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Journal Abstract Search

247 related items for PubMed ID: 26782176

  • 1. The roles of CC2D1A and HTR1A gene expressions in autism spectrum disorders.
    Sener EF, Cıkılı Uytun M, Korkmaz Bayramov K, Zararsiz G, Oztop DB, Canatan H, Ozkul Y.
    Metab Brain Dis; 2016 Jun; 31(3):613-9. PubMed ID: 26782176
    [Abstract] [Full Text] [Related]

  • 2. Altered Global mRNA Expressions of Pain and Aggression Related Genes in the Blood of Children with Autism Spectrum Disorders.
    Sener EF, Taheri S, Sahin MC, Bayramov KK, Marasli MK, Zararsiz G, Mehmetbeyoglu E, Oztop DB, Canpolat M, Canatan H, Ozkul Y.
    J Mol Neurosci; 2019 Jan; 67(1):89-96. PubMed ID: 30519864
    [Abstract] [Full Text] [Related]

  • 3. Novel alterations of CC2D1A as a candidate gene in a Turkish sample of patients with autism spectrum disorder.
    Sener EF, Onal MG, Dal F, Nalbantoglu U, Ozkul Y, Canatan H, Oztop DB.
    Int J Neurosci; 2022 Nov; 132(11):1072-1079. PubMed ID: 33287601
    [Abstract] [Full Text] [Related]

  • 4. Disregulation of Autophagy in the Transgenerational Cc2d1a Mouse Model of Autism.
    Dana H, Bayramov KK, Delibaşı N, Tahtasakal R, Bayramov R, Hamurcu Z, Sener EF.
    Neuromolecular Med; 2020 Jun; 22(2):239-249. PubMed ID: 31721010
    [Abstract] [Full Text] [Related]

  • 5. Autism-Related Cc2d1a Heterozygous Mice: Increased Levels of miRNAs Retained in DNA/RNA Hybrid Profiles (R-Loop).
    Sener EF, Dana H, Tahtasakal R, Taheri S, Rassoulzadegan M.
    Biomolecules; 2024 Sep 20; 14(9):. PubMed ID: 39334949
    [Abstract] [Full Text] [Related]

  • 6. High-Fat Diet Exacerbates Autistic-Like Restricted Repetitive Behaviors and Social Abnormalities in CC2D1A Conditional Knockout Mice.
    Wang YC, Chen CH, Yang CY, Ling P, Hsu KS.
    Mol Neurobiol; 2023 Mar 20; 60(3):1331-1352. PubMed ID: 36445635
    [Abstract] [Full Text] [Related]

  • 7. A novel framework for functional annotation of variants of uncertain significance in ID/ASD risk gene CC2D1A.
    Bhattacharya A, Parlanti P, Cavallo L, Farrow E, Spivey T, Renieri A, Mari F, Manzini MC.
    Hum Mol Genet; 2024 Jul 06; 33(14):1229-1240. PubMed ID: 38652285
    [Abstract] [Full Text] [Related]

  • 8. Cc2d1a Loss of Function Disrupts Functional and Morphological Development in Forebrain Neurons Leading to Cognitive and Social Deficits.
    Oaks AW, Zamarbide M, Tambunan DE, Santini E, Di Costanzo S, Pond HL, Johnson MW, Lin J, Gonzalez DM, Boehler JF, Wu GK, Klann E, Walsh CA, Manzini MC.
    Cereb Cortex; 2017 Feb 01; 27(2):1670-1685. PubMed ID: 26826102
    [Abstract] [Full Text] [Related]

  • 9. Integrated genome-wide Alu methylation and transcriptome profiling analyses reveal novel epigenetic regulatory networks associated with autism spectrum disorder.
    Saeliw T, Tangsuwansri C, Thongkorn S, Chonchaiya W, Suphapeetiporn K, Mutirangura A, Tencomnao T, Hu VW, Sarachana T.
    Mol Autism; 2018 Feb 01; 9():27. PubMed ID: 29686828
    [Abstract] [Full Text] [Related]

  • 10. Autism spectrum disorder and comorbid neurodevelopmental disorders (ASD-NDDs): Clinical and genetic profile of a pediatric cohort.
    Chen S, Xiong J, Chen B, Zhang C, Deng X, He F, Yang L, Chen C, Peng J, Yin F.
    Clin Chim Acta; 2022 Jan 01; 524():179-186. PubMed ID: 34800434
    [Abstract] [Full Text] [Related]

