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

Dept: Molecular, Cellular, Developmental Biology and Genetics

You searched for subject:(Molecular Genetics). Showing records 1 – 30 of 40 total matches.

[1] [2]

Search Limiters

Last 2 Years | English Only

▼ Search Limiters


University of Minnesota

1. Hsu, Wei-Shan. Chromosome cohesion and condensation in Saccharomyces cerevisiae.

Degree: PhD, Molecular, Cellular, Developmental Biology and Genetics, 2011, University of Minnesota

 Sister chromatid cohesion and chromosome condensation are two essential cell cycle processes for maintaining genome stability. Pds1 is the only known regulator for maintaining cohesion… (more)

Subjects/Keywords: Molecular; Cellular; Developmental Biology and Genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hsu, W. (2011). Chromosome cohesion and condensation in Saccharomyces cerevisiae. (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/115898

Chicago Manual of Style (16th Edition):

Hsu, Wei-Shan. “Chromosome cohesion and condensation in Saccharomyces cerevisiae.” 2011. Doctoral Dissertation, University of Minnesota. Accessed July 14, 2020. http://purl.umn.edu/115898.

MLA Handbook (7th Edition):

Hsu, Wei-Shan. “Chromosome cohesion and condensation in Saccharomyces cerevisiae.” 2011. Web. 14 Jul 2020.

Vancouver:

Hsu W. Chromosome cohesion and condensation in Saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. University of Minnesota; 2011. [cited 2020 Jul 14]. Available from: http://purl.umn.edu/115898.

Council of Science Editors:

Hsu W. Chromosome cohesion and condensation in Saccharomyces cerevisiae. [Doctoral Dissertation]. University of Minnesota; 2011. Available from: http://purl.umn.edu/115898


University of Minnesota

2. Rahrmann, Eric Patrick. Identification of novel genes involved in prostate and Schwann cell malignancies utilizing a sleeping beauty transposon somatic cell mutagenesis screen.

Degree: PhD, Molecular, Cellular, Developmental Biology and Genetics, 2011, University of Minnesota

 The focus of this thesis was identification of new genes and genetic pathways altered in prostate cancer and malignant peripheral nerve sheath tumor formation utilizing… (more)

Subjects/Keywords: Cancer; Genetics; Mouse; Prostate; Schwann; Molecular, Cellular, Developmental Biology and Genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Rahrmann, E. P. (2011). Identification of novel genes involved in prostate and Schwann cell malignancies utilizing a sleeping beauty transposon somatic cell mutagenesis screen. (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/112753

Chicago Manual of Style (16th Edition):

Rahrmann, Eric Patrick. “Identification of novel genes involved in prostate and Schwann cell malignancies utilizing a sleeping beauty transposon somatic cell mutagenesis screen.” 2011. Doctoral Dissertation, University of Minnesota. Accessed July 14, 2020. http://purl.umn.edu/112753.

MLA Handbook (7th Edition):

Rahrmann, Eric Patrick. “Identification of novel genes involved in prostate and Schwann cell malignancies utilizing a sleeping beauty transposon somatic cell mutagenesis screen.” 2011. Web. 14 Jul 2020.

Vancouver:

Rahrmann EP. Identification of novel genes involved in prostate and Schwann cell malignancies utilizing a sleeping beauty transposon somatic cell mutagenesis screen. [Internet] [Doctoral dissertation]. University of Minnesota; 2011. [cited 2020 Jul 14]. Available from: http://purl.umn.edu/112753.

Council of Science Editors:

Rahrmann EP. Identification of novel genes involved in prostate and Schwann cell malignancies utilizing a sleeping beauty transposon somatic cell mutagenesis screen. [Doctoral Dissertation]. University of Minnesota; 2011. Available from: http://purl.umn.edu/112753


University of Minnesota

3. Dorr, Casey R. Compounds derived from birch trees that inhibit HIV-1 replication.

Degree: PhD, Molecular, Cellular, Developmental Biology and Genetics, 2011, University of Minnesota

 Human Immunodeficiency Virus type-1 (HIV-1) replication is introduced in Chapter 1 with an emphasis on the late phase of viral replication. Literature about the production… (more)

Subjects/Keywords: Bevirimat; Gag; Maturation; Retrovirus; Triterpene; Molecular, Cellular, Developmental Biology and Genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Dorr, C. R. (2011). Compounds derived from birch trees that inhibit HIV-1 replication. (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/104516

Chicago Manual of Style (16th Edition):

Dorr, Casey R. “Compounds derived from birch trees that inhibit HIV-1 replication.” 2011. Doctoral Dissertation, University of Minnesota. Accessed July 14, 2020. http://purl.umn.edu/104516.

MLA Handbook (7th Edition):

Dorr, Casey R. “Compounds derived from birch trees that inhibit HIV-1 replication.” 2011. Web. 14 Jul 2020.

Vancouver:

Dorr CR. Compounds derived from birch trees that inhibit HIV-1 replication. [Internet] [Doctoral dissertation]. University of Minnesota; 2011. [cited 2020 Jul 14]. Available from: http://purl.umn.edu/104516.

Council of Science Editors:

Dorr CR. Compounds derived from birch trees that inhibit HIV-1 replication. [Doctoral Dissertation]. University of Minnesota; 2011. Available from: http://purl.umn.edu/104516


University of Minnesota

4. Smith, Katherine Laura. Topoisomerase II: characterization of the Topoisomerase II checkpoint and the Classic top2-4 mutant allele.

Degree: PhD, Molecular, Cellular, Developmental Biology and Genetics, 2011, University of Minnesota

 Topoisomerase II (Topo II) is an essential, highly conserved enzyme that is a major component of mitotic chromosomes. Topo II functions as a homodimer to… (more)

Subjects/Keywords: Checkpoint; Topoisomerase II; Molecular, Cellular, Developmental Biology and Genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Smith, K. L. (2011). Topoisomerase II: characterization of the Topoisomerase II checkpoint and the Classic top2-4 mutant allele. (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/116341

Chicago Manual of Style (16th Edition):

Smith, Katherine Laura. “Topoisomerase II: characterization of the Topoisomerase II checkpoint and the Classic top2-4 mutant allele.” 2011. Doctoral Dissertation, University of Minnesota. Accessed July 14, 2020. http://purl.umn.edu/116341.

MLA Handbook (7th Edition):

Smith, Katherine Laura. “Topoisomerase II: characterization of the Topoisomerase II checkpoint and the Classic top2-4 mutant allele.” 2011. Web. 14 Jul 2020.

