T. Tsuda

ORCID: 0000-0003-2975-5311
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About
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Research Areas
  • Alzheimer's disease research and treatments
  • Genetic Neurodegenerative Diseases
  • Mitochondrial Function and Pathology
  • Conducting polymers and applications
  • Organic Electronics and Photovoltaics
  • Amyloidosis: Diagnosis, Treatment, Outcomes
  • Neurological disorders and treatments
  • Plasmonic and Surface Plasmon Research
  • Bioinformatics and Genomic Networks
  • Advanced Photocatalysis Techniques
  • Textile materials and evaluations
  • Organic Light-Emitting Diodes Research
  • Genetics and Neurodevelopmental Disorders
  • Shape Memory Alloy Transformations
  • Crystallization and Solubility Studies
  • RNA and protein synthesis mechanisms
  • Genomics and Rare Diseases
  • Amyotrophic Lateral Sclerosis Research
  • X-ray Diffraction in Crystallography
  • DNA Repair Mechanisms
  • Metal Extraction and Bioleaching
  • Parkinson's Disease Mechanisms and Treatments
  • Gold and Silver Nanoparticles Synthesis and Applications
  • Perovskite Materials and Applications
  • Extraction and Separation Processes

Leibniz Institute of Polymer Research
2018-2024

Technische Universität Dresden
2019-2021

The University of Kitakyushu
2017-2018

University of Hyogo
2018

JTEKT (France)
2014

Kyoto University
2013

Tohoku University
1992-2011

Hiroshima University
2001

Gunma University
1997

Massachusetts General Hospital
1997

Abstract Imprint lithography has emerged as a reliable, reproducible, and rapid method for patterning colloidal nanostructures. As promising alternative to top‐down lithographic approaches, the fabrication of nanodevices thus become effective straightforward. In this study, fusion interference (IL) nanosphere imprint on various target substrates ranging from carbon film transmission electron microscope grid inorganic dopable polymer semiconductor is reported. 1D plasmonic photonic crystals...

10.1002/adfm.202105054 article EN Advanced Functional Materials 2021-06-29

The size of the (CAG)n repeat array in 3′ end MJDI gene and haplotype at a series microsateilite markers surrounding MJD1 were examined large cohort Japanese Caucasian subjects affected with Machado-Joseph disease (MJD). Our data provide five novel observations. First, MJD is associated expansion from normal range 14–37 repeats to 68–84 most subjects, but no observed expansions intermediate between those groups. Second, expanded allele displays inter-generational instability, particularly...

10.1093/hmg/4.7.1137 article EN Human Molecular Genetics 1995-07-01

Machado-Joseph disease (MJD) is an autosomal dominant multisystem neurodegenerative disorder caused by unstable expansion of a CAG repeat in the MJD1 gene at 14q432.1. To identify elements affecting intergenerational instability repeat, we investigated whether CGG/GGG polymorphism 3′ end affects repeat. The [expanded (CAG)n-CGG]/[normal (CAG)n-GGG] haplotypes were found to result significantly greater compared (CAG)n-CGG] or (CAG)nGGG]/[normal haplotypes. Multiple stepwise logistic...

10.1093/hmg/5.7.923 article EN Human Molecular Genetics 1996-07-01

Abstract The challenges in plasmonic charge transfer on a large‐scale and low losses are systematically investigated by optical designs using 1D‐plasmonic lattice structures. These lattices used as couplers to guide the energy an underneath sub‐wavelength titanium dioxide layer, resulting photonic crystal slabs. So far, photodetection is possible at levels close semiconductor bandgap; however, with observed hybrid plasmonic–photonic modes, other wavelengths over broad solar spectrum can be...

10.1002/adfm.202011099 article EN cc-by Advanced Functional Materials 2021-02-28

Abstract We report a patient presenting at age 16 years with postural instability and falls who developed severe generalized dystonia by the of 20 years. He was product consanguineous marriage. Maternal grandfather paternal grandmother (brother sister) living in Azores were both affected Machado‐Joseph disease (MJD) beginning late life. To date neither patient's parents are clinically affected. Linkage studies this family others Azorean descent have confirmed recent mapping MJD gene to...

10.1002/ana.410360318 article EN Annals of Neurology 1994-09-01

We have discovered a new Italian pedigree with autosomal-dominant ALS. The pedigree, at present, comprises 75 members distributed in five generations. ALS was diagnosed eight patients. mean ± SD age of onset the disease 46.8 13.5 years, range 29 to 63 years. duration 11.6 1.7 months. Molecular genetic studies showed missense mutation (Gly→Ser, codon 41) exon 2 Cu/Zn superoxide dismutase gene (SOD1) on chromosome 21 available affected member and 45% at-risk subjects pedigree. This study...

