Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for subject:(Molecular Biology). Showing records 1 – 30 of 12888 total matches.

[1] [2] [3] [4] [5] … [430]

Search Limiters

Last 2 Years | English Only

Degrees

Levels

Languages

Country

▼ Search Limiters


Universiteit Utrecht

1. Hofman, E.G. Plasma membrane organization during EGFR signaling: a FRET-based analysis.

Degree: 2008, Universiteit Utrecht

 Since two decades it has been suggested that the plasma membrane is organized into lipid-separated domains called lipid rafts. A number of functions have been… (more)

Subjects/Keywords: Molecular biology; Life sciences; Cell biology; Biologie/Milieukunde (BIOL); International (English)

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hofman, E. G. (2008). Plasma membrane organization during EGFR signaling: a FRET-based analysis. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/30336

Chicago Manual of Style (16th Edition):

Hofman, E G. “Plasma membrane organization during EGFR signaling: a FRET-based analysis.” 2008. Doctoral Dissertation, Universiteit Utrecht. Accessed August 24, 2019. http://dspace.library.uu.nl:8080/handle/1874/30336.

MLA Handbook (7th Edition):

Hofman, E G. “Plasma membrane organization during EGFR signaling: a FRET-based analysis.” 2008. Web. 24 Aug 2019.

Vancouver:

Hofman EG. Plasma membrane organization during EGFR signaling: a FRET-based analysis. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2008. [cited 2019 Aug 24]. Available from: http://dspace.library.uu.nl:8080/handle/1874/30336.

Council of Science Editors:

Hofman EG. Plasma membrane organization during EGFR signaling: a FRET-based analysis. [Doctoral Dissertation]. Universiteit Utrecht; 2008. Available from: http://dspace.library.uu.nl:8080/handle/1874/30336

2. Verbeeren, Jens. Regulation of the minor spliceosome through alternative splicing and nuclear retention of the U11/U12-65K mRNA.

Degree: Department of Biosciences, 2016, University of Helsinki

The protein coding information in our genome is located on genes which are very often interrupted by non-coding regions called introns. For proper gene expression,… (more)

Subjects/Keywords: molecular Biology; molecular Biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Verbeeren, J. (2016). Regulation of the minor spliceosome through alternative splicing and nuclear retention of the U11/U12-65K mRNA. (Doctoral Dissertation). University of Helsinki. Retrieved from http://hdl.handle.net/10138/159362

Chicago Manual of Style (16th Edition):

Verbeeren, Jens. “Regulation of the minor spliceosome through alternative splicing and nuclear retention of the U11/U12-65K mRNA.” 2016. Doctoral Dissertation, University of Helsinki. Accessed August 24, 2019. http://hdl.handle.net/10138/159362.

MLA Handbook (7th Edition):

Verbeeren, Jens. “Regulation of the minor spliceosome through alternative splicing and nuclear retention of the U11/U12-65K mRNA.” 2016. Web. 24 Aug 2019.

Vancouver:

Verbeeren J. Regulation of the minor spliceosome through alternative splicing and nuclear retention of the U11/U12-65K mRNA. [Internet] [Doctoral dissertation]. University of Helsinki; 2016. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/10138/159362.

Council of Science Editors:

Verbeeren J. Regulation of the minor spliceosome through alternative splicing and nuclear retention of the U11/U12-65K mRNA. [Doctoral Dissertation]. University of Helsinki; 2016. Available from: http://hdl.handle.net/10138/159362

3. Nuhn, Mitchell E. Molecular ecology of Boletinellus merulioides and systematics of the Boletineae.

Degree: 2016, Clark University

  This work focuses on members of the Boletales. This order is comprised of a morphological and ecologically diverse set of species. While the vast… (more)

Subjects/Keywords: Biology; Molecular biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Nuhn, M. E. (2016). Molecular ecology of Boletinellus merulioides and systematics of the Boletineae. (Thesis). Clark University. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=10090330

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):

Nuhn, Mitchell E. “Molecular ecology of Boletinellus merulioides and systematics of the Boletineae.” 2016. Thesis, Clark University. Accessed August 24, 2019. http://pqdtopen.proquest.com/#viewpdf?dispub=10090330.

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

MLA Handbook (7th Edition):

Nuhn, Mitchell E. “Molecular ecology of Boletinellus merulioides and systematics of the Boletineae.” 2016. Web. 24 Aug 2019.

Vancouver:

Nuhn ME. Molecular ecology of Boletinellus merulioides and systematics of the Boletineae. [Internet] [Thesis]. Clark University; 2016. [cited 2019 Aug 24]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=10090330.

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

Council of Science Editors:

Nuhn ME. Molecular ecology of Boletinellus merulioides and systematics of the Boletineae. [Thesis]. Clark University; 2016. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=10090330

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

4. Guo, Lei. The Molecular Mechanisms of Sex Determination in Vertebrates.

Degree: 2017, The University of North Dakota

  Many reptiles display temperature-dependent sex determination (TSD), in which the primary sex is determined by incubation temperatures rather than sex chromosomes. However, temperature is… (more)

Subjects/Keywords: Biology; Molecular biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Guo, L. (2017). The Molecular Mechanisms of Sex Determination in Vertebrates. (Thesis). The University of North Dakota. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=10274673

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):

Guo, Lei. “The Molecular Mechanisms of Sex Determination in Vertebrates.” 2017. Thesis, The University of North Dakota. Accessed August 24, 2019. http://pqdtopen.proquest.com/#viewpdf?dispub=10274673.

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

MLA Handbook (7th Edition):

Guo, Lei. “The Molecular Mechanisms of Sex Determination in Vertebrates.” 2017. Web. 24 Aug 2019.

Vancouver:

Guo L. The Molecular Mechanisms of Sex Determination in Vertebrates. [Internet] [Thesis]. The University of North Dakota; 2017. [cited 2019 Aug 24]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=10274673.

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

Council of Science Editors:

Guo L. The Molecular Mechanisms of Sex Determination in Vertebrates. [Thesis]. The University of North Dakota; 2017. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=10274673

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


Cleveland State University

5. JHA, SUJATA S. Elucidating the Role of Non Random Synonymous Codon Usage in Fine Tuning the Process of Co-translational Protein Folding.

