Seungshin Ha - Related publications

Affiliations: 
Brigham and Women's Hospital and Seattle Children's Research Institute 
Area:
Development of the cerebral cortex
NOTE: We are testing a new system for identifying relevant work based on semantic analysis that identifies similarities between recently published papers and the current author's publications. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches.
50 most relevant papers in past 60 days:
Year Citation  Score
2021 Narayanan RK, Brewer MH, Perez-Siles G, Ellis M, Ly C, Burgess A, Neumann B, Nicholson GA, Vucic S, Kennerson ML. Charcot-Marie-tooth disease causing mutation (p.R158H) in pyruvate dehydrogenase kinase 3 (PDK3) affects synaptic transmission, ATP production and causes neurodegeneration in a CMTX6 C. elegans model. Human Molecular Genetics. PMID 34387338 DOI: 10.1093/hmg/ddab228   
2021 Booth DG, Kozar N, Bradley S, Meijer D. Characterizing the molecular etiology of arthrogryposis multiplex congenita in patients with LGI4 mutations. Glia. PMID 34288120 DOI: 10.1002/glia.24061   
2021 Wilpert NM, Marguet F, Maillard C, Guimiot F, Martinovic J, Drunat S, Attié-Bitach T, Razavi F, Tessier A, Capri Y, Laquerrière A, Bahi-Buisson N. Human neuropathology confirms projection neuron and interneuron defects and delayed oligodendrocyte production and maturation in FOXG1 syndrome. European Journal of Medical Genetics. 64: 104282. PMID 34284163 DOI: 10.1016/j.ejmg.2021.104282   
2021 Wang T, Zhou M, Zhang Q, Zhang C, Peng G. ubtor Mutation Causes Motor Hyperactivity by Activating mTOR Signaling in Zebrafish. Neuroscience Bulletin. PMID 34309811 DOI: 10.1007/s12264-021-00755-z   
2021 Garone MG, Birsa N, Rosito M, Salaris F, Mochi M, de Turris V, Nair RR, Cunningham TJ, Fisher EMC, Morlando M, Fratta P, Rosa A. ALS-related FUS mutations alter axon growth in motoneurons and affect HuD/ELAVL4 and FMRP activity. Communications Biology. 4: 1025. PMID 34471224 DOI: 10.1038/s42003-021-02538-8   
2021 Park YJ, Kim S, Shim HP, Park JH, Lee G, Kim TY, Jo MC, Kwon AY, Lee M, Lee S, Yeo J, Chung HL, Bellen HJ, Kwon SH, Jeon SH. Phosphatidylserine synthase plays an essential role in glia and affects development, as well as the maintenance of neuronal function. Iscience. 24: 102899. PMID 34401677 DOI: 10.1016/j.isci.2021.102899   
2021 Okuda S, Sato M, Kato S, Nagashima S, Inatome R, Yanagi S, Fukuda T. Oscillation of Cdc20-APC/C-mediated CAMDI stability is critical for cortical neuron migration. The Journal of Biological Chemistry. 100986. PMID 34298015 DOI: 10.1016/j.jbc.2021.100986   
2021 Henningsen JB, Soylu-Kucharz R, Björkqvist M, Petersén Å. Effects of excitotoxicity in the hypothalamus in transgenic mouse models of Huntington disease. Heliyon. 7: e07808. PMID 34458633 DOI: 10.1016/j.heliyon.2021.e07808   
2021 de Araújo JAM, Barão S, Mateos-White I, Espinosa A, Costa MR, Gil-Sanz C, Müller U. ZBTB20 is critical for the specification of a subset of callosal projection neurons and astrocytes in the mammalian neocortex. Development (Cambridge, England). PMID 34351428 DOI: 10.1242/dev.196642   
2021 Clark AJ, Kugathasan U, Baskozos G, Priestman DA, Fugger N, Lone MA, Othman A, Chu KH, Blesneac I, Wilson ER, Laurà M, Kalmar B, Greensmith L, Hornemann T, Platt FM, et al. An iPSC model of hereditary sensory neuropathy-1 reveals L-serine-responsive deficits in neuronal ganglioside composition and axoglial interactions. Cell Reports. Medicine. 2: 100345. PMID 34337561 DOI: 10.1016/j.xcrm.2021.100345   
2021 Salamon I, Palsule G, Luo X, Roque A, Tucai S, Khosla I, Volk N, Liu W, Cui H, Pozzo VD, Zalamea P, Jiao X, D'Arcangelo G, Hart RP, Rasin MR, et al. mRNA-Decapping Associated DcpS Enzyme Controls Critical Steps of Neuronal Development. Cerebral Cortex (New York, N.Y. : 1991). PMID 34467373 DOI: 10.1093/cercor/bhab302   