Vancouver:

Smith KL. Topoisomerase II: characterization of the Topoisomerase II checkpoint and the Classic top2-4 mutant allele. [Internet] [Doctoral dissertation]. University of Minnesota; 2011. [cited 2020 Jul 14]. Available from: http://purl.umn.edu/116341.

Council of Science Editors:

Smith KL. Topoisomerase II: characterization of the Topoisomerase II checkpoint and the Classic top2-4 mutant allele. [Doctoral Dissertation]. University of Minnesota; 2011. Available from: http://purl.umn.edu/116341


University of Minnesota

5. Joshi, Preeti Madhav. Histone methylation in polycomb gene silencing.

Degree: PhD, Molecular, Cellular, Developmental Biology and Genetics, 2010, University of Minnesota

 Polycomb (PcG) group proteins are chromatin-modifying factors that collaborate to repress gene expression during development. PcG proteins are crucial for silencing during animal embryogenesis, maintenance… (more)

Subjects/Keywords: Biochemistry; Chromatin Biology; Molecular Genetics; Molecular, Cellular, Developmental Biology and Genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Joshi, P. M. (2010). Histone methylation in polycomb gene silencing. (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/96716

Chicago Manual of Style (16th Edition):

Joshi, Preeti Madhav. “Histone methylation in polycomb gene silencing.” 2010. Doctoral Dissertation, University of Minnesota. Accessed July 14, 2020. http://purl.umn.edu/96716.

MLA Handbook (7th Edition):

Joshi, Preeti Madhav. “Histone methylation in polycomb gene silencing.” 2010. Web. 14 Jul 2020.

Vancouver:

Joshi PM. Histone methylation in polycomb gene silencing. [Internet] [Doctoral dissertation]. University of Minnesota; 2010. [cited 2020 Jul 14]. Available from: http://purl.umn.edu/96716.

Council of Science Editors:

Joshi PM. Histone methylation in polycomb gene silencing. [Doctoral Dissertation]. University of Minnesota; 2010. Available from: http://purl.umn.edu/96716


University of Minnesota

6. Akinci, Ersin. Reprogramming of different cell types into pancreatic beta cells by using transcription factor genes Pdx1, Ngn3 and MafA.

Degree: Molecular, Cellular, Developmental Biology and Genetics, 2012, University of Minnesota

 In this dissertation we studied the effect of the pancreatic transcription factor genes Pdx1, Ngn3 and MafA, all of which were cloned into single adenoviral… (more)

Subjects/Keywords: Beta cells; Insulin; MafA; Ngn3; Pancreas; Pdx1; Molecular, cellular, developmental biology and genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Akinci, E. (2012). Reprogramming of different cell types into pancreatic beta cells by using transcription factor genes Pdx1, Ngn3 and MafA. (Thesis). University of Minnesota. Retrieved from http://hdl.handle.net/11299/166923

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):

Akinci, Ersin. “Reprogramming of different cell types into pancreatic beta cells by using transcription factor genes Pdx1, Ngn3 and MafA.” 2012. Thesis, University of Minnesota. Accessed July 14, 2020. http://hdl.handle.net/11299/166923.

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

MLA Handbook (7th Edition):

Akinci, Ersin. “Reprogramming of different cell types into pancreatic beta cells by using transcription factor genes Pdx1, Ngn3 and MafA.” 2012. Web. 14 Jul 2020.

Vancouver:

Akinci E. Reprogramming of different cell types into pancreatic beta cells by using transcription factor genes Pdx1, Ngn3 and MafA. [Internet] [Thesis]. University of Minnesota; 2012. [cited 2020 Jul 14]. Available from: http://hdl.handle.net/11299/166923.

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

Council of Science Editors:

Akinci E. Reprogramming of different cell types into pancreatic beta cells by using transcription factor genes Pdx1, Ngn3 and MafA. [Thesis]. University of Minnesota; 2012. Available from: http://hdl.handle.net/11299/166923

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


University of Minnesota

7. Bade, Lindsey Kay. FGFR1-induced soluble factors promote mammary tumorigenesis and chemoresistance.

Degree: PhD, Molecular, Cellular, Developmental Biology and Genetics, 2013, University of Minnesota

 The fibroblast growth factor receptor (FGFR) family consists of four receptor tyrosine kinases that are known regulators of cellular processes such as proliferation, migration, survival,… (more)

Subjects/Keywords: AREG; Breast cancer; EGFR; FGFR1; STAT3; Molecular, cellular, developmental biology and genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Bade, L. K. (2013). FGFR1-induced soluble factors promote mammary tumorigenesis and chemoresistance. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/166927

Chicago Manual of Style (16th Edition):

Bade, Lindsey Kay. “FGFR1-induced soluble factors promote mammary tumorigenesis and chemoresistance.” 2013. Doctoral Dissertation, University of Minnesota. Accessed July 14, 2020. http://hdl.handle.net/11299/166927.

MLA Handbook (7th Edition):

Bade, Lindsey Kay. “FGFR1-induced soluble factors promote mammary tumorigenesis and chemoresistance.” 2013. Web. 14 Jul 2020.

Vancouver:

Bade LK. FGFR1-induced soluble factors promote mammary tumorigenesis and chemoresistance. [Internet] [Doctoral dissertation]. University of Minnesota; 2013. [cited 2020 Jul 14]. Available from: http://hdl.handle.net/11299/166927.

Council of Science Editors:

Bade LK. FGFR1-induced soluble factors promote mammary tumorigenesis and chemoresistance. [Doctoral Dissertation]. University of Minnesota; 2013. Available from: http://hdl.handle.net/11299/166927


University of Minnesota

8. Krueger, Katherine Andrea Dick. Molecular and genetic characterization of spinocerebellar ataxia type 5 (SCA5).

Degree: PhD, Molecular, Cellular, Developmental Biology and Genetics, 2008, University of Minnesota

 Spinocerebellar ataxia type 5 (SCA5) is a progressive neurodegenerative disorder, which primarily affects the cerebellum. The disease is inherited in an autosomal dominant pattern, with… (more)

Subjects/Keywords: Molecular; Cellular; Developmental Biology and Genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Krueger, K. A. D. (2008). Molecular and genetic characterization of spinocerebellar ataxia type 5 (SCA5). (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/56777

Chicago Manual of Style (16th Edition):

Krueger, Katherine Andrea Dick. “Molecular and genetic characterization of spinocerebellar ataxia type 5 (SCA5).” 2008. Doctoral Dissertation, University of Minnesota. Accessed July 14, 2020. http://purl.umn.edu/56777.

