Artículos de revistas sobre el tema "CNTNAP2 gene"
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Varea, Olga, Maria Dolores Martin-de-Saavedra, Katherine J. Kopeikina, Britta Schürmann, Hunter J. Fleming, Jessica M. Fawcett-Patel, Anthony Bach et al. "Synaptic abnormalities and cytoplasmic glutamate receptor aggregates in contactin associated protein-like 2/Caspr2 knockout neurons". Proceedings of the National Academy of Sciences 112, n.º 19 (27 de abril de 2015): 6176–81. http://dx.doi.org/10.1073/pnas.1423205112.
Texto completoPapale, Ligia A., Andy Madrid, Qi Zhang, Kailei Chen, Lara Sak, Sündüz Keleş y Reid S. Alisch. "Gene by environment interaction mouse model reveals a functional role for 5-hydroxymethylcytosine in neurodevelopmental disorders". Genome Research 32, n.º 2 (23 de diciembre de 2021): 266–79. http://dx.doi.org/10.1101/gr.276137.121.
Texto completoMemis, Idil, Rahul Mittal, Emily Furar, Isaiah White, Rebecca S. Eshraghi, Jeenu Mittal y Adrien A. Eshraghi. "Altered Blood Brain Barrier Permeability and Oxidative Stress in Cntnap2 Knockout Rat Model". Journal of Clinical Medicine 11, n.º 10 (11 de mayo de 2022): 2725. http://dx.doi.org/10.3390/jcm11102725.
Texto completoAl-Murrani, Amel, Fern Ashton, Salim Aftimos, Alice M. George y Donald R. Love. "Amino-Terminal Microdeletion within theCNTNAP2Gene Associated with Variable Expressivity of Speech Delay". Case Reports in Genetics 2012 (2012): 1–4. http://dx.doi.org/10.1155/2012/172408.
Texto completoFang, Fang, Minxia Ge, Jun Liu, Zengyu Zhang, Hong Yu, Shuilong Zhu, Liwei Xu y Lina Shao. "Association between Genetic Variants in DUSP15, CNTNAP2, and PCDHA Genes and Risk of Childhood Autism Spectrum Disorder". Behavioural Neurology 2021 (28 de junio de 2021): 1–6. http://dx.doi.org/10.1155/2021/4150926.
Texto completoBartolome, Ruby, Tomoko Kaneko-Tarui, Jill Maron y Emily Zimmerman. "The Utility of Speech-Language Biomarkers to Predict Oral Feeding Outcomes in the Premature Newborn". American Journal of Speech-Language Pathology 29, n.º 2S (10 de julio de 2020): 1022–29. http://dx.doi.org/10.1044/2019_ajslp-csw18-19-0027.
Texto completoRanieri, Annaluisa, Iolanda Veneruso, Ilaria La Monica, Maria Grazia Pascale, Lucio Pastore, Valeria D’Argenio y Barbara Lombardo. "Combined aCGH and Exome Sequencing Analysis Improves Autism Spectrum Disorders Diagnosis: A Case Report". Medicina 58, n.º 4 (7 de abril de 2022): 522. http://dx.doi.org/10.3390/medicina58040522.
Texto completoFolia, Vasiliki, Christian Forkstam, Martin Ingvar y Karl Magnus Petersson. "Implicit Artificial Syntax Processing: Genes, Preference, and Bounded Recursion". Biolinguistics 5, n.º 1-2 (27 de junio de 2011): 105–32. http://dx.doi.org/10.5964/bioling.8835.
Texto completoMittal, Rea, Ashutosh Kumar, Roger Ladda, Gayatra Mainali y Ermal Aliu. "Pitt Hopkins-Like Syndrome 1 with Novel CNTNAP2 Mutation in Siblings". Child Neurology Open 8 (enero de 2021): 2329048X2110553. http://dx.doi.org/10.1177/2329048x211055330.
Texto completoDas, Arundhuti, Luca Pagliaroli, Andrea Vereczkei, Eszter Kotyuk, Banrida Langstieh, Zsolt Demetrovics y Csaba Barta. "Association of GDNF and CNTNAP2 gene variants with gambling". Journal of Behavioral Addictions 8, n.º 3 (1 de septiembre de 2019): 471–78. http://dx.doi.org/10.1556/2006.8.2019.40.
