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You searched for subject:(KAP1). Showing records 1 – 6 of 6 total matches.

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University of Southern California

1. Li, Xu. Post-translational modification crosstalk regulates KAP1 co-repressor functions in response to DNA damages.

Degree: PhD, Molecular Pharmacology & Toxicology, 2009, University of Southern California

 As a multifunctional protein, KRAB domain-associated protein 1 (KAP1) is reportedly subjected to multiple protein post-translational modifications, including phosphorylation and SUMOylation. However, gaps exist in… (more)

Subjects/Keywords: DNA damage responses; KAP1; PP1; RNF4; SUMOylation; phosphorylation; ubiquitination; post-translational modifications crosstalk; doxorubicin

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APA (6th Edition):

Li, X. (2009). Post-translational modification crosstalk regulates KAP1 co-repressor functions in response to DNA damages. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/279861/rec/5135

Chicago Manual of Style (16th Edition):

Li, Xu. “Post-translational modification crosstalk regulates KAP1 co-repressor functions in response to DNA damages.” 2009. Doctoral Dissertation, University of Southern California. Accessed May 27, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/279861/rec/5135.

MLA Handbook (7th Edition):

Li, Xu. “Post-translational modification crosstalk regulates KAP1 co-repressor functions in response to DNA damages.” 2009. Web. 27 May 2019.

Vancouver:

Li X. Post-translational modification crosstalk regulates KAP1 co-repressor functions in response to DNA damages. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2019 May 27]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/279861/rec/5135.

Council of Science Editors:

Li X. Post-translational modification crosstalk regulates KAP1 co-repressor functions in response to DNA damages. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/279861/rec/5135


EPFL

2. Ecco, Gabriela. Unraveling the KRAB/KAP1 control of transposable elements in pluripotent and somatic cells.

Degree: 2016, EPFL

 Transposable elements (TEs) are DNA sequences able to change position in the genome, and represent more than 40% of mammalian genetic material. TEs can have… (more)

Subjects/Keywords: transcriptional regulation; epigenetics; transposable element (TE); endogenous retroelement (ERE); KAP1 or TRIM28; KRAB-ZFP; genome evolution.

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APA (6th Edition):

Ecco, G. (2016). Unraveling the KRAB/KAP1 control of transposable elements in pluripotent and somatic cells. (Thesis). EPFL. Retrieved from http://infoscience.epfl.ch/record/219001

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):

Ecco, Gabriela. “Unraveling the KRAB/KAP1 control of transposable elements in pluripotent and somatic cells.” 2016. Thesis, EPFL. Accessed May 27, 2019. http://infoscience.epfl.ch/record/219001.

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

MLA Handbook (7th Edition):

Ecco, Gabriela. “Unraveling the KRAB/KAP1 control of transposable elements in pluripotent and somatic cells.” 2016. Web. 27 May 2019.

Vancouver:

Ecco G. Unraveling the KRAB/KAP1 control of transposable elements in pluripotent and somatic cells. [Internet] [Thesis]. EPFL; 2016. [cited 2019 May 27]. Available from: http://infoscience.epfl.ch/record/219001.

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

Council of Science Editors:

Ecco G. Unraveling the KRAB/KAP1 control of transposable elements in pluripotent and somatic cells. [Thesis]. EPFL; 2016. Available from: http://infoscience.epfl.ch/record/219001

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

3. De Vos, Mike. Interaction fonctionnelle de la Poly(ADP-Ribose) polymérase-1 (PARP1) avec des protéines de l'hétérochromatine : impact sur la fonction de l'hétérochromatine et la réparation de l'ADN : Functional interaction between Poly(ADP-ribose) polymerase-1 (PARPl) and heterochromatin proteins : impact on heterochromatin function and DNA repair.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2014, Université de Strasbourg

Nous avons identifié une association poly(ADP-ribose) (PAR)-dépendante entre PARP1 et UHRF1. UHRF1 est PARylé par PARP1 et lie le PAR de façon non covalente. L’absence… (more)

Subjects/Keywords: PARPs; UHRF1; DNMT1; Hétérochromatine péricentrique; KAP1; HP1; Réparation de l’ADN; PARPs; UHRF1; DNMT1; Pericentric heterochromatin; DNA repair; 572.8

