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- [21] TUBA1A: OUTCOME OF MOSAICISM AND PHENOTYPIC ANALYSISAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2018, 176 (06) : 1471 - 1472Williams, M. S.论文数: 0 引用数: 0 h-index: 0机构: Geisinger Hlth Syst, Danville, PA USA Geisinger Hlth Syst, Danville, PA USAWilliams, J. L.论文数: 0 引用数: 0 h-index: 0机构: Geisinger Hlth Syst, Danville, PA USA Geisinger Hlth Syst, Danville, PA USACrosby, K.论文数: 0 引用数: 0 h-index: 0机构: Childrens Natl Hlth Syst, Washington, DC USA Geisinger Hlth Syst, Danville, PA USADubbs, H.论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA Geisinger Hlth Syst, Danville, PA USAMarsh, E. D.论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA Geisinger Hlth Syst, Danville, PA USALicht, D. J.论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA Geisinger Hlth Syst, Danville, PA USATanpaiboon, P.论文数: 0 引用数: 0 h-index: 0机构: Childrens Natl Hlth Syst, Washington, DC USA Geisinger Hlth Syst, Danville, PA USA
- [22] Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A (TUBA1A)HUMAN MUTATION, 2007, 28 (11) : 1055 - 1064Poirier, Karine论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, Inst Cochin, Dept Genet & Dev, Lab Genet Humaine,CNRS,UMR 8104, F-75014 Paris, FranceKeays, David A.论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, Inst Cochin, Dept Genet & Dev, Lab Genet Humaine,CNRS,UMR 8104, F-75014 Paris, FranceFrancis, Fiona论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, Inst Cochin, Dept Genet & Dev, Lab Genet Humaine,CNRS,UMR 8104, F-75014 Paris, FranceSaillour, Yoann论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, Inst Cochin, Dept Genet & Dev, Lab Genet Humaine,CNRS,UMR 8104, F-75014 Paris, FranceBahi, Nadia论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, Inst Cochin, Dept Genet & Dev, Lab Genet Humaine,CNRS,UMR 8104, F-75014 Paris, FranceManouvrier, Sylvie论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, Inst Cochin, Dept Genet & Dev, Lab Genet Humaine,CNRS,UMR 8104, F-75014 Paris, FranceFallet-Bianco, Catherine论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, Inst Cochin, Dept Genet & Dev, Lab Genet Humaine,CNRS,UMR 8104, F-75014 Paris, FrancePasquier, Laurent论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, Inst Cochin, Dept Genet & Dev, Lab Genet Humaine,CNRS,UMR 8104, F-75014 Paris, FranceToutain, Annick论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, Inst Cochin, Dept Genet & Dev, Lab Genet Humaine,CNRS,UMR 8104, F-75014 Paris, FranceTuy, Françoise Phan Dinh论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, Inst Cochin, Dept Genet & Dev, Lab Genet Humaine,CNRS,UMR 8104, F-75014 Paris, FranceBienvenu, Thierry论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, Inst Cochin, Dept Genet & Dev, Lab Genet Humaine,CNRS,UMR 8104, F-75014 Paris, FranceJoriot, Sylvie论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, Inst Cochin, Dept Genet & Dev, Lab Genet Humaine,CNRS,UMR 8104, F-75014 Paris, FranceOdent, Sylvie论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, Inst Cochin, Dept Genet & Dev, Lab Genet Humaine,CNRS,UMR 8104, F-75014 Paris, FranceVille, Dorothée论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, Inst Cochin, Dept Genet & Dev, Lab Genet Humaine,CNRS,UMR 8104, F-75014 Paris, FranceDesguerre, Isabelle论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, Inst Cochin, Dept Genet & Dev, Lab Genet Humaine,CNRS,UMR 8104, F-75014 Paris, FranceGoldenberg, Alice论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, Inst Cochin, Dept Genet & Dev, Lab Genet Humaine,CNRS,UMR 8104, F-75014 Paris, FranceMoutard, Marie Laure论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, Inst Cochin, Dept Genet & Dev, Lab Genet Humaine,CNRS,UMR 8104, F-75014 Paris, FranceFryns, Jeanpierre论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, Inst Cochin, Dept Genet & Dev, Lab Genet Humaine,CNRS,UMR 8104, F-75014 Paris, FranceVan Esch, Hilde论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, Inst Cochin, Dept Genet & Dev, Lab Genet Humaine,CNRS,UMR 8104, F-75014 Paris, FranceHarvey, Robert J.论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, Inst Cochin, Dept Genet & Dev, Lab Genet Humaine,CNRS,UMR 8104, F-75014 Paris, FranceSiebold, Christian论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, Inst Cochin, Dept Genet & Dev, Lab Genet Humaine,CNRS,UMR 8104, F-75014 Paris, FranceFlint, Jonathan论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, Inst Cochin, Dept Genet & Dev, Lab Genet Humaine,CNRS,UMR 8104, F-75014 Paris, FranceBeldjord, Chérif论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, Inst Cochin, Dept Genet & Dev, Lab Genet Humaine,CNRS,UMR 8104, F-75014 Paris, FranceChelly, Jamel论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, Inst Cochin, Dept Genet & Dev, Lab Genet Humaine,CNRS,UMR 8104, F-75014 Paris, France
- [23] TUBA1A mutation can cause a hydranencephaly-like severe form of cortical dysgenesisSCIENTIFIC REPORTS, 2015, 5Yokoi, Setsuri论文数: 0 引用数: 0 h-index: 0机构: Fujita Hlth Univ, Inst Comprehens Med Sci, Div Mol Genet, Toyoake, Aichi, Japan Nagoya Univ, Grad Sch Med, Dept Pediat, Nagoya, Aichi 4648601, Japan Fujita Hlth Univ, Inst Comprehens Med Sci, Div Mol Genet, Toyoake, Aichi, JapanIshihara, Naoko论文数: 0 引用数: 0 h-index: 0机构: Fujita Hlth Univ, Sch Med, Dept Pediat, Toyoake, Aichi 47011, Japan Nagoya Univ, Grad Sch Med, Dept Pediat, Nagoya, Aichi 4648601, Japan Fujita Hlth Univ, Inst Comprehens Med Sci, Div Mol Genet, Toyoake, Aichi, JapanMiya, Fuyuki论文数: 0 引用数: 0 h-index: 0机构: RIKEN, Ctr Integrat Med Sci, Lab Med Sci Math, Yokohama, Kanagawa, Japan Fujita Hlth Univ, Inst Comprehens Med Sci, Div Mol Genet, Toyoake, Aichi, JapanTsutsumi, Makiko论文数: 0 引用数: 0 h-index: 0机构: Fujita Hlth Univ, Inst Comprehens Med Sci, Div Mol Genet, Toyoake, Aichi, Japan Fujita Hlth Univ, Inst