BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

249 related articles for article (PubMed ID: 25891934)

  • 21. Taking pain out of NGF: a "painless" NGF mutant, linked to hereditary sensory autonomic neuropathy type V, with full neurotrophic activity.
    Capsoni S; Covaceuszach S; Marinelli S; Ceci M; Bernardo A; Minghetti L; Ugolini G; Pavone F; Cattaneo A
    PLoS One; 2011 Feb; 6(2):e17321. PubMed ID: 21387003
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Prdm12 specifies V1 interneurons through cross-repressive interactions with Dbx1 and Nkx6 genes in Xenopus.
    Thélie A; Desiderio S; Hanotel J; Quigley I; Van Driessche B; Rodari A; Borromeo MD; Kricha S; Lahaye F; Croce J; Cerda-Moya G; Ordoño Fernandez J; Bolle B; Lewis KE; Sander M; Pierani A; Schubert M; Johnson JE; Kintner CR; Pieler T; Van Lint C; Henningfeld KA; Bellefroid EJ; Van Campenhout C
    Development; 2015 Oct; 142(19):3416-28. PubMed ID: 26443638
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Transgenic expression of neuronal dystonin isoform 2 partially rescues the disease phenotype of the dystonia musculorum mouse model of hereditary sensory autonomic neuropathy VI.
    Ferrier A; Sato T; De Repentigny Y; Gibeault S; Bhanot K; O'Meara RW; Lynch-Godrei A; Kornfeld SF; Young KG; Kothary R
    Hum Mol Genet; 2014 May; 23(10):2694-710. PubMed ID: 24381311
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Recessive mutations in the neuronal isoforms of DST, encoding dystonin, lead to abnormal actin cytoskeleton organization and HSAN type VI.
    Fortugno P; Angelucci F; Cestra G; Camerota L; Ferraro AS; Cordisco S; Uccioli L; Castiglia D; De Angelis B; Kurth I; Kornak U; Brancati F
    Hum Mutat; 2019 Jan; 40(1):106-114. PubMed ID: 30371979
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Hmx: an evolutionary conserved homeobox gene family expressed in the developing nervous system in mice and Drosophila.
    Wang W; Lo P; Frasch M; Lufkin T
    Mech Dev; 2000 Dec; 99(1-2):123-37. PubMed ID: 11091080
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Swedish Nerve Growth Factor Mutation (NGF
    Sung K; Ferrari LF; Yang W; Chung C; Zhao X; Gu Y; Lin S; Zhang K; Cui B; Pearn ML; Maloney MT; Mobley WC; Levine JD; Wu C
    J Neurosci; 2018 Apr; 38(14):3394-3413. PubMed ID: 29483280
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A missense point mutation in nerve growth factor (NGF
    Yang W; Sung K; Xu W; Rodriguez MJ; Wu AC; Santos SA; Fang S; Uber RK; Dong SX; Guillory BC; Orain X; Raus J; Jolivalt C; Calcutt N; Rissman RA; Ding J; Wu C
    Prog Neurobiol; 2020 Nov; 194():101886. PubMed ID: 32693191
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Understanding pain perception through genetic painlessness diseases: The role of NGF and proNGF.
    Testa G; Cattaneo A; Capsoni S
    Pharmacol Res; 2021 Jul; 169():105662. PubMed ID: 34000361
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Mechanisms of disease in hereditary sensory and autonomic neuropathies.
    Rotthier A; Baets J; Timmerman V; Janssens K
    Nat Rev Neurol; 2012 Jan; 8(2):73-85. PubMed ID: 22270030
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Tlx3 promotes glutamatergic neuronal subtype specification through direct interactions with the chromatin modifier CBP.
    Shimomura A; Patel D; Wilson SM; Koehler KR; Khanna R; Hashino E
    PLoS One; 2015; 10(8):e0135060. PubMed ID: 26258652
    [TBL] [Abstract][Full Text] [Related]  

  • 31. The coexistence of a novel WNK1 variant and a copy number variation causes hereditary sensory and autonomic neuropathy type IIA.
    Wang JJ; Yu B; Li Z
    BMC Med Genet; 2019 May; 20(1):91. PubMed ID: 31132985
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Specification of thermosensory neuron fate in C. elegans requires ttx-1, a homolog of otd/Otx.
    Satterlee JS; Sasakura H; Kuhara A; Berkeley M; Mori I; Sengupta P
    Neuron; 2001 Sep; 31(6):943-56. PubMed ID: 11580895
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Heme and sensory neuropathy: insights from novel mutations in the heme exporter feline leukemia virus subgroup C receptor 1.
    Bertino F; Firestone K; Bellacchio E; Jackson KE; Asamoah A; Hersh J; Fiorito V; Destefanis F; Gonser R; Tucker ME; Altruda F; Tolosano E; Chiabrando D
    Pain; 2019 Dec; 160(12):2766-2775. PubMed ID: 31408049
    [TBL] [Abstract][Full Text] [Related]  

  • 34. From genes to pain: nerve growth factor and hereditary sensory and autonomic neuropathy type V.
    Capsoni S
    Eur J Neurosci; 2014 Feb; 39(3):392-400. PubMed ID: 24494679
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Knockdown of Lingo1b protein promotes myelination and oligodendrocyte differentiation in zebrafish.
    Yin W; Hu B
    Exp Neurol; 2014 Jan; 251():72-83. PubMed ID: 24262204
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Gene methylation in gastric cancer.
    Qu Y; Dang S; Hou P
    Clin Chim Acta; 2013 Sep; 424():53-65. PubMed ID: 23669186
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Prdm12 represses the expression of the visceral neuron determinants Phox2a/b in developing somatosensory ganglia.
    Vermeiren S; Cabochette P; Dannawi M; Desiderio S; San José AS; Achouri Y; Kricha S; Sitte M; Salinas-Riester G; Vanhollebeke B; Brunet JF; Bellefroid EJ
    iScience; 2023 Dec; 26(12):108364. PubMed ID: 38025786
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Dystonin-A3 upregulation is responsible for maintenance of tubulin acetylation in a less severe dystonia musculorum mouse model for hereditary sensory and autonomic neuropathy type VI.
    Lynch-Godrei A; De Repentigny Y; Gagnon S; Trung MT; Kothary R
    Hum Mol Genet; 2018 Oct; 27(20):3598-3611. PubMed ID: 29982604
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 13.