Ror2 knockout mouse as a model for the developmental pathology of autosomal recessive Robinow syndrome (Q28590779)

31 January 2017

title

Ror2 knockout mouse as a model for the developmental pathology of autosomal recessive Robinow syndrome (English)

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Tyrosine-protein kinase transmembrane receptor ROR2

31 January 2017

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GOA release 2020-03-11

Robinow syndrome

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autosomal recessive Robinow syndrome

inferred from title

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8

Stefan Mundlos

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31 January 2017

Abigail S. Tucker

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author name string

Georg C. Schwabe

1

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31 January 2017

Britta Trepczik

2

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31 January 2017

Kathrin Süring

3

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31 January 2017

Norbert Brieske

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31 January 2017

Paul T. Sharpe

6

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31 January 2017

Yasuhiro Minami

7

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31 January 2017

publication date

1 February 2004

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31 January 2017

published in

Developmental Dynamics

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31 January 2017

volume

229

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31 January 2017

issue

2

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31 January 2017

page(s)

400–410

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Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2.

31 January 2017

cites work

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The synpolydactyly homolog (spdh) mutation in the mouse -- a defect in patterning and growth of limb cartilage elements

21 January 2018

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Expression of the Ror1 and Ror2 receptor tyrosine kinase genes during mouse development

21 January 2018

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Wnt3a plays a major role in the segmentation clock controlling somitogenesis

21 January 2018

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Murine cerberus homologue mCer-1: a candidate anterior patterning molecule

21 January 2018

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HedgehogandBmpGenes Are Coexpressed at Many Diverse Sites of Cell–Cell Interaction in the Mouse Embryo

21 January 2018

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Paraxis: a basic helix-loop-helix protein expressed in paraxial mesoderm and developing somites

21 January 2018

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Requirement of the paraxis gene for somite formation and musculoskeletal patterning

21 January 2018

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Ror2, encoding a receptor-like tyrosine kinase, is required for cartilage and growth plate development

21 January 2018

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From head to tail: links between the segmentation clock and antero-posterior patterning of the embryo

21 January 2018

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A C. elegans Ror receptor tyrosine kinase regulates cell motility and asymmetric cell division

21 January 2018

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Mutations in IHH, encoding Indian hedgehog, cause brachydactyly type A-1

21 January 2018

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Homozygous mutations in IHH cause acrocapitofemoral dysplasia, an autosomal recessive disorder with cone-shaped epiphyses in hands and hips

21 January 2018

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Cloning of the T gene required in mesoderm formation in the mouse

21 January 2018

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Expression of three mouse homologs of the Drosophila segment polarity gene cubitus interruptus, Gli, Gli-2, and Gli-3, in ectoderm- and mesoderm-derived tissues suggests multiple roles during postimplantation development

21 January 2018

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Of fingers, toes and penises.

21 January 2018

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Genetic disorders of the skeleton: a developmental approach

21 January 2018

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Cloning and expression analysis of the mouse T-box gene Tbx18.

21 January 2018

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Expression of the receptor tyrosine kinase genes, Ror1 and Ror2, during mouse development.

21 January 2018

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The receptor tyrosine kinase Ror2 associates with the melanoma-associated antigen (MAGE) family protein Dlxin-1 and regulates its intracellular distribution

21 January 2018

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Mutation of HOXA13 in hand-foot-genital syndrome

21 January 2018

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Mouse mutant "rib-vertebrae" (rv): a defect in somite polarity.

21 January 2018

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A positive feedback loop coordinates growth and patterning in the vertebrate limb.

21 January 2018

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Loss of mRor1 enhances the heart and skeletal abnormalities in mRor2-deficient mice: redundant and pleiotropic functions of mRor1 and mRor2 receptor tyrosine kinases

21 January 2018

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A novel Drosophila receptor tyrosine kinase expressed specifically in the nervous system. Unique structural features and implication in developmental signaling

21 January 2018

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Spatio-temporally regulated expression of receptor tyrosine kinases, mRor1, mRor2, during mouse development: implications in development and function of the nervous system

21 January 2018

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Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B

21 January 2018

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21 January 2018

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The Dlx5 and Dlx6 homeobox genes are essential for craniofacial, axial, and appendicular skeletal development

21 January 2018

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Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development

21 January 2018

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Cell signaling by receptor tyrosine kinases

21 January 2018

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Distinct mutations in the receptor tyrosine kinase gene ROR2 cause brachydactyly type B.

21 January 2018

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Recessive Robinow syndrome: with emphasis on endocrine functions

21 January 2018

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Mesp2 initiates somite segmentation through the Notch signalling pathway.

21 January 2018

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Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome

21 January 2018

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Ogon/Secreted Frizzled functions as a negative feedback regulator of Bmp signaling

21 January 2018

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Spondylometaphyseal dysplasia in mice carrying a dominant negative mutation in a matrix protein specific for cartilage-to-bone transition

21 January 2018

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The receptor tyrosine kinase Ror2 is involved in non-canonical Wnt5a/JNK signalling pathway

21 January 2018

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7 January 2021

The Robinow (fetal face) syndrome

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7 January 2021

Mesp2: a novel mouse gene expressed in the presegmented mesoderm and essential for segmentation initiation

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7 January 2021

Indian hedgehog signaling regulates proliferation and differentiation of chondrocytes and is essential for bone formation

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7 January 2021

Wnt-3a regulates somite and tailbud formation in the mouse embryo

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7 January 2021

Mouse Ror2 receptor tyrosine kinase is required for the heart development and limb formation

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7 January 2021

Regulation of rate of cartilage differentiation by Indian hedgehog and PTH-related protein

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7 January 2021

Dror, a potential neurotrophic receptor gene, encodes a Drosophila homolog of the vertebrate Ror family of Trk-related receptor tyrosine kinases

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7 January 2021

Identifiers

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31 January 2017

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