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You searched for subject:(Posttranslational regulation). Showing records 1 – 11 of 11 total matches.

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University of Minnesota

1. Molan, Amy. Regulation of APOBEC3B and the Restriction of HIV-1 in Myeloid Cells.

Degree: PhD, Biochemistry, Molecular Bio, and Biophysics, 2018, University of Minnesota

 The APOBEC3 (A3) DNA cytosine deaminase family comprises a fundamental arm of the innate immune response and is best known for retrovirus restriction. Several A3… (more)

Subjects/Keywords: APOBEC; Cancer; HIV; myeloid; posttranslational regulation; restriction

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APA (6th Edition):

Molan, A. (2018). Regulation of APOBEC3B and the Restriction of HIV-1 in Myeloid Cells. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/200293

Chicago Manual of Style (16th Edition):

Molan, Amy. “Regulation of APOBEC3B and the Restriction of HIV-1 in Myeloid Cells.” 2018. Doctoral Dissertation, University of Minnesota. Accessed November 12, 2019. http://hdl.handle.net/11299/200293.

MLA Handbook (7th Edition):

Molan, Amy. “Regulation of APOBEC3B and the Restriction of HIV-1 in Myeloid Cells.” 2018. Web. 12 Nov 2019.

Vancouver:

Molan A. Regulation of APOBEC3B and the Restriction of HIV-1 in Myeloid Cells. [Internet] [Doctoral dissertation]. University of Minnesota; 2018. [cited 2019 Nov 12]. Available from: http://hdl.handle.net/11299/200293.

Council of Science Editors:

Molan A. Regulation of APOBEC3B and the Restriction of HIV-1 in Myeloid Cells. [Doctoral Dissertation]. University of Minnesota; 2018. Available from: http://hdl.handle.net/11299/200293


Georgia State University

2. Morgan, Julie E. Dynamic Regulation of the Class II Transactivator by Posttranslational Modifications.

Degree: PhD, Biology, 2015, Georgia State University

  The class II Transactivator (CIITA) is the master regulator for Major Histocompatibility Class II (MHC II) molecules. CIITA is dynamically regulated by a series… (more)

Subjects/Keywords: Posttranslational modifications; Ubiquitination; phosphorylation; CIITA; MHC II; transcription regulation

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APA (6th Edition):

Morgan, J. E. (2015). Dynamic Regulation of the Class II Transactivator by Posttranslational Modifications. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/biology_diss/157

Chicago Manual of Style (16th Edition):

Morgan, Julie E. “Dynamic Regulation of the Class II Transactivator by Posttranslational Modifications.” 2015. Doctoral Dissertation, Georgia State University. Accessed November 12, 2019. https://scholarworks.gsu.edu/biology_diss/157.

MLA Handbook (7th Edition):

Morgan, Julie E. “Dynamic Regulation of the Class II Transactivator by Posttranslational Modifications.” 2015. Web. 12 Nov 2019.

Vancouver:

Morgan JE. Dynamic Regulation of the Class II Transactivator by Posttranslational Modifications. [Internet] [Doctoral dissertation]. Georgia State University; 2015. [cited 2019 Nov 12]. Available from: https://scholarworks.gsu.edu/biology_diss/157.

Council of Science Editors:

Morgan JE. Dynamic Regulation of the Class II Transactivator by Posttranslational Modifications. [Doctoral Dissertation]. Georgia State University; 2015. Available from: https://scholarworks.gsu.edu/biology_diss/157


University of Washington

3. Silverman, Julie Michelle. Posttranslational regulation and effector specificity of the type VI secretion system.

Degree: PhD, 2013, University of Washington

 Bacteria mediate interactions with their surroundings by exporting a variety of proteins into the extracellular environment. Gram-negative bacteria have evolved at least six dedicated secretory… (more)

Subjects/Keywords: Bacterial interactions; Posttranslational regulation; Secretion systems; Microbiology; Molecular biology; Biochemistry; microbiology

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APA (6th Edition):

Silverman, J. M. (2013). Posttranslational regulation and effector specificity of the type VI secretion system. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/24205

Chicago Manual of Style (16th Edition):

Silverman, Julie Michelle. “Posttranslational regulation and effector specificity of the type VI secretion system.” 2013. Doctoral Dissertation, University of Washington. Accessed November 12, 2019. http://hdl.handle.net/1773/24205.

MLA Handbook (7th Edition):

Silverman, Julie Michelle. “Posttranslational regulation and effector specificity of the type VI secretion system.” 2013. Web. 12 Nov 2019.