Degree: PhD, College of Sciences and Health Professions, 2014, Cleveland State University

 After decades of research, the exact path any polypeptide follows to achieve its functional conformation in vivo is still an enigma. Protein folding in vivo… (more)

Subjects/Keywords: Biology; Molecular Biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

JHA, S. S. (2014). Elucidating the Role of Non Random Synonymous Codon Usage in Fine Tuning the Process of Co-translational Protein Folding. (Doctoral Dissertation). Cleveland State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=csu1413375693

Chicago Manual of Style (16th Edition):

JHA, SUJATA S. “Elucidating the Role of Non Random Synonymous Codon Usage in Fine Tuning the Process of Co-translational Protein Folding.” 2014. Doctoral Dissertation, Cleveland State University. Accessed August 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=csu1413375693.

MLA Handbook (7th Edition):

JHA, SUJATA S. “Elucidating the Role of Non Random Synonymous Codon Usage in Fine Tuning the Process of Co-translational Protein Folding.” 2014. Web. 24 Aug 2019.

Vancouver:

JHA SS. Elucidating the Role of Non Random Synonymous Codon Usage in Fine Tuning the Process of Co-translational Protein Folding. [Internet] [Doctoral dissertation]. Cleveland State University; 2014. [cited 2019 Aug 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=csu1413375693.

Council of Science Editors:

JHA SS. Elucidating the Role of Non Random Synonymous Codon Usage in Fine Tuning the Process of Co-translational Protein Folding. [Doctoral Dissertation]. Cleveland State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=csu1413375693

6. Clarke, Don Lucas. Development of a Stem Cell Gene Therapy for Sanfilippo Syndrome Type B.

Degree: 2017, California State University, Los Angeles

  Sanfilippo syndrome type B (Mucopolysaccharidosis type IIIB; MPS IIIB) is a lysosomal storage disorder affecting primarily the brain and is characterized by profound intellectual… (more)

Subjects/Keywords: Biology; Molecular biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Clarke, D. L. (2017). Development of a Stem Cell Gene Therapy for Sanfilippo Syndrome Type B. (Thesis). California State University, Los Angeles. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=10278830

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):

Clarke, Don Lucas. “Development of a Stem Cell Gene Therapy for Sanfilippo Syndrome Type B.” 2017. Thesis, California State University, Los Angeles. Accessed August 24, 2019. http://pqdtopen.proquest.com/#viewpdf?dispub=10278830.

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

MLA Handbook (7th Edition):

Clarke, Don Lucas. “Development of a Stem Cell Gene Therapy for Sanfilippo Syndrome Type B.” 2017. Web. 24 Aug 2019.

Vancouver:

Clarke DL. Development of a Stem Cell Gene Therapy for Sanfilippo Syndrome Type B. [Internet] [Thesis]. California State University, Los Angeles; 2017. [cited 2019 Aug 24]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=10278830.

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

Council of Science Editors:

Clarke DL. Development of a Stem Cell Gene Therapy for Sanfilippo Syndrome Type B. [Thesis]. California State University, Los Angeles; 2017. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=10278830

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. Fassas, Scott. Functional characterization of proteins essential for de novo peroxisome biogenesis.

Degree: Biology, 2016, University of California – San Diego

 Recent discoveries suggest a role for the endoplasmic reticulum (ER) in peroxisome formation. Following the intra-ER sorting of peroxisomal membrane proteins (PMPs) to a site… (more)

Subjects/Keywords: Biology; Molecular biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Fassas, S. (2016). Functional characterization of proteins essential for de novo peroxisome biogenesis. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/97j475fd

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):

Fassas, Scott. “Functional characterization of proteins essential for de novo peroxisome biogenesis.” 2016. Thesis, University of California – San Diego. Accessed August 24, 2019. http://www.escholarship.org/uc/item/97j475fd.

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

MLA Handbook (7th Edition):

Fassas, Scott. “Functional characterization of proteins essential for de novo peroxisome biogenesis.” 2016. Web. 24 Aug 2019.

Vancouver:

Fassas S. Functional characterization of proteins essential for de novo peroxisome biogenesis. [Internet] [Thesis]. University of California – San Diego; 2016. [cited 2019 Aug 24]. Available from: http://www.escholarship.org/uc/item/97j475fd.

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

Council of Science Editors:

Fassas S. Functional characterization of proteins essential for de novo peroxisome biogenesis. [Thesis]. University of California – San Diego; 2016. Available from: http://www.escholarship.org/uc/item/97j475fd

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


Universidade Nova

8. Tavares, Débora A. Studies on non-typeability and molecular identification of the pneumococcus.

Degree: 2016, Universidade Nova

Pneumococcus(is(a(major(human(pathogen.(Its(main(virulence(factor(is(the(capsule,( which( is( of( polysaccharide( nature.( The( detection( of( the( capsule( using( specific( antisera( is( used( to( identify( pneumococcus.( Also,( differences( in( structural( and( antigenic(properties(of(the(polysaccharides(composing(the(capsule(have(been(used( to(classify(pneumococcus(into(serotypes.(

info:eu-repo/semantics/publishedVersion

Subjects/Keywords: Biology; Molecular Biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Tavares, D. A. (2016). Studies on non-typeability and molecular identification of the pneumococcus. (Thesis). Universidade Nova. Retrieved from https://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/43668

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):

Tavares, Débora A. “Studies on non-typeability and molecular identification of the pneumococcus.” 2016. Thesis, Universidade Nova. Accessed August 24, 2019. https://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/43668.

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

MLA Handbook (7th Edition):

Tavares, Débora A. “Studies on non-typeability and molecular identification of the pneumococcus.” 2016. Web. 24 Aug 2019.

Vancouver:

Tavares DA. Studies on non-typeability and molecular identification of the pneumococcus. [Internet] [Thesis]. Universidade Nova; 2016. [cited 2019 Aug 24]. Available from: https://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/43668.

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

Council of Science Editors:

Tavares DA. Studies on non-typeability and molecular identification of the pneumococcus. [Thesis]. Universidade Nova; 2016. Available from: https://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/43668

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


University of California – Santa Cruz

9. Kan, Christopher H. Quantifying Introgression at the Gene Level in Strongylocentrotid Urchins.

Degree: Ecology and Evolutionary Biology, 2018, University of California – Santa Cruz

 Introgressive hybridization, the movement of genetic material between species, is increasingly being documented in many taxa. It has largely been studied at 100kb+ level. I… (more)

Subjects/Keywords: Biology; Molecular biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Kan, C. H. (2018). Quantifying Introgression at the Gene Level in Strongylocentrotid Urchins. (Thesis). University of California – Santa Cruz. Retrieved from http://www.escholarship.org/uc/item/6773x4rv

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):

Kan, Christopher H. “Quantifying Introgression at the Gene Level in Strongylocentrotid Urchins.” 2018. Thesis, University of California – Santa Cruz. Accessed August 24, 2019. http://www.escholarship.org/uc/item/6773x4rv.

