胰岛素样生长因子（IGF）-I基因缺失。 - Suppr

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超能文献

Insulin-like growth factor (IGF)-I gene deletion.

作者信息

Camacho-Hübner Cecilia, Woods Katie A, Clark Adrian J L, Savage Martin O

机构信息

Paediatric Endocrinology Section, Department of Endocrinology, St. Bartholomew's Hospital, London, UK.

出版信息

Rev Endocr Metab Disord. 2002 Dec;3(4):357-61. doi: 10.1023/a:1020957809082.

DOI:10.1023/a:1020957809082

PMID:12424437

Abstract

摘要

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本文引用的文献

Growth hormone insensitivity: pathophysiology, diagnosis, clinical variation and future perspectives.

Horm Res. 2001;55 Suppl 2:32-5. doi: 10.1159/000063471.

Insulin-like growth factor -I deficiency.

Horm Res. 2001;55 Suppl 1:17-20. doi: 10.1159/000063457.

Effects of insulin-like growth factor I (IGF-I) therapy on body composition and insulin resistance in IGF-I gene deletion.胰岛素样生长因子I（IGF-I）基因缺失时IGF-I治疗对身体成分和胰岛素抵抗的影响。

J Clin Endocrinol Metab. 2000 Apr;85(4):1407-11. doi: 10.1210/jcem.85.4.6495.

The insulin-like growth factor-I (IGF-I) gene in individuals born small for gestational age (SGA).小于胎龄儿（SGA）个体中的胰岛素样生长因子-I（IGF-I）基因。

Clin Endocrinol (Oxf). 1999 Oct;51(4):423-7. doi: 10.1046/j.1365-2265.1999.00803.x.

Insulin-like growth factor I is essential for postnatal growth in response to growth hormone.胰岛素样生长因子I对于出生后响应生长激素的生长至关重要。

Endocrinology. 1999 Nov;140(11):5178-84. doi: 10.1210/endo.140.11.7151.

Long-term treatment of growth hormone insensitivity syndrome with IGF-I. Results of the European Multicentre Study. The Working Group on Growth Hormone Insensitivity Syndromes.使用胰岛素样生长因子-I对生长激素不敏感综合征进行长期治疗。欧洲多中心研究结果。生长激素不敏感综合征工作组。

Horm Res. 1999;51(3):128-34. doi: 10.1159/000023345.

Liver-derived insulin-like growth factor I (IGF-I) is the principal source of IGF-I in blood but is not required for postnatal body growth in mice.肝脏来源的胰岛素样生长因子I（IGF-I）是血液中IGF-I的主要来源，但对于小鼠出生后的身体生长并非必需。

Proc Natl Acad Sci U S A. 1999 Jun 8;96(12):7088-92. doi: 10.1073/pnas.96.12.7088.

J Clin Endocrinol Metab. 1999 May;84(5):1611-6. doi: 10.1210/jcem.84.5.5649.

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J Clin Endocrinol Metab. 1997 Nov;82(11):3529-35. doi: 10.1210/jcem.82.11.4389.

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