Novel insights into the aetiology and pathogenesis of hypopituitarism (Q34367104)

1 August 2017

1 reference

title

Novel insights into the aetiology and pathogenesis of hypopituitarism (English)

1 reference

1 August 2017

1

Mehul T Dattani

1 reference

1 August 2017

language of work or name

1 reference

1 January 2004

1 reference

1 August 2017

1 reference

1 August 2017

volume

62 Suppl 3

1 reference

1 August 2017

page(s)

1-13

1 reference

Early steps in pituitary organogenesis

1 August 2017

cites work

1 reference

Signaling and transcriptional control of pituitary development.

21 January 2018

1 reference

Signaling and transcriptional mechanisms in pituitary development

21 January 2018

1 reference

Paired-like repression/activation in pituitary development

21 January 2018

1 reference

Pituitary development: regulatory codes in mammalian organogenesis

21 January 2018

1 reference

Molecular basis of combined pituitary hormone deficiencies

21 January 2018

1 reference

The molecular basis for developmental disorders of the pituitary gland in man.

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Signal-specific co-activator domain requirements for Pit-1 activation

21 January 2018

1 reference

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

21 January 2018

1 reference

The Ames dwarf gene, df, is required early in pituitary ontogeny for the extinction of Rpx transcription and initiation of lineage-specific cell proliferation.

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Pituitary homeobox 2, a novel member of the bicoid-related family of homeobox genes, is a potential regulator of anterior structure formation.

21 January 2018

1 reference

Pitx2, a bicoid-type homeobox gene, is involved in a lefty-signaling pathway in determination of left-right asymmetry

21 January 2018

1 reference

Multistep control of pituitary organogenesis.

21 January 2018

1 reference

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

21 January 2018

1 reference

Nuclear receptor DAX-1 recruits nuclear receptor corepressor N-CoR to steroidogenic factor 1

21 January 2018

1 reference

Steroidogenic factor 1 and Dax-1 colocalize in multiple cell lineages: potential links in endocrine development.

21 January 2018

1 reference

The Ames dwarf gene is required for Pit-1 gene activation.

21 January 2018

1 reference

A tissue-specific transcription factor containing a homeodomain specifies a pituitary phenotype

21 January 2018

1 reference

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

21 January 2018

1 reference

Septo-optic dysplasia/optic nerve hypoplasia: data from the National Cooperative Growth Study (NCGS).

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features

21 January 2018

1 reference

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

21 January 2018

1 reference

The molecular basis of hypopituitarism

21 January 2018

1 reference

The PROP1 2-base pair deletion is a common cause of combined pituitary hormone deficiency

21 January 2018

1 reference

Mutations in PROP1 cause familial combined pituitary hormone deficiency

21 January 2018

1 reference

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

21 January 2018

1 reference

A unique case of combined pituitary hormone deficiency caused by a PROP1 gene mutation (R120C) associated with normal height and absent puberty

21 January 2018

1 reference

Adrenocorticotropin deficiency in combined pituitary hormone deficiency patients homozygous for a novel PROP1 deletion

21 January 2018

1 reference

Impaired adrenocorticotropin-adrenal axis in combined pituitary hormone deficiency caused by a two-base pair deletion (301-302delAG) in the prophet of Pit-1 gene

21 January 2018

1 reference

Central hypocortisolism as part of combined pituitary hormone deficiency due to mutations of PROP-1 gene

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Transcription factor SOX3 is involved in X-linked mental retardation with growth hormone deficiency

21 January 2018

1 reference

A novel mechanism for isolated central hypothyroidism: inactivating mutations in the thyrotropin-releasing hormone receptor gene

21 January 2018

1 reference

Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans

21 January 2018

1 reference

Obesity and impaired prohormone processing associated with mutations in the human prohormone convertase 1 gene

21 January 2018

1 reference

Brief report: impaired processing of prohormones associated with abnormalities of glucose homeostasis and adrenal function

21 January 2018

1 reference

Small-intestinal dysfunction accompanies the complex endocrinopathy of human proprotein convertase 1 deficiency

21 January 2018

1 reference

A pituitary cell-restricted T box factor, Tpit, activates POMC transcription in cooperation with Pitx homeoproteins

21 January 2018

1 reference

Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome.

21 January 2018

1 reference

Inherited disorders of GnRH and gonadotropin receptors

21 January 2018

1 reference

Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54

21 January 2018

1 reference

Congenital leptin deficiency is associated with severe early-onset obesity in humans

21 January 2018

1 reference

A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction

21 January 2018

1 reference

Effects of recombinant leptin therapy in a child with congenital leptin deficiency.

21 January 2018

1 reference

Mutant vasopressin precursors that cause autosomal dominant neurohypophyseal diabetes insipidus retain dimerization and impair the secretion of wild-type proteins.

21 January 2018

1 reference

Autosomal recessive familial neurohypophyseal diabetes insipidus with continued secretion of mutant weakly active vasopressin.

21 January 2018

1 reference

The molecular genetics of growth hormone deficiency

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1159/000080493

1 reference

release_oiaswpcmajfktlhxbhc2hcar7u

1 August 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/oiaswpcmajfktlhxbhc2hcar7u

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference