(Q40305537)

19 September 2017

0 references

Diseased G protein-coupled receptors (English)

1 reference

G protein-coupled receptor

19 September 2017

0 references

1

Lefkowitz RJ

1 reference

19 September 2017

Premont RT

2

1 reference

PMC publication ID

288383

19 September 2017

language of work or name

English

0 references

publication date

1 November 1993

1 reference

Journal of Clinical Investigation

19 September 2017

1 reference

19 September 2017

92

1 reference

19 September 2017

5

1 reference

19 September 2017

2089

1 reference

Pigmentation phenotypes of variant extension locus alleles result from point mutations that alter MSH receptor function.

19 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=288383

Hereditary isolated glucocorticoid deficiency is associated with abnormalities of the adrenocorticotropin receptor gene

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=288383

A mutation-induced activated state of the beta 2-adrenergic receptor. Extending the ternary complex model

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=288383

Familial glucocorticoid deficiency associated with point mutation in the adrenocorticotropin receptor

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=288383

G-protein-coupled receptor genes as protooncogenes: constitutively activating mutation of the alpha 1B-adrenergic receptor enhances mitogenesis and tumorigenicity

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=288383

Model systems for the study of seven-transmembrane-segment receptors

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=288383

Characterization of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa. Mutations on the cytoplasmic surface affect transducin activation.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=288383

Nephrogenic diabetes insipidus. A V2 vasopressin receptor unable to stimulate adenylyl cyclase

20 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8227321

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1172/JCI116806

1 reference

19 September 2017

1 reference

PMC publication ID

288383

19 September 2017

PubMed publication ID

8227321

1 reference

PMC publication ID

288383