MLA Handbook (7th Edition):

Krueger, Katherine Andrea Dick. “Molecular and genetic characterization of spinocerebellar ataxia type 5 (SCA5).” 2008. Web. 14 Jul 2020.

Vancouver:

Krueger KAD. Molecular and genetic characterization of spinocerebellar ataxia type 5 (SCA5). [Internet] [Doctoral dissertation]. University of Minnesota; 2008. [cited 2020 Jul 14]. Available from: http://purl.umn.edu/56777.

Council of Science Editors:

Krueger KAD. Molecular and genetic characterization of spinocerebellar ataxia type 5 (SCA5). [Doctoral Dissertation]. University of Minnesota; 2008. Available from: http://purl.umn.edu/56777


University of Minnesota

9. Buckley, Shannon Mychel. Identification of microenvironment factors that regulate hematopoietic stem and progenitor cells.

Degree: PhD, Molecular, Cellular, Developmental Biology and Genetics, 2009, University of Minnesota

 The hematopoietic stem cell (HSC) maintains hematopoiesis throughout life. HSC are used to treat a number of hematopoietic disorders including leukemia and other hematopoietic malignancies,… (more)

Subjects/Keywords: Molecular; Cellular; Developmental Biology and Genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Buckley, S. M. (2009). Identification of microenvironment factors that regulate hematopoietic stem and progenitor cells. (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/99706

Chicago Manual of Style (16th Edition):

Buckley, Shannon Mychel. “Identification of microenvironment factors that regulate hematopoietic stem and progenitor cells.” 2009. Doctoral Dissertation, University of Minnesota. Accessed July 14, 2020. http://purl.umn.edu/99706.

MLA Handbook (7th Edition):

Buckley, Shannon Mychel. “Identification of microenvironment factors that regulate hematopoietic stem and progenitor cells.” 2009. Web. 14 Jul 2020.

Vancouver:

Buckley SM. Identification of microenvironment factors that regulate hematopoietic stem and progenitor cells. [Internet] [Doctoral dissertation]. University of Minnesota; 2009. [cited 2020 Jul 14]. Available from: http://purl.umn.edu/99706.

Council of Science Editors:

Buckley SM. Identification of microenvironment factors that regulate hematopoietic stem and progenitor cells. [Doctoral Dissertation]. University of Minnesota; 2009. Available from: http://purl.umn.edu/99706


University of Minnesota

10. Lane, Andrew Besançon. The extreme C-terminus of human Topoisomerase IΙ alpha defines a novel bi-modular DNA tether essential for the formation of mitotic chromosomes.

Degree: PhD, Molecular, Cellular, Developmental Biology and Genetics, 2012, University of Minnesota

 Topoisomerase II is the target of an important class of anti-cancer drugs, but tumor cells can become resistant by reducing the association of the enzyme… (more)

Subjects/Keywords: Chromosome; DNA; Histone; Localization; Topoisomerase II; Molecular, Cellular, Developmental Biology and Genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lane, A. B. (2012). The extreme C-terminus of human Topoisomerase IΙ alpha defines a novel bi-modular DNA tether essential for the formation of mitotic chromosomes. (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/129501

Chicago Manual of Style (16th Edition):

Lane, Andrew Besançon. “The extreme C-terminus of human Topoisomerase IΙ alpha defines a novel bi-modular DNA tether essential for the formation of mitotic chromosomes.” 2012. Doctoral Dissertation, University of Minnesota. Accessed July 14, 2020. http://purl.umn.edu/129501.

MLA Handbook (7th Edition):

Lane, Andrew Besançon. “The extreme C-terminus of human Topoisomerase IΙ alpha defines a novel bi-modular DNA tether essential for the formation of mitotic chromosomes.” 2012. Web. 14 Jul 2020.

Vancouver:

Lane AB. The extreme C-terminus of human Topoisomerase IΙ alpha defines a novel bi-modular DNA tether essential for the formation of mitotic chromosomes. [Internet] [Doctoral dissertation]. University of Minnesota; 2012. [cited 2020 Jul 14]. Available from: http://purl.umn.edu/129501.

Council of Science Editors:

Lane AB. The extreme C-terminus of human Topoisomerase IΙ alpha defines a novel bi-modular DNA tether essential for the formation of mitotic chromosomes. [Doctoral Dissertation]. University of Minnesota; 2012. Available from: http://purl.umn.edu/129501


University of Minnesota

11. Knutson, Todd Philip. Phosphorylated and SUMO-deficient progesterone receptors drive proliferative gene signatures during breast cancer progression.

Degree: PhD, Molecular, Cellular, Developmental Biology and Genetics, 2012, University of Minnesota

 Introduction: Progesterone receptors (PR) are emerging as important breast cancer drivers. Phosphorylation events common to breast cancer cells impact PR transcriptional activity, in part by… (more)

Subjects/Keywords: Breast cancer; Gene expression; Microarray; Phosphorylation; Progesterone receptor; Sumoylation; Molecular, Cellular, Developmental Biology and Genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Knutson, T. P. (2012). Phosphorylated and SUMO-deficient progesterone receptors drive proliferative gene signatures during breast cancer progression. (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/133773

Chicago Manual of Style (16th Edition):

Knutson, Todd Philip. “Phosphorylated and SUMO-deficient progesterone receptors drive proliferative gene signatures during breast cancer progression.” 2012. Doctoral Dissertation, University of Minnesota. Accessed July 14, 2020. http://purl.umn.edu/133773.

MLA Handbook (7th Edition):

Knutson, Todd Philip. “Phosphorylated and SUMO-deficient progesterone receptors drive proliferative gene signatures during breast cancer progression.” 2012. Web. 14 Jul 2020.

Vancouver:

Knutson TP. Phosphorylated and SUMO-deficient progesterone receptors drive proliferative gene signatures during breast cancer progression. [Internet] [Doctoral dissertation]. University of Minnesota; 2012. [cited 2020 Jul 14]. Available from: http://purl.umn.edu/133773.

Council of Science Editors:

Knutson TP. Phosphorylated and SUMO-deficient progesterone receptors drive proliferative gene signatures during breast cancer progression. [Doctoral Dissertation]. University of Minnesota; 2012. Available from: http://purl.umn.edu/133773


University of Minnesota

12. Pulver, Rebecca. A conservative mechanism of polarization drives hyphal growth in the opportunistic yeast pathogen Candida albicans.

