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You searched for subject:(CARM1). Showing records 1 – 7 of 7 total matches.

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Texas Medical Center

1. Vemulapalli, Vidyasiri. Developing and using methyl-specific antibodies to study the biological roles of arginine methylation.

Degree: PhD, 2016, Texas Medical Center

  Arginine residues can be modified in three different ways to produce asymmetric dimethylarginine (ADMA), symmetric dimethylarginine (SDMA), and monomethylarginine (MMA). These modifications are catalyzed… (more)

Subjects/Keywords: Arginine methylation; PRMT1; CARM1; MED12; ER; Monomethylation; asymmetric dimethylation; CARM1 substrates; Cell Biology; Medicine and Health Sciences; Molecular Biology

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

APA (6th Edition):

Vemulapalli, V. (2016). Developing and using methyl-specific antibodies to study the biological roles of arginine methylation. (Doctoral Dissertation). Texas Medical Center. Retrieved from http://digitalcommons.library.tmc.edu/utgsbs_dissertations/648

Chicago Manual of Style (16th Edition):

Vemulapalli, Vidyasiri. “Developing and using methyl-specific antibodies to study the biological roles of arginine methylation.” 2016. Doctoral Dissertation, Texas Medical Center. Accessed July 15, 2019. http://digitalcommons.library.tmc.edu/utgsbs_dissertations/648.

MLA Handbook (7th Edition):

Vemulapalli, Vidyasiri. “Developing and using methyl-specific antibodies to study the biological roles of arginine methylation.” 2016. Web. 15 Jul 2019.

Vancouver:

Vemulapalli V. Developing and using methyl-specific antibodies to study the biological roles of arginine methylation. [Internet] [Doctoral dissertation]. Texas Medical Center; 2016. [cited 2019 Jul 15]. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/648.

Council of Science Editors:

Vemulapalli V. Developing and using methyl-specific antibodies to study the biological roles of arginine methylation. [Doctoral Dissertation]. Texas Medical Center; 2016. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/648


University of Western Ontario

2. Coughlan, Niamh. The role of the arginine methyltransferase CARM1 in global transcriptional regulation.

Degree: 2014, University of Western Ontario

 Arginine methylation is a prevalent post-translational modification that is found on many nuclear and cytoplasmic proteins, and has been implicated in the regulation of gene… (more)

Subjects/Keywords: Transcriptional regulation; arginine methylation; CARM1; p/CIP (SRC3); cancer; Biochemistry

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APA (6th Edition):

Coughlan, N. (2014). The role of the arginine methyltransferase CARM1 in global transcriptional regulation. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/2013

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):

Coughlan, Niamh. “The role of the arginine methyltransferase CARM1 in global transcriptional regulation.” 2014. Thesis, University of Western Ontario. Accessed July 15, 2019. https://ir.lib.uwo.ca/etd/2013.

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

MLA Handbook (7th Edition):

Coughlan, Niamh. “The role of the arginine methyltransferase CARM1 in global transcriptional regulation.” 2014. Web. 15 Jul 2019.

Vancouver:

Coughlan N. The role of the arginine methyltransferase CARM1 in global transcriptional regulation. [Internet] [Thesis]. University of Western Ontario; 2014. [cited 2019 Jul 15]. Available from: https://ir.lib.uwo.ca/etd/2013.

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

Council of Science Editors:

Coughlan N. The role of the arginine methyltransferase CARM1 in global transcriptional regulation. [Thesis]. University of Western Ontario; 2014. Available from: https://ir.lib.uwo.ca/etd/2013

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

3. Walia, Mannu. La méthylation de CBP détermine des sites de liaison distincts au niveau de la chromatine pour le récepteur nucléaire à l'estradiol : Methylation specifies distinct estrogen-induced binding site repertoires of CBP to chromatin.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2012, Université de Strasbourg

L’oestradiol est l’une des hormones sécrétées par les ovaires. Non seulement impliquée dans le développement des organes sexuels chez les femmes, cette hormone aurait également… (more)

