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You searched for subject:(Molecular biology). Showing records 1 – 30 of 10953 total matches.

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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)

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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 16, 2018. 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. 16 Aug 2018.

Vancouver:

Hofman EG. Plasma membrane organization during EGFR signaling: a FRET-based analysis. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2008. [cited 2018 Aug 16]. 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

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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 16, 2018. 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. 16 Aug 2018.

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 2018 Aug 16]. 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. 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

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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 16, 2018. 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. 16 Aug 2018.

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 2018 Aug 16]. 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

4. 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

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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 16, 2018. 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. 16 Aug 2018.

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 2018 Aug 16]. 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

5. Patitucci, Cecilia. PPARy, a new player in hepatic metabolic adaptation from mouse model to human liver cancer : Relationships Between Microstructural Parameters and Mechanical Properties of a new Nickel Based Superalloy AD730™.

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

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APA (6th Edition):

Patitucci, C. (2016). PPARy, a new player in hepatic metabolic adaptation from mouse model to human liver cancer : Relationships Between Microstructural Parameters and Mechanical Properties of a new Nickel Based Superalloy AD730™. (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 : Relationships Between Microstructural Parameters and Mechanical Properties of a new Nickel Based Superalloy AD730™.” 2016. Doctoral Dissertation, Sorbonne Paris Cité. Accessed August 16, 2018. 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 : Relationships Between Microstructural Parameters and Mechanical Properties of a new Nickel Based Superalloy AD730™.” 2016. Web. 16 Aug 2018.

Vancouver:

Patitucci C. PPARy, a new player in hepatic metabolic adaptation from mouse model to human liver cancer : Relationships Between Microstructural Parameters and Mechanical Properties of a new Nickel Based Superalloy AD730™. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; 2016. [cited 2018 Aug 16]. 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 : Relationships Between Microstructural Parameters and Mechanical Properties of a new Nickel Based Superalloy AD730™. [Doctoral Dissertation]. Sorbonne Paris Cité; 2016. Available from: http://www.theses.fr/2016USPCB056

6. 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

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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 16, 2018. 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. 16 Aug 2018.

Vancouver:

Nuhn ME. Molecular ecology of Boletinellus merulioides and systematics of the Boletineae. [Internet] [Thesis]. Clark University; 2016. [cited 2018 Aug 16]. 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

7. 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

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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 16, 2018. 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. 16 Aug 2018.

Vancouver:

Guo L. The Molecular Mechanisms of Sex Determination in Vertebrates. [Internet] [Thesis]. The University of North Dakota; 2017. [cited 2018 Aug 16]. 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


Florida State University

8. 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

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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 16, 2018. 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. 16 Aug 2018.

Vancouver:

Li J. Functional Characterization of Protein O-glcnacylation in Plants. [Internet] [Masters thesis]. Florida State University; 2015. [cited 2018 Aug 16]. 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 ;


Cleveland State University

9. 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

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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 16, 2018. 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. 16 Aug 2018.

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 2018 Aug 16]. 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

10. 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

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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 16, 2018. 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. 16 Aug 2018.

Vancouver:

Clarke DL. Development of a Stem Cell Gene Therapy for Sanfilippo Syndrome Type B. [Internet] [Thesis]. California State University, Los Angeles; 2017. [cited 2018 Aug 16]. 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

11. 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

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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 16, 2018. 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. 16 Aug 2018.

Vancouver:

Fassas S. Functional characterization of proteins essential for de novo peroxisome biogenesis. [Internet] [Thesis]. University of California – San Diego; 2016. [cited 2018 Aug 16]. 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

12. 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

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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 16, 2018. 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. 16 Aug 2018.

Vancouver:

Tavares DA. Studies on non-typeability and molecular identification of the pneumococcus. [Internet] [Thesis]. Universidade Nova; 2016. [cited 2018 Aug 16]. 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

13. 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

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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 16, 2018. 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. 16 Aug 2018.