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

MLA Handbook (7th Edition):

Kan, Christopher H. “Quantifying Introgression at the Gene Level in Strongylocentrotid Urchins.” 2018. Web. 24 Aug 2019.

Vancouver:

Kan CH. Quantifying Introgression at the Gene Level in Strongylocentrotid Urchins. [Internet] [Thesis]. University of California – Santa Cruz; 2018. [cited 2019 Aug 24]. Available from: http://www.escholarship.org/uc/item/6773x4rv.

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

Council of Science Editors:

Kan CH. Quantifying Introgression at the Gene Level in Strongylocentrotid Urchins. [Thesis]. University of California – Santa Cruz; 2018. Available from: http://www.escholarship.org/uc/item/6773x4rv

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


Columbia University

10. Lewis, Thera Cathy. Serum Regulation of Inhibitor of DNA Binding/Differentiation 1 Expression by a BMP Pathway and BMP Responsive El.

Degree: 2013, Columbia University

 Immediate Early Genes (IEGs) are expressed upon re-entry of quiescent cells into the cell cycle following serum stimulation. These genes are involved in growth control… (more)

Subjects/Keywords: Biology; Molecular biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lewis, T. C. (2013). Serum Regulation of Inhibitor of DNA Binding/Differentiation 1 Expression by a BMP Pathway and BMP Responsive El. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8Q246NR

Chicago Manual of Style (16th Edition):

Lewis, Thera Cathy. “Serum Regulation of Inhibitor of DNA Binding/Differentiation 1 Expression by a BMP Pathway and BMP Responsive El.” 2013. Doctoral Dissertation, Columbia University. Accessed August 24, 2019. https://doi.org/10.7916/D8Q246NR.

MLA Handbook (7th Edition):

Lewis, Thera Cathy. “Serum Regulation of Inhibitor of DNA Binding/Differentiation 1 Expression by a BMP Pathway and BMP Responsive El.” 2013. Web. 24 Aug 2019.

Vancouver:

Lewis TC. Serum Regulation of Inhibitor of DNA Binding/Differentiation 1 Expression by a BMP Pathway and BMP Responsive El. [Internet] [Doctoral dissertation]. Columbia University; 2013. [cited 2019 Aug 24]. Available from: https://doi.org/10.7916/D8Q246NR.

Council of Science Editors:

Lewis TC. Serum Regulation of Inhibitor of DNA Binding/Differentiation 1 Expression by a BMP Pathway and BMP Responsive El. [Doctoral Dissertation]. Columbia University; 2013. Available from: https://doi.org/10.7916/D8Q246NR


University of Wisconsin – Milwaukee

11. Biswas, Sreya. Characterization and Use of Folate Receptor Isoforms for Targeting of Epithelial and Myeloid Cells.

Degree: PhD, Biological Sciences, 2016, University of Wisconsin – Milwaukee

  ABSTRACT CHARACTERIZATION AND USE OF FOLATE RECEPTOR ISOFORMS FOR TARGETING OF EPITHELIAL AND MYELOID CELLS by Sreya Biswas The University of Wisconsin-Milwaukee, 2016 Under… (more)

Subjects/Keywords: Biology; Molecular Biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Biswas, S. (2016). Characterization and Use of Folate Receptor Isoforms for Targeting of Epithelial and Myeloid Cells. (Doctoral Dissertation). University of Wisconsin – Milwaukee. Retrieved from https://dc.uwm.edu/etd/1352

Chicago Manual of Style (16th Edition):

Biswas, Sreya. “Characterization and Use of Folate Receptor Isoforms for Targeting of Epithelial and Myeloid Cells.” 2016. Doctoral Dissertation, University of Wisconsin – Milwaukee. Accessed August 24, 2019. https://dc.uwm.edu/etd/1352.

MLA Handbook (7th Edition):

Biswas, Sreya. “Characterization and Use of Folate Receptor Isoforms for Targeting of Epithelial and Myeloid Cells.” 2016. Web. 24 Aug 2019.

Vancouver:

Biswas S. Characterization and Use of Folate Receptor Isoforms for Targeting of Epithelial and Myeloid Cells. [Internet] [Doctoral dissertation]. University of Wisconsin – Milwaukee; 2016. [cited 2019 Aug 24]. Available from: https://dc.uwm.edu/etd/1352.

Council of Science Editors:

Biswas S. Characterization and Use of Folate Receptor Isoforms for Targeting of Epithelial and Myeloid Cells. [Doctoral Dissertation]. University of Wisconsin – Milwaukee; 2016. Available from: https://dc.uwm.edu/etd/1352


Florida State University

12. Sima, Jiao. Genetic Dissection of Cis-Elements in Spatio-temporal Control of DNA Replication.

Degree: PhD, Biological Science, 2018, Florida State University

DNA replication in all Eukaryotes follows a defined temporal order termed replication-timing program (RT), which is coupled with the spatial separation of chromatin distribution inside… (more)

Subjects/Keywords: Biology; Molecular biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Sima, J. (2018). Genetic Dissection of Cis-Elements in Spatio-temporal Control of DNA Replication. (Doctoral Dissertation). Florida State University. Retrieved from http://purl.flvc.org/fsu/fd/2018_Sp_Sima_fsu_0071E_14411 ;

Chicago Manual of Style (16th Edition):

Sima, Jiao. “Genetic Dissection of Cis-Elements in Spatio-temporal Control of DNA Replication.” 2018. Doctoral Dissertation, Florida State University. Accessed August 24, 2019. http://purl.flvc.org/fsu/fd/2018_Sp_Sima_fsu_0071E_14411 ;.

MLA Handbook (7th Edition):

Sima, Jiao. “Genetic Dissection of Cis-Elements in Spatio-temporal Control of DNA Replication.” 2018. Web. 24 Aug 2019.

Vancouver:

Sima J. Genetic Dissection of Cis-Elements in Spatio-temporal Control of DNA Replication. [Internet] [Doctoral dissertation]. Florida State University; 2018. [cited 2019 Aug 24]. Available from: http://purl.flvc.org/fsu/fd/2018_Sp_Sima_fsu_0071E_14411 ;.