Degree: PhD, Molecular, Cellular, Developmental Biology and Genetics, 2014, University of Minnesota

 In eukaryotes, different cell morphologies are generated by fine-tuning the spatiotemporal regulation of the polarized growth machinery. Studying hyphal growth in the multimorphic opportunistic yeast… (more)

Subjects/Keywords: Candida albicans; Cdc42,; Hyphae; Polarized growth; Rsr1; Molecular, cellular, developmental biology and genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Pulver, R. (2014). A conservative mechanism of polarization drives hyphal growth in the opportunistic yeast pathogen Candida albicans. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/167427

Chicago Manual of Style (16th Edition):

Pulver, Rebecca. “A conservative mechanism of polarization drives hyphal growth in the opportunistic yeast pathogen Candida albicans.” 2014. Doctoral Dissertation, University of Minnesota. Accessed July 14, 2020. http://hdl.handle.net/11299/167427.

MLA Handbook (7th Edition):

Pulver, Rebecca. “A conservative mechanism of polarization drives hyphal growth in the opportunistic yeast pathogen Candida albicans.” 2014. Web. 14 Jul 2020.

Vancouver:

Pulver R. A conservative mechanism of polarization drives hyphal growth in the opportunistic yeast pathogen Candida albicans. [Internet] [Doctoral dissertation]. University of Minnesota; 2014. [cited 2020 Jul 14]. Available from: http://hdl.handle.net/11299/167427.

Council of Science Editors:

Pulver R. A conservative mechanism of polarization drives hyphal growth in the opportunistic yeast pathogen Candida albicans. [Doctoral Dissertation]. University of Minnesota; 2014. Available from: http://hdl.handle.net/11299/167427


University of Minnesota

13. Belanto, Joseph John. A biochemical and molecular analysis of functional differences between dystrophin and utrophin.

Degree: PhD, Molecular, Cellular, Developmental Biology and Genetics, 2013, University of Minnesota

 The DMD gene encodes the protein dystrophin, a 427kD cytoplasmic protein responsible for linking the actin cytoskeleton to the extracellular matrix via the dystrophin-glycoprotein complex.… (more)

Subjects/Keywords: DMD; Duchenne muscular dystrophy; Dystrophin; mdx; Microtubules; Utrophin; Molecular, cellular, developmental biology and genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Belanto, J. J. (2013). A biochemical and molecular analysis of functional differences between dystrophin and utrophin. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/170101

Chicago Manual of Style (16th Edition):

Belanto, Joseph John. “A biochemical and molecular analysis of functional differences between dystrophin and utrophin.” 2013. Doctoral Dissertation, University of Minnesota. Accessed July 14, 2020. http://hdl.handle.net/11299/170101.

MLA Handbook (7th Edition):

Belanto, Joseph John. “A biochemical and molecular analysis of functional differences between dystrophin and utrophin.” 2013. Web. 14 Jul 2020.

Vancouver:

Belanto JJ. A biochemical and molecular analysis of functional differences between dystrophin and utrophin. [Internet] [Doctoral dissertation]. University of Minnesota; 2013. [cited 2020 Jul 14]. Available from: http://hdl.handle.net/11299/170101.

Council of Science Editors:

Belanto JJ. A biochemical and molecular analysis of functional differences between dystrophin and utrophin. [Doctoral Dissertation]. University of Minnesota; 2013. Available from: http://hdl.handle.net/11299/170101


University of Minnesota

14. McCulloch, Katherine Ann. Characterization of the function of the C. elegans heterochronic gene lin-42/per during larval development.

Degree: Molecular, Cellular, Developmental Biology and Genetics, 2013, University of Minnesota

 The heterochronic pathway of C. elegans ensures the appropriate timing of post-embryonic development. Mutations in heterochronic genes cause skipping or reiteration of larval programs, resulting… (more)

Subjects/Keywords: Heterochrony; let-7; lin-42; miRNA; Molecular, cellular, developmental biology and genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

McCulloch, K. A. (2013). Characterization of the function of the C. elegans heterochronic gene lin-42/per during larval development. (Thesis). University of Minnesota. Retrieved from http://hdl.handle.net/11299/171448

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):

McCulloch, Katherine Ann. “Characterization of the function of the C. elegans heterochronic gene lin-42/per during larval development.” 2013. Thesis, University of Minnesota. Accessed July 14, 2020. http://hdl.handle.net/11299/171448.

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

MLA Handbook (7th Edition):

McCulloch, Katherine Ann. “Characterization of the function of the C. elegans heterochronic gene lin-42/per during larval development.” 2013. Web. 14 Jul 2020.

Vancouver:

McCulloch KA. Characterization of the function of the C. elegans heterochronic gene lin-42/per during larval development. [Internet] [Thesis]. University of Minnesota; 2013. [cited 2020 Jul 14]. Available from: http://hdl.handle.net/11299/171448.

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

Council of Science Editors:

McCulloch KA. Characterization of the function of the C. elegans heterochronic gene lin-42/per during larval development. [Thesis]. University of Minnesota; 2013. Available from: http://hdl.handle.net/11299/171448

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


University of Minnesota

15. Talsness, Dana. Biophysical, cellular, and animal models of dystrophin missense mutations.

Degree: PhD, Molecular, Cellular, Developmental Biology and Genetics, 2014, University of Minnesota

 The 427kDa protein dystrophin is expressed in skeletal muscle where it localizes to the costamere and physically links the interior of muscle fibers to the… (more)

Subjects/Keywords: DMD; Duchenne; Dystrophin; Missense mutation; Protein misfolding; Molecular, cellular, developmental biology and genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Talsness, D. (2014). Biophysical, cellular, and animal models of dystrophin missense mutations. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/171764

Chicago Manual of Style (16th Edition):

Talsness, Dana. “Biophysical, cellular, and animal models of dystrophin missense mutations.” 2014. Doctoral Dissertation, University of Minnesota. Accessed July 14, 2020. http://hdl.handle.net/11299/171764.

MLA Handbook (7th Edition):

Talsness, Dana. “Biophysical, cellular, and animal models of dystrophin missense mutations.” 2014. Web. 14 Jul 2020.

Vancouver:

Talsness D. Biophysical, cellular, and animal models of dystrophin missense mutations. [Internet] [Doctoral dissertation]. University of Minnesota; 2014. [cited 2020 Jul 14]. Available from: http://hdl.handle.net/11299/171764.

