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 (1-10 of 51) with videos related to

Pageof 6
Sort By:
Human Mutation|December 19, 2001
Molecular basis of congenital insensitivity to pain with anhidrosis (CIPA): mutations and polymorphisms in TRKA (NTRK1) gene encoding the receptor tyrosine kinase for nerve growth factorY Indo
Clinical Genetics|August 14, 2012
Nerve growth factor and the physiology of pain: lessons from congenital insensitivity to pain with anhidrosisY Indo
Ryoikibetsu Shokogun Shirizu|May 20, 1998
[Maple syrup urine disease]Y Indo, I Matsuda
Nihon Rinsho. Japanese Journal of Clinical Medicine|December 1, 1992
[Recent progress in molecular biology of inherited tubular transport abnormalities]Y Indo, I Matsuda
Progress in Clinical and Biological Research|January 1, 1992
Evolution of the acyl-CoA dehydrogenase/oxidase superfamilyK Tanaka, Y Indo
The Journal of Clinical Investigation|May 1, 1990
Identification of two variant short chain acyl-coenzyme A dehydrogenase alleles, each containing a different point mutation in a patient with short chain acyl-coenzyme A dehydrogenase deficiencyE Naito, Y Indo, K Tanaka
The Journal of Clinical Investigation|November 1, 1989
Short chain acyl-coenzyme A dehydrogenase (SCAD) deficiency. Immunochemical demonstration of molecular heterogeneity due to variant SCAD with differing stabilityE Naito, Y Indo, K Tanaka
Progress in Clinical and Biological Research|January 1, 1992
Molecular characterization of variant alpha-subunit of electron transfer flavoprotein in three patients with glutaric acidemia type II, and identification of glycine substitution for valine 157, producing an unstable mature protein in a patientY Indo, R Glassberg, I Yokota, et al.
Pediatric Research|December 1, 1987
Immunochemical studies of human prolidase with monoclonal and polyclonal antibodies: absence of the subunit of prolidase in erythrocytes from a patient with prolidase deficiencyF Endo, K Motohara, Y Indo, et al.
American Journal of Human Genetics|September 1, 1991
Molecular characterization of variant alpha-subunit of electron transfer flavoprotein in three patients with glutaric acidemia type II--and identification of glycine substitution for valine-157 in the sequence of the precursor, producing an unstable mature protein in a patientY Indo, R Glassberg, I Yokota, et al.
Pageof 6

Showing results (1-10 of 51) with videos related to

Sort By:
Pageof 6
Human Mutation|December 19, 2001
Molecular basis of congenital insensitivity to pain with anhidrosis (CIPA): mutations and polymorphisms in TRKA (NTRK1) gene encoding the receptor tyrosine kinase for nerve growth factorY Indo
Clinical Genetics|August 14, 2012
Nerve growth factor and the physiology of pain: lessons from congenital insensitivity to pain with anhidrosisY Indo
Ryoikibetsu Shokogun Shirizu|May 20, 1998
[Maple syrup urine disease]Y Indo, I Matsuda
Nihon Rinsho. Japanese Journal of Clinical Medicine|December 1, 1992
[Recent progress in molecular biology of inherited tubular transport abnormalities]Y Indo, I Matsuda
Progress in Clinical and Biological Research|January 1, 1992
Evolution of the acyl-CoA dehydrogenase/oxidase superfamilyK Tanaka, Y Indo
The Journal of Clinical Investigation|May 1, 1990
Identification of two variant short chain acyl-coenzyme A dehydrogenase alleles, each containing a different point mutation in a patient with short chain acyl-coenzyme A dehydrogenase deficiencyE Naito, Y Indo, K Tanaka
The Journal of Clinical Investigation|November 1, 1989
Short chain acyl-coenzyme A dehydrogenase (SCAD) deficiency. Immunochemical demonstration of molecular heterogeneity due to variant SCAD with differing stabilityE Naito, Y Indo, K Tanaka
Progress in Clinical and Biological Research|January 1, 1992
Molecular characterization of variant alpha-subunit of electron transfer flavoprotein in three patients with glutaric acidemia type II, and identification of glycine substitution for valine 157, producing an unstable mature protein in a patientY Indo, R Glassberg, I Yokota, et al.
Pediatric Research|December 1, 1987
Immunochemical studies of human prolidase with monoclonal and polyclonal antibodies: absence of the subunit of prolidase in erythrocytes from a patient with prolidase deficiencyF Endo, K Motohara, Y Indo, et al.
American Journal of Human Genetics|September 1, 1991
Molecular characterization of variant alpha-subunit of electron transfer flavoprotein in three patients with glutaric acidemia type II--and identification of glycine substitution for valine-157 in the sequence of the precursor, producing an unstable mature protein in a patientY Indo, R Glassberg, I Yokota, et al.
Pageof 6