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المؤلفون: Murakami, Tetsuro, Qamar, Seema, Lin, Julie Qiaojin, Schierle, Gabriele S. Kaminski, Rees, Eric, Miyashita, Akinori, Costa, Ana R., Dodd, Roger B., Chan, Fiona T.S., Michel, Claire H., Kronenberg-Versteeg, Deborah, Li, Yi, Yang, Seung-Pil, Wakutani, Yosuke, Meadows, William, Ferry, Rodylyn Rose, Dong, Liang, Tartaglia, Gian Gaetano, Favrin, Giorgio, Lin, Wen-Lang, Dickson, Dennis W., Zhen, Mei, Ron, David, Schmitt-Ulms, Gerold, Fraser, Paul E., Shneider, Neil A., Holt, Christine, Vendruscolo, Michele, Kaminski, Clemens F., St George-Hyslop, Peter
المساهمون: Lin, Qiaojin [0000-0002-2669-6478], Rees, Eric [0000-0001-7478-5961], Dodd, Roger [0000-0003-4268-1863], Kronenberg-Versteeg, Deborah [0000-0003-0965-9998], Favrin, Giorgio [0000-0002-1884-7352], Ron, David [0000-0002-3014-5636], Holt, Christine [0000-0003-2829-121X], Vendruscolo, Michele [0000-0002-3616-1610], Kaminski, Clemens [0000-0002-5194-0962], St George-Hyslop, Peter [0000-0003-0796-7209], Apollo - University of Cambridge Repository
المصدر: Neuron
مصطلحات موضوعية: Animal, Neuroscience(all), Messenger, Amyotrophic Lateral Sclerosis, Longevity, Animals, Caenorhabditis elegans, Caenorhabditis elegans Proteins, Cytoplasmic Granules, Disease Models, Animal, Frontotemporal Lobar Degeneration, Motor Activity, Mutation, RNA, Messenger, RNA-Binding Protein FUS, Ribonucleoproteins, Hydrogels, Phase Transition, Article, Disease Models, RNA
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::b366c66fb03b36d81bb0727d2364f832Test
https://pubmed.ncbi.nlm.nih.gov/26651288Test -
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المؤلفون: Miyashita, Akinori, Koike, Asako, Jun, Gyungah, Wang, Li-San, Takahashi, Satoshi, Matsubara, Etsuro, Kawarabayashi, Takeshi, Shoji, Mikio, Tomita, Naoki, Arai, Hiroyuki, Asada, Takashi, Harigaya, Yasuo, Ikeda, Masaki, Amari, Masakuni, Hanyu, Haruo, Ikeuchi, Takeshi, Higuchi, Susumu, Nishizawa, Masatoyo, Suga, Masaichi, Kawase, Yasuhiro, Akatsu, Hiroyasu, Kosaka, Kenji, Yamamoto, Takayuki, Imagawa, Masaki, Yamada, Masahito, Hamaguchi, Tsuyoshi, Moriaha, Takashi, Takeda, Masatoshi, Takao, Takeo, Nakata, Kenji, Fujisawa, Yoshikatsu, Sasaki, Ken, Watanabe, Ken, Nakashima, Kenji, Urakami, Katsuya, Ooya, Terumi, Takahashi, Mitsuo, Yuzuriha, Takefumi, Serikawa, Kayoko, Yoshimoto, Seishi, Nakagawa, Ryuji, Kim, Jong-Won, Ki, Chang-Seok, Won, Hong-Hee, Na, Duk L., Seo, Sang Won, Mook-Jung, Inhee, St. George-Hyslop, Peter, Mayeux, Richard, Haines, Jonathan L., Pericak-Vance, Margaret A., Yoshida, Makiko, Nishida, Nao, Tokunaga, Katsushi, Yamamoto, Ken, Tsuji, Shoji, Kanazawa, Ichiro, Ihara, Yasuo, Schellenberg, Gerard D., Farrer, Lindsay A., Kuwano, Ryozo, Consortium, The Alzheimer Disease Genetics
المصدر: PLoS ONE, Vol 8, Iss 4, p e58618 (2013)
PLoS ONEمصطلحات موضوعية: Epidemiology, SORL1, Gene Identification and Analysis, Genome-wide association study, PICALM, 0302 clinical medicine, Japan, Genotype, Odds Ratio, Genetics, 0303 health sciences, Multidisciplinary, Chromosome Mapping, Neurology, Genetic Epidemiology, Medicine, Research Article, Science, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, White People, Molecular Genetics, 03 medical and health sciences, Asian People, Alzheimer Disease, Republic of Korea, Genome-Wide Association Studies, Humans, SNP, Genetic Predisposition to Disease, Allele, Alleles, LDL-Receptor Related Proteins, 030304 developmental biology, Chromosomes, Human, Pair 11, Haplotype, Membrane Transport Proteins, Human Genetics, Genetics of Disease, Genetic Polymorphism, Dementia, Population Genetics, 030217 neurology & neurosurgery, Genome-Wide Association Study
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39d55942339d4a4b85af9e9317e96edeTest
https://doi.org/10.1371/journal.pone.0058618Test