DAX1: Increasing complexity in the roles of this novel nuclear receptor (Q24671523)

Molecular and Cellular Endocrinology

Europe PubMed Central

title

DAX1: Increasing complexity in the roles of this novel nuclear receptor (English)

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author name string

Edward R B McCabe

series ordinal

1

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language of work or name

English

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publication date

February 2007

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published in

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volume

265-266

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page(s)

179-82

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cites work

Dosage-sensitive sex reversal adrenal hypoplasia congenita critical region on the X chromosome, gene 1 (DAX1) (NR0B1) and small heterodimer partner (SHP) (NR0B2) form homodimers individually, as well as DAX1-SHP heterodimers

1 reference

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Molecular mechanisms of DAX1 action

7 April 2017

1 reference

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DAX1 origin, function, and novel role

7 April 2017

1 reference

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Role of Ahch in gonadal development and gametogenesis

7 April 2017

1 reference

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Dax1 antagonizes Sry action in mammalian sex determination

7 April 2017

1 reference

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

7 April 2017

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Novel role for the orphan nuclear receptor Dax1 in embryogenesis, different from steroidogenesis

7 April 2017

1 reference

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Nr0b1 and its network partners are expressed early in murine embryos prior to steroidogenic axis organogenesis

7 April 2017

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Zebrafish dax1 is required for development of the interrenal organ, the adrenal cortex equivalent

7 April 2017

1 reference

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Generation of two distinct functional isoforms of dosage-sensitive sex reversal-adrenal hypoplasia congenita-critical region on the X chromosome gene 1 (DAX-1) by alternative splicing

28 September 2017

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1847396

DAX1 and its network partners: exploring complexity in development

28 September 2017

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28 September 2017

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Mutations in NR0B1 (DAX1) and NR5A1 (SF1) responsible for adrenal hypoplasia congenita

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1847396

Consequences of complexity within biological networks: robustness and health, or vulnerability and disease

28 September 2017

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Modifier genes convert "simple" Mendelian disorders to complex traits

28 September 2017

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Phenotypes of patients with "simple" Mendelian disorders are complex traits: thresholds, modifiers, and systems dynamics

28 September 2017

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A familial missense mutation in the hinge region of DAX1 associated with late-onset AHC in a prepubertal female.

30 May 2018

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NR0B1A: an alternatively spliced form of NR0B1.

28 November 2018

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Familial occurrence of Addison's disease

28 November 2018

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Nine novel mutations in NR0B1 (DAX1) causing adrenal hypoplasia congenita.

28 November 2018

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Congenital adrenal hypoplasia: clinical spectrum, experience with hormonal diagnosis, and report on new point mutations of the DAX-1 gene.

28 November 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1847396

Glycerol kinase deficiency with neuromuscular, skeletal, and adrenal abnormalities

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17210221

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.MCE.2006.12.017

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4896916

4896916

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1 reference

1 reference