(Q33942188)

30 July 2017

1 reference

title

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

1 reference

30 July 2017

Dattani MT

1

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30 July 2017

Robinson IC

series ordinal

2

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30 July 2017

language of work or name

1 reference

1 May 2000

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30 July 2017

1 reference

30 July 2017

volume

57

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30 July 2017

issue

5

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30 July 2017

page(s)

337-346

1 reference

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

30 July 2017

cites work

1 reference

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Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux.

21 January 2018

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An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome

21 January 2018

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Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene

21 January 2018

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Genomic structure, evolutionary conservation and aniridia mutations in the human PAX6 gene

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A human MSX1 homeodomain missense mutation causes selective tooth agenesis

21 January 2018

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A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis

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21 January 2018

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Mutations in PROP1 cause familial combined pituitary hormone deficiency

21 January 2018

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

21 January 2018

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

21 January 2018

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Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome

21 January 2018

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21 January 2018

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Effects of brain and mesenchyme upon the cytogenesis of rat adenohypophysis in vitro. I. Differentiation of adrenocorticotropes.

21 January 2018

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An organ culture study on the site of determination of ACTH and LH cells in the rat adenohypophysis

21 January 2018

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Effect of the basal diencephalon on the development of Rathke's pouch in rats: a study in combined organ cultures

21 January 2018

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21 January 2018

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21 January 2018

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The T/ebp null mouse: thyroid-specific enhancer-binding protein is essential for the organogenesis of the thyroid, lung, ventral forebrain, and pituitary

21 January 2018

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21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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Otlx2, an Otx-related homeobox gene expressed in the pituitary gland and in a restricted pattern in the forebrain

21 January 2018

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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

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

21 January 2018

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The transcription factor Pitx2 mediates situs-specific morphogenesis in response to left-right asymmetric signals

21 January 2018

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lefty-1 is required for left-right determination as a regulator of lefty-2 and nodal

21 January 2018

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Pitx2 participates in the late phase of the pathway controlling left-right asymmetry

21 January 2018

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Pitx2 determines left-right asymmetry of internal organs in vertebrates.

21 January 2018

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Cloning and expression pattern of chicken Pitx2: a new component in the SHH signaling pathway controlling embryonic heart looping

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

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Specification of pituitary cell lineages by the LIM homeobox gene Lhx3

21 January 2018

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Multistep control of pituitary organogenesis.

21 January 2018

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Multistep signaling requirements for pituitary organogenesis in vivo

21 January 2018

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Early steps in pituitary organogenesis

21 January 2018

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

21 January 2018

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

21 January 2018

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A cell-specific nuclear receptor is essential for adrenal and gonadal development and sexual differentiation.

21 January 2018

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

21 January 2018

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Effects of Prolactin (PRL) on Pituitary and Testicular Function in Mice with Hereditary PRL Deficiency

21 January 2018

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

21 January 2018

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

21 January 2018

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Transcriptional mechanisms in anterior pituitary cell differentiation

21 January 2018

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

21 January 2018

1 reference

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

21 January 2018

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Mutations in the Pit-1 gene in children with combined pituitary hormone deficiency

21 January 2018

1 reference

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Septo-optic dysplasia and pituitary dwarfism

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570503.X

The endocrine spectrum of septo-optic dysplasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570503.X

Evidence for possible Mendelian inheritance of septo-optic dysplasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570503.X

Hypopituitarism and septooptic "dysplasia" in first cousins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570503.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570503.X

Early evolutionary origin of major homeodomain sequence classes

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570503.X

inferred from DOI database lookup

7 January 2021

based on heuristic

A plus-one frameshift mutation in PAX3 alters the entire deduced amino acid sequence of the paired box in a Waardenburg syndrome type 1 (WS1) family

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570503.X

inferred from DOI database lookup

7 January 2021

based on heuristic

Septo-optic Dysplasia

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570503.X

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1034/J.1399-0004.2000.570503.X

1 reference

30 July 2017

1 reference