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You searched for subject:(Enhancer). Showing records 1 – 30 of 275 total matches.

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1. Mihala, Alexandra Gabriela. Studying enhancer function using the Tbx4 locus as a model.

Degree: PhD, Genetics, 2014, University of Georgia

 Key developmental processes in embryogenesis are modulated by transcription factors and signaling molecules whose spatio-temporal expression patterns need to be tightly regulated by cis-regulatory elements… (more)

Subjects/Keywords: Enhancer

…distinct enhancers, hindlimb enhancer A (HLEA) and B (HLEB)… …93 Figure 3.2: Tbx4 limb and genital expression is regulated by hindlimb enhancer B (… …enhancers, hindlimb enhancer A (HLEA) and B (HLEB)… …example, Pitx1 has been shown both in vitro and in vivo to bind a hindlimb specific enhancer of… …substantially in the number of tricomes. They noticed that the enhancer copies from D. sechellia do… 

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APA (6th Edition):

Mihala, A. G. (2014). Studying enhancer function using the Tbx4 locus as a model. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/mihala_alexandra_g_201405_phd

Chicago Manual of Style (16th Edition):

Mihala, Alexandra Gabriela. “Studying enhancer function using the Tbx4 locus as a model.” 2014. Doctoral Dissertation, University of Georgia. Accessed November 22, 2019. http://purl.galileo.usg.edu/uga_etd/mihala_alexandra_g_201405_phd.

MLA Handbook (7th Edition):

Mihala, Alexandra Gabriela. “Studying enhancer function using the Tbx4 locus as a model.” 2014. Web. 22 Nov 2019.

Vancouver:

Mihala AG. Studying enhancer function using the Tbx4 locus as a model. [Internet] [Doctoral dissertation]. University of Georgia; 2014. [cited 2019 Nov 22]. Available from: http://purl.galileo.usg.edu/uga_etd/mihala_alexandra_g_201405_phd.

Council of Science Editors:

Mihala AG. Studying enhancer function using the Tbx4 locus as a model. [Doctoral Dissertation]. University of Georgia; 2014. Available from: http://purl.galileo.usg.edu/uga_etd/mihala_alexandra_g_201405_phd

2. Al-Omairi, Jaafar Ghadeer Khudhair. Functional study of lymphoid specific enhancers : Etude fonctionnelle des enhancers lymphoides.

Degree: Docteur es, Génétique, 2017, Aix Marseille Université

Les amplificateurs (aussi appelés par le terme anglais enhancers) ont été initialement identifiés comme des séquences d'ADN agissant en cis qui augmentent la transcription d'une… (more)

Subjects/Keywords: Promoteur; Enhancer; Lymphocytes; Promoter; Enhancer; Lymphocytes; 572

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APA (6th Edition):

Al-Omairi, J. G. K. (2017). Functional study of lymphoid specific enhancers : Etude fonctionnelle des enhancers lymphoides. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2017AIXM0474

Chicago Manual of Style (16th Edition):

Al-Omairi, Jaafar Ghadeer Khudhair. “Functional study of lymphoid specific enhancers : Etude fonctionnelle des enhancers lymphoides.” 2017. Doctoral Dissertation, Aix Marseille Université. Accessed November 22, 2019. http://www.theses.fr/2017AIXM0474.

MLA Handbook (7th Edition):

Al-Omairi, Jaafar Ghadeer Khudhair. “Functional study of lymphoid specific enhancers : Etude fonctionnelle des enhancers lymphoides.” 2017. Web. 22 Nov 2019.

Vancouver:

Al-Omairi JGK. Functional study of lymphoid specific enhancers : Etude fonctionnelle des enhancers lymphoides. [Internet] [Doctoral dissertation]. Aix Marseille Université 2017. [cited 2019 Nov 22]. Available from: http://www.theses.fr/2017AIXM0474.

Council of Science Editors:

Al-Omairi JGK. Functional study of lymphoid specific enhancers : Etude fonctionnelle des enhancers lymphoides. [Doctoral Dissertation]. Aix Marseille Université 2017. Available from: http://www.theses.fr/2017AIXM0474


University of Iowa

3. Galle, Courtney Searcey. Characterization of Cis-acting partners within the cytomegalovirus major immediate-early enhancer that strengthen MIE gene expression and viral fitness.

Degree: PhD, Molecular and Cellular Biology, 2013, University of Iowa

  Human cytomegalovirus infects approximately 50% of adults in the United States and in most cases is asymptomatic. However, in the case of immune compromised… (more)

Subjects/Keywords: CMV enhancer; cytomegalovirus; HCMV enhancer; herpesvirus; major Immediate early enhancer; Transcription; Cell Biology

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APA (6th Edition):

Galle, C. S. (2013). Characterization of Cis-acting partners within the cytomegalovirus major immediate-early enhancer that strengthen MIE gene expression and viral fitness. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/4985

Chicago Manual of Style (16th Edition):

Galle, Courtney Searcey. “Characterization of Cis-acting partners within the cytomegalovirus major immediate-early enhancer that strengthen MIE gene expression and viral fitness.” 2013. Doctoral Dissertation, University of Iowa. Accessed November 22, 2019. https://ir.uiowa.edu/etd/4985.

MLA Handbook (7th Edition):

Galle, Courtney Searcey. “Characterization of Cis-acting partners within the cytomegalovirus major immediate-early enhancer that strengthen MIE gene expression and viral fitness.” 2013. Web. 22 Nov 2019.

Vancouver:

Galle CS. Characterization of Cis-acting partners within the cytomegalovirus major immediate-early enhancer that strengthen MIE gene expression and viral fitness. [Internet] [Doctoral dissertation]. University of Iowa; 2013. [cited 2019 Nov 22]. Available from: https://ir.uiowa.edu/etd/4985.

Council of Science Editors:

Galle CS. Characterization of Cis-acting partners within the cytomegalovirus major immediate-early enhancer that strengthen MIE gene expression and viral fitness. [Doctoral Dissertation]. University of Iowa; 2013. Available from: https://ir.uiowa.edu/etd/4985

4. Ladam, Franck. Etude du rôle du facteur de transcription Pea3 pendant la morphogenèse et la tumorigenèse mammaires : caractérisation de ses propriétés pro-morphogènes et pro-tumorigènes : étude des mécanismes moléculaires associés : Study of the Pea3 transcription factor involvement during mammary morphogenesis and tumorigenesis : characterization of its morphogenetic and tumorigenic properties : analysis of the molecular mechanisms involving Pea3.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2010, Université Lille II – Droit et Santé

 Les Facteurs de transcription du groupe PEA3 (Pea3, Erm et Er81) font partie de la famille d’oncogènes ETS. Leur expression est souvent observée lors de… (more)

Subjects/Keywords: Pea3; Polyomavirus enhancer activator 3

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APA (6th Edition):

Ladam, F. (2010). Etude du rôle du facteur de transcription Pea3 pendant la morphogenèse et la tumorigenèse mammaires : caractérisation de ses propriétés pro-morphogènes et pro-tumorigènes : étude des mécanismes moléculaires associés : Study of the Pea3 transcription factor involvement during mammary morphogenesis and tumorigenesis : characterization of its morphogenetic and tumorigenic properties : analysis of the molecular mechanisms involving Pea3. (Doctoral Dissertation). Université Lille II – Droit et Santé. Retrieved from http://www.theses.fr/2010LIL2S031

Chicago Manual of Style (16th Edition):

Ladam, Franck. “Etude du rôle du facteur de transcription Pea3 pendant la morphogenèse et la tumorigenèse mammaires : caractérisation de ses propriétés pro-morphogènes et pro-tumorigènes : étude des mécanismes moléculaires associés : Study of the Pea3 transcription factor involvement during mammary morphogenesis and tumorigenesis : characterization of its morphogenetic and tumorigenic properties : analysis of the molecular mechanisms involving Pea3.” 2010. Doctoral Dissertation, Université Lille II – Droit et Santé. Accessed November 22, 2019. http://www.theses.fr/2010LIL2S031.

