Browsing "1. Journal Papers" by Issue Date :

Jump to a point in the index:
  • Sort by:
  • In order:
  • Results/Page
  • Authors/Record:

Showing results 101 to 120 of 663

This table browses all dspace content
Issue DateTitleJournal Title
2017Concise Review: Fate Determination of Stem Cells by Deubiquitinating EnzymesSTEM CELLS
2017Genetic Predisposition to Sporadic Congenital Hearing Loss in a Pediatric Population SCIENTIFIC REPORTS
2017A Review of Modeling Approaches to Predict Drug Response in Clinical Oncology YONSEI MEDICAL JOURNAL
2017Quantitative Assessment of Food Effect on the Pharmacokinetics of Nano-Crystallized Megestrol AcetateBASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY
2017UDP-Induced Phagocytosis and ATP-Stimulated Chemotactic Migration Are Impaired in STIM1-/- Microglia In Vitro and In Vivo MEDIATORS OF INFLAMMATION
2017Sec16A is critical for both conventional and unconventional secretion of CFTR SCIENTIFIC REPORTS
2017Targeted Next-Generation Sequencing for Comprehensive Genetic Profiling of PharmacogenesCLINICAL PHARMACOLOGY & THERAPEUTICS
2017Relationships between Psychosocial Difficulties and Oxidative Stress Biomarkers in Women Subject to Intimate Partner ViolenceHEALTH & SOCIAL WORK
2017Adult-Onset Vitelliform Macular Dystrophy caused by BEST1 p.Ile38Ser Mutation is a Mild Form of Best Vitelliform Macular Dystrophy SCIENTIFIC REPORTS
2017Oxytocin receptor gene polymorphisms exert a modulating effect on the onset age in patients with obsessive-compulsive disorderPSYCHONEUROENDOCRINOLOGY
2017Glutamatergic stimulation of the left dentate gyrus abolishes depressive-like behaviors in a rat learned helplessness paradigmNEUROIMAGE
2017MPSR1 is a cytoplasmic PQC E3 ligase for eliminating emergent misfolded proteins in Arabidopsis thaliana PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
2017Changes in brain metabolic connectivity underlie autistic-like social deficits in a rat model of autism spectrum disorder SCIENTIFIC REPORTS
2017Accuracy of Next-Generation Sequencing for Molecular Diagnosis in Patients With Infantile Nystagmus SyndromeJAMA OPHTHALMOLOGY
2017Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly NATURE GENETICS
2017Mutations in DZIP1L, which encodes a ciliary-transition-zone protein, cause autosomal recessive polycystic kidney disease NATURE GENETICS
2017Genetics of vesicoureteral reflux and congenital anomalies of the kidney and urinary tract INVESTIGATIVE AND CLINICAL UROLOGY
2017RanBPM: a potential therapeutic target for modulating diverse physiological disordersDRUG DISCOVERY TODAY
2017Sustained Mutant KIT Activation in the Golgi Complex Is Mediated by PKC-θ in Gastrointestinal Stromal TumorsCLINICAL CANCER RESEARCH
2017Chronological Change of Right Ventricle by Chronic Intermittent Hypoxia in MiceSLEEP

Browse

Links