Artykuły w czasopismach na temat „CNTNAP2 gene”
Utwórz poprawne odniesienie w stylach APA, MLA, Chicago, Harvard i wielu innych
Sprawdź 50 najlepszych artykułów w czasopismach naukowych na temat „CNTNAP2 gene”.
Przycisk „Dodaj do bibliografii” jest dostępny obok każdej pracy w bibliografii. Użyj go – a my automatycznie utworzymy odniesienie bibliograficzne do wybranej pracy w stylu cytowania, którego potrzebujesz: APA, MLA, Harvard, Chicago, Vancouver itp.
Możesz również pobrać pełny tekst publikacji naukowej w formacie „.pdf” i przeczytać adnotację do pracy online, jeśli odpowiednie parametry są dostępne w metadanych.
Przeglądaj artykuły w czasopismach z różnych dziedzin i twórz odpowiednie bibliografie.
Varea, Olga, Maria Dolores Martin-de-Saavedra, Katherine J. Kopeikina, Britta Schürmann, Hunter J. Fleming, Jessica M. Fawcett-Patel, Anthony Bach i in. "Synaptic abnormalities and cytoplasmic glutamate receptor aggregates in contactin associated protein-like 2/Caspr2 knockout neurons". Proceedings of the National Academy of Sciences 112, nr 19 (27.04.2015): 6176–81. http://dx.doi.org/10.1073/pnas.1423205112.
Pełny tekst źródłaPapale, Ligia A., Andy Madrid, Qi Zhang, Kailei Chen, Lara Sak, Sündüz Keleş i Reid S. Alisch. "Gene by environment interaction mouse model reveals a functional role for 5-hydroxymethylcytosine in neurodevelopmental disorders". Genome Research 32, nr 2 (23.12.2021): 266–79. http://dx.doi.org/10.1101/gr.276137.121.
Pełny tekst źródłaMemis, Idil, Rahul Mittal, Emily Furar, Isaiah White, Rebecca S. Eshraghi, Jeenu Mittal i Adrien A. Eshraghi. "Altered Blood Brain Barrier Permeability and Oxidative Stress in Cntnap2 Knockout Rat Model". Journal of Clinical Medicine 11, nr 10 (11.05.2022): 2725. http://dx.doi.org/10.3390/jcm11102725.
Pełny tekst źródłaAl-Murrani, Amel, Fern Ashton, Salim Aftimos, Alice M. George i 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.
Pełny tekst źródłaFang, Fang, Minxia Ge, Jun Liu, Zengyu Zhang, Hong Yu, Shuilong Zhu, Liwei Xu i Lina Shao. "Association between Genetic Variants in DUSP15, CNTNAP2, and PCDHA Genes and Risk of Childhood Autism Spectrum Disorder". Behavioural Neurology 2021 (28.06.2021): 1–6. http://dx.doi.org/10.1155/2021/4150926.
Pełny tekst źródłaBartolome, Ruby, Tomoko Kaneko-Tarui, Jill Maron i Emily Zimmerman. "The Utility of Speech-Language Biomarkers to Predict Oral Feeding Outcomes in the Premature Newborn". American Journal of Speech-Language Pathology 29, nr 2S (10.07.2020): 1022–29. http://dx.doi.org/10.1044/2019_ajslp-csw18-19-0027.
Pełny tekst źródłaRanieri, Annaluisa, Iolanda Veneruso, Ilaria La Monica, Maria Grazia Pascale, Lucio Pastore, Valeria D’Argenio i Barbara Lombardo. "Combined aCGH and Exome Sequencing Analysis Improves Autism Spectrum Disorders Diagnosis: A Case Report". Medicina 58, nr 4 (7.04.2022): 522. http://dx.doi.org/10.3390/medicina58040522.
Pełny tekst źródłaFolia, Vasiliki, Christian Forkstam, Martin Ingvar i Karl Magnus Petersson. "Implicit Artificial Syntax Processing: Genes, Preference, and Bounded Recursion". Biolinguistics 5, nr 1-2 (27.06.2011): 105–32. http://dx.doi.org/10.5964/bioling.8835.