Council of Science Editors:

Sima J. Genetic Dissection of Cis-Elements in Spatio-temporal Control of DNA Replication. [Doctoral Dissertation]. Florida State University; 2018. Available from: http://purl.flvc.org/fsu/fd/2018_Sp_Sima_fsu_0071E_14411 ;


Florida State University

13. Li, Jie. Functional Characterization of Protein O-glcnacylation in Plants.

Degree: MS, Biological Science, 2015, Florida State University

O-linked β-N-acetylglucosamine (O-GlcNAc) is an abundant and dynamic protein modification in eukaryotes, carried out by O-GlcNAc transferases (OGT). Two OGTs from Arabidopsis, SPINDLY (SPY) and… (more)

Subjects/Keywords: Biology; Molecular biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Li, J. (2015). Functional Characterization of Protein O-glcnacylation in Plants. (Masters Thesis). Florida State University. Retrieved from http://purl.flvc.org/fsu/fd/FSU_migr_etd-9639 ;

Chicago Manual of Style (16th Edition):

Li, Jie. “Functional Characterization of Protein O-glcnacylation in Plants.” 2015. Masters Thesis, Florida State University. Accessed August 24, 2019. http://purl.flvc.org/fsu/fd/FSU_migr_etd-9639 ;.

MLA Handbook (7th Edition):

Li, Jie. “Functional Characterization of Protein O-glcnacylation in Plants.” 2015. Web. 24 Aug 2019.

Vancouver:

Li J. Functional Characterization of Protein O-glcnacylation in Plants. [Internet] [Masters thesis]. Florida State University; 2015. [cited 2019 Aug 24]. Available from: http://purl.flvc.org/fsu/fd/FSU_migr_etd-9639 ;.

Council of Science Editors:

Li J. Functional Characterization of Protein O-glcnacylation in Plants. [Masters Thesis]. Florida State University; 2015. Available from: http://purl.flvc.org/fsu/fd/FSU_migr_etd-9639 ;


West Virginia University

14. Bose, Anasua. Role of protein kinase CK2 and phosphatase PP2A in Notch-mediated lateral inhibition.

Degree: PhD, Biology, 2010, West Virginia University

 The Notch signaling pathway is highly conserved in vertebrates and invertebrates and regulates binary cell fate specifications in diverse developmental contexts. In a process termed… (more)

Subjects/Keywords: Biology; Molecular biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Bose, A. (2010). Role of protein kinase CK2 and phosphatase PP2A in Notch-mediated lateral inhibition. (Doctoral Dissertation). West Virginia University. Retrieved from https://researchrepository.wvu.edu/etd/4565

Chicago Manual of Style (16th Edition):

Bose, Anasua. “Role of protein kinase CK2 and phosphatase PP2A in Notch-mediated lateral inhibition.” 2010. Doctoral Dissertation, West Virginia University. Accessed August 24, 2019. https://researchrepository.wvu.edu/etd/4565.

MLA Handbook (7th Edition):

Bose, Anasua. “Role of protein kinase CK2 and phosphatase PP2A in Notch-mediated lateral inhibition.” 2010. Web. 24 Aug 2019.

Vancouver:

Bose A. Role of protein kinase CK2 and phosphatase PP2A in Notch-mediated lateral inhibition. [Internet] [Doctoral dissertation]. West Virginia University; 2010. [cited 2019 Aug 24]. Available from: https://researchrepository.wvu.edu/etd/4565.

Council of Science Editors:

Bose A. Role of protein kinase CK2 and phosphatase PP2A in Notch-mediated lateral inhibition. [Doctoral Dissertation]. West Virginia University; 2010. Available from: https://researchrepository.wvu.edu/etd/4565

15. Thierry, Eloïse. Caractérisation des voies d’échappement aux inhibiteurs d’intégrase du VIH-1 : Characterisation of escape pathways during HIV-1 integrase inhibitor treatment.

Degree: Docteur es, Science de la vie et de la santé, 2015, Cachan, Ecole normale supérieure

L’intégration est une étape cruciale dans la réplication du VIH-1, assurant la stabilité et l’expression de son génome. Elle est donc la cible d’inhibiteurs de… (more)

Subjects/Keywords: Biologie moléculaire; Virologie; VIH-1; Molecular biology; Virology; HIV-1 genome

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Thierry, E. (2015). Caractérisation des voies d’échappement aux inhibiteurs d’intégrase du VIH-1 : Characterisation of escape pathways during HIV-1 integrase inhibitor treatment. (Doctoral Dissertation). Cachan, Ecole normale supérieure. Retrieved from http://www.theses.fr/2015DENS0030

Chicago Manual of Style (16th Edition):

Thierry, Eloïse. “Caractérisation des voies d’échappement aux inhibiteurs d’intégrase du VIH-1 : Characterisation of escape pathways during HIV-1 integrase inhibitor treatment.” 2015. Doctoral Dissertation, Cachan, Ecole normale supérieure. Accessed August 24, 2019. http://www.theses.fr/2015DENS0030.

MLA Handbook (7th Edition):

Thierry, Eloïse. “Caractérisation des voies d’échappement aux inhibiteurs d’intégrase du VIH-1 : Characterisation of escape pathways during HIV-1 integrase inhibitor treatment.” 2015. Web. 24 Aug 2019.

Vancouver:

Thierry E. Caractérisation des voies d’échappement aux inhibiteurs d’intégrase du VIH-1 : Characterisation of escape pathways during HIV-1 integrase inhibitor treatment. [Internet] [Doctoral dissertation]. Cachan, Ecole normale supérieure; 2015. [cited 2019 Aug 24]. Available from: http://www.theses.fr/2015DENS0030.

Council of Science Editors:

Thierry E. Caractérisation des voies d’échappement aux inhibiteurs d’intégrase du VIH-1 : Characterisation of escape pathways during HIV-1 integrase inhibitor treatment. [Doctoral Dissertation]. Cachan, Ecole normale supérieure; 2015. Available from: http://www.theses.fr/2015DENS0030

16. Conde Perez, Alejandro. Novel implications of β-catenin in melanocyte homeostasis and melanomagenesis : Multiscale evaluation of venom toxins as potential antinociceptive agents.

Degree: Docteur es, Biologie cellulaire et moléculaire, 2014, Université Paris Descartes – Paris V

L’homéostasie des mélanocytes est d'une importance primordiale dans la prévention de la transformation maligne. Les mélanocytes transformés conduisent souvent à un type particulièrement agressif de… (more)

Subjects/Keywords: Biologie cellulaire et moléculaire; Cellular and molecular biology; 616.994

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Conde Perez, A. (2014). Novel implications of β-catenin in melanocyte homeostasis and melanomagenesis : Multiscale evaluation of venom toxins as potential antinociceptive agents. (Doctoral Dissertation). Université Paris Descartes – Paris V. Retrieved from http://www.theses.fr/2014PA05T074

Chicago Manual of Style (16th Edition):

Conde Perez, Alejandro. “Novel implications of β-catenin in melanocyte homeostasis and melanomagenesis : Multiscale evaluation of venom toxins as potential antinociceptive agents.” 2014. Doctoral Dissertation, Université Paris Descartes – Paris V. Accessed August 24, 2019. http://www.theses.fr/2014PA05T074.

