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 +publisher:"Brown University" +contributor:("Freiman, Richard"). Showing records 1 – 30 of 35 total matches.

[1] [2]

Search Limiters

Last 2 Years | English Only

▼ Search Limiters

1. Mori, Megumi. Gene Expression Changes Associated with the Differentiation of Mouse Embryonic Stem Cells to Primordial Germ Cell-Like Cells.

Degree: Department of Molecular Biology, Cell Biology and Biochemistry, 2018, Brown University

 Embryonic stem cells (ESCs) are found early in the developing embryo and from this initial population, all cells in the body are eventually derived. A… (more)

Subjects/Keywords: Cell differentiation

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Mori, M. (2018). Gene Expression Changes Associated with the Differentiation of Mouse Embryonic Stem Cells to Primordial Germ Cell-Like Cells. (Thesis). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:792693/

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):

Mori, Megumi. “Gene Expression Changes Associated with the Differentiation of Mouse Embryonic Stem Cells to Primordial Germ Cell-Like Cells.” 2018. Thesis, Brown University. Accessed January 16, 2021. https://repository.library.brown.edu/studio/item/bdr:792693/.

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

MLA Handbook (7th Edition):

Mori, Megumi. “Gene Expression Changes Associated with the Differentiation of Mouse Embryonic Stem Cells to Primordial Germ Cell-Like Cells.” 2018. Web. 16 Jan 2021.

Vancouver:

Mori M. Gene Expression Changes Associated with the Differentiation of Mouse Embryonic Stem Cells to Primordial Germ Cell-Like Cells. [Internet] [Thesis]. Brown University; 2018. [cited 2021 Jan 16]. Available from: https://repository.library.brown.edu/studio/item/bdr:792693/.

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

Council of Science Editors:

Mori M. Gene Expression Changes Associated with the Differentiation of Mouse Embryonic Stem Cells to Primordial Germ Cell-Like Cells. [Thesis]. Brown University; 2018. Available from: https://repository.library.brown.edu/studio/item/bdr:792693/

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

2. Oxendine, Lauren. PI3K/Akt/mTOR pathway modulation by cAMP and metabotropic glutamate receptors.

Degree: Department of Molecular Pharmacology, Physiology and Biotechnology, 2018, Brown University

 The phosphatidylinositol 3 kinase/protein kinase B/mammalian target of rapamycin (PI3K/AKT/mTOR) pathway is essential for cell survival, growth, proliferation, and differentiation. It is highly conserved and… (more)

Subjects/Keywords: Proteins

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Oxendine, L. (2018). PI3K/Akt/mTOR pathway modulation by cAMP and metabotropic glutamate receptors. (Thesis). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:792763/

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):

Oxendine, Lauren. “PI3K/Akt/mTOR pathway modulation by cAMP and metabotropic glutamate receptors.” 2018. Thesis, Brown University. Accessed January 16, 2021. https://repository.library.brown.edu/studio/item/bdr:792763/.

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

MLA Handbook (7th Edition):

Oxendine, Lauren. “PI3K/Akt/mTOR pathway modulation by cAMP and metabotropic glutamate receptors.” 2018. Web. 16 Jan 2021.

Vancouver:

Oxendine L. PI3K/Akt/mTOR pathway modulation by cAMP and metabotropic glutamate receptors. [Internet] [Thesis]. Brown University; 2018. [cited 2021 Jan 16]. Available from: https://repository.library.brown.edu/studio/item/bdr:792763/.

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

Council of Science Editors:

Oxendine L. PI3K/Akt/mTOR pathway modulation by cAMP and metabotropic glutamate receptors. [Thesis]. Brown University; 2018. Available from: https://repository.library.brown.edu/studio/item/bdr:792763/

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

3. Nixon, Christina Erin. Ubiquitin-Dependent Proteolysis of the Yeast Mating-Type Regulator Matalpha1.

Degree: PhD, Division of Biology and Medicine. Molecular Biology, Cell Biology, and Biochemistry, 2009, Brown University

 Cell type in budding yeast is controlled by the master regulatory transcription factors encoded at the mating-type (MAT) locus Mat?1, Mat?2, and Mata1. In homothallic… (more)

Subjects/Keywords: MATalpha1

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Nixon, C. E. (2009). Ubiquitin-Dependent Proteolysis of the Yeast Mating-Type Regulator Matalpha1. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:224/

Chicago Manual of Style (16th Edition):

Nixon, Christina Erin. “Ubiquitin-Dependent Proteolysis of the Yeast Mating-Type Regulator Matalpha1.” 2009. Doctoral Dissertation, Brown University. Accessed January 16, 2021. https://repository.library.brown.edu/studio/item/bdr:224/.

MLA Handbook (7th Edition):

Nixon, Christina Erin. “Ubiquitin-Dependent Proteolysis of the Yeast Mating-Type Regulator Matalpha1.” 2009. Web. 16 Jan 2021.

Vancouver:

Nixon CE. Ubiquitin-Dependent Proteolysis of the Yeast Mating-Type Regulator Matalpha1. [Internet] [Doctoral dissertation]. Brown University; 2009. [cited 2021 Jan 16]. Available from: https://repository.library.brown.edu/studio/item/bdr:224/.

Council of Science Editors:

Nixon CE. Ubiquitin-Dependent Proteolysis of the Yeast Mating-Type Regulator Matalpha1. [Doctoral Dissertation]. Brown University; 2009. Available from: https://repository.library.brown.edu/studio/item/bdr:224/

4. DeSimone, Alec M. The Dynamic Interactions of the alpha2 Repressor Engender Robust Repression of Developmentally Regulated Genes while Priming them for Rapid Activation.

Degree: PhD, Division of Biology and Medicine. Molecular Biology, Cell Biology, and Biochemistry, 2009, Brown University

 In budding yeast, mating-type identity is determined genetically by the MAT locus, which encodes a set of transcriptional regulators that direct the cell to execute… (more)

Subjects/Keywords: phenotypic switching mating-type switching

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

DeSimone, A. M. (2009). The Dynamic Interactions of the alpha2 Repressor Engender Robust Repression of Developmentally Regulated Genes while Priming them for Rapid Activation. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:200/

Chicago Manual of Style (16th Edition):

DeSimone, Alec M. “The Dynamic Interactions of the alpha2 Repressor Engender Robust Repression of Developmentally Regulated Genes while Priming them for Rapid Activation.” 2009. Doctoral Dissertation, Brown University. Accessed January 16, 2021. https://repository.library.brown.edu/studio/item/bdr:200/.

