(Q24310558)

Nuclear receptor subfamily 0 group B member 1

inferred from title

1 reference

GOA release 2020-03-11

male gonad development

1 reference

hypogonadotropic hypogonadism

GOA release 2020-03-11

1 reference

F Muscatelli

1

0 references

Alfons Meindl

6

object named as

A Meindl

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author name string

T M Strom

2

0 references

A P Walker

3

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E Zanaria

4

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D Récan

5

0 references

B Bardoni

7

0 references

S Guioli

8

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G Zehetner

9

0 references

W Rabl

Failure of adrenal androgen to induce puberty in familial cytomegalic adrenocortical hypoplasia

10

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language of work or name

English

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publication date

15 December 1994

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published in

Nature

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volume

372

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issue

6507

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page(s)

672-6

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cites work

1 reference

7 January 2021

A YAC contig in Xp21 containing the adrenal hypoplasia congenita and glycerol kinase deficiency genes

1 reference

7 January 2021

Yeast artificial chromosome cloning in the glycerol kinase and adrenal hypoplasia congenita region of Xp21.

1 reference

7 January 2021

A dosage sensitive locus at chromosome Xp21 is involved in male to female sex reversal

1 reference

7 January 2021

An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita

1 reference

7 January 2021

Direct solid phase sequencing of genomic and plasmid DNA using magnetic beads as solid support.

1 reference

7 January 2021

Nonsense mutations in the human beta-globin gene affect mRNA metabolism

1 reference

7 January 2021

Analysis of factor VIII mRNA reveals defects in everyone of 28 haemophilia A patients

1 reference

7 January 2021

Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A

1 reference

7 January 2021

Illegitimate transcription: transcription of any gene in any cell type

1 reference

7 January 2021

Endocrinology in preadolescents and adolescents. I. Hormonal changes during normal puberty

1 reference

7 January 2021

A cell-specific nuclear receptor is essential for adrenal and gonadal development and sexual differentiation.

1 reference

7 January 2021

Construction, arraying, and high-density screening of large insert libraries of human chromosomes X and 21: their potential use as reference libraries

1 reference

7 January 2021

A cosmid contig and high resolution restriction map of the 2 megabase region containing the Huntington's disease gene

1 reference

7 January 2021

Analysis of cosmids using linearization by phage lambda terminase

1 reference

7 January 2021

A computer program package for restriction map analysis and manipulation

1 reference

7 January 2021

Mutations in the connexin 32 gene in X-linked dominant Charcot-Marie-Tooth disease (CMTX1)

1 reference

7 January 2021

Isolation of the human Xp21 glycerol kinase gene by positional cloning

1 reference

7 January 2021

Gene deletion causing adrenal hypoplasia congenita and hypogonadotrophic hypogonadism

1 reference

7 January 2021

Familial deletion of Xp21.2 with glycerol kinase deficiency and congenital adrenal hypoplasia

1 reference

7 January 2021

Are cysteine-rich and COOH-terminal domains of dystrophin critical for sarcolemmal localization?

1 reference

7 January 2021

Deletion proximal to DXS68 locus (L1 probe site) in a boy with Duchenne muscular dystrophy, glycerol kinase deficiency, and adrenal hypoplasia.

1 reference

7 January 2021