Texto completoFernandes, Dominique, Sandra D. Santos, Ester Coutinho, Jessica L. Whitt, Nuno Beltrão, Tiago Rondão, M. Isabel Leite, Camilla Buckley, Hey-Kyoung Lee y Ana Luísa Carvalho. "Disrupted AMPA Receptor Function upon Genetic- or Antibody-Mediated Loss of Autism-Associated CASPR2". Cerebral Cortex 29, n.º 12 (4 de marzo de 2019): 4919–31. http://dx.doi.org/10.1093/cercor/bhz032.
Texto completoFriedman, J. I., T. Vrijenhoek, S. Markx, I. M. Janssen, W. A. van der Vliet, B. H. W. Faas, N. V. Knoers et al. "CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy". Molecular Psychiatry 13, n.º 3 (24 de julio de 2007): 261–66. http://dx.doi.org/10.1038/sj.mp.4002049.
Texto completoAlarcón, Maricela, Brett S. Abrahams, Jennifer L. Stone, Jacqueline A. Duvall, Julia V. Perederiy, Jamee M. Bomar, Jonathan Sebat et al. "Linkage, Association, and Gene-Expression Analyses Identify CNTNAP2 as an Autism-Susceptibility Gene". American Journal of Human Genetics 82, n.º 1 (enero de 2008): 150–59. http://dx.doi.org/10.1016/j.ajhg.2007.09.005.
Texto completoSiddiqua, Hafsa, Yasmin Akter, Md Arju Mia, Mst Sharika Ahmed, Mahmood Ahmed Chowdhury y Lolo Wal Marzan. "A case-control study along with an epidemiological approach to CNTNAP2 polymorphism among Bangladeshi ASD children". Asian Journal of Medical and Biological Research 8, n.º 2 (26 de junio de 2022): 79–93. http://dx.doi.org/10.3329/ajmbr.v8i2.59511.
Texto completoGandhi, Tanya, Cade R. Canepa, Tolulope T. Adeyelu, Philip A. Adeniyi y Charles C. Lee. "Neuroanatomical Alterations in the CNTNAP2 Mouse Model of Autism Spectrum Disorder". Brain Sciences 13, n.º 6 (31 de mayo de 2023): 891. http://dx.doi.org/10.3390/brainsci13060891.
Texto completoFriedman, J. I., T. Vrijenhoek, S. Markx, I. M. Janssen, W. A. van der Vliet, B. H. W. Faas, N. V. Knoers et al. "Erratum: CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy". Molecular Psychiatry 15, n.º 11 (20 de abril de 2010): 1121. http://dx.doi.org/10.1038/mp.2010.20.
Texto completoZare, Sahar, Farhad Mashayekhi y Elham Bidabadi. "The association of CNTNAP2 rs7794745 gene polymorphism and autism in Iranian population". Journal of Clinical Neuroscience 39 (mayo de 2017): 189–92. http://dx.doi.org/10.1016/j.jocn.2017.01.008.
Texto completoKaraca, Irmak, Suzan Guven Yilmaz, Melis Palamar, Huseyin Onay, Bilcag Akgun, Burcu Aytacoglu, Ayca Aykut y Feristah Ferda Ozkinay. "Evaluation of CNTNAP2 gene rs2107856 polymorphism in Turkish population with pseudoexfoliation syndrome". International Ophthalmology 39, n.º 1 (19 de diciembre de 2017): 167–73. http://dx.doi.org/10.1007/s10792-017-0800-3.
Texto completoDennis, Emily L., Neda Jahanshad, Jeffrey D. Rudie, Jesse A. Brown, Kori Johnson, Katie L. McMahon, Greig I. de Zubicaray et al. "Altered Structural Brain Connectivity in Healthy Carriers of the Autism Risk Gene,CNTNAP2". Brain Connectivity 1, n.º 6 (diciembre de 2011): 447–59. http://dx.doi.org/10.1089/brain.2011.0064.
Texto completoJurgensen, S. y P. E. Castillo. "Selective Dysregulation of Hippocampal Inhibition in the Mouse Lacking Autism Candidate Gene CNTNAP2". Journal of Neuroscience 35, n.º 43 (28 de octubre de 2015): 14681–87. http://dx.doi.org/10.1523/jneurosci.1666-15.2015.