MLA Handbook (7th Edition):

DeSimone, Alec M. “The Dynamic Interactions of the alpha2 Repressor Engender Robust Repression of Developmentally Regulated Genes while Priming them for Rapid Activation.” 2009. Web. 16 Jan 2021.

Vancouver:

DeSimone AM. The Dynamic Interactions of the alpha2 Repressor Engender Robust Repression of Developmentally Regulated Genes while Priming them for Rapid Activation. [Internet] [Doctoral dissertation]. Brown University; 2009. [cited 2021 Jan 16]. Available from: https://repository.library.brown.edu/studio/item/bdr:200/.

Council of Science Editors:

DeSimone AM. The Dynamic Interactions of the alpha2 Repressor Engender Robust Repression of Developmentally Regulated Genes while Priming them for Rapid Activation. [Doctoral Dissertation]. Brown University; 2009. Available from: https://repository.library.brown.edu/studio/item/bdr:200/

5. Ribeiro, Jennifer R. Molecular and Functional Roles of TAF4B in Ovarian Health and Disease.

Degree: PhD, Pathobiology, 2014, Brown University

 Historically, the TFIID complex has been viewed as part of the general transcriptional apparatus; however, recent studies demonstrate that it is flexible in its constituents… (more)

Subjects/Keywords: ovarian cancer

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Ribeiro, J. R. (2014). Molecular and Functional Roles of TAF4B in Ovarian Health and Disease. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:386237/

Chicago Manual of Style (16th Edition):

Ribeiro, Jennifer R. “Molecular and Functional Roles of TAF4B in Ovarian Health and Disease.” 2014. Doctoral Dissertation, Brown University. Accessed January 16, 2021. https://repository.library.brown.edu/studio/item/bdr:386237/.

MLA Handbook (7th Edition):

Ribeiro, Jennifer R. “Molecular and Functional Roles of TAF4B in Ovarian Health and Disease.” 2014. Web. 16 Jan 2021.

Vancouver:

Ribeiro JR. Molecular and Functional Roles of TAF4B in Ovarian Health and Disease. [Internet] [Doctoral dissertation]. Brown University; 2014. [cited 2021 Jan 16]. Available from: https://repository.library.brown.edu/studio/item/bdr:386237/.

Council of Science Editors:

Ribeiro JR. Molecular and Functional Roles of TAF4B in Ovarian Health and Disease. [Doctoral Dissertation]. Brown University; 2014. Available from: https://repository.library.brown.edu/studio/item/bdr:386237/

6. Berk-Rauch, Hanna E. FMRP Regulates the Expression of Axonal Messages In Vivo.

Degree: PhD, Molecular Biology, Cell Biology, and Biochemistry, 2013, Brown University

 Fragile X syndrome, a leading cause of autism and the most common form of inherited intellectual disability, results from the loss of Fragile X mental… (more)

Subjects/Keywords: cellular biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Berk-Rauch, H. E. (2013). FMRP Regulates the Expression of Axonal Messages In Vivo. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:320509/

Chicago Manual of Style (16th Edition):

Berk-Rauch, Hanna E. “FMRP Regulates the Expression of Axonal Messages In Vivo.” 2013. Doctoral Dissertation, Brown University. Accessed January 16, 2021. https://repository.library.brown.edu/studio/item/bdr:320509/.

MLA Handbook (7th Edition):

Berk-Rauch, Hanna E. “FMRP Regulates the Expression of Axonal Messages In Vivo.” 2013. Web. 16 Jan 2021.

Vancouver:

Berk-Rauch HE. FMRP Regulates the Expression of Axonal Messages In Vivo. [Internet] [Doctoral dissertation]. Brown University; 2013. [cited 2021 Jan 16]. Available from: https://repository.library.brown.edu/studio/item/bdr:320509/.

Council of Science Editors:

Berk-Rauch HE. FMRP Regulates the Expression of Axonal Messages In Vivo. [Doctoral Dissertation]. Brown University; 2013. Available from: https://repository.library.brown.edu/studio/item/bdr:320509/

7. Chery , Jessica. The Function of the CLAMP Zinc Finger Protein in Targeting MSL Complex to the X-chromosome during Dosage Compensation in Drosophila Melanogaster.

Degree: PhD, Molecular Biology, Cell Biology, and Biochemistry, 2014, Brown University

 Coordinate gene regulation is critical to promote normal development and prevent disease. How domains of co-regulation are established in vivo remains poorly understood. X-chromosome dosage… (more)

Subjects/Keywords: CLAMP

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Chery , J. (2014). The Function of the CLAMP Zinc Finger Protein in Targeting MSL Complex to the X-chromosome during Dosage Compensation in Drosophila Melanogaster. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:386293/

Chicago Manual of Style (16th Edition):

Chery , Jessica. “The Function of the CLAMP Zinc Finger Protein in Targeting MSL Complex to the X-chromosome during Dosage Compensation in Drosophila Melanogaster.” 2014. Doctoral Dissertation, Brown University. Accessed January 16, 2021. https://repository.library.brown.edu/studio/item/bdr:386293/.

MLA Handbook (7th Edition):

Chery , Jessica. “The Function of the CLAMP Zinc Finger Protein in Targeting MSL Complex to the X-chromosome during Dosage Compensation in Drosophila Melanogaster.” 2014. Web. 16 Jan 2021.

Vancouver:

Chery J. The Function of the CLAMP Zinc Finger Protein in Targeting MSL Complex to the X-chromosome during Dosage Compensation in Drosophila Melanogaster. [Internet] [Doctoral dissertation]. Brown University; 2014. [cited 2021 Jan 16]. Available from: https://repository.library.brown.edu/studio/item/bdr:386293/.

