| scholarly article | Q13442814 |
| P819 | ADS bibcode | 2007PNAS..10417424M |
| P356 | DOI | 10.1073/PNAS.0708561104 |
| P932 | PMC publication ID | 2077272 |
| P698 | PubMed publication ID | 17962410 |
| P5875 | ResearchGate publication ID | 5884291 |
| P2093 | author name string | Toshiro Fujita | |
| Micheala A Aldred | |||
| Yasuhito Yuasa | |||
| Philippe Rondard | |||
| Noriko Makita | |||
| Taroh Iiri | |||
| Junichiro Sato | |||
| Hiroshi Fukamachi | |||
| Makiko Hashimoto | |||
| 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 |
| Conditional activation defect of a human Gsalpha mutant | Q24323004 | ||
| The GTPase superfamily: conserved structure and molecular mechanism | Q27860524 | ||
| Characterization of Saccharomyces cerevisiae acyl-protein thioesterase 1, the enzyme responsible for G protein alpha subunit deacylation in vivo | Q27939571 | ||
| Regulation of G proteins by covalent modification | Q28213744 | ||
| Palmitoylation is required for signaling functions and membrane attachment of Gq alpha and Gs alpha | Q28255860 | ||
| Palmitoylation of intracellular signaling proteins: regulation and function | Q28266189 | ||
| A Cytoplasmic Acyl-Protein Thioesterase That Removes Palmitate from G Protein α Subunits and p21RAS | Q28273568 | ||
| Palmitoylation: policing protein stability and traffic | Q28280080 | ||
| Causal relationship between the loss of RUNX3 expression and gastric cancer | Q28509530 | ||
| Live cell imaging of Gs and the beta2-adrenergic receptor demonstrates that both alphas and beta1gamma7 internalize upon stimulation and exhibit similar trafficking patterns that differ from that of the beta2-adrenergic receptor | Q28573455 | ||
| Insights into G protein structure, function, and regulation. | Q30336381 | ||
| Mechanisms of disease: the role of GRK4 in the etiology of essential hypertension and salt sensitivity | Q30441976 | ||
| The expanding spectrum of G protein diseases | Q33547178 | ||
| Efficient generation of recombinant adenoviruses using adenovirus DNA-terminal protein complex and a cosmid bearing the full-length virus genome | Q33557797 | ||
| Stimulation of beta-adrenergic receptors of S49 lymphoma cells redistributes the alpha subunit of the stimulatory G protein between cytosol and membranes | Q34312140 | ||
| Pathophysiological roles of G-protein-coupled receptor kinases | Q34418929 | ||
| Seven-transmembrane-spanning receptors and heart function | Q34503394 | ||
| A Gsalpha mutant designed to inhibit receptor signaling through Gs. | Q34817858 | ||
| Inherited diseases involving g proteins and g protein-coupled receptors. | Q35640200 | ||
| An acquired hypocalciuric hypercalcemia autoantibody induces allosteric transition among active human Ca-sensing receptor conformations. | Q35720141 | ||
| Historical review: a brief history and personal retrospective of seven-transmembrane receptors | Q35847116 | ||
| Multi-tasking RGS proteins in the heart: the next therapeutic target? | Q36061193 | ||
| Epithelioid cell cultures from rat small intestine. Characterization by morphologic and immunologic criteria | Q36200458 | ||
| Thematic review series: lipid posttranslational modifications. Lysosomal metabolism of lipid-modified proteins | Q36455039 | ||
| Activation of the alpha subunit of Gs in intact cells alters its abundance, rate of degradation, and membrane avidity | Q36532319 | ||
| Mechanisms of disease: Mutations of G proteins and G-protein-coupled receptors in endocrine diseases. | Q36672702 | ||
| Assembly and trafficking of heterotrimeric G proteins | Q36845087 | ||
| Reciprocal regulation of Gs alpha by palmitate and the beta gamma subunit | Q37045553 | ||
| Activation-induced subcellular redistribution of Gs alpha | Q37381937 | ||
| Nobel Lecture. G proteins and regulation of adenylyl cyclase | Q40424775 | ||
| Runx3-/- gastric epithelial cells differentiate into intestinal type cells | Q40517145 | ||
| A Novel Mutation Adjacent to the Switch III Domain of Gsαin a Patient with Pseudohypoparathyroidism | Q41084237 | ||
