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Cell Transplantation
|
August 7, 2002
In vitro study of encapsulation therapy for Fabry disease using genetically engineered CHO cell line
Y Naganawa, K Ohsugi, R Kase, et al.
Biochemical and Biophysical Research Communications
|
November 30, 1994
Distribution of lysosomal protective protein in human tissues
A Satake, K Itoh, M Shimmoto, et al.
Journal of Human Genetics
|
August 17, 2000
Structural and functional study of K453E mutant protective protein/cathepsin A causing the late infantile form of galactosialidosis
K Takiguchi, K Itoh, M Shimmoto, et al.
Annals of Neurology
|
May 1, 1991
Fabry disease: detection of 13-bp deletion in alpha-galactosidase A gene and its application to gene diagnosis of heterozygotes
S Ishii, H Sakuraba, M Shimmoto, et al.
Clinical Genetics
|
May 1, 1992
GM1-gangliosidosis: tandem duplication within exon 3 of beta-galactosidase gene in an infantile patient
A Oshima, K Yoshida, A Ishizaki, et al.
Developmental Neuroscience
|
January 1, 1991
Clinical and molecular heterogeneity in hereditary beta-galactosidase deficiency
Y Suzuki, H Sakuraba, A Oshima, et al.
Biochemical and Biophysical Research Communications
|
September 25, 1995
Galactose stabilizes various missense mutants of alpha-galactosidase in Fabry disease
T Okumiya, S Ishii, T Takenaka, et al.
Biochemical and Biophysical Research Communications
|
March 27, 1996
A human protective protein gene partially overlaps the gene encoding phospholipid transfer protein on the complementary strand of DNA
M Shimmoto, Y Nakahori, I Matsushita, et al.
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics
|
June 1, 1991
Acid carboxypeptidase deficiency in galactosialidosis
K Itoh, N Takiyama, Y Nagao, et al.
Annals of Neurology
|
January 13, 2000
Endothelin-1 in the brain of patients with galactosialidosis: its abnormal increase and distribution pattern
K Itoh, K Oyanagi, H Takahashi, et al.
Page
of 13
Search research articles
Search
Showing results (61-70 of 128) with videos related to
Sort By:
Page
of 13
Cell Transplantation
|
August 7, 2002
In vitro study of encapsulation therapy for Fabry disease using genetically engineered CHO cell line
Y Naganawa, K Ohsugi, R Kase, et al.
Biochemical and Biophysical Research Communications
|
November 30, 1994
Distribution of lysosomal protective protein in human tissues
A Satake, K Itoh, M Shimmoto, et al.
Journal of Human Genetics
|
August 17, 2000
Structural and functional study of K453E mutant protective protein/cathepsin A causing the late infantile form of galactosialidosis
K Takiguchi, K Itoh, M Shimmoto, et al.
Annals of Neurology
|
May 1, 1991
Fabry disease: detection of 13-bp deletion in alpha-galactosidase A gene and its application to gene diagnosis of heterozygotes
S Ishii, H Sakuraba, M Shimmoto, et al.
Clinical Genetics
|
May 1, 1992
GM1-gangliosidosis: tandem duplication within exon 3 of beta-galactosidase gene in an infantile patient
A Oshima, K Yoshida, A Ishizaki, et al.
Developmental Neuroscience
|
January 1, 1991
Clinical and molecular heterogeneity in hereditary beta-galactosidase deficiency
Y Suzuki, H Sakuraba, A Oshima, et al.
Biochemical and Biophysical Research Communications
|
September 25, 1995
Galactose stabilizes various missense mutants of alpha-galactosidase in Fabry disease
T Okumiya, S Ishii, T Takenaka, et al.
Biochemical and Biophysical Research Communications
|
March 27, 1996
A human protective protein gene partially overlaps the gene encoding phospholipid transfer protein on the complementary strand of DNA
M Shimmoto, Y Nakahori, I Matsushita, et al.
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics
|
June 1, 1991
Acid carboxypeptidase deficiency in galactosialidosis
K Itoh, N Takiyama, Y Nagao, et al.
Annals of Neurology
|
January 13, 2000
Endothelin-1 in the brain of patients with galactosialidosis: its abnormal increase and distribution pattern
K Itoh, K Oyanagi, H Takahashi, et al.
Page
of 13