BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

257 related articles for article (PubMed ID: 28463240)

  • 21. IQSEC2 Deficiency Results in Abnormal Social Behaviors Relevant to Autism by Affecting Functions of Neural Circuits in the Medial Prefrontal Cortex.
    Mehta A; Shirai Y; Kouyama-Suzuki E; Zhou M; Yoshizawa T; Yanagawa T; Mori T; Tabuchi K
    Cells; 2021 Oct; 10(10):. PubMed ID: 34685703
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Immature morphological properties in subcellular-scale structures in the dentate gyrus of Schnurri-2 knockout mice: a model for schizophrenia and intellectual disability.
    Nakao A; Miyazaki N; Ohira K; Hagihara H; Takagi T; Usuda N; Ishii S; Murata K; Miyakawa T
    Mol Brain; 2017 Dec; 10(1):60. PubMed ID: 29233179
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A Christianson syndrome-linked deletion mutation (Δ287ES288) in SLC9A6 impairs hippocampal neuronal plasticity.
    Gao AYL; Ilie A; Chang PKY; Orlowski J; McKinney RA
    Neurobiol Dis; 2019 Oct; 130():104490. PubMed ID: 31175985
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Molecular Insights into IQSEC2 Disease.
    Levy NS; Borisov V; Lache O; Levy AP
    Int J Mol Sci; 2023 Mar; 24(5):. PubMed ID: 36902414
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Remodeling of dendrites and spines in the C1q knockout model of genetic epilepsy.
    Ma Y; Ramachandran A; Ford N; Parada I; Prince DA
    Epilepsia; 2013 Jul; 54(7):1232-9. PubMed ID: 23621154
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Subtle functional defects in the Arf-specific guanine nucleotide exchange factor IQSEC2 cause non-syndromic X-linked intellectual disability.
    Shoubridge C; Walikonis RS; Gécz J; Harvey RJ
    Small GTPases; 2010 Sep; 1(2):98-103. PubMed ID: 21686261
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Impaired Dendritic Development and Memory in Sorbs2 Knock-Out Mice.
    Zhang Q; Gao X; Li C; Feliciano C; Wang D; Zhou D; Mei Y; Monteiro P; Anand M; Itohara S; Dong X; Fu Z; Feng G
    J Neurosci; 2016 Feb; 36(7):2247-60. PubMed ID: 26888934
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Role of numb in dendritic spine development with a Cdc42 GEF intersectin and EphB2.
    Nishimura T; Yamaguchi T; Tokunaga A; Hara A; Hamaguchi T; Kato K; Iwamatsu A; Okano H; Kaibuchi K
    Mol Biol Cell; 2006 Mar; 17(3):1273-85. PubMed ID: 16394100
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Perturbation of dendritic protrusions in intellectual disability.
    Levenga J; Willemsen R
    Prog Brain Res; 2012; 197():153-68. PubMed ID: 22541292
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Xp11.2 microduplications including IQSEC2, TSPYL2 and KDM5C genes in patients with neurodevelopmental disorders.
    Moey C; Hinze SJ; Brueton L; Morton J; McMullan DJ; Kamien B; Barnett CP; Brunetti-Pierri N; Nicholl J; Gecz J; Shoubridge C
    Eur J Hum Genet; 2016 Mar; 24(3):373-80. PubMed ID: 26059843
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Rho GTPase signaling at the synapse: implications for intellectual disability.
    Ba W; van der Raadt J; Nadif Kasri N
    Exp Cell Res; 2013 Sep; 319(15):2368-74. PubMed ID: 23769912
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Differences in Expression of
    Baladron B; Mielu LM; López-Martín E; Barrero MJ; Lopez L; Alvarado JI; Monzón S; Varona S; Cuesta I; Cazorla R; Lara J; Iglesias G; Román E; Ros P; Gomez-Mariano G; Cubillo I; Miguel EH; Rivera D; Alonso J; Bermejo-Sánchez E; Posada M; Martínez-Delgado B
    Int J Mol Sci; 2022 Aug; 23(16):. PubMed ID: 36012761
    [TBL] [Abstract][Full Text] [Related]  

  • 33. The role of IQSEC2 in syndromic intellectual disability: Narrowing the diagnostic odyssey.
    Helm BM; Powis Z; Prada CE; Casasbuenas-Alarcon OL; Balmakund T; Schaefer GB; Kahler SG; Kaylor J; Winter S; Zarate YA; Schrier Vergano SA
    Am J Med Genet A; 2017 Oct; 173(10):2814-2820. PubMed ID: 28815955
    [TBL] [Abstract][Full Text] [Related]  

  • 34.
    Liu X; Zhang S; Wan L; Zhang X; Wang H; Zhang H; Zhu G; Liang Y; Yan H; Zhang B; Yang G
    Front Mol Neurosci; 2022; 15():984776. PubMed ID: 36267700
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Diagnostic exome sequencing identifies two novel IQSEC2 mutations associated with X-linked intellectual disability with seizures: implications for genetic counseling and clinical diagnosis.
    Gandomi SK; Farwell Gonzalez KD; Parra M; Shahmirzadi L; Mancuso J; Pichurin P; Temme R; Dugan S; Zeng W; Tang S
    J Genet Couns; 2014 Jun; 23(3):289-98. PubMed ID: 24306141
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Structural and functional brain-wide alterations in A350V Iqsec2 mutant mice displaying autistic-like behavior.
    Lichtman D; Bergmann E; Kavushansky A; Cohen N; Levy NS; Levy AP; Kahn I
    Transl Psychiatry; 2021 Mar; 11(1):181. PubMed ID: 33753721
    [TBL] [Abstract][Full Text] [Related]  

  • 37. TRIO loss of function is associated with mild intellectual disability and affects dendritic branching and synapse function.
    Ba W; Yan Y; Reijnders MR; Schuurs-Hoeijmakers JH; Feenstra I; Bongers EM; Bosch DG; De Leeuw N; Pfundt R; Gilissen C; De Vries PF; Veltman JA; Hoischen A; Mefford HC; Eichler EE; Vissers LE; Nadif Kasri N; De Vries BB
    Hum Mol Genet; 2016 Mar; 25(5):892-902. PubMed ID: 26721934
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Preliminary Study on Clinical Characteristics and Pathogenesis of
    Ren Y; Luo X; Tong H; Wang S; Yan J; Lin L; Chen Y
    Pharmgenomics Pers Med; 2024; 17():289-318. PubMed ID: 38827181
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The role of glia in the dysregulation of neuronal spinogenesis in Ube3a-dependent ASD.
    Gardner Z; Holbrook O; Tian Y; Odamah K; Man HY
    Exp Neurol; 2024 Jun; 376():114756. PubMed ID: 38508482
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Dendritic spine and dendritic field characteristics of layer V pyramidal neurons in the visual cortex of fragile-X knockout mice.
    Irwin SA; Idupulapati M; Gilbert ME; Harris JB; Chakravarti AB; Rogers EJ; Crisostomo RA; Larsen BP; Mehta A; Alcantara CJ; Patel B; Swain RA; Weiler IJ; Oostra BA; Greenough WT
    Am J Med Genet; 2002 Aug; 111(2):140-6. PubMed ID: 12210340
    [TBL] [Abstract][Full Text] [Related]  

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