BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

260 related articles for article (PubMed ID: 23832105)

  • 1. 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]  

  • 2. Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitability.
    Cacace R; Heeman B; Van Mossevelde S; De Roeck A; Hoogmartens J; De Rijk P; Gossye H; De Vos K; De Coster W; Strazisar M; De Baets G; Schymkowitz J; Rousseau F; Geerts N; De Pooter T; Peeters K; Sieben A; Martin JJ; Engelborghs S; Salmon E; Santens P; Vandenberghe R; Cras P; P De Deyn P; C van Swieten J; M van Duijn C; van der Zee J; Sleegers K; Van Broeckhoven C;
    Acta Neuropathol; 2019 Jun; 137(6):901-918. PubMed ID: 30874922
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Combined deletion of two Condensin II system genes (NCAPG2 and MCPH1) in a case of severe microcephaly and mental deficiency.
    Perche O; Menuet A; Marcos M; Liu L; Pâris A; Utami KH; Kervran D; Cacheux V; Laudier B; Briault S
    Eur J Med Genet; 2013 Nov; 56(11):635-41. PubMed ID: 24013099
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The DYRK1A gene is a cause of syndromic intellectual disability with severe microcephaly and epilepsy.
    Courcet JB; Faivre L; Malzac P; Masurel-Paulet A; Lopez E; Callier P; Lambert L; Lemesle M; Thevenon J; Gigot N; Duplomb L; Ragon C; Marle N; Mosca-Boidron AL; Huet F; Philippe C; Moncla A; Thauvin-Robinet C
    J Med Genet; 2012 Dec; 49(12):731-6. PubMed ID: 23099646
    [TBL] [Abstract][Full Text] [Related]  

  • 5. DPP6 gene disruption in a family with Gilles de la Tourette syndrome.
    Prontera P; Napolioni V; Ottaviani V; Rogaia D; Fusco C; Augello B; Serino D; Parisi V; Bernardini L; Merla G; Cavanna AE; Donti E
    Neurogenetics; 2014 Oct; 15(4):237-42. PubMed ID: 25129042
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Abnormal spindle-like microcephaly gene detection in an autosomal recessive microcephalic Saudi patient with attention deficit hyperactivity disorder and mental retardation.
    Mahmoud AA; Siddiqui IA
    Neurosciences (Riyadh); 2013 Jul; 18(3):278-80. PubMed ID: 23887221
    [No Abstract]   [Full Text] [Related]  

  • 7. 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]  

  • 8. Implication of LRRC4C and DPP6 in neurodevelopmental disorders.
    Maussion G; Cruceanu C; Rosenfeld JA; Bell SC; Jollant F; Szatkiewicz J; Collins RL; Hanscom C; Kolobova I; de Champfleur NM; Blumenthal I; Chiang C; Ota V; Hultman C; O'Dushlaine C; McCarroll S; Alda M; Jacquemont S; Ordulu Z; Marshall CR; Carter MT; Shaffer LG; Sklar P; Girirajan S; Morton CC; Gusella JF; Turecki G; Stavropoulos DJ; Sullivan PF; Scherer SW; Talkowski ME; Ernst C
    Am J Med Genet A; 2017 Feb; 173(2):395-406. PubMed ID: 27759917
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Autosomal dominant microcephaly without mental retardation.
    Rossi LN; Candini G; Scarlatti G; Rossi G; Prina E; Alberti S
    Am J Dis Child; 1987 Jun; 141(6):655-9. PubMed ID: 3578190
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mapping breakpoints of a familial chromosome insertion (18,7) (q22.1; q36.2q21.11) to DPP6 and CACNA2D1 genes in an azoospermic male.
    Li L; Chen H; Yin C; Yang C; Wang B; Zheng S; Zhang J; Fan W
    Gene; 2014 Aug; 547(1):43-9. PubMed ID: 24937803
    [TBL] [Abstract][Full Text] [Related]  

