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Author Details

Kathleen M Scott
University of Michigan ann arbor
1995
18
11
Dexter Pratt (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
35337019A BioID-Derived Proximity Interactome for SARS-CoV-2 Proteins.Viruses2022
35712768The Nucleus Bypasses Obstacles by Deforming Like a Drop with Surface Tension Mediated by Lamin A/C.Adv Sci (Weinh)2022
34580671A BioID-derived proximity interactome for SARS-CoV-2 proteins.bioRxiv2021
32344865Comparative Application of BioID and TurboID for Protein-Proximity Biotinylation.Cells2020
24002674Genome-wide association study and meta-analysis of intraocular pressure.Hum Genet2014
25489230Congenital cataracts: de novo gene conversion event in CRYBB2.Mol Vis2014
22570617Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma.PLoS Genet2012
18195223Effects of timolol on MYOC, OPTN, and WDR36 RNA levels.Arch Ophthalmol2008
17210862Differential expression profile prioritization of positional candidate glaucoma genes: the GLC1C locus.Arch Ophthalmol2007
16541013Gene expression profile of human trabecular meshwork cells in response to long-term dexamethasone exposure.Mol Vis2006
9856502Physical mapping of the nail patella syndrome interval at 9q34: ordering of STSs and ESTs.Hum Genet1998
9618165Loss-of-function mutations in the LIM-homeodomain gene, LMX1B, in nail-patella syndrome.Hum Mol Genet1998
9772276GLC1A mutations point to regions of potential functional importance on the TIGR/MYOC protein.Mol Vis1998
9344665Human bZIP transcription factor gene NRL: structure, genomic sequence, and fine linkage mapping at 14q11.2 and negative mutation analysis in patients with retinal degeneration.Genomics1997
9417917Neuropeptide Y receptor genes mapped in human and mouse: receptors with high affinity for pancreatic polypeptide are not clustered with receptors specific for neuropeptide Y and peptide YY.Genomics1997
8807324Linkage study of Best's vitelliform macular dystrophy (VMD2) in a large North American family.Hum Hered1996
7724183Disruption of conserved rhodopsin disulfide bond by Cys187Tyr mutation causes early and severe autosomal dominant retinitis pigmentosa.Ophthalmology1995
7846071Dark-light: model for nightblindness from the human rhodopsin Gly-90-->Asp mutation.Proc Natl Acad Sci U S A1995
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Collaborators

Sanford School of Medicine, University of South Dakota
Co-authored papers 4
Children's Health Research Center
Co-authored papers 3
The Scripps Research Institute
Co-authored papers 2
Co-authored papers 2
Cleveland Institute for Computational Biology, Case Western Reserve University
Co-authored papers 2
Augusta University
Co-authored papers 2
Johns Hopkins University School of Medicine
Co-authored papers 2
Sanford Burnham Prebys Medical Discovery Institute
Co-authored papers 2
Icahn School of Medicine at Mount Sinai
Co-authored papers 2
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Co-authored papers 2
National Eye Institute, National Institutes of Health
Co-authored papers 2
UC San Diego
Co-authored papers 2
Genentech Inc.
Co-authored papers 2
Harvard University
Co-authored papers 2
South Dakota State University
Co-authored papers 2
Co-authored papers 1
Co-authored papers 1
Broad Institute of Harvard and MIT
Co-authored papers 1
Broad Institute
Co-authored papers 1
Center for Inherited Disease Research, Johns Hopkins School of Medicine
Co-authored papers 1
Co-authored papers 1
University of California
Co-authored papers 1
NYU College of Arts and Sciences
Co-authored papers 1
University of California
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University of Minnesota Medical School, 1035 University Drive duluth
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Regeneron Pharmaceuticals Inc.
Co-authored papers 1
Einhorn Clinical Research Center, New York Eye and Ear Infirmary of Mount Sinai
Co-authored papers 1
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