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Genomics
|
December 1, 1996
Molecular cloning, tissue distribution, and chromosomal localization of human cationic amino acid transporter 2 (HCAT2)
R Hoshide, Y Ikeda, S Karashima, et al.
Journal of Human Genetics
|
June 11, 1998
Molecular basis of intermittent maple syrup urine disease: novel mutations in the E2 gene of the branched-chain alpha-keto acid dehydrogenase complex
M Tsuruta, H Mitsubuchi, S Mardy, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
March 12, 1982
Skin histidase activity and urine formiminoglutamic acid (FIGLU) in patients with histidinemia found by screening newborn infants
I Matsuda, K Matsuo, F Endo, et al.
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology
|
July 1, 1996
[Detection of PEBP2 beta/MYH11 fusion mRNA in acute myelomonocytic leukemia without marrow eosinophilia]
S Morinaga, M Osato, Y Yanabe, et al.
Gan to Kagaku Ryoho. Cancer & Chemotherapy
|
November 22, 2000
[Arterial infusion chemotherapy for liver metastases from colorectal cancer--therapeutic effects of different protocols]
K Mori, A Kosaka, S Yamada, et al.
Clinical Genetics
|
August 1, 1995
Clinical and molecular analysis of a Japanese boy with Morquio B disease
N Ishii, T Oohira, A Oshima, et al.
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology
|
August 1, 1994
[Autoimmune hemolytic anemia associated with multicentric Castleman's disease with a 28-year history]
J Hisatake, T Ishiyama, Y Akimoto, et al.
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology
|
July 1, 1994
Characterization of subspecies of apolipoprotein A-I-containing lipoprotein in homozygotes for familial lecithin:cholesterol acyltransferase deficiency
T Ohta, S Hattori, R Nakamura, et al.
Acta Endocrinologica
|
February 1, 1990
Isolated human growth hormone deficiency due to the hGH-I gene deletion with (type IA) and without (the Israeli-type) hGH antibody formation during hGH therapy
Y Nishi, H Masuda, S Nishimura, et al.
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology
|
October 1, 1995
[Neutropenia in patient with X-linked hyper-IgM syndrome]
M Iwata, H Nunoi, S Nonoyama, et al.
Page
of 44
Search research articles
Search
Showing results (361-370 of 433) with videos related to
Sort By:
Page
of 44
Genomics
|
December 1, 1996
Molecular cloning, tissue distribution, and chromosomal localization of human cationic amino acid transporter 2 (HCAT2)
R Hoshide, Y Ikeda, S Karashima, et al.
Journal of Human Genetics
|
June 11, 1998
Molecular basis of intermittent maple syrup urine disease: novel mutations in the E2 gene of the branched-chain alpha-keto acid dehydrogenase complex
M Tsuruta, H Mitsubuchi, S Mardy, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
March 12, 1982
Skin histidase activity and urine formiminoglutamic acid (FIGLU) in patients with histidinemia found by screening newborn infants
I Matsuda, K Matsuo, F Endo, et al.
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology
|
July 1, 1996
[Detection of PEBP2 beta/MYH11 fusion mRNA in acute myelomonocytic leukemia without marrow eosinophilia]
S Morinaga, M Osato, Y Yanabe, et al.
Gan to Kagaku Ryoho. Cancer & Chemotherapy
|
November 22, 2000
[Arterial infusion chemotherapy for liver metastases from colorectal cancer--therapeutic effects of different protocols]
K Mori, A Kosaka, S Yamada, et al.
Clinical Genetics
|
August 1, 1995
Clinical and molecular analysis of a Japanese boy with Morquio B disease
N Ishii, T Oohira, A Oshima, et al.
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology
|
August 1, 1994
[Autoimmune hemolytic anemia associated with multicentric Castleman's disease with a 28-year history]
J Hisatake, T Ishiyama, Y Akimoto, et al.
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology
|
July 1, 1994
Characterization of subspecies of apolipoprotein A-I-containing lipoprotein in homozygotes for familial lecithin:cholesterol acyltransferase deficiency
T Ohta, S Hattori, R Nakamura, et al.
Acta Endocrinologica
|
February 1, 1990
Isolated human growth hormone deficiency due to the hGH-I gene deletion with (type IA) and without (the Israeli-type) hGH antibody formation during hGH therapy
Y Nishi, H Masuda, S Nishimura, et al.
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology
|
October 1, 1995
[Neutropenia in patient with X-linked hyper-IgM syndrome]
M Iwata, H Nunoi, S Nonoyama, et al.
Page
of 44