MLA Handbook (7th Edition):

Ladam, Franck. “Etude du rôle du facteur de transcription Pea3 pendant la morphogenèse et la tumorigenèse mammaires : caractérisation de ses propriétés pro-morphogènes et pro-tumorigènes : étude des mécanismes moléculaires associés : Study of the Pea3 transcription factor involvement during mammary morphogenesis and tumorigenesis : characterization of its morphogenetic and tumorigenic properties : analysis of the molecular mechanisms involving Pea3.” 2010. Web. 22 Nov 2019.

Vancouver:

Ladam F. Etude du rôle du facteur de transcription Pea3 pendant la morphogenèse et la tumorigenèse mammaires : caractérisation de ses propriétés pro-morphogènes et pro-tumorigènes : étude des mécanismes moléculaires associés : Study of the Pea3 transcription factor involvement during mammary morphogenesis and tumorigenesis : characterization of its morphogenetic and tumorigenic properties : analysis of the molecular mechanisms involving Pea3. [Internet] [Doctoral dissertation]. Université Lille II – Droit et Santé 2010. [cited 2019 Nov 22]. Available from: http://www.theses.fr/2010LIL2S031.

Council of Science Editors:

Ladam F. Etude du rôle du facteur de transcription Pea3 pendant la morphogenèse et la tumorigenèse mammaires : caractérisation de ses propriétés pro-morphogènes et pro-tumorigènes : étude des mécanismes moléculaires associés : Study of the Pea3 transcription factor involvement during mammary morphogenesis and tumorigenesis : characterization of its morphogenetic and tumorigenic properties : analysis of the molecular mechanisms involving Pea3. [Doctoral Dissertation]. Université Lille II – Droit et Santé 2010. Available from: http://www.theses.fr/2010LIL2S031


University of Edinburgh

5. Taylor, Gillian Catherine Agnes. H4K16 acetylation during embryonic stem cell differentiation.

Degree: PhD, 2013, University of Edinburgh

 Eukaryote DNA is organised into the more compact nucleosome by wrapping 147bp of DNA around a histone octamer core. The N-terminal tails of the histones… (more)

Subjects/Keywords: H4K16ac; chromatin; enhancer; histone modification

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APA (6th Edition):

Taylor, G. C. A. (2013). H4K16 acetylation during embryonic stem cell differentiation. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/8069

Chicago Manual of Style (16th Edition):

Taylor, Gillian Catherine Agnes. “H4K16 acetylation during embryonic stem cell differentiation.” 2013. Doctoral Dissertation, University of Edinburgh. Accessed November 22, 2019. http://hdl.handle.net/1842/8069.

MLA Handbook (7th Edition):

Taylor, Gillian Catherine Agnes. “H4K16 acetylation during embryonic stem cell differentiation.” 2013. Web. 22 Nov 2019.

Vancouver:

Taylor GCA. H4K16 acetylation during embryonic stem cell differentiation. [Internet] [Doctoral dissertation]. University of Edinburgh; 2013. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/1842/8069.

Council of Science Editors:

Taylor GCA. H4K16 acetylation during embryonic stem cell differentiation. [Doctoral Dissertation]. University of Edinburgh; 2013. Available from: http://hdl.handle.net/1842/8069


University of Utah

6. Song, Yang. Studies on human epidermal membrane with alternating current.

Degree: MS;, Pharmaceutics & Pharmaceutical Chemistry;, 2001, University of Utah

 Alternating current (AC) electric field was found to be able to induce and keep human epidermal membrane (HEM) electrical conductance constant during iontophoresis. The technique… (more)

Subjects/Keywords: Chemical Enhancer; Electrical

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APA (6th Edition):

Song, Y. (2001). Studies on human epidermal membrane with alternating current. (Masters Thesis). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1610/rec/1099

Chicago Manual of Style (16th Edition):

Song, Yang. “Studies on human epidermal membrane with alternating current.” 2001. Masters Thesis, University of Utah. Accessed November 22, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1610/rec/1099.

MLA Handbook (7th Edition):

Song, Yang. “Studies on human epidermal membrane with alternating current.” 2001. Web. 22 Nov 2019.

Vancouver:

Song Y. Studies on human epidermal membrane with alternating current. [Internet] [Masters thesis]. University of Utah; 2001. [cited 2019 Nov 22]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1610/rec/1099.

Council of Science Editors:

Song Y. Studies on human epidermal membrane with alternating current. [Masters Thesis]. University of Utah; 2001. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1610/rec/1099

7. Viswanathan, Priya. Molecular analysis of the baculovirus enhancer sequence; -.

Degree: Immunology, 2002, Jawaharlal Nehru University

None

Bibilography p.121

Advisors/Committee Members: Hasnain, Seyed E.

Subjects/Keywords: Immunology; Baculovirus; enhancer

Page 1

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APA (6th Edition):

Viswanathan, P. (2002). Molecular analysis of the baculovirus enhancer sequence; -. (Thesis). Jawaharlal Nehru University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/21030

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):

Viswanathan, Priya. “Molecular analysis of the baculovirus enhancer sequence; -.” 2002. Thesis, Jawaharlal Nehru University. Accessed November 22, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/21030.

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

MLA Handbook (7th Edition):

Viswanathan, Priya. “Molecular analysis of the baculovirus enhancer sequence; -.” 2002. Web. 22 Nov 2019.

Vancouver:

Viswanathan P. Molecular analysis of the baculovirus enhancer sequence; -. [Internet] [Thesis]. Jawaharlal Nehru University; 2002. [cited 2019 Nov 22]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/21030.

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

Council of Science Editors:

Viswanathan P. Molecular analysis of the baculovirus enhancer sequence; -. [Thesis]. Jawaharlal Nehru University; 2002. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/21030

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


Case Western Reserve University

8. Akhtar-Zaidi, Batool. DISCOVERY OF NOVEL EPIGENETIC MECHANISMS OF CARCINOGENESIS BY GENOME-WIDE PROFILING OF NON-CODING REGULATORY ELEMENTS.

Degree: PhD, Molecular Medicine, 2013, Case Western Reserve University

 Epigenetic mechanisms are of paramount importance in cancer. Historically, epigenetic studies of cancer have focused on aberrant DNA methylation events. Far less is known about… (more)

Subjects/Keywords: Biomedical Research; Epigenetics; cancer; enhancer elements

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APA (6th Edition):

Akhtar-Zaidi, B. (2013). DISCOVERY OF NOVEL EPIGENETIC MECHANISMS OF CARCINOGENESIS BY GENOME-WIDE PROFILING OF NON-CODING REGULATORY ELEMENTS. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1347020396

Chicago Manual of Style (16th Edition):

Akhtar-Zaidi, Batool. “DISCOVERY OF NOVEL EPIGENETIC MECHANISMS OF CARCINOGENESIS BY GENOME-WIDE PROFILING OF NON-CODING REGULATORY ELEMENTS.” 2013. Doctoral Dissertation, Case Western Reserve University. Accessed November 22, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1347020396.

