(Q24323305)

GOA release 2020-03-11

brain development

1 reference

Homeobox gene expressed in ES cells

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

septo-optic dysplasia

1 reference

J K Wales

9

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author name string

M T Dattani

1

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J P Martinez-Barbera

2

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P Q Thomas

3

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J M Brickman

4

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R Gupta

5

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I L Mårtensson

6

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H Toresson

7

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M Fox

8

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P C Hindmarsh

10

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S Krauss

11

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R S Beddington

12

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I C Robinson

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

13

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language of work or name

English

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publication date

June 1998

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published in

Nature Genetics

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volume

19

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page(s)

125-33

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issue

2

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cites work

1 reference

The early formation of the corpus callosum: a light and electron microscopic study in foetal and neonatal rats.

21 January 2018

1 reference

Sonic hedgehog, a member of a family of putative signaling molecules, is implicated in the regulation of CNS polarity

21 January 2018

1 reference

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

21 January 2018

1 reference

Hesx1, a homeobox gene expressed by murine embryonic stem cells, maps to mouse chromosome 14, bands A3-B.

21 January 2018

1 reference

Evidence for possible Mendelian inheritance of septo-optic dysplasia.

21 January 2018

1 reference

High resolution crystal structure of a paired (Pax) class cooperative homeodomain dimer on DNA

21 January 2018

1 reference

Crystal structure of an engrailed homeodomain-DNA complex at 2.8 A resolution: a framework for understanding homeodomain-DNA interactions

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 Xenopus Brachyury promoter is activated by FGF and low concentrations of activin and suppressed by high concentrations of activin and by paired-type homeodomain proteins

21 January 2018

1 reference

Septo-optic dysplasia and pituitary dwarfism

21 January 2018

1 reference

The endocrine spectrum of septo-optic dysplasia.

21 January 2018

1 reference

Hypopituitarism and septooptic "dysplasia" in first cousins.

21 January 2018

1 reference

Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor

21 January 2018

1 reference

Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly.

21 January 2018

1 reference

The molecular basis of Boston-type craniosynostosis: the Pro148-->His mutation in the N-terminal arm of the MSX2 homeodomain stabilizes DNA binding without altering nucleotide sequence preferences

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

A human MSX1 homeodomain missense mutation causes selective tooth agenesis

21 January 2018

1 reference

A homeodomain point mutation of the Drosophila proboscipedia protein provokes eye loss independently of homeotic function.

21 January 2018

1 reference

Diabetes insipidus with impaired osmotic regulation in septo-optic dysplasia and agenesis of the corpus callosum

21 January 2018

1 reference

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

21 January 2018

1 reference

Wild-type endoderm abrogates the ventral developmental defects associated with GATA-4 deficiency in the mouse.

21 January 2018

1 reference

An Fgf8 mutant allelic series generated by Cre- and Flp-mediated recombination

21 January 2018

1 reference

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

21 January 2018

1 reference

Specification of pituitary cell lineages by the LIM homeobox gene Lhx3

21 January 2018

1 reference

Mutations in PROP1 cause familial combined pituitary hormone deficiency

21 January 2018

1 reference

Determinants of binding-site specificity among yeast C6 zinc cluster proteins

21 January 2018

1 reference

Interactions of a Rel protein with its inhibitor.

21 January 2018

1 reference

Irradiation hybrids for human chromosome 11: characterization and use for generating region-specific markers in 11q14-q23.

21 January 2018

1 reference

21 January 2018

Septo-optic Dysplasia

1 reference

7 January 2021

Hormonal, metabolic, and neuroradiologic abnormalities associated with septo-optic dysplasia

1 reference

7 January 2021

Reciprocal effect of Waardenburg syndrome mutations on DNA binding by the Pax-3 paired domain and homeodomain

1 reference

7 January 2021

Hypothalamic defects in two adult patients with septo-optic dysplasia

1 reference

7 January 2021

Agenesis of the corpus callosum and macrocephaly in siblings.

1 reference

7 January 2021