Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomalies (Q24311933)

GOA release 2020-03-11

eye development

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GOA release 2020-03-11

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Ming Ye

1

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Karyn M Berry-Wynne

2

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Mika Asai-Coakwell

3

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Periasamy Sundaresan

4

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Tim Footz

5

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Curtis R French

6

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Marc Abitbol

7

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Valerie C Fleisch

8

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Nathan Corbett

9

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W Ted Allison

10

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Garry Drummond

11

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Michael A Walter

12

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T Michael Underhill

13

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Andrew J Waskiewicz

14

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Ordan J Lehmann

Generation and characterization of a Gdf1 conditional null allele

15

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language of work or name

English

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publication date

15 January 2010

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published in

Human Molecular Genetics

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volume

19

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issue

2

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page(s)

287-98

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cites work

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SWISS-MODEL and the Swiss-PdbViewer: an environment for comparative protein modeling

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Mutations in GDF6 are associated with vertebral segmentation defects in Klippel-Feil syndrome

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Haploinsufficient phenotypes in Bmp4 heterozygous null mice and modification by mutations in Gli3 and Alx4

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Morpholino oligos: making sense of antisense?

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BMP7 null mutation in mice: developmental defects in skeleton, kidney, and eye.

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Mutations in BMP4 cause eye, brain, and digit developmental anomalies: overlap between the BMP4 and hedgehog signaling pathways

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Mutations in BMP4 are associated with subepithelial, microform, and overt cleft lip.

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Synergistic interaction between Gdf1 and Nodal during anterior axis development

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Distinct and cooperative roles of mammalian Vg1 homologs GDF1 and GDF3 during early embryonic development

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Gdf6a is required for the initiation of dorsal-ventral retinal patterning and lens development.

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A transcript from a Drosophila pattern gene predicts a protein homologous to the transforming growth factor-beta family.

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Regulation of left-right patterning in mice by growth/differentiation factor-1

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A novel type of mutation in the cysteine rich domain of the RET receptor causes ligand independent activation

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An essential role for Radar (Gdf6a) in inducing dorsal fate in the zebrafish retina

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Constitutive Activation of Fibroblast Growth Factor Receptor-2 by a Point Mutation Associated with Crouzon Syndrome

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Functional and molecular characterization of naturally occurring mutations in the oocyte-secreted factors bone morphogenetic protein-15 and growth and differentiation factor-9

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Leptin receptor activation depends on critical cysteine residues in its fibronectin type III subdomains

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Requirement for RAR-mediated gene repression in skeletal progenitor differentiation

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BMP action in skeletogenesis involves attenuation of retinoid signaling

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GDF6, a novel locus for a spectrum of ocular developmental anomalies

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Loss-of-function mutations in growth differentiation factor-1 (GDF1) are associated with congenital heart defects in humans

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Incomplete penetrance and phenotypic variability characterize Gdf6-attributable oculo-skeletal phenotypes

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7 January 2021

Uveal coloboma: clinical and basic science update

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A requirement for bone morphogenetic protein-7 during development of the mammalian kidney and eye

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Evolution and classification of cystine knot-containing hormones and related extracellular signaling molecules

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Deficiency of growth differentiation factor 3 protects against diet-induced obesity by selectively acting on white adipose.

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GDF3, a BMP inhibitor, regulates cell fate in stem cells and early embryos

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7 January 2021

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