MLA Handbook (7th Edition):

Akhtar-Zaidi, Batool. “DISCOVERY OF NOVEL EPIGENETIC MECHANISMS OF CARCINOGENESIS BY GENOME-WIDE PROFILING OF NON-CODING REGULATORY ELEMENTS.” 2013. Web. 22 Nov 2019.

Vancouver:

Akhtar-Zaidi B. DISCOVERY OF NOVEL EPIGENETIC MECHANISMS OF CARCINOGENESIS BY GENOME-WIDE PROFILING OF NON-CODING REGULATORY ELEMENTS. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2013. [cited 2019 Nov 22]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1347020396.

Council of Science Editors:

Akhtar-Zaidi B. DISCOVERY OF NOVEL EPIGENETIC MECHANISMS OF CARCINOGENESIS BY GENOME-WIDE PROFILING OF NON-CODING REGULATORY ELEMENTS. [Doctoral Dissertation]. Case Western Reserve University; 2013. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1347020396

9. Li, Yuan. LUC7L3/CROP inhibits replication of hepatitis B virus via suppressing enhancer II/basal core promoter activity : LUC7L3/CROPはエンハンサーII/ベーサルコアプロモーターを抑制することによりB型肝炎ウイルスの複製を阻害する.

Degree: 博士(医学), 2017, Hamamatsu University School of Medicine / 浜松医科大学

The core promoter of hepatitis B virus (HBV) genome is a critical region for transcriptional initiation of 3.5 kb, pregenome and precore RNAs and for… (more)

Subjects/Keywords: Hepatitis B virus; HBV; replication; promoter; enhancer

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APA (6th Edition):

Li, Y. (2017). LUC7L3/CROP inhibits replication of hepatitis B virus via suppressing enhancer II/basal core promoter activity : LUC7L3/CROPはエンハンサーII/ベーサルコアプロモーターを抑制することによりB型肝炎ウイルスの複製を阻害する. (Thesis). Hamamatsu University School of Medicine / 浜松医科大学. Retrieved from http://hdl.handle.net/10271/3215

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):

Li, Yuan. “LUC7L3/CROP inhibits replication of hepatitis B virus via suppressing enhancer II/basal core promoter activity : LUC7L3/CROPはエンハンサーII/ベーサルコアプロモーターを抑制することによりB型肝炎ウイルスの複製を阻害する.” 2017. Thesis, Hamamatsu University School of Medicine / 浜松医科大学. Accessed November 22, 2019. http://hdl.handle.net/10271/3215.

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

MLA Handbook (7th Edition):

Li, Yuan. “LUC7L3/CROP inhibits replication of hepatitis B virus via suppressing enhancer II/basal core promoter activity : LUC7L3/CROPはエンハンサーII/ベーサルコアプロモーターを抑制することによりB型肝炎ウイルスの複製を阻害する.” 2017. Web. 22 Nov 2019.

Vancouver:

Li Y. LUC7L3/CROP inhibits replication of hepatitis B virus via suppressing enhancer II/basal core promoter activity : LUC7L3/CROPはエンハンサーII/ベーサルコアプロモーターを抑制することによりB型肝炎ウイルスの複製を阻害する. [Internet] [Thesis]. Hamamatsu University School of Medicine / 浜松医科大学; 2017. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/10271/3215.

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

Council of Science Editors:

Li Y. LUC7L3/CROP inhibits replication of hepatitis B virus via suppressing enhancer II/basal core promoter activity : LUC7L3/CROPはエンハンサーII/ベーサルコアプロモーターを抑制することによりB型肝炎ウイルスの複製を阻害する. [Thesis]. Hamamatsu University School of Medicine / 浜松医科大学; 2017. Available from: http://hdl.handle.net/10271/3215

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


University of California – San Diego

10. Suter, Thomas. Enhancer function driving cellular senescence, DNA damage repair, differentiation, and nuclear organization.

Degree: Biology, 2017, University of California – San Diego

 This dissertation, by Thomas Barton Suter, discusses enhancer function driving cellular senescence, DNA damage repair, differentiation, and nuclear organization. Enhancers are a major regulatory feature… (more)

Subjects/Keywords: Molecular biology; Aging; Enhancer; Methylation; Rapamycin; Senescence

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APA (6th Edition):

Suter, T. (2017). Enhancer function driving cellular senescence, DNA damage repair, differentiation, and nuclear organization. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/17t5r581

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):

Suter, Thomas. “Enhancer function driving cellular senescence, DNA damage repair, differentiation, and nuclear organization.” 2017. Thesis, University of California – San Diego. Accessed November 22, 2019. http://www.escholarship.org/uc/item/17t5r581.

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

MLA Handbook (7th Edition):

Suter, Thomas. “Enhancer function driving cellular senescence, DNA damage repair, differentiation, and nuclear organization.” 2017. Web. 22 Nov 2019.

Vancouver:

Suter T. Enhancer function driving cellular senescence, DNA damage repair, differentiation, and nuclear organization. [Internet] [Thesis]. University of California – San Diego; 2017. [cited 2019 Nov 22]. Available from: http://www.escholarship.org/uc/item/17t5r581.

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

Council of Science Editors:

Suter T. Enhancer function driving cellular senescence, DNA damage repair, differentiation, and nuclear organization. [Thesis]. University of California – San Diego; 2017. Available from: http://www.escholarship.org/uc/item/17t5r581

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


University of California – San Diego

11. Yang, Lu. Ligand mediated interactions between ER alpha enhancers on chromosome 21 results in the formation of a “distributed estradiol super enhancer”.

Degree: Biology, 2017, University of California – San Diego

 Discovery of transferable distal genetic elements capable of activating gene transcription was a milestone in the study of transcriptional control. These genetic elements were termed… (more)

Subjects/Keywords: Biology; CRISPR; Enhancer; Estrogen; FISH; Genetics

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APA (6th Edition):

Yang, L. (2017). Ligand mediated interactions between ER alpha enhancers on chromosome 21 results in the formation of a “distributed estradiol super enhancer”. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/5g38r02z

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):

Yang, Lu. “Ligand mediated interactions between ER alpha enhancers on chromosome 21 results in the formation of a “distributed estradiol super enhancer”.” 2017. Thesis, University of California – San Diego. Accessed November 22, 2019. http://www.escholarship.org/uc/item/5g38r02z.

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

MLA Handbook (7th Edition):

Yang, Lu. “Ligand mediated interactions between ER alpha enhancers on chromosome 21 results in the formation of a “distributed estradiol super enhancer”.” 2017. Web. 22 Nov 2019.

Vancouver:

Yang L. Ligand mediated interactions between ER alpha enhancers on chromosome 21 results in the formation of a “distributed estradiol super enhancer”. [Internet] [Thesis]. University of California – San Diego; 2017. [cited 2019 Nov 22]. Available from: http://www.escholarship.org/uc/item/5g38r02z.

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

Council of Science Editors:

Yang L. Ligand mediated interactions between ER alpha enhancers on chromosome 21 results in the formation of a “distributed estradiol super enhancer”. [Thesis]. University of California – San Diego; 2017. Available from: http://www.escholarship.org/uc/item/5g38r02z

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


University of Edinburgh

12. Benabdallah, Suzanne Nezha. New model for long-range chromatin reorganisation upon enhancer-driven gene activation.

Degree: PhD, 2017, University of Edinburgh

 Enhancers are non-coding DNA sequences which are able to activate the expression of a gene in a specific tissue manner and at a precise stage… (more)

Subjects/Keywords: 616; enhancer-promoter communication; chromatin organisation; imaging

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APA (6th Edition):

Benabdallah, S. N. (2017). New model for long-range chromatin reorganisation upon enhancer-driven gene activation. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/23575

Chicago Manual of Style (16th Edition):

Benabdallah, Suzanne Nezha. “New model for long-range chromatin reorganisation upon enhancer-driven gene activation.” 2017. Doctoral Dissertation, University of Edinburgh. Accessed November 22, 2019. http://hdl.handle.net/1842/23575.

