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Dermatology (Basel, Switzerland)
|
August 7, 1998
Angiokeratoma corporis diffusum associated with galactosialidosis
Y Kawachi, K Matsu-ura, H Sakuraba, et al.
Journal of Bioscience and Bioengineering
|
October 20, 2005
Transcriptional regulation of phosphoenolpyruvate synthase by maltose in the hyperthermophilic archaeon, Pyrococcus furiosus
H Sakuraba, E Utsumi, H J Schreier, et al.
Applied and Environmental Microbiology
|
April 3, 2001
Purification, characterization, and application of a novel dye-linked L-proline dehydrogenase from a hyperthermophilic archaeon, Thermococcus profundus
H Sakuraba, Y Takamatsu, T Satomura, et al.
Pediatric Neurology
|
May 1, 1990
Relief of chronic burning pain in Fabry disease with neurotropin
M Inagaki, K Ohno, S Ohta, et al.
Biochemical and Biophysical Research Communications
|
March 27, 1996
Aggregation of the inactive form of human alpha-galactosidase in the endoplasmic reticulum
S Ishii, R Kase, T Okumiya, et al.
Brain & Development
|
September 1, 1991
A screening for dystrophin gene deletions in Japanese patients with Duchenne/Becker muscular dystrophy by the multiplex polymerase chain reaction
H Sakuraba, K Ishii, M Shimmoto, et al.
Biochemical and Biophysical Research Communications
|
June 15, 1993
Characterization of an anti-beta-galactosidase antibody recognizing a precursor but not a mature enzyme in solution
N Takiyama, K Itoh, A Oshima, et al.
Biochemical and Biophysical Research Communications
|
January 8, 1999
Stabilizing effect of lysosomal beta-galactosidase on the catalytic activity of protective protein/cathepsin A secreted by human platelets
K Itoh, Y Naganawa, S Kamei, et al.
Journal of Biochemistry
|
July 1, 1981
Beta-galactosidase-neuraminidase deficiency: restoration of beta-galactosidase activity by protease inhibitors
Y Suzuki, H Sakuraba, K Hayashi, et al.
The Journal of Dermatology
|
August 1, 1992
Two cases of Fabry's disease: a hemizygote with a point mutation in the alpha-galactosidase A gene and his relative
M Inaoki, N Otsuki, S Ishise, et al.
Page
of 13
Search research articles
Search
Showing results (21-30 of 128) with videos related to
Sort By:
Page
of 13
Dermatology (Basel, Switzerland)
|
August 7, 1998
Angiokeratoma corporis diffusum associated with galactosialidosis
Y Kawachi, K Matsu-ura, H Sakuraba, et al.
Journal of Bioscience and Bioengineering
|
October 20, 2005
Transcriptional regulation of phosphoenolpyruvate synthase by maltose in the hyperthermophilic archaeon, Pyrococcus furiosus
H Sakuraba, E Utsumi, H J Schreier, et al.
Applied and Environmental Microbiology
|
April 3, 2001
Purification, characterization, and application of a novel dye-linked L-proline dehydrogenase from a hyperthermophilic archaeon, Thermococcus profundus
H Sakuraba, Y Takamatsu, T Satomura, et al.
Pediatric Neurology
|
May 1, 1990
Relief of chronic burning pain in Fabry disease with neurotropin
M Inagaki, K Ohno, S Ohta, et al.
Biochemical and Biophysical Research Communications
|
March 27, 1996
Aggregation of the inactive form of human alpha-galactosidase in the endoplasmic reticulum
S Ishii, R Kase, T Okumiya, et al.
Brain & Development
|
September 1, 1991
A screening for dystrophin gene deletions in Japanese patients with Duchenne/Becker muscular dystrophy by the multiplex polymerase chain reaction
H Sakuraba, K Ishii, M Shimmoto, et al.
Biochemical and Biophysical Research Communications
|
June 15, 1993
Characterization of an anti-beta-galactosidase antibody recognizing a precursor but not a mature enzyme in solution
N Takiyama, K Itoh, A Oshima, et al.
Biochemical and Biophysical Research Communications
|
January 8, 1999
Stabilizing effect of lysosomal beta-galactosidase on the catalytic activity of protective protein/cathepsin A secreted by human platelets
K Itoh, Y Naganawa, S Kamei, et al.
Journal of Biochemistry
|
July 1, 1981
Beta-galactosidase-neuraminidase deficiency: restoration of beta-galactosidase activity by protease inhibitors
Y Suzuki, H Sakuraba, K Hayashi, et al.
The Journal of Dermatology
|
August 1, 1992
Two cases of Fabry's disease: a hemizygote with a point mutation in the alpha-galactosidase A gene and his relative
M Inaoki, N Otsuki, S Ishise, et al.
Page
of 13