(Q33927296)

30 July 2017

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title

RTK mutations and human syndromeswhen good receptors turn bad. (English)

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30 July 2017

Robertson SC

1

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30 July 2017

Tynan JA

series ordinal

2

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30 July 2017

Donoghue DJ

series ordinal

3

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30 July 2017

publication date

1 June 2000

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30 July 2017

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30 July 2017

volume

16

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30 July 2017

issue

6

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30 July 2017

page(s)

265-271

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Signalling by receptor tyrosine kinases

30 July 2017

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De novo alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndrome

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The transmembrane mutation G380R in fibroblast growth factor receptor 3 uncouples ligand-mediated receptor activation from down-regulation

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

Mutations in the TRKA/NGF receptor gene in patients with congenital insensitivity to pain with anhidrosis

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7 January 2021

Congenital insensitivity to pain with anhidrosis: novel mutations in the TRKA (NTRK1) gene encoding a high-affinity receptor for nerve growth factor

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7 January 2021

A specific inhibitor of the epidermal growth factor receptor tyrosine kinase

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7 January 2021

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

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7 January 2021

10.1016/S0168-9525(00)02021-7

Identifiers

DOI

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30 July 2017

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