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Live cell imaging of β-tubulin mRNA reveals spatiotemporal expression dynamics in the filamentous fungus Aspergillus oryzae.
- Published in:
- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-64531-5
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- Publication type:
- Article
Genetic research of inherited peripheral neuropathies.
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- Neurology & Clinical Neuroscience, 2024, v. 12, n. 3, p. 159, doi. 10.1111/ncn3.12770
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- Publication type:
- Article
A novel homozygous HPDL variant in Japanese siblings with autosomal recessive hereditary spastic paraplegia: case report and literature review.
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- Neurogenetics, 2024, v. 25, n. 2, p. 149, doi. 10.1007/s10048-024-00746-y
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- Publication type:
- Article
Spatial Fluctuation of Central Nervous System Lesions in X-linked Charcot-Marie-Tooth Disease with a Novel GJB1 Mutation.
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- Internal Medicine, 2024, v. 63, n. 4, p. 571, doi. 10.2169/internalmedicine.1713-23
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- Publication type:
- Article
Clinical variability associated with intronic FGF14 GAA repeat expansion in Japan.
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- Annals of Clinical & Translational Neurology, 2024, v. 11, n. 1, p. 96, doi. 10.1002/acn3.51936
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- Publication type:
- Article
Dystonia and Parkinsonism in COA7-related disorders: expanding the phenotypic spectrum.
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- Journal of Neurology, 2024, v. 271, n. 1, p. 419, doi. 10.1007/s00415-023-11998-3
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- Publication type:
- Article
Genetic, electrophysiological, and pathological studies on patients with SCN9A‐related pain disorders.
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- Journal of the Peripheral Nervous System, 2023, v. 28, n. 4, p. 597, doi. 10.1111/jns.12590
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- Publication type:
- Article
Microbleed clustering in thalamus sign in CADASIL patients with NOTCH3 R75P mutation.
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- Frontiers in Neurology, 2023, p. 01, doi. 10.3389/fneur.2023.1241678
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- Publication type:
- Article
Siblings with Cockayne Syndrome B Type III Presenting with Slowly Progressive Cerebellar Ataxia.
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- Internal Medicine, 2023, v. 62, n. 15, p. 2253, doi. 10.2169/internalmedicine.0061-22
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- Publication type:
- Article
Anti-ganglionic acetylcholine receptor antibodies in functional neurological symptom disorder/conversion disorder.
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- Frontiers in Neurology, 2023, v. 14, p. 1, doi. 10.3389/fneur.2023.1137958
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- Publication type:
- Article
Efficacy of l‐Arginine treatment in patients with HTLV‐1‐associated neurological disease.
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- Annals of Clinical & Translational Neurology, 2023, v. 10, n. 2, p. 237, doi. 10.1002/acn3.51715
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- Publication type:
- Article
Gene panel analysis of 119 index patients with suspected periodic paralysis in Japan.
- Published in:
- Frontiers in Neurology, 2023, v. 14, p. 01, doi. 10.3389/fneur.2023.1078195
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- Publication type:
- Article
Genetic spectrum and founder effect of non-dystrophic myotonia: a Japanese case series study.
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- Journal of Neurology, 2022, v. 269, n. 12, p. 6406, doi. 10.1007/s00415-022-11305-6
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- Publication type:
- Article
Prevalence of Fragile X-Associated Tremor/Ataxia Syndrome in Patients with Cerebellar Ataxia in Japan.
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- Cerebellum, 2022, v. 21, n. 5, p. 851, doi. 10.1007/s12311-021-01323-x
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- Publication type:
- Article
Multi-type RFC1 repeat expansions as the most common cause of hereditary sensory and autonomic neuropathy.
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- Frontiers in Neurology, 2022, v. 13, p. 1, doi. 10.3389/fneur.2022.986504
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- Publication type:
- Article
Genetic and clinical features of cerebellar ataxia with RFC1 biallelic repeat expansions in Japan.
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- Frontiers in Neurology, 2022, v. 13, p. 1, doi. 10.3389/fneur.2022.952493
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- Publication type:
- Article
Complex hereditary peripheral neuropathies caused by novel variants in mitochondrial-related nuclear genes.
