「An extremely rare missense mutation of the androgen receptor gene in a Vietnamese family with complete androgen insensitivity syndrome」の関連論文
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尿管癌を契機にリンチ症候群と診断された1例
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Decreased serum phosphate levels are a useful biomarker to predict occurrence and severity of cytokine release syndrome in chimeric antigen receptor T-cell therapy
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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
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Expansion of gastric intestinal metaplasia with copy number aberrations contributes to field cancerization
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Examination of the body composition of patients with Werner syndrome using bioelectrical impedance analysis
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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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Subtype Distribution and Drug Resistance Patterns Among HIV-1 Strains Prevalent in Makassar, Indonesia
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Genomics-based discrimination of 2n gamete formation mechanisms in polyploids: a case study in nonaploid Diospyros kaki ‘Akiou’
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Population genetics of variants in infectious diseases and its application to the prediction of variant replacement
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Genomic stability of mouse spermatogonial stem cells in vitro
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Molecular biological and evolutionary analysis of hybrid weakness in Capsicum annuum x Capsicum chinense
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Studies on quantitative assessment of countermeasures during a hepatitis A virus outbreak using renewal equation model
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Characterisation of an Escherichia coli line that completely lacks ribonucleotide reduction yields insights into the evolution of parasitism and endosymbiosis
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Implications of interleukin-17 in psoriatic lesions as Koebner phenomenon caused by recurrent occupational burns
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Analysis of Anti-metabolic Syndrome Effect of Kaempferol in TSOD Mice
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Pluripotent stem cell model of Shwachman-Diamond syndrome reveals apoptotic predisposition of hemoangiogenic progenitors
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Identification of Quantitative Trait Loci (QTL) for Production Traits in Japanese Quail (Coturnix japonica)
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Clinical Significance of Serum Galectin-9 and Soluble CD155 Levels in Patients with Systemic Sclerosis
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Identification and analysis of mechanisms that bypass the essentiality of Polo, a mitotic regulator
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A proof-of-concept study to construct Bayesian network decision models for supporting the categorization of sudden unexpected infant death
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The generation and insights of an inducible diabetes mellitus mouse model based on MafA and MafB double knockout
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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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Case report : Vascular graft infection due to Aspergillus species presenting with recurrent vascular occlusion
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Case report: Severe non-pigmenting fixed drug eruption showing general symptoms caused by chondroitin sulfate sodium
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Progression of Recurrent Pancreatitis to Chronic Pancreatitis within 3 Years due to SPINK1 Mutation IVS3+2T>C
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Downregulation of endothelial nitric oxide synthase (eNOS) and endothelin-1 (ET-1) in a co-culture system with human stimulated X-linked CGD neutrophils
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Downregulation of endothelial nitric oxide synthase (eNOS) and endothelin-1 (ET-1) in a co-culture system with human stimulated X-linked CGD neutrophils
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Screening method for congenital dysfibrinogenemia using clot waveform analysis with the Clauss method
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Tenascin C Aggravates Autoimmune Myocarditis via Dendritic Cell Activation and Th17 Cell Differentiation
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成獣ライディッヒ細胞における性染色体の機能解析
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In silico study of RNA-seq and H3 Trimethylation ChIP-seq analysis in combination with laser-microdissection on human lung cancer cells
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Ovulatory follicle size investigated by ultrasonography and single artificial insemination with ovulation induction in the Japanese macaque (Macaca fuscata)
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Glucose transporter Glut1 controls diffuse invasion phenotype with perineuronal satellitosis in diffuse glioma microenvironment
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精巣高発現タンパク質の精子形成における機能と応用
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Assessment of the association between the polymorphism rs1256031 of the estrogen receptor β gene and GDM susceptibility
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Risk factors and diagnostic biomarkers for nonalcoholic fatty liver disease-associated hepatocellular carcinoma: Current evidence and future perspectives
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Inherent genomic properties underlie the epigenomic heterogeneity of human induced pluripotent stem cells
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TNFRSF11A-Associated Dysosteosclerosis: A Report of the Second Case and Characterization of the Phenotypic Spectrum
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Individual identification of inbred medaka based on characteristic melanophore spot patterns on the head
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Safety comparisons among monoamine oxidase inhibitors against Parkinson’s disease using FDA adverse event reporting system
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Utility of plasma circulating tumor DNA and tumor DNA profiles in head and neck squamous cell carcinoma
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Identification of T cell receptors targeting a neoantigen derived from recurrently mutated FGFR3
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A genome-wide association study identifying single nucleotide polymorphisms in the PPFIBP2 gene was predictive for interstitial lung disease in rheumatoid arthritis patients
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Postoperative supraventricular tachycardia and polymorphic ventricular tachycardia due to a novel SCN5A variant: a case report of a rare comorbidity that is difficult to diagnose.
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Dysmenorrhea due to undiagnosed obstructed hemi-vagina and ipsilateral renal anomaly syndrome can become a cause of suicide.
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Lionheart LincRNA alleviates cardiac systolic dysfunction under pressure overload
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Expression of urokinase-type plasminogen activator system in non-metastatic prostate cancer
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Gender difference in the transabdominal ultrasound findings of solid-pseudopapillary neoplasm
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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