BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

138 related articles for article (PubMed ID: 19332697)

  • 1. Dpp6 is associated with susceptibility to progressive spinal muscular atrophy.
    van Es MA; van Vught PW; van Kempen G; Blauw HM; Veldink JH; van den Berg LH
    Neurology; 2009 Mar; 72(13):1184-5. PubMed ID: 19332697
    [No Abstract]   [Full Text] [Related]  

  • 2. Genetics. The elusive ALS genes.
    Garber K
    Science; 2008 Jan; 319(5859):20. PubMed ID: 18174402
    [No Abstract]   [Full Text] [Related]  

  • 3. DPP6 gene variability confers increased risk of developing sporadic amyotrophic lateral sclerosis in Italian patients.
    Del Bo R; Ghezzi S; Corti S; Santoro D; Prelle A; Mancuso M; Siciliano G; Briani C; Murri L; Bresolin N; Comi GP
    J Neurol Neurosurg Psychiatry; 2008 Sep; 79(9):1085. PubMed ID: 18708572
    [No Abstract]   [Full Text] [Related]  

  • 4. Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis.
    van Es MA; van Vught PW; Blauw HM; Franke L; Saris CG; Van den Bosch L; de Jong SW; de Jong V; Baas F; van't Slot R; Lemmens R; Schelhaas HJ; Birve A; Sleegers K; Van Broeckhoven C; Schymick JC; Traynor BJ; Wokke JH; Wijmenga C; Robberecht W; Andersen PM; Veldink JH; Ophoff RA; van den Berg LH
    Nat Genet; 2008 Jan; 40(1):29-31. PubMed ID: 18084291
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Association between DPP6 polymorphism and the risk of progressive multiple sclerosis in Northern and Southern Europeans.
    Brambilla P; Esposito F; Lindstrom E; Sorosina M; Giacalone G; Clarelli F; Rodegher M; Colombo B; Moiola L; Ghezzi A; Capra R; Collimedaglia L; Coniglio G; Celius EG; Galimberti D; Sørensen PS; Martinelli V; Oturai AB; Harbo HF; Hillert J; Comi G; Martinelli-Boneschi F
    Neurosci Lett; 2012 Nov; 530(2):155-60. PubMed ID: 23069673
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Lack of evidence supporting a role for DPP6 sequence variants in Alzheimer's disease in the European American population.
    Kirola L; Budde JP; Wang F; Norton J; Morris JC; ; Cruchaga C; Fernández MV
    Acta Neuropathol; 2021 Apr; 141(4):623-624. PubMed ID: 33591372
    [No Abstract]   [Full Text] [Related]  

  • 7. Screening for replication of genome-wide SNP associations in sporadic ALS.
    Cronin S; Tomik B; Bradley DG; Slowik A; Hardiman O
    Eur J Hum Genet; 2009 Feb; 17(2):213-8. PubMed ID: 18987618
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A Genetic Predisposition for Lethal Arrhythmias: No Need for Preventive Treatment?
    van der Does LJ; Burghouwt DE; de Groot NM
    Am J Med Sci; 2015 Oct; 350(4):340-1. PubMed ID: 26252795
    [No Abstract]   [Full Text] [Related]  

  • 9. [Premature sudden death--consider serious familial heart rhythm disturbances].
    Postema PG; Christiaans I; Alders M; Hofman N; Wilde AA
    Ned Tijdschr Geneeskd; 2011; 155(39):A3391. PubMed ID: 21961687
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Reply: Lack of evidence supporting a role for DPP6 sequence variants in Alzheimer's disease in the European American population.
    Cacace R; Van Broeckhoven C
    Acta Neuropathol; 2021 Apr; 141(4):625-626. PubMed ID: 33591373
    [No Abstract]   [Full Text] [Related]  

  • 11. I SA channel complexes include four subunits each of DPP6 and Kv4.2.
    Soh H; Goldstein SA
    J Biol Chem; 2008 May; 283(22):15072-7. PubMed ID: 18364354
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prediction of dipeptidyl peptidase (DP) 8 structure by homology modelling.
    Pitman MR; Menz RI; Abbott CA
    Adv Exp Med Biol; 2006; 575():33-42. PubMed ID: 16700506
    [No Abstract]   [Full Text] [Related]  

  • 13. No association of DPP6 with amyotrophic lateral sclerosis in an Italian population.
    Fogh I; D'Alfonso S; Gellera C; Ratti A; Cereda C; Penco S; Corrado L; Sorarù G; Castellotti B; Tiloca C; Gagliardi S; Cozzi L; Lupton MK; Ticozzi N; Mazzini L; Shaw CE; Al-Chalabi A; Powell J; Silani V
    Neurobiol Aging; 2011 May; 32(5):966-7. PubMed ID: 19525032
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Loss-of-function variation in the DPP6 gene is associated with autosomal dominant microcephaly and mental retardation.
    Liao C; Fu F; Li R; Yang WQ; Liao HY; Yan JR; Li J; Li SY; Yang X; Li DZ
    Eur J Med Genet; 2013 Sep; 56(9):484-9. PubMed ID: 23832105
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A genome-wide association study of sporadic ALS in a homogenous Irish population.
    Cronin S; Berger S; Ding J; Schymick JC; Washecka N; Hernandez DG; Greenway MJ; Bradley DG; Traynor BJ; Hardiman O
    Hum Mol Genet; 2008 Mar; 17(5):768-74. PubMed ID: 18057069
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Expression of DPP6 in Meckel's cartilage and tooth germs during mouse facial development.
    Du J; Fan Z; Ma X; Wu Y; Liu S; Gao Y; Shen Y; Fan M; Wang S
    Biotech Histochem; 2014 Jan; 89(1):14-8. PubMed ID: 23750656
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Haplotype-sharing analysis implicates chromosome 7q36 harboring DPP6 in familial idiopathic ventricular fibrillation.
    Alders M; Koopmann TT; Christiaans I; Postema PG; Beekman L; Tanck MW; Zeppenfeld K; Loh P; Koch KT; Demolombe S; Mannens MM; Bezzina CR; Wilde AA
    Am J Hum Genet; 2009 Apr; 84(4):468-76. PubMed ID: 19285295
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Structure and function in dipeptidyl peptidase IV and related proteins.
    Gorrell MD; Wang XM; Park J; Ajami K; Yu DM; Knott H; Seth D; McCaughan GW
    Adv Exp Med Biol; 2006; 575():45-54. PubMed ID: 16700507
    [No Abstract]   [Full Text] [Related]  

  • 19. Species and tissue differences in the expression of DPPY splicing variants.
    Takimoto K; Hayashi Y; Ren X; Yoshimura N
    Biochem Biophys Res Commun; 2006 Sep; 348(3):1094-100. PubMed ID: 16899223
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A large genome scan for rare CNVs in amyotrophic lateral sclerosis.
    Blauw HM; Al-Chalabi A; Andersen PM; van Vught PW; Diekstra FP; van Es MA; Saris CG; Groen EJ; van Rheenen W; Koppers M; Van't Slot R; Strengman E; Estrada K; Rivadeneira F; Hofman A; Uitterlinden AG; Kiemeney LA; Vermeulen SH; Birve A; Waibel S; Meyer T; Cronin S; McLaughlin RL; Hardiman O; Sapp PC; Tobin MD; Wain LV; Tomik B; Slowik A; Lemmens R; Rujescu D; Schulte C; Gasser T; Brown RH; Landers JE; Robberecht W; Ludolph AC; Ophoff RA; Veldink JH; van den Berg LH
    Hum Mol Genet; 2010 Oct; 19(20):4091-9. PubMed ID: 20685689
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.