Expression of the receptor tyrosine kinase genes, Ror1 and Ror2, during mouse development. (Q43655583)

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9 November 2019

title

Expression of the receptor tyrosine kinase genes, Ror1 and Ror2, during mouse development (English)

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9 November 2019

3

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9 November 2019

Isao Oishi

5

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9 November 2019

Shinji Takada

7

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9 November 2019

author name string

T Matsuda

1

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9 November 2019

M Nomi

2

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9 November 2019

S Kani

4

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9 November 2019

T Terashima

6

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9 November 2019

Y Minami

8

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9 November 2019

publication date

1 July 2001

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Mechanisms of Development

9 November 2019

published in

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9 November 2019

volume

105

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9 November 2019

issue

1-2

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9 November 2019

page(s)

153-156

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

9 November 2019

cites work

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https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900383-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900383-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900383-5

7 January 2021

The Wnt receptor CRD domain is also found in MuSK and related orphan receptor tyrosine kinases.

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900383-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900383-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900383-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900383-5

7 January 2021

Identification of a Frizzled-like cysteine rich domain in the extracellular region of developmental receptor tyrosine kinases

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900383-5

7 January 2021

Direct binding and activation of receptor tyrosine kinases by collagen

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900383-5

7 January 2021

Cell signaling by receptor tyrosine kinases

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900383-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900383-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900383-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900383-5

7 January 2021

Evidence that absence of Wnt-3a signaling promotes neuralization instead of paraxial mesoderm development in the mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900383-5

7 January 2021

10.1016/S0925-4773(01)00383-5

Identifiers

DOI

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9 November 2019

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