Council of Science Editors:

Chery J. The Function of the CLAMP Zinc Finger Protein in Targeting MSL Complex to the X-chromosome during Dosage Compensation in Drosophila Melanogaster. [Doctoral Dissertation]. Brown University; 2014. Available from: https://repository.library.brown.edu/studio/item/bdr:386293/

8. Lovasco, Lindsay A. The Ovarian Requirement for Variant TFIID Subunit, TAF4b, in Mammalian Reproduction.

Degree: PhD, Division of Biology and Medicine. Molecular Biology, Cell Biology, and Biochemistry, 2009, Brown University

 TAF4b is a gonadal-encriched variant of the general transcription factor complex, TFIID. The studies presented here highlight the specific requirement for TAF4b in female mammalian… (more)

Subjects/Keywords: Mammalian

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lovasco, L. A. (2009). The Ovarian Requirement for Variant TFIID Subunit, TAF4b, in Mammalian Reproduction. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:181/

Chicago Manual of Style (16th Edition):

Lovasco, Lindsay A. “The Ovarian Requirement for Variant TFIID Subunit, TAF4b, in Mammalian Reproduction.” 2009. Doctoral Dissertation, Brown University. Accessed January 16, 2021. https://repository.library.brown.edu/studio/item/bdr:181/.

MLA Handbook (7th Edition):

Lovasco, Lindsay A. “The Ovarian Requirement for Variant TFIID Subunit, TAF4b, in Mammalian Reproduction.” 2009. Web. 16 Jan 2021.

Vancouver:

Lovasco LA. The Ovarian Requirement for Variant TFIID Subunit, TAF4b, in Mammalian Reproduction. [Internet] [Doctoral dissertation]. Brown University; 2009. [cited 2021 Jan 16]. Available from: https://repository.library.brown.edu/studio/item/bdr:181/.

Council of Science Editors:

Lovasco LA. The Ovarian Requirement for Variant TFIID Subunit, TAF4b, in Mammalian Reproduction. [Doctoral Dissertation]. Brown University; 2009. Available from: https://repository.library.brown.edu/studio/item/bdr:181/

9. Srivastava, Akash. Transdifferentiation of liver to pancreas.

Degree: PhD, Molecular Biology, Cell Biology, and Biochemistry, 2015, Brown University

 Diabetes mellitus results from gradual decline in pancreatic beta cell mass and function. Cell-based therapies in diabetes research are mainly focused on using stem cells… (more)

Subjects/Keywords: Transdifferentiation

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Srivastava, A. (2015). Transdifferentiation of liver to pancreas. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:419395/

Chicago Manual of Style (16th Edition):

Srivastava, Akash. “Transdifferentiation of liver to pancreas.” 2015. Doctoral Dissertation, Brown University. Accessed January 16, 2021. https://repository.library.brown.edu/studio/item/bdr:419395/.

MLA Handbook (7th Edition):

Srivastava, Akash. “Transdifferentiation of liver to pancreas.” 2015. Web. 16 Jan 2021.

Vancouver:

Srivastava A. Transdifferentiation of liver to pancreas. [Internet] [Doctoral dissertation]. Brown University; 2015. [cited 2021 Jan 16]. Available from: https://repository.library.brown.edu/studio/item/bdr:419395/.

Council of Science Editors:

Srivastava A. Transdifferentiation of liver to pancreas. [Doctoral Dissertation]. Brown University; 2015. Available from: https://repository.library.brown.edu/studio/item/bdr:419395/

10. Moyer, Benjamin James. Perinatal Endocrine Disruption in the Female: Multiple Latent Effects Throughout Murine Life.

Degree: PhD, Pathobiology, 2012, Brown University

 Endocrine disruptors are a broad class of toxicants with the ability to alter and/or interfere with normal endocrine signaling. The perinatal period is particularly vulnerable… (more)

Subjects/Keywords: In Utero

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Moyer, B. J. (2012). Perinatal Endocrine Disruption in the Female: Multiple Latent Effects Throughout Murine Life. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:297567/

Chicago Manual of Style (16th Edition):

Moyer, Benjamin James. “Perinatal Endocrine Disruption in the Female: Multiple Latent Effects Throughout Murine Life.” 2012. Doctoral Dissertation, Brown University. Accessed January 16, 2021. https://repository.library.brown.edu/studio/item/bdr:297567/.

MLA Handbook (7th Edition):

Moyer, Benjamin James. “Perinatal Endocrine Disruption in the Female: Multiple Latent Effects Throughout Murine Life.” 2012. Web. 16 Jan 2021.

Vancouver:

Moyer BJ. Perinatal Endocrine Disruption in the Female: Multiple Latent Effects Throughout Murine Life. [Internet] [Doctoral dissertation]. Brown University; 2012. [cited 2021 Jan 16]. Available from: https://repository.library.brown.edu/studio/item/bdr:297567/.

Council of Science Editors:

Moyer BJ. Perinatal Endocrine Disruption in the Female: Multiple Latent Effects Throughout Murine Life. [Doctoral Dissertation]. Brown University; 2012. Available from: https://repository.library.brown.edu/studio/item/bdr:297567/

11. Lim, Kian Huat. Using positional frequency distribution to identify functional splicing elements and predict pre-mRNA processing defects in human genes.

Degree: PhD, Molecular Biology, Cell Biology, and Biochemistry, 2012, Brown University

 We present an intuitive strategy for predicting the effect of sequence variation on splicing. In contrast to transcriptional elements, splicing elements appear to be strongly… (more)

Subjects/Keywords: alternational splicing

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lim, K. H. (2012). Using positional frequency distribution to identify functional splicing elements and predict pre-mRNA processing defects in human genes. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:297548/

Chicago Manual of Style (16th Edition):

Lim, Kian Huat. “Using positional frequency distribution to identify functional splicing elements and predict pre-mRNA processing defects in human genes.” 2012. Doctoral Dissertation, Brown University. Accessed January 16, 2021. https://repository.library.brown.edu/studio/item/bdr:297548/.

MLA Handbook (7th Edition):

Lim, Kian Huat. “Using positional frequency distribution to identify functional splicing elements and predict pre-mRNA processing defects in human genes.” 2012. Web. 16 Jan 2021.

Vancouver:

Lim KH. Using positional frequency distribution to identify functional splicing elements and predict pre-mRNA processing defects in human genes. [Internet] [Doctoral dissertation]. Brown University; 2012. [cited 2021 Jan 16]. Available from: https://repository.library.brown.edu/studio/item/bdr:297548/.