Texto completoValeeva, Elena V., Ilnur S. Sabirov, Liliya R. Safiullina, Dmitriy O. Nikitin, Irina I. Semina, Tim Rees, Denis O. Fesenko y Ildus I. Ahmetov. "The role of the CNTNAP2 gene in the development of autism spectrum disorder". Research in Autism Spectrum Disorders 114 (junio de 2024): 102409. http://dx.doi.org/10.1016/j.rasd.2024.102409.
Texto completoHoffman, Ellen J., Katherine J. Turner, Joseph M. Fernandez, Daniel Cifuentes, Marcus Ghosh, Sundas Ijaz, Roshan A. Jain et al. "Estrogens Suppress a Behavioral Phenotype in Zebrafish Mutants of the Autism Risk Gene, CNTNAP2". Neuron 89, n.º 4 (febrero de 2016): 725–33. http://dx.doi.org/10.1016/j.neuron.2015.12.039.
Texto completoShimoda, Yasushi, Hidehiro Ueda y Kazutada Watanabe. "Involvement of Caspr2 encoded by neuropsychiatric developmental disorder-susceptibility gene CNTNAP2 in the synaptogenesis". Neuroscience Research 65 (enero de 2009): S99. http://dx.doi.org/10.1016/j.neures.2009.09.427.
Texto completoBocharova, Anna, Kseniya Vagaitseva, Andrey Marusin, Natalia Zhukova, Irina Zhukova, Larisa Minaycheva, Oksana Makeeva y Vadim Stepanov. "Association and Gene–Gene Interactions Study of Late-Onset Alzheimer’s Disease in the Russian Population". Genes 12, n.º 10 (19 de octubre de 2021): 1647. http://dx.doi.org/10.3390/genes12101647.
Texto completoNakabayashi, Kazuhiko y Stephen W. Scherer. "The Human Contactin-Associated Protein-like 2 Gene (CNTNAP2) Spans over 2 Mb of DNA at Chromosome 7q35". Genomics 73, n.º 1 (abril de 2001): 108–12. http://dx.doi.org/10.1006/geno.2001.6517.
Texto completoZhu, Bi, Chuansheng Chen, Gui Xue, Xuemei Lei, Yunxin Wang, Jin Li, Robert K. Moyzis, Jun Li, Qi Dong y Chongde Lin. "Associations between the CNTNAP2 gene, dorsolateral prefrontal cortex, and cognitive performance on the Stroop task". Neuroscience 343 (febrero de 2017): 21–29. http://dx.doi.org/10.1016/j.neuroscience.2016.11.021.
Texto completoRoss, Lars A., Victor A. Del Bene, Sophie Molholm, Young Jae Woo, Gizely N. Andrade, Brett S. Abrahams y John J. Foxe. "Common variation in the autism risk gene CNTNAP2, brain structural connectivity and multisensory speech integration". Brain and Language 174 (noviembre de 2017): 50–60. http://dx.doi.org/10.1016/j.bandl.2017.07.005.
Texto completoWerling, Anna Maria, Elise Bobrowski, Regina Taurines, Ronnie Gundelfinger, Marcel Romanos, Edna Grünblatt y Susanne Walitza. "CNTNAP2 gene in high functioning autism: no association according to family and meta-analysis approaches". Journal of Neural Transmission 123, n.º 3 (11 de noviembre de 2015): 353–63. http://dx.doi.org/10.1007/s00702-015-1458-5.
Texto completoGu, Huaiting, Fang Hou, Lingfei Liu, Xiu Luo, Pauline Denis Nkomola, Xinyan Xie, Xin Li y Ranran Song. "Genetic variants in the CNTNAP2 gene are associated with gender differences among dyslexic children in China". EBioMedicine 34 (agosto de 2018): 165–70. http://dx.doi.org/10.1016/j.ebiom.2018.07.007.
Texto completoChien, Yi-Ling, Yu-Chieh Chen y Susan Shur-Fen Gau. "Altered cingulate structures and the associations with social awareness deficits and CNTNAP2 gene in autism spectrum disorder". NeuroImage: Clinical 31 (2021): 102729. http://dx.doi.org/10.1016/j.nicl.2021.102729.
