Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Y Indo

Showing results (21-30 of 51) with videos related to

Pageof 6
Sort By:
Journal of Inherited Metabolic Disease|January 1, 1987
Immunochemical analysis of prolidase deficiency and molecular cloning of cDNA for prolidase of human liverF Endo, A Hata, Y Indo, et al.
Human Molecular Genetics|February 13, 2001
Congenital insensitivity to pain with anhidrosis (CIPA): effect of TRKA (NTRK1) missense mutations on autophosphorylation of the receptor tyrosine kinase for nerve growth factorS Mardy, Y Miura, F Endo, et al.
Pediatric Research|September 1, 1991
Immunochemical characterization of variant long-chain acyl-CoA dehydrogenase in cultured fibroblasts from nine patients with long-chain acyl-CoA dehydrogenase deficiencyY Indo, P M Coates, D E Hale, et al.
Pediatric Research|July 1, 1993
Identification of very-long-chain acyl-CoA dehydrogenase deficiency in three patients previously diagnosed with long-chain acyl-CoA dehydrogenase deficiencyS Yamaguchi, Y Indo, P M Coates, et al.
The Japanese Journal of Human Genetics|June 1, 1997
Structure and organization of the human TRKA gene encoding a high affinity receptor for nerve growth factorY Indo, S Mardy, M Tsuruta, et al.
Pediatric Research|January 1, 1992
Immunochemical characterization of variant medium-chain acyl-CoA dehydrogenase in fibroblasts from patients with medium-chain acyl-CoA dehydrogenase deficiencyP M Coates, Y Indo, D Young, 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.
No to Shinkei = Brain and Nerve|October 6, 1997
[Basal encephalomeningocele that occurred in adulthood: a case report]T Kato, Y Iwasaki, E Yoshida, et al.
The Journal of Clinical Investigation|April 1, 1991
Maple syrup urine disease caused by a partial deletion in the inner E2 core domain of the branched chain alpha-keto acid dehydrogenase complex due to aberrant splicing. A single base deletion at a 5'-splice donor site of an intron of the E2 gene disrupts the consensus sequence in this regionH Mitsubuchi, Y Nobukuni, I Akaboshi, et al.
Journal of Pediatric Gastroenterology and Nutrition|April 1, 1985
Effects of dietary zinc deficiency on hepatic ornithine carbamoyltransferase and alcohol dehydrogenase activities in ratsY Indo, N Nagata, A Higashi, et al.
Pageof 6

Showing results (21-30 of 51) with videos related to

Sort By:
Pageof 6
Journal of Inherited Metabolic Disease|January 1, 1987
Immunochemical analysis of prolidase deficiency and molecular cloning of cDNA for prolidase of human liverF Endo, A Hata, Y Indo, et al.
Human Molecular Genetics|February 13, 2001
Congenital insensitivity to pain with anhidrosis (CIPA): effect of TRKA (NTRK1) missense mutations on autophosphorylation of the receptor tyrosine kinase for nerve growth factorS Mardy, Y Miura, F Endo, et al.
Pediatric Research|September 1, 1991
Immunochemical characterization of variant long-chain acyl-CoA dehydrogenase in cultured fibroblasts from nine patients with long-chain acyl-CoA dehydrogenase deficiencyY Indo, P M Coates, D E Hale, et al.
Pediatric Research|July 1, 1993
Identification of very-long-chain acyl-CoA dehydrogenase deficiency in three patients previously diagnosed with long-chain acyl-CoA dehydrogenase deficiencyS Yamaguchi, Y Indo, P M Coates, et al.
The Japanese Journal of Human Genetics|June 1, 1997
Structure and organization of the human TRKA gene encoding a high affinity receptor for nerve growth factorY Indo, S Mardy, M Tsuruta, et al.
Pediatric Research|January 1, 1992
Immunochemical characterization of variant medium-chain acyl-CoA dehydrogenase in fibroblasts from patients with medium-chain acyl-CoA dehydrogenase deficiencyP M Coates, Y Indo, D Young, 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.
No to Shinkei = Brain and Nerve|October 6, 1997
[Basal encephalomeningocele that occurred in adulthood: a case report]T Kato, Y Iwasaki, E Yoshida, et al.
The Journal of Clinical Investigation|April 1, 1991
Maple syrup urine disease caused by a partial deletion in the inner E2 core domain of the branched chain alpha-keto acid dehydrogenase complex due to aberrant splicing. A single base deletion at a 5'-splice donor site of an intron of the E2 gene disrupts the consensus sequence in this regionH Mitsubuchi, Y Nobukuni, I Akaboshi, et al.
Journal of Pediatric Gastroenterology and Nutrition|April 1, 1985
Effects of dietary zinc deficiency on hepatic ornithine carbamoyltransferase and alcohol dehydrogenase activities in ratsY Indo, N Nagata, A Higashi, et al.
Pageof 6