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 *

126 related articles for article (PubMed ID: 28970473)

  • 1. Patient-derived hiPSC neurons with heterozygous CNTNAP2 deletions display altered neuronal gene expression and network activity.
    Flaherty E; Deranieh RM; Artimovich E; Lee IS; Siegel AJ; Levy DL; Nestor MW; Brennand KJ
    NPJ Schizophr; 2017 Oct; 3(1):35. PubMed ID: 28970473
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Characterization of molecular and cellular phenotypes associated with a heterozygous
    Lee IS; Carvalho CM; Douvaras P; Ho SM; Hartley BJ; Zuccherato LW; Ladran IG; Siegel AJ; McCarthy S; Malhotra D; Sebat J; Rapoport J; Fossati V; Lupski JR; Levy DL; Brennand KJ
    NPJ Schizophr; 2015 Jun; 1():15019-. PubMed ID: 26985448
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Intragenic
    Poot M
    Mol Syndromol; 2017 May; 8(3):118-130. PubMed ID: 28588433
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1.
    Gregor A; Albrecht B; Bader I; Bijlsma EK; Ekici AB; Engels H; Hackmann K; Horn D; Hoyer J; Klapecki J; Kohlhase J; Maystadt I; Nagl S; Prott E; Tinschert S; Ullmann R; Wohlleber E; Woods G; Reis A; Rauch A; Zweier C
    BMC Med Genet; 2011 Aug; 12():106. PubMed ID: 21827697
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders.
    Toma C; Pierce KD; Shaw AD; Heath A; Mitchell PB; Schofield PR; Fullerton JM
    PLoS Genet; 2018 Dec; 14(12):e1007535. PubMed ID: 30586385
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Loss of CNTNAP2 Alters Human Cortical Excitatory Neuron Differentiation and Neural Network Development.
    St George-Hyslop F; Haneklaus M; Kivisild T; Livesey FJ
    Biol Psychiatry; 2023 Nov; 94(10):780-791. PubMed ID: 37001843
    [TBL] [Abstract][Full Text] [Related]  

  • 7.
    Canali G; Goutebroze L
    J Exp Neurosci; 2018; 12():1179069518809666. PubMed ID: 30450007
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Modelling monogenic autism spectrum disorder using mouse cortical organoids.
    Hali S; Kim J; Kwak TH; Lee H; Shin CY; Han DW
    Biochem Biophys Res Commun; 2020 Jan; 521(1):164-171. PubMed ID: 31653345
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Pitt Hopkins-Like Syndrome 1 with Novel CNTNAP2 Mutation in Siblings.
    Mittal R; Kumar A; Ladda R; Mainali G; Aliu E
    Child Neurol Open; 2021; 8():2329048X211055330. PubMed ID: 34778490
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Altered neurite morphology and cholinergic function of induced pluripotent stem cell-derived neurons from a patient with Kleefstra syndrome and autism.
    Nagy J; Kobolák J; Berzsenyi S; Ábrahám Z; Avci HX; Bock I; Bekes Z; Hodoscsek B; Chandrasekaran A; Téglási A; Dezső P; Koványi B; Vörös ET; Fodor L; Szél T; Németh K; Balázs A; Dinnyés A; Lendvai B; Lévay G; Román V
    Transl Psychiatry; 2017 Jul; 7(7):e1179. PubMed ID: 28742076
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Intronic Variant in
    Falsaperla R; Pappalardo XG; Romano C; Marino SD; Corsello G; Ruggieri M; Parano E; Pavone P
    Front Pediatr; 2020; 8():550. PubMed ID: 33042910
    [No Abstract]   [Full Text] [Related]  

  • 12. Synaptic abnormalities and cytoplasmic glutamate receptor aggregates in contactin associated protein-like 2/Caspr2 knockout neurons.
    Varea O; Martin-de-Saavedra MD; Kopeikina KJ; Schürmann B; Fleming HJ; Fawcett-Patel JM; Bach A; Jang S; Peles E; Kim E; Penzes P
    Proc Natl Acad Sci U S A; 2015 May; 112(19):6176-81. PubMed ID: 25918374
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic variants in autism-related CNTNAP2 impair axonal growth of cortical neurons.
    Canali G; Garcia M; Hivert B; Pinatel D; Goullancourt A; Oguievetskaia K; Saint-Martin M; Girault JA; Faivre-Sarrailh C; Goutebroze L
    Hum Mol Genet; 2018 Jun; 27(11):1941-1954. PubMed ID: 29788201
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular Architecture of Contactin-associated Protein-like 2 (CNTNAP2) and Its Interaction with Contactin 2 (CNTN2).
    Lu Z; Reddy MV; Liu J; Kalichava A; Liu J; Zhang L; Chen F; Wang Y; Holthauzen LM; White MA; Seshadrinathan S; Zhong X; Ren G; Rudenko G
    J Biol Chem; 2016 Nov; 291(46):24133-24147. PubMed ID: 27621318
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders.
    Poot M
    Mol Syndromol; 2015 Feb; 6(1):7-22. PubMed ID: 25852443
    [TBL] [Abstract][Full Text] [Related]  

  • 16. ANK2 loss-of-function variants are associated with epilepsy, and lead to impaired axon initial segment plasticity and hyperactive network activity in hiPSC-derived neuronal networks.
    Teunissen MWA; Lewerissa E; van Hugte EJH; Wang S; Ockeloen CW; Koolen DA; Pfundt R; Marcelis CLM; Brilstra E; Howe JL; Scherer SW; Le Guillou X; Bilan F; Primiano M; Roohi J; Piton A; de Saint Martin A; Baer S; Seiffert S; Platzer K; Jamra RA; Syrbe S; Doering JH; Lakhani S; Nangia S; Gilissen C; Vermeulen RJ; Rouhl RPW; Brunner HG; Willemsen MH; Nadif Kasri N
    Hum Mol Genet; 2023 Jul; 32(14):2373-2385. PubMed ID: 37195288
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A Novel
    Lu P; Wang F; Zhou S; Huang X; Sun H; Zhang YW; Yao Y; Zheng H
    Front Neurol; 2021; 12():712773. PubMed ID: 34737720
    [No Abstract]   [Full Text] [Related]  

  • 18. Learning delays in a mouse model of Autism Spectrum Disorder.
    Rendall AR; Truong DT; Fitch RH
    Behav Brain Res; 2016 Apr; 303():201-7. PubMed ID: 26873041
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Eight further individuals with intellectual disability and epilepsy carrying bi-allelic CNTNAP2 aberrations allow delineation of the mutational and phenotypic spectrum.
    Smogavec M; Cleall A; Hoyer J; Lederer D; Nassogne MC; Palmer EE; Deprez M; Benoit V; Maystadt I; Noakes C; Leal A; Shaw M; Gecz J; Raymond L; Reis A; Shears D; Brockmann K; Zweier C
    J Med Genet; 2016 Dec; 53(12):820-827. PubMed ID: 27439707
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Altered Auditory Processing, Filtering, and Reactivity in the
    Scott KE; Schormans AL; Pacoli KY; De Oliveira C; Allman BL; Schmid S
    J Neurosci; 2018 Oct; 38(40):8588-8604. PubMed ID: 30126973
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.