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APA (6th Edition):

De Vos, M. (2014). Interaction fonctionnelle de la Poly(ADP-Ribose) polymérase-1 (PARP1) avec des protéines de l'hétérochromatine : impact sur la fonction de l'hétérochromatine et la réparation de l'ADN : Functional interaction between Poly(ADP-ribose) polymerase-1 (PARPl) and heterochromatin proteins : impact on heterochromatin function and DNA repair. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2014STRAJ001

Chicago Manual of Style (16th Edition):

De Vos, Mike. “Interaction fonctionnelle de la Poly(ADP-Ribose) polymérase-1 (PARP1) avec des protéines de l'hétérochromatine : impact sur la fonction de l'hétérochromatine et la réparation de l'ADN : Functional interaction between Poly(ADP-ribose) polymerase-1 (PARPl) and heterochromatin proteins : impact on heterochromatin function and DNA repair.” 2014. Doctoral Dissertation, Université de Strasbourg. Accessed May 27, 2019. http://www.theses.fr/2014STRAJ001.

MLA Handbook (7th Edition):

De Vos, Mike. “Interaction fonctionnelle de la Poly(ADP-Ribose) polymérase-1 (PARP1) avec des protéines de l'hétérochromatine : impact sur la fonction de l'hétérochromatine et la réparation de l'ADN : Functional interaction between Poly(ADP-ribose) polymerase-1 (PARPl) and heterochromatin proteins : impact on heterochromatin function and DNA repair.” 2014. Web. 27 May 2019.

Vancouver:

De Vos M. Interaction fonctionnelle de la Poly(ADP-Ribose) polymérase-1 (PARP1) avec des protéines de l'hétérochromatine : impact sur la fonction de l'hétérochromatine et la réparation de l'ADN : Functional interaction between Poly(ADP-ribose) polymerase-1 (PARPl) and heterochromatin proteins : impact on heterochromatin function and DNA repair. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2014. [cited 2019 May 27]. Available from: http://www.theses.fr/2014STRAJ001.

Council of Science Editors:

De Vos M. Interaction fonctionnelle de la Poly(ADP-Ribose) polymérase-1 (PARP1) avec des protéines de l'hétérochromatine : impact sur la fonction de l'hétérochromatine et la réparation de l'ADN : Functional interaction between Poly(ADP-ribose) polymerase-1 (PARPl) and heterochromatin proteins : impact on heterochromatin function and DNA repair. [Doctoral Dissertation]. Université de Strasbourg; 2014. Available from: http://www.theses.fr/2014STRAJ001


University of Canterbury

4. Chen R. P-TEFb: finding its ways to release promoter-proximally paused RNA Polymerase II.

Degree: 2017, University of Canterbury

The release of a paused Pol II depends on the recruitment of P-TEFb. Recent studies showed that both active P-TEFb and inactive P-TEFb (7SK snRNP) can be recruited to the promoter regions of global genes by different mechanisms. Here, we summarize the recent advances on these distinct recruitment mechanisms.

Subjects/Keywords: P-TEFb; 7SK snRNP; Brd4; SEC; KAP1; RNA Pol II; promoter-proximal pausing; transcription elongation; Field of Research::06 - Biological Sciences::0601 - Biochemistry and Cell Biology

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APA (6th Edition):

R, C. (2017). P-TEFb: finding its ways to release promoter-proximally paused RNA Polymerase II. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/15360

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):

R, Chen. “P-TEFb: finding its ways to release promoter-proximally paused RNA Polymerase II.” 2017. Thesis, University of Canterbury. Accessed May 27, 2019. http://hdl.handle.net/10092/15360.

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

MLA Handbook (7th Edition):

R, Chen. “P-TEFb: finding its ways to release promoter-proximally paused RNA Polymerase II.” 2017. Web. 27 May 2019.

Vancouver:

R C. P-TEFb: finding its ways to release promoter-proximally paused RNA Polymerase II. [Internet] [Thesis]. University of Canterbury; 2017. [cited 2019 May 27]. Available from: http://hdl.handle.net/10092/15360.

