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F Endo

Showing results (91-100 of 197) with videos related to

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Endocrinology|August 1, 1983
Insulin-induced receptor loss reduces responsiveness of chick heart cells to insulinJ C Serravezza, F Endo, R L DeHaan, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Mutation of the E1 alpha subunit of the pyruvate dehydrogenase complex, in relation to heterogeneityA Kitano, F Endo, I Matsuda, et al.
Journal of Pediatric Surgery|July 7, 1999
Surgical indications for patients with hyperammonemiaS Ikeda, Y Sera, H Ohshiro, et al.
The Journal of Clinical Investigation|May 1, 1993
Carbamyl phosphate synthetase I deficiency. One base substitution in an exon of the CPS I gene causes a 9-basepair deletion due to aberrant splicingR Hoshide, T Matsuura, Y Haraguchi, et al.
Veterinary Microbiology|February 14, 1998
The effect of Bcg gene on antigen presentation of spleen adherent cells and peritoneal macrophages from Mycobacterium bovis BCG-infected Bcg(s) and Bcg(r) miceD L Xu, Y Goto, F Endo, et al.
Advances in Experimental Medicine and Biology|January 1, 1982
Ornithine transcarbamylase (OTC) in white blood cells and jejunal mucosaN Nagata, I Akaboshi, J Yamamoto, et al.
Tanpakushitsu Kakusan Koso. Protein, Nucleic Acid, Enzyme|December 1, 1995
[Gene therapy for ornithine transcarbamylase deficiency]I Matsuda, K Kiwaki, S Komaki, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Maple syrup urine disease: clinical and biochemical significance of gene analysisY Nobukuni, H Mitsubuchi, I Akaboshi, et al.
The Japanese Journal of Human Genetics|December 1, 1992
Sex-determining region Y (SRY) in a patient with 46,XX true hermaphroditismA Tanoue, T Nakamura, F Endo, et al.
Archives of Dermatology|November 1, 1981
Autosomal recessive prolidase deficiency. Three patients with recalcitrant ulcersA Ogata, S Tanaka, T Tomoda, et al.
Pageof 20

Showing results (91-100 of 197) with videos related to

Sort By:
Pageof 20
Endocrinology|August 1, 1983
Insulin-induced receptor loss reduces responsiveness of chick heart cells to insulinJ C Serravezza, F Endo, R L DeHaan, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Mutation of the E1 alpha subunit of the pyruvate dehydrogenase complex, in relation to heterogeneityA Kitano, F Endo, I Matsuda, et al.
Journal of Pediatric Surgery|July 7, 1999
Surgical indications for patients with hyperammonemiaS Ikeda, Y Sera, H Ohshiro, et al.
The Journal of Clinical Investigation|May 1, 1993
Carbamyl phosphate synthetase I deficiency. One base substitution in an exon of the CPS I gene causes a 9-basepair deletion due to aberrant splicingR Hoshide, T Matsuura, Y Haraguchi, et al.
Veterinary Microbiology|February 14, 1998
The effect of Bcg gene on antigen presentation of spleen adherent cells and peritoneal macrophages from Mycobacterium bovis BCG-infected Bcg(s) and Bcg(r) miceD L Xu, Y Goto, F Endo, et al.
Advances in Experimental Medicine and Biology|January 1, 1982
Ornithine transcarbamylase (OTC) in white blood cells and jejunal mucosaN Nagata, I Akaboshi, J Yamamoto, et al.
Tanpakushitsu Kakusan Koso. Protein, Nucleic Acid, Enzyme|December 1, 1995
[Gene therapy for ornithine transcarbamylase deficiency]I Matsuda, K Kiwaki, S Komaki, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Maple syrup urine disease: clinical and biochemical significance of gene analysisY Nobukuni, H Mitsubuchi, I Akaboshi, et al.
The Japanese Journal of Human Genetics|December 1, 1992
Sex-determining region Y (SRY) in a patient with 46,XX true hermaphroditismA Tanoue, T Nakamura, F Endo, et al.
Archives of Dermatology|November 1, 1981
Autosomal recessive prolidase deficiency. Three patients with recalcitrant ulcersA Ogata, S Tanaka, T Tomoda, et al.
Pageof 20