10.1212/wnl.44.2.347 article EN Neurology 1994-02-01

The present paper reports the fabrication of novel types hybrid fibrous photocatalysts by combining block copolymer (BCP) templating, sol-gel processing, and coaxial electrospinning techniques. Coaxial produces core-shell nanofibers (NFs), which are converted into hollow porous TiO

10.1016/j.jcis.2024.06.133 article EN cc-by-nc Journal of Colloid and Interface Science 2024-06-21

Abstract Allele frequencies for polymorphisms in the aplipoprotein E and apolipoprotein CII genes were determined subjects of Ashkenazi Jewish origin with lateonset Alzheimer's disease unaffected control from same ethnic group. A significant association was observed between late‐onset ε4 (112 Cys→Arg ) allele E; however, no detected CII. These results suggest that is probably not due to linkage disequilibrium.

10.1002/ana.410360118 article EN Annals of Neurology 1994-07-01

Abstract Metal‐semiconductor nanostructures in various configurations are extensively used photodetection, photocatalysis, and photovoltaics. For photodetection purposes, the working principle is straightforward; on illumination, generated charge carriers excess lead to a decrease resistance. Notably, using an interconnected metal‐semiconductor grating, it observed now reported opposite response, increase Such photoresistors fabricated through wrinkle structuring oblique angle material...

10.1002/adfm.202210172 article EN cc-by Advanced Functional Materials 2023-03-14

Abstract In this study, DNA local structures with bulged bases and mismatched base pairs as well ordinary full‐matched by using 19 F NMR spectroscopy F‐labeled oligodeoxynucleotides (ODNs) were monitored. The chemical shift change in the spectra allowed discrimination of structures. Two types ODNs possessing bis(trifluoromethyl)benzene unit (F‐unit) at specified uridines prepared hybridized their complementary or noncomplementary strands to form matched, mismatched, duplexes. By ODN F1,...

10.1002/chem.201302770 article EN Chemistry - A European Journal 2013-09-23

Abstract Here, for the first time, high‐yield (87.6%) robust and facile synthesis of water‐processable donor–acceptor Janus nanoparticles (JNP) that are high potential optoelectronic applications is reported. The JNPs have easily controlled ratios excellent quality, which shown by energy‐filtered transmission electron microscopy. exhibit improved charge separation transfer properties compared to conventional characterized via both steady‐state transient photoluminescence spectroscopy....

10.1002/adom.202101922 article EN Advanced Optical Materials 2022-02-27

Abstract The understanding and applications of electron‐conducting π ‐conjugated polymers with naphtalene diimide (NDI) blocks show remarkable progress in recent years. Such demonstrate a facilitated n‐doping due to the strong electron deficiency main polymer chain presence positively charged side groups stabilizing negative charge n‐doped backbone. Here, n‐type conducting NDI enhanced stability its states for prospective “in‐water” is developed. A combined experimental–theoretical approach...

10.1002/advs.202203530 article EN cc-by Advanced Science 2022-09-05

Some patients with familial Alzheimer's disease (FAD) have mutations in the presenilin-1 (PS-1) gene on chromosome 14. We report a Japanese family AD and an Ala285Val substitution exon 8 of PS-1 gene. FAD this was characterized by relatively late onset (mean age, 50 years) absence myoclonus, seizures, or paratonia. Levels tau were markedly elevated CSF whereas levels amyloid beta protein normal. MRI cranium showed marked linear signal abnormalities within white matter parieto-occipital...

10.1212/wnl.48.4.1118 article EN Neurology 1997-04-01

The <i>c-FOS</i> gene product, a putative transacting transcriptional regulator of the amyloid precursor protein (APP) gene, is candidate locus for familial Alzheimer9s disease (FAD) mutation on chromosome 14 (FAD<sub>14</sub>). In light this functional relationship, we investigated nucleotide sequence and segregation <i>of c-FOS</i> 59 APP promoter. Single-stranded conformational polymorphisms (SSCPs) in revealed that closely cosegregates with FAD<sub>14</sub> but does not show allelic...

10.1212/wnl.43.11.2275 article EN Neurology 1993-11-01

Semiconducting, redox-active and solution-processable: accessing a highly functional Ru–polymetallayne <italic>via</italic> copper-free dehydrohalogenation polymerization.

10.1039/c9py01090d article EN Polymer Chemistry 2019-10-04
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