Home
About
Overview
Sharing Data
ORCID
Help
History (8)
The association of non-alcoholic fatty liver disease and cardiac structure and function-Framingham Heart Study.
X-inactivation status varies in human embryonic stem cell lines.
Novel Oxygen Carrier Slows Infarct Growth in Large Vessel Occlusion Dog Model Based on Magnetic Resonance Imaging Analysis.
Activity-dependent regulome of human GABAergic neurons reveals new patterns of gene regulation and neurological disease heritability.
The Y141C knockin mutation in RDS leads to complex phenotypes in the mouse.
See All 8 Pages
Login
to edit your profile (add a photo, awards, links to other websites, etc.)
Edit My Profile
My Person List (
0
)
Return to Top
The Y141C knockin mutation in RDS leads to complex phenotypes in the mouse.
Stuck MW, Conley SM, Naash MI. The Y141C knockin mutation in RDS leads to complex phenotypes in the mouse. Hum Mol Genet. 2014 Dec 01; 23(23):6260-74.
View in:
PubMed
subject areas
Animals
Eye Proteins
Gene Knock-In Techniques
Membrane Proteins
Mice, Inbred C57BL
Mice, Knockout
Mutation
Peripherins
Phenotype
Retina
Retinal Cone Photoreceptor Cells
Retinal Degeneration
Retinal Rod Photoreceptor Cells
Retinitis Pigmentosa
Tetraspanins
authors with profiles
Michael Wayne Stuck PhD