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You searched for subject:(enhancer). Showing records 1 – 30 of 307 total matches.

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

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 February 26, 2021. 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. 26 Feb 2021.

Vancouver:

Al-Omairi JGK. Functional study of lymphoid specific enhancers : Etude fonctionnelle des enhancers lymphoides. [Internet] [Doctoral dissertation]. Aix Marseille Université 2017. [cited 2021 Feb 26]. 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 Adelaide

2. Thomson, Ella Paulina. Identification and Validation of SOXB1 Bound Developmental Enhancers.

Degree: 2019, University of Adelaide

 Enhancers are regions of non-coding DNA bound by transcription factors that influence gene expression, and are essential for the precise regulation of embryonic development. Many… (more)

Subjects/Keywords: development; CRISPR; enhancer

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APA (6th Edition):

Thomson, E. P. (2019). Identification and Validation of SOXB1 Bound Developmental Enhancers. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/124500

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):

Thomson, Ella Paulina. “Identification and Validation of SOXB1 Bound Developmental Enhancers.” 2019. Thesis, University of Adelaide. Accessed February 26, 2021. http://hdl.handle.net/2440/124500.

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

MLA Handbook (7th Edition):

Thomson, Ella Paulina. “Identification and Validation of SOXB1 Bound Developmental Enhancers.” 2019. Web. 26 Feb 2021.

Vancouver:

Thomson EP. Identification and Validation of SOXB1 Bound Developmental Enhancers. [Internet] [Thesis]. University of Adelaide; 2019. [cited 2021 Feb 26]. Available from: http://hdl.handle.net/2440/124500.

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

Council of Science Editors:

Thomson EP. Identification and Validation of SOXB1 Bound Developmental Enhancers. [Thesis]. University of Adelaide; 2019. Available from: http://hdl.handle.net/2440/124500

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


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 February 26, 2021. 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. 26 Feb 2021.

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 2021 Feb 26]. 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. Vieira, Mathieu. Régulation de l'expression du gène Nodal lors de la différenciation des cellules souches embryonnaires : Regulation of Nodal gene expression during mouse embryonic stem cells differentiation.

Degree: Docteur es, Sciences de la vie et de la santé. Génétique, 2018, Sorbonne Paris Cité

 L'influence des signalisations ACTIVINE/NODAL et FGF sur les cellules souches embryonnaires murines (mESC) déclenchent leurs différenciations en cellules analogues aux EpiSC (EpiLCs). Cette différenciation modifie… (more)

Subjects/Keywords: EpiSC; Amplificateur HBE; Amplificateur ASE; EpiSC; Enhancer HBE; Enhancer ASE

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APA (6th Edition):

Vieira, M. (2018). Régulation de l'expression du gène Nodal lors de la différenciation des cellules souches embryonnaires : Regulation of Nodal gene expression during mouse embryonic stem cells differentiation. (Doctoral Dissertation). Sorbonne Paris Cité. Retrieved from http://www.theses.fr/2018USPCC244

Chicago Manual of Style (16th Edition):

Vieira, Mathieu. “Régulation de l'expression du gène Nodal lors de la différenciation des cellules souches embryonnaires : Regulation of Nodal gene expression during mouse embryonic stem cells differentiation.” 2018. Doctoral Dissertation, Sorbonne Paris Cité. Accessed February 26, 2021. http://www.theses.fr/2018USPCC244.

MLA Handbook (7th Edition):

Vieira, Mathieu. “Régulation de l'expression du gène Nodal lors de la différenciation des cellules souches embryonnaires : Regulation of Nodal gene expression during mouse embryonic stem cells differentiation.” 2018. Web. 26 Feb 2021.

Vancouver:

Vieira M. Régulation de l'expression du gène Nodal lors de la différenciation des cellules souches embryonnaires : Regulation of Nodal gene expression during mouse embryonic stem cells differentiation. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; 2018. [cited 2021 Feb 26]. Available from: http://www.theses.fr/2018USPCC244.

