「Wilson’s disease model establishment from human induced pluripotent stem cells」の関連論文
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Study on Contribution of Trimethyl Guanosine Synthase Tgs1 to Heterochromatin Formation in Fission Yeast
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Characterization of the traditional sake yeast Hiroshima no. 6 and its application to sake yeast cross-breeding.
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Study of Mitochonic Acid 5 to improve neuromuscular dysfunction associated with aging and diseases using C. elegans
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Pharmacogenomic study of anti-tuberculosis drugs-induced liver injury in Thais
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Recursive Vesicle Reproduction System Coupled with Enzymatic Cascade Reactions: Toward Synthetic Minimal Cell
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Presenilin is essential for ApoE secretion, a novel role of presenilin involved in Alzheimer’s disease pathogenesis
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All reported non-canonical splice site variants in GLA cause aberrant splicing
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Studies on Circadian Clock RNA Methylation and Micturition Rhythm
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Analysis of Anti-metabolic Syndrome Effect of Kaempferol in TSOD Mice
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Allosteric regulation accompanied by oligomeric state changes of Trypanosoma brucei GMP reductase through cystathionine-β-synthase domain
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Lack of impact of the ALDH2 rs671 variant on breast cancer development in Japanese BRCA1/2‐mutation carriers
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The association of thyroglobulin single nucleotide polymorphism with miniature dachshunds-specific inflammatory colorectal polyps and its involvement in interleukin-6 amplifier induced chronic inflammation
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DNA methyltransferase 3B plays a protective role against hepatocarcinogenesis caused by chronic inflammation via maintaining mitochondrial homeostasis
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Bmal1 Regulates Prostate Growth via Cell-Cycle Modulation
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Cryo-EM structures of Na⁺-pumping NADH-ubiquinone oxidoreductase from Vibrio cholerae
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Characterisation of an Escherichia coli line that completely lacks ribonucleotide reduction yields insights into the evolution of parasitism and endosymbiosis
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Immunobiochemical, molecular biological, and reverse genetical studies on vitellogenin receptor candidates in medaka, Oryzias latipes [an abstract of entire text]
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Inhibition of autophagy in theca cells induces CYP17A1 and PAI-1 expression via ROS/p38 and JNK signalling during the development of polycystic ovary syndrome
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Mammalian methionine adenosyltransferase 2A promotes rRNA processing and methylation of translation factors to induce translation in an mTORC1-independent manner
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Two sporadic cases of childhood-onset Hailey-Hailey disease with superimposed mosaicism
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Two mouse models carrying truncating mutations in Magel2 show distinct phenotypes
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Analyses of genetic and retinal lesions in Ccdc85c knockout rats: a rat model of genetic hydrocephalus
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Genetic and Physiological Characterization of Tomato F-box Gene HAWAIIAN SKIRT Mutants
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Condensate Formation by Metabolic Enzymes in Saccharomyces cerevisiae
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A Single RET Mutation in Hirschsprung Disease Induces Intestinal Aganglionosis Via a Dominant-Negative Mechanism
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Impairment of DYRK2 by DNMT1-mediated transcription augments carcinogenesis in human colorectal cancer
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STUDY ON SEAWEED CHLOROPHYLLS AND LIPIDS : DISTRIBUTION, BIOAVAILABILITY, AND FUNCTIONALITY [an abstract of entire text]
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Subcellular localization of nucleocapsid protein of severe fever with thrombocytopenia syndrome virus (SFTSV) and characterization of quasi-species of SFTSV
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Networking and Specificity-Changing DNA Methyltransferases in Helicobacter pylori.
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Quantitative Prediction of P-Glycoprotein-Mediated Intestinal Absorption for Molecules Beyond the Rule of Five Using Model Animals
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Combination of target site mutation and associated CYPs confers high-level resistance to pyridaben in Tetranychus urticae
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Molecular genetic study of the FMR1 CGG repeat configurations in the Japanese population and patients with Fragile X-Associated Tremor/Ataxia Syndrome
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Population genetics of variants in infectious diseases and its application to the prediction of variant replacement
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Development of genetic management methods for rice varieties and prediction of spontaneous mutation frequencies using next-generation sequencing technology [an abstract of entire text]
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Immunohistochemical assessment of sex-determining region Y (SRY)-related high mobility group (HMG)-box 2 (Sox2) and Krüppel-like factor 4 (Klf4) in ameloblastomas
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Novel genes and variants associated with congenital pituitary hormone deficiency in the era of next-generation sequencing
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Long-Read Sequence Confirmed a Large Deletion Including MYH6 and MYH7 in an Infant of Atrial Septal Defect and Atrial Arrhythmias.
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Increase in the peripheral blood methylglyoxal levels in 10% of hospitalized chronic schizophrenia patients
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Iinfluence of plasma cytokine levels on the conversion risk from MCI to dementia in the Alzheimer's disease neuroimaging initiative database
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Glucose as a Protein-Condensing Cellular Solute
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The influence of HLA-B51 on clinical manifestations among Japanese patients with Behçet’s disease: A nationwide survey
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Forced expression of α2,3-sialyltransferase IV rescues impaired heart development in α2,6-sialyltransferase I-deficient medaka
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Prophylactic treatment of rapamycin ameliorates naturally developing and episode -induced heterotopic ossification in mice expressing human mutant ACVR1
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Development of a molecular tool for the differentiation of Mycobacterium bovis and molecular characterization of Mycobacterium bovis isolates in Malawi
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Studies on the molecular pathogenesis and the novel disease-associated genes in dogs with inflammatory colorectal polyps [an abstract of entire text]
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Homozygous variant p.Ser427Pro in PNPLA1 is a preventive factor from atopic dermatitis
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Combined landscape of single-nucleotide variants and copy number alterations in clonal hematopoiesis
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Avoiding entry into intracellular protein degradation pathways by signal mutations increases protein secretion in Pichia pastoris
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A novel NCSTN missense mutation in the signal peptide domain causes hidradenitis suppurativa, which has features characteristic of an autoinflammatory keratinization disease
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Clinical efficacy of the combined treatment of anti-PD-L1 rat-bovine chimeric antibody with a COX-2 inhibitor in calves infected with Mycoplasma bovis