Vancouver:

Kan CH. Quantifying Introgression at the Gene Level in Strongylocentrotid Urchins. [Internet] [Thesis]. University of California – Santa Cruz; 2018. [cited 2018 Aug 16]. 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


Universiteit Utrecht

14. Senf, F. The integral inner membrane component XcpS of the Pseudomonas aeruginosa type II secretion system: structure, function and localisation.

Degree: 2008, Universiteit Utrecht

 Type II secretion systems (T2SS) of Gram-negative bacteria are multi-component apparatuses that secrete proteins into the extracellular milieu. These systems have homology to type IV… (more)

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

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APA (6th Edition):

Senf, F. (2008). The integral inner membrane component XcpS of the Pseudomonas aeruginosa type II secretion system: structure, function and localisation. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/27861

Chicago Manual of Style (16th Edition):

Senf, F. “The integral inner membrane component XcpS of the Pseudomonas aeruginosa type II secretion system: structure, function and localisation.” 2008. Doctoral Dissertation, Universiteit Utrecht. Accessed August 16, 2018. http://dspace.library.uu.nl:8080/handle/1874/27861.

MLA Handbook (7th Edition):

Senf, F. “The integral inner membrane component XcpS of the Pseudomonas aeruginosa type II secretion system: structure, function and localisation.” 2008. Web. 16 Aug 2018.

Vancouver:

Senf F. The integral inner membrane component XcpS of the Pseudomonas aeruginosa type II secretion system: structure, function and localisation. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2008. [cited 2018 Aug 16]. Available from: http://dspace.library.uu.nl:8080/handle/1874/27861.

Council of Science Editors:

Senf F. The integral inner membrane component XcpS of the Pseudomonas aeruginosa type II secretion system: structure, function and localisation. [Doctoral Dissertation]. Universiteit Utrecht; 2008. Available from: http://dspace.library.uu.nl:8080/handle/1874/27861


Universiteit Utrecht

15. van Peer, A.F. Structure and function of the septal pore cap of Schizophyllum commune.

Degree: 2008, Universiteit Utrecht

 Filamentous fungi form networks (mycelia) of long, tubular structures (hyphae) that extend at their tip (apex) and branch subapically (behind the tip). Hyphae are compartmentalized… (more)

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

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APA (6th Edition):

van Peer, A. F. (2008). Structure and function of the septal pore cap of Schizophyllum commune. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/30964

Chicago Manual of Style (16th Edition):

van Peer, A F. “Structure and function of the septal pore cap of Schizophyllum commune.” 2008. Doctoral Dissertation, Universiteit Utrecht. Accessed August 16, 2018. http://dspace.library.uu.nl:8080/handle/1874/30964.

MLA Handbook (7th Edition):

van Peer, A F. “Structure and function of the septal pore cap of Schizophyllum commune.” 2008. Web. 16 Aug 2018.

Vancouver:

van Peer AF. Structure and function of the septal pore cap of Schizophyllum commune. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2008. [cited 2018 Aug 16]. Available from: http://dspace.library.uu.nl:8080/handle/1874/30964.

Council of Science Editors:

van Peer AF. Structure and function of the septal pore cap of Schizophyllum commune. [Doctoral Dissertation]. Universiteit Utrecht; 2008. Available from: http://dspace.library.uu.nl:8080/handle/1874/30964


Universiteit Utrecht

16. Grijpstra, J. Capsule biogenesis in Cryptococcus neoformans.

Degree: 2008, Universiteit Utrecht

 Cryptococcus neoformans is a human pathogen that mainly causes disease in immuno-compromised individuals. The yeast cells or basidiospores spread through dissemination from environmental sources, for… (more)

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

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APA (6th Edition):

Grijpstra, J. (2008). Capsule biogenesis in Cryptococcus neoformans. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/31692

Chicago Manual of Style (16th Edition):

Grijpstra, J. “Capsule biogenesis in Cryptococcus neoformans.” 2008. Doctoral Dissertation, Universiteit Utrecht. Accessed August 16, 2018. http://dspace.library.uu.nl:8080/handle/1874/31692.

