Literature DB >> 6283911

Deficiency of hormone receptor-adenylate cyclase coupling protein: basis for hormone resistance in pseudohypoparathyroidism.

A M Spiegel, M A Levine, G D Aurbach, R W Downs, S J Marx, R D Lasker, A M Moses, N A Breslau.   

Abstract

Pseudohypoparathyroidism is an inherited disorder associated with resistance to the action of several hormones, including parathyroid hormone, thyroid-stimulating hormone, follicle-stimulating hormone, and luteinizing hormone. The disorders described under this designation are heterogeneous in regard to the underlying genetic defects, the phenotypic manifestation, and the severity of the defects in hormone action. The majority of affected individuals who also have the characteristic skeletal changes (heredity osteodystrophy) have a defect in the guanine nucleotide regulatory protein (G protein) that is essential for coupling certain cell-surface hormone receptors to the adenylate cyclase system. This defect is probably the cause for resistance to the action of multiple hormones. In the remaining patients the cause for hormone resistance has not been identified.

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Year:  1982        PMID: 6283911     DOI: 10.1152/ajpendo.1982.243.1.E37

Source DB:  PubMed          Journal:  Am J Physiol        ISSN: 0002-9513


  9 in total

1.  Defective dopamine-1 receptor adenylate cyclase coupling in the proximal convoluted tubule from the spontaneously hypertensive rat.

Authors:  S Kinoshita; A Sidhu; R A Felder
Journal:  J Clin Invest       Date:  1989-12       Impact factor: 14.808

Review 2.  Calcium metabolism in thyroid disease.

Authors:  G Benker; N Breuer; R Windeck; D Reinwein
Journal:  J Endocrinol Invest       Date:  1988-01       Impact factor: 4.256

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

Authors:  L S Weinstein; P V Gejman; E Friedman; T Kadowaki; R M Collins; E S Gershon; A M Spiegel
Journal:  Proc Natl Acad Sci U S A       Date:  1990-11       Impact factor: 11.205

4.  Extensive cerebral calcification and retinal changes in pseudohypoparathyroidism.

Authors:  E Ellie; J Julien; X Ferrer; I Riss; M C Durquety
Journal:  J Neurol       Date:  1989-10       Impact factor: 4.849

Review 5.  Nephrogenic diabetes insipidus: clinical symptoms, pathogenesis, genetics and treatment.

Authors:  N Knoers; L A Monnens
Journal:  Pediatr Nephrol       Date:  1992-09       Impact factor: 3.714

6.  Desensitization to parathyroid hormone in renal cells from aged rats is associated with alterations in G-protein activity.

Authors:  H Hanai; C T Liang; L Cheng; B Sacktor
Journal:  J Clin Invest       Date:  1989-01       Impact factor: 14.808

7.  A variant of nephrogenic diabetes insipidus: V2 receptor abnormality restricted to the kidney.

Authors:  N Knoers; L A Monnens
Journal:  Eur J Pediatr       Date:  1991-03       Impact factor: 3.183

8.  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.

Authors:  M A Levine; C Eil; R W Downs; A M Spiegel
Journal:  J Clin Invest       Date:  1983-07       Impact factor: 14.808

9.  Pseudohypoparathyroidism type 1a and insulin resistance in a child.

Authors:  Benjamin U Nwosu; Mary M Lee
Journal:  Nat Rev Endocrinol       Date:  2009-06       Impact factor: 43.330

  9 in total

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