A mouse model of human familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism-Reference-Cited by-同舟云学术

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A mouse model of human familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism

Published:1995-12 Issue:4 Volume:11 Page:389-394
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Ho Chrystal,Conner David A.,Pollak Martin R.,Ladd Daniel J.,Kifor Olga,Warren Henry B.,Brown Edward M.,Seidman J.G.,Seidman Christine E.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1295-389.pdf

Reference24 articles.

1. Brown, E.M. et al. Cloning, expression, and characterization of an extracellular Ca2+ sensing receptor from bovine parathyroid. Nature 366, 575–580 (1993).

2. Riccardi, D. et al. Cloning and functional expression of a rat kidney extracellular calcium-sensing receptor. Proc. natn. Acad. Sci. U.S.A. 92, 131–135 (1994).

3. Ruat, M., Molliver, M.E., Snowman, A.M. & Snyder, S.H. Calcium sensing receptor molecular cloning in rat and localization to nerve terminals. Proc. natn. Acad. Sci. U.S.A. 92, 3161–3165 (1995).

4. Pollak, M.R. et al. Mutations in the human Ca2+-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. Cell 75, 1297–1303 (1993).

5. Pollak, M.R. et al. Autosomal dominant hypocalcaemia caused by a Ca2+-sensing receptor gene mutation. Nature Genet. 8, 303–307 (1994).

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1. Rare genetic disorders that impair parathyroid hormone synthesis, secretion, or bioactivity provide insights into the diagnostic utility of different parathyroid hormone assays;Current Opinion in Nephrology & Hypertension;2024-05-03

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4. Exploring Adaptive Phenotypes for the Human Calcium-Sensing Receptor Polymorphism R990G;Molecular Biology and Evolution;2024-01-29

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