Subjects/Keywords: Protéine CBP; Oestradiol; Cancer; Facteur de croissance; CARM1; 572.8

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APA (6th Edition):

Walia, M. (2012). La méthylation de CBP détermine des sites de liaison distincts au niveau de la chromatine pour le récepteur nucléaire à l'estradiol : Methylation specifies distinct estrogen-induced binding site repertoires of CBP to chromatin. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2012STRAJ006

Chicago Manual of Style (16th Edition):

Walia, Mannu. “La méthylation de CBP détermine des sites de liaison distincts au niveau de la chromatine pour le récepteur nucléaire à l'estradiol : Methylation specifies distinct estrogen-induced binding site repertoires of CBP to chromatin.” 2012. Doctoral Dissertation, Université de Strasbourg. Accessed July 15, 2019. http://www.theses.fr/2012STRAJ006.

MLA Handbook (7th Edition):

Walia, Mannu. “La méthylation de CBP détermine des sites de liaison distincts au niveau de la chromatine pour le récepteur nucléaire à l'estradiol : Methylation specifies distinct estrogen-induced binding site repertoires of CBP to chromatin.” 2012. Web. 15 Jul 2019.

Vancouver:

Walia M. La méthylation de CBP détermine des sites de liaison distincts au niveau de la chromatine pour le récepteur nucléaire à l'estradiol : Methylation specifies distinct estrogen-induced binding site repertoires of CBP to chromatin. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2012. [cited 2019 Jul 15]. Available from: http://www.theses.fr/2012STRAJ006.

Council of Science Editors:

Walia M. La méthylation de CBP détermine des sites de liaison distincts au niveau de la chromatine pour le récepteur nucléaire à l'estradiol : Methylation specifies distinct estrogen-induced binding site repertoires of CBP to chromatin. [Doctoral Dissertation]. Université de Strasbourg; 2012. Available from: http://www.theses.fr/2012STRAJ006


University of Ottawa

4. Haghandish, Amir. Characterizing the Role of HuR in Skeletal Muscle of Mice with Spinal Muscular Atrophy .

Degree: 2017, University of Ottawa

 Spinal muscular atrophy (SMA) is a debilitating neuromuscular disorder characterized by insufficient SMN protein, resulting in motoneuron death. Initially, it was thought that motoneuronal death… (more)

Subjects/Keywords: Spinal Muscular Atrophy; HuR; CARM1; SMA; Skeletal Muscle; Differentiation

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APA (6th Edition):

Haghandish, A. (2017). Characterizing the Role of HuR in Skeletal Muscle of Mice with Spinal Muscular Atrophy . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/36746

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):

Haghandish, Amir. “Characterizing the Role of HuR in Skeletal Muscle of Mice with Spinal Muscular Atrophy .” 2017. Thesis, University of Ottawa. Accessed July 15, 2019. http://hdl.handle.net/10393/36746.

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

MLA Handbook (7th Edition):

Haghandish, Amir. “Characterizing the Role of HuR in Skeletal Muscle of Mice with Spinal Muscular Atrophy .” 2017. Web. 15 Jul 2019.

Vancouver:

Haghandish A. Characterizing the Role of HuR in Skeletal Muscle of Mice with Spinal Muscular Atrophy . [Internet] [Thesis]. University of Ottawa; 2017. [cited 2019 Jul 15]. Available from: http://hdl.handle.net/10393/36746.

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

Council of Science Editors:

Haghandish A. Characterizing the Role of HuR in Skeletal Muscle of Mice with Spinal Muscular Atrophy . [Thesis]. University of Ottawa; 2017. Available from: http://hdl.handle.net/10393/36746

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

5. Mailliot, Justine. Étude structurale de l’histoneméthyltransférase « CARM1 » et de ses complexes biologiquement significatifs : des structures 3D vers la conception rationnelle de composés à action pharmacologique : Structural study of CARM1 a histone methyltransferase and its biologically significant complexes : from 3D structures to rational conception of pharmacologically active compounds.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2013, Université de Strasbourg

