Genetic diseases associated with heterotrimeric G proteins
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Regulation of cAMP responses by the G12/13 pathway converges on adenylyl cyclase VIIKrüppel-like factor 11 regulates the expression of metabolic genes via an evolutionarily conserved protein interaction domain functionally disrupted in maturity onset diabetes of the young.The C825T polymorphism of the G-protein β3 subunit gene and its association with hypertension and stroke: an updated meta-analysis.DNA sequence polymorphisms within the bovine guanine nucleotide-binding protein Gs subunit alpha (Gsα)-encoding (GNAS) genomic imprinting domain are associated with performance traitsGNAS gene variants affect β-blocker-related survival after coronary artery bypass grafting.The D153del mutation in GNB3 gene causes tissue specific signalling patterns and an abnormal renal morphology in Rge chickens.The role of GNAS and other imprinted genes in the development of obesity.A mouse model for osseous heteroplasiaPaternal uniparental isodisomy of the entire chromosome 20 as a molecular cause of pseudohypoparathyroidism type Ib (PHP-Ib)Technologies for the synthesis of mRNA-encoding libraries and discovery of bioactive natural product-inspired non-traditional macrocyclic peptides.Effects of deficiency of the G protein Gsα on energy and glucose homeostasisGsα enhances commitment of mesenchymal progenitors to the osteoblast lineage but restrains osteoblast differentiation in mice.Increased methylation at differentially methylated region of GNAS in infants born to gestational diabetes.Extra-long Gαs variant XLαs protein escapes activation-induced subcellular redistribution and is able to provide sustained signalingThe role of G protein gene GNB3 C825T polymorphism in HIV-1 acquisition, progression and immune activation.G-Protein α-Subunit Gsα Is Required for Craniofacial Morphogenesis.Thyrocyte-specific Gq/G11 deficiency impairs thyroid function and prevents goiter development.Paternally inherited gsα mutation impairs adipogenesis and potentiates a lean phenotype in vivo.Gsα deficiency in the paraventricular nucleus of the hypothalamus partially contributes to obesity associated with Gsα mutationsDevelopment and treatment of tertiary hyperparathyroidism in patients with pseudohypoparathyroidism type 1BGβ3 is required for normal light ON responses and synaptic maintenanceInherited human diseases of heterotopic bone formation.Heterozygous inactivation of Gnas in adipose-derived mesenchymal progenitor cells enhances osteoblast differentiation and promotes heterotopic ossificationSorting nexin 27 couples PTHR trafficking to retromer for signal regulation in osteoblasts during bone growth.Biallelic Mutations in GNB3 Cause a Unique Form of Autosomal-Recessive Congenital Stationary Night BlindnessDesign of cyclic peptides that bind protein surfaces with antibody-like affinity.Association of the GNAS locus with severe malaria.Reduced insulin sensitivity in adults with pseudohypoparathyroidism type 1a.Estimation of the relationship between the polymorphisms of selected genes: ACE, AGTR1, TGFβ1 and GNB3 with the occurrence of primary vesicoureteral reflux.Pharmacogenomics of beta-adrenergic receptors and their accessory signaling proteins in heart failure.Adrenergic signaling polymorphisms and their impact on cardiovascular disease.Epac, in synergy with cAMP-dependent protein kinase (PKA), is required for cAMP-mediated mitogenesis.Different roles of GNAS and cAMP signaling during early and late stages of osteogenic differentiation.The role of G protein β3 subunit polymorphisms C825T, C1429T, and G5177A in Turkish subjects with essential hypertension.A novel, evolutionarily conserved enhancer of cone photoreceptor-specific expression.Role of a heterotrimeric G-protein, Gi2, in the corticogenesis: possible involvement in periventricular nodular heterotopia and intellectual disability.Overexpression of Gα11 in Osteoblast Lineage Cells Suppresses the Osteoanabolic Response to Intermittent PTH and Exercise.Elevated Gα11 expression in osteoblast lineage cells promotes osteoclastogenesis and leads to enhanced trabecular bone accrual in response to pamidronate.Improvement of Non-Steroidal Anti-Inflammatory Drug-Induced Gastrointestinal Symptoms during Proton Pump Inhibitor Treatment: Are G-Protein β3 Subunit Genotype, Helicobacter pylori Status, and Environmental Factors Response Modifiers?Are elite endurance athletes genetically predisposed to lower disease risk?
P2860
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P2860
Genetic diseases associated with heterotrimeric G proteins
description
2006 nî lūn-bûn
@nan
2006 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Genetic diseases associated with heterotrimeric G proteins
@ast
Genetic diseases associated with heterotrimeric G proteins
@en
Genetic diseases associated with heterotrimeric G proteins
@nl
type
label
Genetic diseases associated with heterotrimeric G proteins
@ast
Genetic diseases associated with heterotrimeric G proteins
@en
Genetic diseases associated with heterotrimeric G proteins
@nl
prefLabel
Genetic diseases associated with heterotrimeric G proteins
@ast
Genetic diseases associated with heterotrimeric G proteins
@en
Genetic diseases associated with heterotrimeric G proteins
@nl
P2093
P1476
Genetic diseases associated with heterotrimeric G proteins
@en
P2093
P304
P356
10.1016/J.TIPS.2006.03.005
P407
P577
2006-04-05T00:00:00Z