2021 Cariboni A, Balasubramanian R. Kallmann syndrome and idiopathic hypogonadotropic hypogonadism: The role of semaphorin signaling on GnRH neurons. Handbook of Clinical Neurology. 182: 307-315. PMID 34266601 DOI: 10.1016/B978-0-12-819973-2.00022-8   
2021 Singh A, Upadhayay S, Mehan S. Understanding Abnormal c-JNK/p38MAPK Signaling Overactivation Involved in the Progression of Multiple Sclerosis: Possible Therapeutic Targets and Impact on Neurodegenerative Diseases. Neurotoxicity Research. PMID 34432262 DOI: 10.1007/s12640-021-00401-6   
2021 Dumrongprechachan V, Salisbury RB, Soto G, Kumar M, MacDonald ML, Kozorovitskiy Y. Cell-type and subcellular compartment-specific APEX2 proximity labeling reveals activity-dependent nuclear proteome dynamics in the striatum. Nature Communications. 12: 4855. PMID 34381044 DOI: 10.1038/s41467-021-25144-y   
2021 Tay SH, Ellieyana EN, Le Y, Sarusie MV, Grimm C, Ohmer J, Mathuru A, Fischer U, Winkler C. A novel zebrafish model for intermediate type spinal muscular atrophy demonstrates importance of Smn for maintenance of mature motor neurons. Human Molecular Genetics. PMID 34302176 DOI: 10.1093/hmg/ddab212   
2021 Tay SH, Ellieyana EN, Le Y, Sarusie MV, Grimm C, Ohmer J, Mathuru A, Fischer U, Winkler C. A novel zebrafish model for intermediate type spinal muscular atrophy demonstrates importance of Smn for maintenance of mature motor neurons. Human Molecular Genetics. PMID 34302176 DOI: 10.1093/hmg/ddab212   
2021 Kray KM, McGovern VL, Chugh D, Arnold WD, Burghes AHM. Dual SMN inducing therapies can rescue survival and motor unit function in symptomatic ∆7SMA mice. Neurobiology of Disease. 159: 105488. PMID 34425216 DOI: 10.1016/j.nbd.2021.105488   
2021 Shen H, Zhao X, Chen J, Qu W, Huang X, Wang M, Shao Z, Shu Q, Li X. O-GlcNAc transferase Ogt regulates embryonic neuronal development through modulating Wnt/β-catenin signaling. Human Molecular Genetics. PMID 34346496 DOI: 10.1093/hmg/ddab223   
2021 Komuro Y, Galas L, Morozov YM, Fahrion JK, Raoult E, Lebon A, Tilot AK, Kikuchi S, Ohno N, Vaudry D, Rakic P, Komuro H. The Role of Galanin in Cerebellar Granule Cell Migration in the Early Postnatal Mouse during Normal Development and After Injury. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 34462307 DOI: 10.1523/JNEUROSCI.0900-15.2021   
2021 Talley MJ, Nardini D, Shabbir N, Ehrman LA, Prada CE, Waclaw RR. Generation of a Mouse Model to Study the Noonan Syndrome Gene in the Telencephalon. Frontiers in Cell and Developmental Biology. 9: 673995. PMID 34222248 DOI: 10.3389/fcell.2021.673995   
2021 Talley MJ, Nardini D, Shabbir N, Ehrman LA, Prada CE, Waclaw RR. Generation of a Mouse Model to Study the Noonan Syndrome Gene in the Telencephalon. Frontiers in Cell and Developmental Biology. 9: 673995. PMID 34222248 DOI: 10.3389/fcell.2021.673995   
2021 Fulton RE, Pearson-Smith JN, Huynh CQ, Fabisiak T, Liang LP, Aivazidis S, High BA, Buscaglia G, Corrigan T, Valdez R, Shimizu T, Patel MN. Neuron-specific mitochondrial oxidative stress results in epilepsy, glucose dysregulation and a striking astrocyte response. Neurobiology of Disease. 105470. PMID 34371143 DOI: 10.1016/j.nbd.2021.105470   
2021 Derksen A, Mirchi A, Tran LT, Cao-Lei L, Oskoui M, Srour M, Poulin C, , Bernard G. A Novel Variant in Causes Spinal Muscular Atrophy Lower Extremity Predominant in Identical Twins: A Case Report. Child Neurology Open. 8: 2329048X211027438. PMID 34368388 DOI: 10.1177/2329048X211027438   
2021 Hsia HE, Tüshaus J, Feng X, Hofmann LI, Wefers B, Marciano DK, Wurst W, Lichtenthaler SF. Endoglycan (PODXL2) is proteolytically processed by ADAM10 (a disintegrin and metalloprotease 10) and controls neurite branching in primary neurons. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 35: e21813. PMID 34390512 DOI: 10.1096/fj.202100475R   
