(Q57632581)

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The degree of external genitalia virilization in girls with 21-hydroxylase deficiency appears to be influenced by the CAG repeats in the androgen receptor gene

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The degree of external genitalia virilization in girls with 21-hydroxylase deficiency appears to be influenced by the CAG repeats in the androgen receptor gene (English)

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Emilia Modolo Pinto

object named as

Emília M. Pinto

3

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author name string

Rosana O. Rocha

1

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Ana Elisa C. Billerbeck

2

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Karla F. S. Melo

4

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Chin J. Lin

5

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Carlos A. Longui

6

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Berenice B. Mendonca

7

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Tânia A. S. S. Bachega

8

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publication date

4 September 2007

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Clinical Endocrinology

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0

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070907132242006-???

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The nuclear receptor superfamily: the second decade

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https://api.crossref.org/works/10.1111%2FJ.1365-2265.2007.03023.X

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The length and location of CAG trinucleotide repeats in the androgen receptor N-terminal domain affect transactivation function

1 reference

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21 January 2018

Long Polyglutamine Tracts in the Androgen Receptor Are Associated with Reduced Trans-Activation, Impaired Sperm Production, and Male Infertility

1 reference

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Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy

1 reference

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The CAG repeat within the androgen receptor gene and its relationship to prostate cancer

1 reference

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Effect of the androgen receptor CAG repeat polymorphism on transcriptional activity: specificity in prostate and non-prostate cell lines

1 reference

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Androgen receptor gene CAG length polymorphism in women with polycystic ovary syndrome

1 reference

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Androgen receptor gene CAG repeat polymorphism in the development of ovarian hyperandrogenism.

1 reference

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Three novel mutations in CYP21 gene in Brazilian patients with the classical form of 21-hydroxylase deficiency due to a founder effect

1 reference

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Structure of human steroid 21-hydroxylase genes

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2007.03023.X

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A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2007.03023.X

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Skewed X-chromosome inactivation is common in fetuses or newborns associated with confined placental mosaicism

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2007.03023.X

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X-inactivation analysis in the 1990s: promise and potential problems

1 reference

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High frequency of skewed X inactivation in young breast cancer patients

1 reference

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X-inactivation patterns in human embryonic and extra-embryonic tissues.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2007.03023.X

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Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2007.03023.X

21 January 2018

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10.1111/J.1365-2265.2007.03023.X

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