ISWI Proteins SNF2H and SNF2L in Ovarian Folliculogenesis .” 2011. Thesis, University of Ottawa. Accessed April 14, 2021. http://hdl.handle.net/10393/19840.

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

MLA Handbook (7th Edition):

Pépin, David. “The Role of the ISWI Proteins SNF2H and SNF2L in Ovarian Folliculogenesis .” 2011. Web. 14 Apr 2021.

Vancouver:

Pépin D. The Role of the ISWI Proteins SNF2H and SNF2L in Ovarian Folliculogenesis . [Internet] [Thesis]. University of Ottawa; 2011. [cited 2021 Apr 14]. Available from: http://hdl.handle.net/10393/19840.

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

Council of Science Editors:

Pépin D. The Role of the ISWI Proteins SNF2H and SNF2L in Ovarian Folliculogenesis . [Thesis]. University of Ottawa; 2011. Available from: http://hdl.handle.net/10393/19840

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


University of Edinburgh

2. Huang, Rui. Roles of HDACs in chromatin remodelling and response to chemotherapy in cancer.

Degree: PhD, 2014, University of Edinburgh

 Background: The higher-order structure of chromatin changes in response to extracellular and environmental signals. We observed nuclear morphological changes in biopsied cancer tissue after chemotherapy.… (more)

Subjects/Keywords: 616.99; HDAC; chromatin remodeling; chemotherapy

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APA (6th Edition):

Huang, R. (2014). Roles of HDACs in chromatin remodelling and response to chemotherapy in cancer. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/9626

Chicago Manual of Style (16th Edition):

Huang, Rui. “Roles of HDACs in chromatin remodelling and response to chemotherapy in cancer.” 2014. Doctoral Dissertation, University of Edinburgh. Accessed April 14, 2021. http://hdl.handle.net/1842/9626.

MLA Handbook (7th Edition):

Huang, Rui. “Roles of HDACs in chromatin remodelling and response to chemotherapy in cancer.” 2014. Web. 14 Apr 2021.

Vancouver:

Huang R. Roles of HDACs in chromatin remodelling and response to chemotherapy in cancer. [Internet] [Doctoral dissertation]. University of Edinburgh; 2014. [cited 2021 Apr 14]. Available from: http://hdl.handle.net/1842/9626.

Council of Science Editors:

Huang R. Roles of HDACs in chromatin remodelling and response to chemotherapy in cancer. [Doctoral Dissertation]. University of Edinburgh; 2014. Available from: http://hdl.handle.net/1842/9626


Texas State University – San Marcos

3. Bonnard, April. Histone variant H2A.Z substitution mediated by the SWR1-like complex is a novel transcriptional regulatory mechanism controlling defense genes and immunity in plants.

Degree: MS, Biology, 2016, Texas State University – San Marcos

 Plants have evolved a complex immune system as a result of an evolutionary arms race between the host and various pathogens. One of the most… (more)

Subjects/Keywords: Plant immunity; Chromatin remodeling; Epigenetics

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APA (6th Edition):

Bonnard, A. (2016). Histone variant H2A.Z substitution mediated by the SWR1-like complex is a novel transcriptional regulatory mechanism controlling defense genes and immunity in plants. (Masters Thesis). Texas State University – San Marcos. Retrieved from https://digital.library.txstate.edu/handle/10877/7744

Chicago Manual of Style (16th Edition):

Bonnard, April. “Histone variant H2A.Z substitution mediated by the SWR1-like complex is a novel transcriptional regulatory mechanism controlling defense genes and immunity in plants.” 2016. Masters Thesis, Texas State University – San Marcos. Accessed April 14, 2021. https://digital.library.txstate.edu/handle/10877/7744.

MLA Handbook (7th Edition):

Bonnard, April. “Histone variant H2A.Z substitution mediated by the SWR1-like complex is a novel transcriptional regulatory mechanism controlling defense genes and immunity in plants.” 2016. Web. 14 Apr 2021.

Vancouver:

Bonnard A. Histone variant H2A.Z substitution mediated by the SWR1-like complex is a novel transcriptional regulatory mechanism controlling defense genes and immunity in plants. [Internet] [Masters thesis]. Texas State University – San Marcos; 2016. [cited 2021 Apr 14]. Available from: https://digital.library.txstate.edu/handle/10877/7744.

Council of Science Editors:

Bonnard A. Histone variant H2A.Z substitution mediated by the SWR1-like complex is a novel transcriptional regulatory mechanism controlling defense genes and immunity in plants. [Masters Thesis]. Texas State University – San Marcos; 2016. Available from: https://digital.library.txstate.edu/handle/10877/7744


University of Toronto

4. Dorman, Kathryn. The Role of CtBP in Pituitary Tumorigenesis.

Degree: 2010, University of Toronto

C-terminal Binding Protein (CtBP) is a transcriptional co-repressor that plays an important role in mammalian development and tumorigenesis. CtBP is known to interact with Ikaros,… (more)

Subjects/Keywords: Pituitary; CtBP; Chromatin Remodeling; Ikaros; 0307

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APA (6th Edition):

Dorman, K. (2010). The Role of CtBP in Pituitary Tumorigenesis. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/25555

Chicago Manual of Style (16th Edition):

Dorman, Kathryn. “The Role of CtBP in Pituitary Tumorigenesis.” 2010. Masters Thesis, University of Toronto. Accessed April 14, 2021. http://hdl.handle.net/1807/25555.

MLA Handbook (7th Edition):

Dorman, Kathryn. “The Role of CtBP in Pituitary Tumorigenesis.” 2010. Web. 14 Apr 2021.

Vancouver:

Dorman K. The Role of CtBP in Pituitary Tumorigenesis. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2021 Apr 14]. Available from: http://hdl.handle.net/1807/25555.

Council of Science Editors:

Dorman K. The Role of CtBP in Pituitary Tumorigenesis. [Masters Thesis]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/25555


University of California – San Francisco

5. Leonard, John Duncan. Mechanism of Nucleosome Sliding by the Human Chromatin Remodeling Enzyme SNF2h.

Degree: Biochemistry and Molecular Biology, 2014, University of California – San Francisco

Chromatin remodelers are molecular motors that reposition and restructure nucleosomes to regulate gene expression and genome organization. The human ATP-dependent chromatin assembly factor (ACF) is… (more)

Subjects/Keywords: Biochemistry; ATPase; chromatin; chromatin remodeling; molecular motor; nucleosome

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APA (6th Edition):

Leonard, J. D. (2014). Mechanism of Nucleosome Sliding by the Human Chromatin Remodeling Enzyme SNF2h. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/9rk47666

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):

Leonard, John Duncan. “Mechanism of Nucleosome Sliding by the Human Chromatin Remodeling Enzyme SNF2h.” 2014. Thesis, University of California – San Francisco. Accessed April 14, 2021. http://www.escholarship.org/uc/item/9rk47666.

