Functional heterogeneity of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa

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Functional heterogeneity of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa is …
instance of (P31):
scholarly articleQ13442814

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P819ADS bibcode1991PNAS...88.8840S
P356DOI10.1073/PNAS.88.19.8840
P8608Fatcat IDrelease_f5zmrot52zgudbpx37qgbqtrsq
P932PMC publication ID52606
P698PubMed publication ID1924344
P5875ResearchGate publication ID21232334

P2093author name stringN Agarwal
J Nathans
C H Sung
D S Papermaster
B G Schneider
P2860cites workMolecular genetics of human color vision: the genes encoding blue, green, and red pigmentsQ24294339
Rhodopsin mutations in autosomal dominant retinitis pigmentosaQ24564252
A 3-bp deletion in the rhodopsin gene in a family with autosomal dominant retinitis pigmentosaQ24669855
Assembly of asparagine-linked oligosaccharidesQ28131690
“Western Blotting”: Electrophoretic transfer of proteins from sodium dodecyl sulfate-polyacrylamide gels to unmodified nitrocellulose and radiographic detection with antibody and radioiodinated protein AQ28131712
Isolation and nucleotide sequence of the gene encoding human rhodopsinQ28609991
Role of the intradiscal domain in rhodopsin assembly and functionQ33656119
A point mutation of the rhodopsin gene in one form of retinitis pigmentosaQ34168407
Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosaQ34239582
Immunocytochemical localization of opsin in outer segments and Golgi zones of frog photoreceptor cells. An electron microscope analysis of cross-linked albumin-embedded retinasQ36199130
In vitro biosynthesis, core glycosylation, and membrane integration of opsinQ36204957
Rapid embedding of tissues in Lowicryl K4M for immunoelectron microscopyQ36605377
The LDL receptor locus in familial hypercholesterolemia: mutational analysis of a membrane proteinQ37794678
Protein degradation in the endoplasmic reticulumQ37947738
Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosisQ41714520
Production of bovine rhodopsin by mammalian cell lines expressing cloned cDNA: spectrophotometry and subcellular localizationQ45154048
Use of peptides to select for anti-rhodopsin antibodies with desired amino acid sequence specificities.Q53790290
Assembly of functional rhodopsin requires a disulfide bond between cysteine residues 110 and 187.Q55054124
Human rhodopsinQ57088986
Determinants of visual pigment absorbance: role of charged amino acids in the putative transmembrane segmentsQ67290885
Preparation of cultured mammalian cells for transmission and scanning electron microscopy using Aclar filmQ67971823
Antigen-antibody interaction. Synthetic peptides define linear antigenic determinants recognized by monoclonal antibodies directed to the cytoplasmic carboxyl terminus of rhodopsinQ69034628
Immunocytochemistry of retinal membrane protein biosynthesis at the electron microscopic level by the albumin embedding techniqueQ70309705
P433issue19
P407language of work or nameEnglishQ1860
P921main subjectheterogeneityQ928498
P304page(s)8840-8844
P577publication date1991-10-01
P1433published inProceedings of the National Academy of Sciences of the United States of AmericaQ1146531
P1476titleFunctional heterogeneity of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa
P478volume88