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Human Genetics
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June 1, 1995
Characteristics of gene mutations among 32 unrelated Japanese Gaucher disease patients: absence of the common Jewish 84GG and 1226G mutations
H Ida, K Iwasawa, H Kawame, et al.
Blood
|
May 29, 2000
Reduction of lysosomal storage in murine mucopolysaccharidosis type VII by transplantation of normal and genetically modified macrophages
T Ohashi, T Yokoo, S Iizuka, et al.
Gene Therapy
|
September 1, 1995
Successful transduction of oligodendrocytes and restoration of arylsulfatase A deficiency in metachromatic leukodystrophy fibroblasts using an adenovirus vector
T Ohashi, K Watabe, Y Sato, et al.
Human Genetics
|
August 1, 1996
Mutation screening of 17 Japanese patients with neuropathic Gaucher disease
H Ida, O M Rennert, H Kawame, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 18, 1997
Adenovirus-mediated gene transfer and expression of human beta-glucuronidase gene in the liver, spleen, and central nervous system in mucopolysaccharidosis type VII mice
T Ohashi, K Watabe, K Uehara, et al.
Annals of Neurology
|
May 11, 2000
Three novel mutations (G27E, insAAC, R179X) in the ORNT1 gene of Japanese patients with hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome
S Tsujino, N Kanazawa, T Ohashi, et al.
No to Hattatsu = Brain and Development
|
August 1, 2000
[A patient with epilepsy, congenital alopecia and mental retardation: combination of atypical absence in waking and nocturnal partial seizure]
J Arita, K Maekawa, H Matsushima, et al.
Biochemical and Biophysical Research Communications
|
February 14, 1990
Activin A stimulates meiotic maturation of the rat oocyte in vitro
M Itoh, M Igarashi, K Yamada, et al.
The Kurume Medical Journal
|
January 1, 1983
Natural and unnatural histories of the pulmonary vascular circulation with a ventricular septal defect (VSD)
K Yokochi, Y Eto, T Mikazima, et al.
Endocrinology
|
June 1, 1994
Effect of activin on luteinizing hormone-human chorionic gonadotropin receptor messenger ribonucleic acid in granulosa cells
K Nakamura, M Nakamura, S Igarashi, et al.
Page
of 31
Search research articles
Search
Showing results (191-200 of 307) with videos related to
Sort By:
Page
of 31
Human Genetics
|
June 1, 1995
Characteristics of gene mutations among 32 unrelated Japanese Gaucher disease patients: absence of the common Jewish 84GG and 1226G mutations
H Ida, K Iwasawa, H Kawame, et al.
Blood
|
May 29, 2000
Reduction of lysosomal storage in murine mucopolysaccharidosis type VII by transplantation of normal and genetically modified macrophages
T Ohashi, T Yokoo, S Iizuka, et al.
Gene Therapy
|
September 1, 1995
Successful transduction of oligodendrocytes and restoration of arylsulfatase A deficiency in metachromatic leukodystrophy fibroblasts using an adenovirus vector
T Ohashi, K Watabe, Y Sato, et al.
Human Genetics
|
August 1, 1996
Mutation screening of 17 Japanese patients with neuropathic Gaucher disease
H Ida, O M Rennert, H Kawame, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 18, 1997
Adenovirus-mediated gene transfer and expression of human beta-glucuronidase gene in the liver, spleen, and central nervous system in mucopolysaccharidosis type VII mice
T Ohashi, K Watabe, K Uehara, et al.
Annals of Neurology
|
May 11, 2000
Three novel mutations (G27E, insAAC, R179X) in the ORNT1 gene of Japanese patients with hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome
S Tsujino, N Kanazawa, T Ohashi, et al.
No to Hattatsu = Brain and Development
|
August 1, 2000
[A patient with epilepsy, congenital alopecia and mental retardation: combination of atypical absence in waking and nocturnal partial seizure]
J Arita, K Maekawa, H Matsushima, et al.
Biochemical and Biophysical Research Communications
|
February 14, 1990
Activin A stimulates meiotic maturation of the rat oocyte in vitro
M Itoh, M Igarashi, K Yamada, et al.
The Kurume Medical Journal
|
January 1, 1983
Natural and unnatural histories of the pulmonary vascular circulation with a ventricular septal defect (VSD)
K Yokochi, Y Eto, T Mikazima, et al.
Endocrinology
|
June 1, 1994
Effect of activin on luteinizing hormone-human chorionic gonadotropin receptor messenger ribonucleic acid in granulosa cells
K Nakamura, M Nakamura, S Igarashi, et al.
Page
of 31