X Q Song|T Fukao - JoVE Visualize

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Pediatric Research|June 1, 1996

Immunotitration analysis of cytosolic acetoacetyl-coenzyme A thiolase activity in human fibroblastsT Fukao, X Q Song, S Yamaguchi, et al.

Biochemical and Biophysical Research Communications|May 30, 1994

Molecular cloning and nucleotide sequence of complementary DNA for human hepatic cytosolic acetoacetyl-coenzyme A thiolaseX Q Song, T Fukao, S Yamaguchi, et al.

Prenatal Diagnosis|March 1, 1996

Prenatal diagnosis of adrenoleukodystrophy by means of mutation analysisA Imamura, Y Suzuki, X Q Song, et al.

Prenatal Diagnosis|April 1, 1995

Prenatal diagnosis in a family with mitochondrial acetoacetyl-coenzyme A thiolase deficiency with the use of the polymerase chain reaction followed by the heteroduplex detection methodT Fukao, A Wakazono, X Q Song, et al.

Pediatric Research|October 6, 1997

Enzymes of ketone body utilization in human tissues: protein and messenger RNA levels of succinyl-coenzyme A (CoA):3-ketoacid CoA transferase and mitochondrial and cytosolic acetoacetyl-CoA thiolasesT Fukao, X Q Song, G A Mitchell, et al.

The Tohoku Journal of Experimental Medicine|June 2, 1998

Practical assay method of cytosolic acetoacetyl-CoA thiolase by rapid release of cytosolic enzymes from cultured lymphocytes using digitoninH Watanabe, S Yamaguchi, M Kimura, et al.

Human Mutation|January 1, 1995

Mucopolysaccharidosis type II (Hunter disease): identification and characterization of eight point mutations in the iduronate-2-sulfatase gene in Japanese patientsK Sukegawa, S Tomatsu, T Fukao, et al.

Prenatal Diagnosis|May 1, 1996

Prenatal diagnosis of succinyl-coenzyme A:3-ketoacid coenzyme A transferase deficiencyT Fukao, X Q Song, H Watanabe, et al.

Biochemical and Biophysical Research Communications|January 28, 1994

Identification of a nonsense mutation in ALD protein cDNA from a patient with adrenoleukodystrophyA Uchiyama, Y Suzuki, X Q Song, et al.

Journal of Inherited Metabolic Disease|March 21, 1998

Mutation analysis in the iduronate-2-sulphatase gene in 43 Japanese patients with mucopolysaccharidosis type II (Hunter disease)K Isogai, K Sukegawa, S Tomatsu, et al.

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Showing results (1-10 of 135) with videos related to

Sort By:

Pageof 14

Pediatric Research|June 1, 1996

Immunotitration analysis of cytosolic acetoacetyl-coenzyme A thiolase activity in human fibroblastsT Fukao, X Q Song, S Yamaguchi, et al.

Biochemical and Biophysical Research Communications|May 30, 1994

Molecular cloning and nucleotide sequence of complementary DNA for human hepatic cytosolic acetoacetyl-coenzyme A thiolaseX Q Song, T Fukao, S Yamaguchi, et al.

Prenatal Diagnosis|March 1, 1996

Prenatal diagnosis of adrenoleukodystrophy by means of mutation analysisA Imamura, Y Suzuki, X Q Song, et al.

Prenatal Diagnosis|April 1, 1995

Prenatal diagnosis in a family with mitochondrial acetoacetyl-coenzyme A thiolase deficiency with the use of the polymerase chain reaction followed by the heteroduplex detection methodT Fukao, A Wakazono, X Q Song, et al.

Pediatric Research|October 6, 1997

Enzymes of ketone body utilization in human tissues: protein and messenger RNA levels of succinyl-coenzyme A (CoA):3-ketoacid CoA transferase and mitochondrial and cytosolic acetoacetyl-CoA thiolasesT Fukao, X Q Song, G A Mitchell, et al.

The Tohoku Journal of Experimental Medicine|June 2, 1998

Practical assay method of cytosolic acetoacetyl-CoA thiolase by rapid release of cytosolic enzymes from cultured lymphocytes using digitoninH Watanabe, S Yamaguchi, M Kimura, et al.

Human Mutation|January 1, 1995

Mucopolysaccharidosis type II (Hunter disease): identification and characterization of eight point mutations in the iduronate-2-sulfatase gene in Japanese patientsK Sukegawa, S Tomatsu, T Fukao, et al.

Prenatal Diagnosis|May 1, 1996

Prenatal diagnosis of succinyl-coenzyme A:3-ketoacid coenzyme A transferase deficiencyT Fukao, X Q Song, H Watanabe, et al.

Biochemical and Biophysical Research Communications|January 28, 1994

Identification of a nonsense mutation in ALD protein cDNA from a patient with adrenoleukodystrophyA Uchiyama, Y Suzuki, X Q Song, et al.

Journal of Inherited Metabolic Disease|March 21, 1998

Mutation analysis in the iduronate-2-sulphatase gene in 43 Japanese patients with mucopolysaccharidosis type II (Hunter disease)K Isogai, K Sukegawa, S Tomatsu, et al.

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