Literature DB >> 8269505

Mutations in G protein-linked receptors: novel insights on disease.

D E Clapham1.   

Abstract

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Year:  1993        PMID： 8269505     DOI： 10.1016/0092-8674(93)90609-t

Source DB:  PubMed          Journal:  Cell        ISSN： 0092-8674            Impact factor:   41.582


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  9 in total

Review 1.  Genetics of vasopressin receptors.

Authors:  Marc Thibonnier
Journal:  Curr Hypertens Rep       Date:  2004-02       Impact factor: 5.369

2.  Truncated, desensitization-defective neurokinin receptors mediate sustained MAP kinase activation, cell growth and transformation by a Ras-independent mechanism.

Authors:  J Alblas; I van Etten; W H Moolenaar
Journal:  EMBO J       Date:  1996-07-01       Impact factor: 11.598

3.  Platelet signal transduction defect with Galpha subunit dysfunction and diminished Galphaq in a patient with abnormal platelet responses.

Authors:  J Gabbeta; X Yang; M A Kowalska; L Sun; N Dhanasekaran; A K Rao
Journal:  Proc Natl Acad Sci U S A       Date:  1997-08-05       Impact factor: 11.205

4.  Alanine-261 in intracellular loop III of the human gonadotropin-releasing hormone receptor is crucial for G-protein coupling and receptor internalization.

Authors:  D B Myburgh; R P Millar; J P Hapgood
Journal:  Biochem J       Date:  1998-05-01       Impact factor: 3.857

5.  Identification of constitutively activating mutation of the luteinising hormone receptor in a family with male limited gonadotrophin independent precocious puberty (testotoxicosis).

Authors:  N Kawate; G B Kletter; B E Wilson; M L Netzloff; K M Menon
Journal:  J Med Genet       Date:  1995-07       Impact factor: 6.318

Review 6.  Molecular basis of pituitary oncogenesis.

Authors:  M Tada; H Kobayashi; T Moriuchi
Journal:  J Neurooncol       Date:  1999       Impact factor: 4.130

Review 7.  Familial benign hypercalcemia--from clinical description to molecular genetics.

Authors:  H Heath
Journal:  West J Med       Date:  1994-06

8.  Arg60 to Leu mutation of the human thromboxane A2 receptor in a dominantly inherited bleeding disorder.

Authors:  T Hirata; A Kakizuka; F Ushikubi; I Fuse; M Okuma; S Narumiya
Journal:  J Clin Invest       Date:  1994-10       Impact factor: 14.808

9.  Heterogeneous AVPR2 gene mutations in congenital nephrogenic diabetes insipidus.

Authors:  R S Wildin; M J Antush; R L Bennett; J M Schoof; C R Scott
Journal:  Am J Hum Genet       Date:  1994-08       Impact factor: 11.025
  9 in total

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