Search research articles
Contact Us
Filters
Showing results (1-10 of 128) with videos related to
Page
of 13
Sort By:
Rinsho Byori. the Japanese Journal of Clinical Pathology
|
June 1, 1994
[Molecular genetics of inherited metabolic diseases--its application to the investigation of pathogenesis and the diagnosis of Fabry disease]
H Sakuraba
Brain & Development
|
January 1, 1983
Biochemical analysis of cerebrum of fetal rat X-irradiated in utero--DNA, RNA, superoxide dismutase and lipid peroxide--
H Sakuraba, H Tanaka
Nihon Rinsho. Japanese Journal of Clinical Medicine
|
December 1, 1995
[Fabry disease (alpha-galactosidase deficiency)]
T Okumiya, H Sakuraba
The Journal of Biological Chemistry
|
January 6, 1995
Alcohol:NAD+ oxidoreductase is present in rat liver peroxisomes
H Sakuraba, T Noguchi
American Journal of Hematology
|
May 1, 1986
Activation of platelet function in Fabry's disease
T Igarashi, H Sakuraba, Y Suzuki
Archives of Biochemistry and Biophysics
|
May 1, 1994
Identification of chicken liver mitochondrial alanine:2-oxoglutarate aminotransferase and its response to starvation
S Fujiwara, H Sakuraba, T Noguchi
Biochemical and Biophysical Research Communications
|
June 15, 1989
Alanine:glyoxylate aminotransferase is present as the apoenzyme in the peroxisomes of chicken kidney
H Sakuraba, S Fujiwara, T Noguchi
Human Genetics
|
April 1, 1992
Point mutations in the upstream region of the alpha-galactosidase A gene exon 6 in an atypical variant of Fabry disease
S Ishii, H Sakuraba, Y Suzuki
Biochemical and Biophysical Research Communications
|
May 15, 1991
Intraperoxisomal form of alanine:glyoxylate aminotransferase in the peroxisomes of bird kidney
H Sakuraba, S Fujiwara, T Noguchi
Biochemical and Biophysical Research Communications
|
November 30, 1989
Response of hepatic alanine:glyoxylate aminotransferase 1 to hormone differs among mammalia
S Hayashi, H Sakuraba, T Noguchi
Page
of 13
Search research articles
Search
Showing results (1-10 of 128) with videos related to
Sort By:
Page
of 13
Rinsho Byori. the Japanese Journal of Clinical Pathology
|
June 1, 1994
[Molecular genetics of inherited metabolic diseases--its application to the investigation of pathogenesis and the diagnosis of Fabry disease]
H Sakuraba
Brain & Development
|
January 1, 1983
Biochemical analysis of cerebrum of fetal rat X-irradiated in utero--DNA, RNA, superoxide dismutase and lipid peroxide--
H Sakuraba, H Tanaka
Nihon Rinsho. Japanese Journal of Clinical Medicine
|
December 1, 1995
[Fabry disease (alpha-galactosidase deficiency)]
T Okumiya, H Sakuraba
The Journal of Biological Chemistry
|
January 6, 1995
Alcohol:NAD+ oxidoreductase is present in rat liver peroxisomes
H Sakuraba, T Noguchi
American Journal of Hematology
|
May 1, 1986
Activation of platelet function in Fabry's disease
T Igarashi, H Sakuraba, Y Suzuki
Archives of Biochemistry and Biophysics
|
May 1, 1994
Identification of chicken liver mitochondrial alanine:2-oxoglutarate aminotransferase and its response to starvation
S Fujiwara, H Sakuraba, T Noguchi
Biochemical and Biophysical Research Communications
|
June 15, 1989
Alanine:glyoxylate aminotransferase is present as the apoenzyme in the peroxisomes of chicken kidney
H Sakuraba, S Fujiwara, T Noguchi
Human Genetics
|
April 1, 1992
Point mutations in the upstream region of the alpha-galactosidase A gene exon 6 in an atypical variant of Fabry disease
S Ishii, H Sakuraba, Y Suzuki
Biochemical and Biophysical Research Communications
|
May 15, 1991
Intraperoxisomal form of alanine:glyoxylate aminotransferase in the peroxisomes of bird kidney
H Sakuraba, S Fujiwara, T Noguchi
Biochemical and Biophysical Research Communications
|
November 30, 1989
Response of hepatic alanine:glyoxylate aminotransferase 1 to hormone differs among mammalia
S Hayashi, H Sakuraba, T Noguchi
Page
of 13