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Nihon Gan Chiryo Gakkai Shi
|
May 20, 1986
[Clinical evaluation of tumor markers in patients with lung cancer, laying stress on tissue polypeptide antigen (TPA)]
Y Matsubara, K Ninomiya, Y Yasuda, et al.
The Journal of Biological Chemistry
|
July 25, 1987
Molecular cloning and nucleotide sequence of cDNA encoding the entire precursor of rat liver medium chain acyl coenzyme A dehydrogenase
Y Matsubara, J P Kraus, H Ozasa, et al.
Kansenshogaku Zasshi. the Journal of the Japanese Association for Infectious Diseases
|
July 1, 1987
[Comparison of clinical efficacy of norfloxacin (NFLX) and pipemidic acid (PPA) in the treatment of infectious enteritis by a double-blind method. The Japan Research Committee of Norfloxacin Research Group Enteritis]
T Aoki, N Shimizu, I Tomizawa, et al.
Kyobu Geka. the Japanese Journal of Thoracic Surgery
|
July 1, 1979
[N-factor in the surgical treatment of lung cancer in relation to mediastinoscopy and to the presence of anti-tumor-specific antibody in mediastinal lymph nodes (author's transl)]
Y Matsubara, T Funatsu, R Hatakenaka, et al.
Nihon Gan Chiryo Gakkai Shi
|
May 20, 1989
[Evaluation of sialyl SSEA-1 antigen in patients with lung cancer]
T Shiota, Y Matsubara, S Ikeda, et al.
Human Genetics
|
May 26, 1998
A missense mutation (His42Arg) in the T-protein gene from a large Israeli-Arab kindred with nonketotic hyperglycinemia
S Kure, H Mandel, M O Rolland, et al.
Journal of Human Genetics
|
February 24, 2001
Haplotype analysis suggests that the two predominant mutations in Japanese patients with holocarboxylase synthetase deficiency are founder mutations
X Yang, Y Aoki, X Li, et al.
The Journal of Pediatrics
|
September 15, 1999
Tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency
S Kure, D C Hou, T Ohura, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1990
Molecular analysis of dihydropteridine reductase deficiency and restoration of the enzyme activity by gene transfer
H Mikami, Y Matsubara, K Hayasaka, et al.
The Journal of Pediatrics
|
August 10, 2000
Glycogen storage disease type Ib without neutropenia
S Kure, D C Hou, Y Suzuki, et al.
Page
of 37
Search research articles
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Showing results (301-310 of 367) with videos related to
Sort By:
Page
of 37
Nihon Gan Chiryo Gakkai Shi
|
May 20, 1986
[Clinical evaluation of tumor markers in patients with lung cancer, laying stress on tissue polypeptide antigen (TPA)]
Y Matsubara, K Ninomiya, Y Yasuda, et al.
The Journal of Biological Chemistry
|
July 25, 1987
Molecular cloning and nucleotide sequence of cDNA encoding the entire precursor of rat liver medium chain acyl coenzyme A dehydrogenase
Y Matsubara, J P Kraus, H Ozasa, et al.
Kansenshogaku Zasshi. the Journal of the Japanese Association for Infectious Diseases
|
July 1, 1987
[Comparison of clinical efficacy of norfloxacin (NFLX) and pipemidic acid (PPA) in the treatment of infectious enteritis by a double-blind method. The Japan Research Committee of Norfloxacin Research Group Enteritis]
T Aoki, N Shimizu, I Tomizawa, et al.
Kyobu Geka. the Japanese Journal of Thoracic Surgery
|
July 1, 1979
[N-factor in the surgical treatment of lung cancer in relation to mediastinoscopy and to the presence of anti-tumor-specific antibody in mediastinal lymph nodes (author's transl)]
Y Matsubara, T Funatsu, R Hatakenaka, et al.
Nihon Gan Chiryo Gakkai Shi
|
May 20, 1989
[Evaluation of sialyl SSEA-1 antigen in patients with lung cancer]
T Shiota, Y Matsubara, S Ikeda, et al.
Human Genetics
|
May 26, 1998
A missense mutation (His42Arg) in the T-protein gene from a large Israeli-Arab kindred with nonketotic hyperglycinemia
S Kure, H Mandel, M O Rolland, et al.
Journal of Human Genetics
|
February 24, 2001
Haplotype analysis suggests that the two predominant mutations in Japanese patients with holocarboxylase synthetase deficiency are founder mutations
X Yang, Y Aoki, X Li, et al.
The Journal of Pediatrics
|
September 15, 1999
Tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency
S Kure, D C Hou, T Ohura, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1990
Molecular analysis of dihydropteridine reductase deficiency and restoration of the enzyme activity by gene transfer
H Mikami, Y Matsubara, K Hayasaka, et al.
The Journal of Pediatrics
|
August 10, 2000
Glycogen storage disease type Ib without neutropenia
S Kure, D C Hou, Y Suzuki, et al.
Page
of 37