Council of Science Editors:

Vieira M. Régulation de l'expression du gène Nodal lors de la différenciation des cellules souches embryonnaires : Regulation of Nodal gene expression during mouse embryonic stem cells differentiation. [Doctoral Dissertation]. Sorbonne Paris Cité; 2018. Available from: http://www.theses.fr/2018USPCC244

5. 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 February 26, 2021. 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. 26 Feb 2021.

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 2021 Feb 26]. 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

6. 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 February 26, 2021. 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. 26 Feb 2021.

Vancouver:

Suter T. Enhancer function driving cellular senescence, DNA damage repair, differentiation, and nuclear organization. [Internet] [Thesis]. University of California – San Diego; 2017. [cited 2021 Feb 26]. 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

7. 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 February 26, 2021. 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. 26 Feb 2021.

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 2021 Feb 26]. 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 Utah

8. 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 February 26, 2021. 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. 26 Feb 2021.

Vancouver:

Song Y. Studies on human epidermal membrane with alternating current. [Internet] [Masters thesis]. University of Utah; 2001. [cited 2021 Feb 26]. 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

9. 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 February 26, 2021. 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. 26 Feb 2021.

Vancouver:

Viswanathan P. Molecular analysis of the baculovirus enhancer sequence; -. [Internet] [Thesis]. Jawaharlal Nehru University; 2002. [cited 2021 Feb 26]. 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


Vanderbilt University

10. Chen, Ling. UNDERSTANDING THE EVOLUTION AND SEQUENCE ARCHITECTURE OF GENE REGULATORY ELEMENTS THROUGH MACHINE LEARNING.

Degree: PhD, Biological Sciences, 2019, Vanderbilt University

 Enhancers are genomic regions distal to promoters that bind transcription factors (TFs) to regulate the dynamic spatiotemporal patterns of gene expression required for proper differentiation… (more)

Subjects/Keywords: regulatory genome; deep learning; enhancer; machine learning

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APA (6th Edition):

Chen, L. (2019). UNDERSTANDING THE EVOLUTION AND SEQUENCE ARCHITECTURE OF GENE REGULATORY ELEMENTS THROUGH MACHINE LEARNING. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14530

Chicago Manual of Style (16th Edition):

Chen, Ling. “UNDERSTANDING THE EVOLUTION AND SEQUENCE ARCHITECTURE OF GENE REGULATORY ELEMENTS THROUGH MACHINE LEARNING.” 2019. Doctoral Dissertation, Vanderbilt University. Accessed February 26, 2021. http://hdl.handle.net/1803/14530.

MLA Handbook (7th Edition):

Chen, Ling. “UNDERSTANDING THE EVOLUTION AND SEQUENCE ARCHITECTURE OF GENE REGULATORY ELEMENTS THROUGH MACHINE LEARNING.” 2019. Web. 26 Feb 2021.

Vancouver:

Chen L. UNDERSTANDING THE EVOLUTION AND SEQUENCE ARCHITECTURE OF GENE REGULATORY ELEMENTS THROUGH MACHINE LEARNING. [Internet] [Doctoral dissertation]. Vanderbilt University; 2019. [cited 2021 Feb 26]. Available from: http://hdl.handle.net/1803/14530.

Council of Science Editors:

Chen L. UNDERSTANDING THE EVOLUTION AND SEQUENCE ARCHITECTURE OF GENE REGULATORY ELEMENTS THROUGH MACHINE LEARNING. [Doctoral Dissertation]. Vanderbilt University; 2019. Available from: http://hdl.handle.net/1803/14530


University of California – San Diego

11. 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 (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 February 26, 2021. 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. 26 Feb 2021.

Vancouver:

Oh S. Enhancer Activation, Release and Retargeting in Transcription. [Internet] [Thesis]. University of California – San Diego; 2018. [cited 2021 Feb 26]. 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 Debrecen

12. 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 (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 February 26, 2021. 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. 26 Feb 2021.

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 2021 Feb 26]. 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.