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

MLA Handbook (7th Edition):

Leonard, John Duncan. “Mechanism of Nucleosome Sliding by the Human Chromatin Remodeling Enzyme SNF2h.” 2014. Web. 14 Apr 2021.

Vancouver:

Leonard JD. Mechanism of Nucleosome Sliding by the Human Chromatin Remodeling Enzyme SNF2h. [Internet] [Thesis]. University of California – San Francisco; 2014. [cited 2021 Apr 14]. Available from: http://www.escholarship.org/uc/item/9rk47666.

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

Council of Science Editors:

Leonard JD. Mechanism of Nucleosome Sliding by the Human Chromatin Remodeling Enzyme SNF2h. [Thesis]. University of California – San Francisco; 2014. Available from: http://www.escholarship.org/uc/item/9rk47666

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


Princeton University

6. Dann, Geoffrey Paul. Diverse Regulation of ISWI Family ATP-dependent Chromatin Remodeling Enzymes by Nucleosome Modifications .

Degree: PhD, 2017, Princeton University

 ATP-dependent chromatin remodelers regulate access to genetic information by controlling nucleosome positions in vivo. However, the mechanism by which remodelers discriminate between different nucleosome substrates… (more)

Subjects/Keywords: Chemical Biology; Chromatin Biology; Chromatin Remodeling; Epigenetics; Histones; Post-translational modifications

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APA (6th Edition):

Dann, G. P. (2017). Diverse Regulation of ISWI Family ATP-dependent Chromatin Remodeling Enzymes by Nucleosome Modifications . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp01j9602327k

Chicago Manual of Style (16th Edition):

Dann, Geoffrey Paul. “Diverse Regulation of ISWI Family ATP-dependent Chromatin Remodeling Enzymes by Nucleosome Modifications .” 2017. Doctoral Dissertation, Princeton University. Accessed April 14, 2021. http://arks.princeton.edu/ark:/88435/dsp01j9602327k.

MLA Handbook (7th Edition):

Dann, Geoffrey Paul. “Diverse Regulation of ISWI Family ATP-dependent Chromatin Remodeling Enzymes by Nucleosome Modifications .” 2017. Web. 14 Apr 2021.

Vancouver:

Dann GP. Diverse Regulation of ISWI Family ATP-dependent Chromatin Remodeling Enzymes by Nucleosome Modifications . [Internet] [Doctoral dissertation]. Princeton University; 2017. [cited 2021 Apr 14]. Available from: http://arks.princeton.edu/ark:/88435/dsp01j9602327k.

Council of Science Editors:

Dann GP. Diverse Regulation of ISWI Family ATP-dependent Chromatin Remodeling Enzymes by Nucleosome Modifications . [Doctoral Dissertation]. Princeton University; 2017. Available from: http://arks.princeton.edu/ark:/88435/dsp01j9602327k


Université de Grenoble

7. Aguilar Gurrieri, Carmen. Etudes structurales sur l'assemblage du nucléosome : Structural studies of Nucleosome Assembly.

Degree: Docteur es, Biologie structurale et nanobiologie, 2013, Université de Grenoble

Au sein du noyau, l'ADN est organise en chromatine dont l'unité de base est le nucléosome. La structure de la chromatine est très dynamique, ce… (more)

Subjects/Keywords: Nucleosome; Histone chaperone; Histones; Nucleosome assembly; Chromatin remodeling; Nap1; Nucleosome; Histone chaperone; Histones; Nucleosome assembly; Chromatin remodeling; Nap1

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APA (6th Edition):

Aguilar Gurrieri, C. (2013). Etudes structurales sur l'assemblage du nucléosome : Structural studies of Nucleosome Assembly. (Doctoral Dissertation). Université de Grenoble. Retrieved from http://www.theses.fr/2013GRENV017

Chicago Manual of Style (16th Edition):

Aguilar Gurrieri, Carmen. “Etudes structurales sur l'assemblage du nucléosome : Structural studies of Nucleosome Assembly.” 2013. Doctoral Dissertation, Université de Grenoble. Accessed April 14, 2021. http://www.theses.fr/2013GRENV017.

MLA Handbook (7th Edition):

Aguilar Gurrieri, Carmen. “Etudes structurales sur l'assemblage du nucléosome : Structural studies of Nucleosome Assembly.” 2013. Web. 14 Apr 2021.

Vancouver:

Aguilar Gurrieri C. Etudes structurales sur l'assemblage du nucléosome : Structural studies of Nucleosome Assembly. [Internet] [Doctoral dissertation]. Université de Grenoble; 2013. [cited 2021 Apr 14]. Available from: http://www.theses.fr/2013GRENV017.

Council of Science Editors:

Aguilar Gurrieri C. Etudes structurales sur l'assemblage du nucléosome : Structural studies of Nucleosome Assembly. [Doctoral Dissertation]. Université de Grenoble; 2013. Available from: http://www.theses.fr/2013GRENV017


University of Illinois – Urbana-Champaign

8. Echtenkamp, Frank. Characterization of the p23 interaction network.

Degree: PhD, 4094, 2015, University of Illinois – Urbana-Champaign

 Molecular chaperones have evolved to support the general stability and maintenance of the cellular proteome. Through their broad binding capacity, transient interactions, and high cellular… (more)

Subjects/Keywords: molecular chaperones; p23; Hsp90; chromatin remodeling; Remodels the Structure of Chromatin (RSC); Chaperone Interaction Network

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APA (6th Edition):

Echtenkamp, F. (2015). Characterization of the p23 interaction network. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/73034

Chicago Manual of Style (16th Edition):

Echtenkamp, Frank. “Characterization of the p23 interaction network.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed April 14, 2021. http://hdl.handle.net/2142/73034.

MLA Handbook (7th Edition):

Echtenkamp, Frank. “Characterization of the p23 interaction network.” 2015. Web. 14 Apr 2021.

Vancouver:

Echtenkamp F. Characterization of the p23 interaction network. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2021 Apr 14]. Available from: http://hdl.handle.net/2142/73034.

