「FKRP mutations cause congenital muscular dystrophy 1C and limb-girdle muscular dystrophy 2I in Asian patients」の関連論文
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Ribosomal DNA gene copies are increased in blood and brain of Japanese schizophrenia patients
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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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Studies on quantitative assessment of countermeasures during a hepatitis A virus outbreak using renewal equation model
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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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Primary functional brain connections associated with melancholic major depressive disorder and modulation by antidepressants
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Primary functional brain connections associated with melancholic major depressive disorder and modulation by antidepressants
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Multidisciplinary diagnostic approach for fulminant myocarditis related to coronavirus disease 2019 messenger RNA vaccines: a case report
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Complete resection and untethering of the cervical and thoracic spinal dermal sinus tracts in adult patients
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Analysis of Anti-metabolic Syndrome Effect of Kaempferol in TSOD Mice
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Tumour-immune microenvironment in duodenal-type follicular lymphoma
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Association of usual sleep quality and glycemic control in type 2 diabetes in Japanese: a cross sectional study. Sleep and Food Registry in Kanagawa(SOREKA)
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Efficacy of endoscopic cricopharyngeal myotomy using a curved rigid laryngoscope in patients with sporadic inclusion body myositis: four retrospective case reviews
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A mixed methods study on health-seeking behaviors in a malaria endemic district in Lao People's Democratic Republic
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Molecular epidemiology of Enterobacter cloacae complex isolates with reduced carbapenem susceptibility recovered by blood culture
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Consumption of coffee and antioxidant vitamins and risk of lung cancer in Japan
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Timing of therapeutic interventions against infection-triggered encephalopathy syndrome: a scoping review of the pediatric literature
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Reasons for Undergoing CT During Childhood : Can CT-Exposed and CT-Naïve Populations Be Compared?
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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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Two effects of GATA2 enhancer repositioning by 3q chromosomal rearrangements.
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Testosterone deficiency syndrome among males with type 2 diabetes mellitus in East Malaysia
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食習慣や代謝疾患に関連したインドネシア人の腸内マイクロバイオームおよびメタボロームについての研究
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Implications of interleukin-17 in psoriatic lesions as Koebner phenomenon caused by recurrent occupational burns
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Is Generalized and Segmental Dystonia Accompanied by Impairments in the Dopaminergic System?
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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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Disease modeling of pulmonary fibrosis using human pluripotent stem cell-derived alveolar organoids
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HSP47 levels determine the degree of body adiposity
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Development of Remote Inflammation through Interneuron Network in the Spinal Cord
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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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Pediatric Respiratory Virus Infections During the COVID-19 Pandemic in a Region Without Active Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Circulation
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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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A prospective cohort study of the association between the Apgar score and developmental status at 3 years of age: the Japan Environment and Children’s Study (JECS)
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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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Generation of two human induced pluripotent stem cell lines derived from two X-linked adrenoleukodystrophy patients with ABCD1 mutations
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Effect of Avoiding Cow's Milk Formula at Birth on Prevention of Asthma or Recurrent Wheeze Among Young Children: Extended Follow-up From the ABC Randomized Clinical Trial
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Immunohistochemically Detected Expression of ATRX, TSC2, and PTEN Predicts Clinical Outcomes in Patients With Grade 1 and 2 Pancreatic Neuroendocrine Tumors
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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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Associations of pulmonary and extrapulmonary computed tomographic manifestations with impaired physical activity in symptomatic patients with chronic obstructive pulmonary disease
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Association of Socio-Demographic and Climatic Factors with the Duration of Hospital Stay of Under-Five Children with Severe Pneumonia in Urban Bangladesh: An Observational Study.
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Association of Socio-Demographic and Climatic Factors with the Duration of Hospital Stay of Under-Five Children with Severe Pneumonia in Urban Bangladesh: An Observational Study.
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Study on the control of high pathogenicity and low pathogenicity avian influenza in Vietnam [an abstract of entire text]
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Repurposing bromocriptine for Aβ metabolism in Alzheimer’s disease (REBRAnD) study: randomised placebo-controlled double-blind comparative trial and open-label extension trial to investigate the safety and efficacy of bromocriptine in Alzheimer’s disease with presenilin 1 (PSEN1) mutations
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The impact of diabetic polyneuropathy on toe grip strength in patients with type 2 diabetes mellitus: a cross-sectional study
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Pulmonary syphilis with a cicatricial variant of organizing pneumonia: a case report
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Interventions to improve locomotive syndrome: a systematic review and meta-analysis of randomized controlled trials
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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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The Immunology of Takotsubo Syndrome
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The relationship between DRD2 Taq1A polymorphism and white matter structure in healthy young adults.
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Underestimation of Trisomy 18 and 13 Syndromes in Vital Statistics from Inadequate Death Certificates.
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Overdispersion of SARS-CoV-2 transmission in Japan: Demographic characteristics and temporal change
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iPSC-derived type IV collagen α5-expressing kidney organoids model Alport syndrome