Growth hormone and IGF-1. (Q35668780)

9 August 2017

1 reference

title

Growth hormone and IGF-1. (English)

1 reference

9 August 2017

Roberto Salvatori

1

1 reference

9 August 2017

publication date

1 March 2004

1 reference

Reviews in Endocrine and Metabolic Disorders

9 August 2017

published in

1 reference

9 August 2017

volume

5

1 reference

9 August 2017

issue

1

1 reference

9 August 2017

page(s)

15-23

1 reference

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

9 August 2017

cites work

1 reference

12 December 2020

Magnetic resonance imaging study of pituitary morphology in subjects homozygous and heterozygous for a null mutation of the GHRH receptor gene

1 reference

12 December 2020

Brief report: short stature caused by a mutant growth hormone

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Three new mutations in the gene for the growth hormone (gh)-releasing hormone receptor in familial isolated gh deficiency type ib.

1 reference

12 December 2020

Biologically inactive growth hormone caused by an amino acid substitution

1 reference

12 December 2020

Endocrine function and morphological findings in patients with disorders of the hypothalamo-pituitary area: a study with magnetic resonance

1 reference

12 December 2020

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

1 reference

12 December 2020

Familial isolated growth hormone deficiency is associated with increased systolic blood pressure, central obesity, and dyslipidemia.

1 reference

12 December 2020

Detection of a recurring mutation in the human growth hormone-releasing hormone receptor gene

1 reference

12 December 2020

Prevalence of Human GH-1 Gene Alterations in Patients with Isolated Growth Hormone Deficiency

1 reference

12 December 2020

Ghrelin is a growth-hormone-releasing acylated peptide from stomach

1 reference

12 December 2020

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

1 reference

12 December 2020

A novel IVS2 -2A>T splicing mutation in the GH-1 gene in familial isolated growth hormone deficiency type II in the spectrum of other splicing mutations in the Russian population

1 reference

12 December 2020

Growth hormone (GH) insensitivity due to primary GH receptor deficiency

1 reference

12 December 2020

Autosomal dominant growth hormone (GH) deficiency type II: the Del32-71-GH deletion mutant suppresses secretion of wild-type GH.

1 reference

12 December 2020

Novel mutations of the growth hormone 1 (GH1) gene disclosed by modulation of the clinical selection criteria for individuals with short stature

1 reference

12 December 2020

Serum GH response to pharmacological stimuli and physical exercise in two siblings with two new inactivating mutations in the GH-releasing hormone receptor gene

1 reference

12 December 2020

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

1 reference

12 December 2020

Deletions of the homeobox gene SHOX (short stature homeobox) are an important cause of growth failure in children with short stature

1 reference

12 December 2020

A new missense mutation in the growth hormone-releasing hormone receptor gene in familial isolated GH deficiency.

1 reference

12 December 2020

Autosomal dominant growth hormone deficiency disrupts secretory vesicles in vitro and in vivo in transgenic mice.

1 reference

12 December 2020

Neuroendocrine control of growth hormone secretion

1 reference

12 December 2020

Growth hormone receptor and serum binding protein: purification, cloning and expression

1 reference

12 December 2020

Genetic pituitary dwarfism with high serum concentation of growth hormone--a new inborn error of metabolism?

1 reference

12 December 2020

Pituitary size in patients with Laron syndrome (primary GH insensitivity).

1 reference

12 December 2020

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

1 reference

12 December 2020

Growth failure with normal serum RIA-GH and low somatomedin activity: somatomedin restoration and growth acceleration after exogenous GH

1 reference

12 December 2020

Pseudoexon activation as a novel mechanism for disease resulting in atypical growth-hormone insensitivity

1 reference

12 December 2020

An exon splice enhancer mutation causes autosomal dominant GH deficiency

1 reference

12 December 2020

MR imaging in idiopathic growth hormone deficiency.

1 reference

12 December 2020

Identification of Binding Domains of the Growth Hormone-Releasing Hormone Receptor by Analysis of Mutant and Chimeric Receptor Proteins

1 reference

12 December 2020

Pituitary hypoplasia in patients with a mutation in the growth hormone-releasing hormone receptor gene

1 reference

12 December 2020

Growth hormone-releasing peptide-2 stimulates GH secretion in GH-deficient patients with mutated GH-releasing hormone receptor

1 reference

12 December 2020

Decreased expression of the GHRH receptor gene due to a mutation in a Pit-1 binding site.

1 reference

12 December 2020

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

1 reference

12 December 2020

Abnormal GH receptor signaling in children with idiopathic short stature

1 reference

12 December 2020

Four contiguous amino acid substitutions, identified in patients with Laron syndrome, differently affect the binding affinity and intracellular trafficking of the growth hormone receptor

1 reference

12 December 2020

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

1 reference

12 December 2020

Phenotype: Genotype Relationships in Growth Hormone Insensitivity Syndrome1

1 reference

12 December 2020

Pulsatile growth hormone secretion persists in genetic growth hormone-releasing hormone resistance.

1 reference

12 December 2020

Isolated growth hormone (GH) deficiency due to compound heterozygosity for two new mutations in the GH-releasing hormone receptor gene

1 reference

12 December 2020

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

12 December 2020

Hot spots for growth hormone gene deletions in homologous regions outside of Alu repeats

1 reference

12 December 2020

In vitro and in vivo responses to short-term recombinant human insulin-like growth factor-1 (IGF-I) in a severely growth-retarded girl with ring chromosome 15 and deletion of a single allele for the type 1 IGF receptor gene.

1 reference

12 December 2020

Signal transduction via the growth hormone receptor

1 reference

12 December 2020

Normal pituitary size in two patients with growth hormone gene deletion

1 reference

12 December 2020

[Isolated GH deficiency due to inactivating mutation of GHRH receptor]

1 reference

12 December 2020

Growth hormone (GH) secretion in patients with an inactivating defect of the GH-releasing hormone (GHRH) receptor is pulsatile: evidence for a role for non-GHRH inputs into the generation of GH pulses

1 reference

12 December 2020

Stature in Ecuadorians heterozygous for growth hormone receptor gene E180 splice mutation does not differ from that of homozygous normal relatives

1 reference

12 December 2020

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

1 reference

12 December 2020

Growth hormone insensitivity associated with a STAT5b mutation

1 reference

12 December 2020

The essential role of IGF-I: lessons from the long-term study and treatment of children and adults with Laron syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Extensive Phenotypic Analysis of a Family with Growth Hormone (GH) Deficiency Caused by a Mutation in the GH-Releasing Hormone Receptor Gene1

1 reference

12 December 2020

Molecular basis for familial isolated growth hormone deficiency

1 reference

12 December 2020

Isolated GH deficiency (IGHD) type II: imaging of the pituitary gland by magnetic resonance reveals characteristic differences in comparison with severe IGHD of unknown origin

1 reference

12 December 2020

10.1023/B:REMD.0000016121.58762.6D

Identifiers

DOI

1 reference

Dimensions Publication ID

9 August 2017

1029357601

0 references

1 reference