Council of Science Editors:

Echtenkamp F. Characterization of the p23 interaction network. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/73034


University of Pennsylvania

9. Kuhn, Terra. Nuclear Pore Proteins In Regulation Of Chromatin State And Gene Expression.

Degree: 2019, University of Pennsylvania

 Nuclear pore complexes are best known for their regulation of nucleocytoplasmic transport as integral components of the eukaryotic nuclear envelope. Over the years, their importance… (more)

Subjects/Keywords: Chromatin; Chromatin Remodeling; Chromatin Structure; Decondensation; Nuclear Pore Complex; Nuclear Pore Protein; Cell Biology; Genetics; Molecular Biology

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APA (6th Edition):

Kuhn, T. (2019). Nuclear Pore Proteins In Regulation Of Chromatin State And Gene Expression. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/3656

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):

Kuhn, Terra. “Nuclear Pore Proteins In Regulation Of Chromatin State And Gene Expression.” 2019. Thesis, University of Pennsylvania. Accessed April 14, 2021. https://repository.upenn.edu/edissertations/3656.

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

MLA Handbook (7th Edition):

Kuhn, Terra. “Nuclear Pore Proteins In Regulation Of Chromatin State And Gene Expression.” 2019. Web. 14 Apr 2021.

Vancouver:

Kuhn T. Nuclear Pore Proteins In Regulation Of Chromatin State And Gene Expression. [Internet] [Thesis]. University of Pennsylvania; 2019. [cited 2021 Apr 14]. Available from: https://repository.upenn.edu/edissertations/3656.

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

Council of Science Editors:

Kuhn T. Nuclear Pore Proteins In Regulation Of Chromatin State And Gene Expression. [Thesis]. University of Pennsylvania; 2019. Available from: https://repository.upenn.edu/edissertations/3656

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


Universiteit Utrecht

10. Soete, G.A.J. Cell fate determination in the Caenorhabditis elegans epidermal lineages.

Degree: 2007, Universiteit Utrecht

 The starting point for this work was to use the hypodermal seam of C. elegans as a model system to study cell fate determination. Even… (more)

Subjects/Keywords: Biologie; C. elegans; cell fate; patterning; chromatin remodeling; trithorax; cancer

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APA (6th Edition):

Soete, G. A. J. (2007). Cell fate determination in the Caenorhabditis elegans epidermal lineages. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/21400

Chicago Manual of Style (16th Edition):

Soete, G A J. “Cell fate determination in the Caenorhabditis elegans epidermal lineages.” 2007. Doctoral Dissertation, Universiteit Utrecht. Accessed April 14, 2021. http://dspace.library.uu.nl:8080/handle/1874/21400.

MLA Handbook (7th Edition):

Soete, G A J. “Cell fate determination in the Caenorhabditis elegans epidermal lineages.” 2007. Web. 14 Apr 2021.

Vancouver:

Soete GAJ. Cell fate determination in the Caenorhabditis elegans epidermal lineages. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2007. [cited 2021 Apr 14]. Available from: http://dspace.library.uu.nl:8080/handle/1874/21400.

Council of Science Editors:

Soete GAJ. Cell fate determination in the Caenorhabditis elegans epidermal lineages. [Doctoral Dissertation]. Universiteit Utrecht; 2007. Available from: http://dspace.library.uu.nl:8080/handle/1874/21400


University of Alberta

11. Van de Vosse, David W. A role for the nuclear pore complex protein Nup170p in defining chromatin structure and regulating gene expression.

Degree: PhD, Department of Cell Biology, 2012, University of Alberta

 The spatial organization of chromosomal loci within the nucleus can have a significant influence on transcriptional activity. Transcriptionally active genes are generally positioned within the… (more)

Subjects/Keywords: chromatin remodeling; telomere; heterochromatin; yeast; nuclear pore complex; epigenetic gene regulation

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APA (6th Edition):

Van de Vosse, D. W. (2012). A role for the nuclear pore complex protein Nup170p in defining chromatin structure and regulating gene expression. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/fj2362335

Chicago Manual of Style (16th Edition):

Van de Vosse, David W. “A role for the nuclear pore complex protein Nup170p in defining chromatin structure and regulating gene expression.” 2012. Doctoral Dissertation, University of Alberta. Accessed April 14, 2021. https://era.library.ualberta.ca/files/fj2362335.

MLA Handbook (7th Edition):

Van de Vosse, David W. “A role for the nuclear pore complex protein Nup170p in defining chromatin structure and regulating gene expression.” 2012. Web. 14 Apr 2021.

Vancouver:

Van de Vosse DW. A role for the nuclear pore complex protein Nup170p in defining chromatin structure and regulating gene expression. [Internet] [Doctoral dissertation]. University of Alberta; 2012. [cited 2021 Apr 14]. Available from: https://era.library.ualberta.ca/files/fj2362335.

Council of Science Editors:

Van de Vosse DW. A role for the nuclear pore complex protein Nup170p in defining chromatin structure and regulating gene expression. [Doctoral Dissertation]. University of Alberta; 2012. Available from: https://era.library.ualberta.ca/files/fj2362335


Vanderbilt University

12. Burns, Laura Titus. Nuclear Structure in Budding yeast: Impacts of Chromatin Organization and Gene Expression.

Degree: PhD, Cell and Developmental Biology, 2013, Vanderbilt University

 The genome of a eukaryotic cell tightly packed within the nucleus with a high degree of structural organization. Two mechanisms accounting for nuclear structure and… (more)

Subjects/Keywords: nuclear structure; transcription; chromatin remodeling; MAP kinase signalling

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APA (6th Edition):

Burns, L. T. (2013). Nuclear Structure in Budding yeast: Impacts of Chromatin Organization and Gene Expression. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14815

Chicago Manual of Style (16th Edition):

Burns, Laura Titus. “Nuclear Structure in Budding yeast: Impacts of Chromatin Organization and Gene Expression.” 2013. Doctoral Dissertation, Vanderbilt University. Accessed April 14, 2021. http://hdl.handle.net/1803/14815.

MLA Handbook (7th Edition):

Burns, Laura Titus. “Nuclear Structure in Budding yeast: Impacts of Chromatin Organization and Gene Expression.” 2013. Web. 14 Apr 2021.

Vancouver:

Burns LT. Nuclear Structure in Budding yeast: Impacts of Chromatin Organization and Gene Expression. [Internet] [Doctoral dissertation]. Vanderbilt University; 2013. [cited 2021 Apr 14]. Available from: http://hdl.handle.net/1803/14815.

Council of Science Editors:

Burns LT. Nuclear Structure in Budding yeast: Impacts of Chromatin Organization and Gene Expression. [Doctoral Dissertation]. Vanderbilt University; 2013. Available from: http://hdl.handle.net/1803/14815

13. 조, 수진. A functional role of chromatin remodeling factor, Rsf-1 in the DNA damage signaling pathway.

