Literature DB >> 10090906

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

A Greco, R Villa, B Tubino, L Romano, D Penso, M A Pierotti.   

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Year:  1999        PMID： 10090906      PMCID： PMC1377845          DOI： 10.1086/302319

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  10 in total

Review 1.  Mechanisms of disease in hereditary sensory and autonomic neuropathies.

Authors:  Annelies Rotthier; Jonathan Baets; Vincent Timmerman; Katrien Janssens
Journal:  Nat Rev Neurol       Date:  2012-01-24       Impact factor: 42.937

2.  The TPM3-NTRK1 rearrangement is a recurring event in colorectal carcinoma and is associated with tumor sensitivity to TRKA kinase inhibition.

Authors:  Elena Ardini; Roberta Bosotti; Andrea Lombardi Borgia; Cristina De Ponti; Alessio Somaschini; Rosaria Cammarota; Nadia Amboldi; Laura Raddrizzani; Andrea Milani; Paola Magnaghi; Dario Ballinari; Daniele Casero; Fabio Gasparri; Patrizia Banfi; Nilla Avanzi; Maria B Saccardo; Rachele Alzani; Tiziano Bandiera; Eduard Felder; Daniele Donati; Enrico Pesenti; Andrea Sartore-Bianchi; Marcello Gambacorta; Marco A Pierotti; Salvatore Siena; Silvio Veronese; Arturo Galvani; Antonella Isacchi
Journal:  Mol Oncol       Date:  2014-06-12       Impact factor: 6.603

Review 3.  Exploring Missense Mutations in Tyrosine Kinases Implicated with Neurodegeneration.

Authors:  Neha Sami; Vijay Kumar; Asimul Islam; Sher Ali; Faizan Ahmad; Imtaiyaz Hassan
Journal:  Mol Neurobiol       Date:  2016-08-20       Impact factor: 5.590

4.  Recurrent NTRK1 Gene Fusions Define a Novel Subset of Locally Aggressive Lipofibromatosis-like Neural Tumors.

Authors:  Narasimhan P Agaram; Lei Zhang; Yun-Shao Sung; Chun-Liang Chen; Catherine T Chung; Cristina R Antonescu; Christopher Dm Fletcher
Journal:  Am J Surg Pathol       Date:  2016-10       Impact factor: 6.394

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

Authors:  Beyhan Tüysüz; Fatih Bayrakli; Michael L DiLuna; Kaya Bilguvar; Yasar Bayri; Cengiz Yalcinkaya; Aysegul Bursali; Elif Ozdamar; Baris Korkmaz; Christopher E Mason; Ali K Ozturk; Richard P Lifton; Matthew W State; Murat Gunel
Journal:  Neurogenetics       Date:  2008-03-06       Impact factor: 2.660

6.  A novel lymphocyte signaling defect: trk A mutation in the syndrome of congenital insensitivity to pain and anhidrosis (CIPA).

Authors:  I Melamed; J Levy; R Parvari; E W Gelfand
Journal:  J Clin Immunol       Date:  2004-07       Impact factor: 8.317

7.  Estrogen Receptor α- and β-Interacting Proteins Contain Consensus Secondary Structures: An Insilico Study.

Authors:  Vijay Paramanik; Harini Krishnan; Mahendra Kumar Thakur
Journal:  Ann Neurosci       Date:  2017-10-23

8.  Congenital insensitivity to pain with anhidrosis in an Iranian patient.

Authors:  Nasrollah Saleh-Gohari; Marzye Mohammadi-Anaie
Journal:  Basic Clin Neurosci       Date:  2013

9.  A Comprehensive Functional Analysis of NTRK1 Missense Mutations Causing Hereditary Sensory and Autonomic Neuropathy Type IV (HSAN IV).

Authors:  Samiha S Shaikh; Ya-Chun Chen; Sally-Anne Halsall; Michael S Nahorski; Kiyoyuki Omoto; Gareth T Young; Anne Phelan; Christopher Geoffrey Woods
Journal:  Hum Mutat       Date:  2016-11-26       Impact factor: 4.878

10.  An Inversion Disrupting FAM134B Is Associated with Sensory Neuropathy in the Border Collie Dog Breed.

Authors:  Oliver P Forman; Rebekkah J Hitti; Louise Pettitt; Christopher A Jenkins; Dennis P O'Brien; G Diane Shelton; Luisa De Risio; Rodrigo Gutierrez Quintana; Elsa Beltran; Cathryn Mellersh
Journal:  G3 (Bethesda)       Date:  2016-09-08       Impact factor: 3.542
  10 in total

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