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Electronic Theses & Dissertations
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Actin genes
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Allelomorphism
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Cell culture
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Deaf dogs
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Deafness in animals
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Dogs--Diseases--Genetic aspects
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Dogs--Genetics
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Gene mapping
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Human chromosome abnormalities
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Human genetics--Research
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Myosin
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Protein folding
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Exploring molecular mechanisms of human genetic diseases--two examples : autosomal dominant hearing loss (DFNA20/26) and autosomal recessive lysosomal storage disease, beta-mannosidosis
Zhu, Mei
Text (2007)
Part of
Electronic Theses & Dissertations
Hereditary deafness and mast cell tumors in dogs : sequence analysis of candidate genes from the melanocyte development pathway
Zemke, Daniel
Text (2003)
Part of
Electronic Theses & Dissertations
Molecular cloning of an unconventional myosin MYO15 and the identification of mutations of MYO15 responsible for human nonsyndromic deafness DFNB3
Wang, Aihui
Text (1999)
Part of
Electronic Theses & Dissertations
Mapping a new autosomal dominant hearing loss locus, DFNA20, ON 17Q25 and searching for the disease causing gene(s)
Wei, Sainan
Text (2002)
Part of
Electronic Theses & Dissertations
Mapping, mutation identification and expression study of DFNB3, a gene for human recessive deafnes [i.e. deafness]
Liang, Yong
Text (1999)
Part of
Electronic Theses & Dissertations
Functional analysis of cytoplasmic [gamma]-actin mutations causing non-syndromic, progressive autosomal dominant hearing loss
Korrapati, Soumya
Text (2009)
Part of
Electronic Theses & Dissertations
Investigating DFNA20 mutations in {OCLCbr#DE}-actin : studies in yeast, cell culture, and mouse
Drummond, Meghan Chapman
Text (2010)
Part of
Electronic Theses & Dissertations
Characterization of a DFNB1 deletion allele in a Michigan kindred of German descent
Wilch, Ellen Shields
Text (2010)
Part of
Electronic Theses & Dissertations
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