「Rescue of recurrent deep intronic mutation underlying cell type-dependent quantitative NEMO deficiency」の関連論文
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Establishment and Application of Anti-CD20 Monoclonal Antibodies using the Cell-based Immunization and Screening Method for the Detection of B Cells
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Clinical and serological features of dermatomyositis and systemic lupus erythematosus patients with autoantibodies to ADAR1
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Study on the role of CtBP2 in pancreatic β cell
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Elucidation of Hair Growth and Hair Pigmentation Promotion Effect of 3,4,5-Tri-O-Caffeoylquinic Acid
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Failure of internal fixation for ankle joint Charcot neuroarthropathy with beta(2)-microglobulin amyloidosis: a case report
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Interactions of amyloid coaggregates with biomolecules and its relevance to neurodegeneration
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Implications of interleukin-17 in psoriatic lesions as Koebner phenomenon caused by recurrent occupational burns
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Optimized sonoreactor for accelerative amyloid-fibril assays through enhancement of primary nucleation and fragmentation
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Combined Hypophysitis and Type 1 Diabetes Mellitus Related to Immune Checkpoint Inhibitors
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Stability and Oligomerization of Mutated SMN Protein Determine Clinical Severity of Spinal Muscular Atrophy
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卵巣低異型度漿液性癌のin vitro発癌モデル
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Dermal fibroblast-like cells reprogrammed directly from adipocytes in mouse (本文)
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Paraproteinemia and neuropathy
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Generation and evaluation of a transgenic zebrafish for tissue-specific expression of a dominant-negative Rho-associated protein kinase-2
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Usefulness of functional splicing analysis to confirm precise disease pathogenesis in Diamond-Blackfan anemia caused by intronic variants in RPS19
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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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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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Usefulness of interleukin-18 as a diagnostic biomarker to differentiate adult-onset Still’s disease with/without macrophage activation syndrome from other secondary hemophagocytic lymphohistiocytosis in adults
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MDGA1-deficiency attenuates prepulse inhibition with alterations of dopamine and serotonin metabolism : An ex vivo HPLC-ECD analysis
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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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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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Increase of tissue factor expression on the surface of peripheral monocytes of patients with chronic spontaneous urticaria
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Increase of tissue factor expression on the surface of peripheral monocytes of patients with chronic spontaneous urticaria
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Unique reticular hyperkeratotic eruptions seen in a patient with Darier's disease and attention deficit hyperactivity disorder
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Natural genetic transformation mediates MRSA emergence
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Molecular Mechanism of Quinclorac Resistance in Multiple-Herbicide Resistant Echinochloa phyllopogon
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Ndufs4 ablation shows an elevated GFAP and a decreased synaptophysin expression in mouse hippocampus.
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Pluripotent stem cell model of Shwachman-Diamond syndrome reveals apoptotic predisposition of hemoangiogenic progenitors
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The ocular involvement did not accompany with the genital ulcer or the gastrointestinal symptoms at the early stage Behcet’s disease
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Lusutrombopag effectively promotes the growth and differentiation of megakaryocytic cells from patients with myelodysplastic syndrome
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Molecular and pathologic characterization of avian adenovirus isolated from the oviducts of laying hens in eastern Japan
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Mineralocorticoid and glucocorticoid receptors and 11beta-hydroxysteroid dehydrogenases in human breast lesions
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RUNX1 rearrangement in mature B-cell acute lymphoblastic leukemia with non-L3 morphology
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Autism-associated mutation in Hevin/Sparcl1 induces endoplasmic reticulum stress through structural instability
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Bmal1 Regulates Prostate Growth via Cell-Cycle Modulation
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JNK and Yorkie drive tumor malignancy by inducing L-amino acid transporter 1 in Drosophila
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Involvement of Transcription Factor 21 in the Pathogenesis of Fibrosis in Endometriosis
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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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A case of Erdheim–Chester disease with the BRAF V600E mutation diagnosed via endoscopic sinus surgery
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Systematic Review of Clinical Characteristics and Genotype-Phenotype Correlation in LAMB2-Associated Disease
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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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Large-scale discovery of male reproductive tract-specific genes through analysis of RNA-seq datasets
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Analysis of aging-related epigenetic modifications in murine male germline cells
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Cryptic insertion of CBFB into MYH11 leading to a type D fusion in acute myeloid leukemia with normal karyotype
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The role of autophagy in Arabidopsis plants exposed to ultraviolet-B or high temperature stress
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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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Increased CaV1.2 late current by a CACNA1C p.R412M variant causes an atypical Timothy syndrome without syndactyly
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Differentiation of hypertrophic chondrocytes from human iPSCs for the in vitro modeling of chondrodysplasias