  • 11. Effects of the Cc2d1a/Freud-1 Knockdown in the Hippocampus of BTBR Mice on the Autistic-Like Behavior, Expression of Serotonin 5-HT1A and D2 Dopamine Receptors, and CREB and NF-kB Intracellular Signaling.
    Belokopytova II, Kondaurova EM, Kulikova EA, Ilchibaeva TV, Naumenko VS, Popova NK.
    Biochemistry (Mosc); 2022 Oct 01; 87(10):1206-1218. PubMed ID: 36273889
    [Abstract] [Full Text] [Related]

  • 12. Salivary miRNA profiles identify children with autism spectrum disorder, correlate with adaptive behavior, and implicate ASD candidate genes involved in neurodevelopment.
    Hicks SD, Ignacio C, Gentile K, Middleton FA.
    BMC Pediatr; 2016 Apr 22; 16():52. PubMed ID: 27105825
    [Abstract] [Full Text] [Related]

  • 13. Genotype-phenotype analysis of 18q12.1-q12.2 copy number variation in autism.
    Wang P, Carrion P, Qiao Y, Tyson C, Hrynchak M, Calli K, Lopez-Rangel E, Andrieux J, Delobel B, Duban-Bedu B, Thuresson AC, Annerén G, Liu X, Rajcan-Separovic E, Suzanne Lewis ME.
    Eur J Med Genet; 2013 Aug 22; 56(8):420-5. PubMed ID: 23727450
    [Abstract] [Full Text] [Related]

  • 14. Loss of the Intellectual Disability and Autism Gene Cc2d1a and Its Homolog Cc2d1b Differentially Affect Spatial Memory, Anxiety, and Hyperactivity.
    Zamarbide M, Oaks AW, Pond HL, Adelman JS, Manzini MC.
    Front Genet; 2018 Aug 22; 9():65. PubMed ID: 29552027
    [Abstract] [Full Text] [Related]

  • 15. DNA repair gene XPD Asp312Asn and XRCC4 G-1394T polymorphisms and the risk of autism spectrum disorder.
    Dasdemir S, Guven M, Pekkoc KC, Ulucan H, Dogangun B, Kirtas E, Kadak MT, Kucur M, Seven M.
    Cell Mol Biol (Noisy-le-grand); 2016 Mar 20; 62(3):46-50. PubMed ID: 27064873
    [Abstract] [Full Text] [Related]

  • 16. Homozygous 2p11.2 deletion supports the implication of ELMOD3 in hearing loss and reveals the potential association of CAPG with ASD/ID etiology.
    Lahbib S, Leblond CS, Hamza M, Regnault B, Lemée L, Mathieu A, Jaouadi H, Mkaouar R, Youssef-Turki IB, Belhadj A, Kraoua I, Bourgeron T, Abdelhak S.
    J Appl Genet; 2019 Feb 20; 60(1):49-56. PubMed ID: 30284680
    [Abstract] [Full Text] [Related]

  • 17. Male-Specific cAMP Signaling in the Hippocampus Controls Spatial Memory Deficits in a Mouse Model of Autism and Intellectual Disability.
    Zamarbide M, Mossa A, Muñoz-Llancao P, Wilkinson MK, Pond HL, Oaks AW, Manzini MC.
    Biol Psychiatry; 2019 May 01; 85(9):760-768. PubMed ID: 30732858
    [Abstract] [Full Text] [Related]

  • 18. CHD8 intragenic deletion associated with autism spectrum disorder.
    Stolerman ES, Smith B, Chaubey A, Jones JR.
    Eur J Med Genet; 2016 Apr 01; 59(4):189-94. PubMed ID: 26921529
    [Abstract] [Full Text] [Related]

  • 19. Identification of a Novel Variant in CC2D1A Gene Linked to Autosomal Recessive Intellectual Disability 3 in an Iranian Family and Investigating the Structure and Pleiotropic Effects of this Gene.
    Rashvand Z, Najmabadi H, Kahrizi K, Mozhdehipanah H, Moradi M, Estaki Z, Taherkhani K, Nikzat N, Najafipour R, Omrani MD.
    Iran J Child Neurol; 2024 Apr 01; 18(1):25-41. PubMed ID: 38375126
    [Abstract] [Full Text] [Related]

  • 20. Loss of CC2D1A in Glutamatergic Neurons Results in Autistic-Like Features in Mice.
    Yang CY, Hung YC, Cheng KH, Ling P, Hsu KS.
    Neurotherapeutics; 2021 Jul 01; 18(3):2021-2039. PubMed ID: 34132974
    [Abstract] [Full Text] [Related]

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