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- Journal of Neurology, 2022, v. 269, n. 8, p. 4129, doi. 10.1007/s00415-022-11026-w
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- Publication type:
- Article
Novel heterozygous variants of SLC12A6 in Japanese families with Charcot–Marie–Tooth disease.
- Published in:
- Annals of Clinical & Translational Neurology, 2022, v. 9, n. 7, p. 902, doi. 10.1002/acn3.51603
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- Publication type:
- Article
Comprehensive Genetic Analyses of Inherited Peripheral Neuropathies in Japan: Making Early Diagnosis Possible.
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- Biomedicines, 2022, v. 10, n. 7, p. N.PAG, doi. 10.3390/biomedicines10071546
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- Publication type:
- Article
Novel de novo POLR3B mutations responsible for demyelinating Charcot–Marie–Tooth disease in Japan.
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- Annals of Clinical & Translational Neurology, 2022, v. 9, n. 5, p. 747, doi. 10.1002/acn3.51555
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- Publication type:
- Article
The first case of infantile-onset multisystem neurologic, endocrine, and pancreatic disease caused by novel PTRH2 mutation in Japan.
- Published in:
- 2022
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- Publication type:
- Letter
Overexpression of cell-wall GPI-anchored proteins restores cell growth of N-glycosylation-defective och1 mutants in Schizosaccharomyces pombe.
- Published in:
- Applied Microbiology & Biotechnology, 2021, v. 105, n. 23, p. 8771, doi. 10.1007/s00253-021-11649-5
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- Publication type:
- Article
Traditional and Latest Researches on Aspergillus oryzae and Related Koji Molds.
- Published in:
- 2021
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- Publication type:
- Editorial
Substrate specificities of α1,2- and α1,3-galactosyltransferases and characterization of Gmh1p and Otg1p in Schizosaccharomyces pombe.
- Published in:
- Glycobiology, 2021, v. 31, n. 8, p. 1037, doi. 10.1093/glycob/cwab028
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- Publication type:
- Article
Membrane Traffic in Aspergillus oryzae and Related Filamentous Fungi.
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- Journal of Fungi, 2021, v. 7, n. 7, p. 1, doi. 10.3390/jof7070534
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- Publication type:
- Article
Membrane traffic related to endosome dynamics and protein secretion in filamentous fungi.
- Published in:
- Bioscience, Biotechnology & Biochemistry, 2021, v. 85, n. 5, p. 1038, doi. 10.1093/bbb/zbab004
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- Publication type:
- Article
Genetic spectrum of Charcot–Marie–Tooth disease associated with myelin protein zero gene variants in Japan.
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- Clinical Genetics, 2021, v. 99, n. 3, p. 359, doi. 10.1111/cge.13881
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- Publication type:
- Article
Single-Molecule FISH Reveals Subcellular Localization of α-Amylase and Actin mRNAs in the Filamentous Fungus Aspergillus oryzae.
- Published in:
- Frontiers in Microbiology, 2020, v. 11, p. N.PAG, doi. 10.3389/fmicb.2020.578862
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- Publication type:
- Article
Clinical features of inherited neuropathy with BSCL2 mutations in Japan.
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- Journal of the Peripheral Nervous System, 2020, v. 25, n. 2, p. 125, doi. 10.1111/jns.12369
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- Publication type:
- Article
Author Correction: Characterization of novel endo-β-N-acetylglucosaminidases from Sphingobacterium species, Beauveria bassiana and Cordyceps militaris that specifically hydrolyze fucose-containing oligosaccharides and human IgG.
- Published in:
- 2020
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- Publication type:
- Correction Notice
Author Correction: Identification and characterization of a novel β-D-galactosidase that releases pyruvylated galactose.
- Published in:
- 2020
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- Publication type:
- Correction Notice
Catechol O-methyltransferase homologs in Schizosaccharomyces pombe are response factors to alkaline and salt stress.
- Published in:
- Applied Microbiology & Biotechnology, 2019, v. 103, n. 12, p. 4881, doi. 10.1007/s00253-019-09858-0
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- Publication type:
- Article
Identification and characterization of a novel β-D-galactosidase that releases pyruvylated galactose.
- Published in:
- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-30508-4
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- Publication type:
- Article
Mutations in COA7 cause spinocerebellar ataxia with axonal neuropathy.
