| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1152/AJPRENAL.2000.278.4.F507 |
| P698 | PubMed publication ID | 10751211 |
| P2093 | author name string | S Yu | |
| C A Ecelbarger | |||
| L S Weinstein | |||
| P2860 | cites work | A novel mutation in the switch 3 region of Gsalpha in a patient with Albright hereditary osteodystrophy impairs GDP binding and receptor activation | Q24310441 |
| XL alpha s is a new type of G protein | Q24311320 | ||
| Absence of functional receptors for parathyroid hormone and parathyroid hormone-related peptide in Blomstrand chondrodysplasia | Q24564439 | ||
| Differential expression of novel Gs alpha signal transduction protein cDNA species | Q28118286 | ||
| Mutation in the gene encoding the stimulatory G protein of adenylate cyclase in Albright's hereditary osteodystrophy | Q28298978 | ||
| Aquaporin-3 water channel localization and regulation in rat kidney | Q28639847 | ||
| Isolation and characterization of the human Gs alpha gene | Q28646194 | ||
| Cloning and characterization of kidney-specific promoter of human PTH/PTHrP receptor gene: absence of mutation in patients with pseudohypoparathyroidism type Ib. | Q32030051 | ||
| G protein regulation of adenylate cyclase | Q33547895 | ||
| Bidirectional imprinting of a single gene: GNAS1 encodes maternally, paternally, and biallelically derived proteins | Q33591397 | ||
| Imprinting in Albright's hereditary osteodystrophy | Q33594945 | ||
| Parental origin of Gs alpha gene mutations in Albright's hereditary osteodystrophy. | Q33596161 | ||
| Parental origin of transcription from the human GNAS1 gene. | Q33674736 | ||
| Deficient guanine nucleotide regulatory unit activity in cultured fibroblast membranes from patients with pseudohypoparathyroidism type I. A cause of impaired synthesis of 3',5'-cyclic AMP by intact and broken cells | Q33821910 | ||
| Mutations of the Gs alpha-subunit gene in Albright hereditary osteodystrophy detected by denaturing gradient gel electrophoresis | Q33862158 | ||
| Differential activity of maternally and paternally derived chromosome regions in mice | Q34198480 | ||
| Reduced expression of multiple forms of the alpha subunit of the stimulatory GTP-binding protein in pseudohypoparathyroidism type Ia | Q34354981 | ||
| Splice variants of the alpha subunit of the G protein Gs activate both adenylyl cyclase and calcium channels | Q34446263 | ||
| Genomic imprinting in mammals. | Q34453750 | ||
| Molecular physiology of urinary concentrating mechanism: regulation of aquaporin water channels by vasopressin | Q34738098 | ||
| Pseudohypoparathyroidism: defective excretion of 3',5'-AMP in response to parathyroid hormone | Q35573411 | ||
| Regulation of collecting duct water channel expression by vasopressin in Brattleboro rat | Q35757345 | ||
| Increased expression of adenylylcyclase type VI proportionately increases beta-adrenergic receptor-stimulated production of cAMP in neonatal rat cardiac myocytes | Q35785891 | ||
| 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 | Q36214949 | ||
| The human GNAS1 gene is imprinted and encodes distinct paternally and biallelically expressed G proteins | Q36283882 | ||
| The gene responsible for pseudohypoparathyroidism type Ib is paternally imprinted and maps in four unrelated kindreds to chromosome 20q13.3. | Q36321841 | ||
| A cluster of oppositely imprinted transcripts at the Gnas locus in the distal imprinting region of mouse chromosome 2 | Q36452285 | ||
| Molecular cloning and characterization of NESP55, a novel chromogranin-like precursor of a peptide with 5-HT1B receptor antagonist activity | Q36855078 | ||
| Effect of vasopressin on electrical potential difference and chloride transport in mouse medullary thick ascending limb of Henle's loop | Q37027623 | ||
| Genetic deficiency of the alpha subunit of the guanine nucleotide-binding protein Gs as the molecular basis for Albright hereditary osteodystrophy. | Q37483952 | ||
| Cloning and kidney cell-specific activity of the promoter of the murine renal Na-K-C1 cotransporter gene | Q38358838 | ||
| Deficient activity of receptor-cyclase coupling protein in platelets of patients with pseudohypoparathyroidism | Q41549169 | ||
| Fibroblast Defect in Pseudohypoparathyroidism, Type I: Reduced Activity of Receptor-Cyclase Coupling Protein* | Q41551225 | ||
| Deficient Activity of Receptor-Cyclase Coupling Protein in Transformed Lymphoblasts of Patients with Pseudohypoparathyroidism, Type I* | Q41553025 | ||