Comprehens Med Sci, Div Mol Genet, Toyoake, Aichi, JapanYanagihara, Itaru论文数: 0 引用数: 0 h-index: 0机构: Osaka Med Ctr Maternal & Child Hlth, Res Inst, Dept Dev Med, Izumi, Japan Fujita Hlth Univ, Inst Comprehens Med Sci, Div Mol Genet, Toyoake, Aichi, JapanFujita, Naoko论文数: 0 引用数: 0 h-index: 0机构: Fujita Hlth Univ, Inst Comprehens Med Sci, Div Mol Genet, Toyoake, Aichi, Japan Fujita Hlth Univ, Inst Comprehens Med Sci, Div Mol Genet, Toyoake, Aichi, JapanYamamoto, Hiroyuki论文数: 0 引用数: 0 h-index: 0机构: Nagoya Univ, Grad Sch Med, Dept Pediat, Nagoya, Aichi 4648601, Japan Fujita Hlth Univ, Inst Comprehens Med Sci, Div Mol Genet, Toyoake, Aichi, JapanKato, Mitsuhiro论文数: 0 引用数: 0 h-index: 0机构: Yamagata Univ, Fac Med, Dept Pediat, Yamagata 990, Japan Fujita Hlth Univ, Inst Comprehens Med Sci, Div Mol Genet, Toyoake, Aichi, JapanOkamoto, Nobuhiko论文数: 0 引用数: 0 h-index: 0机构: Osaka Med Ctr, Dept Med Genet, Osaka, Japan Res Inst Maternal & Child Hlth, Osaka, Japan Fujita Hlth Univ, Inst Comprehens Med Sci, Div Mol Genet, Toyoake, Aichi, JapanTsunoda, Tatsuhiko论文数: 0 引用数: 0 h-index: 0机构: RIKEN, Ctr Integrat Med Sci, Lab Med Sci Math, Yokohama, Kanagawa, Japan Fujita Hlth Univ, Inst Comprehens Med Sci, Div Mol Genet, Toyoake, Aichi, JapanYamasaki, Mami论文数: 0 引用数: 0 h-index: 0机构: Takatsuki Gen Hosp, Dept Neurosurg, Osaka, Japan Fujita Hlth Univ, Inst Comprehens Med Sci, Div Mol Genet, Toyoake, Aichi, JapanKanemura, Yonehiro论文数: 0 引用数: 0 h-index: 0机构: Osaka Natl Hosp, Natl Hosp Org, Inst Clin Res, Div Regenerat Med, Osaka, Japan Osaka Natl Hosp, Natl Hosp Org, Dept Neurosurg, Osaka, Japan Fujita Hlth Univ, Inst Comprehens Med Sci, Div Mol Genet, Toyoake, Aichi, JapanKosaki, Kenjiro论文数: 0 引用数: 0 h-index: 0机构: Keio Univ, Sch Med, Ctr Med Genet, Tokyo, Japan Fujita Hlth Univ, Inst Comprehens Med Sci, Div Mol Genet, Toyoake, Aichi, JapanKojima, Seiji论文数: 0 引用数: 0 h-index: 0机构: Nagoya Univ, Grad Sch Med, Dept Pediat, Nagoya, Aichi 4648601, Japan Fujita Hlth Univ, Inst Comprehens Med Sci, Div Mol Genet, Toyoake, Aichi, JapanSaitoh, Shinji论文数: 0 引用数: 0 h-index: 0机构: Nagoya City Univ, Grad Sch Med Sci, Dept Pediat & Neonatol, Nagoya, Aichi, Japan Fujita Hlth Univ, Inst Comprehens Med Sci, Div Mol Genet, Toyoake, Aichi, Japan论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:
- [24] TUBA1A mutation can cause a hydranencephaly-like severe form of cortical dysgenesisScientific Reports, 5Setsuri Yokoi论文数: 0 引用数: 0 h-index: 0机构: Institute for Comprehensive Medical Science,Division of Molecular GeneticsNaoko Ishihara论文数: 0 引用数: 0 h-index: 0机构: Institute for Comprehensive Medical Science,Division of Molecular GeneticsFuyuki Miya论文数: 0 引用数: 0 h-index: 0机构: Institute for Comprehensive Medical Science,Division of Molecular GeneticsMakiko Tsutsumi论文数: 0 引用数: 0 h-index: 0机构: Institute for Comprehensive Medical Science,Division of Molecular GeneticsItaru Yanagihara论文数: 0 引用数: 0 h-index: 0机构: Institute for Comprehensive Medical Science,Division of Molecular GeneticsNaoko Fujita论文数: 0 引用数: 0 h-index: 0机构: Institute for Comprehensive Medical Science,Division of Molecular GeneticsHiroyuki Yamamoto论文数: 0 引用数: 0 h-index: 0机构: Institute for Comprehensive Medical Science,Division of Molecular GeneticsMitsuhiro Kato论文数: 0 引用数: 0 h-index: 0机构: Institute for Comprehensive Medical Science,Division of Molecular GeneticsNobuhiko Okamoto论文数: 0 引用数: 0 h-index: 0机构: Institute for Comprehensive Medical Science,Division of Molecular GeneticsTatsuhiko Tsunoda论文数: 0 引用数: 0 h-index: 0机构: Institute for Comprehensive Medical Science,Division of Molecular GeneticsMami Yamasaki论文数: 0 引用数: 0 h-index: 0机构: Institute for Comprehensive Medical Science,Division of Molecular GeneticsYonehiro Kanemura论文数: 0 引用数: 0 h-index: 0机构: Institute for Comprehensive Medical Science,Division of Molecular GeneticsKenjiro Kosaki论文数: 0 引用数: 0 h-index: 0机构: Institute for Comprehensive Medical Science,Division of Molecular GeneticsSeiji Kojima论文数: 0 引用数: 0 h-index: 0机构: Institute for Comprehensive Medical Science,Division of Molecular GeneticsShinji Saitoh论文数: 0 引用数: 0 h-index: 0机构: Institute for Comprehensive Medical Science,Division of Molecular GeneticsHiroki Kurahashi论文数: 0 引用数: 0 h-index: 0机构: Institute for Comprehensive Medical Science,Division of Molecular GeneticsJun Natsume论文数: 0 引用数: 0 h-index: 0机构: Institute for Comprehensive Medical Science,Division of Molecular Genetics
- [25] Immediate Therapeutic Response to Vigabatrin in Lissencephaly-Related Epileptic Spasms due to TUBA1A R402H VariantAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2025,Nagata, Toru论文数: 0 引用数: 0 h-index: 0机构: Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Pediat Neurol, Okayama, Japan Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Pediat Neurol, Okayama, JapanShibata, Takashi论文数: 0 引用数: 0 h-index: 0机构: Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Pediat Neurol, Okayama, Japan Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Pediat Neurol, Okayama, JapanTsuchiya, Hiroki论文数: 0 引用数: 0 h-index: 0机构: Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Pediat Neurol, Okayama, Japan Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Pediat Neurol, Okayama, JapanAkiyama, Mari论文数: 0 引用数: 0 h-index: 0机构: Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Pediat Neurol, Okayama, Japan Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Pediat Neurol, Okayama, JapanKato, Mitsuhiro论文数: 0 引用数: 0 h-index: 0机构: Showa Univ, Sch Med, Dept Pediat, Tokyo, Japan Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Pediat Neurol, Okayama, JapanAkiyama, Tomoyuki论文数: 0 引用数: 0 h-index: 0机构: Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Pediat Neurol, Okayama, Japan Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Pediat Neurol, Okayama, JapanTakenouchi, Toshiki论文数: 0 引用数: 0 h-index: 0机构: Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Pediat Neurol, Okayama, Japan Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Pediat Neurol, Okayama, Japan
- [26] TUBA1A mutations cause wide spectrum lissencephaly (smooth brain) and suggest that multiple neuronal migration pathways converge on alpha tubulinsHUMAN MOLECULAR GENETICS, 2010, 19 (14) : 2817 - 2827Kumar, Ravinesh A.论文数: 0 引用数: 0 h-index: 0机构: Univ Chicago, Dept Human Genet, Chicago, IL 60637 USA Univ Chicago, Dept Human Genet, Chicago, IL 60637 USAPilz, Daniela T.论文数: 0 引用数: 0 h-index: 0机构: Univ Wales Hosp, Inst Med Genet, Cardiff CF14 4XW, Wales Univ Chicago, Dept Human Genet, Chicago, IL 60637 USABabatz, Timothy D.论文数: 0 引用数: 0 h-index: 0机构: Univ Chicago, Dept Human Genet, Chicago, IL 60637 USA Univ Chicago, Dept Human Genet, Chicago, IL 60637 USACushion, Thomas D.论文数: 0 引用数: 0 h-index: 0机构: Swansea Univ, Sch Med, Inst Life Sci, Swansea SA2 8PP, W Glam, Wales Univ Chicago, Dept Human Genet, Chicago, IL 60637 USAHarvey, Kirsten论文数: 0 引用数: 0 h-index: 0机构: Sch Pharm, Dept Pharmacol, London WC1N 1AX, England Univ Chicago, Dept Human Genet, Chicago, IL 60637 USATopf, Maya论文数: 0 引用数: 0 h-index: 0机构: Univ London, Birkbeck Coll, Inst Struct & Mol Biol Crystallog, London WC1E 7HX, England Univ Chicago, Dept Human Genet, Chicago, IL 60637 USAYates, Laura论文数: 0 引用数: 0 h-index: 0机构: Int Ctr Life, Inst Human Genet, Newcastle Upon Tyne NE1 3BZ, Tyne & Wear, England Univ Chicago, Dept Human Genet, Chicago, IL 60637 USARobb, Stephanie论文数: 0 引用数: 0 h-index: 0机构: Great Ormond St Hosp Sick Children, Dubowitz Neuromuscular Ctr, London WC1N 3JN, England Univ Chicago, Dept Human Genet, Chicago, IL 60637 USAUyanik, Goekhan论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Hamburg Eppendorf, Inst Human Genet, Hamburg, Germany Univ Chicago, Dept Human Genet, Chicago, IL 60637 USAMancini, Gracia M. S.论文数: 0 引用数: 0 h-index: 0机构: Erasmus Univ, Med Ctr, Dept Clin Genet, NL-3000CA Rotterdam, Netherlands Univ Chicago, Dept Human Genet, Chicago, IL 60637 USARees, Mark I.论文数: 0 引用数: 0 h-index: 0机构: Univ Wales Hosp, Inst Med Genet, Cardiff CF14 4XW, Wales Swansea Univ, Sch Med, Inst Life Sci, Swansea SA2 8PP, W Glam, Wales Univ Chicago, Dept Human Genet, Chicago, IL 60637 USAHarvey, Robert J.论文数: 0 引用数: 0 h-index: 0机构: Sch Pharm, Dept Pharmacol, London WC1N 1AX, England Univ Chicago, Dept Human Genet, Chicago, IL 60637 USADobyns, William B.论文数: 0 引用数: 0 h-index: 0机构: Univ Chicago, Dept Human Genet, Chicago, IL 60637 USA Univ Chicago, Dept Neurol, Chicago, IL 60637 USA Univ Chicago, Dept Pediat, Chicago, IL 60637 USA Univ Chicago, Dept Human Genet, Chicago, IL 60637 USA