MLA Handbook (7th Edition):

Conde Perez, Alejandro. “Novel implications of β-catenin in melanocyte homeostasis and melanomagenesis : Multiscale evaluation of venom toxins as potential antinociceptive agents.” 2014. Web. 24 Aug 2019.

Vancouver:

Conde Perez A. Novel implications of β-catenin in melanocyte homeostasis and melanomagenesis : Multiscale evaluation of venom toxins as potential antinociceptive agents. [Internet] [Doctoral dissertation]. Université Paris Descartes – Paris V; 2014. [cited 2019 Aug 24]. Available from: http://www.theses.fr/2014PA05T074.

Council of Science Editors:

Conde Perez A. Novel implications of β-catenin in melanocyte homeostasis and melanomagenesis : Multiscale evaluation of venom toxins as potential antinociceptive agents. [Doctoral Dissertation]. Université Paris Descartes – Paris V; 2014. Available from: http://www.theses.fr/2014PA05T074

17. Giraud, Andréas. Développement d’une approche de thérapie cellulaire de l’anévrisme de l’aorte abdominale utilisant les fibroblastes gingivaux chez la souris : Development of abdominal aortic aneurysm cell-based therapy approach using gingival fibroblast in mouse model.

Degree: Docteur es, Biologie cellulaire et moléculaire, 2016, Sorbonne Paris Cité

L’anévrisme de l’aorte abdominale (AAA) correspond à une dilatation progressive de l’aorte dont la complication principale, et potentiellement mortelle, est la rupture. La physiopathologie de… (more)

Subjects/Keywords: Biologie cellulaire et moléculaire; Cell and molecular biology; 571.6

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Giraud, A. (2016). Développement d’une approche de thérapie cellulaire de l’anévrisme de l’aorte abdominale utilisant les fibroblastes gingivaux chez la souris : Development of abdominal aortic aneurysm cell-based therapy approach using gingival fibroblast in mouse model. (Doctoral Dissertation). Sorbonne Paris Cité. Retrieved from http://www.theses.fr/2016USPCB029

Chicago Manual of Style (16th Edition):

Giraud, Andréas. “Développement d’une approche de thérapie cellulaire de l’anévrisme de l’aorte abdominale utilisant les fibroblastes gingivaux chez la souris : Development of abdominal aortic aneurysm cell-based therapy approach using gingival fibroblast in mouse model.” 2016. Doctoral Dissertation, Sorbonne Paris Cité. Accessed August 24, 2019. http://www.theses.fr/2016USPCB029.

MLA Handbook (7th Edition):

Giraud, Andréas. “Développement d’une approche de thérapie cellulaire de l’anévrisme de l’aorte abdominale utilisant les fibroblastes gingivaux chez la souris : Development of abdominal aortic aneurysm cell-based therapy approach using gingival fibroblast in mouse model.” 2016. Web. 24 Aug 2019.

Vancouver:

Giraud A. Développement d’une approche de thérapie cellulaire de l’anévrisme de l’aorte abdominale utilisant les fibroblastes gingivaux chez la souris : Development of abdominal aortic aneurysm cell-based therapy approach using gingival fibroblast in mouse model. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; 2016. [cited 2019 Aug 24]. Available from: http://www.theses.fr/2016USPCB029.

Council of Science Editors:

Giraud A. Développement d’une approche de thérapie cellulaire de l’anévrisme de l’aorte abdominale utilisant les fibroblastes gingivaux chez la souris : Development of abdominal aortic aneurysm cell-based therapy approach using gingival fibroblast in mouse model. [Doctoral Dissertation]. Sorbonne Paris Cité; 2016. Available from: http://www.theses.fr/2016USPCB029

18. Patitucci, Cecilia. PPARy, a new player in hepatic metabolic adaptation from mouse model to human liver cancer : Myosin-based motility in actin filament networks of controlled architecture in vitro.

Degree: Docteur es, Biologie cellulaire et moléculaire, 2016, Sorbonne Paris Cité

 La tumorigenèse est influencée par des facteurs génétiques et environmentaux. La surnutrition est une cause d'obésité et d'accumulation pathologique de lipides dans le foie, la… (more)

Subjects/Keywords: Biologie cellulaire et moléculaire; Cell and molecular biology; 571.6

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Patitucci, C. (2016). PPARy, a new player in hepatic metabolic adaptation from mouse model to human liver cancer : Myosin-based motility in actin filament networks of controlled architecture in vitro. (Doctoral Dissertation). Sorbonne Paris Cité. Retrieved from http://www.theses.fr/2016USPCB056

Chicago Manual of Style (16th Edition):

Patitucci, Cecilia. “PPARy, a new player in hepatic metabolic adaptation from mouse model to human liver cancer : Myosin-based motility in actin filament networks of controlled architecture in vitro.” 2016. Doctoral Dissertation, Sorbonne Paris Cité. Accessed August 24, 2019. http://www.theses.fr/2016USPCB056.

MLA Handbook (7th Edition):

Patitucci, Cecilia. “PPARy, a new player in hepatic metabolic adaptation from mouse model to human liver cancer : Myosin-based motility in actin filament networks of controlled architecture in vitro.” 2016. Web. 24 Aug 2019.

Vancouver:

Patitucci C. PPARy, a new player in hepatic metabolic adaptation from mouse model to human liver cancer : Myosin-based motility in actin filament networks of controlled architecture in vitro. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; 2016. [cited 2019 Aug 24]. Available from: http://www.theses.fr/2016USPCB056.

Council of Science Editors:

Patitucci C. PPARy, a new player in hepatic metabolic adaptation from mouse model to human liver cancer : Myosin-based motility in actin filament networks of controlled architecture in vitro. [Doctoral Dissertation]. Sorbonne Paris Cité; 2016. Available from: http://www.theses.fr/2016USPCB056

19. Menara, Mélanie. Étude de l'implication de la matrice extracellulaire dans la malignité des phéochromocytomes et des paragangliomes SDHB-dépendants : Study of extracellular matrix involvement in malignancy of SDHB-related pheochromocytomas and paragangliomas.