MLA Handbook (7th Edition):

Grijpstra, J. “Capsule biogenesis in Cryptococcus neoformans.” 2008. Web. 16 Aug 2018.

Vancouver:

Grijpstra J. Capsule biogenesis in Cryptococcus neoformans. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2008. [cited 2018 Aug 16]. Available from: http://dspace.library.uu.nl:8080/handle/1874/31692.

Council of Science Editors:

Grijpstra J. Capsule biogenesis in Cryptococcus neoformans. [Doctoral Dissertation]. Universiteit Utrecht; 2008. Available from: http://dspace.library.uu.nl:8080/handle/1874/31692

17. 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.

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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 16, 2018. 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. 16 Aug 2018.

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 2018 Aug 16]. 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

18. 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.

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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 16, 2018. 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. 16 Aug 2018.

Vancouver:

Dhaliwal R. Roles of Cyclin A and Cyclin B in Drosophila Female Meiosis. [Internet] [Masters thesis]. National Library of Canada; 2011. [cited 2018 Aug 16]. 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

19. 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

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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 16, 2018. 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. 16 Aug 2018.

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 2018 Aug 16]. 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

20. 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

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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 16, 2018. 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. 16 Aug 2018.

Vancouver:

Bishop SC. Long primer extension by a novel inverse PCR method. [Internet] [Thesis]. University of Kansas; 2009. [cited 2018 Aug 16]. 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

21. 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

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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 16, 2018. 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. 16 Aug 2018.

Vancouver:

Murthy N. hIws1 structural elucidation and protein interactions. [Internet] [Thesis]. University of California, San Diego; 2009. [cited 2018 Aug 16]. 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

22. 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

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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 16, 2018. 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. 16 Aug 2018.

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 2018 Aug 16]. 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

23. 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

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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 16, 2018. 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. 16 Aug 2018.

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 2018 Aug 16]. 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

24. 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

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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 16, 2018. 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. 16 Aug 2018.

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 2018 Aug 16]. 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

25. 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

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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 16, 2018. 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. 16 Aug 2018.

Vancouver:

Si Y. Determination of the causal potential of histone modifications on transcription and chromatin structure. [Internet] [Thesis]. University of Southern California; 2012. [cited 2018 Aug 16]. 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

26. 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

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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 16, 2018. 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. 16 Aug 2018.

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 2018 Aug 16]. 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


University of South Florida

27. Shor, Audrey Cathryn. Src kinase inhibitors for the treatment of sarcomas| Cellular and molecular mechanisms of action.

Degree: 2007, University of South Florida

  Sarcomas are rare mesenchymally-derived tumors with limited treatment options. Tyrosine kinases may serve as potential targets for sarcoma therapy because many are mutated or… (more)

Subjects/Keywords: Biology; Molecular

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APA (6th Edition):

Shor, A. C. (2007). Src kinase inhibitors for the treatment of sarcomas| Cellular and molecular mechanisms of action. (Thesis). University of South Florida. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=3260112

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):

Shor, Audrey Cathryn. “Src kinase inhibitors for the treatment of sarcomas| Cellular and molecular mechanisms of action.” 2007. Thesis, University of South Florida. Accessed August 16, 2018. http://pqdtopen.proquest.com/#viewpdf?dispub=3260112.

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

MLA Handbook (7th Edition):

Shor, Audrey Cathryn. “Src kinase inhibitors for the treatment of sarcomas| Cellular and molecular mechanisms of action.” 2007. Web. 16 Aug 2018.

Vancouver:

Shor AC. Src kinase inhibitors for the treatment of sarcomas| Cellular and molecular mechanisms of action. [Internet] [Thesis]. University of South Florida; 2007. [cited 2018 Aug 16]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3260112.