Council of Science Editors:

Lim KH. Using positional frequency distribution to identify functional splicing elements and predict pre-mRNA processing defects in human genes. [Doctoral Dissertation]. Brown University; 2012. Available from: https://repository.library.brown.edu/studio/item/bdr:297548/

12. Grive, Kathryn J. Taf4b Controls Oocyte-Specific Gene Regulatory Networks and Primordial Follicle Development.

Degree: PhD, Molecular Biology, Cell Biology, and Biochemistry, 2016, Brown University

 Primary ovarian insufficiency (POI) affects 1% of women under 40, and can be induced by ovarian follicle disruption or depletion. Taf4b is a gonadal-enriched subunit… (more)

Subjects/Keywords: oocyte

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Grive, K. J. (2016). Taf4b Controls Oocyte-Specific Gene Regulatory Networks and Primordial Follicle Development. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:674153/

Chicago Manual of Style (16th Edition):

Grive, Kathryn J. “Taf4b Controls Oocyte-Specific Gene Regulatory Networks and Primordial Follicle Development.” 2016. Doctoral Dissertation, Brown University. Accessed January 16, 2021. https://repository.library.brown.edu/studio/item/bdr:674153/.

MLA Handbook (7th Edition):

Grive, Kathryn J. “Taf4b Controls Oocyte-Specific Gene Regulatory Networks and Primordial Follicle Development.” 2016. Web. 16 Jan 2021.

Vancouver:

Grive KJ. Taf4b Controls Oocyte-Specific Gene Regulatory Networks and Primordial Follicle Development. [Internet] [Doctoral dissertation]. Brown University; 2016. [cited 2021 Jan 16]. Available from: https://repository.library.brown.edu/studio/item/bdr:674153/.

Council of Science Editors:

Grive KJ. Taf4b Controls Oocyte-Specific Gene Regulatory Networks and Primordial Follicle Development. [Doctoral Dissertation]. Brown University; 2016. Available from: https://repository.library.brown.edu/studio/item/bdr:674153/

13. Catlin, Natasha Rene. The Stage-Specific Apoptotic Response of the Rat Testis to Low Dose Co-Exposures.

Degree: PhD, Pathobiology, 2014, Brown University

 Human exposure to mixtures of environmental chemicals occurs daily, leading to challenges regarding risk assessment due to limited information on these interactions. This dissertation developed… (more)

Subjects/Keywords: 2; 5-hexanedione

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Catlin, N. R. (2014). The Stage-Specific Apoptotic Response of the Rat Testis to Low Dose Co-Exposures. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:386159/

Chicago Manual of Style (16th Edition):

Catlin, Natasha Rene. “The Stage-Specific Apoptotic Response of the Rat Testis to Low Dose Co-Exposures.” 2014. Doctoral Dissertation, Brown University. Accessed January 16, 2021. https://repository.library.brown.edu/studio/item/bdr:386159/.

MLA Handbook (7th Edition):

Catlin, Natasha Rene. “The Stage-Specific Apoptotic Response of the Rat Testis to Low Dose Co-Exposures.” 2014. Web. 16 Jan 2021.

Vancouver:

Catlin NR. The Stage-Specific Apoptotic Response of the Rat Testis to Low Dose Co-Exposures. [Internet] [Doctoral dissertation]. Brown University; 2014. [cited 2021 Jan 16]. Available from: https://repository.library.brown.edu/studio/item/bdr:386159/.

Council of Science Editors:

Catlin NR. The Stage-Specific Apoptotic Response of the Rat Testis to Low Dose Co-Exposures. [Doctoral Dissertation]. Brown University; 2014. Available from: https://repository.library.brown.edu/studio/item/bdr:386159/

14. Booker, Anne B. The Long and Short of the Fragile X Mental Retardation 1 Gene.

Degree: PhD, Neuroscience, 2009, Brown University

 Fragile X Syndrome (FXS) is the leading cause of inherited mental retardation, due to mutations in the Fragile X Mental Retardation 1 (FMR1) gene. Almost… (more)

Subjects/Keywords: fragile X

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Booker, A. B. (2009). The Long and Short of the Fragile X Mental Retardation 1 Gene. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:121/

Chicago Manual of Style (16th Edition):

Booker, Anne B. “The Long and Short of the Fragile X Mental Retardation 1 Gene.” 2009. Doctoral Dissertation, Brown University. Accessed January 16, 2021. https://repository.library.brown.edu/studio/item/bdr:121/.

MLA Handbook (7th Edition):

Booker, Anne B. “The Long and Short of the Fragile X Mental Retardation 1 Gene.” 2009. Web. 16 Jan 2021.

Vancouver:

Booker AB. The Long and Short of the Fragile X Mental Retardation 1 Gene. [Internet] [Doctoral dissertation]. Brown University; 2009. [cited 2021 Jan 16]. Available from: https://repository.library.brown.edu/studio/item/bdr:121/.

Council of Science Editors:

Booker AB. The Long and Short of the Fragile X Mental Retardation 1 Gene. [Doctoral Dissertation]. Brown University; 2009. Available from: https://repository.library.brown.edu/studio/item/bdr:121/

15. Hagan, Elizabeth P. Novel Role of Xeroderma Pigmentosum Group A Protein in Nucleolar Responses to Proteotoxic Stress.

Degree: PhD, Division of Biology and Medicine. Pathobiology, 2009, Brown University

 Xeroderma pigmentosum Group A protein (XPA) is essential in the nucleotide excision repair (NER) pathway. Patients without functional XPA have extreme sensitivity to ultraviolet (UV)… (more)

Subjects/Keywords: XPA

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hagan, E. P. (2009). Novel Role of Xeroderma Pigmentosum Group A Protein in Nucleolar Responses to Proteotoxic Stress. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:172/

Chicago Manual of Style (16th Edition):

Hagan, Elizabeth P. “Novel Role of Xeroderma Pigmentosum Group A Protein in Nucleolar Responses to Proteotoxic Stress.” 2009. Doctoral Dissertation, Brown University. Accessed January 16, 2021. https://repository.library.brown.edu/studio/item/bdr:172/.

MLA Handbook (7th Edition):

Hagan, Elizabeth P. “Novel Role of Xeroderma Pigmentosum Group A Protein in Nucleolar Responses to Proteotoxic Stress.” 2009. Web. 16 Jan 2021.

Vancouver:

Hagan EP. Novel Role of Xeroderma Pigmentosum Group A Protein in Nucleolar Responses to Proteotoxic Stress. [Internet] [Doctoral dissertation]. Brown University; 2009. [cited 2021 Jan 16]. Available from: https://repository.library.brown.edu/studio/item/bdr:172/.

