(Q37242244)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18697996%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

review article

1 reference

title

Physiological dysfunctions associated with mutations of the imprinted Gnas locus (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18697996%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18697996%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

author name string

Stefan Krechowec

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18697996%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

language of work or name

1 reference

1 August 2008

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18697996%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18697996%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

volume

23

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18697996%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

page(s)

221-229

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18697996%20AND%20SRC:MED&resulttype=core&format=json

Constitutional deletion of chromosome 20q in two patients affected with albright hereditary osteodystrophy.

12 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Cell microarrays and RNA interference chip away at gene function

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Receptor-mediated adenylyl cyclase activation through XLalpha(s), the extra-large variant of the stimulatory G protein alpha-subunit.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Skeletal abnormalities and extra-skeletal ossification in mice with restricted Gsalpha deletion caused by a renin promoter-Cre transgene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Differential activity of maternally and paternally derived chromosome regions in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Genomic imprinting, growth control and the allocation of nutritional resources: consequences for postnatal life

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Regulation of renin in mice with Cre recombinase-mediated deletion of G protein Gsalpha in juxtaglomerular cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Alternative Gnas gene products have opposite effects on glucose and lipid metabolism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Increased glucose tolerance and reduced adiposity in the absence of fasting hypoglycemia in mice with liver-specific Gs alpha deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Maternal UPD 20 in a hyperactive child with severe growth retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

21 January 2018

Resourceful imprinting.

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Imprinting in Albright's hereditary osteodystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Mechanisms regulating imprinted genes in clusters.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Identification of interstitial maternal uniparental disomy (UPD) (14) and complete maternal UPD(20) in a cohort of growth retarded patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Neuroendocrine secretory protein 55: a novel marker for the constitutive secretory pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Paternal deletion of the GNAS imprinted locus (including Gnasxl) in two girls presenting with severe pre- and post-natal growth retardation and intractable feeding difficulties

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

A mouse model of albright hereditary osteodystrophy generated by targeted disruption of exon 1 of the Gnas gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Genomic imprinting and kinship: how good is the evidence?

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Petulant cellular acts: destroying the ECM rather than creating it.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

An imprinted antisense transcript at the human GNAS1 locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

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

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

XL alpha s is a new type of G protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Identification of imprinted loci by methylation-sensitive representational difference analysis: application to mouse distal chromosome 2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Characterization of the extra-large G protein alpha-subunit XLalphas. II. Signal transduction properties.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Clinical spectrum and pathogenesis of pseudohypoparathyroidism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Coding GNAS mutations leading to hormone resistance impair in vitro agonist- and cholera toxin-induced adenosine cyclic 3',5'-monophosphate formation mediated by human XLalphas.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Identification of the control region for tissue-specific imprinting of the stimulatory G protein alpha-subunit

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

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

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Identification of a methylation imprint mark within the mouse Gnas locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Body mass index differences in pseudohypoparathyroidism type 1a versus pseudopseudohypoparathyroidism may implicate paternal imprinting of Galpha(s) in the development of human obesity

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Relative amounts and molecular forms of NESP55 in various bovine tissues.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Biallelic expression of the Gsalpha gene in human bone and adipose tissue.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

A census of mammalian imprinting.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Expression of the extra-large G protein alpha-subunit XLalphas in neuroepithelial cells and young neurons during development of the rat nervous system.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Silencing by imprinted noncoding RNAs: is transcription the answer?

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Imprinting control within the compact Gnas locus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Control of imprinting at the Gnas cluster

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Imprinted Nesp55 influences behavioral reactivity to novel environments

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Imprinting the Gnas locus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Physiological functions of the imprinted Gnas locus and its protein variants Galpha(s) and XLalpha(s) in human and mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Genomic imprinting: parental influence on the genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Deficiency of the G-protein alpha-subunit G(s)alpha in osteoblasts leads to differential effects on trabecular and cortical bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Maternal UPD 20 in an infant from a pregnancy with mosaic trisomy 20.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

The imprinted oedematous-small mutation on mouse chromosome 2 identifies new roles for Gnas and Gnasxl in development

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Regulation of growth and metabolism by imprinted genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Zac1 regulates an imprinted gene network critically involved in the control of embryonic growth

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Maternal uniparental isodisomy 20 in a foetus with trisomy 20 mosaicism: clinical, cytogenetic and molecular analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Studies of the regulation and function of the Gs alpha gene Gnas using gene targeting technology

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Mammalian G proteins and their cell type specific functions

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Identification of an imprinting control region affecting the expression of all transcripts in the Gnas cluster.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Genomic imprinting in mammals: emerging themes and established theories

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Beta cell-specific deficiency of the stimulatory G protein alpha-subunit Gsalpha leads to reduced beta cell mass and insulin-deficient diabetes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

The alternative stimulatory G protein alpha-subunit XLalphas is a critical regulator of energy and glucose metabolism and sympathetic nerve activity in adult mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Increased insulin sensitivity in Gsalpha knockout mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

Paternal versus maternal transmission of a stimulatory G-protein alpha subunit knockout produces opposite effects on energy metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008

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

https://api.crossref.org/works/10.1152%2FPHYSIOL.00010.2008