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28 in total

Review 1. Tumour necrosis factor gene polymorphisms as severity markers in rheumatoid arthritis.

Authors: C L Verweij
Journal: Ann Rheum Dis Date: 1999-11 Impact factor: 19.103

2. Distribution of deletions and seven point mutations on CYP21B genes in three clinical forms of steroid 21-hydroxylase deficiency.

Authors: E Mornet; P Crété; F Kuttenn; M C Raux-Demay; J Boué; P C White; A Boué
Journal: Am J Hum Genet Date: 1991-01 Impact factor: 11.025

3. Function and membrane topology of wild-type and mutated cytochrome P-450c21.

Authors: M C Hu; L C Hsu; N C Hsu; B C Chung
Journal: Biochem J Date: 1996-05-15 Impact factor: 3.857

Review 4. The molecular biology, biochemistry, and physiology of human steroidogenesis and its disorders.

Authors: Walter L Miller; Richard J Auchus
Journal: Endocr Rev Date: 2010-11-04 Impact factor: 19.871

5. Intersection of the Roles of Cytochrome P450 Enzymes with Xenobiotic and Endogenous Substrates: Relevance to Toxicity and Drug Interactions.

Authors: F Peter Guengerich
Journal: Chem Res Toxicol Date: 2016-08-11 Impact factor: 3.739

6. Extraadrenal 21-hydroxylation by CYP2C19 and CYP3A4: effect on 21-hydroxylase deficiency.

Authors: Larissa G Gomes; Ningwu Huang; Vishal Agrawal; Berenice B Mendonça; Tania A S S Bachega; Walter L Miller
Journal: J Clin Endocrinol Metab Date: 2008-10-28 Impact factor: 5.958

Review 7. Androgen synthesis in adrenarche.

Authors: Walter L Miller
Journal: Rev Endocr Metab Disord Date: 2009-03 Impact factor: 6.514

8. Haplotypes of the steroid 21-hydroxylase gene region encoding mild steroid 21-hydroxylase deficiency.

Authors: B Haglund-Stengler; E Martin Ritzén; J Gustafsson; H Luthman
Journal: Proc Natl Acad Sci U S A Date: 1991-10-01 Impact factor: 11.205

9. Substitution of Ile-172 to Asn in the steroid 21-hydroxylase B (P450c21B) gene in a Finnish patient with the simple virilizing form of congenital adrenal hyperplasia.

Authors: J Partanen; R D Campbell
Journal: Hum Genet Date: 1991-10 Impact factor: 4.132

10. Molecular analysis of patient and carrier genes with congenital steroid 21-hydroxylase deficiency by using polymerase chain reaction and single strand conformation polymorphism.

Authors: T Tajima; K Fujieda; K Nakayama; Y Fujii-Kuriyama
Journal: J Clin Invest Date: 1993-11 Impact factor: 14.808