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The American Journal of Physiology|March 1, 1991
Several cation transporters and volume regulation in high-K dog red blood cellsH Fujise, I Yamada, M Masuda, et al.Cell Growth & Differentiation : the Molecular Biology Journal of the American Association for Cancer Research|March 1, 1990
A ubiquitous repressor interacting with an F9 cell-specific silencer and its functional suppression by differentiated cell-specific positive factorsK Furukawa, Y Yamaguchi, E Ogawa, et al.Journal of Cardiothoracic and Vascular Anesthesia|August 4, 2006
Platelet dysfunction during cardiopulmonary bypass assessed by a novel whole-blood aggregometerYoshifumi Kotake, Naomi E Ogawa, Nobuyuki Katori, et al.The American Journal of Pathology|September 15, 1998
Correlation of reduction in MRP-1/CD9 and KAI1/CD82 expression with recurrences in breast cancer patientsC I Huang, N Kohno, E Ogawa, et al.Journal of Human Genetics|September 25, 1999
Molecular analysis of Japanese patients with steroid 21-hydroxylase deficiencyA Asanuma, T Ohura, E Ogawa, et al.Human Genetics|December 6, 2001
A novel intronic mutation of the TAZ ( G4.5) gene in a patient with Barth syndrome: creation of a 5' splice donor site with variant GC consensus and elongation of the upstream exonO Sakamoto, T Ohura, Y Katsushima, et al.Pediatric Research|October 25, 2000
Mutation analysis of the GLUT2 gene in patients with Fanconi-Bickel syndromeO Sakamoto, E Ogawa, T Ohura, et al.Fukuoka Shika Daigaku Gakkai Zasshi|January 1, 1989
[Clinical observation following the use of neotriozinc pasta as root canal filling pasta]Y Haraga, A Ueno, M Miyake, et al.European Journal of Neurology|May 28, 2009
Cutaneous accumulation of abnormal polyglutamine proteins of patients with dentatorubral-pallidoluysian atrophyM Ohta, R Okuyama, E Ogawa, et al.Journal of Human Genetics|October 24, 2000
Novel mutation of L718X in the ATP7A gene in a Japanese patient with classical Menkes disease, and four novel polymorphisms in the Japanese populationA Ogawa, S Yamamoto, M Kanazawa, et al.Pageof 9