「Automated screening procedure for the phenotypes of congenital fibrinogen disorders using novel parameters, |min1|c and Ac/|min1|c, obtained from clot waveform analysis using the Clauss method」の関連論文
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Persistent elevation of lysophosphatidylcholine promotes radiation brain necrosis with microglial recruitment by P2RX4 activation
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Elucidation of cause and natural feature of cheating rhizobia, and host defense mechanism against them
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Identification of Virus Receptors
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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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Universal screening for familial hypercholesterolemia in children in Kagawa, Japan
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Biosynthetic study of miuraenamide A, an antifungal antibiotic of a slightly halophilic myxobacterium
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Identification of an Anti-Integrin αvβ6 Autoantibody in Patients With Ulcerative Colitis
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大気圧酸素プラズマ照射によるT細胞の活性制御に関する研究
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Subtype Distribution and Drug Resistance Patterns Among HIV-1 Strains Prevalent in Makassar, Indonesia
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Gut bacteria identified in colorectal cancer patients promote tumourigenesis via butyrate secretion
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Physiological and Pathological Mitochondrial Clearance Is Related to Pectoralis Major Muscle Pathogenesis in Broilers With Wooden Breast Syndrome
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Identification and analysis of mechanisms that bypass the essentiality of Polo, a mitotic regulator
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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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Immunobiochemical, molecular biological, and reverse genetical studies on vitellogenin receptor candidates in medaka, Oryzias latipes [an abstract of entire text]
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Exploring the landscape of ectodomain shedding by quantitative protein terminomics
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Structural insights into tetraspanin CD9 function
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Study on serological diagnostic assays for Crimean-Congo hemorrhagic fever
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A novel variant fibrinogen, AαE11del, demonstrating the importance of AαE11 residue in thrombin binding
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Genetic basis of female-limited polymorphism of the damselfly Ischnura senegalensis
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Functional studies of the egg cortical alveolus proteases on fertilization of medaka
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STUDY ON SEAWEED CHLOROPHYLLS AND LIPIDS : DISTRIBUTION, BIOAVAILABILITY, AND FUNCTIONALITY [an abstract of entire text]
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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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Studies on the prevention of influenza by vitamin D metabolite and vaccine in mice
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Paraneoplastic isolated adrenocorticotropic hormone deficiency revealed after immune checkpoint inhibitors therapy: new insights into anti-corticotroph antibody
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Genetic and Physiological Characterization of Tomato F-box Gene HAWAIIAN SKIRT Mutants
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Relationship between gene mutations and clinicopathological features in nonampullary duodenal epithelial tumors
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Azacitidine is a potential therapeutic drug for pyridoxine-refractory female X-linked sideroblastic anemia
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Involvement of Transcription Factor 21 in the Pathogenesis of Fibrosis in Endometriosis
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Study on the role of CtBP2 in pancreatic β cell
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Embryonal erythropoiesis and aging exploit ferroptosis
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PML-RARαはMED1との結合を介して全トランス型レチノイン酸依存性の転写活性化を誘導する
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Isolation of a human SARS-CoV-2 neutralizing antibody from a synthetic phage library and its conversion to fluorescent biosensors
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Studies on the Transport Mechanism and Physiological Roles of a Cargo Protein of Extracellular Membrane Vesicles from Shewanella vesiculosa HM13
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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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Glucose transporter Glut1 controls diffuse invasion phenotype with perineuronal satellitosis in diffuse glioma microenvironment
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硬骨魚類における補体成分C4アイソタイプの機能的多様性
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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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Prophylactic treatment of rapamycin ameliorates naturally developing and episode -induced heterotopic ossification in mice expressing human mutant ACVR1
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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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Large-scale discovery of male reproductive tract-specific genes through analysis of RNA-seq datasets
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Redesigning the enzymatic synthetic pathway of adrenaline to produce non-natural compound, Phenylephrine [an abstract of entire text]
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Severe neurodevelopmental disorder caused by an MEF2C nonsense mutation
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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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Allosteric regulation accompanied by oligomeric state changes of Trypanosoma brucei GMP reductase through cystathionine-β-synthase domain
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Functional analysis of Rab7D small GTPase of Entamoeba histolytica
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The landscape of genetic aberrations in myxofibrosarcoma
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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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Pathological mechanisms in Crohn’s disease via dysbiosis triggered by Paneth cell α-defensin misfolding
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Molecular characterization of Staphylococcus aureus isolated from skin infection