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Author Details
Full Name
Kathleen M Scott
Affiliation
University of Michigan ann arbor
ORCID
Career Start Year
1995
Papers
18
H Index
11
Expertise
CM4AI Collaborator
Dexter Pratt (CM4AI)
PMID
Paper Title
Journal Title
Published Year
35337019
A BioID-Derived Proximity Interactome for SARS-CoV-2 Proteins.
Viruses
2022
35712768
The Nucleus Bypasses Obstacles by Deforming Like a Drop with Surface Tension Mediated by Lamin A/C.
Adv Sci (Weinh)
2022
34580671
A BioID-derived proximity interactome for SARS-CoV-2 proteins.
bioRxiv
2021
32344865
Comparative Application of BioID and TurboID for Protein-Proximity Biotinylation.
Cells
2020
24002674
Genome-wide association study and meta-analysis of intraocular pressure.
Hum Genet
2014
25489230
Congenital cataracts: de novo gene conversion event in CRYBB2.
Mol Vis
2014
22570617
Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma.
PLoS Genet
2012
18195223
Effects of timolol on MYOC, OPTN, and WDR36 RNA levels.
Arch Ophthalmol
2008
17210862
Differential expression profile prioritization of positional candidate glaucoma genes: the GLC1C locus.
Arch Ophthalmol
2007
16541013
Gene expression profile of human trabecular meshwork cells in response to long-term dexamethasone exposure.
Mol Vis
2006
9856502
Physical mapping of the nail patella syndrome interval at 9q34: ordering of STSs and ESTs.
Hum Genet
1998
9618165
Loss-of-function mutations in the LIM-homeodomain gene, LMX1B, in nail-patella syndrome.
Hum Mol Genet
1998
9772276
GLC1A mutations point to regions of potential functional importance on the TIGR/MYOC protein.
Mol Vis
1998
9344665
Human bZIP transcription factor gene NRL: structure, genomic sequence, and fine linkage mapping at 14q11.2 and negative mutation analysis in patients with retinal degeneration.
Genomics
1997
9417917
Neuropeptide 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.
Genomics
1997
8807324
Linkage study of Best's vitelliform macular dystrophy (VMD2) in a large North American family.
Hum Hered
1996
7724183
Disruption of conserved rhodopsin disulfide bond by Cys187Tyr mutation causes early and severe autosomal dominant retinitis pigmentosa.
Ophthalmology
1995
7846071
Dark-light: model for nightblindness from the human rhodopsin Gly-90-->Asp mutation.
Proc Natl Acad Sci U S A
1995
1 - 18 of 18
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