(Q40917020)

English

The Gly571Arg mutation, associated with the autonomic and sensory disorder congenital insensitivity to pain with anhidrosis, causes the inactivation of the NTRK1/nerve growth factor receptor

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

The Gly571Arg mutation, associated with the autonomic and sensory disorder congenital insensitivity to pain with anhidrosis, causes the inactivation of the NTRK1/nerve growth factor receptor (English)

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

congenital disorder

0 references

congenital insensitivity to pain with anhidrosis

0 references

author name string

A Greco

1

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

R Villa

2

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

L Fusetti

3

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

R Orlandi

4

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

M A Pierotti

5

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

language of work or name

1 reference

based on heuristic

inferred from title

publication date

1 January 2000

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

Journal of Cellular Physiology

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

182

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

127-133

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

TrkA receptor ectodomain cleavage generates a tyrosine-phosphorylated cell-associated fragment

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-4652%28200001%29182%3A1%3C127%3A%3AAID-JCP14%3E3.0.CO%3B2-0

21 January 2018

Mice lacking nerve growth factor display perinatal loss of sensory and sympathetic neurons yet develop basal forebrain cholinergic neurons

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-4652%28200001%29182%3A1%3C127%3A%3AAID-JCP14%3E3.0.CO%3B2-0

21 January 2018

A novel NTRK1 mutation associated with congenital insensitivity to pain with anhidrosis

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-4652%28200001%29182%3A1%3C127%3A%3AAID-JCP14%3E3.0.CO%3B2-0

21 January 2018

Role of the TFG N-terminus and coiled-coil domain in the transforming activity of the thyroid TRK-T3 oncogene

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-4652%28200001%29182%3A1%3C127%3A%3AAID-JCP14%3E3.0.CO%3B2-0

21 January 2018

The DNA rearrangement that generates the TRK-T3 oncogene involves a novel gene on chromosome 3 whose product has a potential coiled-coil domain

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-4652%28200001%29182%3A1%3C127%3A%3AAID-JCP14%3E3.0.CO%3B2-0

21 January 2018

p140trk mRNA marks NGF-responsive forebrain neurons: evidence that trk gene expression is induced by NGF

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-4652%28200001%29182%3A1%3C127%3A%3AAID-JCP14%3E3.0.CO%3B2-0

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-4652%28200001%29182%3A1%3C127%3A%3AAID-JCP14%3E3.0.CO%3B2-0

21 January 2018

The trk Proto-Oncogene Product: a Signal Transducing Receptor for Nerve Growth Factor

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-4652%28200001%29182%3A1%3C127%3A%3AAID-JCP14%3E3.0.CO%3B2-0

21 January 2018

The trk proto-oncogene encodes a receptor for nerve growth factor

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-4652%28200001%29182%3A1%3C127%3A%3AAID-JCP14%3E3.0.CO%3B2-0

21 January 2018

Targeted mutation of the gene encoding the low affinity NGF receptor p75 leads to deficits in the peripheral sensory nervous system

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-4652%28200001%29182%3A1%3C127%3A%3AAID-JCP14%3E3.0.CO%3B2-0

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-4652%28200001%29182%3A1%3C127%3A%3AAID-JCP14%3E3.0.CO%3B2-0

21 January 2018

Expression of the trk proto-oncogene is restricted to the sensory cranial and spinal ganglia of neural crest origin in mouse development

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-4652%28200001%29182%3A1%3C127%3A%3AAID-JCP14%3E3.0.CO%3B2-0

21 January 2018

RET mutations in human disease

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-4652%28200001%29182%3A1%3C127%3A%3AAID-JCP14%3E3.0.CO%3B2-0

21 January 2018

Congenital insensitivity to pain with anhidrosis (hereditary sensory and autonomic neuropathy type IV)

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-4652%28200001%29182%3A1%3C127%3A%3AAID-JCP14%3E3.0.CO%3B2-0

21 January 2018

Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-4652%28200001%29182%3A1%3C127%3A%3AAID-JCP14%3E3.0.CO%3B2-0

21 January 2018

Severe sensory and sympathetic neuropathies in mice carrying a disrupted Trk/NGF receptor gene.

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-4652%28200001%29182%3A1%3C127%3A%3AAID-JCP14%3E3.0.CO%3B2-0

21 January 2018

High-affinity nerve growth factor receptor (Trk) immunoreactivity is localized in cholinergic neurons of the basal forebrain and striatum in the adult rat brain

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-4652%28200001%29182%3A1%3C127%3A%3AAID-JCP14%3E3.0.CO%3B2-0

21 January 2018

FGFR activation in skeletal disorders: too much of a good thing

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-4652%28200001%29182%3A1%3C127%3A%3AAID-JCP14%3E3.0.CO%3B2-0

21 January 2018

Rapid physical mapping of the human trk protooncogene (NTRK1) to human chromosome 1q21–q22 by P1 clone selection, fluorescence in situ hybridization (FISH), and computer-assisted microscopy

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-4652%28200001%29182%3A1%3C127%3A%3AAID-JCP14%3E3.0.CO%3B2-0

21 January 2018

A novel point mutation affecting the tyrosine kinase domain of the TRKA gene in a family with congenital insensitivity to pain with anhidrosis

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-4652%28200001%29182%3A1%3C127%3A%3AAID-JCP14%3E3.0.CO%3B2-0

21 January 2018

Eccrine sweat glands are not innervated in hereditary sensory neuropathy type IV. An electron-microscopic study

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-4652%28200001%29182%3A1%3C127%3A%3AAID-JCP14%3E3.0.CO%3B2-0

21 January 2018

Identifiers

10.1002/(SICI)1097-4652(200001)182:1<127::AID-JCP14>3.0.CO;2-0

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q40917020&oldid=2092583652"