Council of Science Editors:

Hagan EP. Novel Role of Xeroderma Pigmentosum Group A Protein in Nucleolar Responses to Proteotoxic Stress. [Doctoral Dissertation]. Brown University; 2009. Available from: https://repository.library.brown.edu/studio/item/bdr:172/

16. Magruder, Hilary. Signaling Effectors Required for G Protein-Coupled Estrogen Receptor-, GPER, Induced Events Associated with Breast Cancer Progression.

Degree: PhD, Pathobiology, 2014, Brown University

 Stimulation of estrogen receptor (ER)-negative human breast cancer cells with 17β-estradiol (E2β) results in fibronectin (FN) matrix assembly and transactivation of the epidermal growth factor… (more)

Subjects/Keywords: estrogen receptor (ER)

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Magruder, H. (2014). Signaling Effectors Required for G Protein-Coupled Estrogen Receptor-, GPER, Induced Events Associated with Breast Cancer Progression. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:386260/

Chicago Manual of Style (16th Edition):

Magruder, Hilary. “Signaling Effectors Required for G Protein-Coupled Estrogen Receptor-, GPER, Induced Events Associated with Breast Cancer Progression.” 2014. Doctoral Dissertation, Brown University. Accessed January 16, 2021. https://repository.library.brown.edu/studio/item/bdr:386260/.

MLA Handbook (7th Edition):

Magruder, Hilary. “Signaling Effectors Required for G Protein-Coupled Estrogen Receptor-, GPER, Induced Events Associated with Breast Cancer Progression.” 2014. Web. 16 Jan 2021.

Vancouver:

Magruder H. Signaling Effectors Required for G Protein-Coupled Estrogen Receptor-, GPER, Induced Events Associated with Breast Cancer Progression. [Internet] [Doctoral dissertation]. Brown University; 2014. [cited 2021 Jan 16]. Available from: https://repository.library.brown.edu/studio/item/bdr:386260/.

Council of Science Editors:

Magruder H. Signaling Effectors Required for G Protein-Coupled Estrogen Receptor-, GPER, Induced Events Associated with Breast Cancer Progression. [Doctoral Dissertation]. Brown University; 2014. Available from: https://repository.library.brown.edu/studio/item/bdr:386260/

17. Gasparovic, Megan L. Viral and Host-Cell Factors Critical for JC Virus Infection.

Degree: PhD, Division of Biology and Medicine. Molecular Biology, Cell Biology, and Biochemistry, 2009, Brown University

 JC virus (JCV) is the causative agent of Progressive Multifocal Leukoencephalopathy, a fatal demyelinating disease of the central nervous system (CNS). This disease is caused… (more)

Subjects/Keywords: JC virus

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Gasparovic, M. L. (2009). Viral and Host-Cell Factors Critical for JC Virus Infection. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:84/

Chicago Manual of Style (16th Edition):

Gasparovic, Megan L. “Viral and Host-Cell Factors Critical for JC Virus Infection.” 2009. Doctoral Dissertation, Brown University. Accessed January 16, 2021. https://repository.library.brown.edu/studio/item/bdr:84/.

MLA Handbook (7th Edition):

Gasparovic, Megan L. “Viral and Host-Cell Factors Critical for JC Virus Infection.” 2009. Web. 16 Jan 2021.

Vancouver:

Gasparovic ML. Viral and Host-Cell Factors Critical for JC Virus Infection. [Internet] [Doctoral dissertation]. Brown University; 2009. [cited 2021 Jan 16]. Available from: https://repository.library.brown.edu/studio/item/bdr:84/.

Council of Science Editors:

Gasparovic ML. Viral and Host-Cell Factors Critical for JC Virus Infection. [Doctoral Dissertation]. Brown University; 2009. Available from: https://repository.library.brown.edu/studio/item/bdr:84/

18. Donovan, Diana J. The Genetic and Biochemical Analysis of the Chromatin-Targeting Protein BRD2 in Mammalian Development.

Degree: PhD, Molecular Biology, Cell Biology, and Biochemistry, 2013, Brown University

 The regulation of gene expression in eukaryotic cells is controlled by both chromatin dynamics and the actions of myriad components of the transcriptional machinery. While… (more)

Subjects/Keywords: BRD2

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Donovan, D. J. (2013). The Genetic and Biochemical Analysis of the Chromatin-Targeting Protein BRD2 in Mammalian Development. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:320567/

Chicago Manual of Style (16th Edition):

Donovan, Diana J. “The Genetic and Biochemical Analysis of the Chromatin-Targeting Protein BRD2 in Mammalian Development.” 2013. Doctoral Dissertation, Brown University. Accessed January 16, 2021. https://repository.library.brown.edu/studio/item/bdr:320567/.

MLA Handbook (7th Edition):

Donovan, Diana J. “The Genetic and Biochemical Analysis of the Chromatin-Targeting Protein BRD2 in Mammalian Development.” 2013. Web. 16 Jan 2021.

Vancouver:

Donovan DJ. The Genetic and Biochemical Analysis of the Chromatin-Targeting Protein BRD2 in Mammalian Development. [Internet] [Doctoral dissertation]. Brown University; 2013. [cited 2021 Jan 16]. Available from: https://repository.library.brown.edu/studio/item/bdr:320567/.

Council of Science Editors:

Donovan DJ. The Genetic and Biochemical Analysis of the Chromatin-Targeting Protein BRD2 in Mammalian Development. [Doctoral Dissertation]. Brown University; 2013. Available from: https://repository.library.brown.edu/studio/item/bdr:320567/

19. LaRocca, Jessica Lyn. Growth and Proliferation Signaling in Mammary Gland Development and Cancer.

Degree: PhD, Pathobiology, 2012, Brown University

 Breast cancer is the second most frequently diagnosed cancer and the second leading cause of cancer death in U.S. women. The studies presented in this… (more)

Subjects/Keywords: development

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

LaRocca, J. L. (2012). Growth and Proliferation Signaling in Mammary Gland Development and Cancer. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:297565/

Chicago Manual of Style (16th Edition):

LaRocca, Jessica Lyn. “Growth and Proliferation Signaling in Mammary Gland Development and Cancer.” 2012. Doctoral Dissertation, Brown University. Accessed January 16, 2021. https://repository.library.brown.edu/studio/item/bdr:297565/.

