「Two mouse models carrying truncating mutations in Magel2 show distinct phenotypes<Abstract of dissertation>」の関連論文
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Evolutionary histories of breast cancer and related clones
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FGF5 and EPAS1 gene polymorphisms are associated with high-altitude adaptation in Nepalese goat breeds
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Glucose transporter Glut1 controls diffuse invasion phenotype with perineuronal satellitosis in diffuse glioma microenvironment
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Tenascin C Aggravates Autoimmune Myocarditis via Dendritic Cell Activation and Th17 Cell Differentiation
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Mice with exonic RELN deletion identified from a patient with schizophrenia have impaired visual discrimination learning and reversal learning in touchscreen operant tasks
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Severe neurodevelopmental disorder caused by an MEF2C nonsense mutation
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Comprehensive analysis of full-length transcripts reveals novel splicing abnormalities and oncogenic transcripts in liver cancer
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Molecular Mechanism of Quinclorac Resistance in Multiple-Herbicide Resistant Echinochloa phyllopogon
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Dilated cardiomyopathy-linked heat shock protein family D member 1 mutations cause up-regulation of reactive oxygen species and autophagy through mitochondrial dysfunction (本文)
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Constitutively active signaling of MDA5 in Treg cells causes apoptosis of Treg cells and results in autoimmune diseases
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Trp53 Mutation in Keratin 5 (Krt5)-Expressing Basal Cells Facilitates the Development of Basal Squamous-Like Invasive Bladder Cancer in the Chemical Carcinogenesis of Mouse Bladder
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A cerebrospinal fluid microRNA analysis: Progressive supranuclear palsy
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Transcription of MERVL retrotransposons is required for preimplantation embryo development (本文)
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Comprehensive behavioral analysis of the mice deficient in Akain1, a novel protein kinase A-binding protein.
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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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Tooth Loss Induces Memory Impairment and Gliosis in App Knock-in Mouse Models of Alzheimer's disease
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Study on the role of CtBP2 in pancreatic β cell
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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 PDGF receptor alpha signal regulates the senescence of neural stem cells and their niche via the close functional correlation with NAD
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A clinical and genetic study of SPG31 in Japan
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Conserved Double Translation Initiation Site for Δ160p53 Protein Hints at Isoform’s Key Role in Mammalian Physiology
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Cellular senescence in white matter microglia is induced during ageing in mice and exacerbates the neuroinflammatory phenotype
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Patient-derived ovarian cancer organoids capture the genomic profiles of primary tumours applicable for drug sensitivity and resistance testing (本文)
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Elucidation of cause and natural feature of cheating rhizobia, and host defense mechanism against them
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Establishment and analysis of a mouse model conditionally expressing the Helicobacter pylori CagA oncoprotein
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Analysis of Anti-metabolic Syndrome Effect of Kaempferol in TSOD Mice
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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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Lineage tracing analysis defines erythropoietin-producing cells as a distinct subpopulation of resident fibroblasts with unique behaviors
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A case of Cockayne syndrome with unusually mild clinical manifestations
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CRISPR/Cas9-mediated genome-edited mice reveal 10 testis-enriched genes are dispensable for male fecundity
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The landscape of genetic aberrations in myxofibrosarcoma
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Role of Dopamine D2 Receptor/Fatty Acid-Binding Protein 3 Signaling in Nicotine-Induced Addiction
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Homozygous variant p.Ser427Pro in PNPLA1 is a preventive factor from atopic dermatitis
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Genomic analysis of multiple myeloma using targeted capture sequencing in the Japanese cohort
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Neuronal glutathione loss leads to neurodegeneration involving gasdermin activation
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Analysis of absolute amounts of two meiotic cohesin subunits, RAD21L and REC8, in mouse spermatocytes
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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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Studies on the transcriptional regulation of genes involved in adult development in insects
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Studies on multifunctional genome elements functioning in mouse spermatogenesis [an abstract of entire text]
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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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Study on Contribution of Trimethyl Guanosine Synthase Tgs1 to Heterochromatin Formation in Fission Yeast
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CEBPγ facilitates lamellipodia formation and cancer cell migration through CERS6 upregulation
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A RUNX-targeted gene switch-off approach modulates the BIRC5/PIF1-p21 pathway and reduces glioblastoma growth in mice
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Pitfalls in establishing mouse model of female infertility by immunization with human centromere protein
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Novel SLC30A2 mutations in the pathogenesis of transient neonatal zinc deficiency
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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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Cryptotanshinone is a candidate therapeutic agent for interstitial lung disease associated with a BRICHOS-domain mutation of SFTPC
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Clinical and genetic features of cystic fibrosis in Japan