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

Council of Science Editors:

Shor AC. Src kinase inhibitors for the treatment of sarcomas| Cellular and molecular mechanisms of action. [Thesis]. University of South Florida; 2007. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3260112

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

28. He, Ti. Molecular regulation of Pax5-mediated biological functions.

Degree: 2009, The University of Alabama at Birmingham

  B lineage cells are major players in the adaptive immune system. Pax5 is essential for B lineage cell development and function. Pax5 controls B… (more)

Subjects/Keywords: Biology; Molecular

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

APA (6th Edition):

He, T. (2009). Molecular regulation of Pax5-mediated biological functions. (Thesis). The University of Alabama at Birmingham. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=3339168

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):

He, Ti. “Molecular regulation of Pax5-mediated biological functions.” 2009. Thesis, The University of Alabama at Birmingham. Accessed August 16, 2018. http://pqdtopen.proquest.com/#viewpdf?dispub=3339168.

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

MLA Handbook (7th Edition):

He, Ti. “Molecular regulation of Pax5-mediated biological functions.” 2009. Web. 16 Aug 2018.

Vancouver:

He T. Molecular regulation of Pax5-mediated biological functions. [Internet] [Thesis]. The University of Alabama at Birmingham; 2009. [cited 2018 Aug 16]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3339168.

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

Council of Science Editors:

He T. Molecular regulation of Pax5-mediated biological functions. [Thesis]. The University of Alabama at Birmingham; 2009. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3339168

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


University of California, Riverside

29. Karr, Stephen John. A novel approach to functional genomic studies of the superfamily of receptor-like kinases (RLKs) in Arabidopsis thaliana.

Degree: 2009, University of California, Riverside

  Receptor-like kinases (RLKs) form a large monophyletic gene family of approximately 600 members in Arabidopsis. They consist of proteins that contain a single extracellular… (more)

Subjects/Keywords: Biology; Molecular

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Karr, S. J. (2009). A novel approach to functional genomic studies of the superfamily of receptor-like kinases (RLKs) in Arabidopsis thaliana. (Thesis). University of California, Riverside. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=3345263

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):

Karr, Stephen John. “A novel approach to functional genomic studies of the superfamily of receptor-like kinases (RLKs) in Arabidopsis thaliana.” 2009. Thesis, University of California, Riverside. Accessed August 16, 2018. http://pqdtopen.proquest.com/#viewpdf?dispub=3345263.

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

MLA Handbook (7th Edition):

Karr, Stephen John. “A novel approach to functional genomic studies of the superfamily of receptor-like kinases (RLKs) in Arabidopsis thaliana.” 2009. Web. 16 Aug 2018.

Vancouver:

Karr SJ. A novel approach to functional genomic studies of the superfamily of receptor-like kinases (RLKs) in Arabidopsis thaliana. [Internet] [Thesis]. University of California, Riverside; 2009. [cited 2018 Aug 16]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3345263.

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

Council of Science Editors:

Karr SJ. A novel approach to functional genomic studies of the superfamily of receptor-like kinases (RLKs) in Arabidopsis thaliana. [Thesis]. University of California, Riverside; 2009. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3345263

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


Stanford University

30. Truong, Amy Bidong. Control of epidermal proliferation and differentiation by p63.

Degree: 2009, Stanford University

  p63 is a p53 family member consisting of six isoforms, broadly characterized by the presence (TA) or absence (ΔN) or an amino-terminal transactivation domain.… (more)

Subjects/Keywords: Biology; Molecular

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Truong, A. B. (2009). Control of epidermal proliferation and differentiation by p63. (Thesis). Stanford University. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=3351495

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):

Truong, Amy Bidong. “Control of epidermal proliferation and differentiation by p63.” 2009. Thesis, Stanford University. Accessed August 16, 2018. http://pqdtopen.proquest.com/#viewpdf?dispub=3351495.

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

MLA Handbook (7th Edition):

Truong, Amy Bidong. “Control of epidermal proliferation and differentiation by p63.” 2009. Web. 16 Aug 2018.

Vancouver:

Truong AB. Control of epidermal proliferation and differentiation by p63. [Internet] [Thesis]. Stanford University; 2009. [cited 2018 Aug 16]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3351495.

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

Council of Science Editors:

Truong AB. Control of epidermal proliferation and differentiation by p63. [Thesis]. Stanford University; 2009. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3351495

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

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