(Q41496210)

English

Analysis of mouse models carrying the I26T and R160C substitutions in the transcriptional repressor HESX1 as models for septo-optic dysplasia and hypopituitarism

scientific article published on 6 November 2008

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

1 October 2017

Analysis of mouse models carrying the I26T and R160C substitutions in the transcriptional repressor HESX1 as models for septo-optic dysplasia and hypopituitarism (English)

1 reference

Europe PubMed Central

PMC publication ID

1 October 2017

septo-optic dysplasia

1 reference

based on heuristic

inferred from title

Cynthia L Andoniadou

object named as

Cynthia L Andoniadou

4

0 references

Juan Pedro Martinez-Barbera

object named as

Juan Pedro Martinez-Barbera

10

0 references

Heather Etchevers

object named as

Heather C Etchevers

7

0 references

Carles Gaston-Massuet

2

object named as

Carles Gaston-Massuet

1 reference

Europe PubMed Central

PMC publication ID

1 October 2017

Daniel Kelberman

5

object named as

Daniel Kelberman

1 reference

Europe PubMed Central

PMC publication ID

1 October 2017

Mehul T Dattani

9

object named as

Mehul T Dattani

1 reference

Europe PubMed Central

PMC publication ID

1 October 2017

Dianne Gerrelli

8

object named as

Dianne Gerrelli

1 reference

Europe PubMed Central

PMC publication ID

1 October 2017

author name string

Ezat Sajedi

1

1 reference

Europe PubMed Central

PMC publication ID

1 October 2017

Massimo Signore

3

1 reference

Europe PubMed Central

PMC publication ID

1 October 2017

Sandra Castro

6

1 reference

Europe PubMed Central

PMC publication ID

1 October 2017

publication date

6 November 2008

1 reference

Europe PubMed Central

PMC publication ID

1 October 2017

Disease Models & Mechanisms

1 reference

Europe PubMed Central

PMC publication ID

1 October 2017

1

1 reference

Europe PubMed Central

PMC publication ID

1 October 2017

4-5

1 reference

Europe PubMed Central

PMC publication ID

1 October 2017

241-254

1 reference

Europe PubMed Central

PMC publication ID

1 October 2017

Genetic interaction between the homeobox transcription factors HESX1 and SIX3 is required for normal pituitary development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

11 June 2018

DNMT1 interacts with the developmental transcriptional repressor HESX1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

11 June 2018

The role of transcription factors implicated in anterior pituitary development in the aetiology of congenital hypopituitarism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

11 June 2018

Lack of the murine homeobox gene Hesx1 leads to a posterior transformation of the anterior forebrain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

11 June 2018

HESX1 mutations are an uncommon cause of septooptic dysplasia and hypopituitarism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

11 June 2018

Novel HESX1 mutations associated with a life-threatening neonatal phenotype, pituitary aplasia, but normally located posterior pituitary and no optic nerve abnormalities

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

11 June 2018

Mutations within Sox2/SOX2 are associated with abnormalities in the hypothalamo-pituitary-gonadal axis in mice and humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

11 June 2018

Homeodomain-mediated beta-catenin-dependent switching events dictate cell-lineage determination

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

11 June 2018

A pharyngeal and ectopic hypophysis in a neonate with craniofacial abnormalities: a case report and review of development and structure

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

11 June 2018

Pituitary hypoplasia and respiratory distress syndrome in Prop1 knockout mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

11 June 2018

WNT5A signaling affects pituitary gland shape

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

11 June 2018

SOX3 is required during the formation of the hypothalamo-pituitary axis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

11 June 2018

A homozygous mutation in HESX1 is associated with evolving hypopituitarism due to impaired repressor-corepressor interaction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

11 June 2018

Enhanced repression by HESX1 as a cause of hypopituitarism and septooptic dysplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

11 June 2018

Six3 repression of Wnt signaling in the anterior neuroectoderm is essential for vertebrate forebrain development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

11 June 2018

Sporadic heterozygous frameshift mutation of HESX1 causing pituitary and optic nerve hypoplasia and combined pituitary hormone deficiency in a Japanese patient

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

11 June 2018

Six3 and Six6 activity is modulated by members of the groucho family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

11 June 2018

Molecular effects of novel mutations in Hesx1/HESX1 associated with human pituitary disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

11 June 2018

Temporal regulation of a paired-like homeodomain repressor/TLE corepressor complex and a related activator is required for pituitary organogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

11 June 2018

Molecular basis of pituitary dysfunction in mouse and human.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

11 June 2018

The homeobox gene Hesx1 is required in the anterior neural ectoderm for normal forebrain formation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

11 June 2018

Generalized lacZ expression with the ROSA26 Cre reporter strain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

11 June 2018

Multistep signaling requirements for pituitary organogenesis in vivo

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

11 June 2018

Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

11 June 2018

An Fgf8 mutant allelic series generated by Cre- and Flp-mediated recombination

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

11 June 2018

Pax2 contributes to inner ear patterning and optic nerve trajectory

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

11 June 2018

Anterior primitive endoderm may be responsible for patterning the anterior neural plate in the mouse embryo

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

11 June 2018

Role of Pit-1 in the gene expression of growth hormone, prolactin, and thyrotropin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

11 June 2018

Specification of pituitary cell lineages by the LIM homeobox gene Lhx3

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

11 June 2018

The mouse Fgf8 gene encodes a family of polypeptides and is expressed in regions that direct outgrowth and patterning in the developing embryo

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

11 June 2018

High resolution crystal structure of a paired (Pax) class cooperative homeodomain dimer on DNA

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

11 June 2018

Winged helix transcription factor BF-1 is essential for the development of the cerebral hemispheres

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

11 June 2018

The Wnt-1 (int-1) proto-oncogene is required for development of a large region of the mouse brain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

11 June 2018

Pax-6, a murine paired box gene, is expressed in the developing CNS

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

11 June 2018

Alu-element insertion in the homeodomain of HESX1 and aplasia of the anterior pituitary.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

19 August 2018

Fate map of the chicken neural plate at stage 4.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

19 August 2018

Ectopic Wnt signal determines the eyeless phenotype of zebrafish masterblind mutant.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

19 August 2018

Heterozygous HESX1 mutations associated with isolated congenital pituitary hypoplasia and septo-optic dysplasia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

19 August 2018

The prenatal pituitary gland--hidden and forgotten.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

19 August 2018

A comparison of Notch, Hes and Grg expression during murine embryonic and post-natal development.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

19 August 2018

Evolution of homeobox genes: Q50 Paired-like genes founded the Paired class

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

19 August 2018

Xwnt-8 and lithium can act upon either dorsal mesodermal or neurectodermal cells to cause a loss of forebrain in Xenopus embryos.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

19 August 2018

Rpx: a novel anterior-restricted homeobox gene progressively activated in the prechordal plate, anterior neural plate and Rathke's pouch of the mouse embryo.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

19 August 2018

Utah Growth Study: growth standards and the prevalence of growth hormone deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2590837

19 August 2018

The molecular genetics of growth hormone deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/19093031

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of severe growth hormone deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/19093031

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Geographical Distribution of Optic Nerve Hypoplasia and Septo-optic Dysplasia in Northwest England

1 reference

https://pubmed.ncbi.nlm.nih.gov/19093031

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Panhypopituitarism: genetic versus acquired etiological factors

1 reference

https://pubmed.ncbi.nlm.nih.gov/19093031

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1242/DMM.000711

1 reference

Europe PubMed Central

PMC publication ID

1 October 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

1 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

1 October 2017

ResearchGate publication ID

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