Vancouver:

Silverman JM. Posttranslational regulation and effector specificity of the type VI secretion system. [Internet] [Doctoral dissertation]. University of Washington; 2013. [cited 2019 Nov 12]. Available from: http://hdl.handle.net/1773/24205.

Council of Science Editors:

Silverman JM. Posttranslational regulation and effector specificity of the type VI secretion system. [Doctoral Dissertation]. University of Washington; 2013. Available from: http://hdl.handle.net/1773/24205


University of Illinois – Chicago

4. Orozco-Nunnelly, Danielle A. Determining the Role of Pirin1 in Light-Regulated Growth and Cellular Responses in Arabidopsis thaliana.

Degree: 2015, University of Illinois – Chicago

 As photoautotrophic and sessile organisms, plants are both reliant upon, and vulnerable to abiotic signals. Different wavelengths of light provide information for plant development, but… (more)

Subjects/Keywords: Arabidopsis; G protein pathway; Light signaling; Photomorphogenesis; Pirin; Plant transgenes; Posttranslational modification; Quercetin; Regulation of transcript and protein; Seedling development

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APA (6th Edition):

Orozco-Nunnelly, D. A. (2015). Determining the Role of Pirin1 in Light-Regulated Growth and Cellular Responses in Arabidopsis thaliana. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/19577

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):

Orozco-Nunnelly, Danielle A. “Determining the Role of Pirin1 in Light-Regulated Growth and Cellular Responses in Arabidopsis thaliana.” 2015. Thesis, University of Illinois – Chicago. Accessed November 12, 2019. http://hdl.handle.net/10027/19577.

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

MLA Handbook (7th Edition):

Orozco-Nunnelly, Danielle A. “Determining the Role of Pirin1 in Light-Regulated Growth and Cellular Responses in Arabidopsis thaliana.” 2015. Web. 12 Nov 2019.

Vancouver:

Orozco-Nunnelly DA. Determining the Role of Pirin1 in Light-Regulated Growth and Cellular Responses in Arabidopsis thaliana. [Internet] [Thesis]. University of Illinois – Chicago; 2015. [cited 2019 Nov 12]. Available from: http://hdl.handle.net/10027/19577.

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

Council of Science Editors:

Orozco-Nunnelly DA. Determining the Role of Pirin1 in Light-Regulated Growth and Cellular Responses in Arabidopsis thaliana. [Thesis]. University of Illinois – Chicago; 2015. Available from: http://hdl.handle.net/10027/19577

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


Universitat Pompeu Fabra

5. Iturbide Martínez de Albéniz, Ane, 1989-. Identification of new LOXL2 substrates : a role for lysine oxidation in embryonic stem cell differentiation.

Degree: Departament de Ciències Experimentals i de la Salut, 2016, Universitat Pompeu Fabra

 La funció de les proteïnes és sovint regulada i controlada per modificacions post-traduccionals, com ara l’oxidació. Encara que l’oxidació ha sigut principalment considerada com una… (more)

Subjects/Keywords: Posttranslational modifications; Transcriptional regulation; Embryonic stem cells (ESCs); LOXL2; TAF10; Modificacions post-traduccionals; Regulació de la transcripció; Cèl·lules mare embrionàries; 576

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APA (6th Edition):

Iturbide Martínez de Albéniz, Ane, 1. (2016). Identification of new LOXL2 substrates : a role for lysine oxidation in embryonic stem cell differentiation. (Thesis). Universitat Pompeu Fabra. Retrieved from http://hdl.handle.net/10803/456678

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):

Iturbide Martínez de Albéniz, Ane, 1989-. “Identification of new LOXL2 substrates : a role for lysine oxidation in embryonic stem cell differentiation.” 2016. Thesis, Universitat Pompeu Fabra. Accessed November 12, 2019. http://hdl.handle.net/10803/456678.

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

MLA Handbook (7th Edition):

Iturbide Martínez de Albéniz, Ane, 1989-. “Identification of new LOXL2 substrates : a role for lysine oxidation in embryonic stem cell differentiation.” 2016. Web. 12 Nov 2019.

Vancouver:

Iturbide Martínez de Albéniz, Ane 1. Identification of new LOXL2 substrates : a role for lysine oxidation in embryonic stem cell differentiation. [Internet] [Thesis]. Universitat Pompeu Fabra; 2016. [cited 2019 Nov 12]. Available from: http://hdl.handle.net/10803/456678.

