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Biochemical and Biophysical Research Communications
|
May 25, 1995
Adrenoleukodystrophy: the restoration of peroxisomal beta-oxidation by transfection of normal cDNA
N Shinnoh, T Yamada, T Yoshimura, et al.
The Journal of Pediatrics
|
November 1, 1988
Zellweger-like syndrome with detectable hepatic peroxisomes: a variant form of peroxisomal disorder
Y Suzuki, N Shimozawa, T Orii, et al.
Clinical Transplantation
|
August 17, 2000
Usefulness of quantitative real-time polymerase chain reaction in following up patients with Epstein-Barr virus infection after liver transplantation
T Orii, N Ohkohchi, H Kikuchi, et al.
Clinical Genetics
|
August 1, 1995
Clinical and molecular analysis of a Japanese boy with Morquio B disease
N Ishii, T Oohira, A Oshima, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
April 1, 1983
Activities of sulfatases for the degradation of acidic glycosaminoglycans in cultured skin fibroblasts from two siblings with multiple sulfatase deficiency
R Minami, S Fujibayashi, N Tachi, et al.
Genomics
|
March 1, 1994
Mucopolysaccharidosis IV A: molecular cloning of the human N-acetylgalactosamine-6-sulfatase gene (GALNS) and analysis of the 5'-flanking region
Y Nakashima, S Tomatsu, T Hori, et al.
Biochemical and Biophysical Research Communications
|
March 16, 1992
Intermediate form of mucopolysaccharidosis type II (Hunter disease): a C1327 to T substitution in the iduronate sulfatase gene
K Sukegawa, S Tomatsu, K Tamai, et al.
The Journal of Allergy and Clinical Immunology
|
February 1, 1993
The role of T lymphocytes in patients with food-sensitive atopic dermatitis
N Kondo, O Fukutomi, H Agata, 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 patients
K Sukegawa, S Tomatsu, T Fukao, et al.
Human Genetics
|
March 1, 1992
Complementation study of peroxisome-deficient disorders by immunofluorescence staining and characterization of fused cells
S Yajima, Y Suzuki, N Shimozawa, et al.
Page
of 28
Search research articles
Search
Showing results (201-210 of 276) with videos related to
Sort By:
Page
of 28
Biochemical and Biophysical Research Communications
|
May 25, 1995
Adrenoleukodystrophy: the restoration of peroxisomal beta-oxidation by transfection of normal cDNA
N Shinnoh, T Yamada, T Yoshimura, et al.
The Journal of Pediatrics
|
November 1, 1988
Zellweger-like syndrome with detectable hepatic peroxisomes: a variant form of peroxisomal disorder
Y Suzuki, N Shimozawa, T Orii, et al.
Clinical Transplantation
|
August 17, 2000
Usefulness of quantitative real-time polymerase chain reaction in following up patients with Epstein-Barr virus infection after liver transplantation
T Orii, N Ohkohchi, H Kikuchi, et al.
Clinical Genetics
|
August 1, 1995
Clinical and molecular analysis of a Japanese boy with Morquio B disease
N Ishii, T Oohira, A Oshima, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
April 1, 1983
Activities of sulfatases for the degradation of acidic glycosaminoglycans in cultured skin fibroblasts from two siblings with multiple sulfatase deficiency
R Minami, S Fujibayashi, N Tachi, et al.
Genomics
|
March 1, 1994
Mucopolysaccharidosis IV A: molecular cloning of the human N-acetylgalactosamine-6-sulfatase gene (GALNS) and analysis of the 5'-flanking region
Y Nakashima, S Tomatsu, T Hori, et al.
Biochemical and Biophysical Research Communications
|
March 16, 1992
Intermediate form of mucopolysaccharidosis type II (Hunter disease): a C1327 to T substitution in the iduronate sulfatase gene
K Sukegawa, S Tomatsu, K Tamai, et al.
The Journal of Allergy and Clinical Immunology
|
February 1, 1993
The role of T lymphocytes in patients with food-sensitive atopic dermatitis
N Kondo, O Fukutomi, H Agata, 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 patients
K Sukegawa, S Tomatsu, T Fukao, et al.
Human Genetics
|
March 1, 1992
Complementation study of peroxisome-deficient disorders by immunofluorescence staining and characterization of fused cells
S Yajima, Y Suzuki, N Shimozawa, et al.
Page
of 28