Pełny tekst źródłaMittal, Rea, Ashutosh Kumar, Roger Ladda, Gayatra Mainali i Ermal Aliu. "Pitt Hopkins-Like Syndrome 1 with Novel CNTNAP2 Mutation in Siblings". Child Neurology Open 8 (styczeń 2021): 2329048X2110553. http://dx.doi.org/10.1177/2329048x211055330.
Pełny tekst źródłaDas, Arundhuti, Luca Pagliaroli, Andrea Vereczkei, Eszter Kotyuk, Banrida Langstieh, Zsolt Demetrovics i Csaba Barta. "Association of GDNF and CNTNAP2 gene variants with gambling". Journal of Behavioral Addictions 8, nr 3 (1.09.2019): 471–78. http://dx.doi.org/10.1556/2006.8.2019.40.
Pełny tekst źródłaFernandes, Dominique, Sandra D. Santos, Ester Coutinho, Jessica L. Whitt, Nuno Beltrão, Tiago Rondão, M. Isabel Leite, Camilla Buckley, Hey-Kyoung Lee i Ana Luísa Carvalho. "Disrupted AMPA Receptor Function upon Genetic- or Antibody-Mediated Loss of Autism-Associated CASPR2". Cerebral Cortex 29, nr 12 (4.03.2019): 4919–31. http://dx.doi.org/10.1093/cercor/bhz032.
Pełny tekst źródłaFriedman, J. I., T. Vrijenhoek, S. Markx, I. M. Janssen, W. A. van der Vliet, B. H. W. Faas, N. V. Knoers i in. "CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy". Molecular Psychiatry 13, nr 3 (24.07.2007): 261–66. http://dx.doi.org/10.1038/sj.mp.4002049.
Pełny tekst źródłaAlarcón, Maricela, Brett S. Abrahams, Jennifer L. Stone, Jacqueline A. Duvall, Julia V. Perederiy, Jamee M. Bomar, Jonathan Sebat i in. "Linkage, Association, and Gene-Expression Analyses Identify CNTNAP2 as an Autism-Susceptibility Gene". American Journal of Human Genetics 82, nr 1 (styczeń 2008): 150–59. http://dx.doi.org/10.1016/j.ajhg.2007.09.005.
Pełny tekst źródłaSiddiqua, Hafsa, Yasmin Akter, Md Arju Mia, Mst Sharika Ahmed, Mahmood Ahmed Chowdhury i 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, nr 2 (26.06.2022): 79–93. http://dx.doi.org/10.3329/ajmbr.v8i2.59511.
Pełny tekst źródłaGandhi, Tanya, Cade R. Canepa, Tolulope T. Adeyelu, Philip A. Adeniyi i Charles C. Lee. "Neuroanatomical Alterations in the CNTNAP2 Mouse Model of Autism Spectrum Disorder". Brain Sciences 13, nr 6 (31.05.2023): 891. http://dx.doi.org/10.3390/brainsci13060891.
Pełny tekst źródłaFriedman, J. I., T. Vrijenhoek, S. Markx, I. M. Janssen, W. A. van der Vliet, B. H. W. Faas, N. V. Knoers i in. "Erratum: CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy". Molecular Psychiatry 15, nr 11 (20.04.2010): 1121. http://dx.doi.org/10.1038/mp.2010.20.
Pełny tekst źródłaZare, Sahar, Farhad Mashayekhi i Elham Bidabadi. "The association of CNTNAP2 rs7794745 gene polymorphism and autism in Iranian population". Journal of Clinical Neuroscience 39 (maj 2017): 189–92. http://dx.doi.org/10.1016/j.jocn.2017.01.008.
Pełny tekst źródłaKaraca, Irmak, Suzan Guven Yilmaz, Melis Palamar, Huseyin Onay, Bilcag Akgun, Burcu Aytacoglu, Ayca Aykut i Feristah Ferda Ozkinay. "Evaluation of CNTNAP2 gene rs2107856 polymorphism in Turkish population with pseudoexfoliation syndrome". International Ophthalmology 39, nr 1 (19.12.2017): 167–73. http://dx.doi.org/10.1007/s10792-017-0800-3.
