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Beverly L. Davidson, PhD, University of Michigan

Affiliations: 
1999-2014 Internal Medicine University of Iowa, Iowa City, IA 
 2014- University of Pennsylvania, Philadelphia, PA, United States 
Area:
inherited genetic diseases
Website:
https://www.med.upenn.edu/apps/faculty/index.php/g275/p8762892
Google:
"Beverly L. Davidson"
Bio:

https://curealz.org/people/beverly-davidson
http://www.biomedexperts.com/Profile.bme/292624/Beverly_L_Davidson
https://medicine.umich.edu/dept/biochem/beverly-l-davidson-phd
http://www.springerlink.com/index/R503N38026722318.pdf

Mean distance: 10686.6
 
Cross-listing: GenetiTree - Cell & Gene Therapy Tree

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Parents

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William N. Kelley grad student 1988 University of Michigan (Cell & Gene Therapy Tree)
 (The Genetic Basis of Hypoxanthine Guanine Phosphoribosyltransferase Deficiency States in Humans)

Children

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Lane K. Law grad student 2003 University of Iowa
Gumei Liu grad student 2005 University of Iowa
Glen M. Borchert grad student 2007 University of Iowa (Cell Biology Tree)
Ryan L. Boudreau grad student 2008 University of Iowa
Sarah K. Fineberg grad student 2010 University of Iowa
Aislinn Williams grad student 2010 University of Iowa
Amy N. Dubinsky grad student 2011 University of Iowa
Megan K. Keiser grad student 2013 University of Iowa
Hayley S. McLoughlin grad student 2013 University of Iowa
Ryan M. Spengler grad student 2013 University of Iowa
Mark L Schultz grad student 2008-2013 University of Iowa (Cell & Gene Therapy Tree)
Pavitra S. Ramachandran grad student 2014 University of Iowa
Stephanie M Hughes post-doc (Cell & Gene Therapy Tree)
Jodi McBride post-doc
David Leib post-doc 2018- Penn
Scott Q. Harper post-doc 2002-2007 (Cell & Gene Therapy Tree)

Collaborators

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BETA: Related publications

Publications

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Gall-Duncan T, Luo J, Jurkovic CM, et al. (2023) Antagonistic roles of canonical and Alternative-RPA in disease-associated tandem CAG repeat instability. Cell
Fang L, Monteys AM, Dürr A, et al. (2023) Erratum: Haplotyping SNPs for allele-specific gene editing of the expanded huntingtin allele using long-read sequencing. Hgg Advances. 4: 100212
Ranum PT, Tecedor L, Keiser MS, et al. (2023) Cochlear transduction via cerebrospinal fluid delivery of AAV in non-human primates. Molecular Therapy : the Journal of the American Society of Gene Therapy
Fang L, Monteys AM, Dürr A, et al. (2022) Haplotyping SNPs for allele-specific gene editing of the expanded huntingtin allele using long-read sequencing. Hgg Advances. 4: 100146
Carrell EM, Keiser MS, Robbins AB, et al. (2022) Combined overexpression of ATXN1L and mutant ATXN1 knockdown by AAV rescue motor phenotypes and gene signatures in SCA1 mice. Molecular Therapy. Methods & Clinical Development. 25: 333-343
Keller CG, Shin Y, Monteys AM, et al. (2022) An orally available, brain penetrant, small molecule lowers huntingtin levels by enhancing pseudoexon inclusion. Nature Communications. 13: 1150
Leib D, Chen YH, Monteys AM, et al. (2022) Limited astrocyte-to-neuron conversion in the mouse brain using NeuroD1 overexpression. Molecular Therapy : the Journal of the American Society of Gene Therapy
Prezelski K, Keiser M, Stein JM, et al. (2021) Design and Validation of a Multi-Point Injection Technology for MR-Guided Convection Enhanced Delivery in the Brain. Frontiers in Medical Technology. 3: 725844
Keiser MS, Ranum PT, Yrigollen CM, et al. (2021) Toxicity after AAV delivery of RNAi expression constructs into nonhuman primate brain. Nature Medicine. 27: 1982-1989
Pluciennik A, Liu Y, Molotsky E, et al. (2020) Deubiquitinase USP7 contributes to the pathogenicity of spinal and bulbar muscular atrophy. The Journal of Clinical Investigation
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