Degree: 2014, Ajou University

As a member of imitation switch (ISWI) family in ATP-dependent chromatin remodeling factors, RSF complex consists of SNF2h ATPase and Rsf-1. Although it has been… (more)

Subjects/Keywords: DNA damage; chromatin remodeling factor; Rsf-1; PARP1; DNA damage checkpoint

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APA (6th Edition):

조, . (2014). A functional role of chromatin remodeling factor, Rsf-1 in the DNA damage signaling pathway. (Thesis). Ajou University. Retrieved from http://repository.ajou.ac.kr/handle/201003/10857 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000016596

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):

조, 수진. “A functional role of chromatin remodeling factor, Rsf-1 in the DNA damage signaling pathway.” 2014. Thesis, Ajou University. Accessed April 14, 2021. http://repository.ajou.ac.kr/handle/201003/10857 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000016596.

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

MLA Handbook (7th Edition):

조, 수진. “A functional role of chromatin remodeling factor, Rsf-1 in the DNA damage signaling pathway.” 2014. Web. 14 Apr 2021.

Vancouver:

조 . A functional role of chromatin remodeling factor, Rsf-1 in the DNA damage signaling pathway. [Internet] [Thesis]. Ajou University; 2014. [cited 2021 Apr 14]. Available from: http://repository.ajou.ac.kr/handle/201003/10857 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000016596.

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

Council of Science Editors:

조 . A functional role of chromatin remodeling factor, Rsf-1 in the DNA damage signaling pathway. [Thesis]. Ajou University; 2014. Available from: http://repository.ajou.ac.kr/handle/201003/10857 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000016596

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


University of Ottawa

14. Nguyen, Thinh. CDX2 Regulates Gene Expression Through Recruitment of BRG1-Associated SWI/SNF Chromatin Remodeling Activity .

Degree: 2016, University of Ottawa

 The packaging of genomic DNA into nucleosomes creates a barrier to transcription which can be relieved through ATP-dependent chromatin remodeling via complexes such as the… (more)

Subjects/Keywords: Cdx2; transcription; Brg1; SWI/SNF; Chromatin Remodeling; development

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APA (6th Edition):

Nguyen, T. (2016). CDX2 Regulates Gene Expression Through Recruitment of BRG1-Associated SWI/SNF Chromatin Remodeling Activity . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/35377

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):

Nguyen, Thinh. “CDX2 Regulates Gene Expression Through Recruitment of BRG1-Associated SWI/SNF Chromatin Remodeling Activity .” 2016. Thesis, University of Ottawa. Accessed April 14, 2021. http://hdl.handle.net/10393/35377.

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

MLA Handbook (7th Edition):

Nguyen, Thinh. “CDX2 Regulates Gene Expression Through Recruitment of BRG1-Associated SWI/SNF Chromatin Remodeling Activity .” 2016. Web. 14 Apr 2021.

Vancouver:

Nguyen T. CDX2 Regulates Gene Expression Through Recruitment of BRG1-Associated SWI/SNF Chromatin Remodeling Activity . [Internet] [Thesis]. University of Ottawa; 2016. [cited 2021 Apr 14]. Available from: http://hdl.handle.net/10393/35377.

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

Council of Science Editors:

Nguyen T. CDX2 Regulates Gene Expression Through Recruitment of BRG1-Associated SWI/SNF Chromatin Remodeling Activity . [Thesis]. University of Ottawa; 2016. Available from: http://hdl.handle.net/10393/35377

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


University of Washington

15. Lee, Laura Jane. Regulation of chromatin structure in genome stability.

Degree: PhD, 2016, University of Washington

 In eukaryotic cells, DNA is tightly packaged into chromatin. Because chromatin is inhibitory to DNA-binding proteins, it must be modified so that necessary DNA-protein interactions… (more)

Subjects/Keywords: chromatin remodeling; genome stability; Molecular biology; molecular and cellular biology

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APA (6th Edition):

Lee, L. J. (2016). Regulation of chromatin structure in genome stability. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/35621

Chicago Manual of Style (16th Edition):

Lee, Laura Jane. “Regulation of chromatin structure in genome stability.” 2016. Doctoral Dissertation, University of Washington. Accessed April 14, 2021. http://hdl.handle.net/1773/35621.

MLA Handbook (7th Edition):

Lee, Laura Jane. “Regulation of chromatin structure in genome stability.” 2016. Web. 14 Apr 2021.

Vancouver:

Lee LJ. Regulation of chromatin structure in genome stability. [Internet] [Doctoral dissertation]. University of Washington; 2016. [cited 2021 Apr 14]. Available from: http://hdl.handle.net/1773/35621.

Council of Science Editors:

Lee LJ. Regulation of chromatin structure in genome stability. [Doctoral Dissertation]. University of Washington; 2016. Available from: http://hdl.handle.net/1773/35621

16. LIU CHANG. Regulation of Floral Patterning By Flowering Time Genes.

Degree: 2009, National University of Singapore

Subjects/Keywords: Floral patterning; MADS; chromatin remodeling

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APA (6th Edition):

CHANG, L. (2009). Regulation of Floral Patterning By Flowering Time Genes. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/16279

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):

CHANG, LIU. “Regulation of Floral Patterning By Flowering Time Genes.” 2009. Thesis, National University of Singapore. Accessed April 14, 2021. http://scholarbank.nus.edu.sg/handle/10635/16279.

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

MLA Handbook (7th Edition):

CHANG, LIU. “Regulation of Floral Patterning By Flowering Time Genes.” 2009. Web. 14 Apr 2021.

Vancouver:

CHANG L. Regulation of Floral Patterning By Flowering Time Genes. [Internet] [Thesis]. National University of Singapore; 2009. [cited 2021 Apr 14]. Available from: http://scholarbank.nus.edu.sg/handle/10635/16279.

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

Council of Science Editors:

CHANG L. Regulation of Floral Patterning By Flowering Time Genes. [Thesis]. National University of Singapore; 2009. Available from: http://scholarbank.nus.edu.sg/handle/10635/16279

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


University of Edinburgh

17. Burrage, Joseph. Analysis of the function of LSH in DNA damage repair.

Degree: PhD, 2013, University of Edinburgh

 DNA damage from both normal metabolic activities and environmental factors such as UV and radiation can cause as many as 1 million individual lesions to… (more)

Subjects/Keywords: 572.8; chromatin remodeling; DNA damage; lymphoid sepcific helicase; LSH

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APA (6th Edition):

Burrage, J. (2013). Analysis of the function of LSH in DNA damage repair. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/9416

Chicago Manual of Style (16th Edition):

Burrage, Joseph. “Analysis of the function of LSH in DNA damage repair.” 2013. Doctoral Dissertation, University of Edinburgh. Accessed April 14, 2021. http://hdl.handle.net/1842/9416.