Council of Science Editors:

Talsness D. Biophysical, cellular, and animal models of dystrophin missense mutations. [Doctoral Dissertation]. University of Minnesota; 2014. Available from: http://hdl.handle.net/11299/171764


University of Minnesota

16. LeClere, Andrea Ruth. Minisatellites in meiosis: crossover regulation and stability of repetitive DNA.

Degree: PhD, Molecular, Cellular, Developmental Biology and Genetics, 2012, University of Minnesota

 The minisatellite associated with the human HRAS1 proto-oncogene has an enhancer effect on HRAS1 expression. Rare minisatellite alleles have stronger enhancer activity and are frequently… (more)

Subjects/Keywords: Crossovers; Large loop repair; Meiosis; Minisatellite; Recombination; Molecular, Cellular, Developmental Biology and Genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

LeClere, A. R. (2012). Minisatellites in meiosis: crossover regulation and stability of repetitive DNA. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/126297

Chicago Manual of Style (16th Edition):

LeClere, Andrea Ruth. “Minisatellites in meiosis: crossover regulation and stability of repetitive DNA.” 2012. Doctoral Dissertation, University of Minnesota. Accessed July 14, 2020. http://hdl.handle.net/11299/126297.

MLA Handbook (7th Edition):

LeClere, Andrea Ruth. “Minisatellites in meiosis: crossover regulation and stability of repetitive DNA.” 2012. Web. 14 Jul 2020.

Vancouver:

LeClere AR. Minisatellites in meiosis: crossover regulation and stability of repetitive DNA. [Internet] [Doctoral dissertation]. University of Minnesota; 2012. [cited 2020 Jul 14]. Available from: http://hdl.handle.net/11299/126297.

Council of Science Editors:

LeClere AR. Minisatellites in meiosis: crossover regulation and stability of repetitive DNA. [Doctoral Dissertation]. University of Minnesota; 2012. Available from: http://hdl.handle.net/11299/126297


University of Minnesota

17. Hamline, Michelle Yvonne. The BCL6 transcriptional corepressor (BCOR) is required for multiple aspects of murine embryonic development.

Degree: PhD, Molecular, Cellular, Developmental Biology and Genetics, 2011, University of Minnesota

 The BCL6 transcriptional corepressor (BCOR) is mutated in the human multisystemic developmental disorder Oculofaciocardiodental syndrome (OFCD). The aim of this thesis is to understand the… (more)

Subjects/Keywords: BCOR; Cardiovascular development; Craniofacial development; Oculofaciocardiodental syndrome; OFCD; Transcriptional repression; Molecular, Cellular, Developmental Biology and Genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hamline, M. Y. (2011). The BCL6 transcriptional corepressor (BCOR) is required for multiple aspects of murine embryonic development. (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/107820

Chicago Manual of Style (16th Edition):

Hamline, Michelle Yvonne. “The BCL6 transcriptional corepressor (BCOR) is required for multiple aspects of murine embryonic development.” 2011. Doctoral Dissertation, University of Minnesota. Accessed July 14, 2020. http://purl.umn.edu/107820.

MLA Handbook (7th Edition):

Hamline, Michelle Yvonne. “The BCL6 transcriptional corepressor (BCOR) is required for multiple aspects of murine embryonic development.” 2011. Web. 14 Jul 2020.

Vancouver:

Hamline MY. The BCL6 transcriptional corepressor (BCOR) is required for multiple aspects of murine embryonic development. [Internet] [Doctoral dissertation]. University of Minnesota; 2011. [cited 2020 Jul 14]. Available from: http://purl.umn.edu/107820.

Council of Science Editors:

Hamline MY. The BCL6 transcriptional corepressor (BCOR) is required for multiple aspects of murine embryonic development. [Doctoral Dissertation]. University of Minnesota; 2011. Available from: http://purl.umn.edu/107820

18. Kim, Dong-Hwan. Investigation on the mechanistic roles of Tom1 and Dia2 in DNA replication and cell cycle.

Degree: PhD, Molecular, Cellular, Developmental Biology and Genetics, 2012, University of Minnesota

 As cells duplicate and divide, the inheritance of accurate genetic information is critical to maintaining cell viability and preventing the generation of cancer-causing mutations. Thus,… (more)

Subjects/Keywords: Molecular; cellular; deve biology and genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Kim, D. (2012). Investigation on the mechanistic roles of Tom1 and Dia2 in DNA replication and cell cycle. (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/142733

Chicago Manual of Style (16th Edition):

Kim, Dong-Hwan. “Investigation on the mechanistic roles of Tom1 and Dia2 in DNA replication and cell cycle.” 2012. Doctoral Dissertation, University of Minnesota. Accessed July 14, 2020. http://purl.umn.edu/142733.

MLA Handbook (7th Edition):

Kim, Dong-Hwan. “Investigation on the mechanistic roles of Tom1 and Dia2 in DNA replication and cell cycle.” 2012. Web. 14 Jul 2020.

Vancouver:

Kim D. Investigation on the mechanistic roles of Tom1 and Dia2 in DNA replication and cell cycle. [Internet] [Doctoral dissertation]. University of Minnesota; 2012. [cited 2020 Jul 14]. Available from: http://purl.umn.edu/142733.

Council of Science Editors:

Kim D. Investigation on the mechanistic roles of Tom1 and Dia2 in DNA replication and cell cycle. [Doctoral Dissertation]. University of Minnesota; 2012. Available from: http://purl.umn.edu/142733

19. Fong, Chi Meng. Dia2 mediates Mrc1 degradation to promote checkpoint recovery from DNA damage in Saccharomyces cerevisiae.

Degree: PhD, Molecular, Cellular, Developmental Biology and Genetics, 2012, University of Minnesota

 Cell cycle progression is monitored by checkpoint pathways that pause the cell cycle when stress arises to threaten the integrity of the genome. Although activation… (more)

Subjects/Keywords: Molecular; Cellular; Developmental Biology and Genetics

…study because 1) genetic, cellular, and molecular biology tools are well developed for… 

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Fong, C. M. (2012). Dia2 mediates Mrc1 degradation to promote checkpoint recovery from DNA damage in Saccharomyces cerevisiae. (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/136871

Chicago Manual of Style (16th Edition):

Fong, Chi Meng. “Dia2 mediates Mrc1 degradation to promote checkpoint recovery from DNA damage in Saccharomyces cerevisiae.” 2012. Doctoral Dissertation, University of Minnesota. Accessed July 14, 2020. http://purl.umn.edu/136871.

MLA Handbook (7th Edition):

Fong, Chi Meng. “Dia2 mediates Mrc1 degradation to promote checkpoint recovery from DNA damage in Saccharomyces cerevisiae.” 2012. Web. 14 Jul 2020.

