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The human GNAS1 gene is imprinted and encodes distinct paternally and biallelically expressed G proteins

Data up to Jan 2025

Published1998
Citations264
References25

Total Citations Per Year

Abstract

References (25)

p57KIP2, a structurally distinct member of the p21CIP1 Cdk inhibitor family, is a candidate tumor suppressor gene.

1995 • 956 citations

Cloning of p57KIP2, a cyclin-dependent kinase inhibitor with unique domain structure and tissue distribution.

1995 • 910 citations

Mutation in the Gene Encoding the Stimulatory G Protein of Adenylate Cyclase in Albright's Hereditary Osteodystrophy

1990 • 402 citations

An imprinted gene p57KIP2 is mutated in Beckwith–Wiedemann syndrome

1996 • 390 citations

Isolation and characterization of the human Gs alpha gene.

1988 • 379 citations

A genomic scanning method for higher organisms using restriction sites as landmarks.

1991 • 351 citations

Imprinting in Albright's hereditary osteodystrophy.

1993 • 306 citations

Genomic imprinting of p57KIP2, a cyclin–dependent kinase inhibitor, in mouse

1995 • 288 citations

Mutations of the Gs alpha-subunit gene in Albright hereditary osteodystrophy detected by denaturing gradient gel electrophoresis.

1990 • 257 citations

Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene.

1996 • 234 citations

XLαs is a new type of G protein

1994 • 223 citations

Identification of an imprinted U2af binding protein related sequence on mouse chromosome 11 using the RLGS method

1994 • 219 citations

Identification of Grf1 on mouse chromosome 9 as an imprinted gene by RLGS–M

1996 • 195 citations

Genetic deficiency of the alpha subunit of the guanine nucleotide-binding protein Gs as the molecular basis for Albright hereditary osteodystrophy.

1988 • 145 citations

A human parthenogenetic chimaera

1995 • 138 citations

Parental origin of transcription from the human GNAS1 gene.

1994 • 120 citations

Conservation of a maternal-specific methylation signal at the human IGF2R locus

1995 • 116 citations

Oppositely imprinted genes H19 and insulin-like growth factor 2 are coexpressed in human androgenetic trophoblast.

1993 • 79 citations

Differential expression of novel Gsα signal transduction protein cDNA species

1991 • 78 citations

Glomerular-Specific Imprinting of the Mouse Gsα Gene: How Does This Relate to Hormone Resistance in Albright Hereditary Osteodystrophy?

1996 • 55 citations

Neural expression of a novel alternatively spliced and polyadenylated Gs alpha transcript

1993 • 50 citations

Clinical and Biological Heterogeneity in Pseudohypoparathyroidism Syndrome

1997 • 49 citations

Direct detection and isolation of restriction landmark genomic scanning (RLGS) spot DNA markers tightly linked to a specific trait by using the RLGS spot-bombing method.

1995 • 29 citations

Quantitative and qualitative genetic variation in two‐dimensional DNA gels of human lymphocytoid cell lines

1995 • 24 citations

Genetic mapping and systematic screening of mouse endogenously imprinted loci detected with restriction landmark genome scanning method (RLGS)

1994 • 19 citations

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The human GNAS1 gene is imprinted and encodes distinct paternally and biallelically… (1998) – Proceedings of the National Academy of Sciences | Metascience Observatory Explorer