MLA Handbook (7th Edition):

Burrage, Joseph. “Analysis of the function of LSH in DNA damage repair.” 2013. Web. 14 Apr 2021.

Vancouver:

Burrage J. Analysis of the function of LSH in DNA damage repair. [Internet] [Doctoral dissertation]. University of Edinburgh; 2013. [cited 2021 Apr 14]. Available from: http://hdl.handle.net/1842/9416.

Council of Science Editors:

Burrage J. Analysis of the function of LSH in DNA damage repair. [Doctoral Dissertation]. University of Edinburgh; 2013. Available from: http://hdl.handle.net/1842/9416


Louisiana State University

18. Avva, S. V. Satya Prakash. Characterization of Boundary Element-Associated Factors BEAF-32A and BEAF-32B and Identification of Novel Interaction Partners in Drosophila Melanogaster.

Degree: PhD, 2016, Louisiana State University

 Regulatory elements are DNA sequences which have specialized activities that coordinate the functions of the genome. Promoters, enhancers, locus control regions, boundary elements (or insulator… (more)

Subjects/Keywords: BEAF-32; Chromatin Remodeling; Insulators; Topologically Associating Domains (TADs)

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APA (6th Edition):

Avva, S. V. S. P. (2016). Characterization of Boundary Element-Associated Factors BEAF-32A and BEAF-32B and Identification of Novel Interaction Partners in Drosophila Melanogaster. (Doctoral Dissertation). Louisiana State University. Retrieved from etd-07072016-122243 ; https://digitalcommons.lsu.edu/gradschool_dissertations/617

Chicago Manual of Style (16th Edition):

Avva, S V Satya Prakash. “Characterization of Boundary Element-Associated Factors BEAF-32A and BEAF-32B and Identification of Novel Interaction Partners in Drosophila Melanogaster.” 2016. Doctoral Dissertation, Louisiana State University. Accessed April 14, 2021. etd-07072016-122243 ; https://digitalcommons.lsu.edu/gradschool_dissertations/617.

MLA Handbook (7th Edition):

Avva, S V Satya Prakash. “Characterization of Boundary Element-Associated Factors BEAF-32A and BEAF-32B and Identification of Novel Interaction Partners in Drosophila Melanogaster.” 2016. Web. 14 Apr 2021.

Vancouver:

Avva SVSP. Characterization of Boundary Element-Associated Factors BEAF-32A and BEAF-32B and Identification of Novel Interaction Partners in Drosophila Melanogaster. [Internet] [Doctoral dissertation]. Louisiana State University; 2016. [cited 2021 Apr 14]. Available from: etd-07072016-122243 ; https://digitalcommons.lsu.edu/gradschool_dissertations/617.

Council of Science Editors:

Avva SVSP. Characterization of Boundary Element-Associated Factors BEAF-32A and BEAF-32B and Identification of Novel Interaction Partners in Drosophila Melanogaster. [Doctoral Dissertation]. Louisiana State University; 2016. Available from: etd-07072016-122243 ; https://digitalcommons.lsu.edu/gradschool_dissertations/617


University of Kansas

19. Al-Ani, Gada K. Elucidation of the Mechanisms of Nucleosome Binding and Repositioning by a Chromatin Remodeler: Monomeric ISWI Remodels Nucleosomes Through a Random Walk.

Degree: PhD, Molecular Biosciences, 2014, University of Kansas

 The regulation of chromatin structure is controlled by a family of molecular motors called chromatin remodelers. The ability of these enzymes to remodel chromatin structure… (more)

Subjects/Keywords: Biology; Biochemistry; Molecular biology; ATPase; Chromatin; ISWI; Nuclesomes; Remodeling; Repositioning

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APA (6th Edition):

Al-Ani, G. K. (2014). Elucidation of the Mechanisms of Nucleosome Binding and Repositioning by a Chromatin Remodeler: Monomeric ISWI Remodels Nucleosomes Through a Random Walk. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/16838

Chicago Manual of Style (16th Edition):

Al-Ani, Gada K. “Elucidation of the Mechanisms of Nucleosome Binding and Repositioning by a Chromatin Remodeler: Monomeric ISWI Remodels Nucleosomes Through a Random Walk.” 2014. Doctoral Dissertation, University of Kansas. Accessed April 14, 2021. http://hdl.handle.net/1808/16838.

MLA Handbook (7th Edition):

Al-Ani, Gada K. “Elucidation of the Mechanisms of Nucleosome Binding and Repositioning by a Chromatin Remodeler: Monomeric ISWI Remodels Nucleosomes Through a Random Walk.” 2014. Web. 14 Apr 2021.

Vancouver:

Al-Ani GK. Elucidation of the Mechanisms of Nucleosome Binding and Repositioning by a Chromatin Remodeler: Monomeric ISWI Remodels Nucleosomes Through a Random Walk. [Internet] [Doctoral dissertation]. University of Kansas; 2014. [cited 2021 Apr 14]. Available from: http://hdl.handle.net/1808/16838.

Council of Science Editors:

Al-Ani GK. Elucidation of the Mechanisms of Nucleosome Binding and Repositioning by a Chromatin Remodeler: Monomeric ISWI Remodels Nucleosomes Through a Random Walk. [Doctoral Dissertation]. University of Kansas; 2014. Available from: http://hdl.handle.net/1808/16838


Georgia State University

20. Carter, Christie. The RNA Helicase p68 Regulates Transcription by Facilitating Chromatin Remodeling.

Degree: PhD, Biology, 2009, Georgia State University

  P68 is a prototypical member of the DEAD box RNA helicase family. Implicated in numerous functions such as cell proliferation, cancer metastasis, transcription regulation… (more)

Subjects/Keywords: chromatin remodeling; transcription; p68; Biology

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

APA (6th Edition):

Carter, C. (2009). The RNA Helicase p68 Regulates Transcription by Facilitating Chromatin Remodeling. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/biology_diss/60

Chicago Manual of Style (16th Edition):

Carter, Christie. “The RNA Helicase p68 Regulates Transcription by Facilitating Chromatin Remodeling.” 2009. Doctoral Dissertation, Georgia State University. Accessed April 14, 2021. https://scholarworks.gsu.edu/biology_diss/60.

MLA Handbook (7th Edition):

Carter, Christie. “The RNA Helicase p68 Regulates Transcription by Facilitating Chromatin Remodeling.” 2009. Web. 14 Apr 2021.

