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Fujiki

Showing results (891-900 of 2,384) with videos related to

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European Heart Journal|August 16, 2003
Proportion and prognosis of healthy people with coved or saddle-back type ST segment elevation in the right precordial leads during 10 years follow-upMasao Sakabe, Akira Fujiki, Masanao Tani, et al.
Carcinogenesis|December 1, 1992
Hyperphosphorylation of cytokeratins 8 and 18 by microcystin-LR, a new liver tumor promoter, in primary cultured rat hepatocytesT Ohta, R Nishiwaki, J Yatsunami, et al.
Carcinogenesis|September 1, 1988
A radioimmunoassay for the teleocidins using 26 (2'-aminoethylthio)-tetrahydroteleocidin A-2 as haptenL Levine, H Fujiki, S Sakai, et al.
The Japanese Journal of Psychiatry and Neurology|June 1, 1987
Neuro-Behçet disease and magnetic resonance imagingK Tashiro, N Fujiki, F Moriwaka, et al.
Molecular and Cellular Biology|January 1, 1989
Peroxisome targeting signal of rat liver acyl-coenzyme A oxidase resides at the carboxy terminusS Miyazawa, T Osumi, T Hashimoto, et al.
The Japanese Journal of Thoracic and Cardiovascular Surgery : Official Publication of the Japanese Association for Thoracic Surgery = Nihon Kyobu Geka Gakkai Zasshi|March 26, 1998
[Two cases of surgical treatment of recrudescent Stanford type A dissection after early thrombogenic closure without intimal tear]H Ide, M Sato, T Fujiki, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1986
Presence of the peroxisomal 22-kDa integral membrane protein in the liver of a person lacking recognizable peroxisomes (Zellweger syndrome)P B Lazarow, Y Fujiki, G M Small, et al.
Japanese Circulation Journal|December 30, 1999
Electrophysiological mechanisms of conversion of typical to atypical atrioventricular nodal reentrant tachycardia occurring after radiofrequency catheter ablation of the slow pathwayA Fujiki, M Usui, K Mizumaki, et al.
American Journal of Human Genetics|September 1, 2000
PEX3 is the causal gene responsible for peroxisome membrane assembly-defective Zellweger syndrome of complementation group GK Ghaedi, M Honsho, N Shimozawa, et al.
European Journal of Immunology|March 31, 2000
Molecular cloning and protein analysis of divergent forms of the complement component C3 from a bony fish, the common carp (Cyprinus carpio): presence of variants lacking the catalytic histidineM Nakao, J Mutsuro, R Obo, et al.
Pageof 239

Showing results (891-900 of 2,384) with videos related to

Sort By:
Pageof 239
European Heart Journal|August 16, 2003
Proportion and prognosis of healthy people with coved or saddle-back type ST segment elevation in the right precordial leads during 10 years follow-upMasao Sakabe, Akira Fujiki, Masanao Tani, et al.
Carcinogenesis|December 1, 1992
Hyperphosphorylation of cytokeratins 8 and 18 by microcystin-LR, a new liver tumor promoter, in primary cultured rat hepatocytesT Ohta, R Nishiwaki, J Yatsunami, et al.
Carcinogenesis|September 1, 1988
A radioimmunoassay for the teleocidins using 26 (2'-aminoethylthio)-tetrahydroteleocidin A-2 as haptenL Levine, H Fujiki, S Sakai, et al.
The Japanese Journal of Psychiatry and Neurology|June 1, 1987
Neuro-Behçet disease and magnetic resonance imagingK Tashiro, N Fujiki, F Moriwaka, et al.
Molecular and Cellular Biology|January 1, 1989
Peroxisome targeting signal of rat liver acyl-coenzyme A oxidase resides at the carboxy terminusS Miyazawa, T Osumi, T Hashimoto, et al.
The Japanese Journal of Thoracic and Cardiovascular Surgery : Official Publication of the Japanese Association for Thoracic Surgery = Nihon Kyobu Geka Gakkai Zasshi|March 26, 1998
[Two cases of surgical treatment of recrudescent Stanford type A dissection after early thrombogenic closure without intimal tear]H Ide, M Sato, T Fujiki, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1986
Presence of the peroxisomal 22-kDa integral membrane protein in the liver of a person lacking recognizable peroxisomes (Zellweger syndrome)P B Lazarow, Y Fujiki, G M Small, et al.
Japanese Circulation Journal|December 30, 1999
Electrophysiological mechanisms of conversion of typical to atypical atrioventricular nodal reentrant tachycardia occurring after radiofrequency catheter ablation of the slow pathwayA Fujiki, M Usui, K Mizumaki, et al.
American Journal of Human Genetics|September 1, 2000
PEX3 is the causal gene responsible for peroxisome membrane assembly-defective Zellweger syndrome of complementation group GK Ghaedi, M Honsho, N Shimozawa, et al.
European Journal of Immunology|March 31, 2000
Molecular cloning and protein analysis of divergent forms of the complement component C3 from a bony fish, the common carp (Cyprinus carpio): presence of variants lacking the catalytic histidineM Nakao, J Mutsuro, R Obo, et al.
Pageof 239