2021 Stergas HR, Kalbag Z, St Clair RM, Talbot JC, Ballif BA, Ebert AM. Crk adaptor proteins are necessary for the development of the zebrafish retina. Developmental Dynamics : An Official Publication of the American Association of Anatomists. PMID 34268820 DOI: 10.1002/dvdy.402   
2021 Zhang M, Wang J, Zhang K, Lu G, Liu Y, Ren K, Wang W, Xin D, Xu L, Mao H, Xing J, Gao X, Jin W, Berry K, Mikoshiba K, et al. Ten-eleven translocation 1 mediated-DNA hydroxymethylation is required for myelination and remyelination in the mouse brain. Nature Communications. 12: 5091. PMID 34429415 DOI: 10.1038/s41467-021-25353-5   
2021 Mi Z, Liu H, Rose ME, Ma J, Reay DP, Ma X, Henchir JJ, Edward Dixon C, Graham SH. Mutation of a ubiquitin carboxy terminal hydrolase L1 lipid binding site alleviates cell death, axonal injury, and behavioral deficits after traumatic brain injury in mice. Neuroscience. PMID 34508847 DOI: 10.1016/j.neuroscience.2021.09.001   
2021 Takahashi H, Asahina R, Fujioka M, Matsui TK, Kato S, Mori E, Hioki H, Yamamoto T, Kobayashi K, Tsuboi A. Ras-like Gem GTPase induced by Npas4 promotes activity-dependent neuronal tolerance for ischemic stroke. Proceedings of the National Academy of Sciences of the United States of America. 118. PMID 34349016 DOI: 10.1073/pnas.2018850118   
2021 Kato Y, Sakamoto K. Niclosamide affects intracellular TDP-43 distribution in motor neurons, activates mitophagy, and attenuates morphological changes under stress. Journal of Bioscience and Bioengineering. PMID 34429248 DOI: 10.1016/j.jbiosc.2021.06.015   
2021 Levenga J, Wong H, Milstead R, LaPlante L, Hoeffer CA. Immunohistological Examination of AKT Isoforms in the Brain: Cell-Type Specificity That May Underlie AKT's Role in Complex Brain Disorders and Neurological Disease. Cerebral Cortex Communications. 2: tgab036. PMID 34296180 DOI: 10.1093/texcom/tgab036   
2021 Levenga J, Wong H, Milstead R, LaPlante L, Hoeffer CA. Immunohistological Examination of AKT Isoforms in the Brain: Cell-Type Specificity That May Underlie AKT's Role in Complex Brain Disorders and Neurological Disease. Cerebral Cortex Communications. 2: tgab036. PMID 34296180 DOI: 10.1093/texcom/tgab036   
2021 Appel SH, Beers DR, Zhao W. Amyotrophic lateral sclerosis is a systemic disease: peripheral contributions to inflammation-mediated neurodegeneration. Current Opinion in Neurology. PMID 34402459 DOI: 10.1097/WCO.0000000000000983   
2021 Barthelemy A, Demais V, Stancu IC, Vasile E, Houben T, Reber M, Pallottini V, Perraut M, Reibel S, Pfrieger FW. Glial contribution to cyclodextrin-mediated reversal of cholesterol accumulation in murine NPC1-deficient neurons in vivo. Neurobiology of Disease. 105469. PMID 34364974 DOI: 10.1016/j.nbd.2021.105469   
2021 Parcerisas A, Ortega-Gascó A, Hernaiz-Llorens M, Odena MA, Ulloa F, de Oliveira E, Bosch M, Pujadas L, Soriano E. New Partners Identified by Mass Spectrometry Assay Reveal Functions of NCAM2 in Neural Cytoskeleton Organization. International Journal of Molecular Sciences. 22. PMID 34299022 DOI: 10.3390/ijms22147404   
2021 Gafner M, Michelson M, Argilli E, Yosovich K, Sherr EH, Parks KC, England EM, Hady-Cohen R, Leibovitz Z, Lev D, Michaeli-Yosef Y, Lerman-Sagie T, Blumkin L. Major brain malformations: corpus callosum dysgenesis, agenesis of septum pellucidum and polymicrogyria in patients with BCORL1-related disorders. Journal of Human Genetics. PMID 34400773 DOI: 10.1038/s10038-021-00971-5   
2021 Yamazaki Y, Abe Y, Fujii S, Tanaka KF. Oligodendrocytic Na-K-Cl co-transporter 1 activity facilitates axonal conduction and restores plasticity in the adult mouse brain. Nature Communications. 12: 5146. PMID 34446732 DOI: 10.1038/s41467-021-25488-5   