Vancouver:

Carter C. The RNA Helicase p68 Regulates Transcription by Facilitating Chromatin Remodeling. [Internet] [Doctoral dissertation]. Georgia State University; 2009. [cited 2021 Apr 14]. Available from: https://scholarworks.gsu.edu/biology_diss/60.

Council of Science Editors:

Carter C. The RNA Helicase p68 Regulates Transcription by Facilitating Chromatin Remodeling. [Doctoral Dissertation]. Georgia State University; 2009. Available from: https://scholarworks.gsu.edu/biology_diss/60


University of California – San Francisco

21. Alexander, Jeffrey M. Stage-specific Chromatin Modification and Regulation in Cardiomyocyte Differentiation.

Degree: Biomedical Sciences, 2012, University of California – San Francisco

 Development of a properly formed heart is vital to life and defects in cardiogenesis lead to congenital heart disease. Central to this process is the… (more)

Subjects/Keywords: Developmental biology; Cellular biology; Molecular biology; Brg1; Cardiomyocyte differentiation; Chromatin; Chromatin remodeling; Embryonic stem cells; Histone modifications

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APA (6th Edition):

Alexander, J. M. (2012). Stage-specific Chromatin Modification and Regulation in Cardiomyocyte Differentiation. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/4z40n0ft

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):

Alexander, Jeffrey M. “Stage-specific Chromatin Modification and Regulation in Cardiomyocyte Differentiation.” 2012. Thesis, University of California – San Francisco. Accessed April 14, 2021. http://www.escholarship.org/uc/item/4z40n0ft.

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

MLA Handbook (7th Edition):

Alexander, Jeffrey M. “Stage-specific Chromatin Modification and Regulation in Cardiomyocyte Differentiation.” 2012. Web. 14 Apr 2021.

Vancouver:

Alexander JM. Stage-specific Chromatin Modification and Regulation in Cardiomyocyte Differentiation. [Internet] [Thesis]. University of California – San Francisco; 2012. [cited 2021 Apr 14]. Available from: http://www.escholarship.org/uc/item/4z40n0ft.

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

Council of Science Editors:

Alexander JM. Stage-specific Chromatin Modification and Regulation in Cardiomyocyte Differentiation. [Thesis]. University of California – San Francisco; 2012. Available from: http://www.escholarship.org/uc/item/4z40n0ft

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


Texas A&M University

22. Jessen, Walter Joseph. Chromatin dynamics at the Saccharomyces cerevisiae PHO5 promoter.

Degree: PhD, Biochemistry, 2006, Texas A&M University

 In eukaryotes, the organization of DNA into chromatin is a primary determinant of gene expression. Positioned nucleosomes in promoter regions are frequently found to regulate… (more)

Subjects/Keywords: PHO5; promoter; chromatin; remodeling; nucleosome; accessibility

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APA (6th Edition):

Jessen, W. J. (2006). Chromatin dynamics at the Saccharomyces cerevisiae PHO5 promoter. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/3306

Chicago Manual of Style (16th Edition):

Jessen, Walter Joseph. “Chromatin dynamics at the Saccharomyces cerevisiae PHO5 promoter.” 2006. Doctoral Dissertation, Texas A&M University. Accessed April 14, 2021. http://hdl.handle.net/1969.1/3306.

MLA Handbook (7th Edition):

Jessen, Walter Joseph. “Chromatin dynamics at the Saccharomyces cerevisiae PHO5 promoter.” 2006. Web. 14 Apr 2021.

Vancouver:

Jessen WJ. Chromatin dynamics at the Saccharomyces cerevisiae PHO5 promoter. [Internet] [Doctoral dissertation]. Texas A&M University; 2006. [cited 2021 Apr 14]. Available from: http://hdl.handle.net/1969.1/3306.

Council of Science Editors:

Jessen WJ. Chromatin dynamics at the Saccharomyces cerevisiae PHO5 promoter. [Doctoral Dissertation]. Texas A&M University; 2006. Available from: http://hdl.handle.net/1969.1/3306


Penn State University

23. Chandy, Mark. HISTONE MODIFICATIONS INFLUENCE CHROMATIN MODIFYING AND CHROMATIN REMODELING COMPLEXES .

Degree: 2008, Penn State University

Chromatin condenses DNA and packages it into the nucleus. The fundamental unit of chromatin is the nucleosome, which compacts and forms higher order structures. Chromatin(more)

Subjects/Keywords: SAGA; SWI/SNF; chromatin remodeling; bromodomain

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APA (6th Edition):

Chandy, M. (2008). HISTONE MODIFICATIONS INFLUENCE CHROMATIN MODIFYING AND CHROMATIN REMODELING COMPLEXES . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/6926

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):

Chandy, Mark. “HISTONE MODIFICATIONS INFLUENCE CHROMATIN MODIFYING AND CHROMATIN REMODELING COMPLEXES .” 2008. Thesis, Penn State University. Accessed April 14, 2021. https://submit-etda.libraries.psu.edu/catalog/6926.

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

MLA Handbook (7th Edition):

Chandy, Mark. “HISTONE MODIFICATIONS INFLUENCE CHROMATIN MODIFYING AND CHROMATIN REMODELING COMPLEXES .” 2008. Web. 14 Apr 2021.

Vancouver:

Chandy M. HISTONE MODIFICATIONS INFLUENCE CHROMATIN MODIFYING AND CHROMATIN REMODELING COMPLEXES . [Internet] [Thesis]. Penn State University; 2008. [cited 2021 Apr 14]. Available from: https://submit-etda.libraries.psu.edu/catalog/6926.

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

Council of Science Editors:

Chandy M. HISTONE MODIFICATIONS INFLUENCE CHROMATIN MODIFYING AND CHROMATIN REMODELING COMPLEXES . [Thesis]. Penn State University; 2008. Available from: https://submit-etda.libraries.psu.edu/catalog/6926

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

24. Sandoz, Jérémy. Rôles de TFIIH dans l’ouverture du promoteur et le remodelage de la chromatine lors la transcription des gènes de classe II : Roles of TFIIH in promoter opening and chromatin remodeling during class II genes transcription.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2019, Université de Strasbourg

La synthèse des ARN messagers est un processus hautement régulé. Pendant l’initiation de la transcription, un nombre important de protéines est recruté au niveau du… (more)

Subjects/Keywords: TFIIH; XPB; Ouverture du promoteur; Remodelage chromatinien; TFIIH; XPB; Promoter opening; Chromatin remodeling; 572.8

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APA (6th Edition):

Sandoz, J. (2019). Rôles de TFIIH dans l’ouverture du promoteur et le remodelage de la chromatine lors la transcription des gènes de classe II : Roles of TFIIH in promoter opening and chromatin remodeling during class II genes transcription. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2019STRAJ027

Chicago Manual of Style (16th Edition):

Sandoz, Jérémy. “Rôles de TFIIH dans l’ouverture du promoteur et le remodelage de la chromatine lors la transcription des gènes de classe II : Roles of TFIIH in promoter opening and chromatin remodeling during class II genes transcription.” 2019. Doctoral Dissertation, Université de Strasbourg. Accessed April 14, 2021. http://www.theses.fr/2019STRAJ027.