MLA Handbook (7th Edition):

LaRocca, Jessica Lyn. “Growth and Proliferation Signaling in Mammary Gland Development and Cancer.” 2012. Web. 16 Jan 2021.

Vancouver:

LaRocca JL. Growth and Proliferation Signaling in Mammary Gland Development and Cancer. [Internet] [Doctoral dissertation]. Brown University; 2012. [cited 2021 Jan 16]. Available from: https://repository.library.brown.edu/studio/item/bdr:297565/.

Council of Science Editors:

LaRocca JL. Growth and Proliferation Signaling in Mammary Gland Development and Cancer. [Doctoral Dissertation]. Brown University; 2012. Available from: https://repository.library.brown.edu/studio/item/bdr:297565/

20. Hofmann, Jeffrey W. The Role of Myc in Aging and Longevity in Mice.

Degree: PhD, Molecular Biology, Cell Biology, and Biochemistry, 2014, Brown University

 Abstract of “The Role of Myc in Aging and Longevity in Mice” by Jeffrey W. Hofmann, Ph.D., Brown University, May 2014 The gene Myc encodes… (more)

Subjects/Keywords: Myc

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hofmann, J. W. (2014). The Role of Myc in Aging and Longevity in Mice. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:386199/

Chicago Manual of Style (16th Edition):

Hofmann, Jeffrey W. “The Role of Myc in Aging and Longevity in Mice.” 2014. Doctoral Dissertation, Brown University. Accessed January 16, 2021. https://repository.library.brown.edu/studio/item/bdr:386199/.

MLA Handbook (7th Edition):

Hofmann, Jeffrey W. “The Role of Myc in Aging and Longevity in Mice.” 2014. Web. 16 Jan 2021.

Vancouver:

Hofmann JW. The Role of Myc in Aging and Longevity in Mice. [Internet] [Doctoral dissertation]. Brown University; 2014. [cited 2021 Jan 16]. Available from: https://repository.library.brown.edu/studio/item/bdr:386199/.

Council of Science Editors:

Hofmann JW. The Role of Myc in Aging and Longevity in Mice. [Doctoral Dissertation]. Brown University; 2014. Available from: https://repository.library.brown.edu/studio/item/bdr:386199/

21. Hagan, Nellwyn A. The Spatial and Temporal Control of Gene Expression in Cerebellum Development.

Degree: PhD, Neuroscience, 2012, Brown University

 The primary objective of this thesis is to spatially and temporally dissect the role of WNT1 in cerebellum (Cb) development. During embryogenesis, the Cb is… (more)

Subjects/Keywords: Development

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hagan, N. A. (2012). The Spatial and Temporal Control of Gene Expression in Cerebellum Development. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:297694/

Chicago Manual of Style (16th Edition):

Hagan, Nellwyn A. “The Spatial and Temporal Control of Gene Expression in Cerebellum Development.” 2012. Doctoral Dissertation, Brown University. Accessed January 16, 2021. https://repository.library.brown.edu/studio/item/bdr:297694/.

MLA Handbook (7th Edition):

Hagan, Nellwyn A. “The Spatial and Temporal Control of Gene Expression in Cerebellum Development.” 2012. Web. 16 Jan 2021.

Vancouver:

Hagan NA. The Spatial and Temporal Control of Gene Expression in Cerebellum Development. [Internet] [Doctoral dissertation]. Brown University; 2012. [cited 2021 Jan 16]. Available from: https://repository.library.brown.edu/studio/item/bdr:297694/.

Council of Science Editors:

Hagan NA. The Spatial and Temporal Control of Gene Expression in Cerebellum Development. [Doctoral Dissertation]. Brown University; 2012. Available from: https://repository.library.brown.edu/studio/item/bdr:297694/

22. Gyuris, Aron. Transcriptional regulation of Drosophila melanogaster courtship behavior by fruitless and dissatisfaction.

Degree: PhD, Molecular Biology, Cell Biology, and Biochemistry, 2014, Brown University

 Genetically determined, fixed action pattern behaviors offer a useful model for studying how developmental gene expression programs lay down a neuroanatomical architecture that underlies these… (more)

Subjects/Keywords: Courtship Behavior

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Gyuris, A. (2014). Transcriptional regulation of Drosophila melanogaster courtship behavior by fruitless and dissatisfaction. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:386201/

Chicago Manual of Style (16th Edition):

Gyuris, Aron. “Transcriptional regulation of Drosophila melanogaster courtship behavior by fruitless and dissatisfaction.” 2014. Doctoral Dissertation, Brown University. Accessed January 16, 2021. https://repository.library.brown.edu/studio/item/bdr:386201/.

MLA Handbook (7th Edition):

Gyuris, Aron. “Transcriptional regulation of Drosophila melanogaster courtship behavior by fruitless and dissatisfaction.” 2014. Web. 16 Jan 2021.

Vancouver:

Gyuris A. Transcriptional regulation of Drosophila melanogaster courtship behavior by fruitless and dissatisfaction. [Internet] [Doctoral dissertation]. Brown University; 2014. [cited 2021 Jan 16]. Available from: https://repository.library.brown.edu/studio/item/bdr:386201/.

Council of Science Editors:

Gyuris A. Transcriptional regulation of Drosophila melanogaster courtship behavior by fruitless and dissatisfaction. [Doctoral Dissertation]. Brown University; 2014. Available from: https://repository.library.brown.edu/studio/item/bdr:386201/

23. Santos Ahmed, Jeena M. The Effect of Transient Neonatal Goitrogen Exposure on Akt1-Dependent Testicular Development and Gene Expression in the C57/Bl6 Mouse.

Degree: PhD, Pathobiology, 2011, Brown University

 The Sertoli cell is the "support cell" of the testis. The number of Sertoli cells which populate the testis during peri-pubertal development dictate the number… (more)

Subjects/Keywords: Akt

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Santos Ahmed, J. M. (2011). The Effect of Transient Neonatal Goitrogen Exposure on Akt1-Dependent Testicular Development and Gene Expression in the C57/Bl6 Mouse. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:11350/

Chicago Manual of Style (16th Edition):

Santos Ahmed, Jeena M. “The Effect of Transient Neonatal Goitrogen Exposure on Akt1-Dependent Testicular Development and Gene Expression in the C57/Bl6 Mouse.” 2011. Doctoral Dissertation, Brown University. Accessed January 16, 2021. https://repository.library.brown.edu/studio/item/bdr:11350/.