University of Cambridge

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

Degree: PhD, 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. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/293838

Chicago Manual of Style (16th Edition):

Vojtasova, Erika. “HIF2a regulates ccRCC tumorigenesis through activation of cell cycle regulators.” 2019. Doctoral Dissertation, University of Cambridge. Accessed February 26, 2021. https://www.repository.cam.ac.uk/handle/1810/293838.

MLA Handbook (7th Edition):

Vojtasova, Erika. “HIF2a regulates ccRCC tumorigenesis through activation of cell cycle regulators.” 2019. Web. 26 Feb 2021.

Vancouver:

Vojtasova E. HIF2a regulates ccRCC tumorigenesis through activation of cell cycle regulators. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2021 Feb 26]. Available from: https://www.repository.cam.ac.uk/handle/1810/293838.

Council of Science Editors:

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


University of Bath

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

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 February 26, 2021. 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. 26 Feb 2021.

Vancouver:

Wu X. The impact of splicing related constraints on exonic evolution. [Internet] [Doctoral dissertation]. University of Bath; 2016. [cited 2021 Feb 26]. 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 Southern California

15. 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/2941

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 February 26, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/220618/rec/2941.

MLA Handbook (7th Edition):

Mendoza-Fandiño, Gustavo Alfonso. “Functional characterization of colorectal cancer GWAS loci.” 2013. Web. 26 Feb 2021.

Vancouver:

Mendoza-Fandiño GA. Functional characterization of colorectal cancer GWAS loci. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2021 Feb 26]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/220618/rec/2941.

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/2941


University of Edinburgh

16. 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: 572; 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 February 26, 2021. http://hdl.handle.net/1842/8069.

MLA Handbook (7th Edition):

Taylor, Gillian Catherine Agnes. “H4K16 acetylation during embryonic stem cell differentiation.” 2013. Web. 26 Feb 2021.

Vancouver:

Taylor GCA. H4K16 acetylation during embryonic stem cell differentiation. [Internet] [Doctoral dissertation]. University of Edinburgh; 2013. [cited 2021 Feb 26]. 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 Cambridge

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

Degree: PhD, 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. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.40950 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.782848

Chicago Manual of Style (16th Edition):

Vojtasova, Erika. “HIF2a regulates ccRCC tumorigenesis through activation of cell cycle regulators.” 2019. Doctoral Dissertation, University of Cambridge. Accessed February 26, 2021. https://doi.org/10.17863/CAM.40950 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.782848.

MLA Handbook (7th Edition):

Vojtasova, Erika. “HIF2a regulates ccRCC tumorigenesis through activation of cell cycle regulators.” 2019. Web. 26 Feb 2021.

Vancouver:

Vojtasova E. HIF2a regulates ccRCC tumorigenesis through activation of cell cycle regulators. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2021 Feb 26]. Available from: https://doi.org/10.17863/CAM.40950 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.782848.

Council of Science Editors:

Vojtasova E. HIF2a regulates ccRCC tumorigenesis through activation of cell cycle regulators. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://doi.org/10.17863/CAM.40950 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.782848

18. Ghosh Dastidar, Sayantani. Molecular Mechanisms Of Transcriptional Responses In Stress-Induced Human Cells.

Degree: PhD, Biomedical Sciences, 2020, University of North Dakota

  Precise regulation of gene expression is essential for maintaining cell homeostasis and survival. Rapid responses to intracellular or extracellular stimuli involve highly regulated genome-wide… (more)

Subjects/Keywords: Enhancer; Heat Shock; Histones; Inflammation; Promoter; Transcription

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APA (6th Edition):

Ghosh Dastidar, S. (2020). Molecular Mechanisms Of Transcriptional Responses In Stress-Induced Human Cells. (Doctoral Dissertation). University of North Dakota. Retrieved from https://commons.und.edu/theses/3097

Chicago Manual of Style (16th Edition):

Ghosh Dastidar, Sayantani. “Molecular Mechanisms Of Transcriptional Responses In Stress-Induced Human Cells.” 2020. Doctoral Dissertation, University of North Dakota. Accessed February 26, 2021. https://commons.und.edu/theses/3097.