Les "protéine arginine méthyltransférases" (PRMT) sont impliquées dans de nombreux processus cellulaires : transcription, maturation et transport des ARN, traduction, transduction du signal, réplication et… (more)

Subjects/Keywords: CARM1; Coactivator-associated arginine methyltransferase 1; Coactivateurs des récepteurs nucléaires; PRMT; Biologie structurale; CARM1; Coactivator-associated arginine methyltransferase 1; Nuclear receptor coactivator; PRMT; Structural biology; 572.8

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

APA (6th Edition):

Mailliot, J. (2013). Étude structurale de l’histoneméthyltransférase « CARM1 » et de ses complexes biologiquement significatifs : des structures 3D vers la conception rationnelle de composés à action pharmacologique : Structural study of CARM1 a histone methyltransferase and its biologically significant complexes : from 3D structures to rational conception of pharmacologically active compounds. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2013STRAJ015

Chicago Manual of Style (16th Edition):

Mailliot, Justine. “Étude structurale de l’histoneméthyltransférase « CARM1 » et de ses complexes biologiquement significatifs : des structures 3D vers la conception rationnelle de composés à action pharmacologique : Structural study of CARM1 a histone methyltransferase and its biologically significant complexes : from 3D structures to rational conception of pharmacologically active compounds.” 2013. Doctoral Dissertation, Université de Strasbourg. Accessed July 15, 2019. http://www.theses.fr/2013STRAJ015.

MLA Handbook (7th Edition):

Mailliot, Justine. “Étude structurale de l’histoneméthyltransférase « CARM1 » et de ses complexes biologiquement significatifs : des structures 3D vers la conception rationnelle de composés à action pharmacologique : Structural study of CARM1 a histone methyltransferase and its biologically significant complexes : from 3D structures to rational conception of pharmacologically active compounds.” 2013. Web. 15 Jul 2019.

Vancouver:

Mailliot J. Étude structurale de l’histoneméthyltransférase « CARM1 » et de ses complexes biologiquement significatifs : des structures 3D vers la conception rationnelle de composés à action pharmacologique : Structural study of CARM1 a histone methyltransferase and its biologically significant complexes : from 3D structures to rational conception of pharmacologically active compounds. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2013. [cited 2019 Jul 15]. Available from: http://www.theses.fr/2013STRAJ015.

Council of Science Editors:

Mailliot J. Étude structurale de l’histoneméthyltransférase « CARM1 » et de ses complexes biologiquement significatifs : des structures 3D vers la conception rationnelle de composés à action pharmacologique : Structural study of CARM1 a histone methyltransferase and its biologically significant complexes : from 3D structures to rational conception of pharmacologically active compounds. [Doctoral Dissertation]. Université de Strasbourg; 2013. Available from: http://www.theses.fr/2013STRAJ015


Université de Lorraine

6. Akoum, Rania El. La phosphorylation de CARM1 empêche l'interaction entre PRMT1 et CARM1, deux « Protein Arginine MethylTransférases » impliquées dans la prolifération dans le cancer du poumon : CARM1 phosphorylation prevents interaction between PRMT1 and CARM1, two <<protein arginine methyltransferases>> involved in proliferation in lung cancer.

Degree: Docteur es, Sciences de la vie et de la santé, 2013, Université de Lorraine

CARM1 et PRMT1 sont 2 Protein Arginine MethylTransferases (PRMTs) impliquées dans la prolifération et dérégulées dans le cancer. La dimérisation est une caractéristique commune aux… (more)

Subjects/Keywords: CARM1; PRMT1; Phosphorylation; Prolifération; Différenciation; Cancer du poumon à non petites cellules; CARM1; PRMT1; Phosphorylation; Proliferation; Differentiation; Non-small cell lung cancer; 616.994 2406

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APA (6th Edition):

Akoum, R. E. (2013). La phosphorylation de CARM1 empêche l'interaction entre PRMT1 et CARM1, deux « Protein Arginine MethylTransférases » impliquées dans la prolifération dans le cancer du poumon : CARM1 phosphorylation prevents interaction between PRMT1 and CARM1, two <<protein arginine methyltransferases>> involved in proliferation in lung cancer. (Doctoral Dissertation). Université de Lorraine. Retrieved from http://www.theses.fr/2013LORR0128