2021 Vahdat S, Pendharkar AV, Chiang T, Harvey S, Uchino H, Cao Z, Kim A, Choy M, Chen H, Lee HJ, Cheng MY, Lee JH, Steinberg GK. Brain-wide neural dynamics of poststroke recovery induced by optogenetic stimulation. Science Advances. 7. PMID 34380610 DOI: 10.1126/sciadv.abd9465   
2021 Li H, Li QQ, Hong Y. Global Gene Expression Signatures in Response to Citrate-coated Silver Nanoparticles Exposure. Toxicology. 152898. PMID 34403730 DOI: 10.1016/j.tox.2021.152898   
2021 Follis RM, Tep C, Genaro-Mattos TC, Kim ML, Ryu JC, Morrison VE, Chan JR, Porter N, Carter BD, Yoon SO. Metabolic control of sensory neuron survival by the p75 neurotrophin receptor in Schwann cells. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 34507952 DOI: 10.1523/JNEUROSCI.3243-20.2021   
2021 Koh A, Sarusie MV, Ohmer J, Fischer U, Winkler C, Wohland T. Fluorescence Correlation Spectroscopy Reveals Survival Motor Neuron Oligomerization but No Active Transport in Motor Axons of a Zebrafish Model for Spinal Muscular Atrophy. Frontiers in Cell and Developmental Biology. 9: 639904. PMID 34458251 DOI: 10.3389/fcell.2021.639904   
2021 Gorostieta-Salas E, Moreno-Blas D, Gerónimo-Olvera C, Cisneros B, Court FA, Castro-Obregón S. Enhanced Activity of Exportin-1/CRM1 in Neurons Contributes to Autophagy Dysfunction and Senescent Features in Old Mouse Brain. Oxidative Medicine and Cellular Longevity. 2021: 6682336. PMID 34434486 DOI: 10.1155/2021/6682336   
2021 Pereira JD, DuBreuil DM, Devlin AC, Held A, Sapir Y, Berezovski E, Hawrot J, Dorfman K, Chander V, Wainger BJ. Human sensorimotor organoids derived from healthy and amyotrophic lateral sclerosis stem cells form neuromuscular junctions. Nature Communications. 12: 4744. PMID 34362895 DOI: 10.1038/s41467-021-24776-4   
2021 Tatomir A, Beltrand A, Nguyen V, Courneya JP, Boodhoo D, Cudrici C, Muresanu DF, Rus V, Badea TC, Rus H. RGC-32 Acts as a Hub to Regulate the Transcriptomic Changes Associated With Astrocyte Development and Reactive Astrocytosis. Frontiers in Immunology. 12: 705308. PMID 34394104 DOI: 10.3389/fimmu.2021.705308   
2021 Orcinha C, Kilias A, Paschen E, Follo M, Haas CA. Reelin Is Required for Maintenance of Granule Cell Lamination in the Healthy and Epileptic Hippocampus. Frontiers in Molecular Neuroscience. 14: 730811. PMID 34483838 DOI: 10.3389/fnmol.2021.730811   
2021 Fujitani M, Otani Y, Miyajima H. Pathophysiological Roles of Abnormal Axon Initial Segments in Neurodevelopmental Disorders. Cells. 10. PMID 34440880 DOI: 10.3390/cells10082110   
2021 Irfan M, Evonuk KS, DeSilva TM. Microglia phagocytose oligodendrocyte progenitor cells and synapses during early postnatal development: implications for white versus gray matter maturation. The Febs Journal. PMID 34496137 DOI: 10.1111/febs.16190   
2021 Coyne AN, Rothstein JD. The ESCRT-III protein VPS4, but not CHMP4B or CHMP2B, is pathologically increased in familial and sporadic ALS neuronal nuclei. Acta Neuropathologica Communications. 9: 127. PMID 34281622 DOI: 10.1186/s40478-021-01228-0   
2021 Markworth R, Bähr M, Burk K. Held Up in Traffic-Defects in the Trafficking Machinery in Charcot-Marie-Tooth Disease. Frontiers in Molecular Neuroscience. 14: 695294. PMID 34483837 DOI: 10.3389/fnmol.2021.695294   
2021 Al Mamun A, Ngwa C, Qi S, Honarpisheh P, Datar S, Sharmeen R, Xu Y, McCullough LD, Liu F. Neuronal CD200 Signaling Is Protective in the Acute Phase of Ischemic Stroke. Stroke. STROKEAHA120032374. PMID 34353112 DOI: 10.1161/STROKEAHA.120.032374   
2021 Zhang L, Fang Y, Zhao X, Zheng Y, Ma Y, Li S, Huang Z, Li L. BRUCE silencing leads to axonal dystrophy by repressing autophagosome-lysosome fusion in Alzheimer's disease. Translational Psychiatry. 11: 421. PMID 34354038 DOI: 10.1038/s41398-021-01427-2