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

Council of Science Editors:

Iturbide Martínez de Albéniz, Ane 1. Identification of new LOXL2 substrates : a role for lysine oxidation in embryonic stem cell differentiation. [Thesis]. Universitat Pompeu Fabra; 2016. Available from: http://hdl.handle.net/10803/456678

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


University of Oxford

6. Lercher, Lukas A. Chemical tools for the study of epigenetic mechanisms.

Degree: PhD, 2014, University of Oxford

 The overall goal of my work was to develop and apply new chemical methods for the study of epigenetic DNA and protein modifications. In Chapter… (more)

Subjects/Keywords: 572.8; Chemical biology; Protein chemistry; Organic chemistry; NMR spectroscopy; Molecular biophysics (biochemistry); Epigenetic regulation; posttranslational modifications; DNA modification; protein NMR

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APA (6th Edition):

Lercher, L. A. (2014). Chemical tools for the study of epigenetic mechanisms. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:8fec2af6-573b-464a-865e-a70d31fa1c41 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.629538

Chicago Manual of Style (16th Edition):

Lercher, Lukas A. “Chemical tools for the study of epigenetic mechanisms.” 2014. Doctoral Dissertation, University of Oxford. Accessed November 12, 2019. http://ora.ox.ac.uk/objects/uuid:8fec2af6-573b-464a-865e-a70d31fa1c41 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.629538.

MLA Handbook (7th Edition):

Lercher, Lukas A. “Chemical tools for the study of epigenetic mechanisms.” 2014. Web. 12 Nov 2019.

Vancouver:

Lercher LA. Chemical tools for the study of epigenetic mechanisms. [Internet] [Doctoral dissertation]. University of Oxford; 2014. [cited 2019 Nov 12]. Available from: http://ora.ox.ac.uk/objects/uuid:8fec2af6-573b-464a-865e-a70d31fa1c41 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.629538.

Council of Science Editors:

Lercher LA. Chemical tools for the study of epigenetic mechanisms. [Doctoral Dissertation]. University of Oxford; 2014. Available from: http://ora.ox.ac.uk/objects/uuid:8fec2af6-573b-464a-865e-a70d31fa1c41 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.629538


The Ohio State University

7. Dearth, Lawrence. Characterization of C/EBPs in Mammary Epithelial Cell Biology.

Degree: PhD, Molecular, Cellular, and Developmental Biology, 2002, The Ohio State University

 Work from this dissertation has demonstrated that C/EBPbeta is the predominant C/EBPbeta isoform expressed in the normal mouse mammary gland and mouse mammary tumors in… (more)

Subjects/Keywords: Biology, Molecular; C/EBPs; mammary epithelial cells; posttranscriptional regulation; posttranslational regulation

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APA (6th Edition):

Dearth, L. (2002). Characterization of C/EBPs in Mammary Epithelial Cell Biology. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1038840268

Chicago Manual of Style (16th Edition):

Dearth, Lawrence. “Characterization of C/EBPs in Mammary Epithelial Cell Biology.” 2002. Doctoral Dissertation, The Ohio State University. Accessed November 12, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1038840268.

MLA Handbook (7th Edition):

Dearth, Lawrence. “Characterization of C/EBPs in Mammary Epithelial Cell Biology.” 2002. Web. 12 Nov 2019.

Vancouver:

Dearth L. Characterization of C/EBPs in Mammary Epithelial Cell Biology. [Internet] [Doctoral dissertation]. The Ohio State University; 2002. [cited 2019 Nov 12]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1038840268.

Council of Science Editors:

Dearth L. Characterization of C/EBPs in Mammary Epithelial Cell Biology. [Doctoral Dissertation]. The Ohio State University; 2002. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1038840268


Université de Grenoble

8. Casabona, Maria Guillermina. Mécanismes moléculaires impliqués dans la régulation post-traductionnelle du système de sécrétion du type VI chez Pseudomonas aeruginosa : Molecular mechanisms involved in the post-translational regulation of type VI secretion system in Pseudomonas aeruginosa.

