「Mechanism-Based Personalized Medicine for Cystic Fibrosis by Suppressing Pseudo Exon Inclusion」の関連論文
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Chemical biology studies on nucleic acid recognition, modification, and secondary structures
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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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Generation of two human induced pluripotent stem cell lines derived from two X-linked adrenoleukodystrophy patients with ABCD1 mutations
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Cell migration is impaired in XPA-deficient cells
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A clinical and genetic study of SPG31 in Japan
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HER2 G776S mutation promotes oncogenic potential in colorectal cancer cells when accompanied by loss of APC function
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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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Circulatory C-type natriuretic peptide reduces mucopolysaccharidosis-associated craniofacial hypoplasia in vivo
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Two sporadic cases of childhood-onset Hailey-Hailey disease with superimposed mosaicism
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Evolutionary genetics of socioemotional behavior in humans and other mammals
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Identification of FMRP target genes expressed during corticogenesis: Implication for common phenotypes among neurodevelopmental disorders
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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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Morphea in a Crohn's disease patient undergoing ustekinumab treatment
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FKRP mutations cause congenital muscular dystrophy 1C and limb-girdle muscular dystrophy 2I in Asian patients
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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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Nucleolar stress: Molecular mechanisms and related human diseases
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CCL2-CCR2 signaling in the skin drives surfactant-induced irritant contact dermatitis via IL-1β-mediated neutrophil accumulation
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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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Functional and genomic characterization of patient-derived xenograft model to study adaptation to mTORC1 inhibitor in clear cell renal cell carcinoma
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Clinical and serological features of dermatomyositis and systemic lupus erythematosus patients with autoantibodies to ADAR1
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In situ vaccination using unique TLR9 ligand K3-SPG induces long-lasting systemic immune response and synergizes with systemic and local immunotherapy
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iPSC-derived type IV collagen α5-expressing kidney organoids model Alport syndrome
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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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A muscle fatigue-like contractile decline was recapitulated using skeletal myotubes from Duchenne muscular dystrophy patient-derived iPSCs
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A cerebrospinal fluid microRNA analysis: Progressive supranuclear palsy
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Malfunctioning CD106-positive, short-term hematopoietic stem cells trigger diabetic neuropathy in mice by cell fusion.
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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
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Antiviral R Genes of Plants May Have Experienced Different "Selections" in Nature and in Crop Fields
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Loss of Arid1a and Pten in Pancreatic Ductal Cells Induces Intraductal Tubulopapillary Neoplasm via the YAP/TAZ Pathway
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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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Inherited CARD9 Deficiency in a Child with Invasive Disease Due to Exophiala dermatitidis and Two Older but Asymptomatic Siblings
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Inherited CARD9 Deficiency in a Child with Invasive Disease Due to Exophiala dermatitidis and Two Older but Asymptomatic Siblings
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Cross-ancestry genome-wide analysis of atrial fibrillation unveils disease biology and enables cardioembolic risk prediction
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Cooperative participation of epigenomic and genomic alterations in the clinicopathological diversity of gastric adenocarcinomas : significance of cell adhesion and epithelial–mesenchymal transition-related signaling pathways (本文)
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Polo-like kinase 4 and stromal antigen 3 are not associated with recurrent pregnancy loss caused by embryonic aneuploidy
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De Novo T790M Mutation in an L858R Epidermal Growth Factor Receptor Mutant-Associated Lung Adenocarcinoma
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Neural Isoforms of Agrin Are Generated by Reduced PTBP1−RNA Interaction Network Spanning the Neuron−Specific Splicing Regions in AGRN
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MECHANISTIC ANALYSIS OF THE INITIATION OF RETROVIRAL GENE SILENCING BY REPROGRAMMING FACTORS
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Remote solid cancers rewire hepatic nitrogen metabolism via host nicotinamide-N-methyltransferase
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Role of serotonin 4 receptor in the growth of axon and dendrites of hippocampal neurons during the embryonic development in mice
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Eighteen-years follow-up of congenital hypothyroidism by TSHR gene p.Arg109Gln and p.Arg450His variants
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A novel phosphodiesterase 4 inhibitor, AA6216, reduces macrophage activity and fibrosis in the lung
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Hippo-TAZ signaling is the master regulator of the onset of triple-negative basal-like breast cancers
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Everolimus delayed and suppressed cytomegalovirus DNA synthesis and the spread of infection and alleviated cytomegalovirus infection
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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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Study of the Effects of Inhibition of Epigenetic Regulators on the Proliferation of Hematological Malignant Tumor Cells
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Gut bacteria identified in colorectal cancer patients promote tumourigenesis via butyrate secretion
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Lung fibrogenic microenvironment in mouse reconstitutes human alveolar structure and lung tumor
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Pluripotent stem cell-based therapies and their path to the clinic
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The generation and insights of an inducible diabetes mellitus mouse model based on MafA and MafB double knockout