(Q34144132)

31 July 2017

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

1 reference

Andrew Oliver Mungo Wilkie

31 July 2017

8

1 reference

31 July 2017

G C Schwabe

1

1 reference

31 July 2017

S Tinschert

2

1 reference

31 July 2017

C Buschow

3

1 reference

31 July 2017

P Meinecke

4

1 reference

31 July 2017

G Wolff

5

1 reference

31 July 2017

G Gillessen-Kaesbach

6

1 reference

31 July 2017

M Oldridge

7

1 reference

31 July 2017

R Kömec

9

1 reference

31 July 2017

S Mundlos

10

1 reference

31 July 2017

language of work or name

English

0 references

publication date

12 September 2000

1 reference

American Journal of Human Genetics

31 July 2017

1 reference

31 July 2017

67

1 reference

31 July 2017

822-831

1 reference

31 July 2017

4

1 reference

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

31 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287887

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287887

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287887

Genetics of limb anomalies in humans

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287887

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287887

A perfect message: RNA surveillance and nonsense-mediated decay

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287887

Brachydactyly type B: linkage to chromosome 9q22 and evidence for genetic heterogeneity

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287887

Brachydactyly type B: clinical description, genetic mapping to chromosome 9q, and evidence for a shared ancestral mutation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287887

At least one intron is required for the nonsense-mediated decay of triosephosphate isomerase mRNA: a possible link between nuclear splicing and cytoplasmic translation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287887

Limb development: molecular dysmorphology is at hand!

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287887

Binary specification of nonsense codons by splicing and cytoplasmic translation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287887

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287887

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287887

Regulation of signal transduction and signal diversity by receptor oligomerization

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287887

A novel family of cell surface receptors with tyrosine kinase-like domain

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287887

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287887

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

28 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10986040

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/303084

1 reference

31 July 2017

1 reference

31 July 2017

1 reference