Texto completoScott-Van Zeeland, A. A., B. S. Abrahams, A. I. Alvarez-Retuerto, L. I. Sonnenblick, J. D. Rudie, D. Ghahremani, J. A. Mumford et al. "Altered Functional Connectivity in Frontal Lobe Circuits Is Associated with Variation in the Autism Risk Gene CNTNAP2". Science Translational Medicine 2, n.º 56 (3 de noviembre de 2010): 56ra80. http://dx.doi.org/10.1126/scitranslmed.3001344.
Texto completoLiska, Adam, Alice Bertero, Ryszard Gomolka, Mara Sabbioni, Alberto Galbusera, Noemi Barsotti, Stefano Panzeri, Maria Luisa Scattoni, Massimo Pasqualetti y Alessandro Gozzi. "Homozygous Loss of Autism-Risk Gene CNTNAP2 Results in Reduced Local and Long-Range Prefrontal Functional Connectivity". Cerebral Cortex 28, n.º 4 (10 de febrero de 2017): 1141–53. http://dx.doi.org/10.1093/cercor/bhx022.
Texto completoBai, Tongjian, Long Zhang, Xiaohui Xie, Guixian Xiao, Wanling Huang, Dandan Li, Meidan Zu et al. "Common variant of CNTNAP2 gene modulate the social performances and functional connectivity of posterior right temporoparietal junction". Social Cognitive and Affective Neuroscience 14, n.º 12 (diciembre de 2019): 1297–305. http://dx.doi.org/10.1093/scan/nsaa008.
Texto completoPetrin, Aline L., Célia M. Giacheti, Luciana P. Maximino, Dagma V. M. Abramides, Sthella Zanchetta, Natalia F. Rossi, Antônio Richieri-Costa y Jeffrey C. Murray. "Identification of a microdeletion at the 7q33-q35 disrupting the CNTNAP2 gene in a Brazilian stuttering case". American Journal of Medical Genetics Part A 152A, n.º 12 (24 de noviembre de 2010): 3164–72. http://dx.doi.org/10.1002/ajmg.a.33749.
Texto completoVorn, Rany, Katie A. Edwards, James Hentig, Sijung Yun, Hyung-Suk Kim, Chen Lai, Christina Devoto et al. "A Pilot Study of Whole-Blood Transcriptomic Analysis to Identify Genes Associated with Repetitive Low-Level Blast Exposure in Career Breachers". Biomedicines 10, n.º 3 (17 de marzo de 2022): 690. http://dx.doi.org/10.3390/biomedicines10030690.
Texto completoSchaafsma, Sara M., Khatuna Gagnidze, Anny Reyes, Natalie Norstedt, Karl Månsson, Kerel Francis y Donald W. Pfaff. "Sex-specific gene–environment interactions underlying ASD-like behaviors". Proceedings of the National Academy of Sciences 114, n.º 6 (23 de enero de 2017): 1383–88. http://dx.doi.org/10.1073/pnas.1619312114.
Texto completoUddén, Julia, Tineke M. Snijders, Simon E. Fisher y Peter Hagoort. "A common variant of the CNTNAP2 gene is associated with structural variation in the left superior occipital gyrus". Brain and Language 172 (septiembre de 2017): 16–21. http://dx.doi.org/10.1016/j.bandl.2016.02.003.
Texto completoPaduano, Francesco, Emma Colao, Sara Loddo, Valeria Orlando, Francesco Trapasso, Antonio Novelli, Nicola Perrotti y Rodolfo Iuliano. "7q35 Microdeletion and 15q13.3 and Xp22.33 Microduplications in a Patient with Severe Myoclonic Epilepsy, Microcephaly, Dysmorphisms, Severe Psychomotor Delay and Intellectual Disability". Genes 11, n.º 5 (8 de mayo de 2020): 525. http://dx.doi.org/10.3390/genes11050525.
Texto completoBrignoni, Lucía, Mónica Cappetta, Valentina Colistro, Mónica Sans, Nora Artagaveytia, Carolina Bonilla y Bernardo Bertoni. "Genomic Diversity in Sporadic Breast Cancer in a Latin American Population". Genes 11, n.º 11 (28 de octubre de 2020): 1272. http://dx.doi.org/10.3390/genes11111272.
Texto completoHsu, Michelle, Mehek Dedhia, Wim E. Crusio y Anna Delprato. "Sex differences in gene expression patterns associated with the APOE4 allele". F1000Research 8 (23 de julio de 2019): 387. http://dx.doi.org/10.12688/f1000research.18671.2.