Degree: Docteur es, Médecine, 2013, Université de Grenoble

La bactérie à Gram-négatif Pseudomonas aeruginosa est un pathogène humain opportuniste qui peut causer des infections chroniques pouvant conduire à la mort des patients, et… (more)

Subjects/Keywords: Pseudomonas aeruginosa; SST6; Régulation post-traductionnelle; Protéomique à haut débit; Sous-protéome; Pseudomonas aeruginosa; T6SS; Posttranslational regulation; Shotgun proteomics; IM-OM sub-proteomes

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APA (6th Edition):

Casabona, M. G. (2013). Mécanismes moléculaires impliqués dans la régulation post-traductionnelle du système de sécrétion du type VI chez Pseudomonas aeruginosa : Molecular mechanisms involved in the post-translational regulation of type VI secretion system in Pseudomonas aeruginosa. (Doctoral Dissertation). Université de Grenoble. Retrieved from http://www.theses.fr/2013GRENV009

Chicago Manual of Style (16th Edition):

Casabona, Maria Guillermina. “Mécanismes moléculaires impliqués dans la régulation post-traductionnelle du système de sécrétion du type VI chez Pseudomonas aeruginosa : Molecular mechanisms involved in the post-translational regulation of type VI secretion system in Pseudomonas aeruginosa.” 2013. Doctoral Dissertation, Université de Grenoble. Accessed November 12, 2019. http://www.theses.fr/2013GRENV009.

MLA Handbook (7th Edition):

Casabona, Maria Guillermina. “Mécanismes moléculaires impliqués dans la régulation post-traductionnelle du système de sécrétion du type VI chez Pseudomonas aeruginosa : Molecular mechanisms involved in the post-translational regulation of type VI secretion system in Pseudomonas aeruginosa.” 2013. Web. 12 Nov 2019.

Vancouver:

Casabona MG. Mécanismes moléculaires impliqués dans la régulation post-traductionnelle du système de sécrétion du type VI chez Pseudomonas aeruginosa : Molecular mechanisms involved in the post-translational regulation of type VI secretion system in Pseudomonas aeruginosa. [Internet] [Doctoral dissertation]. Université de Grenoble; 2013. [cited 2019 Nov 12]. Available from: http://www.theses.fr/2013GRENV009.

Council of Science Editors:

Casabona MG. Mécanismes moléculaires impliqués dans la régulation post-traductionnelle du système de sécrétion du type VI chez Pseudomonas aeruginosa : Molecular mechanisms involved in the post-translational regulation of type VI secretion system in Pseudomonas aeruginosa. [Doctoral Dissertation]. Université de Grenoble; 2013. Available from: http://www.theses.fr/2013GRENV009

9. Drecourt, Anthony. Mécanisme physiopathologique des neurodégénérescences avec accumulation de fer dans le cerveau et de l’ataxie de Friedreich : Pathophysiological mechanism of neurodegeneration with brain iron accumulation and Friedreich ataxia.

Degree: Docteur es, Génétique, 2016, Sorbonne Paris Cité

Les neurodégénérescences avec accumulation de fer dans le cerveau (Neurodegeneration with Brain Iron Accumulation, NBIA) sont des maladies neurodégénératives progressives, génétiquement hétérogènes. On connait actuellement… (more)

Subjects/Keywords: NBIA; Ataxie de Friedreich; Maladies neurodégénératives; Transferrine; Homéostasie du fer; Régulation post-traductionnelle; NBIA; Friedreich ataxia; Neurodegenerative disorders; Transferrin; Iron homeostasis; Posttranslational regulation; 599.935

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APA (6th Edition):

Drecourt, A. (2016). Mécanisme physiopathologique des neurodégénérescences avec accumulation de fer dans le cerveau et de l’ataxie de Friedreich : Pathophysiological mechanism of neurodegeneration with brain iron accumulation and Friedreich ataxia. (Doctoral Dissertation). Sorbonne Paris Cité. Retrieved from http://www.theses.fr/2016USPCB061

Chicago Manual of Style (16th Edition):

Drecourt, Anthony. “Mécanisme physiopathologique des neurodégénérescences avec accumulation de fer dans le cerveau et de l’ataxie de Friedreich : Pathophysiological mechanism of neurodegeneration with brain iron accumulation and Friedreich ataxia.” 2016. Doctoral Dissertation, Sorbonne Paris Cité. Accessed November 12, 2019. http://www.theses.fr/2016USPCB061.

MLA Handbook (7th Edition):

Drecourt, Anthony. “Mécanisme physiopathologique des neurodégénérescences avec accumulation de fer dans le cerveau et de l’ataxie de Friedreich : Pathophysiological mechanism of neurodegeneration with brain iron accumulation and Friedreich ataxia.” 2016. Web. 12 Nov 2019.

Vancouver:

Drecourt A. Mécanisme physiopathologique des neurodégénérescences avec accumulation de fer dans le cerveau et de l’ataxie de Friedreich : Pathophysiological mechanism of neurodegeneration with brain iron accumulation and Friedreich ataxia. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; 2016. [cited 2019 Nov 12]. Available from: http://www.theses.fr/2016USPCB061.

