The forkhead/winged helix gene Mf1 is disrupted in the pleiotropic mouse mutation congenital hydrocephalus (Q28511312)

25 January 2017

title

The forkhead/winged helix gene Mf1 is disrupted in the pleiotropic mouse mutation congenital hydrocephalus (English)

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25 January 2017

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GOA release 2020-03-11

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T. Kume

1

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25 January 2017

K. Y. Deng

2

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25 January 2017

V. Winfrey

3

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25 January 2017

D. B. Gould

4

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25 January 2017

M. A. Walter

5

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25 January 2017

B. L. Hogan

6

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25 January 2017

language of work or name

English

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publication date

12 June 1998

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25 January 2017

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25 January 2017

volume

93

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25 January 2017

issue

6

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25 January 2017

page(s)

985–996

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Partial deletion of chromosome 6p: autopsy findings in a premature infant and review of the literature

25 January 2017

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Co-crystal structure of the HNF-3/fork head DNA-recognition motif resembles histone H5

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TWH regulates the development of subsets of spinal cord neurons

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15-Deoxy-delta 12, 14-prostaglandin J2 is a ligand for the adipocyte determination factor PPAR gamma

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Autosomal dominant Axenfeld-Rieger anomaly maps to 6p25

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The developmental effects of congenital hydrocephalus (ch) in the mouse

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Essential role of stromal mesenchyme in kidney morphogenesis revealed by targeted disruption of Winged Helix transcription factor BF-2

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Developmental expression of murine Beta-trace in embryos and adult animals suggests a function in maturation and maintenance of blood-tissue barriers

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Familial glaucoma iridogoniodysplasia maps to a 6p25 region implicated in primary congenital glaucoma and iridogoniodysgenesis anomaly

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The mesenchymal winged helix transcription factor Fkh6 is required for the control of gastrointestinal proliferation and differentiation

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Five years on the wings of fork head

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The mouse short ear skeletal morphogenesis locus is associated with defects in a bone morphogenetic member of the TGF beta superfamily

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A prostaglandin J2 metabolite binds peroxisome proliferator-activated receptor gamma and promotes adipocyte differentiation

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The chromosomal mapping of four genes encoding winged helix proteins expressed early in mouse development

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Chromosomal localization of six human forkhead genes, freac-1 (FKHL5), -3 (FKHL7), -4 (FKHL8), -5 (FKHL9), -6 (FKHL10), and -8 (FKHL12)

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Colocalization of BMP 7 and BMP 2 RNAs suggests that these factors cooperatively mediate tissue interactions during murine development

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An active tissue-specific enhancer and bound transcription factors existing in a precisely positioned nucleosomal array.

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New member of the winged-helix protein family disrupted in mouse and rat nude mutations

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7 January 2021

Ultrastructure of the mouse leptomeninx

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7 January 2021

The Fork head transcription factor DAF-16 transduces insulin-like metabolic and longevity signals in C. elegans

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7 January 2021

Cloning and characterization of seven human forkhead proteins: binding site specificity and DNA bending

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

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7 January 2021

Autosomal-dominant iridogoniodysgenesis and Axenfeld-Rieger syndrome are genetically distinct

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7 January 2021

The homeotic gene fork head encodes a nuclear protein and is expressed in the terminal regions of the Drosophila embryo

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7 January 2021

The winged-helix transcription factor HNF-3 beta is required for notochord development in the mouse embryo

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7 January 2021

The winged helix transcription factor MFH1 is required for proliferation and patterning of paraxial mesoderm in the mouse embryo

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7 January 2021

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7 January 2021

Winged helix transcription factor BF-1 is essential for the development of the cerebral hemispheres

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7 January 2021

Distal deletion of the short arm of chromosome 6

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7 January 2021

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Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

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Consolidated OpenCitations Corpus – April 2017