ScholarWorks@Gachon: Eva, Bagyinszky

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Eva, Bagyinszky (Bagyinszky Eva)

Graduate School (Department of Nano Science and Technology)

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Tel 031-750-8591
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s disease:26||Alzheimer&apos:24||mutation:12||Mutation:10||PSEN1:6||diagnosis:6||Alzheimer’s disease:5||prion:5||presenilin1:4||Next generation sequencing:3||SARSCoV2:3||presenilin2:3||EOAD:3||genetics:3||sequencing:3||risk modifiers:2||Novel mutation:2||haploinsufficiency:2||therapy:2||GRN:2||Structural prediction:2||APOE:2||mutations:2||Dementia:2||whole exome sequencing:2||biomarkers:2||Diagnosis:2||ARSACS:2||neurodegeneration:2||Thailand:2||dementia:2||COVID19:2||Presenilin1:2||Presenilin1:2||Inflammation:2||early onset Alzheimer's disease:2||Neurodegeneration:2||PSEN1 mutation:2||frontotemporal dementia:2||Alzheimer's disease:2||amyloid precursor protein:2||Semen:2||MAPT:1||MRI:1||Modelling:1||Mutations:1||NGS:1||Neurodegenerative genes:1||Neuroprotection:1||Novel APP Val669Leu mutation:1||O157:1||Omicron:1||Oxidative stress:1||P.Ala285Val:1||PET:1||PGRN:1||PRNP:1||PRNP Val180Ile mutation:1||PRNP gene:1||PSEN1 Thr116Ile mutation:1||PSEN2:1||PSEN2 TM5:1||PSEN2 mutation:1||Parkinsonism:1||Pathogenic:1||Pittsburgh compound B:1||Ployphen2:1||Presenilin 1:1||Presenilin 1 mutation:1||Presenilin 1 protein structure:1||Presenilin 2:1||Presenilin 2 mutation:1||Presenilin 2 protein structure:1||RNA array:1||RNA sequencing:1||SACS:1||SIFT:1||SORL1:1||SVD:1||Sacsin:1||Seminal vesicles:1||Splice site mutation:1||Strategies:1||TARDBP:1||TNFAIP3 gene:1||TOMM40:1||Testes:1||Therapy:1||Thr119Ile mutation:1||Trp165Cys:1||Tumornecrosis factor:1||Tyr225Cys mutation:1||V604M:1||VCP:1||VOCs:1||Whole Exome Sequence (WES) analysis:1||Wholeexome sequencing:1||Wuhan:1||acne inversa:1||alternative splicing:1||amyotrophic lateral sclerosis:1||animal models:1||apolipoprotein E:1||apolipoprotein structure:1||atypical CreutzfeldtJakob disease:1||autoimmunity:1||3D modeling:1||biomarker:1||cerebrospinal fluid:1||copy number variant:1||dementia with Lewy bodies:1||differently expressed genes:1||dilated cardiomyopathy:1||diseases:1||early onset AD:1||early onset Alzheimer&apos:1||earlyonset Alzheimer&apos:1||familial:1||fatal familial insomnia:1||fatal familial insomnia (FFI):1||gammasecretase:1||gene interactions:1||genetic biomarker:1||genetic factors:1||genetic molecular analysis:1||genetic testing:1||hallucination:1||immune dysfunctions:1||in silico modeling:1||ischemic stroke:1||loss of function:1||mild cognitive impairment:1||motor diseases:1||multiplex PCR:1||neurodegenerative disorders:1||neuroprotection:1||next generation sequencing:1||nextgeneration sequencing:1||noncoding RNA:1||novel mutation:1||p.Gly417Ala:1||p.His169Asn mutation:1||pathogenesis:1||pathogenic Escherichia coli:1||presenilin:1||presenilin 1:1||presenilin 2:1||prophage:1||proteomic markers:1||protocol:1||rectal cancer:1||risk factor:1||risk factors:1||risk modifier:1||s dementia:1||sacsinopathy:1||small vessel disease:1||structure prediction:1||trancriptome:1||typing:1||vaccine development:1||vascular cognitive impairment:1||vascular dementia:1||wholeexome sequencing:1||young onset Alzheimer&apos:1||youngonset stroke:1||bioinformatic analysis:1||50 genes:1||A beta 42/40 ratio:1||A20 haploinsufficiency:1||ABCA7:1||ACE2:1||ACMGAMP guidelines:1||AD:1||APP:1||Alzheimer’s diseases:1||Amyloid beta:1||Amyloid precursor protein:1||Asia:1||Asian:1||Ataxia:1||Biomarkers:1||C9orf72:1||CADASIL:1||CARASAL:1||CARASIL:1||CHMP2B:1||CRISPRCas9:1||Coronavirus:1||CreutzfeldtJakob disease:1||CreutzfeldtJakob disease (CJD):1||Creutzfelt Jakob disease:1||EHEC:1||Early onset:1||FTD:1||FUS:1||Gene panel:1||Genetics:1||GerstmannStrausslerScheinker disease:1||GerstmannStrausslerScheinker disease (GSS):1||GerstmannStrausslerScheinker syndrome:1||HDLS:1||Interferon:1||Interleukin:1||Korean:1||L232P mutation:1||Leu159Pro:1||LowDensity Lipoprotein Receptor (LDLR):1||

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1342, Seongnam-daero, Sujeong-gu, Seongnam-si, Gyeonggi-do, Republic of Korea(13120)031-750-5114

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