Council of Science Editors:

Drecourt A. Mécanisme physiopathologique des neurodégénérescences avec accumulation de fer dans le cerveau et de l’ataxie de Friedreich : Pathophysiological mechanism of neurodegeneration with brain iron accumulation and Friedreich ataxia. [Doctoral Dissertation]. Sorbonne Paris Cité; 2016. Available from: http://www.theses.fr/2016USPCB061


Université Paris-Sud – Paris XI

10. Waltz, Fanny. Etude du transport de l'iode par chémogénomique : A chemogenomics study of iodide transport.

Degree: Docteur es, Chimie organique et biochimie, 2011, Université Paris-Sud – Paris XI

 Une importante avancée dans la compréhension des mécanismes gouvernant le processus de transport des ions iodures à l’intérieur des cellules thyroïdiennes a été le clonage… (more)

Subjects/Keywords: Transport d’iodures; Thyroïde; Inhibiteurs; Mécanismes de régulation posttraductionnels; Identification de protéine; Protéomique; Spectrométrie de masse; Sonde photoactivable; Biotine; Desthiobiotine; Iodide transport; Thyroid; Inhibitors; Posttranslational regulation mechanisms; Protein identification; Proteomics; Mass spectrometry; Photoactivable probe; Biotin; Desthiobiotin

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APA (6th Edition):

Waltz, F. (2011). Etude du transport de l'iode par chémogénomique : A chemogenomics study of iodide transport. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2011PA112214

Chicago Manual of Style (16th Edition):

Waltz, Fanny. “Etude du transport de l'iode par chémogénomique : A chemogenomics study of iodide transport.” 2011. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed November 12, 2019. http://www.theses.fr/2011PA112214.

MLA Handbook (7th Edition):

Waltz, Fanny. “Etude du transport de l'iode par chémogénomique : A chemogenomics study of iodide transport.” 2011. Web. 12 Nov 2019.

Vancouver:

Waltz F. Etude du transport de l'iode par chémogénomique : A chemogenomics study of iodide transport. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2011. [cited 2019 Nov 12]. Available from: http://www.theses.fr/2011PA112214.

Council of Science Editors:

Waltz F. Etude du transport de l'iode par chémogénomique : A chemogenomics study of iodide transport. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2011. Available from: http://www.theses.fr/2011PA112214

11. Vujatovic, Olivera, 1981-. Functional analysis of Drosophila melanogaster linker histone dH1.

Degree: Departament de Ciències Experimentals i de la Salut, 2012, Universitat Pompeu Fabra

 We did functional characterisation of Drosophila melanogaster linker histone, dH1. In the mutant state for this protein, we observed structural changes in polytene chromosomes chromocenter… (more)

Subjects/Keywords: Histona H1; Drosophila melanogaster; Regulación de la expressión genética; Elementos transponibles; Estabilidad Genómica; Modificaciones postranslacionales; Linker histone; Gene expression regulation; Transposable elements; Genome stability; Posttranslational modifications; 575

…expression regulation. We determined effects of dH1 loss in different types of chromatin and we… …proteins that organize DNA into more compact structures. A role in regulation of transcription… …proposed. It is also becoming clear that posttranslational modifications of linker histone can… …posttranslational modification and DNA was of defined sequence. The main part of the structure was… …posttranslational histone modifications, histone variants and irregular nucleosome spacing. Bases for… 

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APA (6th Edition):

Vujatovic, Olivera, 1. (2012). Functional analysis of Drosophila melanogaster linker histone dH1. (Thesis). Universitat Pompeu Fabra. Retrieved from http://hdl.handle.net/10803/91286

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):

Vujatovic, Olivera, 1981-. “Functional analysis of Drosophila melanogaster linker histone dH1.” 2012. Thesis, Universitat Pompeu Fabra. Accessed November 12, 2019. http://hdl.handle.net/10803/91286.

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

MLA Handbook (7th Edition):

Vujatovic, Olivera, 1981-. “Functional analysis of Drosophila melanogaster linker histone dH1.” 2012. Web. 12 Nov 2019.

Vancouver:

Vujatovic, Olivera 1. Functional analysis of Drosophila melanogaster linker histone dH1. [Internet] [Thesis]. Universitat Pompeu Fabra; 2012. [cited 2019 Nov 12]. Available from: http://hdl.handle.net/10803/91286.

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

Council of Science Editors:

Vujatovic, Olivera 1. Functional analysis of Drosophila melanogaster linker histone dH1. [Thesis]. Universitat Pompeu Fabra; 2012. Available from: http://hdl.handle.net/10803/91286

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

.