نتایج جستجو برای: insensitivity syndrome

تعداد نتایج: 626376  

Journal: :Steroids 1996
H T Brüggenwirth A L Boehmer M C Verleun-Mooijman T Hoogenboezem W J Kleijer B J Otten J Trapman A O Brinkmann

Mutations in the androgen receptor gene in 46,XY individuals can be associated with the androgen insensitivity syndrome, of which the phenotype can vary from a female phenotype to an undervirilized or infertile male phenotype. We have studied the androgen receptor gene of androgen insensitivity patients to get information about amino acid residues or regions involved in DNA binding and transcri...

2016
N. C. Hornig M. Ukat H. U. Schweikert O. Hiort R. Werner S. L. S. Drop M. Cools I. A. Hughes L. Audi S. F. Ahmed J. Demiri P. Rodens L. Worch G. Wehner A. E. Kulle D. Dunstheimer E. Müller-Roßberg T. Reinehr A. T. Hadidi A. K. Eckstein C. van der Horst C. Seif R. Siebert O. Ammerpohl P.-M. Holterhus

CONTEXT Only approximately 85% of patients with a clinical diagnosis complete androgen insensitivity syndrome and less than 30% with partial androgen insensitivity syndrome can be explained by inactivating mutations in the androgen receptor (AR) gene. OBJECTIVE The objective of the study was to clarify this discrepancy by in vitro determination of AR transcriptional activity in individuals wi...

Journal: :Archives of disease in childhood 1993
J A Batch H R Davies B A Evans I A Hughes M N Patterson

The partial androgen insensitivity syndrome occurs in 46,XY subjects with phenotypes ranging from perineoscrotal hypospadias with cryptorchidism and micropenis (mild undervirilisation) to clitoromegaly and partial labial fusion (marked undervirilisation). Within an affected family, wide variation in the degree of genital ambiguity between individuals can be seen. Two cousins of a previously rep...

Journal: :International Journal of Environmental Research and Public Health 2019

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