MLA Handbook (7th Edition):

Santos Ahmed, Jeena M. “The Effect of Transient Neonatal Goitrogen Exposure on Akt1-Dependent Testicular Development and Gene Expression in the C57/Bl6 Mouse.” 2011. Web. 16 Jan 2021.

Vancouver:

Santos Ahmed JM. The Effect of Transient Neonatal Goitrogen Exposure on Akt1-Dependent Testicular Development and Gene Expression in the C57/Bl6 Mouse. [Internet] [Doctoral dissertation]. Brown University; 2011. [cited 2021 Jan 16]. Available from: https://repository.library.brown.edu/studio/item/bdr:11350/.

Council of Science Editors:

Santos Ahmed JM. The Effect of Transient Neonatal Goitrogen Exposure on Akt1-Dependent Testicular Development and Gene Expression in the C57/Bl6 Mouse. [Doctoral Dissertation]. Brown University; 2011. Available from: https://repository.library.brown.edu/studio/item/bdr:11350/

24. Zins, Stephen R. Human defensins and innate immune control of JC Polyomavirus infection.

Degree: PhD, Pathobiology, 2015, Brown University

 This dissertation attempted to elucidate the role of - and -defensins in JCPyV infection, determine a mechanism of action of HD5-mediated JCPyV neutralization, and to… (more)

Subjects/Keywords: JC Polyomavirus

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Zins, S. R. (2015). Human defensins and innate immune control of JC Polyomavirus infection. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:419472/

Chicago Manual of Style (16th Edition):

Zins, Stephen R. “Human defensins and innate immune control of JC Polyomavirus infection.” 2015. Doctoral Dissertation, Brown University. Accessed January 16, 2021. https://repository.library.brown.edu/studio/item/bdr:419472/.

MLA Handbook (7th Edition):

Zins, Stephen R. “Human defensins and innate immune control of JC Polyomavirus infection.” 2015. Web. 16 Jan 2021.

Vancouver:

Zins SR. Human defensins and innate immune control of JC Polyomavirus infection. [Internet] [Doctoral dissertation]. Brown University; 2015. [cited 2021 Jan 16]. Available from: https://repository.library.brown.edu/studio/item/bdr:419472/.

Council of Science Editors:

Zins SR. Human defensins and innate immune control of JC Polyomavirus infection. [Doctoral Dissertation]. Brown University; 2015. Available from: https://repository.library.brown.edu/studio/item/bdr:419472/

25. Brown, Stephen D. Genetic Approaches to Understand the Timing of Gene Expression and Lineage Allocation in the Mouse Auditory System.

Degree: PhD, Molecular Biology, Cell Biology, and Biochemistry, 2011, Brown University

 l to the function of any organ system is the proper specification and distribution of cell types during development. This is especially true for the… (more)

Subjects/Keywords: development

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Brown, S. D. (2011). Genetic Approaches to Understand the Timing of Gene Expression and Lineage Allocation in the Mouse Auditory System. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:11356/

Chicago Manual of Style (16th Edition):

Brown, Stephen D. “Genetic Approaches to Understand the Timing of Gene Expression and Lineage Allocation in the Mouse Auditory System.” 2011. Doctoral Dissertation, Brown University. Accessed January 16, 2021. https://repository.library.brown.edu/studio/item/bdr:11356/.

MLA Handbook (7th Edition):

Brown, Stephen D. “Genetic Approaches to Understand the Timing of Gene Expression and Lineage Allocation in the Mouse Auditory System.” 2011. Web. 16 Jan 2021.

Vancouver:

Brown SD. Genetic Approaches to Understand the Timing of Gene Expression and Lineage Allocation in the Mouse Auditory System. [Internet] [Doctoral dissertation]. Brown University; 2011. [cited 2021 Jan 16]. Available from: https://repository.library.brown.edu/studio/item/bdr:11356/.

Council of Science Editors:

Brown SD. Genetic Approaches to Understand the Timing of Gene Expression and Lineage Allocation in the Mouse Auditory System. [Doctoral Dissertation]. Brown University; 2011. Available from: https://repository.library.brown.edu/studio/item/bdr:11356/

26. Heger, Nicholas E. A Fetal Testis Xenograft Bioassay to Assess Human Susceptibility to Phthalate-Induced Endocrine Disruption.

Degree: PhD, Pathobiology, 2012, Brown University

 Recent increases in the incidence of congenital (hypospadias, cryptorchidism) and adult-onset (testis germ cell cancer, lowered sperm counts) diseases of the male reproductive tract are… (more)

Subjects/Keywords: phthalate

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Heger, N. E. (2012). A Fetal Testis Xenograft Bioassay to Assess Human Susceptibility to Phthalate-Induced Endocrine Disruption. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:297570/

Chicago Manual of Style (16th Edition):

Heger, Nicholas E. “A Fetal Testis Xenograft Bioassay to Assess Human Susceptibility to Phthalate-Induced Endocrine Disruption.” 2012. Doctoral Dissertation, Brown University. Accessed January 16, 2021. https://repository.library.brown.edu/studio/item/bdr:297570/.

MLA Handbook (7th Edition):

Heger, Nicholas E. “A Fetal Testis Xenograft Bioassay to Assess Human Susceptibility to Phthalate-Induced Endocrine Disruption.” 2012. Web. 16 Jan 2021.

Vancouver:

Heger NE. A Fetal Testis Xenograft Bioassay to Assess Human Susceptibility to Phthalate-Induced Endocrine Disruption. [Internet] [Doctoral dissertation]. Brown University; 2012. [cited 2021 Jan 16]. Available from: https://repository.library.brown.edu/studio/item/bdr:297570/.

Council of Science Editors:

Heger NE. A Fetal Testis Xenograft Bioassay to Assess Human Susceptibility to Phthalate-Induced Endocrine Disruption. [Doctoral Dissertation]. Brown University; 2012. Available from: https://repository.library.brown.edu/studio/item/bdr:297570/

27. Vantangoli, Marguerite May. Assessment of Morphologic and Molecular Effects of Estrogen Exposure Using MCF-7 3D Microtissues.

