Isolation, Tissue Localization, and Cellular Characterization of Progenitors Derived from Adult Human Salivary Glands

Ayumi Sato, Kenji Okumura, Shirou Matsumoto, +4

Cloning and Stem Cells

Intracellular distribution of the Wilson’s disease gene product (atpase7b) after in vitro and in vivo exogenous expression in hepatocytes from the LEC rat, an animal model of Wilson’s disease

Koji Nagano, Kimitoshi Nakamura, Ken-Ich Urakami, +7

Hepatology

Complete Rescue of Lethal Albino c Mice by Null Mutation of 4-Hydroxyphenylpyruvate Dioxygenase and Induction of Apoptosis of Hepatocytes in These Mice by in VivoRetrieval of the Tyrosine Catabolic Pathway

Fumio Endo, Shuji Kubo, Hisataka Awata, +9

Journal of Biological Chemistry

Complete RescueGeneticsApoptosisLipid PeroxidationCell Death +20

In situ evaluation of podocin in normal and glomerular diseases

Izumi Horinouchi, Hitoshi Nakazato, Tomoyasu Kawano, +7

Kidney International

Glomerular DiseaseGlomerulonephritisRenal FunctionKidney FailureChronic Kidney Disease +5

Mutations in the CLCN5 gene in Japanese patients with familial idiopathic low-molecular-weight proteinuria

Hitoshi Nakazato, Shinzaburo Hattori, Akio Furuse, +6

Kidney International

Mendelian DisorderGenetic DisorderGeneticsInherited Metabolic DiseaseGenetic Epidemiology +8

A Mouse Model of Renal Tubular Injury of Tyrosinemia Type 1

MAO-SEN SUN, Shinzaburo Hattori, Shuji Kubo, +3

Journal of the American Society of Nephrology

GeneticsRenal PathologyRenal InflammationCell DeathDisease Gene Identification +25

Arrhythmia induced by spatiotemporal overexpression of calreticulin in the heart

Kiyoko Hattori, Kimitoshi Nakamura, Yuichiro Hisatomi, +8

Molecular Genetics and Metabolism

Cardiac MuscleSpatiotemporal OverexpressionCardiomyopathyPhysiologyElectrophysiology +5

Developmental changes in carbonic anhydrase II in the rat kidney

Shinnyo Karashima, Shinzaburo Hattori, Tadashi Ushijima, +3

Pediatric Nephrology

Renal FunctionDevelopmental BiologyBiochemistryPhysiologyCarbonic Anhydrase Ii +5

Chloride channel CLCN5 mutations in Japanese children with familial idiopathic low molecular weight proteinuria

Hitoshi Nakazato, Junichiro Yoshimuta, Shinnyo Karashima, +4

Kidney International

Japanese ChildrenGenetic DisorderGeneticsInherited Metabolic DiseaseGenetic Epidemiology +6

Quantitative and qualitative changes of apolipoprotein AI-containing lipoproteins in patients on continuous ambulatory peritoneal dialysis

Takao Ohta, Shinzaburo Hattori, Soroku Nishiyama, +2

Metabolism

HemodialysisUrologyRenal FunctionMedicineDialysis +7