BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

146 related articles for article (PubMed ID: 11241480)

  • 1. Congenital insensitivity to pain with anhidrosis: an NGF/TrkA-related disorder.
    Toscano E; Andria G
    Am J Med Genet; 2001 Mar; 99(2):164-5. PubMed ID: 11241480
    [No Abstract]   [Full Text] [Related]  

  • 2. Congenital insensitivity to pain with anhidrosis (CIPA): effect of TRKA (NTRK1) missense mutations on autophosphorylation of the receptor tyrosine kinase for nerve growth factor.
    Mardy S; Miura Y; Endo F; Matsuda I; Indo Y
    Hum Mol Genet; 2001 Feb; 10(3):179-88. PubMed ID: 11159935
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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.
    Shatzky S; Moses S; Levy J; Pinsk V; Hershkovitz E; Herzog L; Shorer Z; Luder A; Parvari R
    Am J Med Genet; 2000 Jun; 92(5):353-60. PubMed ID: 10861667
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutations in the TRKA/NGF receptor gene in patients with congenital insensitivity to pain with anhidrosis.
    Indo Y; Tsuruta M; Hayashida Y; Karim MA; Ohta K; Kawano T; Mitsubuchi H; Tonoki H; Awaya Y; Matsuda I
    Nat Genet; 1996 Aug; 13(4):485-8. PubMed ID: 8696348
    [TBL] [Abstract][Full Text] [Related]  

  • 5. NGF-dependent neurons and neurobiology of emotions and feelings: Lessons from congenital insensitivity to pain with anhidrosis.
    Indo Y
    Neurosci Biobehav Rev; 2018 Apr; 87():1-16. PubMed ID: 29407522
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Decreased first phase insulin response in children with congenital insensitivity to pain with anhidrosis.
    Schreiber R; Levy J; Loewenthal N; Pinsk V; Hershkovitz E
    J Pediatr Endocrinol Metab; 2005 Sep; 18(9):873-7. PubMed ID: 16279365
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Nerve growth factor, pain, itch and inflammation: lessons from congenital insensitivity to pain with anhidrosis.
    Indo Y
    Expert Rev Neurother; 2010 Nov; 10(11):1707-24. PubMed ID: 20977328
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Complete paternal uniparental isodisomy for chromosome 1 revealed by mutation analyses of the TRKA (NTRK1) gene encoding a receptor tyrosine kinase for nerve growth factor in a patient with congenital insensitivity to pain with anhidrosis.
    Miura Y; Hiura M; Torigoe K; Numata O; Kuwahara A; Matsunaga M; Hasegawa S; Boku N; Ino H; Mardy S; Endo F; Matsuda I; Indo Y
    Hum Genet; 2000 Sep; 107(3):205-9. PubMed ID: 11071380
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutations in TrkA Causing Congenital Insensitivity to Pain with Anhidrosis (CIPA) Induce Misfolding, Aggregation, and Mutation-dependent Neurodegeneration by Dysfunction of the Autophagic Flux.
    Franco ML; Melero C; Sarasola E; Acebo P; Luque A; Calatayud-Baselga I; García-Barcina M; Vilar M
    J Biol Chem; 2016 Oct; 291(41):21363-21374. PubMed ID: 27551041
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Novel pathogenic mechanisms of congenital insensitivity to pain with anhidrosis genetic disorder unveiled by functional analysis of neurotrophic tyrosine receptor kinase type 1/nerve growth factor receptor mutations.
    Miranda C; Di Virgilio M; Selleri S; Zanotti G; Pagliardini S; Pierotti MA; Greco A
    J Biol Chem; 2002 Feb; 277(8):6455-62. PubMed ID: 11719521
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Congenital insensitivity to pain with anhidrosis: novel mutations in the TRKA (NTRK1) gene encoding a high-affinity receptor for nerve growth factor.
    Mardy S; Miura Y; Endo F; Matsuda I; Sztriha L; Frossard P; Moosa A; Ismail EA; Macaya A; Andria G; Toscano E; Gibson W; Graham GE; Indo Y
    Am J Hum Genet; 1999 Jun; 64(6):1570-9. PubMed ID: 10330344
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Skoura - a genetic island for congenital insensitivity to pain and anhidrosis among Moroccan Jews, as determined by a novel mutation in the NTRK1 gene.
    Suriu C; Khayat M; Weiler M; Kfir N; Cohen C; Zinger A; Aslanidis C; Schmitz G; Falik-Zaccai TC
    Clin Genet; 2009 Mar; 75(3):230-6. PubMed ID: 19250380
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Congenital insensitivity to pain with anhidrosis associated with congenital myasthenic syndrome].
    Raspall-Chaure M; Del Toro-Riera M; Gratacós M; Cuenca-León E; Ferrer I; Indo Y; Roig-Quilis M; Macaya-Ruiz A
    Rev Neurol; 2005 Aug 16-31; 41(4):218-22. PubMed ID: 16075400
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel point mutation affecting the tyrosine kinase domain of the TRKA gene in a family with congenital insensitivity to pain with anhidrosis.
    Yotsumoto S; Setoyama M; Hozumi H; Mizoguchi S; Fukumaru S; Kobayashi K; Saheki T; Kanzaki T
    J Invest Dermatol; 1999 May; 112(5):810-4. PubMed ID: 10233776
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Multisystem involvement in congenital insensitivity to pain with anhidrosis (CIPA), a nerve growth factor receptor(Trk A)-related disorder.
    Toscano E; della Casa R; Mardy S; Gaetaniello L; Sadile F; Indo Y; Pignata C; Andria G
    Neuropediatrics; 2000 Feb; 31(1):39-41. PubMed ID: 10774995
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Congenital insensitivity to pain with Anhidrosis (NTRK1 mutation) and early onset renal disease: clinical report on three sibs with a 25-year follow-up in one of them.
    Barone R; Lempereur L; Anastasi M; Parano E; Pavone P
    Neuropediatrics; 2005 Aug; 36(4):270-3. PubMed ID: 16138253
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Humoral immunodeficiency in congenital insensitivity to pain with anhidrosis.
    Kilic SS; Ozturk R; Sarisozen B; Rotthier A; Baets J; Timmerman V
    Neurogenetics; 2009 Apr; 10(2):161-5. PubMed ID: 19089473
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel mutation in the SCN9A gene associated with congenital insensitivity to pain, anhidrosis, and mild cognitive impairment.
    Romagnuolo M; Moltrasio C; Cavalli R; Brena M; Tadini G
    Pediatr Dermatol; 2024; 41(1):80-83. PubMed ID: 37345838
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Structural analysis of TrkA mutations in patients with congenital insensitivity to pain reveals PLCγ as an analgesic drug target.
    Moraes BC; Ribeiro-Filho HV; Roldão AP; Toniolo EF; Carretero GPB; Sgro GG; Batista FAH; Berardi DE; Oliveira VRS; Tomasin R; Vieceli FM; Pramio DT; Cardoso AB; Figueira ACM; Farah SC; Devi LA; Dale CS; de Oliveira PSL; Schechtman D
    Sci Signal; 2022 Apr; 15(731):eabm6046. PubMed ID: 35471943
    [TBL] [Abstract][Full Text] [Related]  

  • 20. An infant with primary tooth loss and palmar hyperkeratosis: a novel mutation in the NTRK1 gene causing congenital insensitivity to pain with anhidrosis.
    Bonkowsky JL; Johnson J; Carey JC; Smith AG; Swoboda KJ
    Pediatrics; 2003 Sep; 112(3 Pt 1):e237-41. PubMed ID: 12949319
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.