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Y Sugahara

Showing results (1-10 of 48) with videos related to

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Thrombosis and Haemostasis|March 1, 1993
Intracellular transport-deficient mutants causing hereditary deficiencies of factors involved in coagulation and fibrinolysisO Miura, Y Sugahara, N Aoki
The Journal of Biological Chemistry|October 25, 1989
Hereditary alpha 2-plasmin inhibitor deficiency caused by a transport-deficient mutation (alpha 2-PI-Okinawa). Deletion of Glu137 by a trinucleotide deletion blocks intracellular transportO Miura, Y Sugahara, N Aoki
[Kango Gijutsu] : [Nursing Technique]|February 1, 1971
[Customs concerning terminal care and death. Observation in local public health nursing activities]M Shigamura, Y Sugahara, R Takemura
Psychiatry and Clinical Neurosciences|October 24, 2000
Lithium carbonate in prophylaxis of reappearing catatonic stupor: case reportY Sugahara, H Tsukamoto, T Sasaki
Internal Medicine (Tokyo, Japan)|September 1, 1995
Evolution of severe aplastic anemia to myelodysplasia with monosomy 7 following granulocyte colony-stimulating factor, erythropoietin and high-dose methylprednisolone combination therapyA Ohsaka, Y Sugahara, Y Imai, et al.
Thrombosis Research|May 15, 1992
Purification of human alpha 2-plasmin inhibitor by a one-step immunoaffinity chromatography procedureT Koyama, Y Koike, Y Sugahara, et al.
Blood|July 1, 1992
Protein C deficiency Hong Kong 1 and 2: hereditary protein C deficiency caused by two mutant alleles, a 5-nucleotide deletion and a missense mutationY Sugahara, O Miura, P Yuen, et al.
Thrombosis and Haemostasis|December 1, 1994
Compound heterozygous protein C deficiency caused by two mutations, Arg-178 to Gln and Cys-331 to Arg, leading to impaired secretion of mutant protein CY Sugahara, O Miura, S Hirosawa, et al.
Journal of Biochemistry|October 1, 1987
pH-dependent membrane fusion activity of a synthetic twenty amino acid peptide with the same sequence as that of the hydrophobic segment of influenza virus hemagglutininM Murata, Y Sugahara, S Takahashi, et al.
Journal of Biochemistry|October 1, 1983
Hydrolysis of phenylthiazolones of p-guanidinophenylalanine and arginine by trypsin and related enzymesH Tsunematsu, Y Hatanaka, Y Sugahara, et al.
Pageof 5

Showing results (1-10 of 48) with videos related to

Sort By:
Pageof 5
Thrombosis and Haemostasis|March 1, 1993
Intracellular transport-deficient mutants causing hereditary deficiencies of factors involved in coagulation and fibrinolysisO Miura, Y Sugahara, N Aoki
The Journal of Biological Chemistry|October 25, 1989
Hereditary alpha 2-plasmin inhibitor deficiency caused by a transport-deficient mutation (alpha 2-PI-Okinawa). Deletion of Glu137 by a trinucleotide deletion blocks intracellular transportO Miura, Y Sugahara, N Aoki
[Kango Gijutsu] : [Nursing Technique]|February 1, 1971
[Customs concerning terminal care and death. Observation in local public health nursing activities]M Shigamura, Y Sugahara, R Takemura
Psychiatry and Clinical Neurosciences|October 24, 2000
Lithium carbonate in prophylaxis of reappearing catatonic stupor: case reportY Sugahara, H Tsukamoto, T Sasaki
Internal Medicine (Tokyo, Japan)|September 1, 1995
Evolution of severe aplastic anemia to myelodysplasia with monosomy 7 following granulocyte colony-stimulating factor, erythropoietin and high-dose methylprednisolone combination therapyA Ohsaka, Y Sugahara, Y Imai, et al.
Thrombosis Research|May 15, 1992
Purification of human alpha 2-plasmin inhibitor by a one-step immunoaffinity chromatography procedureT Koyama, Y Koike, Y Sugahara, et al.
Blood|July 1, 1992
Protein C deficiency Hong Kong 1 and 2: hereditary protein C deficiency caused by two mutant alleles, a 5-nucleotide deletion and a missense mutationY Sugahara, O Miura, P Yuen, et al.
Thrombosis and Haemostasis|December 1, 1994
Compound heterozygous protein C deficiency caused by two mutations, Arg-178 to Gln and Cys-331 to Arg, leading to impaired secretion of mutant protein CY Sugahara, O Miura, S Hirosawa, et al.
Journal of Biochemistry|October 1, 1987
pH-dependent membrane fusion activity of a synthetic twenty amino acid peptide with the same sequence as that of the hydrophobic segment of influenza virus hemagglutininM Murata, Y Sugahara, S Takahashi, et al.
Journal of Biochemistry|October 1, 1983
Hydrolysis of phenylthiazolones of p-guanidinophenylalanine and arginine by trypsin and related enzymesH Tsunematsu, Y Hatanaka, Y Sugahara, et al.
Pageof 5