MLA Handbook (7th Edition):

Sandoz, Jérémy. “Rôles de TFIIH dans l’ouverture du promoteur et le remodelage de la chromatine lors la transcription des gènes de classe II : Roles of TFIIH in promoter opening and chromatin remodeling during class II genes transcription.” 2019. Web. 14 Apr 2021.

Vancouver:

Sandoz J. Rôles de TFIIH dans l’ouverture du promoteur et le remodelage de la chromatine lors la transcription des gènes de classe II : Roles of TFIIH in promoter opening and chromatin remodeling during class II genes transcription. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2019. [cited 2021 Apr 14]. Available from: http://www.theses.fr/2019STRAJ027.

Council of Science Editors:

Sandoz J. Rôles de TFIIH dans l’ouverture du promoteur et le remodelage de la chromatine lors la transcription des gènes de classe II : Roles of TFIIH in promoter opening and chromatin remodeling during class II genes transcription. [Doctoral Dissertation]. Université de Strasbourg; 2019. Available from: http://www.theses.fr/2019STRAJ027


Freie Universität Berlin

25. Schlesinger, Jenny. Transkriptionelle und epigenetische Regulation kardialer Genexpression und Identifikation eines neuen Chromatin Remodeling Faktors.

Degree: 2011, Freie Universität Berlin

 Für die Entwicklung und Aufrechterhaltung aller eukaryotischen Organismen muss die zeitliche und zellspezifische Expression von Genen durch einen umfassenden Satz von verschiedenen zellulären Mechanismen reguliert… (more)

Subjects/Keywords: heart; gene regulation; histone modifications; chromatin remodeling; 500 Naturwissenschaften und Mathematik::570 Biowissenschaften; Biologie

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APA (6th Edition):

Schlesinger, J. (2011). Transkriptionelle und epigenetische Regulation kardialer Genexpression und Identifikation eines neuen Chromatin Remodeling Faktors. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-9808

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):

Schlesinger, Jenny. “Transkriptionelle und epigenetische Regulation kardialer Genexpression und Identifikation eines neuen Chromatin Remodeling Faktors.” 2011. Thesis, Freie Universität Berlin. Accessed April 14, 2021. http://dx.doi.org/10.17169/refubium-9808.

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

MLA Handbook (7th Edition):

Schlesinger, Jenny. “Transkriptionelle und epigenetische Regulation kardialer Genexpression und Identifikation eines neuen Chromatin Remodeling Faktors.” 2011. Web. 14 Apr 2021.

Vancouver:

Schlesinger J. Transkriptionelle und epigenetische Regulation kardialer Genexpression und Identifikation eines neuen Chromatin Remodeling Faktors. [Internet] [Thesis]. Freie Universität Berlin; 2011. [cited 2021 Apr 14]. Available from: http://dx.doi.org/10.17169/refubium-9808.

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

Council of Science Editors:

Schlesinger J. Transkriptionelle und epigenetische Regulation kardialer Genexpression und Identifikation eines neuen Chromatin Remodeling Faktors. [Thesis]. Freie Universität Berlin; 2011. Available from: http://dx.doi.org/10.17169/refubium-9808

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

26. 민, 선우. The role of RSF1 in DNA damage signaling pathway and DSB-induced transcriptional regulation.

Degree: 2018, Ajou University

Chromatin remodeling factors are known as a key determinant of chromatin modification in DNA replication, transcription, and double strand break (DSB) repair. As a member… (more)

Subjects/Keywords: DNA damage response; DNA repair; Chromatin remodeling factor; DSB-induced transcriptional silencing

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APA (6th Edition):

민, . (2018). The role of RSF1 in DNA damage signaling pathway and DSB-induced transcriptional regulation. (Thesis). Ajou University. Retrieved from http://repository.ajou.ac.kr/handle/201003/16567 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000027270

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):

민, 선우. “The role of RSF1 in DNA damage signaling pathway and DSB-induced transcriptional regulation.” 2018. Thesis, Ajou University. Accessed April 14, 2021. http://repository.ajou.ac.kr/handle/201003/16567 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000027270.

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

MLA Handbook (7th Edition):

민, 선우. “The role of RSF1 in DNA damage signaling pathway and DSB-induced transcriptional regulation.” 2018. Web. 14 Apr 2021.

Vancouver:

민 . The role of RSF1 in DNA damage signaling pathway and DSB-induced transcriptional regulation. [Internet] [Thesis]. Ajou University; 2018. [cited 2021 Apr 14]. Available from: http://repository.ajou.ac.kr/handle/201003/16567 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000027270.

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

Council of Science Editors:

민 . The role of RSF1 in DNA damage signaling pathway and DSB-induced transcriptional regulation. [Thesis]. Ajou University; 2018. Available from: http://repository.ajou.ac.kr/handle/201003/16567 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000027270

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

27. G. Barbagiovanni. NEURONAL TRANSDIFFERENTIATION: UNCOVERING THE ROLE OF MLL1 AND MLL2 DURING LINEAGE CONVERSION.

Degree: 2017, Università degli Studi di Milano

 Neuronal transdifferentiation entails the direct conversion between mouse embryonic fibroblasts (MEFs) and induced neuronal cells (iNs), through the expression of the neuronal-specific transcription factors Brn2,… (more)

Subjects/Keywords: Transdifferentiation; Trithorax; MLL2; MLL1; Neurons; Chromatin remodeling; Epigenetics; Settore BIO/11 - Biologia Molecolare

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APA (6th Edition):

Barbagiovanni, G. (2017). NEURONAL TRANSDIFFERENTIATION: UNCOVERING THE ROLE OF MLL1 AND MLL2 DURING LINEAGE CONVERSION. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/468287

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):

Barbagiovanni, G.. “NEURONAL TRANSDIFFERENTIATION: UNCOVERING THE ROLE OF MLL1 AND MLL2 DURING LINEAGE CONVERSION.” 2017. Thesis, Università degli Studi di Milano. Accessed April 14, 2021. http://hdl.handle.net/2434/468287.

