These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

194 related articles for article (PubMed ID: 30201336)

  • 1. Identification of a novel mutation of the NTRK1 gene in patients with congenital insensitivity to pain with anhidrosis (CIPA).
    Wang WB; Cao YJ; Lyu SS; Zuo RT; Zhang ZL; Kang QL
    Gene; 2018 Dec; 679():253-259. PubMed ID: 30201336
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Recurrent and novel mutations in the NTRK1 gene lead to rare congenital insensitivity to pain with anhidrosis in two Chinese patients.
    Lv F; Xu XJ; Song YW; Li LJ; Wang O; Jiang Y; Xia WB; Xing XP; Gao P; Li M
    Clin Chim Acta; 2017 May; 468():39-45. PubMed ID: 28192073
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Novel NTRK1 mutations in Chinese patients with congenital insensitivity to pain with anhidrosis.
    Geng X; Liu Y; Ren X; Guan Y; Wang Y; Mao B; Zhao X; Zhang X
    Mol Pain; 2018; 14():1744806918781140. PubMed ID: 29770739
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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.
    Miura Y; Mardy S; Awaya Y; Nihei K; Endo F; Matsuda I; Indo Y
    Hum Genet; 2000 Jan; 106(1):116-24. PubMed ID: 10982191
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical and genetic analysis of Korean patients with congenital insensitivity to pain with anhidrosis.
    Lee ST; Lee J; Lee M; Kim JW; Ki CS
    Muscle Nerve; 2009 Nov; 40(5):855-9. PubMed ID: 19618435
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetics of congenital insensitivity to pain with anhidrosis (CIPA) or hereditary sensory and autonomic neuropathy type IV. Clinical, biological and molecular aspects of mutations in TRKA(NTRK1) gene encoding the receptor tyrosine kinase for nerve growth factor.
    Indo Y
    Clin Auton Res; 2002 May; 12 Suppl 1():I20-32. PubMed ID: 12102460
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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.
    Indo Y; Mardy S; Miura Y; Moosa A; Ismail EA; Toscano E; Andria G; Pavone V; Brown DL; Brooks A; Endo F; Matsuda I
    Hum Mutat; 2001 Oct; 18(4):308-18. PubMed ID: 11668614
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identification of a novel nonsense mutation of the neurotrophic tyrosine kinase receptor type 1 gene in two siblings with congenital insensitivity to pain with anhidrosis.
    Wang T; Li H; Xiang J; Wei B; Zhang Q; Zhu Q; Liu M; Sun M; Li H
    J Int Med Res; 2017 Apr; 45(2):549-555. PubMed ID: 28345382
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel NTRK1 mutations associated with congenital insensitivity to pain with anhidrosis verified by functional studies.
    Nam TS; Li W; Yoon S; Eom GH; Kim MK; Jung ST; Choi SY
    J Peripher Nerv Syst; 2017 Jun; 22(2):92-99. PubMed ID: 28177573
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Novel nonsense and frameshift NTRK1 gene mutations in Chinese patients with congenital insensitivity to pain with anhidrosis.
    Li M; Liang JY; Sun ZH; Zhang H; Yao ZR
    Genet Mol Res; 2012 Aug; 11(3):2156-62. PubMed ID: 22653642
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Mutation analysis of NTRK1 gene in a family affected with congenital insensitivity to pain with anhidrosis].
    Li B; Zhang Z; Wu X; Chen W; Chen J; Lyu Q; Liu G
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Oct; 34(5):646-649. PubMed ID: 28981924
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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.
    Indo Y
    Hum Mutat; 2001 Dec; 18(6):462-71. PubMed ID: 11748840
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A short in-frame deletion in NTRK1 tyrosine kinase domain caused by a novel splice site mutation in a patient with congenital insensitivity to pain with anhidrosis.
    Sarasola E; Rodríguez JA; Garrote E; Arístegui J; García-Barcina MJ
    BMC Med Genet; 2011 Jun; 12():86. PubMed ID: 21708027
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical and genetic characteristics of three patients with congenital insensitivity to pain with anhidrosis: Case reports and a review of the literature.
    Cho JH; Hwang S; Kwak YH; Yum MS; Seo GH; Koh JY; Ju YS; Yoon JH; Kang M; Do HS; Kim S; Kim GH; Bae H; Lee BH
    Mol Genet Genomic Med; 2024 Apr; 12(4):e2430. PubMed ID: 38581121
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel and novel de novo mutations in NTRK1 associated with congenital insensitivity to pain with anhidrosis: a case report.
    Wang Q; Guo S; Duan G; Xiang G; Ying Y; Zhang Y; Zhang X
    Medicine (Baltimore); 2015 May; 94(19):e871. PubMed ID: 25984678
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Novel NTRK1 Frameshift Mutation in Congenital Insensitivity to Pain With Anhidrosis.
    Liu S; Wu N; Liu J; Ming X; Chen J; Pavelec D; Su X; Qiu G; Tian Y; Giampietro P; Wu Z
    J Child Neurol; 2015 Sep; 30(10):1357-61. PubMed ID: 25316729
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Congenital insensitivity to pain with anhidrosis: A report of two siblings with a novel mutation in (TrkA) NTRK1 gene in a Saudi family.
    Algahtani H; Naseer MI; Al-Qahtani M; Abdulrahman SA; Boker F; Shirah B
    J Neurol Sci; 2016 Nov; 370():35-38. PubMed ID: 27772781
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Exome sequencing identifies novel NTRK1 mutations in patients with HSAN-IV phenotype.
    Altassan R; Saud HA; Masoodi TA; Dosssari HA; Khalifa O; Al-Zaidan H; Sakati N; Rhabeeni Z; Al-Hassnan Z; Binamer Y; Alhashemi N; Wade W; Al-Zayed Z; Al-Sayed M; Al-Muhaizea MA; Meyer B; Al-Owain M; Wakil SM
    Am J Med Genet A; 2017 Apr; 173(4):1009-1016. PubMed ID: 28328124
    [TBL] [Abstract][Full Text] [Related]  

  • 19. NTRK1 gene-related congenital insensitivity to pain with anhidrosis: a nationwide multicenter retrospective study.
    Echaniz-Laguna A; Altuzarra C; Verloes A; De La Banda MGG; Quijano-Roy S; Tudorache RA; Jaxybayeva A; Myrzaliyeva B; Tazir M; Vallat JM; Francou B; Urtizberea JA
    Neurogenetics; 2021 Oct; 22(4):333-341. PubMed ID: 34405299
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of founder and novel mutations that cause congenital insensitivity to pain (CIP) in palestinian patients.
    Khaled B; Alzahayqa M; Jaffal A; Sallam H; Thawabta R; Mansour M; Alian A; Salah Z
    BMC Med Genomics; 2023 May; 16(1):120. PubMed ID: 37248554
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.