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M Soejima

Showing results (51-60 of 64) with videos related to

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Diabetologia|August 22, 2002
Haptoglobin genotype and diabetic microangiopathies in Japanese diabetic patientsY Koda, M Soejima, S Yamagishi, et al.
Genetics|June 19, 2001
Contrasting patterns of polymorphisms at the ABO-secretor gene (FUT2) and plasma alpha(1,3)fucosyltransferase gene (FUT6) in human populationsY Koda, H Tachida, H Pang, et al.
Clinical Nephrology|December 21, 2006
Idiopathic retroperitoneal fibrosis associated with Hashimoto's thyroiditis: a long-term follow-upT Sanai, M Hirakawa, M Yokoyama, et al.
Human Genetics|August 14, 1998
Five novel missense mutations of the Lewis gene (FUT3) in African (Xhosa) and Caucasian populations in South AfricaH Pang, Y Liu, Y Koda, et al.
Clinical Rheumatology|March 27, 2009
Selective expression of MHC class I in the affected muscle of a patient with idiopathic inflammatory myopathyT Gono, Y Katsumata, Y Kawaguchi, et al.
Medical Hypotheses|March 5, 2003
Polymorphisms of sorbitol dehydrogenase (SDH) gene and susceptibility to diabetic retinopathyS Amano, S Yamagishi, Y Koda, et al.
Nephron|January 1, 1989
Waldenström's macroglobulinemia associated with amyloidosis and crescentic glomerulonephritisY Ogami, M Takasugi, M Soejima, et al.
Nihon Jinzo Gakkai Shi|November 1, 1984
[Gentamicin pharmacokinetics during hemodialysis]M Takasugi, O Hasegawa, M Soejima, et al.
Blood|February 9, 2000
Simple PCR detection of haptoglobin gene deletion in anhaptoglobinemic patients with antihaptoglobin antibody that causes anaphylactic transfusion reactionsY Koda, Y Watanabe, M Soejima, et al.
Journal of Human Genetics|May 13, 1999
The fusion gene at the ABO-secretor locus (FUT2): absence in Chinese populationsY H Liu, Y Koda, M Soejima, et al.
Pageof 7

Showing results (51-60 of 64) with videos related to

Sort By:
Pageof 7
Diabetologia|August 22, 2002
Haptoglobin genotype and diabetic microangiopathies in Japanese diabetic patientsY Koda, M Soejima, S Yamagishi, et al.
Genetics|June 19, 2001
Contrasting patterns of polymorphisms at the ABO-secretor gene (FUT2) and plasma alpha(1,3)fucosyltransferase gene (FUT6) in human populationsY Koda, H Tachida, H Pang, et al.
Clinical Nephrology|December 21, 2006
Idiopathic retroperitoneal fibrosis associated with Hashimoto's thyroiditis: a long-term follow-upT Sanai, M Hirakawa, M Yokoyama, et al.
Human Genetics|August 14, 1998
Five novel missense mutations of the Lewis gene (FUT3) in African (Xhosa) and Caucasian populations in South AfricaH Pang, Y Liu, Y Koda, et al.
Clinical Rheumatology|March 27, 2009
Selective expression of MHC class I in the affected muscle of a patient with idiopathic inflammatory myopathyT Gono, Y Katsumata, Y Kawaguchi, et al.
Medical Hypotheses|March 5, 2003
Polymorphisms of sorbitol dehydrogenase (SDH) gene and susceptibility to diabetic retinopathyS Amano, S Yamagishi, Y Koda, et al.
Nephron|January 1, 1989
Waldenström's macroglobulinemia associated with amyloidosis and crescentic glomerulonephritisY Ogami, M Takasugi, M Soejima, et al.
Nihon Jinzo Gakkai Shi|November 1, 1984
[Gentamicin pharmacokinetics during hemodialysis]M Takasugi, O Hasegawa, M Soejima, et al.
Blood|February 9, 2000
Simple PCR detection of haptoglobin gene deletion in anhaptoglobinemic patients with antihaptoglobin antibody that causes anaphylactic transfusion reactionsY Koda, Y Watanabe, M Soejima, et al.
Journal of Human Genetics|May 13, 1999
The fusion gene at the ABO-secretor locus (FUT2): absence in Chinese populationsY H Liu, Y Koda, M Soejima, et al.
Pageof 7