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- 2018
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- Publication type:
- journal article
Clinical and genetic features of Charcot‐Marie‐Tooth disease 2F and hereditary motor neuropathy 2B in Japan.
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- Journal of the Peripheral Nervous System, 2018, v. 23, n. 1, p. 40, doi. 10.1111/jns.12252
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- Publication type:
- Article
Clinical and genetic diversities of Charcot-Marie-Tooth disease with MFN2 mutations in a large case study.
- Published in:
- Journal of the Peripheral Nervous System, 2017, v. 22, n. 3, p. 191, doi. 10.1111/jns.12228
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- Publication type:
- Article
Characterization of a PA14 domain-containing galactofuranose-specific β- d -galactofuranosidase from Streptomyces sp.
- Published in:
- Bioscience, Biotechnology & Biochemistry, 2017, v. 81, n. 7, p. 1314, doi. 10.1080/09168451.2017.1300518
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- Publication type:
- Article
Neuron-specific knockdown of the Drosophila fat induces reduction of life span, deficient locomotive ability, shortening of motoneuron terminal branches and defects in axonal targeting.
- Published in:
- Genes to Cells, 2017, v. 22, n. 7, p. 662, doi. 10.1111/gtc.12500
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- Publication type:
- Article
Highly efficient transglycosylation of sialo-complex-type oligosaccharide using Coprinopsis cinerea endoglycosidase and sugar oxazoline.
- Published in:
- Biotechnology Letters, 2017, v. 39, n. 1, p. 157, doi. 10.1007/s10529-016-2230-0
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- Publication type:
- Article
Histopathological features of a patient with Charcot-Marie-Tooth disease type 2U/AD-CMTax- MARS.
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- Journal of the Peripheral Nervous System, 2016, v. 21, n. 4, p. 370, doi. 10.1111/jns.12193
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- Publication type:
- Article
Reply.
- Published in:
- 2016
- By:
- Publication type:
- letter
Adult-onset Krabbe disease presenting with an isolated form of peripheral neuropathy.
- Published in:
- 2016
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- Publication type:
- journal article
A rationally engineered yeast pyruvyltransferase Pvg1p introduces sialylation-like properties in neo-human-type complex oligosaccharide.
- Published in:
- Scientific Reports, 2016, p. 26349, doi. 10.1038/srep26349
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- Publication type:
- Article
Mutations in MME cause an autosomal-recessive Charcot-Marie-Tooth disease type 2.
- Published in:
- 2016
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- Publication type:
- journal article
Identification and Characterization of a Novel Galactofuranose-Specific β-D-Galactofuranosidase from Streptomyces Species.
- Published in:
- PLoS ONE, 2015, v. 10, n. 9, p. 1, doi. 10.1371/journal.pone.0137230
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- Publication type:
- Article
Transglycosylation Activity of Glycosynthase Mutants of Endo-β-N-Acetylglucosaminidase from Coprinopsis cinerea.
- Published in:
- PLoS ONE, 2015, v. 10, n. 7, p. 1, doi. 10.1371/journal.pone.0132859
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- Publication type:
- Article
Clinicopathological features of the first Asian family having vocal cord and pharyngeal weakness with distal myopathy due to a MATR3 mutation.
- Published in:
- Neuropathology & Applied Neurobiology, 2015, v. 41, n. 3, p. 391, doi. 10.1111/nan.12179
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- Publication type:
- Article
Neurofilament light mutation causes hereditary motor and sensory neuropathy with pyramidal signs.
- Published in:
- Journal of the Peripheral Nervous System, 2014, v. 19, n. 4, p. 311, doi. 10.1111/jns.12102
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- Publication type:
- Article
Long-distance endosome trafficking drives fungal effector production during plant infection.
- Published in:
- Nature Communications, 2014, v. 5, n. 10, p. 5097, doi. 10.1038/ncomms6097
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- Publication type:
- Article
Novel mutation in the replication focus targeting sequence domain of DNMT1 causes hereditary sensory and autonomic neuropathy IE.
- Published in:
- Journal of the Peripheral Nervous System, 2013, v. 18, n. 1, p. 89, doi. 10.1111/jns5.12012
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- Publication type:
- Article