Congenital hereditary lymphedema caused by a mutation that inactivates VEGFR3 tyrosine kinase (Q24538742)

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English	Congenital hereditary lymphedema caused by a mutation that inactivates VEGFR3 tyrosine kinase	scientific article

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instance of

scholarly article

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stated in

Europe PubMed Central

PMC publication ID

1287178

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10856194%20AND%20SRC:MED&resulttype=core&format=json

retrieved

7 November 2019

title

Congenital hereditary lymphedema caused by a mutation that inactivates VEGFR3 tyrosine kinase (English)

1 reference

stated in

Europe PubMed Central

PMC publication ID

1287178

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10856194%20AND%20SRC:MED&resulttype=core&format=json

retrieved

7 November 2019

main subject

congenital disorder

0 references

hereditary lymphedema

1 reference

based on heuristic

inferred from title

author

Miikka Vikkula

series ordinal

5

1 reference

stated in

Europe PubMed Central

PMC publication ID

1287178

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10856194%20AND%20SRC:MED&resulttype=core&format=json

retrieved

7 November 2019

Kari Alitalo

series ordinal

4

1 reference

stated in

Europe PubMed Central

PMC publication ID

1287178

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10856194%20AND%20SRC:MED&resulttype=core&format=json

retrieved

7 November 2019

author name string

Irrthum A

series ordinal

1

1 reference

stated in

Europe PubMed Central

PMC publication ID

1287178

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10856194%20AND%20SRC:MED&resulttype=core&format=json

retrieved

7 November 2019

Karkkainen MJ

series ordinal

2

1 reference

stated in

Europe PubMed Central

PMC publication ID

1287178

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10856194%20AND%20SRC:MED&resulttype=core&format=json

retrieved

7 November 2019

Devriendt K

series ordinal

3

1 reference

stated in

Europe PubMed Central

PMC publication ID

1287178

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10856194%20AND%20SRC:MED&resulttype=core&format=json

retrieved

7 November 2019

language of work or name

English

0 references

publication date

9 June 2000

1 reference

stated in

Europe PubMed Central

PMC publication ID

1287178

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10856194%20AND%20SRC:MED&resulttype=core&format=json

retrieved

7 November 2019

published in

American Journal of Human Genetics

1 reference

stated in

Europe PubMed Central

PMC publication ID

1287178

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10856194%20AND%20SRC:MED&resulttype=core&format=json

retrieved

7 November 2019

volume

67

1 reference

stated in

Europe PubMed Central

PMC publication ID

1287178

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10856194%20AND%20SRC:MED&resulttype=core&format=json

retrieved

7 November 2019

issue

2

1 reference

stated in

Europe PubMed Central

PMC publication ID

1287178

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10856194%20AND%20SRC:MED&resulttype=core&format=json

retrieved

7 November 2019

page(s)

295-301

1 reference

stated in

Europe PubMed Central

PMC publication ID

1287178

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10856194%20AND%20SRC:MED&resulttype=core&format=json

retrieved

7 November 2019

cites work

A gene for lymphedema-distichiasis maps to 16q24.3.

1 reference

stated in

PubMed Central

reference URL

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A gene for inherited cutaneous venous anomalies ("glomangiomas") localizes to chromosome 1p21-22.

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24 March 2017

Mapping of primary congenital lymphedema to the 5q35.3 region

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PubMed Central

reference URL

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24 March 2017

Crystal structure of the kinase domain of human vascular endothelial growth factor receptor 2: a key enzyme in angiogenesis

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PubMed Central

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24 March 2017

Strategies for multilocus linkage analysis in humans

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PubMed Central

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24 March 2017

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24 March 2017

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24 March 2017

Assignment of a locus for dominantly inherited venous malformations to chromosome 9p

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PubMed Central

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24 March 2017

Cardiovascular failure in mouse embryos deficient in VEGF receptor-3

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Signalling properties of FLT4, a proteolytically processed receptor tyrosine kinase related to two VEGF receptors

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PubMed Central

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24 March 2017

CONGENITAL HEREDITARY LYMPHOEDEMA.

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287178

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27 September 2017

Endothelial receptor tyrosine kinases activate the STAT signaling pathway: mutant Tie-2 causing venous malformations signals a distinct STAT activation response

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27 September 2017

Hereditary lymphedema: evidence for linkage and genetic heterogeneity

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PubMed Central

reference URL

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27 September 2017

Expression of the fms-like tyrosine kinase 4 gene becomes restricted to lymphatic endothelium during development.

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Lymphatic endothelium and Kaposi's sarcoma spindle cells detected by antibodies against the vascular endothelial growth factor receptor-3

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10856194

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

On congenital lymphedema

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10856194

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel Mutations of the KIT (Mast/Stem Cell Growth Factor Receptor) Proto-Oncogene in Human Piebaldism

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10856194

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12 December 2020

based on heuristic

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Universal cloning method by TA strategy

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10856194

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The eukaryotic protein kinase superfamily: kinase (catalytic) domain structure and classification 1

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1086%2F303019

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

DOI

10.1086/303019

1 reference

stated in

Europe PubMed Central

PMC publication ID

1287178

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10856194%20AND%20SRC:MED&resulttype=core&format=json

retrieved

7 November 2019

Fatcat ID

release_2x3ft6kdfffpjd4ax4qjfysavq

0 references

OpenCitations bibliographic resource ID

321916

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

321916

PMC publication ID

1287178

1 reference

stated in

Europe PubMed Central

PMC publication ID

1287178

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10856194%20AND%20SRC:MED&resulttype=core&format=json

retrieved

7 November 2019

PubMed publication ID

10856194

1 reference

stated in

Europe PubMed Central

PMC publication ID

1287178

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10856194%20AND%20SRC:MED&resulttype=core&format=json

retrieved

7 November 2019

ResearchGate publication ID

12462854

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