MLA Handbook (7th Edition):

Benabdallah, Suzanne Nezha. “New model for long-range chromatin reorganisation upon enhancer-driven gene activation.” 2017. Web. 22 Nov 2019.

Vancouver:

Benabdallah SN. New model for long-range chromatin reorganisation upon enhancer-driven gene activation. [Internet] [Doctoral dissertation]. University of Edinburgh; 2017. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/1842/23575.

Council of Science Editors:

Benabdallah SN. New model for long-range chromatin reorganisation upon enhancer-driven gene activation. [Doctoral Dissertation]. University of Edinburgh; 2017. Available from: http://hdl.handle.net/1842/23575


University of California – San Diego

13. Oh, Soohwan. Enhancer Activation, Release and Retargeting in Transcription.

Degree: Biology, 2018, University of California – San Diego

 This dissertation, by Soohwan Oh, discusses the general mechanisms how enhancers bring target genes activation in various stimuli. Enhancers are cis-regulatory DNA sequences that can… (more)

Subjects/Keywords: Molecular biology; chromatin; enhancer; promoter; transcription

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

APA (6th Edition):

Oh, S. (2018). Enhancer Activation, Release and Retargeting in Transcription. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/1vs5g8vh

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):

Oh, Soohwan. “Enhancer Activation, Release and Retargeting in Transcription.” 2018. Thesis, University of California – San Diego. Accessed November 22, 2019. http://www.escholarship.org/uc/item/1vs5g8vh.

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

MLA Handbook (7th Edition):

Oh, Soohwan. “Enhancer Activation, Release and Retargeting in Transcription.” 2018. Web. 22 Nov 2019.

Vancouver:

Oh S. Enhancer Activation, Release and Retargeting in Transcription. [Internet] [Thesis]. University of California – San Diego; 2018. [cited 2019 Nov 22]. Available from: http://www.escholarship.org/uc/item/1vs5g8vh.

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

Council of Science Editors:

Oh S. Enhancer Activation, Release and Retargeting in Transcription. [Thesis]. University of California – San Diego; 2018. Available from: http://www.escholarship.org/uc/item/1vs5g8vh

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


University of Cambridge

14. Vojtasova, Erika. HIF2a regulates ccRCC tumorigenesis through activation of cell cycle regulators .

Degree: 2019, University of Cambridge

 Clear cell renal cell carcinoma (ccRCC) is the most frequent type of kidney cancer, with 50% 5-year survival. Genetically, ccRCCs are characterised by inactivation of… (more)

Subjects/Keywords: tumour maintenance; cell cycle regulators; enhancer; ccRCC

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APA (6th Edition):

Vojtasova, E. (2019). HIF2a regulates ccRCC tumorigenesis through activation of cell cycle regulators . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/293838

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):

Vojtasova, Erika. “HIF2a regulates ccRCC tumorigenesis through activation of cell cycle regulators .” 2019. Thesis, University of Cambridge. Accessed November 22, 2019. https://www.repository.cam.ac.uk/handle/1810/293838.

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

MLA Handbook (7th Edition):

Vojtasova, Erika. “HIF2a regulates ccRCC tumorigenesis through activation of cell cycle regulators .” 2019. Web. 22 Nov 2019.

Vancouver:

Vojtasova E. HIF2a regulates ccRCC tumorigenesis through activation of cell cycle regulators . [Internet] [Thesis]. University of Cambridge; 2019. [cited 2019 Nov 22]. Available from: https://www.repository.cam.ac.uk/handle/1810/293838.

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

Council of Science Editors:

Vojtasova E. HIF2a regulates ccRCC tumorigenesis through activation of cell cycle regulators . [Thesis]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/293838

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


University of Connecticut

15. Xing, Jian. Epigenetic Profiling of Active Enhancers in Mouse Retinal Ganglion Cells.

Degree: MS, Biomedical Engineering, 2018, University of Connecticut

  Retinal ganglion cells (RGCs) are projection neurons of the eye, which process and pass visual information collected in the eyes to the brain. However,… (more)

Subjects/Keywords: Epigenetic profile; Enhancer; Retinal ganglion cells

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APA (6th Edition):

Xing, J. (2018). Epigenetic Profiling of Active Enhancers in Mouse Retinal Ganglion Cells. (Masters Thesis). University of Connecticut. Retrieved from https://opencommons.uconn.edu/gs_theses/1268

Chicago Manual of Style (16th Edition):

Xing, Jian. “Epigenetic Profiling of Active Enhancers in Mouse Retinal Ganglion Cells.” 2018. Masters Thesis, University of Connecticut. Accessed November 22, 2019. https://opencommons.uconn.edu/gs_theses/1268.

MLA Handbook (7th Edition):

Xing, Jian. “Epigenetic Profiling of Active Enhancers in Mouse Retinal Ganglion Cells.” 2018. Web. 22 Nov 2019.

Vancouver:

Xing J. Epigenetic Profiling of Active Enhancers in Mouse Retinal Ganglion Cells. [Internet] [Masters thesis]. University of Connecticut; 2018. [cited 2019 Nov 22]. Available from: https://opencommons.uconn.edu/gs_theses/1268.

Council of Science Editors:

Xing J. Epigenetic Profiling of Active Enhancers in Mouse Retinal Ganglion Cells. [Masters Thesis]. University of Connecticut; 2018. Available from: https://opencommons.uconn.edu/gs_theses/1268


University of Southern California

16. Mendoza-Fandiño, Gustavo Alfonso. Functional characterization of colorectal cancer GWAS loci.

Degree: PhD, Biochemistry and Molecular Biology, 2013, University of Southern California

 Genome-wide association studies (GWAS) have provided a powerful approach to identify CRC common disease variants. As of June 2012, 18 CRC loci have been identified… (more)

Subjects/Keywords: GWAS; common variant; functional variant; enhancer elements

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APA (6th Edition):

Mendoza-Fandiño, G. A. (2013). Functional characterization of colorectal cancer GWAS loci. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/220618/rec/2937

Chicago Manual of Style (16th Edition):

Mendoza-Fandiño, Gustavo Alfonso. “Functional characterization of colorectal cancer GWAS loci.” 2013. Doctoral Dissertation, University of Southern California. Accessed November 22, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/220618/rec/2937.

MLA Handbook (7th Edition):

Mendoza-Fandiño, Gustavo Alfonso. “Functional characterization of colorectal cancer GWAS loci.” 2013. Web. 22 Nov 2019.

Vancouver:

Mendoza-Fandiño GA. Functional characterization of colorectal cancer GWAS loci. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2019 Nov 22]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/220618/rec/2937.

