(Q33838238)

29 July 2017

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title

Genetic defects of the growth hormone-insulin-like growth factor axis (English)

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29 July 2017

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3

Rosenfeld RG

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29 July 2017

López-Bermejo A

1

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29 July 2017

Buckway CK

series ordinal

2

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29 July 2017

publication date

1 March 2000

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Trends in Endocrinology and Metabolism

29 July 2017

published in

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29 July 2017

volume

11

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29 July 2017

issue

2

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29 July 2017

page(s)

39-49

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

29 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Compound heterozygous deletion of the PROP-1 gene in children with combined pituitary hormone deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Mutations in PROP1 cause familial combined pituitary hormone deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

The Pit-1 transcription factor gene is a candidate for the murine Snell dwarf mutation.

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Rarity of PIT1 involvement in children from Russia with combined pituitary hormone deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Autosomal dominant transmission of isolated growth hormone deficiency in iris-dental dysplasia (Rieger's syndrome).

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

The molecular genetics of growth hormone deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

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%2FS1043-2760%2899%2900226-X

7 January 2021

Extensive Phenotypic Analysis of a Family with Growth Hormone (GH) Deficiency Caused by a Mutation in the GH-Releasing Hormone Receptor Gene

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

The Dwarfs of Sindh: severe growth hormone (GH) deficiency caused by a mutation in the GH-releasing hormone receptor gene.

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Familial dwarfism due to a novel mutation of the growth hormone-releasing hormone receptor gene

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Isolated growth hormone deficiency: testing the little mouse hypothesis in man and exclusion of mutations within the extracellular domain of the growth hormone-releasing hormone receptor

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

X-linked hypogammaglobulinemia and isolated growth hormone deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Brief report: short stature caused by a mutant growth hormone

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Biologically inactive growth hormone caused by an amino acid substitution

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

IGF-I deficiency due to GH receptor deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

A single amino acid substitution in the exoplasmic domain of the human growth hormone (GH) receptor confers familial GH resistance (Laron syndrome) with positive GH-binding activity by abolishing receptor homodimerization

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Intronic mutation in the growth hormone (GH) receptor gene from a girl with Laron syndrome and extremely high serum GH binding protein: extended phenotypic study in a very large pedigree

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

A dominant-negative mutation of the growth hormone receptor causes familial short stature

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Growth hormone (GH) insensitivity syndrome with high serum GH-binding protein levels caused by a heterozygous splice site mutation of the GH receptor gene producing a lack of intracellular domain

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Intrauterine growth retardation and postnatal growth failure associated with deletion of the insulin-like growth factor I gene

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Effects of recombinant human insulin-like growth factor I (IGF-I) therapy on the growth hormone-IGF system of a patient with a partial IGF-I gene deletion.

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

The hypothalamic-pituitary axis: co-development of two organs

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

How many homeobox genes does it take to make a pituitary gland?

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

The PTX family of homeodomain transcription factors during pituitary developments.

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

A model for the development of the hypothalamic-pituitary axis: transcribing the hypophysis

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Early steps in pituitary organogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Transcription Factors and Hypopituitarism

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Genealogy of the Anterior Pituitary Gland: Tracing a Family Tree.

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Exclusion of growth hormone (GH)-releasing hormone gene mutations in familial isolated GH deficiency by linkage and single strand conformation analysis.

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Anterior pituitary hypoplasia and dwarfism in mice lacking the dopamine transporter

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Gsh-1, an orphan Hox gene, is required for normal pituitary development

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Multistep signaling requirements for pituitary organogenesis in vivo

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Reciprocal interactions of Pit1 and GATA2 mediate signaling gradient-induced determination of pituitary cell types

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Ptx1, a bicoid-related homeo box transcription factor involved in transcription of the pro-opiomelanocortin gene

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

P-OTX: a PIT-1-interacting homeodomain factor expressed during anterior pituitary gland development

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Role of the Bicoid-related homeodomain factor Pitx1 in specifying hindlimb morphogenesis and pituitary development

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Specification of pituitary cell lineages by the LIM homeobox gene Lhx3

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Multistep control of pituitary organogenesis.

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

P-Lim, a LIM homeodomain factor, is expressed during pituitary organ and cell commitment and synergizes with Pit-1.

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

A family of LIM domain-associated cofactors confer transcriptional synergism between LIM and Otx homeodomain proteins

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Identification of a novel zinc finger protein binding a conserved element critical for Pit-1-dependent growth hormone gene expression

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Multiple pituitary and ovarian defects in Krox-24 (NGFI-A, Egr-1)-targeted mice.

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Growth hormone deficiency with ectopic neurohypophysis: anatomical variations and relationship between the visibility of the pituitary stalk asserted by magnetic resonance imaging and anterior pituitary function

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Hypothalamic-pituitary function in patients with craniopharyngiomas

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Short stature associated with high circulating insulin-like growth factor (IGF)-binding protein-1 and low circulating IGF-II: effect of growth hormone therapy.

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Serum levels of insulin-like growth factor binding proteins in Ecuadorean children with growth hormone insensitivity

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Insulin-like growth factor-I resistance

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

GHRH receptor of little mice contains a missense mutation in the extracellular domain that disrupts receptor function

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Molecular basis of the little mouse phenotype and implications for cell type-specific growth

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Molecular mechanism of growth hormone (GH) deficiency in the spontaneous dwarf rat: detection of abnormal splicing of GH messenger ribonucleic acid by the polymerase chain reaction

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

A mammalian model for Laron syndrome produced by targeted disruption of the mouse growth hormone receptor/binding protein gene (the Laron mouse)

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Laron dwarfism and mutations of the growth hormone-receptor gene

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Characterization of the human growth hormone receptor gene and demonstration of a partial gene deletion in two patients with Laron-type dwarfism

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Gsh-4 encodes a LIM-type homeodomain, is expressed in the developing central nervous system and is required for early postnatal survival

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Jak2 is essential for signaling through a variety of cytokine receptors

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

Requirement of STAT5b for sexual dimorphism of body growth rates and liver gene expression

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2899%2900226-X

7 January 2021

10.1016/S1043-2760(99)00226-X

Identifiers

DOI

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29 July 2017

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