(Q35668777)

9 August 2017

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title

From panhypopituitarism to combined pituitary deficiencies: do we need the anterior pituitary? (English)

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9 August 2017

Catherine Carrière

1

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9 August 2017

Anatoli Gleiberman

series ordinal

2

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9 August 2017

Chijen R Lin

series ordinal

3

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9 August 2017

Michael G Rosenfeld

series ordinal

4

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9 August 2017

language of work or name

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1 March 2004

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Reviews in Endocrine and Metabolic Disorders

9 August 2017

published in

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9 August 2017

volume

5

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9 August 2017

issue

1

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9 August 2017

page(s)

5-13

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An important role for the IIIb isoform of fibroblast growth factor receptor 2 (FGFR2) in mesenchymal-epithelial signalling during mouse organogenesis.

9 August 2017

cites work

1 reference

12 December 2020

Functional analyses of two newly identified PITX2 mutants reveal a novel molecular mechanism for Axenfeld-Rieger syndrome

1 reference

12 December 2020

Molecular basis of combined pituitary hormone deficiencies

1 reference

12 December 2020

Evolutionary medicine: from dwarf model systems to healthy centenarians?

1 reference

12 December 2020

Integrated FGF and BMP signaling controls the progression of progenitor cell differentiation and the emergence of pattern in the embryonic anterior pituitary

1 reference

12 December 2020

A familial syndrome of isolated "aplasia" of the anterior pituitary. Diagnostic studies and treatment in the neonatal period

1 reference

12 December 2020

The pituitary-specific transcription factor GHF-1 is a homeobox-containing protein

1 reference

12 December 2020

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

1 reference

12 December 2020

Hedgehog signaling is required for pituitary gland development

1 reference

12 December 2020

LHX3 transcription factor mutations associated with combined pituitary hormone deficiency impair the activation of pituitary target genes

1 reference

12 December 2020

Function of Rieger syndrome gene in left-right asymmetry and craniofacial development

1 reference

12 December 2020

The LIM domain: regulation by association

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12 December 2020

Tbx19, a tissue-selective regulator of POMC gene expression

1 reference

12 December 2020

Signaling and transcriptional mechanisms in pituitary development

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12 December 2020

Identification of a Wnt/Dvl/beta-Catenin --> Pitx2 pathway mediating cell-type-specific proliferation during development

1 reference

12 December 2020

The role of SF1 in adrenal and reproductive function: insight from naturally occurring mutations in humans

1 reference

12 December 2020

Specification of pituitary cell lineages by the LIM homeobox gene Lhx3

1 reference

12 December 2020

The mouse homeoprotein mLIM-3 is expressed early in cells derived from the neuroepithelium and persists in adult pituitary.

1 reference

12 December 2020

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

1 reference

12 December 2020

Pitx2 regulates lung asymmetry, cardiac positioning and pituitary and tooth morphogenesis

1 reference

12 December 2020

Identification of a dominant negative homeodomain mutation in Rieger syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Gonadotropin secretion, synthesis, and gene expression in human growth hormone transgenic mice and in Ames dwarf mice

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Developmental origin of the rat adenohypophysis prior to the formation of Rathke's pouch.

1 reference

12 December 2020

Pitx2 is required at multiple stages of pituitary organogenesis: pituitary primordium formation and cell specification.

1 reference

12 December 2020

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

1 reference

12 December 2020

Multistep signaling requirements for pituitary organogenesis in vivo

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12 December 2020

Multistep control of pituitary organogenesis

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12 December 2020

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

12 December 2020

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

1 reference

12 December 2020

T-box genes: what they do and how they do it.

1 reference

12 December 2020

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

1 reference

12 December 2020

A point mutation in the LIM domain of Lhx3 reduces activation of the glycoprotein hormone alpha-subunit promoter

1 reference

12 December 2020

Mutations in PROP1 cause familial combined pituitary hormone deficiency

1 reference

12 December 2020

A tissue-specific enhancer confers Pit-1-dependent morphogen inducibility and autoregulation on the pit-1 gene.

1 reference

12 December 2020

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

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12 December 2020

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

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12 December 2020

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

1 reference

12 December 2020

Development of the ectopically transplanted primordium of epithelial hypophysis (anterior neural ridge) in Bufo japonicus embryos

1 reference

12 December 2020

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

1 reference

12 December 2020

Pituitary ontogeny of the Snell dwarf mouse reveals Pit-1-independent and Pit-1-dependent origins of the thyrotrope.

1 reference

12 December 2020

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

1 reference

12 December 2020

Human Prop-1: cloning, mapping, genomic structure. Mutations in familial combined pituitary hormone deficiency

1 reference

12 December 2020

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

1 reference

12 December 2020

Molecular genetics of Axenfeld-Rieger malformations

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12 December 2020

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

1 reference

12 December 2020

LIM homeodomain factors Lhx3 and Lhx4 assign subtype identities for motor neurons

1 reference

12 December 2020

Tissue interactions in the induction of anterior pituitary: role of the ventral diencephalon, mesenchyme, and notochord

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12 December 2020

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

1 reference

12 December 2020

Steroidogenic factor 1 (SF1) is essential for pituitary gonadotrope function.

1 reference

12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Mapping of the early neural primordium in quail-chick chimeras. II. The prosencephalic neural plate and neural folds: implications for the genesis of cephalic human congenital abnormalities

1 reference

12 December 2020

FGF10 acts as a major ligand for FGF receptor 2 IIIb in mouse multi-organ development

1 reference

12 December 2020

Combined pituitary hormone deficiency due to the F135C human Pit-1 (pituitary-specific factor 1) gene mutation: functional and structural correlates

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12 December 2020

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

1 reference

12 December 2020

The molecular genetics of growth hormone deficiency

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12 December 2020

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

1 reference

12 December 2020

Identification of members of the Wnt signaling pathway in the embryonic pituitary gland

1 reference

12 December 2020

10.1023/B:REMD.0000016120.84792.54

Identifiers

DOI

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Dimensions Publication ID

9 August 2017

1023510376

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