Pełny tekst źródłaDennis, Emily L., Neda Jahanshad, Jeffrey D. Rudie, Jesse A. Brown, Kori Johnson, Katie L. McMahon, Greig I. de Zubicaray i in. "Altered Structural Brain Connectivity in Healthy Carriers of the Autism Risk Gene,CNTNAP2". Brain Connectivity 1, nr 6 (grudzień 2011): 447–59. http://dx.doi.org/10.1089/brain.2011.0064.
Pełny tekst źródłaJurgensen, S., i P. E. Castillo. "Selective Dysregulation of Hippocampal Inhibition in the Mouse Lacking Autism Candidate Gene CNTNAP2". Journal of Neuroscience 35, nr 43 (28.10.2015): 14681–87. http://dx.doi.org/10.1523/jneurosci.1666-15.2015.
Pełny tekst źródłaValeeva, Elena V., Ilnur S. Sabirov, Liliya R. Safiullina, Dmitriy O. Nikitin, Irina I. Semina, Tim Rees, Denis O. Fesenko i Ildus I. Ahmetov. "The role of the CNTNAP2 gene in the development of autism spectrum disorder". Research in Autism Spectrum Disorders 114 (czerwiec 2024): 102409. http://dx.doi.org/10.1016/j.rasd.2024.102409.
Pełny tekst źródłaHoffman, Ellen J., Katherine J. Turner, Joseph M. Fernandez, Daniel Cifuentes, Marcus Ghosh, Sundas Ijaz, Roshan A. Jain i in. "Estrogens Suppress a Behavioral Phenotype in Zebrafish Mutants of the Autism Risk Gene, CNTNAP2". Neuron 89, nr 4 (luty 2016): 725–33. http://dx.doi.org/10.1016/j.neuron.2015.12.039.
Pełny tekst źródłaShimoda, Yasushi, Hidehiro Ueda i Kazutada Watanabe. "Involvement of Caspr2 encoded by neuropsychiatric developmental disorder-susceptibility gene CNTNAP2 in the synaptogenesis". Neuroscience Research 65 (styczeń 2009): S99. http://dx.doi.org/10.1016/j.neures.2009.09.427.
Pełny tekst źródłaBocharova, Anna, Kseniya Vagaitseva, Andrey Marusin, Natalia Zhukova, Irina Zhukova, Larisa Minaycheva, Oksana Makeeva i Vadim Stepanov. "Association and Gene–Gene Interactions Study of Late-Onset Alzheimer’s Disease in the Russian Population". Genes 12, nr 10 (19.10.2021): 1647. http://dx.doi.org/10.3390/genes12101647.
Pełny tekst źródłaNakabayashi, Kazuhiko, i Stephen W. Scherer. "The Human Contactin-Associated Protein-like 2 Gene (CNTNAP2) Spans over 2 Mb of DNA at Chromosome 7q35". Genomics 73, nr 1 (kwiecień 2001): 108–12. http://dx.doi.org/10.1006/geno.2001.6517.
Pełny tekst źródłaZhu, Bi, Chuansheng Chen, Gui Xue, Xuemei Lei, Yunxin Wang, Jin Li, Robert K. Moyzis, Jun Li, Qi Dong i Chongde Lin. "Associations between the CNTNAP2 gene, dorsolateral prefrontal cortex, and cognitive performance on the Stroop task". Neuroscience 343 (luty 2017): 21–29. http://dx.doi.org/10.1016/j.neuroscience.2016.11.021.
Pełny tekst źródłaRoss, Lars A., Victor A. Del Bene, Sophie Molholm, Young Jae Woo, Gizely N. Andrade, Brett S. Abrahams i John J. Foxe. "Common variation in the autism risk gene CNTNAP2, brain structural connectivity and multisensory speech integration". Brain and Language 174 (listopad 2017): 50–60. http://dx.doi.org/10.1016/j.bandl.2017.07.005.
Pełny tekst źródłaWerling, Anna Maria, Elise Bobrowski, Regina Taurines, Ronnie Gundelfinger, Marcel Romanos, Edna Grünblatt i Susanne Walitza. "CNTNAP2 gene in high functioning autism: no association according to family and meta-analysis approaches". Journal of Neural Transmission 123, nr 3 (11.11.2015): 353–63. http://dx.doi.org/10.1007/s00702-015-1458-5.
