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A Review of Pharmacological Strategy for Cognitive Deficits in Schizophrenia

Jeon DW, Jung DU, Kong BG, Kang JW, Moon JJ, Shim JC

Cognitive deficit is frequently observed in patients with schizophrenia. It is significantly associated with functional outcome. In the past 20 years, due to significant advances on the concept of schizophrenia,...
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Effect of K+-channel blockers on the muscarinic- and A|1-adenosine-receptor coupled regulation of electrically evoked acetylcholine release in the rat hippocampus

Yu BS, Kim DK, Choi BK

  • KMID: 1562314
  • Korean J Physiol Pharmacol.
  • 1998 Apr;2(2):147-154.
It was attempted to clarify the participation of K+ channels in the post-receptor mechanisms of the muscarinic and A1-adenosine receptor-mediated control of acetylcholine (ACh) release in the present study. Slices from the rat...
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Regulation of Gastric Electrical and Mechanical Activity by Cholinesterases in Mice

Worth AA, Forrest AS, Peri LE, Ward SM, Hennig GW, Sanders KM

  • KMID: 2381252
  • J Neurogastroenterol Motil.
  • 2015 Apr;21(2):200-216.
  • doi: 10.5056/jnm14120
BACKGROUND/AIMS: Gastric peristalsis begins in the orad corpus and propagates to the pylorus. Directionality of peristalsis depends upon orderly generation and propagation of electrical slow waves and a frequency gradient...
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Malakoplakia in a healthy young female patient

Hyun KH, Shin HD, Kim DH

Malakoplakia is a rare granulomatous disease that occurs commonly in the urinary tract and secondarily in the gastrointestinal tract. Most reported cases of malakoplakia are associated with immunosuppressive diseases or...
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Expression of Ca2+-dependent Synaptotagmin Isoforms in Mouse and Rat Parotid Acinar Cells

Jo H, Byun HM, Kim JH, Kim MS, Kim SH, Hong JH, Seo JT, Lee SI, Shin DM, Son HK

Synaptotagmin is a Ca2+ sensing protein, which triggers a fusion of synaptic vesicles in neuronal transmission. Little is known regarding the expression of Ca2+ - dependent synaptotagmin isoforms and their...
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Cystic Fibrosis in Korean Children: A Case Report Identified by a Quantitative Pilocarpine Iontophoresis Sweat Test and Genetic Analysis

Ahn KM, Park HY, Lee JH, Lee MG, Kim JH, Kang IJ, Lee SI

Cystic fibrosis (CF) is inherited as an autosomal recessive trait, and the mutations in cystic fibrosis transmembrane conductance regulator (CFTR) gene contributes to the CF syndrome. Although CF is common...
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