Chicago Manual of Style (16th Edition):

Akoum, Rania El. “La phosphorylation de CARM1 empêche l'interaction entre PRMT1 et CARM1, deux « Protein Arginine MethylTransférases » impliquées dans la prolifération dans le cancer du poumon : CARM1 phosphorylation prevents interaction between PRMT1 and CARM1, two <<protein arginine methyltransferases>> involved in proliferation in lung cancer.” 2013. Doctoral Dissertation, Université de Lorraine. Accessed July 15, 2019. http://www.theses.fr/2013LORR0128.

MLA Handbook (7th Edition):

Akoum, Rania El. “La phosphorylation de CARM1 empêche l'interaction entre PRMT1 et CARM1, deux « Protein Arginine MethylTransférases » impliquées dans la prolifération dans le cancer du poumon : CARM1 phosphorylation prevents interaction between PRMT1 and CARM1, two <<protein arginine methyltransferases>> involved in proliferation in lung cancer.” 2013. Web. 15 Jul 2019.

Vancouver:

Akoum RE. La phosphorylation de CARM1 empêche l'interaction entre PRMT1 et CARM1, deux « Protein Arginine MethylTransférases » impliquées dans la prolifération dans le cancer du poumon : CARM1 phosphorylation prevents interaction between PRMT1 and CARM1, two <<protein arginine methyltransferases>> involved in proliferation in lung cancer. [Internet] [Doctoral dissertation]. Université de Lorraine; 2013. [cited 2019 Jul 15]. Available from: http://www.theses.fr/2013LORR0128.

Council of Science Editors:

Akoum RE. La phosphorylation de CARM1 empêche l'interaction entre PRMT1 et CARM1, deux « Protein Arginine MethylTransférases » impliquées dans la prolifération dans le cancer du poumon : CARM1 phosphorylation prevents interaction between PRMT1 and CARM1, two <<protein arginine methyltransferases>> involved in proliferation in lung cancer. [Doctoral Dissertation]. Université de Lorraine; 2013. Available from: http://www.theses.fr/2013LORR0128


University of Southern California

7. Ou, Chen-Yin. Differential role of two coactivators, CCAR1 and CARM1, for dysregulated beta-catenin activity in colorectal cancer cell growth and gene expression.

Degree: PhD, Genetic, Molecular & Cellular Biology, 2012, University of Southern California

 Aberrant activation of Wnt/beta-catenin signaling is recognized as a critical factor in the etiology of colorectal cancer. Evidence has suggested that dysregulated beta-catenin activity is… (more)

Subjects/Keywords: colorectal cancer; colon cancer; transcriptional regulation; Wnt signaling; beta-catenin; CARM1; CCAR1; coactivator

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

APA (6th Edition):

Ou, C. (2012). Differential role of two coactivators, CCAR1 and CARM1, for dysregulated beta-catenin activity in colorectal cancer cell growth and gene expression. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/310293/rec/1987

Chicago Manual of Style (16th Edition):

Ou, Chen-Yin. “Differential role of two coactivators, CCAR1 and CARM1, for dysregulated beta-catenin activity in colorectal cancer cell growth and gene expression.” 2012. Doctoral Dissertation, University of Southern California. Accessed July 15, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/310293/rec/1987.

MLA Handbook (7th Edition):

Ou, Chen-Yin. “Differential role of two coactivators, CCAR1 and CARM1, for dysregulated beta-catenin activity in colorectal cancer cell growth and gene expression.” 2012. Web. 15 Jul 2019.

Vancouver:

Ou C. Differential role of two coactivators, CCAR1 and CARM1, for dysregulated beta-catenin activity in colorectal cancer cell growth and gene expression. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2019 Jul 15]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/310293/rec/1987.

Council of Science Editors:

Ou C. Differential role of two coactivators, CCAR1 and CARM1, for dysregulated beta-catenin activity in colorectal cancer cell growth and gene expression. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/310293/rec/1987

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