Degree: Docteur es, Biologie cellulaire et moléculaire, 2016, Sorbonne Paris Cité

 Les phéochromocytomes et les paragangliomes (PPGL) sont des tumeurs neuroendocrines rares qui se développent aux dépens des paraganglions et qui sont identiquement déterminées dans 40%… (more)

Subjects/Keywords: Biologie cellulaire et moleculaire; Cellular and molecular biology; 616.994 8

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Menara, M. (2016). Étude de l'implication de la matrice extracellulaire dans la malignité des phéochromocytomes et des paragangliomes SDHB-dépendants : Study of extracellular matrix involvement in malignancy of SDHB-related pheochromocytomas and paragangliomas. (Doctoral Dissertation). Sorbonne Paris Cité. Retrieved from http://www.theses.fr/2016USPCB096

Chicago Manual of Style (16th Edition):

Menara, Mélanie. “Étude de l'implication de la matrice extracellulaire dans la malignité des phéochromocytomes et des paragangliomes SDHB-dépendants : Study of extracellular matrix involvement in malignancy of SDHB-related pheochromocytomas and paragangliomas.” 2016. Doctoral Dissertation, Sorbonne Paris Cité. Accessed August 24, 2019. http://www.theses.fr/2016USPCB096.

MLA Handbook (7th Edition):

Menara, Mélanie. “Étude de l'implication de la matrice extracellulaire dans la malignité des phéochromocytomes et des paragangliomes SDHB-dépendants : Study of extracellular matrix involvement in malignancy of SDHB-related pheochromocytomas and paragangliomas.” 2016. Web. 24 Aug 2019.

Vancouver:

Menara M. Étude de l'implication de la matrice extracellulaire dans la malignité des phéochromocytomes et des paragangliomes SDHB-dépendants : Study of extracellular matrix involvement in malignancy of SDHB-related pheochromocytomas and paragangliomas. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; 2016. [cited 2019 Aug 24]. Available from: http://www.theses.fr/2016USPCB096.

Council of Science Editors:

Menara M. Étude de l'implication de la matrice extracellulaire dans la malignité des phéochromocytomes et des paragangliomes SDHB-dépendants : Study of extracellular matrix involvement in malignancy of SDHB-related pheochromocytomas and paragangliomas. [Doctoral Dissertation]. Sorbonne Paris Cité; 2016. Available from: http://www.theses.fr/2016USPCB096

20. Valenti-Lehrter, Véronique. Développement d’outils moléculaires au service de la systématique : application à des Ecdysozoaires parasites et vecteurs : Development of molecular tools for systematics : application to a few Ecdysozoa parasites and vectors.

Degree: Docteur es, Pharmacie - STS, 2018, Reims

Les Ecdysozoaires sont des organismes caractérisés par une croissance discontinue composée de plusieurs stades morphologiques séparés par des mues. Parmi eux, certains groupes présentent un… (more)

Subjects/Keywords: Biologie moléculaire; Parasite; Systématique; Vecteur; Molecular biology; Vector; Systematics; Parasite; 610

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Valenti-Lehrter, V. (2018). Développement d’outils moléculaires au service de la systématique : application à des Ecdysozoaires parasites et vecteurs : Development of molecular tools for systematics : application to a few Ecdysozoa parasites and vectors. (Doctoral Dissertation). Reims. Retrieved from http://www.theses.fr/2018REIMP203

Chicago Manual of Style (16th Edition):

Valenti-Lehrter, Véronique. “Développement d’outils moléculaires au service de la systématique : application à des Ecdysozoaires parasites et vecteurs : Development of molecular tools for systematics : application to a few Ecdysozoa parasites and vectors.” 2018. Doctoral Dissertation, Reims. Accessed August 24, 2019. http://www.theses.fr/2018REIMP203.

MLA Handbook (7th Edition):

Valenti-Lehrter, Véronique. “Développement d’outils moléculaires au service de la systématique : application à des Ecdysozoaires parasites et vecteurs : Development of molecular tools for systematics : application to a few Ecdysozoa parasites and vectors.” 2018. Web. 24 Aug 2019.

Vancouver:

Valenti-Lehrter V. Développement d’outils moléculaires au service de la systématique : application à des Ecdysozoaires parasites et vecteurs : Development of molecular tools for systematics : application to a few Ecdysozoa parasites and vectors. [Internet] [Doctoral dissertation]. Reims; 2018. [cited 2019 Aug 24]. Available from: http://www.theses.fr/2018REIMP203.

Council of Science Editors:

Valenti-Lehrter V. Développement d’outils moléculaires au service de la systématique : application à des Ecdysozoaires parasites et vecteurs : Development of molecular tools for systematics : application to a few Ecdysozoa parasites and vectors. [Doctoral Dissertation]. Reims; 2018. Available from: http://www.theses.fr/2018REIMP203

21. Cucullo, Jessica. The role of mammalian WDR1 and its truncated isoform in cell migration and cofilin signalling.

Degree: MS, Biological Sciences, 2010, National Library of Canada

 Directed cellular migration is a normal process which involves the actin cytoskeleton and actin-binding proteins such as WDR1 and cofilin. WDR1 promotes actin filament depolymerization… (more)

Subjects/Keywords: Biology; Molecular.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Cucullo, J. (2010). The role of mammalian WDR1 and its truncated isoform in cell migration and cofilin signalling. (Masters Thesis). National Library of Canada. Retrieved from http://scholar.uwindsor.ca/etd/281

Chicago Manual of Style (16th Edition):

Cucullo, Jessica. “The role of mammalian WDR1 and its truncated isoform in cell migration and cofilin signalling.” 2010. Masters Thesis, National Library of Canada. Accessed August 24, 2019. http://scholar.uwindsor.ca/etd/281.

MLA Handbook (7th Edition):

Cucullo, Jessica. “The role of mammalian WDR1 and its truncated isoform in cell migration and cofilin signalling.” 2010. Web. 24 Aug 2019.

Vancouver:

Cucullo J. The role of mammalian WDR1 and its truncated isoform in cell migration and cofilin signalling. [Internet] [Masters thesis]. National Library of Canada; 2010. [cited 2019 Aug 24]. Available from: http://scholar.uwindsor.ca/etd/281.

Council of Science Editors:

Cucullo J. The role of mammalian WDR1 and its truncated isoform in cell migration and cofilin signalling. [Masters Thesis]. National Library of Canada; 2010. Available from: http://scholar.uwindsor.ca/etd/281

22. Dhaliwal, Rajdeep. Roles of Cyclin A and Cyclin B in Drosophila Female Meiosis.

Degree: MA, Biological Sciences, 2011, National Library of Canada

 Cyclin Dependent Kinase 1 (CDK1) is a key mitotic regulator that associates with Cyclin proteins to form active Cyclin-CDK1 complexes. The mitotic roles of Cyclin-CDK1… (more)

Subjects/Keywords: Molecular biology.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Dhaliwal, R. (2011). Roles of Cyclin A and Cyclin B in Drosophila Female Meiosis. (Masters Thesis). National Library of Canada. Retrieved from http://scholar.uwindsor.ca/etd/67

Chicago Manual of Style (16th Edition):

Dhaliwal, Rajdeep. “Roles of Cyclin A and Cyclin B in Drosophila Female Meiosis.” 2011. Masters Thesis, National Library of Canada. Accessed August 24, 2019. http://scholar.uwindsor.ca/etd/67.

