Parental origin of transcription from the human GNAS1 gene.

Author:

Campbell R,Gosden C M,Bonthron D T

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference29 articles.

1. Mutation in the gene taken. Not only was this experiment free from possible maternal contamination effects, but it encoding the stimulatory G protein of adenylate cyclase in Albright's hereditary osteodystrophy;Patten, J.L.; Johns, D.R.; Valle, D.;N Engl J Med,1990

2. Mutations of the Gs alpha-subunit gene in Albright's hereditary osteodystrophy detected by;Weinstein, L.S.; Gejman, P.V.; Freidman, E.;denaturing gel electrophoresis. Proc ental genotypes were; Natl Acad Sci USA; revealed. Table 3 shows that a reproducible difference in expression,1990

3. Studies in pseudohypoparathyroidism. Two new cases with a levels between the maternal and paternal probable selective deficiency of thyrotropin;Zisman, E.; Lotz, M.; Jenkins, M.E.; Bartter, F.C.;Am J Med; alleles was not obtained in this experiment,1969

4. Raz-If GNAS1 imprinting is a tissue specific dan AK, Kim MH. Partial gonadotropin-resistance in pseudohypoparathyroidism;Wolfsdorf, J.I.; Rosenfeild, R.L.; Fang, V.S.; Kobayashi, R.;Acta Endocrinol,1978

5. Resistance to multiple hormones in patients with pseudohypoparathyrtissues might be involved. These would inoidism;Levine, M.A.; Downs, R.W.; Moses, A.M.;Am J Med; clude PTH target tissues and other endocrine,1983

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