Council of Science Editors:

Mendoza-Fandiño GA. Functional characterization of colorectal cancer GWAS loci. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/220618/rec/2937


University of Bath

17. Wu, Xianming. The impact of splicing related constraints on exonic evolution.

Degree: PhD, 2016, University of Bath

 Regulation of pre-mRNA splicing is a key process for most if not all eukaryotes. The process can, in the abstract, be considered as a series… (more)

Subjects/Keywords: 572.8; Exonic splicing enhancer; Synonymous mutation; SNP

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APA (6th Edition):

Wu, X. (2016). The impact of splicing related constraints on exonic evolution. (Doctoral Dissertation). University of Bath. Retrieved from https://researchportal.bath.ac.uk/en/studentthesis/the-impact-of-splicing-related-constraints-on-exonic-evolution(971e3d7d-0b22-4078-98c7-be4a57a8792f).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.687321

Chicago Manual of Style (16th Edition):

Wu, Xianming. “The impact of splicing related constraints on exonic evolution.” 2016. Doctoral Dissertation, University of Bath. Accessed November 22, 2019. https://researchportal.bath.ac.uk/en/studentthesis/the-impact-of-splicing-related-constraints-on-exonic-evolution(971e3d7d-0b22-4078-98c7-be4a57a8792f).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.687321.

MLA Handbook (7th Edition):

Wu, Xianming. “The impact of splicing related constraints on exonic evolution.” 2016. Web. 22 Nov 2019.

Vancouver:

Wu X. The impact of splicing related constraints on exonic evolution. [Internet] [Doctoral dissertation]. University of Bath; 2016. [cited 2019 Nov 22]. Available from: https://researchportal.bath.ac.uk/en/studentthesis/the-impact-of-splicing-related-constraints-on-exonic-evolution(971e3d7d-0b22-4078-98c7-be4a57a8792f).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.687321.

Council of Science Editors:

Wu X. The impact of splicing related constraints on exonic evolution. [Doctoral Dissertation]. University of Bath; 2016. Available from: https://researchportal.bath.ac.uk/en/studentthesis/the-impact-of-splicing-related-constraints-on-exonic-evolution(971e3d7d-0b22-4078-98c7-be4a57a8792f).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.687321


University of Debrecen

18. Sümegi, Ádám Ferenc. Intronok szerepe a génexpresszió szabályozásában .

Degree: DE – Természettudományi és Technológiai Kar – Biológiai és Ökológiai Intézet, University of Debrecen

 A transzkripció végtermékeként létrejövő pre-mRNS a kódoló régiókon túl (exonok) nem kódoló régiókat (intonok) is tartalmaz, ezek a pre-mRNS érése során háromlépéses folyamatban kivágódnak. Szakdolgozatomban… (more)

Subjects/Keywords: intron; génexpresszió; enhancer

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

APA (6th Edition):

Sümegi, . F. (n.d.). Intronok szerepe a génexpresszió szabályozásában . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/259511

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Sümegi, Ádám Ferenc. “Intronok szerepe a génexpresszió szabályozásában .” Thesis, University of Debrecen. Accessed November 22, 2019. http://hdl.handle.net/2437/259511.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Sümegi, Ádám Ferenc. “Intronok szerepe a génexpresszió szabályozásában .” Web. 22 Nov 2019.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Sümegi F. Intronok szerepe a génexpresszió szabályozásában . [Internet] [Thesis]. University of Debrecen; [cited 2019 Nov 22]. Available from: http://hdl.handle.net/2437/259511.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

Sümegi F. Intronok szerepe a génexpresszió szabályozásában . [Thesis]. University of Debrecen; Available from: http://hdl.handle.net/2437/259511

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

19. Scionti, Isabella. Epigenetic Regulation of Skeletal Muscle Differentiation : Régulation épigénétique de la différenciation du muscle squelettique.

Degree: Docteur es, Biologie, 2017, Lyon

LSD1 et PHF2 sont des déméthylases de lysines capables de déméthyler à la fois les protéines histones qui influencent l’expression génique et les protéines non… (more)

Subjects/Keywords: LSD1; PHF2; MyoD; ARN enhancer; Muscle; Différenciation; LSD1; PHF2; MyoD; RNA enhancer; Muscle; Differenciation

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

APA (6th Edition):

Scionti, I. (2017). Epigenetic Regulation of Skeletal Muscle Differentiation : Régulation épigénétique de la différenciation du muscle squelettique. (Doctoral Dissertation). Lyon. Retrieved from http://www.theses.fr/2017LYSEN084

Chicago Manual of Style (16th Edition):

Scionti, Isabella. “Epigenetic Regulation of Skeletal Muscle Differentiation : Régulation épigénétique de la différenciation du muscle squelettique.” 2017. Doctoral Dissertation, Lyon. Accessed November 22, 2019. http://www.theses.fr/2017LYSEN084.

MLA Handbook (7th Edition):

Scionti, Isabella. “Epigenetic Regulation of Skeletal Muscle Differentiation : Régulation épigénétique de la différenciation du muscle squelettique.” 2017. Web. 22 Nov 2019.

Vancouver:

Scionti I. Epigenetic Regulation of Skeletal Muscle Differentiation : Régulation épigénétique de la différenciation du muscle squelettique. [Internet] [Doctoral dissertation]. Lyon; 2017. [cited 2019 Nov 22]. Available from: http://www.theses.fr/2017LYSEN084.

Council of Science Editors:

Scionti I. Epigenetic Regulation of Skeletal Muscle Differentiation : Régulation épigénétique de la différenciation du muscle squelettique. [Doctoral Dissertation]. Lyon; 2017. Available from: http://www.theses.fr/2017LYSEN084

20. Gobe, Clara. Régulation épigénétique de l’expression de FOXL2 et voies activées en aval de ce gène dans la gonade : FOXL2 : Epigenetic regulation of its expression and downstream activated pathways in the gonad.

Degree: Docteur es, Sciences de la vie et de la santé, 2018, Paris Saclay

FOXL2 constitue un gène majeur de la différenciation et de la fonction ovarienne. Chez l’Homme, l’haploinsuffisance de ce gène induit des malformations palpébrales qui peuvent… (more)

Subjects/Keywords: Gonades; Dmxl2; Spermatogénèse; Epigénétique; Enhancer; CRISPR/dCas9; Gonads; Dmxl2; Spermatogenesis; Epigenetics; Enhancer; CRISPR/dCas9

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APA (6th Edition):

Gobe, C. (2018). Régulation épigénétique de l’expression de FOXL2 et voies activées en aval de ce gène dans la gonade : FOXL2 : Epigenetic regulation of its expression and downstream activated pathways in the gonad. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2018SACLS476

Chicago Manual of Style (16th Edition):

Gobe, Clara. “Régulation épigénétique de l’expression de FOXL2 et voies activées en aval de ce gène dans la gonade : FOXL2 : Epigenetic regulation of its expression and downstream activated pathways in the gonad.” 2018. Doctoral Dissertation, Paris Saclay. Accessed November 22, 2019. http://www.theses.fr/2018SACLS476.

MLA Handbook (7th Edition):

Gobe, Clara. “Régulation épigénétique de l’expression de FOXL2 et voies activées en aval de ce gène dans la gonade : FOXL2 : Epigenetic regulation of its expression and downstream activated pathways in the gonad.” 2018. Web. 22 Nov 2019.

Vancouver:

Gobe C. Régulation épigénétique de l’expression de FOXL2 et voies activées en aval de ce gène dans la gonade : FOXL2 : Epigenetic regulation of its expression and downstream activated pathways in the gonad. [Internet] [Doctoral dissertation]. Paris Saclay; 2018. [cited 2019 Nov 22]. Available from: http://www.theses.fr/2018SACLS476.

