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1دورية أكاديمية
المؤلفون: Renato O. Santos, Rodrigo Secolin, Patrícia G. Barbalho, Mariana S. Silva-Alves, Marina K. M. Alvim, Clarissa L. Yasuda, Fábio Rogerio, Tonicarlo R. Velasco, Americo C. Sakamoto, Antonio L. Teixeira, Fernando Cendes, Claudia V. Maurer-Morelli, Iscia Lopes-Cendes
المصدر: Frontiers in Neurology, Vol 12 (2021)
مصطلحات موضوعية: mesial temporal sclerosis, hippocampal atrophy, association study, gene expression, neuroinflammation, Neurology. Diseases of the nervous system, RC346-429
العلاقة: https://www.frontiersin.org/articles/10.3389/fneur.2021.690847/fullTest; https://doaj.org/toc/1664-2295Test; https://doaj.org/article/b476dc37fe14460aacf656f18a4ab0c4Test
الإتاحة: https://doi.org/10.3389/fneur.2021.690847Test
https://doaj.org/article/b476dc37fe14460aacf656f18a4ab0c4Test -
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المؤلفون: Sheng-Jia Lin, Barbara Vona, Patricia G. Barbalho, Rauan Kaiyrzhanov, Reza Maroofian, Cassidy Petree, Mariasavina Severino, Valentina Stanley, Pratishtha Varshney, Paulina Bahena, Fatema Alzahrani, Amal Alhashem, Alistair T. Pagnamenta, Gudrun Aubertin, Juvianee I. Estrada-Veras, Héctor Adrián Díaz Hernández, Neda Mazaheri, Andrea Oza, Jenny Thies, Deborah L. Renaud, Sanmati Dugad, Jennifer McEvoy, Tipu Sultan, Lynn S. Pais, Brahim Tabarki, Daniel Villalobos-Ramirez, Aboulfazl Rad, J.C. Ambrose, P. Arumugam, M. Bleda, F. Boardman-Pretty, C.R. Boustred, H. Brittain, M.J. Caulfield, G.C. Chan, T. Fowler, A. Giess, A. Hamblin, S. Henderson, T.J.P. Hubbard, R. Jackson, L.J. Jones, D. Kasperaviciute, M. Kayikci, A. Kousathanas, L. Lahnstein, S.E.A. Leigh, I.U.S. Leong, F.J. Lopez, F. Maleady-Crowe, L. Moutsianas, M. Mueller, N. Murugaesu, A.C. Need, P. O‘Donovan, C.A. Odhams, C. Patch, D. Perez-Gil, M.B. Pereira, J. Pullinger, T. Rahim, A. Rendon, T. Rogers, K. Savage, K. Sawant, R.H. Scott, A. Siddiq, A. Sieghart, S.C. Smith, A. Sosinsky, A. Stuckey, M. Tanguy, E.R.A. Thomas, S.R. Thompson, A. Tucci, E. Walsh, M.J. Welland, E. Williams, K. Witkowska, S.M. Wood, Hamid Galehdari, Farah Ashrafzadeh, Afsaneh Sahebzamani, Kolsoum Saeidi, Erin Torti, Houda Z. Elloumi, Sara Mora, Timothy B. Palculict, Hui Yang, Jonathan D. Wren, null Ben Fowler, Manali Joshi, Martine Behra, Shawn M. Burgess, Swapan K. Nath, Michael G. Hanna, Margaret Kenna, J. Lawrence Merritt, Henry Houlden, Ehsan Ghayoor Karimiani, Maha S. Zaki, Thomas Haaf, Fowzan S. Alkuraya, Joseph G. Gleeson, Gaurav K. Varshney
المصدر: Genetics in medicine : official journal of the American College of Medical Genetics. 23(10)
مصطلحات موضوعية: Genetics, Lysine-tRNA Ligase, biology, Disease, biology.organism_classification, medicine.disease, Phenotype, Human genetics, Disease Models, Animal, Neurodevelopmental Disorders, medicine, Missense mutation, Autism, Animals, Humans, Allele, Hearing Loss, Zebrafish, Genetics (clinical), Gene knockout, Alleles
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91f3ae350cc512f0b956a6e8d9210c51Test
https://pubmed.ncbi.nlm.nih.gov/34172899Test -
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المؤلفون: Renato O. Santos (3615728), Rodrigo Secolin (763751), Patrícia G. Barbalho (11234868), Mariana S. Silva-Alves (3615719), Marina K. M. Alvim (3615716), Clarissa L. Yasuda (7948010), Fábio Rogerio (11234871), Tonicarlo R. Velasco (11234874), Americo C. Sakamoto (11234877), Antonio L. Teixeira (5933072), Fernando Cendes (515175), Claudia V. Maurer-Morelli (3615731), Iscia Lopes-Cendes (255345)
مصطلحات موضوعية: Neurology and Neuromuscular Diseases, Neurogenetics, mesial temporal sclerosis, hippocampal atrophy, association study, gene expression, neuroinflammation