Pełny tekst źródłaGu, Huaiting, Fang Hou, Lingfei Liu, Xiu Luo, Pauline Denis Nkomola, Xinyan Xie, Xin Li i Ranran Song. "Genetic variants in the CNTNAP2 gene are associated with gender differences among dyslexic children in China". EBioMedicine 34 (sierpień 2018): 165–70. http://dx.doi.org/10.1016/j.ebiom.2018.07.007.
Pełny tekst źródłaChien, Yi-Ling, Yu-Chieh Chen i 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.
Pełny tekst źródłaScott-Van Zeeland, A. A., B. S. Abrahams, A. I. Alvarez-Retuerto, L. I. Sonnenblick, J. D. Rudie, D. Ghahremani, J. A. Mumford i in. "Altered Functional Connectivity in Frontal Lobe Circuits Is Associated with Variation in the Autism Risk Gene CNTNAP2". Science Translational Medicine 2, nr 56 (3.11.2010): 56ra80. http://dx.doi.org/10.1126/scitranslmed.3001344.
Pełny tekst źródłaLiska, Adam, Alice Bertero, Ryszard Gomolka, Mara Sabbioni, Alberto Galbusera, Noemi Barsotti, Stefano Panzeri, Maria Luisa Scattoni, Massimo Pasqualetti i Alessandro Gozzi. "Homozygous Loss of Autism-Risk Gene CNTNAP2 Results in Reduced Local and Long-Range Prefrontal Functional Connectivity". Cerebral Cortex 28, nr 4 (10.02.2017): 1141–53. http://dx.doi.org/10.1093/cercor/bhx022.
Pełny tekst źródłaBai, Tongjian, Long Zhang, Xiaohui Xie, Guixian Xiao, Wanling Huang, Dandan Li, Meidan Zu i in. "Common variant of CNTNAP2 gene modulate the social performances and functional connectivity of posterior right temporoparietal junction". Social Cognitive and Affective Neuroscience 14, nr 12 (grudzień 2019): 1297–305. http://dx.doi.org/10.1093/scan/nsaa008.
Pełny tekst źródłaPetrin, Aline L., Célia M. Giacheti, Luciana P. Maximino, Dagma V. M. Abramides, Sthella Zanchetta, Natalia F. Rossi, Antônio Richieri-Costa i 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, nr 12 (24.11.2010): 3164–72. http://dx.doi.org/10.1002/ajmg.a.33749.
Pełny tekst źródłaVorn, Rany, Katie A. Edwards, James Hentig, Sijung Yun, Hyung-Suk Kim, Chen Lai, Christina Devoto i in. "A Pilot Study of Whole-Blood Transcriptomic Analysis to Identify Genes Associated with Repetitive Low-Level Blast Exposure in Career Breachers". Biomedicines 10, nr 3 (17.03.2022): 690. http://dx.doi.org/10.3390/biomedicines10030690.
Pełny tekst źródłaSchaafsma, Sara M., Khatuna Gagnidze, Anny Reyes, Natalie Norstedt, Karl Månsson, Kerel Francis i Donald W. Pfaff. "Sex-specific gene–environment interactions underlying ASD-like behaviors". Proceedings of the National Academy of Sciences 114, nr 6 (23.01.2017): 1383–88. http://dx.doi.org/10.1073/pnas.1619312114.
Pełny tekst źródłaUddén, Julia, Tineke M. Snijders, Simon E. Fisher i Peter Hagoort. "A common variant of the CNTNAP2 gene is associated with structural variation in the left superior occipital gyrus". Brain and Language 172 (wrzesień 2017): 16–21. http://dx.doi.org/10.1016/j.bandl.2016.02.003.
Pełny tekst źródłaPaduano, Francesco, Emma Colao, Sara Loddo, Valeria Orlando, Francesco Trapasso, Antonio Novelli, Nicola Perrotti i 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, nr 5 (8.05.2020): 525. http://dx.doi.org/10.3390/genes11050525.
