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Human Genetics
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March 1, 1997
Human orosomucoid polymorphism: molecular basis of the three common ORM1 alleles, ORM1*F1, ORM1*F2, and ORM1*S
I Yuasa, K Umetsu, U Vogt, et al.
The Japanese Journal of Human Genetics
|
June 1, 1993
PI*S(iiyama), a deficiency gene of alpha 1-antitrypsin: evidence for the occurrence in western Japan
I Yuasa, Y Sugimoto, M Ichinose, et al.
Electrophoresis
|
March 1, 1988
PI Mtoyoura: a new PI M subtype found by separator and hybrid isoelectric focusing
I Yuasa, K Suenaga, K Umetsu, et al.
Research Communications in Molecular Pathology and Pharmacology
|
April 2, 1998
Mutation in the exon 10 (R173W) of the hydroxymethylbilane synthase gene in two unrelated Japanese families with acute intermittent porphyria
Y Tomie, Y Horie, F Tajima, et al.
Journal of Forensic Sciences
|
September 1, 1990
Paternity testing: blood group systems and DNA analysis by variable number of tandem repeat markers
A Akane, K Matsubara, H Shiono, et al.
Journal of Human Genetics
|
October 6, 2001
Characterization of genomic rearrangements of the alpha1-acid glycoprotein/orosomucoid gene in Ghanaians
I Yuasa, H Nakamura, L Henke, et al.
Human Genetics
|
May 1, 1995
Characterization of mutants of the vitamin D-binding protein/group-specific component: molecular evolution of GC*1A2 and GC*1A3, common in some Asian populations
I Yuasa, A Kofler, A Braun, et al.
International Journal of Legal Medicine
|
February 24, 2001
Molecular analysis of the human orosomucoid gene ORM1*Q0köln responsible for incompatibility in a German paternity case
H Nakamura, I Yuasa, K Umetsu, et al.
Human Genetics
|
October 1, 1996
Identification of the nucleotide substitution that generates the fourth polymorphic site in human deoxyribonuclease I (DNase I)
R Iida, T Yasuda, H Takeshita, et al.
Journal of Thrombosis and Haemostasis : JTH
|
May 9, 2009
Distinct C-terminus of the B subunit of factor XIII in a population-associated major phenotype: the first case of complete allele-specific alternative splicing products in the coagulation and fibrinolytic systems
H Iwata, T Kitano, K Umetsu, et al.
Page
of 10
Search research articles
Search
Showing results (61-70 of 98) with videos related to
Sort By:
Page
of 10
Human Genetics
|
March 1, 1997
Human orosomucoid polymorphism: molecular basis of the three common ORM1 alleles, ORM1*F1, ORM1*F2, and ORM1*S
I Yuasa, K Umetsu, U Vogt, et al.
The Japanese Journal of Human Genetics
|
June 1, 1993
PI*S(iiyama), a deficiency gene of alpha 1-antitrypsin: evidence for the occurrence in western Japan
I Yuasa, Y Sugimoto, M Ichinose, et al.
Electrophoresis
|
March 1, 1988
PI Mtoyoura: a new PI M subtype found by separator and hybrid isoelectric focusing
I Yuasa, K Suenaga, K Umetsu, et al.
Research Communications in Molecular Pathology and Pharmacology
|
April 2, 1998
Mutation in the exon 10 (R173W) of the hydroxymethylbilane synthase gene in two unrelated Japanese families with acute intermittent porphyria
Y Tomie, Y Horie, F Tajima, et al.
Journal of Forensic Sciences
|
September 1, 1990
Paternity testing: blood group systems and DNA analysis by variable number of tandem repeat markers
A Akane, K Matsubara, H Shiono, et al.
Journal of Human Genetics
|
October 6, 2001
Characterization of genomic rearrangements of the alpha1-acid glycoprotein/orosomucoid gene in Ghanaians
I Yuasa, H Nakamura, L Henke, et al.
Human Genetics
|
May 1, 1995
Characterization of mutants of the vitamin D-binding protein/group-specific component: molecular evolution of GC*1A2 and GC*1A3, common in some Asian populations
I Yuasa, A Kofler, A Braun, et al.
International Journal of Legal Medicine
|
February 24, 2001
Molecular analysis of the human orosomucoid gene ORM1*Q0köln responsible for incompatibility in a German paternity case
H Nakamura, I Yuasa, K Umetsu, et al.
Human Genetics
|
October 1, 1996
Identification of the nucleotide substitution that generates the fourth polymorphic site in human deoxyribonuclease I (DNase I)
R Iida, T Yasuda, H Takeshita, et al.
Journal of Thrombosis and Haemostasis : JTH
|
May 9, 2009
Distinct C-terminus of the B subunit of factor XIII in a population-associated major phenotype: the first case of complete allele-specific alternative splicing products in the coagulation and fibrinolytic systems
H Iwata, T Kitano, K Umetsu, et al.
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of 10