Search research articles
Contact Us
Filters
Showing results (161-170 of 276) with videos related to
Page
of 28
Sort By:
The Tohoku Journal of Experimental Medicine
|
June 1, 1992
Further analysis of mutant thiolase protein in fibroblasts from a Japanese boy with 3-ketothiolase deficiency
S Yamaguchi, T Fukao, M Kano, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
August 24, 2007
Natural history of extensive Mongolian spots in mucopolysaccharidosis type II (Hunter syndrome): a survey among 52 Japanese patients
T Ochiai, Y Suzuki, T Kato, et al.
Journal of Biochemistry
|
August 1, 1989
Molecular cloning and nucleotide sequence of cDNA encoding the entire precursor of rat mitochondrial acetoacetyl-CoA thiolase
T Fukao, K Kamijo, T Osumi, et al.
Human Genetics
|
September 1, 1993
Mucopolysaccharidosis type II (Hunter disease): 13 gene mutations in 52 Japanese patients and carrier detection in four families
Y Yamada, S Tomatsu, K Sukegawa, et al.
Prenatal Diagnosis
|
March 1, 1996
Prenatal diagnosis of adrenoleukodystrophy by means of mutation analysis
A Imamura, Y Suzuki, X Q Song, et al.
Pacing and Clinical Electrophysiology : PACE
|
December 1, 1995
Abnormal response to exercise, face immersion, and isoproterenol in children with the long QT syndrome
M Katagiri-Kawade, T Ohe, Y Arakaki, 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 method
T Fukao, A Wakazono, X Q Song, et al.
Brain & Development
|
November 1, 1994
Effects of erucic acid therapy on Japanese patients with X-linked adrenoleukodystrophy
J Asano, Y Suzuki, S Yajima, et al.
European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics
|
April 1, 1994
A wild-type mu s C-terminal gene is expressed in Bloom's syndrome cells
T Ozawa, N Kondo, Y Kato, et al.
Cell Structure and Function
|
February 1, 1992
Different intracellular localization of peroxisomal proteins in fibroblasts from patients with aberrant peroxisome assembly
Y Suzuki, N Shimozawa, S Yajima, et al.
Page
of 28
Search research articles
Search
Showing results (161-170 of 276) with videos related to
Sort By:
Page
of 28
The Tohoku Journal of Experimental Medicine
|
June 1, 1992
Further analysis of mutant thiolase protein in fibroblasts from a Japanese boy with 3-ketothiolase deficiency
S Yamaguchi, T Fukao, M Kano, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
August 24, 2007
Natural history of extensive Mongolian spots in mucopolysaccharidosis type II (Hunter syndrome): a survey among 52 Japanese patients
T Ochiai, Y Suzuki, T Kato, et al.
Journal of Biochemistry
|
August 1, 1989
Molecular cloning and nucleotide sequence of cDNA encoding the entire precursor of rat mitochondrial acetoacetyl-CoA thiolase
T Fukao, K Kamijo, T Osumi, et al.
Human Genetics
|
September 1, 1993
Mucopolysaccharidosis type II (Hunter disease): 13 gene mutations in 52 Japanese patients and carrier detection in four families
Y Yamada, S Tomatsu, K Sukegawa, et al.
Prenatal Diagnosis
|
March 1, 1996
Prenatal diagnosis of adrenoleukodystrophy by means of mutation analysis
A Imamura, Y Suzuki, X Q Song, et al.
Pacing and Clinical Electrophysiology : PACE
|
December 1, 1995
Abnormal response to exercise, face immersion, and isoproterenol in children with the long QT syndrome
M Katagiri-Kawade, T Ohe, Y Arakaki, 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 method
T Fukao, A Wakazono, X Q Song, et al.
Brain & Development
|
November 1, 1994
Effects of erucic acid therapy on Japanese patients with X-linked adrenoleukodystrophy
J Asano, Y Suzuki, S Yajima, et al.
European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics
|
April 1, 1994
A wild-type mu s C-terminal gene is expressed in Bloom's syndrome cells
T Ozawa, N Kondo, Y Kato, et al.
Cell Structure and Function
|
February 1, 1992
Different intracellular localization of peroxisomal proteins in fibroblasts from patients with aberrant peroxisome assembly
Y Suzuki, N Shimozawa, S Yajima, et al.
Page
of 28