Council of Science Editors:

Gobe C. Régulation épigénétique de l’expression de FOXL2 et voies activées en aval de ce gène dans la gonade : FOXL2 : Epigenetic regulation of its expression and downstream activated pathways in the gonad. [Doctoral Dissertation]. Paris Saclay; 2018. Available from: http://www.theses.fr/2018SACLS476

21. Dao, Thi Mai Lan. Découverte des nouvelles classes d'éléments cis-régulateurs par une approche gène-rapporteur à haut débit : Discovery of new classes of cis-regulatory elements by high-throughput reporter assay.

Degree: Docteur es, Biologie, 2016, Aix Marseille Université

L'étape initiale dans l'expression génique est la transcription de l'ADN génomique du gène en ARN. La transcription être initiée par l'assemblage d'ARN pol II autour… (more)

Subjects/Keywords: Promoteurs; Amplificateurs; Epromoter; Essai amplificateurs reporter à haut débit; CapStarr-Seq; Promoter; Enhancer; Epromoter; High-Throughput enhancer assays; CapStarr-Seq; 570

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APA (6th Edition):

Dao, T. M. L. (2016). Découverte des nouvelles classes d'éléments cis-régulateurs par une approche gène-rapporteur à haut débit : Discovery of new classes of cis-regulatory elements by high-throughput reporter assay. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2016AIXM4036

Chicago Manual of Style (16th Edition):

Dao, Thi Mai Lan. “Découverte des nouvelles classes d'éléments cis-régulateurs par une approche gène-rapporteur à haut débit : Discovery of new classes of cis-regulatory elements by high-throughput reporter assay.” 2016. Doctoral Dissertation, Aix Marseille Université. Accessed November 22, 2019. http://www.theses.fr/2016AIXM4036.

MLA Handbook (7th Edition):

Dao, Thi Mai Lan. “Découverte des nouvelles classes d'éléments cis-régulateurs par une approche gène-rapporteur à haut débit : Discovery of new classes of cis-regulatory elements by high-throughput reporter assay.” 2016. Web. 22 Nov 2019.

Vancouver:

Dao TML. Découverte des nouvelles classes d'éléments cis-régulateurs par une approche gène-rapporteur à haut débit : Discovery of new classes of cis-regulatory elements by high-throughput reporter assay. [Internet] [Doctoral dissertation]. Aix Marseille Université 2016. [cited 2019 Nov 22]. Available from: http://www.theses.fr/2016AIXM4036.

Council of Science Editors:

Dao TML. Découverte des nouvelles classes d'éléments cis-régulateurs par une approche gène-rapporteur à haut débit : Discovery of new classes of cis-regulatory elements by high-throughput reporter assay. [Doctoral Dissertation]. Aix Marseille Université 2016. Available from: http://www.theses.fr/2016AIXM4036


University of Helsinki

22. Määttä, Juha. Uusi rotan beeta-tropomyosiinigeenin enhancer-elementti.

Degree: 1993, University of Helsinki

Subjects/Keywords: enhancer; geeninsäätely; rotta; tropomyosiini; Biokemia; enhancer; geeninsäätely; rotta; tropomyosiini

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APA (6th Edition):

Määttä, J. (1993). Uusi rotan beeta-tropomyosiinigeenin enhancer-elementti. (Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/157974

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):

Määttä, Juha. “Uusi rotan beeta-tropomyosiinigeenin enhancer-elementti.” 1993. Thesis, University of Helsinki. Accessed November 22, 2019. http://hdl.handle.net/10138/157974.

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

MLA Handbook (7th Edition):

Määttä, Juha. “Uusi rotan beeta-tropomyosiinigeenin enhancer-elementti.” 1993. Web. 22 Nov 2019.

Vancouver:

Määttä J. Uusi rotan beeta-tropomyosiinigeenin enhancer-elementti. [Internet] [Thesis]. University of Helsinki; 1993. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/10138/157974.

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

Council of Science Editors:

Määttä J. Uusi rotan beeta-tropomyosiinigeenin enhancer-elementti. [Thesis]. University of Helsinki; 1993. Available from: http://hdl.handle.net/10138/157974

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

23. Roure, Agnes. Mécanismes de régulations transcriptionnelles contrôlant la régionalisation de l'épiderme au cours du développement chez l'Ascidie Ciona intestinalis : Transcriptional regulation mecanisms specifying tail epidermis patterning in Ciona intestinalis development.

Degree: Docteur es, Biologie du developpement, 2013, Aix Marseille Université

3 domaines cellulaires définissent l'épiderme de la queue de Ciona intestinalis. Le domaine des lignes médianes, donne naissance à deux structures différenciées larvaires, la nageoire… (more)

Subjects/Keywords: Ciona intestinalis; Épiderme; Système nerveux périphérique; Régulation transcriptionnelle; Enhancer; Ciona intestinalis; Epidermis; Peripheral nervous system; Transcriptional regulation; Enhancer; 571.8

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APA (6th Edition):

Roure, A. (2013). Mécanismes de régulations transcriptionnelles contrôlant la régionalisation de l'épiderme au cours du développement chez l'Ascidie Ciona intestinalis : Transcriptional regulation mecanisms specifying tail epidermis patterning in Ciona intestinalis development. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2013AIXM4111

Chicago Manual of Style (16th Edition):

Roure, Agnes. “Mécanismes de régulations transcriptionnelles contrôlant la régionalisation de l'épiderme au cours du développement chez l'Ascidie Ciona intestinalis : Transcriptional regulation mecanisms specifying tail epidermis patterning in Ciona intestinalis development.” 2013. Doctoral Dissertation, Aix Marseille Université. Accessed November 22, 2019. http://www.theses.fr/2013AIXM4111.

MLA Handbook (7th Edition):

Roure, Agnes. “Mécanismes de régulations transcriptionnelles contrôlant la régionalisation de l'épiderme au cours du développement chez l'Ascidie Ciona intestinalis : Transcriptional regulation mecanisms specifying tail epidermis patterning in Ciona intestinalis development.” 2013. Web. 22 Nov 2019.

Vancouver:

Roure A. Mécanismes de régulations transcriptionnelles contrôlant la régionalisation de l'épiderme au cours du développement chez l'Ascidie Ciona intestinalis : Transcriptional regulation mecanisms specifying tail epidermis patterning in Ciona intestinalis development. [Internet] [Doctoral dissertation]. Aix Marseille Université 2013. [cited 2019 Nov 22]. Available from: http://www.theses.fr/2013AIXM4111.

Council of Science Editors:

Roure A. Mécanismes de régulations transcriptionnelles contrôlant la régionalisation de l'épiderme au cours du développement chez l'Ascidie Ciona intestinalis : Transcriptional regulation mecanisms specifying tail epidermis patterning in Ciona intestinalis development. [Doctoral Dissertation]. Aix Marseille Université 2013. Available from: http://www.theses.fr/2013AIXM4111


University of Vienna

24. Ahmad, Zabidi Muhammad Mamduh. Enhancer-responsiveness and -specificity of Core Promoters in gene transcription.

Degree: 2017, University of Vienna

Differenzielle Genexpression ist entscheidend für die Entwicklung mehrzelliger Lebewesen wie Menschen und Tiere und muss daher streng kontrolliert werden. Gene werden beginnend von einer etwa… (more)

Subjects/Keywords: 42.13 Molekularbiologie; 42.20 Genetik; Kernpromotor / Enhancer / Transkription / Genregulation / Genexpression; core promoter / enhancer / transcription / gene regulation / gene expression

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APA (6th Edition):

Ahmad, Z. M. M. (2017). Enhancer-responsiveness and -specificity of Core Promoters in gene transcription. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/46663/

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):

Ahmad, Zabidi Muhammad Mamduh. “Enhancer-responsiveness and -specificity of Core Promoters in gene transcription.” 2017. Thesis, University of Vienna. Accessed November 22, 2019. http://othes.univie.ac.at/46663/.