| Selective resistance to parathyroid hormone in cultured skin fibroblasts from patients with pseudohypoparathyroidism type Ib. | Q42508120 | ||
| Quantitative analysis of renal medullary anatomy in rats and rabbits | Q42595803 | ||
| Action of ADH on isolated medullary thick ascending limb of the Brattleboro rat. | Q44647642 | ||
| Genetic mapping of the Gs-alpha subunit gene (GNAS1) to the distal long arm of chromosome 20 using a polymorphism detected by denaturing gradient gel electrophoresis. | Q45036339 | ||
| Mapping of the gene encoding the alpha subunit of the stimulatory G protein of adenylyl cyclase (GNAS1) to 20q13.2----q13.3 in human by in situ hybridization | Q45712605 | ||
| Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons | Q48045480 | ||
| NaCl transport in mouse medullary thick ascending limbs. I. Functional nephron heterogeneity and ADH-stimulated NaCl cotransport | Q48664469 | ||
| Imprinting mechanisms. | Q52184196 | ||
| Oxytocin as an antidiuretic hormone. I. Concentration dependence of action. | Q52338002 | ||
| Decreased renal Na-K-2Cl cotransporter abundance in mice with heterozygous disruption of the G(s)alpha gene. | Q52536017 | ||
| Immunochemical analysis of the alpha-subunit of the stimulatory G-protein of adenylyl cyclase in patients with Albright's hereditary osteodystrophy. | Q54312916 | ||
| Responses to glucagon infusion in pseudohypoparathyroidism. | Q54419230 | ||
| Activity of the stimulatory guanine nucleotide-binding protein is reduced in erythrocytes from patients with pseudohypoparathyroidism and pseudopseudohypoparathyroidism: biochemical, endocrine, and genetic analysis of Albright's hereditary osteodyst | Q54432204 | ||
| Evidence for normal antidiuretic responses to endogenous and exogenous arginine vasopressin in patients with guanine nucleotide-binding stimulatory protein-deficient pseudohypoparathyroidism. | Q54438532 | ||
| Defect of Receptor–Cyclase Coupling Protein in Pseudohypoparathyroidism | Q54550049 | ||
| Parental imprinting of the mouse insulin-like growth factor II gene. | Q55052428 | ||
| P433 | issue | 4 | |
| P304 | page(s) | F507-14 | |
| P577 | publication date | 2000-04-01 | |
| P1433 | published in | American Journal of Physiology - Renal Physiology | Q2610177 |
| P1476 | title | Variable imprinting of the heterotrimeric G protein G(s) alpha-subunit within different segments of the nephron | |
| P478 | volume | 278 |
| Q36521099 | Ablation of the Stimulatory G Protein α-Subunit in Renal Proximal Tubules Leads to Parathyroid Hormone-Resistance With Increased Renal Cyp24a1 mRNA Abundance and Reduced Serum 1,25-Dihydroxyvitamin D. |
| Q48711067 | BEGAIN: a novel imprinted gene that generates paternally expressed transcripts in a tissue- and promoter-specific manner in sheep |
| Q33905190 | Discordance between genetic and epigenetic defects in pseudohypoparathyroidism type 1b revealed by inconsistent loss of maternal imprinting at GNAS1 |
| Q33964982 | Identification of a methylation imprint mark within the mouse Gnas locus |
| Q36892948 | Increased Gsα within blood cell membrane lipid microdomains in some depressive disorders: an exploratory study. |
| Q39575659 | LRP6 mediates cAMP generation by G protein-coupled receptors through regulating the membrane targeting of Gα(s). |
| Q92399677 | Management of pseudohypoparathyroidism |
| Q38363924 | Paternal imprinting of Galpha(s) in the human thyroid as the basis of TSH resistance in pseudohypoparathyroidism type 1a. |
| Q37589286 | Postnatal establishment of allelic Gαs silencing as a plausible explanation for delayed onset of parathyroid hormone resistance owing to heterozygous Gαs disruption |
| Q88486673 | Prevalence of Nephrocalcinosis in Pseudohypoparathyroidism: Is Screening Necessary? |
| Q38816341 | Pseudohypoparathyroidism and Gsα-cAMP-linked disorders: current view and open issues. |
| Q35881887 | Quantitative and functional interrogation of parent-of-origin allelic expression biases in the brain |
| Q36076341 | Studies of the regulation and function of the Gs alpha gene Gnas using gene targeting technology |
| Q28593878 | Targeted deletion of the Nesp55 DMR defines another Gnas imprinting control region and provides a mouse model of autosomal dominant PHP-Ib |
| Q33389173 | Transcriptome-wide identification of novel imprinted genes in neonatal mouse brain |
Search more.