MLA Handbook (7th Edition):

Dhaliwal, Rajdeep. “Roles of Cyclin A and Cyclin B in Drosophila Female Meiosis.” 2011. Web. 24 Aug 2019.

Vancouver:

Dhaliwal R. Roles of Cyclin A and Cyclin B in Drosophila Female Meiosis. [Internet] [Masters thesis]. National Library of Canada; 2011. [cited 2019 Aug 24]. Available from: http://scholar.uwindsor.ca/etd/67.

Council of Science Editors:

Dhaliwal R. Roles of Cyclin A and Cyclin B in Drosophila Female Meiosis. [Masters Thesis]. National Library of Canada; 2011. Available from: http://scholar.uwindsor.ca/etd/67


University of South Florida

23. Mitra, Avishek. Sigma Factor N| A Novel Regulator of Acid Resistance and Locus of Enterocyte Effacement in Escherichia coli O157|H7.

Degree: 2014, University of South Florida

  In enterohemorrhagic <i>E. coli</i> (EHEC) sigma factor N (σ N) regulates glutamate-dependent acid resistance (GDAR) and the locus of enterocyte effacement (LEE), discrete genetic… (more)

Subjects/Keywords: Biology; Molecular

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Mitra, A. (2014). Sigma Factor N| A Novel Regulator of Acid Resistance and Locus of Enterocyte Effacement in Escherichia coli O157|H7. (Thesis). University of South Florida. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=3617860

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):

Mitra, Avishek. “Sigma Factor N| A Novel Regulator of Acid Resistance and Locus of Enterocyte Effacement in Escherichia coli O157|H7.” 2014. Thesis, University of South Florida. Accessed August 24, 2019. http://pqdtopen.proquest.com/#viewpdf?dispub=3617860.

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

MLA Handbook (7th Edition):

Mitra, Avishek. “Sigma Factor N| A Novel Regulator of Acid Resistance and Locus of Enterocyte Effacement in Escherichia coli O157|H7.” 2014. Web. 24 Aug 2019.

Vancouver:

Mitra A. Sigma Factor N| A Novel Regulator of Acid Resistance and Locus of Enterocyte Effacement in Escherichia coli O157|H7. [Internet] [Thesis]. University of South Florida; 2014. [cited 2019 Aug 24]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3617860.

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

Council of Science Editors:

Mitra A. Sigma Factor N| A Novel Regulator of Acid Resistance and Locus of Enterocyte Effacement in Escherichia coli O157|H7. [Thesis]. University of South Florida; 2014. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3617860

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


University of Kansas

24. Bishop, Stephanie Cara. Long primer extension by a novel inverse PCR method.

Degree: 2009, University of Kansas

  An inverse polymerase chain reaction (PCR) was employed to construct an engineered F1-ATPase by means of inserting the repressor of primer (Rop) DNA sequence… (more)

Subjects/Keywords: Biology; Molecular

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Bishop, S. C. (2009). Long primer extension by a novel inverse PCR method. (Thesis). University of Kansas. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=1465374

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):

Bishop, Stephanie Cara. “Long primer extension by a novel inverse PCR method.” 2009. Thesis, University of Kansas. Accessed August 24, 2019. http://pqdtopen.proquest.com/#viewpdf?dispub=1465374.

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

MLA Handbook (7th Edition):

Bishop, Stephanie Cara. “Long primer extension by a novel inverse PCR method.” 2009. Web. 24 Aug 2019.

Vancouver:

Bishop SC. Long primer extension by a novel inverse PCR method. [Internet] [Thesis]. University of Kansas; 2009. [cited 2019 Aug 24]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=1465374.

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

Council of Science Editors:

Bishop SC. Long primer extension by a novel inverse PCR method. [Thesis]. University of Kansas; 2009. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=1465374

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


University of California, San Diego

25. Murthy, Nevin. hIws1 structural elucidation and protein interactions.

Degree: 2009, University of California, San Diego

  There are a number of nuclear factors that play an integral role in transcriptional elongation. Once such factor is hIws1, a nuclear protein first… (more)

Subjects/Keywords: Biology; Molecular

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Murthy, N. (2009). hIws1 structural elucidation and protein interactions. (Thesis). University of California, San Diego. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=1467930

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):

Murthy, Nevin. “hIws1 structural elucidation and protein interactions.” 2009. Thesis, University of California, San Diego. Accessed August 24, 2019. http://pqdtopen.proquest.com/#viewpdf?dispub=1467930.

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

MLA Handbook (7th Edition):

Murthy, Nevin. “hIws1 structural elucidation and protein interactions.” 2009. Web. 24 Aug 2019.

Vancouver:

Murthy N. hIws1 structural elucidation and protein interactions. [Internet] [Thesis]. University of California, San Diego; 2009. [cited 2019 Aug 24]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=1467930.

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

Council of Science Editors:

Murthy N. hIws1 structural elucidation and protein interactions. [Thesis]. University of California, San Diego; 2009. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=1467930

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


University of Southern California

26. Parakh, Sejal. Genetic engineering of thermally sensitive elastin-like polypeptide and its expression in HEK 293 cells.

Degree: 2010, University of Southern California

  Substantial efforts have been to design drug carriers for targeted drug delivery to tumor sites in order to spare the normal tissue from the… (more)

Subjects/Keywords: Biology; Molecular

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Parakh, S. (2010). Genetic engineering of thermally sensitive elastin-like polypeptide and its expression in HEK 293 cells. (Thesis). University of Southern California. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=1479997

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):

Parakh, Sejal. “Genetic engineering of thermally sensitive elastin-like polypeptide and its expression in HEK 293 cells.” 2010. Thesis, University of Southern California. Accessed August 24, 2019. http://pqdtopen.proquest.com/#viewpdf?dispub=1479997.

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

MLA Handbook (7th Edition):

Parakh, Sejal. “Genetic engineering of thermally sensitive elastin-like polypeptide and its expression in HEK 293 cells.” 2010. Web. 24 Aug 2019.

Vancouver:

Parakh S. Genetic engineering of thermally sensitive elastin-like polypeptide and its expression in HEK 293 cells. [Internet] [Thesis]. University of Southern California; 2010. [cited 2019 Aug 24]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=1479997.