MLA Handbook (7th Edition):

Ghosh Dastidar, Sayantani. “Molecular Mechanisms Of Transcriptional Responses In Stress-Induced Human Cells.” 2020. Web. 26 Feb 2021.

Vancouver:

Ghosh Dastidar S. Molecular Mechanisms Of Transcriptional Responses In Stress-Induced Human Cells. [Internet] [Doctoral dissertation]. University of North Dakota; 2020. [cited 2021 Feb 26]. Available from: https://commons.und.edu/theses/3097.

Council of Science Editors:

Ghosh Dastidar S. Molecular Mechanisms Of Transcriptional Responses In Stress-Induced Human Cells. [Doctoral Dissertation]. University of North Dakota; 2020. Available from: https://commons.und.edu/theses/3097

19. 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 School of Graduate Studies

 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 School of Graduate Studies. 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 School of Graduate Studies. Accessed February 26, 2021. 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. 26 Feb 2021.

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 School of Graduate Studies; 2013. [cited 2021 Feb 26]. 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 School of Graduate Studies; 2013. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1347020396

20. 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 (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 February 26, 2021. 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. 26 Feb 2021.

Vancouver:

Scionti I. Epigenetic Regulation of Skeletal Muscle Differentiation : Régulation épigénétique de la différenciation du muscle squelettique. [Internet] [Doctoral dissertation]. Lyon; 2017. [cited 2021 Feb 26]. 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

21. Amoretti Villa, Rocio. Transcriptional regulation of the IgH locus during class switch recombination : Régulation transcriptionnelle du locus IgH lors de la commutation isotypique.

Degree: Docteur es, Immunologie, 2019, Université de Strasbourg

La commutation isotypique (CI) des immunoglobulines (Ig) a lieu au locus constant de la chaîne lourde (IgH) de l'immunoglobuline lors de l'activation des cellules B… (more)

Subjects/Keywords: Commutation isotypique; Enhancer; Transcription; Locus IgH; Class switch recombination; Enhancer; Transcription; IgH locus; 571.96; 572.8

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APA (6th Edition):

Amoretti Villa, R. (2019). Transcriptional regulation of the IgH locus during class switch recombination : Régulation transcriptionnelle du locus IgH lors de la commutation isotypique. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2019STRAJ078

Chicago Manual of Style (16th Edition):

Amoretti Villa, Rocio. “Transcriptional regulation of the IgH locus during class switch recombination : Régulation transcriptionnelle du locus IgH lors de la commutation isotypique.” 2019. Doctoral Dissertation, Université de Strasbourg. Accessed February 26, 2021. http://www.theses.fr/2019STRAJ078.

MLA Handbook (7th Edition):

Amoretti Villa, Rocio. “Transcriptional regulation of the IgH locus during class switch recombination : Régulation transcriptionnelle du locus IgH lors de la commutation isotypique.” 2019. Web. 26 Feb 2021.

Vancouver:

Amoretti Villa R. Transcriptional regulation of the IgH locus during class switch recombination : Régulation transcriptionnelle du locus IgH lors de la commutation isotypique. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2019. [cited 2021 Feb 26]. Available from: http://www.theses.fr/2019STRAJ078.

Council of Science Editors:

Amoretti Villa R. Transcriptional regulation of the IgH locus during class switch recombination : Régulation transcriptionnelle du locus IgH lors de la commutation isotypique. [Doctoral Dissertation]. Université de Strasbourg; 2019. Available from: http://www.theses.fr/2019STRAJ078


KTH

22. Dong, Xue. Systematic comparison of gene regulatory datasets using experimentally validated enhancers.

Degree: Biotechnology and Health (CBH), 2020, KTH

  Promoter-enhancer interactions are essential for gene regulating, Capture Hi-C is a chromosome conformation capture method to map promoter-enhancer interactions at high resolution. We have… (more)

Subjects/Keywords: Capture Hi-C; ChIP-seq; enhancer; promoter-enhancer interactions; eQTLs; Medical Biotechnology; Medicinsk bioteknologi

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APA (6th Edition):

Dong, X. (2020). Systematic comparison of gene regulatory datasets using experimentally validated enhancers. (Thesis). KTH. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-281957

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):

Dong, Xue. “Systematic comparison of gene regulatory datasets using experimentally validated enhancers.” 2020. Thesis, KTH. Accessed February 26, 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-281957.