Vancouver:

Fong CM. Dia2 mediates Mrc1 degradation to promote checkpoint recovery from DNA damage in Saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. University of Minnesota; 2012. [cited 2020 Jul 14]. Available from: http://purl.umn.edu/136871.

Council of Science Editors:

Fong CM. Dia2 mediates Mrc1 degradation to promote checkpoint recovery from DNA damage in Saccharomyces cerevisiae. [Doctoral Dissertation]. University of Minnesota; 2012. Available from: http://purl.umn.edu/136871


University of Minnesota

20. Tseng, Yuen-Yi. Adjacent long non-coding RNA PVT1 and MYC co-operate in breast cancer with gain of 8q24.

Degree: PhD, Molecular, Cellular, Developmental Biology and Genetics, 2013, University of Minnesota

 Copy number gain of 8q24 is a common structural abnormality in human cancers. Although MYC is usually assumed to be responsible for 8q24 gain cancer,… (more)

Subjects/Keywords: 8q24; Breast cancer; Copy number gain; Mouse model; MYC; PVT1; Molecular, cellular, developmental biology and genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Tseng, Y. (2013). Adjacent long non-coding RNA PVT1 and MYC co-operate in breast cancer with gain of 8q24. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/167655

Chicago Manual of Style (16th Edition):

Tseng, Yuen-Yi. “Adjacent long non-coding RNA PVT1 and MYC co-operate in breast cancer with gain of 8q24.” 2013. Doctoral Dissertation, University of Minnesota. Accessed July 14, 2020. http://hdl.handle.net/11299/167655.

MLA Handbook (7th Edition):

Tseng, Yuen-Yi. “Adjacent long non-coding RNA PVT1 and MYC co-operate in breast cancer with gain of 8q24.” 2013. Web. 14 Jul 2020.

Vancouver:

Tseng Y. Adjacent long non-coding RNA PVT1 and MYC co-operate in breast cancer with gain of 8q24. [Internet] [Doctoral dissertation]. University of Minnesota; 2013. [cited 2020 Jul 14]. Available from: http://hdl.handle.net/11299/167655.

Council of Science Editors:

Tseng Y. Adjacent long non-coding RNA PVT1 and MYC co-operate in breast cancer with gain of 8q24. [Doctoral Dissertation]. University of Minnesota; 2013. Available from: http://hdl.handle.net/11299/167655


University of Minnesota

21. Kretzschmar, Daniel Alan. Purification of bacterially-expressed chick NSD3-SET that is active in an in vitro methyltransferase assay.

Degree: MS, Molecular, Cellular, Developmental Biology and Genetics, 2014, University of Minnesota

 The lysine methyltransferase NSD3, which belongs to a family of histone H3 lysine 36 methyltransferases that are conserved among vertebrates and overexpressed in many cancers,… (more)

Subjects/Keywords: Lysine methyltransferase; Neural crest cell migration; NSD3; Purification; Vertebrate; whsc1l1; Molecular, cellular, developmental biology and genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Kretzschmar, D. A. (2014). Purification of bacterially-expressed chick NSD3-SET that is active in an in vitro methyltransferase assay. (Masters Thesis). University of Minnesota. Retrieved from http://hdl.handle.net/11299/170656

Chicago Manual of Style (16th Edition):

Kretzschmar, Daniel Alan. “Purification of bacterially-expressed chick NSD3-SET that is active in an in vitro methyltransferase assay.” 2014. Masters Thesis, University of Minnesota. Accessed July 14, 2020. http://hdl.handle.net/11299/170656.

MLA Handbook (7th Edition):

Kretzschmar, Daniel Alan. “Purification of bacterially-expressed chick NSD3-SET that is active in an in vitro methyltransferase assay.” 2014. Web. 14 Jul 2020.

Vancouver:

Kretzschmar DA. Purification of bacterially-expressed chick NSD3-SET that is active in an in vitro methyltransferase assay. [Internet] [Masters thesis]. University of Minnesota; 2014. [cited 2020 Jul 14]. Available from: http://hdl.handle.net/11299/170656.

Council of Science Editors:

Kretzschmar DA. Purification of bacterially-expressed chick NSD3-SET that is active in an in vitro methyltransferase assay. [Masters Thesis]. University of Minnesota; 2014. Available from: http://hdl.handle.net/11299/170656


University of Minnesota

22. Webber, Beau. Identification of novel signatures of murine definitive hematopoiesis.

Degree: PhD, Molecular, Cellular, Developmental Biology and Genetics, 2014, University of Minnesota

 Pluripotent stem cells (PSC) are a tantalizing prospect for a renewable source of patient-specific hematopoietic stem cells (HSC), however efforts to obtain PSC derived HSC… (more)

Subjects/Keywords: DNA methylation; Hematopoiesis; Hematopoietic stem cell; Pluripotent stem cell; Promoter; Runx1; Molecular, cellular, developmental biology and genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Webber, B. (2014). Identification of novel signatures of murine definitive hematopoiesis. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/172078

Chicago Manual of Style (16th Edition):

Webber, Beau. “Identification of novel signatures of murine definitive hematopoiesis.” 2014. Doctoral Dissertation, University of Minnesota. Accessed July 14, 2020. http://hdl.handle.net/11299/172078.

MLA Handbook (7th Edition):

Webber, Beau. “Identification of novel signatures of murine definitive hematopoiesis.” 2014. Web. 14 Jul 2020.

Vancouver:

Webber B. Identification of novel signatures of murine definitive hematopoiesis. [Internet] [Doctoral dissertation]. University of Minnesota; 2014. [cited 2020 Jul 14]. Available from: http://hdl.handle.net/11299/172078.

Council of Science Editors:

Webber B. Identification of novel signatures of murine definitive hematopoiesis. [Doctoral Dissertation]. University of Minnesota; 2014. Available from: http://hdl.handle.net/11299/172078


University of Minnesota

23. Goraksha-Hicks, Pankuri. Identification and characterization of novel positive regulators of the Target of Rapamycin (TOR) pathway in Drosophila melanogaster.