| Reversible palmitoylation of signaling proteins | Q41382874 | ||
| Rapid GDP release from Gs alpha in patients with gain and loss of endocrine function | Q41442871 | ||
| Activation and depalmitoylation of Gs alpha | Q41459257 | ||
| Separate GTP binding and GTPase activating domains of a G alpha subunit | Q41508279 | ||
| Modification of the function of pertussis toxin substrate GTP-binding protein by cholera toxin-catalyzed ADP-ribosylation | Q41643635 | ||
| Chemotactic peptide receptor-supported ADP-ribosylation of a pertussis toxin substrate GTP-binding protein by cholera toxin in neutrophil-type HL-60 cells | Q41758298 | ||
| 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. | Q42490986 | ||
| Germline mosaicism for a GNAS1 mutation and Albright hereditary osteodystrophy | Q43076226 | ||
| Reconstitution of agonist-stimulated phosphatidylinositol 4,5-bisphosphate hydrolysis using purified m1 muscarinic receptor, Gq/11, and phospholipase C-beta 1 | Q43508385 | ||
| The McCune-Albright syndrome: a lethal gene surviving by mosaicism | Q43628624 | ||
| Real-time visualization of a fluorescent G(alpha)(s): dissociation of the activated G protein from plasma membrane | Q43865607 | ||
| The effect of GTP and Mg2+ on the GTPase activity and the fluorescent properties of Go. | Q45202534 | ||
| G-protein diseases furnish a model for the turn-on switch | Q46345189 | ||
| Synthesis in Escherichia coli of GTPase-deficient mutants of Gs alpha | Q54724996 | ||
| GNAS1 lesions in pseudohypoparathyroidism Ia and Ic: genotype phenotype relationship and evidence of the maternal transmission of the hormonal resistance | Q55670473 | ||
| Cholera | Q57119004 | ||
| Effects of Mg2+ and the beta gamma-subunit complex on the interactions of guanine nucleotides with G proteins | Q70322245 | ||
| Pseudohypoparathyroidism, a novel mutation in the betagamma-contact region of Gsalpha impairs receptor stimulation | Q71245866 | ||
| A novel Gs alpha mutant in a patient with Albright hereditary osteodystrophy uncouples cell surface receptors from adenylyl cyclase | Q71650722 | ||
| P433 | issue | 44 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | diarrhea | Q40878 |
| Albright's hereditary osteodystrophy | Q4712685 | ||
| P304 | page(s) | 17424-17429 | |
| P577 | publication date | 2007-10-25 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | Human G(salpha) mutant causes pseudohypoparathyroidism type Ia/neonatal diarrhea, a potential cell-specific role of the palmitoylation cycle | |
| P478 | volume | 104 |
| Q37192455 | A Novel T55A Variant of Gs α Associated with Impaired cAMP Production, Bone Fragility, and Osteolysis |
| Q42380620 | Analysis of the V2 Vasopressin Receptor (V2R) Mutations Causing Partial Nephrogenic Diabetes Insipidus Highlights a Sustainable Signaling by a Non-peptide V2R Agonist |
| Q54467570 | Attenuated Desensitization of β-Adrenergic Receptor by Water-Soluble N-Nitrosamines That Induce S-Nitrosylation Without NO Release |
| Q93162304 | Cinacalcet corrects biased allosteric modulation of CaSR by AHH autoantibody |
| Q35515532 | Extra-long Gαs variant XLαs protein escapes activation-induced subcellular redistribution and is able to provide sustained signaling |
| Q35563016 | GNAS Spectrum of Disorders |
| Q35125525 | Identification of a novel mutation in a pseudohypoparathyroidism family |
| Q39593006 | Molecular basis of a novel oncogenic mutation in GNAO1 |
| Q37359990 | Protein acyl thioesterases (Review). |
| Q37912382 | Protein palmitoylation and subcellular trafficking |
| Q28577831 | Regulation of RhoA signaling by the cAMP-dependent phosphorylation of RhoGDIα |
| Q26852157 | The GNAS complex locus and human diseases associated with loss-of-function mutations or epimutations within this imprinted gene |
| Q40649339 | V2 Vasopressin Receptor (V2R) Mutations in Partial Nephrogenic Diabetes Insipidus Highlight Protean Agonism of V2R Antagonists |
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