(Q51574823)

English

Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish population.

scientific article published on 6 March 2008

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Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/18322713

Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish population. (English)

1 reference

Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/18322713

hereditary sensory and autonomic neuropathy

0 references

autonomic neuropathy

1 reference

based on heuristic

inferred from title

Cengiz Yalcinkaya

6

1 reference

Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/18322713

4

object named as

Kaya Bilguvar

1 reference

Europe PubMed Central

PubMed publication ID

7 April 2018

Christopher E. Mason

10

object named as

Christopher E Mason

1 reference

Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/18322713

author name string

Beyhan Tüysüz

1

1 reference

Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/18322713

Fatih Bayrakli

2

1 reference

Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/18322713

Michael L DiLuna

3

1 reference

Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/18322713

Yasar Bayri

5

1 reference

Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/18322713

Aysegul Bursali

7

1 reference

Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/18322713

Elif Ozdamar

8

1 reference

Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/18322713

Baris Korkmaz

9

1 reference

Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/18322713

Ali K Ozturk

11

1 reference

Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/18322713

Richard P Lifton

12

1 reference

Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/18322713

Matthew W State

13

1 reference

Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/18322713

Murat Gunel

14

1 reference

Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/18322713

publication date

6 March 2008

1 reference

Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/18322713

1 reference

Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/18322713

9

1 reference

Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/18322713

2

1 reference

Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/18322713

119-125

1 reference

Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/18322713

https://scigraph.springernature.com/pub.10.1007/s10048-008-0121-9

0 references

Congenital insensitivity to pain with anhydrosis. A unique syndrome in two male siblings

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0121-9

21 January 2018

Cutaneous innervation in hereditary sensory and autonomic neuropathy type IV.

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0121-9

21 January 2018

Molecular basis of congenital insensitivity to pain with anhidrosis (CIPA): mutations and polymorphisms in TRKA (NTRK1) gene encoding the receptor tyrosine kinase for nerve growth factor

1 reference

https://pubmed.ncbi.nlm.nih.gov/18322713

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18322713

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic organization of the human NTRK1 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/18322713

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18322713

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel TRK A (NTRK1) mutation associated with hereditary sensory and autonomic neuropathy type V.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18322713

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two novel mutant alleles of the gene encoding neurotrophic tyrosine kinase receptor type 1 (NTRK1) in a patient with congenital insensitivity to pain with anhidrosis: a splice junction mutation in intron 5 and cluster of four mutations in exon 15

1 reference

https://pubmed.ncbi.nlm.nih.gov/18322713

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

TrkA alternative splicing: a regulated tumor-promoting switch in human neuroblastoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/18322713

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital insensitivity to pain with anhidrosis in a 2-month-old boy

1 reference

https://pubmed.ncbi.nlm.nih.gov/18322713

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital insensitivity to pain with anhidrosis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18322713

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel frameshift and splice site mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with hereditary sensory neuropathy type IV.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18322713

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital insensitivity to pain with anhidrosis (CIPA): novel mutations of the TRKA (NTRK1) gene, a putative uniparental disomy, and a linkage of the mutant TRKA and PKLR genes in a family with CIPA and pyruvate kinase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/18322713

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18322713

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital insensitivity to pain with anhidrosis: lack of eccrine sweat gland innervation confirmed

1 reference

https://pubmed.ncbi.nlm.nih.gov/18322713

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation and polymorphism analysis of the TRKA (NTRK1) gene encoding a high-affinity receptor for nerve growth factor in congenital insensitivity to pain with anhidrosis (CIPA) families.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18322713

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18322713

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ABSENCE OF LISSAUER'S TRACT AND SMALL DORSAL ROOT AXONS IN FAMILIAL, CONGENITAL, UNIVERSAL INSENSITIVITY TO PAIN

1 reference

https://pubmed.ncbi.nlm.nih.gov/18322713

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Disease mechanisms in hereditary sensory and autonomic neuropathies

1 reference

https://pubmed.ncbi.nlm.nih.gov/18322713

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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://pubmed.ncbi.nlm.nih.gov/18322713

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Serial magnetic resonance images in a patient with congenital sensory neuropathy with anhidrosis and complications resembling heat stroke

1 reference

https://pubmed.ncbi.nlm.nih.gov/18322713

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital insensitivity to pain with anhidrosis (CIPA) in Israeli-Bedouins: genetic heterogeneity, novel mutations in the TRKA/NGF receptor gene, clinical findings, and results of nerve conduction studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/18322713

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital familial sensory neuropathy with anhidrosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/18322713

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital insensitivity to pain with anhidrosis (CIPA): effect of TRKA (NTRK1) missense mutations on autophosphorylation of the receptor tyrosine kinase for nerve growth factor

1 reference

https://pubmed.ncbi.nlm.nih.gov/18322713

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18322713

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recent advances in hereditary sensory and autonomic neuropathies

1 reference

https://pubmed.ncbi.nlm.nih.gov/18322713

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10048-008-0121-9

1 reference

Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/18322713

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/18322713

ResearchGate publication ID

0 references

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