  • 11. DPP6 as a candidate gene for neuroleptic-induced tardive dyskinesia.
    Tanaka S; Syu A; Ishiguro H; Inada T; Horiuchi Y; Ishikawa M; Koga M; Noguchi E; Ozaki N; Someya T; Kakita A; Takahashi H; Nawa H; Arinami T
    Pharmacogenomics J; 2013 Feb; 13(1):27-34. PubMed ID: 21826085
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutations in MEF2C from the 5q14.3q15 microdeletion syndrome region are a frequent cause of severe mental retardation and diminish MECP2 and CDKL5 expression.
    Zweier M; Gregor A; Zweier C; Engels H; Sticht H; Wohlleber E; Bijlsma EK; Holder SE; Zenker M; Rossier E; Grasshoff U; Johnson DS; Robertson L; Firth HV; ; Ekici AB; Reis A; Rauch A
    Hum Mutat; 2010 Jun; 31(6):722-33. PubMed ID: 20513142
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Microcephalic children without mental retardation].
    Przytycki A; Burgin R
    Harefuah; 1992 May; 122(9):566-8, 615. PubMed ID: 1382036
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Dipeptidyl peptidase-like protein 6 is required for normal electrophysiological properties of cerebellar granule cells.
    Nadin BM; Pfaffinger PJ
    J Neurosci; 2010 Jun; 30(25):8551-65. PubMed ID: 20573902
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel DPP6 variant in Chinese families causes early repolarization syndrome.
    Ji CC; Yao FJ; Cheng YJ; Yao H; Fan J; Chen XM; Zheng ZH; Dong YG; Wu SH
    Exp Cell Res; 2019 Nov; 384(1):111561. PubMed ID: 31476289
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Neuronal Differentiation of Induced Pluripotent Stem Cells from Schizophrenia Patients in Two-Dimensional and in Three-Dimensional Cultures Reveals Increased Expression of the Kv4.2 Subunit DPP6 That Contributes to Decreased Neuronal Activity.
    Naujock M; Speidel A; Fischer S; Kizner V; Dorner-Ciossek C; Gillardon F
    Stem Cells Dev; 2020 Dec; 29(24):1577-1587. PubMed ID: 33143549
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Gonadal mosaicism of large terminal de novo duplication and deletion in siblings with variable intellectual disability phenotypes.
    Rahman MM; Uddin KF; Al Jezawi NK; Karuvantevida N; Akter H; Dity NJ; Rahaman MA; Begum M; Rahaman MA; Baqui MA; Salwa Z; Islam S; Woodbury-Smith M; Basiruzzaman M; Uddin M
    Mol Genet Genomic Med; 2019 Oct; 7(10):e00954. PubMed ID: 31475484
    [TBL] [Abstract][Full Text] [Related]  

  • 18. MCPH1 deletion in a newborn with severe microcephaly and premature chromosome condensation.
    Pfau RB; Thrush DL; Hamelberg E; Bartholomew D; Botes S; Pastore M; Tan C; del Gaudio D; Gastier-Foster JM; Astbury C
    Eur J Med Genet; 2013 Nov; 56(11):609-13. PubMed ID: 24080358
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Autosomal dominant microcephaly with mental retardation.
    Bawle E; Horton M
    Am J Med Genet; 1989 Jul; 33(3):382-4. PubMed ID: 2801773
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability.
    Noor A; Whibley A; Marshall CR; Gianakopoulos PJ; Piton A; Carson AR; Orlic-Milacic M; Lionel AC; Sato D; Pinto D; Drmic I; Noakes C; Senman L; Zhang X; Mo R; Gauthier J; Crosbie J; Pagnamenta AT; Munson J; Estes AM; Fiebig A; Franke A; Schreiber S; Stewart AF; Roberts R; McPherson R; Guter SJ; Cook EH; Dawson G; Schellenberg GD; Battaglia A; Maestrini E; ; Jeng L; Hutchison T; Rajcan-Separovic E; Chudley AE; Lewis SM; Liu X; Holden JJ; Fernandez B; Zwaigenbaum L; Bryson SE; Roberts W; Szatmari P; Gallagher L; Stratton MR; Gecz J; Brady AF; Schwartz CE; Schachar RJ; Monaco AP; Rouleau GA; Hui CC; Lucy Raymond F; Scherer SW; Vincent JB
    Sci Transl Med; 2010 Sep; 2(49):49ra68. PubMed ID: 20844286
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.