Degree: PhD, Molecular, Cellular, Developmental Biology and Genetics, 2008, University of Minnesota

 Target of Rapamycin (TOR) is an evolutionary conserved pathway in eukaryotes for growth and proliferation. TOR pathway plays an important role for growth homeostasis by… (more)

Subjects/Keywords: Growth; Rag GTPases; Screen; TOR; Molecular, Cellular, Developmental Biology and Genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Goraksha-Hicks, P. (2008). Identification and characterization of novel positive regulators of the Target of Rapamycin (TOR) pathway in Drosophila melanogaster. (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/47026

Chicago Manual of Style (16th Edition):

Goraksha-Hicks, Pankuri. “Identification and characterization of novel positive regulators of the Target of Rapamycin (TOR) pathway in Drosophila melanogaster.” 2008. Doctoral Dissertation, University of Minnesota. Accessed July 14, 2020. http://purl.umn.edu/47026.

MLA Handbook (7th Edition):

Goraksha-Hicks, Pankuri. “Identification and characterization of novel positive regulators of the Target of Rapamycin (TOR) pathway in Drosophila melanogaster.” 2008. Web. 14 Jul 2020.

Vancouver:

Goraksha-Hicks P. Identification and characterization of novel positive regulators of the Target of Rapamycin (TOR) pathway in Drosophila melanogaster. [Internet] [Doctoral dissertation]. University of Minnesota; 2008. [cited 2020 Jul 14]. Available from: http://purl.umn.edu/47026.

Council of Science Editors:

Goraksha-Hicks P. Identification and characterization of novel positive regulators of the Target of Rapamycin (TOR) pathway in Drosophila melanogaster. [Doctoral Dissertation]. University of Minnesota; 2008. Available from: http://purl.umn.edu/47026


University of Minnesota

24. Jensen, Philip Anthony. The activin ligand dawdle links diet and metabolism via receptor isoform-specific signaling in Drosophila.

Degree: PhD, Molecular, Cellular, Developmental Biology and Genetics, 2009, University of Minnesota

Abstract not available.

Subjects/Keywords: Activin; Diet; Drosophila; Insulin; Isoform; Metabolism; Molecular, Cellular, Developmental Biology and Genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Jensen, P. A. (2009). The activin ligand dawdle links diet and metabolism via receptor isoform-specific signaling in Drosophila. (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/53650

Chicago Manual of Style (16th Edition):

Jensen, Philip Anthony. “The activin ligand dawdle links diet and metabolism via receptor isoform-specific signaling in Drosophila.” 2009. Doctoral Dissertation, University of Minnesota. Accessed July 14, 2020. http://purl.umn.edu/53650.

MLA Handbook (7th Edition):

Jensen, Philip Anthony. “The activin ligand dawdle links diet and metabolism via receptor isoform-specific signaling in Drosophila.” 2009. Web. 14 Jul 2020.

Vancouver:

Jensen PA. The activin ligand dawdle links diet and metabolism via receptor isoform-specific signaling in Drosophila. [Internet] [Doctoral dissertation]. University of Minnesota; 2009. [cited 2020 Jul 14]. Available from: http://purl.umn.edu/53650.

Council of Science Editors:

Jensen PA. The activin ligand dawdle links diet and metabolism via receptor isoform-specific signaling in Drosophila. [Doctoral Dissertation]. University of Minnesota; 2009. Available from: http://purl.umn.edu/53650


University of Minnesota

25. Breshears, Laura Marie. An unconventional myosin is necessary for chemotaxis in Dictyostellium discoideum.

Degree: PhD, Molecular, Cellular, Developmental Biology and Genetics, 2009, University of Minnesota

 Directed cell migration (chemotaxis) is a fundamental biological process necessary for embryonic development, wound healing, and proper function of the immune system. Chemotaxis also plays… (more)

Subjects/Keywords: Actin; Chemotaxis; Cytoskeleton; Development; Dictyostelium; Myosin; Molecular, Cellular, Developmental Biology and Genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Breshears, L. M. (2009). An unconventional myosin is necessary for chemotaxis in Dictyostellium discoideum. (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/54107

Chicago Manual of Style (16th Edition):

Breshears, Laura Marie. “An unconventional myosin is necessary for chemotaxis in Dictyostellium discoideum.” 2009. Doctoral Dissertation, University of Minnesota. Accessed July 14, 2020. http://purl.umn.edu/54107.

MLA Handbook (7th Edition):

Breshears, Laura Marie. “An unconventional myosin is necessary for chemotaxis in Dictyostellium discoideum.” 2009. Web. 14 Jul 2020.

Vancouver:

Breshears LM. An unconventional myosin is necessary for chemotaxis in Dictyostellium discoideum. [Internet] [Doctoral dissertation]. University of Minnesota; 2009. [cited 2020 Jul 14]. Available from: http://purl.umn.edu/54107.

Council of Science Editors:

Breshears LM. An unconventional myosin is necessary for chemotaxis in Dictyostellium discoideum. [Doctoral Dissertation]. University of Minnesota; 2009. Available from: http://purl.umn.edu/54107


University of Minnesota

26. Score, Paul Rodrick. Characterization of the Sleeping Beauty transposon system for gene therapy applications.

Degree: PhD, Molecular, Cellular, Developmental Biology and Genetics, 2008, University of Minnesota

 Science and medicine are merging in development of gene therapy techniques that will likely become a recognized method for the treatment of human disease within… (more)

Subjects/Keywords: Gene therapy; Sleeping Beauty transposon; Molecular, Cellular, Developmental Biology and Genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Score, P. R. (2008). Characterization of the Sleeping Beauty transposon system for gene therapy applications. (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/91493

Chicago Manual of Style (16th Edition):

Score, Paul Rodrick. “Characterization of the Sleeping Beauty transposon system for gene therapy applications.” 2008. Doctoral Dissertation, University of Minnesota. Accessed July 14, 2020. http://purl.umn.edu/91493.

MLA Handbook (7th Edition):

Score, Paul Rodrick. “Characterization of the Sleeping Beauty transposon system for gene therapy applications.” 2008. Web. 14 Jul 2020.

Vancouver:

Score PR. Characterization of the Sleeping Beauty transposon system for gene therapy applications. [Internet] [Doctoral dissertation]. University of Minnesota; 2008. [cited 2020 Jul 14]. Available from: http://purl.umn.edu/91493.

Council of Science Editors:

Score PR. Characterization of the Sleeping Beauty transposon system for gene therapy applications. [Doctoral Dissertation]. University of Minnesota; 2008. Available from: http://purl.umn.edu/91493


University of Minnesota

27. Offer, Steven. Variations in multiple genes associate with CVID and IgAD.

Degree: PhD, Molecular, Cellular, Developmental Biology and Genetics, 2009, University of Minnesota

 A diverse antibody repertoire is paramount to an effective adaptive immune response in higher eukaryotes. This diversity is generated through the orchestrated introduction of somatic… (more)

Subjects/Keywords: Common variable immunodeficiency; CVID; IgAD; IgA deficiency; Molecular, Cellular, Developmental Biology and Genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Offer, S. (2009). Variations in multiple genes associate with CVID and IgAD. (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/98994

Chicago Manual of Style (16th Edition):

Offer, Steven. “Variations in multiple genes associate with CVID and IgAD.” 2009. Doctoral Dissertation, University of Minnesota. Accessed July 14, 2020. http://purl.umn.edu/98994.

