(Q35197885)

7 August 2017

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title

DNA testing in patients with GH deficiency at the time of transition (English)

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7 August 2017

Dattani MT

1

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7 August 2017

publication date

1 August 2003

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Growth Hormone & I G F Research

7 August 2017

published in

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7 August 2017

volume

13 Suppl A

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7 August 2017

page(s)

S122-9

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Signaling mechanisms in pituitary morphogenesis and cell fate determination

7 August 2017

cites work

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Mapping of the presumptive brain regions in the neural plate of Xenopus laevis

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7 January 2021

Multistep control of pituitary organogenesis

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7 January 2021

Multistep signaling requirements for pituitary organogenesis in vivo

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7 January 2021

Early steps in pituitary organogenesis

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7 January 2021

Signaling and transcriptional control of pituitary development.

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7 January 2021

Pituitary cell phenotypes involve cell-specific Pit-1 mRNA translation and synergistic interactions with other classes of transcription factors

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7 January 2021

In situ hybridization analysis of anterior pituitary hormone gene expression during fetal mouse development

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7 January 2021

Dwarf locus mutants lacking three pituitary cell types result from mutations in the POU-domain gene pit-1.

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7 January 2021

The nuclear receptor steroidogenic factor 1 acts at multiple levels of the reproductive axis

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7 January 2021

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

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7 January 2021

Sequence, genomic organization, and expression of the novel homeobox gene Hesx1.

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7 January 2021

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

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7 January 2021

Septo-optic dysplasia and pituitary dwarfism

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7 January 2021

Hormonal, metabolic, and neuroradiologic abnormalities associated with septo-optic dysplasia

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7 January 2021

The endocrine spectrum of septo-optic dysplasia

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7 January 2021

Sexual precocity in association with septo-optic dysplasia and hypothalamic hypopituitarism

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7 January 2021

Hypothalamic defects in two adult patients with septo-optic dysplasia

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7 January 2021

Growth hormone deficiency of hypothalamic origin in septo-optic dysplasia.

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7 January 2021

Why is the retention of gonadotrophin secretion common in children with panhypopituitarism due to septo-optic dysplasia?

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7 January 2021

Evidence for possible Mendelian inheritance of septo-optic dysplasia.

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7 January 2021

Hypopituitarism and septooptic "dysplasia" in first cousins

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7 January 2021

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

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7 January 2021

Expression pattern of the murine LIM class homeobox gene Lhx3 in subsets of neural and neuroendocrine tissues

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7 January 2021

Specification of pituitary cell lineages by the LIM homeobox gene Lhx3

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7 January 2021

Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency

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7 January 2021

Syndromic short stature in patients with a germline mutation in the LIM homeobox LHX4.

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7 January 2021

Cretinism with combined hormone deficiency caused by a mutation in the PIT1 gene

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7 January 2021

A mutation in the POU-homeodomain of Pit-1 responsible for combined pituitary hormone deficiency

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7 January 2021

Mutation of the POU-specific domain of Pit-1 and hypopituitarism without pituitary hypoplasia

1 reference

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7 January 2021

The POU domain: a large conserved region in the mammalian pit-1, oct-1, oct-2, and Caenorhabditis elegans unc-86 gene products

1 reference

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7 January 2021

Pituitary lineage determination by the Prophet of Pit-1 homeodomain factor defective in Ames dwarfism

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7 January 2021

Mutations in PROP1 cause familial combined pituitary hormone deficiency

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7 January 2021

"Hot spot" in the PROP1 gene responsible for combined pituitary hormone deficiency

1 reference

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7 January 2021

Longitudinal hormonal and pituitary imaging changes in two females with combined pituitary hormone deficiency due to deletion of A301,G302 in the PROP1 gene

1 reference

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7 January 2021

The molecular genetics of growth hormone deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS1096-6374%2803%2900068-6

7 January 2021

Brief report: short stature caused by a mutant growth hormone

1 reference

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7 January 2021

Autosomal dominant GH deficiency due to an Arg183His GH-1 gene mutation: clinical and molecular evidence of impaired regulated GH secretion

1 reference

https://api.crossref.org/works/10.1016%2FS1096-6374%2803%2900068-6

7 January 2021

Nonsense mutation in the human growth hormone-releasing hormone receptor causes growth failure analogous to the little (lit) mouse

1 reference

https://api.crossref.org/works/10.1016%2FS1096-6374%2803%2900068-6

7 January 2021

Phenotype and genetic analysis of a syndrome caused by an inactivating mutation in the growth hormone-releasing hormone receptor: Dwarfism of Sindh

1 reference

https://api.crossref.org/works/10.1016%2FS1096-6374%2803%2900068-6

7 January 2021

10.1016/S1096-6374(03)00068-6

Identifiers

DOI

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7 August 2017

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