Degree: PhD, Pathobiology, 2016, Brown University

 Toxicity testing is undergoing a revolution, as the reliance on animal models has resulted in a large backlog of chemicals that have not been adequately… (more)

Subjects/Keywords: endocrine disruption

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Vantangoli, M. M. (2016). Assessment of Morphologic and Molecular Effects of Estrogen Exposure Using MCF-7 3D Microtissues. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:674246/

Chicago Manual of Style (16th Edition):

Vantangoli, Marguerite May. “Assessment of Morphologic and Molecular Effects of Estrogen Exposure Using MCF-7 3D Microtissues.” 2016. Doctoral Dissertation, Brown University. Accessed January 16, 2021. https://repository.library.brown.edu/studio/item/bdr:674246/.

MLA Handbook (7th Edition):

Vantangoli, Marguerite May. “Assessment of Morphologic and Molecular Effects of Estrogen Exposure Using MCF-7 3D Microtissues.” 2016. Web. 16 Jan 2021.

Vancouver:

Vantangoli MM. Assessment of Morphologic and Molecular Effects of Estrogen Exposure Using MCF-7 3D Microtissues. [Internet] [Doctoral dissertation]. Brown University; 2016. [cited 2021 Jan 16]. Available from: https://repository.library.brown.edu/studio/item/bdr:674246/.

Council of Science Editors:

Vantangoli MM. Assessment of Morphologic and Molecular Effects of Estrogen Exposure Using MCF-7 3D Microtissues. [Doctoral Dissertation]. Brown University; 2016. Available from: https://repository.library.brown.edu/studio/item/bdr:674246/

28. Volle, Catherine B. The Trouble with Triples:Elucidating the Behavior of Trinucleotide Repeats in Chromatin.

Degree: PhD, Molecular Biology, Cell Biology, and Biochemistry, 2014, Brown University

 Trinucleotide repeats (TNRs) occur throughout the genome and their expansion can affect varied cellular processes such as gene expression, mRNA processing, and protein folding. TNR… (more)

Subjects/Keywords: Nucleosome

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Volle, C. B. (2014). The Trouble with Triples:Elucidating the Behavior of Trinucleotide Repeats in Chromatin. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:386117/

Chicago Manual of Style (16th Edition):

Volle, Catherine B. “The Trouble with Triples:Elucidating the Behavior of Trinucleotide Repeats in Chromatin.” 2014. Doctoral Dissertation, Brown University. Accessed January 16, 2021. https://repository.library.brown.edu/studio/item/bdr:386117/.

MLA Handbook (7th Edition):

Volle, Catherine B. “The Trouble with Triples:Elucidating the Behavior of Trinucleotide Repeats in Chromatin.” 2014. Web. 16 Jan 2021.

Vancouver:

Volle CB. The Trouble with Triples:Elucidating the Behavior of Trinucleotide Repeats in Chromatin. [Internet] [Doctoral dissertation]. Brown University; 2014. [cited 2021 Jan 16]. Available from: https://repository.library.brown.edu/studio/item/bdr:386117/.

Council of Science Editors:

Volle CB. The Trouble with Triples:Elucidating the Behavior of Trinucleotide Repeats in Chromatin. [Doctoral Dissertation]. Brown University; 2014. Available from: https://repository.library.brown.edu/studio/item/bdr:386117/

29. Aldrich, Maryanna M. A BMP-dependent feedback loop regulates dpp expression by direct and indirect mechanisms in the Drosophila wing imaginal disc.

Degree: PhD, Molecular Biology, Cell Biology, and Biochemistry, 2012, Brown University

 Morphogen activity gradients assign positional information within fields of cells in a concentration-dependent manner. As transcriptional changes respond to signaling activity thresholds, cells must encounter… (more)

Subjects/Keywords: BMP signaling

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Aldrich, M. M. (2012). A BMP-dependent feedback loop regulates dpp expression by direct and indirect mechanisms in the Drosophila wing imaginal disc. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:297551/

Chicago Manual of Style (16th Edition):

Aldrich, Maryanna M. “A BMP-dependent feedback loop regulates dpp expression by direct and indirect mechanisms in the Drosophila wing imaginal disc.” 2012. Doctoral Dissertation, Brown University. Accessed January 16, 2021. https://repository.library.brown.edu/studio/item/bdr:297551/.

MLA Handbook (7th Edition):

Aldrich, Maryanna M. “A BMP-dependent feedback loop regulates dpp expression by direct and indirect mechanisms in the Drosophila wing imaginal disc.” 2012. Web. 16 Jan 2021.

Vancouver:

Aldrich MM. A BMP-dependent feedback loop regulates dpp expression by direct and indirect mechanisms in the Drosophila wing imaginal disc. [Internet] [Doctoral dissertation]. Brown University; 2012. [cited 2021 Jan 16]. Available from: https://repository.library.brown.edu/studio/item/bdr:297551/.

Council of Science Editors:

Aldrich MM. A BMP-dependent feedback loop regulates dpp expression by direct and indirect mechanisms in the Drosophila wing imaginal disc. [Doctoral Dissertation]. Brown University; 2012. Available from: https://repository.library.brown.edu/studio/item/bdr:297551/

30. Saunders, Ann Catherine E. The Role of p57kip2 in Placental Development and Disease.

Degree: PhD, Pathobiology, 2016, Brown University

 The placenta is the first complex mammalian organ to develop and is as site of gas and nutrient exchange between the mother and fetus. The… (more)

Subjects/Keywords: p57

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Saunders, A. C. E. (2016). The Role of p57kip2 in Placental Development and Disease. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:674132/

Chicago Manual of Style (16th Edition):

Saunders, Ann Catherine E. “The Role of p57kip2 in Placental Development and Disease.” 2016. Doctoral Dissertation, Brown University. Accessed January 16, 2021. https://repository.library.brown.edu/studio/item/bdr:674132/.

MLA Handbook (7th Edition):

Saunders, Ann Catherine E. “The Role of p57kip2 in Placental Development and Disease.” 2016. Web. 16 Jan 2021.

Vancouver:

Saunders ACE. The Role of p57kip2 in Placental Development and Disease. [Internet] [Doctoral dissertation]. Brown University; 2016. [cited 2021 Jan 16]. Available from: https://repository.library.brown.edu/studio/item/bdr:674132/.

Council of Science Editors:

Saunders ACE. The Role of p57kip2 in Placental Development and Disease. [Doctoral Dissertation]. Brown University; 2016. Available from: https://repository.library.brown.edu/studio/item/bdr:674132/

[1] [2]

.