MLA Handbook (7th Edition):

Offer, Steven. “Variations in multiple genes associate with CVID and IgAD.” 2009. Web. 14 Jul 2020.

Vancouver:

Offer S. Variations in multiple genes associate with CVID and IgAD. [Internet] [Doctoral dissertation]. University of Minnesota; 2009. [cited 2020 Jul 14]. Available from: http://purl.umn.edu/98994.

Council of Science Editors:

Offer S. Variations in multiple genes associate with CVID and IgAD. [Doctoral Dissertation]. University of Minnesota; 2009. Available from: http://purl.umn.edu/98994


University of Minnesota

28. Armbrust, Karen Rose. Murine models of spinocerebellar ataxia type 5.

Degree: PhD, Molecular, Cellular, Developmental Biology and Genetics, 2009, University of Minnesota

 Spinocerebellar ataxia type 5 (SCA5) is a slowly progressive neurodegenerative disease of the cerebellum caused by mutations in the SPTBN2 gene, which encodes the protein… (more)

Subjects/Keywords: Ataxia; EAAT4; mGluR1; Mouse; SCA; Spectrin; Molecular, Cellular, Developmental Biology and Genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Armbrust, K. R. (2009). Murine models of spinocerebellar ataxia type 5. (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/109346

Chicago Manual of Style (16th Edition):

Armbrust, Karen Rose. “Murine models of spinocerebellar ataxia type 5.” 2009. Doctoral Dissertation, University of Minnesota. Accessed July 14, 2020. http://purl.umn.edu/109346.

MLA Handbook (7th Edition):

Armbrust, Karen Rose. “Murine models of spinocerebellar ataxia type 5.” 2009. Web. 14 Jul 2020.

Vancouver:

Armbrust KR. Murine models of spinocerebellar ataxia type 5. [Internet] [Doctoral dissertation]. University of Minnesota; 2009. [cited 2020 Jul 14]. Available from: http://purl.umn.edu/109346.

Council of Science Editors:

Armbrust KR. Murine models of spinocerebellar ataxia type 5. [Doctoral Dissertation]. University of Minnesota; 2009. Available from: http://purl.umn.edu/109346


University of Minnesota

29. Wamstad, Joseph Alan. The role of the transcriptional corepressor Bcor in embryonic stem cells and mouse development.

Degree: Molecular, Cellular, Developmental Biology and Genetics, 2009, University of Minnesota

 Mutations in the transcriptional corepressor BCOR results in X-linked MCOPS2 (microphthalmia syndromic 2) disorders, including Oculofaciocardiodental syndrome (OFCD) and MAA2-associated Lenz microphthalmia. BCOR regulates gene… (more)

Subjects/Keywords: Bcor; Chromatin; Development; Epigenetics; Fbxl10; Ring1b; Molecular, Cellular, Developmental Biology and Genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Wamstad, J. A. (2009). The role of the transcriptional corepressor Bcor in embryonic stem cells and mouse development. (Thesis). University of Minnesota. Retrieved from http://purl.umn.edu/109543

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):

Wamstad, Joseph Alan. “The role of the transcriptional corepressor Bcor in embryonic stem cells and mouse development.” 2009. Thesis, University of Minnesota. Accessed July 14, 2020. http://purl.umn.edu/109543.

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

MLA Handbook (7th Edition):

Wamstad, Joseph Alan. “The role of the transcriptional corepressor Bcor in embryonic stem cells and mouse development.” 2009. Web. 14 Jul 2020.

Vancouver:

Wamstad JA. The role of the transcriptional corepressor Bcor in embryonic stem cells and mouse development. [Internet] [Thesis]. University of Minnesota; 2009. [cited 2020 Jul 14]. Available from: http://purl.umn.edu/109543.

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

Council of Science Editors:

Wamstad JA. The role of the transcriptional corepressor Bcor in embryonic stem cells and mouse development. [Thesis]. University of Minnesota; 2009. Available from: http://purl.umn.edu/109543

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

30. Moriarity, Branden Scott. Cancer gene discovery using somatic transposon mutagenesis in the mouse and systems for validation of identified candidate cancer genes and pathways.

Degree: PhD, Molecular, Cellular, Developmental Biology and Genetics, 2012, University of Minnesota

 The conditional Sleeping Beauty (SB) transposon mutagenesis system has proven to be a successful method for cancer gene identification in solid tumors. Using tissue specific… (more)

Subjects/Keywords: Cancer; Osteosarcoma; Sleeping Beauty; Molecular, Cellular, Developmental Biology and Genetics

…Department of Genetics, Cell Biology and Development, and Pediatrics, Center for Genome 2 3… 

Page 1 Page 2 Page 3 Page 4 Page 5 Page 6 Page 7

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Moriarity, B. S. (2012). Cancer gene discovery using somatic transposon mutagenesis in the mouse and systems for validation of identified candidate cancer genes and pathways. (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/134503

Chicago Manual of Style (16th Edition):

Moriarity, Branden Scott. “Cancer gene discovery using somatic transposon mutagenesis in the mouse and systems for validation of identified candidate cancer genes and pathways.” 2012. Doctoral Dissertation, University of Minnesota. Accessed July 14, 2020. http://purl.umn.edu/134503.

MLA Handbook (7th Edition):

Moriarity, Branden Scott. “Cancer gene discovery using somatic transposon mutagenesis in the mouse and systems for validation of identified candidate cancer genes and pathways.” 2012. Web. 14 Jul 2020.

Vancouver:

Moriarity BS. Cancer gene discovery using somatic transposon mutagenesis in the mouse and systems for validation of identified candidate cancer genes and pathways. [Internet] [Doctoral dissertation]. University of Minnesota; 2012. [cited 2020 Jul 14]. Available from: http://purl.umn.edu/134503.

Council of Science Editors:

Moriarity BS. Cancer gene discovery using somatic transposon mutagenesis in the mouse and systems for validation of identified candidate cancer genes and pathways. [Doctoral Dissertation]. University of Minnesota; 2012. Available from: http://purl.umn.edu/134503

[1] [2]

.