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

Council of Science Editors:

Parakh S. Genetic engineering of thermally sensitive elastin-like polypeptide and its expression in HEK 293 cells. [Thesis]. University of Southern California; 2010. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=1479997

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


East Carolina University

27. Shah, Maitri Yogen. Effects of 5-fluorouracil drug treatment on the expression profile of microRNAs in MCF7 breast cancer cells.

Degree: 2010, East Carolina University

  Breast cancer is one of the leading causes of deaths in women worldwide. 5-flourouracil (5-FU) is a classic chemotherapeutic drug that has been widely… (more)

Subjects/Keywords: Biology; Molecular

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Shah, M. Y. (2010). Effects of 5-fluorouracil drug treatment on the expression profile of microRNAs in MCF7 breast cancer cells. (Thesis). East Carolina University. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=1480459

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):

Shah, Maitri Yogen. “Effects of 5-fluorouracil drug treatment on the expression profile of microRNAs in MCF7 breast cancer cells.” 2010. Thesis, East Carolina University. Accessed August 24, 2019. http://pqdtopen.proquest.com/#viewpdf?dispub=1480459.

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

MLA Handbook (7th Edition):

Shah, Maitri Yogen. “Effects of 5-fluorouracil drug treatment on the expression profile of microRNAs in MCF7 breast cancer cells.” 2010. Web. 24 Aug 2019.

Vancouver:

Shah MY. Effects of 5-fluorouracil drug treatment on the expression profile of microRNAs in MCF7 breast cancer cells. [Internet] [Thesis]. East Carolina University; 2010. [cited 2019 Aug 24]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=1480459.

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

Council of Science Editors:

Shah MY. Effects of 5-fluorouracil drug treatment on the expression profile of microRNAs in MCF7 breast cancer cells. [Thesis]. East Carolina University; 2010. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=1480459

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

28. Susilarini, Ni Ketut. Interaction of Kaposi's sarcoma-associated herpesvirus ORF59 with oriLyt is dependent upon binding with K-Rta.

Degree: 2011, University of Nevada, Reno

  There are six Kaposi Sarcoma-associated Herpesvirus (KSHV/HHV-8) viral-encoded core proteins required for lytic origin-dependent DNA replication. They are: ORF9 (DNA polymerase), ORF6 (single-stranded DNA… (more)

Subjects/Keywords: Biology; Molecular

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Susilarini, N. K. (2011). Interaction of Kaposi's sarcoma-associated herpesvirus ORF59 with oriLyt is dependent upon binding with K-Rta. (Thesis). University of Nevada, Reno. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=1484051

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):

Susilarini, Ni Ketut. “Interaction of Kaposi's sarcoma-associated herpesvirus ORF59 with oriLyt is dependent upon binding with K-Rta.” 2011. Thesis, University of Nevada, Reno. Accessed August 24, 2019. http://pqdtopen.proquest.com/#viewpdf?dispub=1484051.

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

MLA Handbook (7th Edition):

Susilarini, Ni Ketut. “Interaction of Kaposi's sarcoma-associated herpesvirus ORF59 with oriLyt is dependent upon binding with K-Rta.” 2011. Web. 24 Aug 2019.

Vancouver:

Susilarini NK. Interaction of Kaposi's sarcoma-associated herpesvirus ORF59 with oriLyt is dependent upon binding with K-Rta. [Internet] [Thesis]. University of Nevada, Reno; 2011. [cited 2019 Aug 24]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=1484051.

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

Council of Science Editors:

Susilarini NK. Interaction of Kaposi's sarcoma-associated herpesvirus ORF59 with oriLyt is dependent upon binding with K-Rta. [Thesis]. University of Nevada, Reno; 2011. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=1484051

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


University of Southern California

29. Si, Yuchen. Determination of the causal potential of histone modifications on transcription and chromatin structure.

Degree: 2012, University of Southern California

  Histone modification is a major epigenetic regulatory mechanism that controls chromatin structure and gene expression potential. However, the causal potential of individual histone modifications… (more)

Subjects/Keywords: Biology; Molecular

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Si, Y. (2012). Determination of the causal potential of histone modifications on transcription and chromatin structure. (Thesis). University of Southern California. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=1529054

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):

Si, Yuchen. “Determination of the causal potential of histone modifications on transcription and chromatin structure.” 2012. Thesis, University of Southern California. Accessed August 24, 2019. http://pqdtopen.proquest.com/#viewpdf?dispub=1529054.

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

MLA Handbook (7th Edition):

Si, Yuchen. “Determination of the causal potential of histone modifications on transcription and chromatin structure.” 2012. Web. 24 Aug 2019.

Vancouver:

Si Y. Determination of the causal potential of histone modifications on transcription and chromatin structure. [Internet] [Thesis]. University of Southern California; 2012. [cited 2019 Aug 24]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=1529054.

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

Council of Science Editors:

Si Y. Determination of the causal potential of histone modifications on transcription and chromatin structure. [Thesis]. University of Southern California; 2012. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=1529054

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

30. Pao, Christina S. Mechanism of G protein-coupled receptor kinase binding and activation by G protein-coupled receptors.

Degree: 2007, Thomas Jefferson University

  G protein-coupled receptors (GPCRs) are regulated through the process of desensitization, where the receptor becomes refractory to agonist stimulation. The first step in desensitization… (more)

Subjects/Keywords: Biology; Molecular

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Pao, C. S. (2007). Mechanism of G protein-coupled receptor kinase binding and activation by G protein-coupled receptors. (Thesis). Thomas Jefferson University. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=3240653

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):

Pao, Christina S. “Mechanism of G protein-coupled receptor kinase binding and activation by G protein-coupled receptors.” 2007. Thesis, Thomas Jefferson University. Accessed August 24, 2019. http://pqdtopen.proquest.com/#viewpdf?dispub=3240653.

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

MLA Handbook (7th Edition):

Pao, Christina S. “Mechanism of G protein-coupled receptor kinase binding and activation by G protein-coupled receptors.” 2007. Web. 24 Aug 2019.

Vancouver:

Pao CS. Mechanism of G protein-coupled receptor kinase binding and activation by G protein-coupled receptors. [Internet] [Thesis]. Thomas Jefferson University; 2007. [cited 2019 Aug 24]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3240653.

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

Council of Science Editors:

Pao CS. Mechanism of G protein-coupled receptor kinase binding and activation by G protein-coupled receptors. [Thesis]. Thomas Jefferson University; 2007. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3240653

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

[1] [2] [3] [4] [5] … [430]

.