Molecular genetics of endocrine disorders
著者
書誌事項
Molecular genetics of endocrine disorders
Chapman & Hall Medical, 1997
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内容説明・目次
内容説明
In recent years important advances in endocrinology and metabolism have resulted from the application of the methods of molecular biology. This book provides a succinct, readable version of these advances, specifically for physicians who are involved in endocrinology and metabolism. In addition to providing this, the book is well referenced, to support the authoritative accounts which are written by leaders in their field.
目次
Molecular genetics and inherited human disease
Molecular pathology of pituitary hormone deficiency syndromes
Kallmann's sydrome
Diabetes insipidus
Molecular aetiology of thyroid cancers
Thyroid hormone resistance syndromes
Molecular aetiology of the parathyroid disorders
Cloning of the gene causing Lowe's syndrome
Abnormalities of structure and function resulting from mutations in the steroid hormone receptors
Parathyroid hormone-related protein and the humoral hypercalcaemia of malignancy
G proteins
Insulin receptor defects
The genetics of adrenal steroid synthesis
Pheochromocytomas
Molecular basis of human hypertension: role of angiotensinogen
The control of gonadal cell death and aetiology of gonadal tumours
Disorders of sexual development and infertility
The genetics of the hyperlipidaemic disorders
Immunogenetics
Cloning of the calcitrophic receptors - parathyroid hormone and parathyroid hormone-related peptide, and calcitonin
Adrenoleukodystrophy.
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