(Q28235038)

Pseudohypoparathyroidism. New insights into an old disease

21 January 2018

1 reference

Growth hormone-releasing hormone resistance in pseudohypoparathyroidism type ia: new evidence for imprinting of the Gs alpha gene.

21 January 2018

1 reference

Growth hormone deficiency in pseudohypoparathyroidism type 1a: another manifestation of multihormone resistance

21 January 2018

1 reference

Variable and tissue-specific hormone resistance in heterotrimeric Gs protein alpha-subunit (Gsalpha) knockout mice is due to tissue-specific imprinting of the gsalpha gene

21 January 2018

1 reference

Paternally inherited inactivating mutations of the GNAS1 gene in progressive osseous heteroplasia.

21 January 2018

1 reference

GNAS1Mutations and Progressive Osseous Heteroplasia

21 January 2018

1 reference

Differential activity of maternally and paternally derived chromosome regions in mice

21 January 2018

1 reference

Galphas transcripts are biallelically expressed in the human kidney cortex: implications for pseudohypoparathyroidism type 1b.

21 January 2018

1 reference

The gsalpha gene: predominant maternal origin of transcription in human thyroid gland and gonads.

21 January 2018

1 reference

Paternal imprinting of Galpha(s) in the human thyroid as the basis of TSH resistance in pseudohypoparathyroidism type 1a.

21 January 2018

1 reference

The stimulatory G protein alpha-subunit Gs alpha is imprinted in human thyroid glands: implications for thyroid function in pseudohypoparathyroidism types 1A and 1B.

21 January 2018

1 reference

Stimulatory G protein directly regulates hypertrophic differentiation of growth plate cartilage in vivo.

21 January 2018

1 reference

A cluster of oppositely imprinted transcripts at the Gnas locus in the distal imprinting region of mouse chromosome 2

21 January 2018

1 reference

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

21 January 2018

1 reference

XL alpha s is a new type of G protein

21 January 2018

1 reference

Molecular cloning and characterization of NESP55, a novel chromogranin-like precursor of a peptide with 5-HT1B receptor antagonist activity

21 January 2018

1 reference

Bidirectional imprinting of a single gene: GNAS1 encodes maternally, paternally, and biallelically derived proteins

21 January 2018

1 reference

Identification of a methylation imprint mark within the mouse Gnas locus

21 January 2018

1 reference

An imprinted antisense transcript at the human GNAS1 locus

21 January 2018

1 reference

An imprinted transcript, antisense to Nesp, adds complexity to the cluster of imprinted genes at the mouse Gnas locus

21 January 2018

1 reference

The imprinted signaling protein XL alpha s is required for postnatal adaptation to feeding.

21 January 2018

1 reference

Paternal uniparental isodisomy of chromosome 20q--and the resulting changes in GNAS1 methylation--as a plausible cause of pseudohypoparathyroidism

21 January 2018

1 reference

Positional dissociation between the genetic mutation responsible for pseudohypoparathyroidism type Ib and the associated methylation defect at exon A/B: evidence for a long-range regulatory element within the imprinted GNAS1 locus.

21 January 2018

1 reference

The gene responsible for pseudohypoparathyroidism type Ib is paternally imprinted and maps in four unrelated kindreds to chromosome 20q13.3.

21 January 2018

1 reference

Syntaxin-16, a putative Golgi t-SNARE

21 January 2018

1 reference

Molecular cloning and localization of human syntaxin 16, a member of the syntaxin family of SNARE proteins

21 January 2018

1 reference

Prader-Willi and Angelman syndromes: sister imprinted disorders

21 January 2018

1 reference

Epigenetic properties and identification of an imprint mark in the Nesp-Gnasxl domain of the mouse Gnas imprinted locus.

21 January 2018

1 reference

Tissue-specific expression of antisense and sense transcripts at the imprinted Gnas locus.

21 January 2018

1 reference