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

Council of Science Editors:

R C. P-TEFb: finding its ways to release promoter-proximally paused RNA Polymerase II. [Thesis]. University of Canterbury; 2017. Available from: http://hdl.handle.net/10092/15360

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

5. P. Mita. ANALYSIS OF RPB5 BINDING PROTEIN (RMP/URI) MEDIATED TRANSCRIPTIONAL REPRESSION IN PROSTATE CELLS.

Degree: 2012, Università degli Studi di Milano

 Unconventional prefoldin RPB5 Interactor (URI) was identified as a protein that binds the RPB5 subunit of polymerases and functions as a transcriptional repressor (Dorjsuren N.,… (more)

Subjects/Keywords: Unconventional prefoldin RPB5 interactor; androgen receptor; prostate cancer; Art-27; transcriptional repressor; KAP1; R2TP/prefoldin-like complex; Settore BIO/11 - Biologia Molecolare; Settore BIO/12 - Biochimica Clinica e Biologia Molecolare Clinica

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

APA (6th Edition):

Mita, P. (2012). ANALYSIS OF RPB5 BINDING PROTEIN (RMP/URI) MEDIATED TRANSCRIPTIONAL REPRESSION IN PROSTATE CELLS. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/203784

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):

Mita, P.. “ANALYSIS OF RPB5 BINDING PROTEIN (RMP/URI) MEDIATED TRANSCRIPTIONAL REPRESSION IN PROSTATE CELLS.” 2012. Thesis, Università degli Studi di Milano. Accessed May 27, 2019. http://hdl.handle.net/2434/203784.

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

MLA Handbook (7th Edition):

Mita, P.. “ANALYSIS OF RPB5 BINDING PROTEIN (RMP/URI) MEDIATED TRANSCRIPTIONAL REPRESSION IN PROSTATE CELLS.” 2012. Web. 27 May 2019.

Vancouver:

Mita P. ANALYSIS OF RPB5 BINDING PROTEIN (RMP/URI) MEDIATED TRANSCRIPTIONAL REPRESSION IN PROSTATE CELLS. [Internet] [Thesis]. Università degli Studi di Milano; 2012. [cited 2019 May 27]. Available from: http://hdl.handle.net/2434/203784.

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

Council of Science Editors:

Mita P. ANALYSIS OF RPB5 BINDING PROTEIN (RMP/URI) MEDIATED TRANSCRIPTIONAL REPRESSION IN PROSTATE CELLS. [Thesis]. Università degli Studi di Milano; 2012. Available from: http://hdl.handle.net/2434/203784

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


University of Southern California

6. Lee, Yung-Kang. A regulatory transcription module of ZBRK1/KAP1 complex and its signaling network in regulating DNA damage-responsive genes expression.

Degree: PhD, Molecular Pharmacology & Toxicology, 2006, University of Southern California

 In pursuit of new SUMOylation targets that regulate the activities of cell cycle progression and mediate cellular apoptosis, a proteomic screening that combined affinity chromatography… (more)

Subjects/Keywords: KAP1 SUMOylation; histone acetylation methylation; DNA double strand break damage; Doxorubicin; ATM ATR; SUMO-specific protease SENP

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

APA (6th Edition):

Lee, Y. (2006). A regulatory transcription module of ZBRK1/KAP1 complex and its signaling network in regulating DNA damage-responsive genes expression. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/18937/rec/336

Chicago Manual of Style (16th Edition):

Lee, Yung-Kang. “A regulatory transcription module of ZBRK1/KAP1 complex and its signaling network in regulating DNA damage-responsive genes expression.” 2006. Doctoral Dissertation, University of Southern California. Accessed May 27, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/18937/rec/336.

MLA Handbook (7th Edition):

Lee, Yung-Kang. “A regulatory transcription module of ZBRK1/KAP1 complex and its signaling network in regulating DNA damage-responsive genes expression.” 2006. Web. 27 May 2019.

Vancouver:

Lee Y. A regulatory transcription module of ZBRK1/KAP1 complex and its signaling network in regulating DNA damage-responsive genes expression. [Internet] [Doctoral dissertation]. University of Southern California; 2006. [cited 2019 May 27]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/18937/rec/336.

Council of Science Editors:

Lee Y. A regulatory transcription module of ZBRK1/KAP1 complex and its signaling network in regulating DNA damage-responsive genes expression. [Doctoral Dissertation]. University of Southern California; 2006. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/18937/rec/336

.