「Rescue of recurrent deep intronic mutation underlying cell type-dependent quantitative NEMO deficiency」の関連論文
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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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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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ニワトリにおけるTRPV1の酸感受性とその制御機構
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Studies on Thermoregulation and Growth Performance in Chicks with av-UCP mutation
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Combination of tumor necrosis factor-α and epidermal growth factor induces the adrenergic-to-mesenchymal transdifferentiation in SH-SY5Y neuroblastoma cells
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Severe neurodevelopmental disorder caused by an MEF2C nonsense mutation
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Single-cell transcriptomics of human cholesteatoma identifies an activin A-producing osteoclastogenic fibroblast subset inducing bone destruction
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The landscape of genetic aberrations in myxofibrosarcoma
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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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Conformational change of RNA‐helicase DHX30 by ALS/FTD‐linked FUS induces mitochondrial dysfunction and cytosolic aggregates
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Cell migration is impaired in XPA-deficient cells
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MECHANISTIC ANALYSIS OF THE INITIATION OF RETROVIRAL GENE SILENCING BY REPROGRAMMING FACTORS
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A cerebrospinal fluid microRNA analysis: Progressive supranuclear palsy
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A case of Cockayne syndrome with unusually mild clinical manifestations
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Inactivation of the PD-1-dependent immunoregulation in mice exacerbates contact hypersensitivity resembling immune-related adverse events
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Studies on Cytotoxic Effects of Tumor Necrosis Factor-Related Apoptosis Inducing Ligand (TRAIL) to Canine Cell Lines Derived from Hemangiosarcoma and Mammary Epithelial Tumor
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Cardio- and reno-protective effects of dipeptidyl peptidase III in diabetic mice.
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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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Study on Accessory Gene Regulator(AGR)Variants in Staphylococcus aureus
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Genomic stability of mouse spermatogonial stem cells in vitro
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Oncogenic FGFR1 mutation and amplification in common cellular origin in a composite tumor with neuroblastoma and pheochromocytoma
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Beneficial screening of Fabry disease in patients with hypohidrosis
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Population genetics of variants in infectious diseases and its application to the prediction of variant replacement
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MAGI-2 orchestrates the localization of backbone proteins in the slit diaphragm of podocytes
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Sarcomatoid mesothelioma diagnosed in a patient with mesothelioma in situ: a case report on morphologic differences after 9-month interval with details analysis of cytology in early-stage mesothelioma
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Genome-wide association studies on hepatocellular carcinoma after eradication of hepatitis C virus in Japanese and on chronic hepatitis B in Thai
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Horizontally Transferred DNA in the Genome of the Fungus Pyricularia oryzae is Associated With Repressive Histone Modifications
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Networking and Specificity-Changing DNA Methyltransferases in Helicobacter pylori.
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Observing the nonvectorial yet cotranslational folding of a multidomain protein, LDL receptor, in the ER of mammalian cells.
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Complex roles of the actin-binding protein Girdin/GIV in DNA damage-induced apoptosis of cancer cells
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Research for elucidation of immune evasion mechanisms and development of a novel immunotherapy for cancer in dogs [an abstract of entire text]
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Persistent elevation of lysophosphatidylcholine promotes radiation brain necrosis with microglial recruitment by P2RX4 activation
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Amplified EPOR/JAK2 Genes Define a Unique Subtype of Acute Erythroid Leukemia
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Comprehensive genomics in androgen receptor-dependent castration-resistant prostate cancer identifies an adaptation pathway mediated by opioid receptor kappa 1
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Novel Therapeutic Impact of Isorhamnetin for the Upstream Treatment of Atrial Fibrillation
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Indoleamine 2,3-Dioxygenase 2 Deficiency Exacerbates Imiquimod-Induced Psoriasis-Like Skin Inflammation
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Individual Differences in Autistic Traits are Associated with Serotonin Transporter Gene Polymorphism Through Medial Prefrontal Function: A Study Using NIRS
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Individual Differences in Autistic Traits are Associated with Serotonin Transporter Gene Polymorphism Through Medial Prefrontal Function: A Study Using NIRS
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The relationship between DRD2 Taq1A polymorphism and white matter structure in healthy young adults.
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Safety comparisons among monoamine oxidase inhibitors against Parkinson’s disease using FDA adverse event reporting system
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Downregulation of lncRNA PVT1 inhibits proliferation and migration of mesothelioma cells by targeting FOXM1
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Downregulation of lncRNA PVT1 inhibits proliferation and migration of mesothelioma cells by targeting FOXM1
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Characterization of the Anticancer Activities of Some Natural and Synthetic Compounds: Molecular Targets and Mechanism
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成獣ライディッヒ細胞における性染色体の機能解析
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Distinctive roles of syntaxin binding protein 4 and its action target, TP63, in lung squamous cell carcinoma: a theranostic study for the precision medicine
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Partial Epithelial-Mesenchymal Transition Was Observed Under p63 Expression in Acquired Middle Ear Cholesteatoma and Congenital Cholesteatoma.
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A motor neuron disease-associated mutation produces non-glycosylated Seipin that induces ER stress and apoptosis by inactivating SERCA2b
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Analysis of Anti-metabolic Syndrome Effect of Kaempferol in TSOD Mice
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Myh9 R702C is associated with erythroid abnormality with splenomegaly in mice
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Screening method for congenital dysfibrinogenemia using clot waveform analysis with the Clauss method