Clinical and molecular evidence for the role of androgens and WT1 in testis descent (Q28209893)

Molecular and Cellular Endocrinology

Europe PubMed Central

title

Clinical and molecular evidence for the role of androgens and WT1 in testis descent (English)

0 references

author name string

H N Lim

series ordinal

1

0 references

I A Hughes

series ordinal

2

0 references

J R Hawkins

series ordinal

3

0 references

language of work or name

English

0 references

publication date

20 December 2001

0 references

published in

0 references

volume

185

0 references

issue

1-2

0 references

page(s)

43-50

0 references

cites work

Phenotypic features, androgen receptor binding, and mutational analysis in 278 clinical cases reported as androgen insensitivity syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

WT1 mutations associated with incomplete Denys-Drash syndrome define a domain predicted to behave in a dominant-negative fashion

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Testicular position in the androgen insensitivity syndrome: implications for the role of androgens in testicular descent

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

A stochastic model of temporally regulated generation of oligodendrocytes in cell culture.

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Functional characterization of naturally occurring mutant androgen receptors from subjects with complete androgen insensitivity

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Germline intronic and exonic mutations in the Wilms' tumour gene (WT1) affecting urogenital development

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Studies of the androgen receptor in dispersed fibroblasts: investigation of patients with androgen insensitivity.

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Testicular feminization: a model for testicular descent in mice and men

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Single amino acid substitution (840Arg-->His) in the hormone-binding domain of the androgen receptor leads to incomplete androgen insensitivity syndrome associated with a thermolabile androgen receptor

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

The diagnosis of 5 alpha-reductase deficiency in infancy

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Bilateral Wilms tumor in a boy with severe hypospadias and cryptochidism due to a heterozygous mutation in the WT1 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

A clinical overview of WT1 gene mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Evidence that WT1 mutations in Denys — Drash syndrome patients may act in a dominant-negative fashion

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Male pseudohermaphroditism, partial androgen receptors defect, 11p13 deletion: indication of gene localization

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Wilms' tumor 1 and Dax-1 modulate the orphan nuclear receptor SF-1 in sex-specific gene expression

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Cryptorchidism in mice mutant for Insl3

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

WT1 mutations in patients with Denys-Drash syndrome: a novel mutation in exon 8 and paternal allele origin

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Constitutional and somatic mutations in theWTI gene in wilms' tumor patients

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

A novel insertional mutation at the third zinc finger coding region of the WT1 gene in Denys-Drash syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Dihydrotestosterone and Its Relationship to Testosterone in Infancy and Childhood*

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumour

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Stochastic mechanism of cellular aging--abrupt telomere shortening as a model for stochastic nature of cellular aging

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Exon skipping due to a mutation in a donor splice site in the WT-1 gene is associated with Wilms' tumor and severe genital malformations

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Correlation of germ-line mutations and two-hit inactivation of the WT1 gene with Wilms tumors of stromal-predominant histology

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

1 reference

7 January 2021

Partial androgen receptor deficiency and mixed gonadal dysgenesis in Drash syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Pituitary-Gonadal Relations in Infancy: 2. Patterns of Serum Gonadal Steroid Concentrations in Man from Birth to Two Years of Age

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Targeted disruption of the Insl3 gene causes bilateral cryptorchidism

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021