Pełny tekst źródłaBrignoni, Lucía, Mónica Cappetta, Valentina Colistro, Mónica Sans, Nora Artagaveytia, Carolina Bonilla i Bernardo Bertoni. "Genomic Diversity in Sporadic Breast Cancer in a Latin American Population". Genes 11, nr 11 (28.10.2020): 1272. http://dx.doi.org/10.3390/genes11111272.
Pełny tekst źródłaHsu, Michelle, Mehek Dedhia, Wim E. Crusio i Anna Delprato. "Sex differences in gene expression patterns associated with the APOE4 allele". F1000Research 8 (23.07.2019): 387. http://dx.doi.org/10.12688/f1000research.18671.2.
Pełny tekst źródłaToma, Claudio, Kerrie D. Pierce, Alex D. Shaw, Anna Heath, Philip B. Mitchell, Peter R. Schofield i 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, nr 12 (26.12.2018): e1007535. http://dx.doi.org/10.1371/journal.pgen.1007535.
Pełny tekst źródłaBelloso, Jose M., Iben Bache, Miriam Guitart, Maria Rosa Caballin, Christina Halgren, Maria Kirchhoff, Hans-Hilger Ropers, Niels Tommerup i 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, nr 6 (28.03.2007): 711–13. http://dx.doi.org/10.1038/sj.ejhg.5201824.
Pełny tekst źródłaWittekind, Dirk Alexander, Markus Scholz, Jürgen Kratzsch, Markus Löffler, Katrin Horn, Holger Kirsten, Veronica Witte, Arno Villringer i Michael Kluge. "Genome-wide association and transcriptome analysis suggests total serum ghrelin to be linked with GFRAL". European Journal of Endocrinology 184, nr 6 (1.06.2021): 847–56. http://dx.doi.org/10.1530/eje-20-1220.
Pełny tekst źródłaLi, Dandan, Long Zhang, Tongjian Bai, Wanling Huang, Gong-Jun Ji, Tingting Yang, Yifan Zhang, Yanghua Tian, Bensheng Qiu i 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 (lipiec 2021): 113319. http://dx.doi.org/10.1016/j.bbr.2021.113319.
Pełny tekst źródłaMa, Yi-Nu, Ting-Yu Xie i Xue-Yi Chen. "Multiple Gene Polymorphisms Associated with Exfoliation Syndrome in the Uygur Population". Journal of Ophthalmology 2019 (2.05.2019): 1–8. http://dx.doi.org/10.1155/2019/9687823.
Pełny tekst źródłaUddin, Mohammad Sarowar, Atkia Azima, Md Abdul Aziz, Tutun Das Aka, Sarah Jafrin, Md Shalahuddin Millat, Shafayet Ahmed Siddiqui, Md Giash Uddin, Md Saddam Hussain i 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, nr 5 (5.05.2021): 1410–23. http://dx.doi.org/10.1007/s13577-021-00546-8.
Pełny tekst źródłaKim, Sang Yoon, Seung Min Lee, Jonghoon Shin, Ji Eun Lee i 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, nr 7 (15.07.2021): 1003–7. http://dx.doi.org/10.3341/jkos.2021.62.7.1003.
Pełny tekst źródłaLewis-Smith, David, Donald Craig i Rhys Thomas. "094 The adult phenotypes of paediatric-onset genetic epilepsies". Journal of Neurology, Neurosurgery & Psychiatry 90, nr 12 (14.11.2019): A29.3—A29. http://dx.doi.org/10.1136/jnnp-2019-abn-2.97.
Pełny tekst źródłaIakoubov, Leonid, Malgorzata Mossakowska, Malgorzata Szwed i Monika Puzianowska-Kuznicka. "A Common Copy Number Variation Polymorphism in the CNTNAP2 Gene: Sexual Dimorphism in Association with Healthy Aging and Disease". Gerontology 61, nr 1 (18.08.2014): 24–31. http://dx.doi.org/10.1159/000363320.
Pełny tekst źródłaMaccaroni, Klizia, Elisa Balzano, Federica Mirimao, Simona Giunta i Franca Pelliccia. "Impaired Replication Timing Promotes Tissue-Specific Expression of Common Fragile Sites". Genes 11, nr 3 (19.03.2020): 326. http://dx.doi.org/10.3390/genes11030326.
Pełny tekst źródła