Texto completoToma, Claudio, Kerrie D. Pierce, Alex D. Shaw, Anna Heath, Philip B. Mitchell, Peter R. Schofield y Janice M. Fullerton. "Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders". PLOS Genetics 14, n.º 12 (26 de diciembre de 2018): e1007535. http://dx.doi.org/10.1371/journal.pgen.1007535.
Texto completoBelloso, Jose M., Iben Bache, Miriam Guitart, Maria Rosa Caballin, Christina Halgren, Maria Kirchhoff, Hans-Hilger Ropers, Niels Tommerup y Zeynep Tümer. "Disruption of the CNTNAP2 gene in a t(7;15) translocation family without symptoms of Gilles de la Tourette syndrome". European Journal of Human Genetics 15, n.º 6 (28 de marzo de 2007): 711–13. http://dx.doi.org/10.1038/sj.ejhg.5201824.
Texto completoWittekind, Dirk Alexander, Markus Scholz, Jürgen Kratzsch, Markus Löffler, Katrin Horn, Holger Kirsten, Veronica Witte, Arno Villringer y Michael Kluge. "Genome-wide association and transcriptome analysis suggests total serum ghrelin to be linked with GFRAL". European Journal of Endocrinology 184, n.º 6 (1 de junio de 2021): 847–56. http://dx.doi.org/10.1530/eje-20-1220.
Texto completoLi, Dandan, Long Zhang, Tongjian Bai, Wanling Huang, Gong-Jun Ji, Tingting Yang, Yifan Zhang, Yanghua Tian, Bensheng Qiu y Kai Wang. "Common variants of the autism-associated CNTNAP2 gene contribute to the modulatory effect of social function mediated by temporal cortex". Behavioural Brain Research 409 (julio de 2021): 113319. http://dx.doi.org/10.1016/j.bbr.2021.113319.
Texto completoMa, Yi-Nu, Ting-Yu Xie y Xue-Yi Chen. "Multiple Gene Polymorphisms Associated with Exfoliation Syndrome in the Uygur Population". Journal of Ophthalmology 2019 (2 de mayo de 2019): 1–8. http://dx.doi.org/10.1155/2019/9687823.
Texto completoUddin, Mohammad Sarowar, Atkia Azima, Md Abdul Aziz, Tutun Das Aka, Sarah Jafrin, Md Shalahuddin Millat, Shafayet Ahmed Siddiqui, Md Giash Uddin, Md Saddam Hussain y Mohammad Safiqul Islam. "CNTNAP2 gene polymorphisms in autism spectrum disorder and language impairment among Bangladeshi children: a case–control study combined with a meta-analysis". Human Cell 34, n.º 5 (5 de mayo de 2021): 1410–23. http://dx.doi.org/10.1007/s13577-021-00546-8.
Texto completoKim, Sang Yoon, Seung Min Lee, Jonghoon Shin, Ji Eun Lee y Su Jin Kim. "Two Cases of Ocular Manifestations in Patients with Microdeletion of the Chromosome 7 Long Arm". Journal of the Korean Ophthalmological Society 62, n.º 7 (15 de julio de 2021): 1003–7. http://dx.doi.org/10.3341/jkos.2021.62.7.1003.
Texto completoLewis-Smith, David, Donald Craig y Rhys Thomas. "094 The adult phenotypes of paediatric-onset genetic epilepsies". Journal of Neurology, Neurosurgery & Psychiatry 90, n.º 12 (14 de noviembre de 2019): A29.3—A29. http://dx.doi.org/10.1136/jnnp-2019-abn-2.97.
Texto completoIakoubov, Leonid, Malgorzata Mossakowska, Malgorzata Szwed y Monika Puzianowska-Kuznicka. "A Common Copy Number Variation Polymorphism in the CNTNAP2 Gene: Sexual Dimorphism in Association with Healthy Aging and Disease". Gerontology 61, n.º 1 (18 de agosto de 2014): 24–31. http://dx.doi.org/10.1159/000363320.
Texto completoMaccaroni, Klizia, Elisa Balzano, Federica Mirimao, Simona Giunta y Franca Pelliccia. "Impaired Replication Timing Promotes Tissue-Specific Expression of Common Fragile Sites". Genes 11, n.º 3 (19 de marzo de 2020): 326. http://dx.doi.org/10.3390/genes11030326.
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