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

MLA Handbook (7th Edition):

Ahmad, Zabidi Muhammad Mamduh. “Enhancer-responsiveness and -specificity of Core Promoters in gene transcription.” 2017. Web. 22 Nov 2019.

Vancouver:

Ahmad ZMM. Enhancer-responsiveness and -specificity of Core Promoters in gene transcription. [Internet] [Thesis]. University of Vienna; 2017. [cited 2019 Nov 22]. Available from: http://othes.univie.ac.at/46663/.

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

Council of Science Editors:

Ahmad ZMM. Enhancer-responsiveness and -specificity of Core Promoters in gene transcription. [Thesis]. University of Vienna; 2017. Available from: http://othes.univie.ac.at/46663/

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

25. Brunelle, Mylène. Étude de l'influence du variant d'histone H2A.Z sur l'organisation des nucléosomes aux enhancers liés par le récepteur alpha de l'oestrogène.

Degree: PhD, Biologie, 2016, Université de Sherbrooke

 L'identité et la réactivité cellulaires sont établies, maintenues et modulées grâce à l'orchestration de programmes transcriptionnels spécifiques. Les éléments régulateurs, des régions particulières de la… (more)

Subjects/Keywords: Enhancer; H2A.Z; Transcription; Nucléosome; Récepteur alpha des oestrogènes

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APA (6th Edition):

Brunelle, M. (2016). Étude de l'influence du variant d'histone H2A.Z sur l'organisation des nucléosomes aux enhancers liés par le récepteur alpha de l'oestrogène. (Doctoral Dissertation). Université de Sherbrooke. Retrieved from http://www.collectionscanada.gc.ca/obj/thesescanada/vol2/QSHERU/TC-QSHERU-11143_8867.pdf ; http://savoirs.usherbrooke.ca/bitstream/11143/8867/1/Brunelle_Mylene_PhD_2016.pdf

Chicago Manual of Style (16th Edition):

Brunelle, Mylène. “Étude de l'influence du variant d'histone H2A.Z sur l'organisation des nucléosomes aux enhancers liés par le récepteur alpha de l'oestrogène.” 2016. Doctoral Dissertation, Université de Sherbrooke. Accessed November 22, 2019. http://www.collectionscanada.gc.ca/obj/thesescanada/vol2/QSHERU/TC-QSHERU-11143_8867.pdf ; http://savoirs.usherbrooke.ca/bitstream/11143/8867/1/Brunelle_Mylene_PhD_2016.pdf.

MLA Handbook (7th Edition):

Brunelle, Mylène. “Étude de l'influence du variant d'histone H2A.Z sur l'organisation des nucléosomes aux enhancers liés par le récepteur alpha de l'oestrogène.” 2016. Web. 22 Nov 2019.

Vancouver:

Brunelle M. Étude de l'influence du variant d'histone H2A.Z sur l'organisation des nucléosomes aux enhancers liés par le récepteur alpha de l'oestrogène. [Internet] [Doctoral dissertation]. Université de Sherbrooke; 2016. [cited 2019 Nov 22]. Available from: http://www.collectionscanada.gc.ca/obj/thesescanada/vol2/QSHERU/TC-QSHERU-11143_8867.pdf ; http://savoirs.usherbrooke.ca/bitstream/11143/8867/1/Brunelle_Mylene_PhD_2016.pdf.

Council of Science Editors:

Brunelle M. Étude de l'influence du variant d'histone H2A.Z sur l'organisation des nucléosomes aux enhancers liés par le récepteur alpha de l'oestrogène. [Doctoral Dissertation]. Université de Sherbrooke; 2016. Available from: http://www.collectionscanada.gc.ca/obj/thesescanada/vol2/QSHERU/TC-QSHERU-11143_8867.pdf ; http://savoirs.usherbrooke.ca/bitstream/11143/8867/1/Brunelle_Mylene_PhD_2016.pdf


Case Western Reserve University

26. Cohen, Andrea. Characterization of Altered Enhancer Usage Across the Human Colorectal Cancer Epigenome.

Degree: PhD, Genetics, 2017, Case Western Reserve University

 Cancer is often considered a disease of the genome, with aberrant gene expression patterns driven by underlying DNA mutations. However, cells natively control gene expression… (more)

Subjects/Keywords: Genetics; colorectal cancer; CRC; epigenetics; epigenome; enhancer; genomics

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

APA (6th Edition):

Cohen, A. (2017). Characterization of Altered Enhancer Usage Across the Human Colorectal Cancer Epigenome. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1491332948235594

Chicago Manual of Style (16th Edition):

Cohen, Andrea. “Characterization of Altered Enhancer Usage Across the Human Colorectal Cancer Epigenome.” 2017. Doctoral Dissertation, Case Western Reserve University. Accessed November 22, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1491332948235594.

MLA Handbook (7th Edition):

Cohen, Andrea. “Characterization of Altered Enhancer Usage Across the Human Colorectal Cancer Epigenome.” 2017. Web. 22 Nov 2019.

Vancouver:

Cohen A. Characterization of Altered Enhancer Usage Across the Human Colorectal Cancer Epigenome. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2017. [cited 2019 Nov 22]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1491332948235594.

Council of Science Editors:

Cohen A. Characterization of Altered Enhancer Usage Across the Human Colorectal Cancer Epigenome. [Doctoral Dissertation]. Case Western Reserve University; 2017. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1491332948235594

27. 八巻, 努. Caco-2細胞sheetにおけるpoly-L-arginineの水溶性高分子薬物の透過促進機構に関する研究 : Caco-2 サイボウ sheet ニ オケル poly-L-arginine ノ スイヨウセイ コウブンシ ヤクブツ ノ トウカ ソクシン キコウ ニ カンスル ケンキュウ; Mechanism of permeation enhancement of hydrophilic macromolecules by poly-L-arginine in Caco-2 cell sheet.

Degree: 博士(薬学), 2013, Josai University / 城西大学

学位授与機関:城西大学 学位記番号:博甲第60号,学位の種別:博士(薬学), 学位授与年月日: 平成25年(2013年) 3月19日 (90p.) 2013 – 08-01以降公開

Subjects/Keywords: poly-L-arginine; absorption enhancer; tight junction; hydrophilic; macromolecules; drug delivery

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

APA (6th Edition):

八巻, . (2013). Caco-2細胞sheetにおけるpoly-L-arginineの水溶性高分子薬物の透過促進機構に関する研究 : Caco-2 サイボウ sheet ニ オケル poly-L-arginine ノ スイヨウセイ コウブンシ ヤクブツ ノ トウカ ソクシン キコウ ニ カンスル ケンキュウ; Mechanism of permeation enhancement of hydrophilic macromolecules by poly-L-arginine in Caco-2 cell sheet. (Thesis). Josai University / 城西大学. Retrieved from http://libir.josai.ac.jp/il/meta_pub/G0000284repository_JOS-PhDK60

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):

八巻, 努. “Caco-2細胞sheetにおけるpoly-L-arginineの水溶性高分子薬物の透過促進機構に関する研究 : Caco-2 サイボウ sheet ニ オケル poly-L-arginine ノ スイヨウセイ コウブンシ ヤクブツ ノ トウカ ソクシン キコウ ニ カンスル ケンキュウ; Mechanism of permeation enhancement of hydrophilic macromolecules by poly-L-arginine in Caco-2 cell sheet.” 2013. Thesis, Josai University / 城西大学. Accessed November 22, 2019. http://libir.josai.ac.jp/il/meta_pub/G0000284repository_JOS-PhDK60.

