Y Matsubara|K Narisawa|K Tada - JoVE Visualize

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European Journal of Pediatrics|March 1, 1992

Medium-chain acyl-CoA dehydrogenase deficiency: molecular aspectsY Matsubara, K Narisawa, K Tada

Acta Paediatrica Japonica : Overseas Edition|June 1, 1994

Rapid detection of phenylketonuria mutations by non-radioactive single-strand conformation polymorphism analysisY Yao, Y Matsubara, K Narisawa

Journal of Human Genetics|June 11, 1998

A one-base deletion (183delC) and a missense mutation (D276H) in the T-protein gene from a Japanese family with nonketotic hyperglycinemiaS Kure, T Shinka, Y Sakata, et al.

Prenatal Diagnosis|August 19, 1999

Prenatal diagnosis of non-ketotic hyperglycinaemia: enzymatic diagnosis in 28 families and DNA diagnosis detecting prevalent Finnish and Israeli-Arab mutationsS Kure, M O Rolland, J Leisti, et al.

The Journal of Pediatrics|January 1, 1992

Enzymatic diagnosis of nonketotic hyperglycinemia with lymphoblastsS Kure, K Narisawa, K Tada

Enzyme|January 1, 1987

Glycogen storage disease type 1b: genetic disorder involving the transport system of intracellular membraneK Narisawa, Y Igarashi, K Tada

The Japanese Journal of Human Genetics|March 1, 1997

Nonketotic hyperglycinemia: biochemical, molecular, and neurological aspectsS Kure, K Tada, K Narisawa

Biochemical and Biophysical Research Communications|February 14, 1991

Structural and expression analyses of normal and mutant mRNA encoding glycine decarboxylase: three-base deletion in mRNA causes nonketotic hyperglycinemiaS Kure, K Narisawa, K Tada

Human Genetics|May 8, 2000

Human glycine decarboxylase gene (GLDC) and its highly conserved processed pseudogene (psiGLDC): their structure and expression, and the identification of a large deletion in a family with nonketotic hyperglycinemiaM Takayanagi, S Kure, Y Sakata, et al.

Human Molecular Genetics|June 1, 1994

Identification of two novel mutations in the methylmalonyl-CoA mutase gene with decreased levels of mutant mRNA in methylmalonic acidemiaM Ogasawara, Y Matsubara, H Mikami, et al.

Pageof 75

Showing results (1-10 of 743) with videos related to

Sort By:

Pageof 75

European Journal of Pediatrics|March 1, 1992

Medium-chain acyl-CoA dehydrogenase deficiency: molecular aspectsY Matsubara, K Narisawa, K Tada

Acta Paediatrica Japonica : Overseas Edition|June 1, 1994

Rapid detection of phenylketonuria mutations by non-radioactive single-strand conformation polymorphism analysisY Yao, Y Matsubara, K Narisawa

Journal of Human Genetics|June 11, 1998

A one-base deletion (183delC) and a missense mutation (D276H) in the T-protein gene from a Japanese family with nonketotic hyperglycinemiaS Kure, T Shinka, Y Sakata, et al.

Prenatal Diagnosis|August 19, 1999

Prenatal diagnosis of non-ketotic hyperglycinaemia: enzymatic diagnosis in 28 families and DNA diagnosis detecting prevalent Finnish and Israeli-Arab mutationsS Kure, M O Rolland, J Leisti, et al.

The Journal of Pediatrics|January 1, 1992

Enzymatic diagnosis of nonketotic hyperglycinemia with lymphoblastsS Kure, K Narisawa, K Tada

Enzyme|January 1, 1987

Glycogen storage disease type 1b: genetic disorder involving the transport system of intracellular membraneK Narisawa, Y Igarashi, K Tada

The Japanese Journal of Human Genetics|March 1, 1997

Nonketotic hyperglycinemia: biochemical, molecular, and neurological aspectsS Kure, K Tada, K Narisawa

Biochemical and Biophysical Research Communications|February 14, 1991

Structural and expression analyses of normal and mutant mRNA encoding glycine decarboxylase: three-base deletion in mRNA causes nonketotic hyperglycinemiaS Kure, K Narisawa, K Tada

Human Genetics|May 8, 2000

Human glycine decarboxylase gene (GLDC) and its highly conserved processed pseudogene (psiGLDC): their structure and expression, and the identification of a large deletion in a family with nonketotic hyperglycinemiaM Takayanagi, S Kure, Y Sakata, et al.

Human Molecular Genetics|June 1, 1994

Identification of two novel mutations in the methylmalonyl-CoA mutase gene with decreased levels of mutant mRNA in methylmalonic acidemiaM Ogasawara, Y Matsubara, H Mikami, et al.

Pageof 75