- [27] In vitro characterization of neurite extension using induced pluripotent stem cells derived from lissencephaly patients with TUBA1A missense mutationsMOLECULAR BRAIN, 2016, 9Bamba, Yohei论文数: 0 引用数: 0 h-index: 0机构: Keio Univ, Sch Med, Dept Physiol, Shinjuku Ku, 35 Shinanomachi, Tokyo 1608582, Japan Natl Hosp Org, Osaka Natl Hosp, Inst Clin Res, Div Regenerat Med,Chuo Ku, 2-1-14 Hoenzaka, Osaka 5400006, Japan Keio Univ, Sch Med, Dept Physiol, Shinjuku Ku, 35 Shinanomachi, Tokyo 1608582, JapanShofuda, Tomoko论文数: 0 引用数: 0 h-index: 0机构: Natl Hosp Org, Osaka Natl Hosp, Inst Clin Res, Div Stem Cell Res, Osaka, Japan Keio Univ, Sch Med, Dept Physiol, Shinjuku Ku, 35 Shinanomachi, Tokyo 1608582, JapanKato, Mitsuhiro论文数: 0 引用数: 0 h-index: 0机构: Yamagata Univ, Fac Med, Dept Pediat, 2-2-2 Iida Nishi, Yamagata, Yamagata 9909585, Japan Keio Univ, Sch Med, Dept Physiol, Shinjuku Ku, 35 Shinanomachi, Tokyo 1608582, JapanPooh, Ritsuko K.论文数: 0 引用数: 0 h-index: 0机构: CRIFM Clin Res Inst, Fetal Med Pooh Matern Clin, 7-1-24 Uehommachi, Tennoji, Osaka 5430001, Japan Keio Univ, Sch Med, Dept Physiol, Shinjuku Ku, 35 Shinanomachi, Tokyo 1608582, JapanTateishi, Yoko论文数: 0 引用数: 0 h-index: 0机构: Natl Hosp Org, Okayama Med Ctr, Dept Obstet & Gynecol, 1711-1 Tamasu, Okayama, Japan Keio Univ, Sch Med, Dept Physiol, Shinjuku Ku, 35 Shinanomachi, Tokyo 1608582, JapanTakanashi, Jun-ichi论文数: 0 引用数: 0 h-index: 0机构: Tokyo Womens Med Univ, Yachiyo Med Ctr, Dept Pediat, Yachiyo 2768524, Japan Keio Univ, Sch Med, Dept Physiol, Shinjuku Ku, 35 Shinanomachi, Tokyo 1608582, JapanUtsunomiya, Hidetsuna论文数: 0 引用数: 0 h-index: 0机构: Int Univ Hlth & Welf, Grad Sch, Dept Radiol Sci, Sawara Ku, 2-4-16 Momochihama, Fukuoka 8140001, Japan Keio Univ, Sch Med, Dept Physiol, Shinjuku Ku, 35 Shinanomachi, Tokyo 1608582, JapanSumida, Miho论文数: 0 引用数: 0 h-index: 0机构: Natl Hosp Org, Osaka Natl Hosp, Inst Clin Res, Div Regenerat Med,Chuo Ku, 2-1-14 Hoenzaka, Osaka 5400006, Japan Keio Univ, Sch Med, Dept Physiol, Shinjuku Ku, 35 Shinanomachi, Tokyo 1608582, JapanKanematsu, Daisuke论文数: 0 引用数: 0 h-index: 0机构: Natl Hosp Org, Osaka Natl Hosp, Inst Clin Res, Div Regenerat Med,Chuo Ku, 2-1-14 Hoenzaka, Osaka 5400006, Japan Keio Univ, Sch Med, Dept Physiol, Shinjuku Ku, 35 Shinanomachi, Tokyo 1608582, JapanSuemizu, Hiroshi论文数: 0 引用数: 0 h-index: 0机构: Cent Inst Expt Anim, Lab Anim Res Dept, Kawasaki Ku, 3-25-12 Tonomachi, Kawasaki, Kanagawa 2100821, Japan Keio Univ, Sch Med, Dept Physiol, Shinjuku Ku, 35 Shinanomachi, Tokyo 1608582, JapanHiguchi, Yuichiro论文数: 0 引用数: 0 h-index: 0机构: Cent Inst Expt Anim, Lab Anim Res Dept, Kawasaki Ku, 3-25-12 Tonomachi, Kawasaki, Kanagawa 2100821, Japan Keio Univ, Sch Med, Dept Physiol, Shinjuku Ku, 35 Shinanomachi, Tokyo 1608582, JapanAkamatsu, Wado论文数: 0 引用数: 0 h-index: 0机构: Keio Univ, Sch Med, Dept Physiol, Shinjuku Ku, 35 Shinanomachi, Tokyo 1608582, Japan Keio Univ, Sch Med, Dept Physiol, Shinjuku Ku, 35 Shinanomachi, Tokyo 1608582, JapanGallagher, Denis论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Program Neurosci & Mental Hlth, Toronto, ON M5G 0A7, Canada Univ Hlth Network, McEwen Ctr Regenerat Med, Toronto, ON M5G 0A7, Canada Univ Toronto, Dept Mol Genet, Toronto, ON M5G 1X5, Canada Keio Univ, Sch Med, Dept Physiol, Shinjuku Ku, 35 Shinanomachi, Tokyo 1608582, JapanMiller, Freda D.