「Ribosomal DNA gene copies are increased in blood and brain of Japanese schizophrenia patients」の関連論文
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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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Iinfluence of plasma cytokine levels on the conversion risk from MCI to dementia in the Alzheimer's disease neuroimaging initiative database
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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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Landscape of driver mutations and their clinical impacts in pediatric B-cell precursor acute lymphoblastic leukemia
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Gut bacteria identified in colorectal cancer patients promote tumourigenesis via butyrate secretion
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A novel urinary microRNA biomarker panel for detecting gastric cancer
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Cross-ancestry genome-wide analysis of atrial fibrillation unveils disease biology and enables cardioembolic risk prediction
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A proteome signature of umbilical cord serum associated with congenital diaphragmatic hernia
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Behavior problems and dysfunctional parenting : Cross-sectional study in Japan.
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Analysis of aging-related epigenetic modifications in murine male germline cells
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Association of two variable number of tandem repeats in the monoamine oxidase A gene promoter with suicide completion: The present study and meta-analysis
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Hereditary Congenital Methemoglobinemia Diagnosed at the Age of 79 Years: A Case Report
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Factors Associated With Prediabetes and Diabetes Among Public Employees in Northern Ethiopia
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Sex-specific regional grey matter volume correlates of daily activities
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Establishment of induced pluripotent stem cells from schizophrenia discordant fraternal twins
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Factors causing a relapse of major depressive disorders following successful electroconvulsive therapy : A retrospective cohort study
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Structural brain changes in severe and enduring anorexia nervosa: A multimodal magnetic resonance imaging study of gray matter volume, cortical thickness, and white matter integrity
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Real-life progression of the use of a genetic panel in to diagnose neonatal cholestasis
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Urinary MicroRNA-Based Diagnostic Model for Central Nervous System Tumors Using Nanowire Scaffolds
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Constitutive activation of mTORC1 signaling induced by biallelic loss-of-function mutations in SZT2 underlies a discernible neurodevelopmental disease
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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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FKRP mutations cause congenital muscular dystrophy 1C and limb-girdle muscular dystrophy 2I in Asian patients
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Statin Use Influence on the Occurrence of Acute Kidney Injury in Patients with Peripheral Arterial Disease
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Oral carriage of Streptococcus mutans harboring the cnm gene relates to an increased incidence of cerebral microbleeds (本文)
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The association of thyroglobulin single nucleotide polymorphism with miniature dachshunds-specific inflammatory colorectal polyps and its involvement in interleukin-6 amplifier induced chronic inflammation
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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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A large-scale targeted proteomics of plasma extracellular vesicles shows utility for prognosis prediction subtyping in colorectal cancer
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Instability of speech in Parkinson disease patients with subthalamic nucleus deep brain stimulation
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Genomic analysis for the prediction of prognosis in small-bowel cancer
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Genomic analysis for the prediction of prognosis in small-bowel cancer
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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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Circulating plasmablasts and follicular helper T-cell subsets are associated with antibody-positive autoimmune epilepsy
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Combination of RERG and ZNF671 methylation rates in circulating cell-free DNA: A novel biomarker for screening of nasopharyngeal carcinoma
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Tumor Shrinkage by Metyrapone in Cushing Disease Exhibiting Glucocorticoid-Induced Positive Feedback
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Cutaneous T-cell-attracting chemokine as a novel biomarker for predicting prognosis of idiopathic pulmonary fibrosis: a prospective observational study
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Study on the incidence of interventions for diabetic retinopathy and serious lower-limb complications and its related factors in patients with diabetes using real-world large claims database
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Increased blood group 2 innate lymphoid cells are associated with the clinical severity of Kimura disease.
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Gender difference in the transabdominal ultrasound findings of solid-pseudopapillary neoplasm
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Mucosa-associated gut microbiome in Japanese patients with functional constipation.
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The association between chronic deciduitis and preeclampsia.
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EYS is a major gene involved in retinitis pigmentosa in Japan: Genetic landscapes revealed by stepwise genetic screening.
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Examination of the prefrontal cortex hemodynamic responses to the Fist-Edge-Palm task in naïve subjects using functional Near-Infrared Spectroscopy
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Resting Heart Rate Variability Is Associated With Subsequent Orthostatic Hypotension: Comparison Between Healthy Older People and Patients With Rapid Eye Movement Sleep Behavior Disorder.
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PCR-Based Screening of Spinal Muscular Atrophy for Newborn Infants in Hyogo Prefecture, Japan
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Testosterone deficiency syndrome among males with type 2 diabetes mellitus in East Malaysia
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Evolutionary genetics of socioemotional behavior in humans and other mammals
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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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The relationship between DRD2 Taq1A polymorphism and white matter structure in healthy young adults.
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Safety comparisons among monoamine oxidase inhibitors against Parkinson’s disease using FDA adverse event reporting system
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Autoantibodies against the plakin family proteins as a novel marker for chronic graft-versus-host disease of the lung