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

MLA Handbook (7th Edition):

八巻, 努. “Caco-2細胞sheetにおけるpoly-L-arginineの水溶性高分子薬物の透過促進機構に関する研究 : Caco-2 サイボウ sheet ニ オケル poly-L-arginine ノ スイヨウセイ コウブンシ ヤクブツ ノ トウカ ソクシン キコウ ニ カンスル ケンキュウ; Mechanism of permeation enhancement of hydrophilic macromolecules by poly-L-arginine in Caco-2 cell sheet.” 2013. Web. 22 Nov 2019.

Vancouver:

八巻 . Caco-2細胞sheetにおけるpoly-L-arginineの水溶性高分子薬物の透過促進機構に関する研究 : Caco-2 サイボウ sheet ニ オケル poly-L-arginine ノ スイヨウセイ コウブンシ ヤクブツ ノ トウカ ソクシン キコウ ニ カンスル ケンキュウ; Mechanism of permeation enhancement of hydrophilic macromolecules by poly-L-arginine in Caco-2 cell sheet. [Internet] [Thesis]. Josai University / 城西大学; 2013. [cited 2019 Nov 22]. Available from: http://libir.josai.ac.jp/il/meta_pub/G0000284repository_JOS-PhDK60.

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

Council of Science Editors:

八巻 . Caco-2細胞sheetにおけるpoly-L-arginineの水溶性高分子薬物の透過促進機構に関する研究 : Caco-2 サイボウ sheet ニ オケル poly-L-arginine ノ スイヨウセイ コウブンシ ヤクブツ ノ トウカ ソクシン キコウ ニ カンスル ケンキュウ; Mechanism of permeation enhancement of hydrophilic macromolecules by poly-L-arginine in Caco-2 cell sheet. [Thesis]. Josai University / 城西大学; 2013. Available from: http://libir.josai.ac.jp/il/meta_pub/G0000284repository_JOS-PhDK60

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


Temple University

28. Li, Cong. The preformulation and formulation development for the transungual delivery of the antifungal drug econazole nitrate.

Degree: PhD, 2015, Temple University

Pharmaceutical Sciences

Onychomycosis is fungal infection of toe nails or fingernails caused by a fungal microbe that invades the nail bed. It is the most… (more)

Subjects/Keywords: Pharmaceutical sciences;

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

APA (6th Edition):

Li, C. (2015). The preformulation and formulation development for the transungual delivery of the antifungal drug econazole nitrate. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,340105

Chicago Manual of Style (16th Edition):

Li, Cong. “The preformulation and formulation development for the transungual delivery of the antifungal drug econazole nitrate.” 2015. Doctoral Dissertation, Temple University. Accessed November 22, 2019. http://digital.library.temple.edu/u?/p245801coll10,340105.

MLA Handbook (7th Edition):

Li, Cong. “The preformulation and formulation development for the transungual delivery of the antifungal drug econazole nitrate.” 2015. Web. 22 Nov 2019.

Vancouver:

Li C. The preformulation and formulation development for the transungual delivery of the antifungal drug econazole nitrate. [Internet] [Doctoral dissertation]. Temple University; 2015. [cited 2019 Nov 22]. Available from: http://digital.library.temple.edu/u?/p245801coll10,340105.

Council of Science Editors:

Li C. The preformulation and formulation development for the transungual delivery of the antifungal drug econazole nitrate. [Doctoral Dissertation]. Temple University; 2015. Available from: http://digital.library.temple.edu/u?/p245801coll10,340105


Texas Medical Center

29. Nolte, Mark J. Targeted Deletion Of Functionally Validated Enhancers Defines Their Role in Mouse Limb Development.

Degree: PhD, 2013, Texas Medical Center

  Transcriptional enhancers are genomic DNA sequences that contain clustered transcription factor (TF) binding sites. When combinations of TFs bind to enhancer sequences they act… (more)

Subjects/Keywords: enhancer; limb; mouse; development; p300; functional genetics; Medicine and Health Sciences

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

APA (6th Edition):

Nolte, M. J. (2013). Targeted Deletion Of Functionally Validated Enhancers Defines Their Role in Mouse Limb Development. (Doctoral Dissertation). Texas Medical Center. Retrieved from http://digitalcommons.library.tmc.edu/utgsbs_dissertations/388

Chicago Manual of Style (16th Edition):

Nolte, Mark J. “Targeted Deletion Of Functionally Validated Enhancers Defines Their Role in Mouse Limb Development.” 2013. Doctoral Dissertation, Texas Medical Center. Accessed November 22, 2019. http://digitalcommons.library.tmc.edu/utgsbs_dissertations/388.

MLA Handbook (7th Edition):

Nolte, Mark J. “Targeted Deletion Of Functionally Validated Enhancers Defines Their Role in Mouse Limb Development.” 2013. Web. 22 Nov 2019.

Vancouver:

Nolte MJ. Targeted Deletion Of Functionally Validated Enhancers Defines Their Role in Mouse Limb Development. [Internet] [Doctoral dissertation]. Texas Medical Center; 2013. [cited 2019 Nov 22]. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/388.

Council of Science Editors:

Nolte MJ. Targeted Deletion Of Functionally Validated Enhancers Defines Their Role in Mouse Limb Development. [Doctoral Dissertation]. Texas Medical Center; 2013. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/388


University of Oxford

30. Becker, Philipp Werner. Transcriptional regulators of arterial-specific endothelial and mural cell development.

Degree: PhD, 2015, University of Oxford

 The vertebrate vasculature is formed by populations of endothelial and mural cells that arrange into functionally and molecularly distinct arterial, venous and capillary beds. Although… (more)

Subjects/Keywords: 611; Biology; Developmental Biology; Vascular Biology; Enhancer; Transcription Factor

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

APA (6th Edition):

Becker, P. W. (2015). Transcriptional regulators of arterial-specific endothelial and mural cell development. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:01ac5c84-2e3b-4401-82ec-32331079e784 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.664810

Chicago Manual of Style (16th Edition):

Becker, Philipp Werner. “Transcriptional regulators of arterial-specific endothelial and mural cell development.” 2015. Doctoral Dissertation, University of Oxford. Accessed November 22, 2019. http://ora.ox.ac.uk/objects/uuid:01ac5c84-2e3b-4401-82ec-32331079e784 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.664810.

MLA Handbook (7th Edition):

Becker, Philipp Werner. “Transcriptional regulators of arterial-specific endothelial and mural cell development.” 2015. Web. 22 Nov 2019.

Vancouver:

Becker PW. Transcriptional regulators of arterial-specific endothelial and mural cell development. [Internet] [Doctoral dissertation]. University of Oxford; 2015. [cited 2019 Nov 22]. Available from: http://ora.ox.ac.uk/objects/uuid:01ac5c84-2e3b-4401-82ec-32331079e784 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.664810.

Council of Science Editors:

Becker PW. Transcriptional regulators of arterial-specific endothelial and mural cell development. [Doctoral Dissertation]. University of Oxford; 2015. Available from: http://ora.ox.ac.uk/objects/uuid:01ac5c84-2e3b-4401-82ec-32331079e784 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.664810

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