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

MLA Handbook (7th Edition):

Barbagiovanni, G.. “NEURONAL TRANSDIFFERENTIATION: UNCOVERING THE ROLE OF MLL1 AND MLL2 DURING LINEAGE CONVERSION.” 2017. Web. 14 Apr 2021.

Vancouver:

Barbagiovanni G. NEURONAL TRANSDIFFERENTIATION: UNCOVERING THE ROLE OF MLL1 AND MLL2 DURING LINEAGE CONVERSION. [Internet] [Thesis]. Università degli Studi di Milano; 2017. [cited 2021 Apr 14]. Available from: http://hdl.handle.net/2434/468287.

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

Council of Science Editors:

Barbagiovanni G. NEURONAL TRANSDIFFERENTIATION: UNCOVERING THE ROLE OF MLL1 AND MLL2 DURING LINEAGE CONVERSION. [Thesis]. Università degli Studi di Milano; 2017. Available from: http://hdl.handle.net/2434/468287

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


University of California – San Francisco

28. Stewart, Kathleen Marie. The Role of SWI/SNF Chromatin Remodeling in Breast Tumorigenesis.

Degree: Biomedical Sciences, 2010, University of California – San Francisco

 Mammary epithelial cell (MEC)-extracellular matrix (ECM) interactions are critical for normal breast tissue development, differentiation and homeostasis by engaging a repertoire of ECM adhesion receptors… (more)

Subjects/Keywords: Biology, Cell; Biology, Molecular; Breast; Breast Cancer; Chromatin remodeling; Integrin; SWI/SNF

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APA (6th Edition):

Stewart, K. M. (2010). The Role of SWI/SNF Chromatin Remodeling in Breast Tumorigenesis. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/0645d0zw

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):

Stewart, Kathleen Marie. “The Role of SWI/SNF Chromatin Remodeling in Breast Tumorigenesis.” 2010. Thesis, University of California – San Francisco. Accessed April 14, 2021. http://www.escholarship.org/uc/item/0645d0zw.

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

MLA Handbook (7th Edition):

Stewart, Kathleen Marie. “The Role of SWI/SNF Chromatin Remodeling in Breast Tumorigenesis.” 2010. Web. 14 Apr 2021.

Vancouver:

Stewart KM. The Role of SWI/SNF Chromatin Remodeling in Breast Tumorigenesis. [Internet] [Thesis]. University of California – San Francisco; 2010. [cited 2021 Apr 14]. Available from: http://www.escholarship.org/uc/item/0645d0zw.

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

Council of Science Editors:

Stewart KM. The Role of SWI/SNF Chromatin Remodeling in Breast Tumorigenesis. [Thesis]. University of California – San Francisco; 2010. Available from: http://www.escholarship.org/uc/item/0645d0zw

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


University of California – San Francisco

29. Engel, Karin Buser. Participation of Regulatory Factors and the Coregulator Brm in the Combinatorial Control of Transcription.

Degree: Chemistry and Chemical Biology, 2011, University of California – San Francisco

 Metazoan transcriptional regulation is governed by combinatorial control, in which distinct multifactor regulatory complexes composed of various combinations of factors assemble at different genomic sites.… (more)

Subjects/Keywords: Molecular Biology; chromatin remodeling; combinatorial control; glucocorticoid receptor; NFkappaB; Swi/Snf; transcriptional regulation

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

APA (6th Edition):

Engel, K. B. (2011). Participation of Regulatory Factors and the Coregulator Brm in the Combinatorial Control of Transcription. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/1c55146w

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):

Engel, Karin Buser. “Participation of Regulatory Factors and the Coregulator Brm in the Combinatorial Control of Transcription.” 2011. Thesis, University of California – San Francisco. Accessed April 14, 2021. http://www.escholarship.org/uc/item/1c55146w.

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

MLA Handbook (7th Edition):

Engel, Karin Buser. “Participation of Regulatory Factors and the Coregulator Brm in the Combinatorial Control of Transcription.” 2011. Web. 14 Apr 2021.

Vancouver:

Engel KB. Participation of Regulatory Factors and the Coregulator Brm in the Combinatorial Control of Transcription. [Internet] [Thesis]. University of California – San Francisco; 2011. [cited 2021 Apr 14]. Available from: http://www.escholarship.org/uc/item/1c55146w.

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

Council of Science Editors:

Engel KB. Participation of Regulatory Factors and the Coregulator Brm in the Combinatorial Control of Transcription. [Thesis]. University of California – San Francisco; 2011. Available from: http://www.escholarship.org/uc/item/1c55146w

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


University of Illinois – Chicago

30. Chase, Kayla A. Histone Methyltransferases (GLP, G9a, SETDB1) and H3K9me2; Regulation in Psychiatric Disorders.

Degree: 2012, University of Illinois – Chicago

 Histone Methyltransferases and Restrictive Chromatin; Regulation in Psychiatric Disorders Kayla A. Chase, Ph.D. Department of Neuroscience University of Illinois at Chicago Chicago, Illinois (2013) Dissertation… (more)

Subjects/Keywords: Schizophrenia; Epigenetics; Chromatin; Remodeling; Histone; Neuron; Lymphocyte; Culture; Nicotine; HDAC; Valproic Acid; Trichostatin A; Cortex

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

APA (6th Edition):

Chase, K. A. (2012). Histone Methyltransferases (GLP, G9a, SETDB1) and H3K9me2; Regulation in Psychiatric Disorders. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/9301

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):

Chase, Kayla A. “Histone Methyltransferases (GLP, G9a, SETDB1) and H3K9me2; Regulation in Psychiatric Disorders.” 2012. Thesis, University of Illinois – Chicago. Accessed April 14, 2021. http://hdl.handle.net/10027/9301.

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

MLA Handbook (7th Edition):

Chase, Kayla A. “Histone Methyltransferases (GLP, G9a, SETDB1) and H3K9me2; Regulation in Psychiatric Disorders.” 2012. Web. 14 Apr 2021.

Vancouver:

Chase KA. Histone Methyltransferases (GLP, G9a, SETDB1) and H3K9me2; Regulation in Psychiatric Disorders. [Internet] [Thesis]. University of Illinois – Chicago; 2012. [cited 2021 Apr 14]. Available from: http://hdl.handle.net/10027/9301.

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

Council of Science Editors:

Chase KA. Histone Methyltransferases (GLP, G9a, SETDB1) and H3K9me2; Regulation in Psychiatric Disorders. [Thesis]. University of Illinois – Chicago; 2012. Available from: http://hdl.handle.net/10027/9301

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

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