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

MLA Handbook (7th Edition):

Dong, Xue. “Systematic comparison of gene regulatory datasets using experimentally validated enhancers.” 2020. Web. 26 Feb 2021.

Vancouver:

Dong X. Systematic comparison of gene regulatory datasets using experimentally validated enhancers. [Internet] [Thesis]. KTH; 2020. [cited 2021 Feb 26]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-281957.

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

Council of Science Editors:

Dong X. Systematic comparison of gene regulatory datasets using experimentally validated enhancers. [Thesis]. KTH; 2020. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-281957

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

23. 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, Université Paris-Saclay (ComUE)

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). Université Paris-Saclay (ComUE). 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, Université Paris-Saclay (ComUE). Accessed February 26, 2021. 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. 26 Feb 2021.

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]. Université Paris-Saclay (ComUE); 2018. [cited 2021 Feb 26]. 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]. Université Paris-Saclay (ComUE); 2018. Available from: http://www.theses.fr/2018SACLS476


University of Helsinki

24. 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 February 26, 2021. 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. 26 Feb 2021.

Vancouver:

Määttä J. Uusi rotan beeta-tropomyosiinigeenin enhancer-elementti. [Internet] [Thesis]. University of Helsinki; 1993. [cited 2021 Feb 26]. 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

25. 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 February 26, 2021. 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. 26 Feb 2021.

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 2021 Feb 26]. 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

26. 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 February 26, 2021. 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. 26 Feb 2021.

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 2021 Feb 26]. 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

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

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 February 26, 2021. 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. 26 Feb 2021.

Vancouver:

Ahmad ZMM. Enhancer-responsiveness and -specificity of Core Promoters in gene transcription. [Internet] [Thesis]. University of Vienna; 2017. [cited 2021 Feb 26]. 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

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

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 February 26, 2021. 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. 26 Feb 2021.

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 2021 Feb 26]. 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

29. 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 February 26, 2021. 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. 26 Feb 2021.

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 2021 Feb 26]. 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


University of California – San Diego

30. Hu, Yiren. Dissecting Enhancer Functions in Signal Induced Transcription Programs.

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

 This dissertation, by Yiren Hu, discusses how enhancer activity is regulated to drive rapid, coordinated transcriptional response to signals like estrogen and inflammatory stimuli. Enhancer(more)

Subjects/Keywords: Biology; Breast Cancer; Condensin; Enhancer; Estrogen; Inflammation; JMJD6

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

APA (6th Edition):

Hu, Y. (2018). Dissecting Enhancer Functions in Signal Induced Transcription Programs. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/0n31q74b

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):

Hu, Yiren. “Dissecting Enhancer Functions in Signal Induced Transcription Programs.” 2018. Thesis, University of California – San Diego. Accessed February 26, 2021. http://www.escholarship.org/uc/item/0n31q74b.

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

MLA Handbook (7th Edition):

Hu, Yiren. “Dissecting Enhancer Functions in Signal Induced Transcription Programs.” 2018. Web. 26 Feb 2021.

Vancouver:

Hu Y. Dissecting Enhancer Functions in Signal Induced Transcription Programs. [Internet] [Thesis]. University of California – San Diego; 2018. [cited 2021 Feb 26]. Available from: http://www.escholarship.org/uc/item/0n31q74b.

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

Council of Science Editors:

Hu Y. Dissecting Enhancer Functions in Signal Induced Transcription Programs. [Thesis]. University of California – San Diego; 2018. Available from: http://www.escholarship.org/uc/item/0n31q74b

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

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