Protein tyrosine phosphatase PTPN14 is a regulator of lymphatic function and choanal development in humans (Q24299089)

Fms related receptor tyrosine kinase 4

1 reference

receptor tyrosine kinase binding

1 reference

Protein tyrosine phosphatase, non-receptor type 14

1 reference

author name string

Audrey C Au

1

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Paolo A Hernandez

2

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Ernest Lieber

3

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Ali M Nadroo

4

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Yu-Ming Shen

5

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Kevin A Kelley

6

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Bruce D Gelb

7

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George A Diaz

American Journal of Human Genetics

8

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language of work or name

English

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publication date

10 September 2010

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published in

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volume

87

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issue

3

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page(s)

436-44

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cites work

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Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome

19 March 2017

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Translocation of protein tyrosine phosphatase Pez/PTPD2/PTP36 to the nucleus is associated with induction of cell proliferation

19 March 2017

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

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Missense mutations interfere with VEGFR-3 signalling in primary lymphoedema

19 March 2017

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VEGF-C receptor binding and pattern of expression with VEGFR-3 suggests a role in lymphatic vascular development

19 March 2017

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19 March 2017

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Src kinase associates with a member of a distinct subfamily of protein-tyrosine phosphatases containing an ezrin-like domain

19 March 2017

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Hyperplasia of lymphatic vessels in VEGF-C transgenic mice

19 March 2017

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Linkage of pycnodysostosis to chromosome 1q21 by homozygosity mapping

19 March 2017

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27 September 2017

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Phosphatase-defective LEOPARD syndrome mutations in PTPN11 gene have gain-of-function effects during Drosophila development

27 September 2017

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27 September 2017

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Gorham's disease: an osseous disease of lymphangiogenesis?

27 September 2017

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Jak2 FERM domain interaction with the erythropoietin receptor regulates Jak2 kinase activity

27 September 2017

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27 September 2017

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Noonan syndrome and related disorders: dysregulated RAS-mitogen activated protein kinase signal transduction

27 September 2017

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Milroy disease and the VEGFR-3 mutation phenotype

27 September 2017

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27 September 2017

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27 September 2017

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Signalling via vascular endothelial growth factor receptor-3 is sufficient for lymphangiogenesis in transgenic mice

27 September 2017

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Regulation of phosphorylation level and distribution of PTP36, a putative protein tyrosine phosphatase, by cell-substrate adhesion

27 September 2017

1 reference

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Effects of overexpression of PTP36, a putative protein tyrosine phosphatase, on cell adhesion, cell growth, and cytoskeletons in HeLa cells

27 September 2017

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Hereditary lymphedema: evidence for linkage and genetic heterogeneity

27 September 2017

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Compensation for a gene trap mutation in the murine microtubule-associated protein 4 locus by alternative polyadenylation and alternative splicing

27 September 2017

1 reference

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cDNA cloning of a novel protein tyrosine phosphatase with homology to cytoskeletal protein 4.1 and its expression in T-lineage cells

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2933336

Protein-tyrosine phosphatase PTPD1 regulates focal adhesion kinase autophosphorylation and cell migration.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2933336

H-, N- and Kras cooperatively regulate lymphatic vessel growth by modulating VEGFR3 expression in lymphatic endothelial cells in mice.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2933336

Defective valves and abnormal mural cell recruitment underlie lymphatic vascular failure in lymphedema distichiasis.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2933336

FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2933336

Somatic mutations in PTPN11 in juvenile myelomonocytic leukemia, myelodysplastic syndromes and acute myeloid leukemia

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2933336

Inheritance of posterior choanal atresia

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2933336

Choanal atresia and lymphedema

29 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20826270

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Efficiency assessment of the gene trap approach

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20826270

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Aplasia of superficial lymphatic capillaries in hereditary and connatal lymphedema (Milroy's disease)

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20826270