「Stability and Oligomerization of Mutated SMN Protein Determine Clinical Severity of Spinal Muscular Atrophy」の関連論文
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Robust and efficient knock-in in embryonic stem cells and early-stage embryos of the common marmoset using the CRISPR-Cas9 system (本文)
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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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GPR64, Screened from Ewing Sarcoma Cells, Is a Potential Target for Antibody-Based Therapy for Various Sarcomas
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Validity of the cell‐extracted proteome as a substrate pool for exploring phosphorylation motifs of kinases
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Insights from a computational analysis of the SARS-CoV-2 Omicron variant: Host-pathogen interaction, pathogenicity, and possible drug therapeutics
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Role of α2δ3 in Cellular Synchronization of the Suprachiasmatic Nucleus Under Constant Light Conditions
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Combined landscape of single-nucleotide variants and copy number alterations in clonal hematopoiesis
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p53 deficiency augments nucleolar instability after ionizing irradiation
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Osteocalcin is necessary for the alignment of apatite crystallites, but not glucose metabolism, testosterone synthesis, or muscle mass
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Identification of anti-citrullinated osteopontin antibodies and increased inflammatory response by enhancement of osteopontin binding to fibroblast-like synoviocytes in rheumatoid arthritis
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Chitinase 3-like 1 secreted from cancer-associated fibroblasts promotes tumor angiogenesis via interleukin-8 secretion in colorectal cancer
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TDO2 Overexpression Is Associated with Cancer Stem Cells and Poor Prognosis in Esophageal Squamous Cell Carcinoma
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TDO2 Overexpression Is Associated with Cancer Stem Cells and Poor Prognosis in Esophageal Squamous Cell Carcinoma
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Studies on Circadian Clock RNA Methylation and Micturition Rhythm
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Calcium-Binding Protein S100A4 Is Upregulated in Carotid Atherosclerotic Plaques and Contributes to Expansive Remodeling
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De novo Selection of Macrocyclic Peptides Binding to TMEPAI family by Means of Random Non-standard Peptides Integrated Discovery System
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Failure of DNA double-strand break repair by tau mediates Alzheimer's disease pathology in vitro
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FGF5 and EPAS1 gene polymorphisms are associated with high-altitude adaptation in Nepalese goat breeds
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Lusutrombopag effectively promotes the growth and differentiation of megakaryocytic cells from patients with myelodysplastic syndrome
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A VCP modulator, KUS121, as a promising therapeutic agent for post-traumatic osteoarthritis
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GLT1 gene delivery based on bone marrow-derived cells ameliorates motor function and survival in a mouse model of ALS.
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An experience in prenatal diagnosis via QF-PCR of a female child with a 9.9 Mb pure deletion at 18p11.32–11.22
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Di-lysine motif-like sequences formed by deleting the C-terminal domain of aquaporin-4 prevent its trafficking to the plasma membrane (本文)
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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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The transcription factor ZFP64 facilitates climbing-fiber synapse elimination along signaling pathway mediated by P/Q-type voltage-dependent Ca2+ channel in the developing cerebellum
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Acquired dysfibrinogenemia: monoclonal λ-type IgA binding to fibrinogen caused lower functional plasma fibrinogen level and abnormal clot formation
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KANPHOS: A Database of Kinase-Associated Neural Protein Phosphorylation in the Brain
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Comparative analysis of plant isochorismate synthases reveals structural mechanisms underlying their distinct biochemical properties
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Effects of knockout of CO2-responsive CCT protein, a regulator of starch synthesis on physiological characteristics of rice
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Screening method for congenital dysfibrinogenemia using clot waveform analysis with the Clauss method
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FIGNL1 AAA+ ATPase remodels RAD51 and DMC1 filaments in pre-meiotic DNA replication and meiotic recombination
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in vitroおよびin silico分析によるアディポネクチン受容体アゴニストジ・トリペプチドに関する研究
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Study on serological diagnostic assays for Crimean-Congo hemorrhagic fever
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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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Mature Myotubes Generated From Human-Induced Pluripotent Stem Cells Without Forced Gene Expression
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The CST complex facilitates cell survival under oxidative genotoxic stress
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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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Three-dimensional human placenta-like bud synthesized from induced pluripotent stem cells
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Establishment of a mouse model of troglitazone-induced liver injury and analysis of its hepatotoxic mechanism
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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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Osteocrin ameliorates adriamycin nephropathy via p38 mitogen-activated protein kinase inhibition
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Homozygous variant p.Ser427Pro in PNPLA1 is a preventive factor from atopic dermatitis
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PCR-Based Screening of Spinal Muscular Atrophy for Newborn Infants in Hyogo Prefecture, Japan
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Exploring the landscape of ectodomain shedding by quantitative protein terminomics
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Diagnostic significance of apical membranous and cytoplasmic dot-like CD26 expression in encapsulated follicular variant of papillary thyroid carcinoma : a useful marker for capsular invasion
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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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Generation of two human induced pluripotent stem cell lines derived from two X-linked adrenoleukodystrophy patients with ABCD1 mutations
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Hamster PIWI proteins bind to piRNAs with stage-specific size variations during oocyte maturation (本文)
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Origin of diverse phosphorylation patterns in the ERBB system
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Tsga8 is required for spermatid morphogenesis and male fertility in mice