论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Program Neurosci & Mental Hlth, Toronto, ON M5G 0A7, Canada Univ Toronto, Dept Mol Genet, Toronto, ON M5G 1X5, Canada Univ Toronto, Dept Physiol, Toronto, ON M5G 1X5, Canada Keio Univ, Sch Med, Dept Physiol, Shinjuku Ku, 35 Shinanomachi, Tokyo 1608582, JapanYamasaki, Mami论文数: 0 引用数: 0 h-index: 0机构: Takatsuki Gen Hosp, Dept Pediat Neurosurg, 1-3-13 Kosobe Cho, Takatsuki, Osaka 5691192, Japan Natl Hosp Org, Osaka Natl Hosp, Inst Clin Res, Div Mol Med, Osaka, Japan Keio Univ, Sch Med, Dept Physiol, Shinjuku Ku, 35 Shinanomachi, Tokyo 1608582, JapanKanemura, Yonehiro论文数: 0 引用数: 0 h-index: 0机构: Natl Hosp Org, Osaka Natl Hosp, Inst Clin Res, Div Regenerat Med,Chuo Ku, 2-1-14 Hoenzaka, Osaka 5400006, Japan Natl Hosp Org, Osaka Natl Hosp, Dept Neurosurg, Osaka, Japan Keio Univ, Sch Med, Dept Physiol, Shinjuku Ku, 35 Shinanomachi, Tokyo 1608582, Japan论文数: 引用数: h-index:机构:
- [28] In vitro characterization of neurite extension using induced pluripotent stem cells derived from lissencephaly patients with TUBA1A missense mutationsMolecular Brain, 9Yohei Bamba论文数: 0 引用数: 0 h-index: 0机构: Keio University School of Medicine,Department of PhysiologyTomoko Shofuda论文数: 0 引用数: 0 h-index: 0机构: Keio University School of Medicine,Department of PhysiologyMitsuhiro Kato论文数: 0 引用数: 0 h-index: 0机构: Keio University School of Medicine,Department of PhysiologyRitsuko K. Pooh论文数: 0 引用数: 0 h-index: 0机构: Keio University School of Medicine,Department of PhysiologyYoko Tateishi论文数: 0 引用数: 0 h-index: 0机构: Keio University School of Medicine,Department of PhysiologyJun-ichi Takanashi论文数: 0 引用数: 0 h-index: 0机构: Keio University School of Medicine,Department of PhysiologyHidetsuna Utsunomiya论文数: 0 引用数: 0 h-index: 0机构: Keio University School of Medicine,Department of PhysiologyMiho Sumida论文数: 0 引用数: 0 h-index: 0机构: Keio University School of Medicine,Department of PhysiologyDaisuke Kanematsu论文数: 0 引用数: 0 h-index: 0机构: Keio University School of Medicine,Department of PhysiologyHiroshi Suemizu论文数: 0 引用数: 0 h-index: 0机构: Keio University School of Medicine,Department of PhysiologyYuichiro Higuchi论文数: 0 引用数: 0 h-index: 0机构: Keio University School of Medicine,Department of PhysiologyWado Akamatsu论文数: 0 引用数: 0 h-index: 0机构: Keio University School of Medicine,Department of PhysiologyDenis Gallagher论文数: 0 引用数: 0 h-index: 0机构: Keio University School of Medicine,Department of PhysiologyFreda D. Miller论文数: 0 引用数: 0 h-index: 0机构: Keio University School of Medicine,Department of PhysiologyMami Yamasaki论文数: 0 引用数: 0 h-index: 0机构: Keio University School of Medicine,Department of PhysiologyYonehiro Kanemura论文数: 0 引用数: 0 h-index: 0机构: Keio University School of Medicine,Department of PhysiologyHideyuki Okano论文数: 0 引用数: 0 h-index: 0机构: Keio University School of Medicine,Department of Physiology
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