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T Shigekiyo

Showing results (1-10 of 49) with videos related to

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Ryoikibetsu Shokogun Shirizu|December 2, 1998
[Congenital histidine-rich glycoprotein deficiency]T Shigekiyo
International Journal of Hematology|August 1, 1992
Replacement therapy in a patient with congenital prekallikrein deficiency undergoing surgeryT Shigekiyo, O Fujino
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|April 1, 1993
[Gammaglobulin infusion therapy in a patient with antiphospholipid syndrome]M Takagi, T Shigekiyo
Ryoikibetsu Shokogun Shirizu|December 16, 1998
[Congenital hypoplasminogenemia and dysplasminogenemia (type I and type II congenital plasminogen deficiency)]T Shigekiyo, H Azuma
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|March 1, 1990
[Congenital plasminogen deficiency in a Japanese family]Y Uno, T Shigekiyo, S Saito
Central European Journal of Public Health|January 1, 1995
High level of plasma thrombomodulin (TM) concentration and correlation with endothelin (ET)-1 in vibration-exposed patientsN Toibana, M Kanazuka, T Shigekiyo
Journal of Biochemistry|August 2, 2000
Intracellular degradation of histidine-rich glycoprotein mutants: tokushima-1 and 2 mutants are degraded by different proteolytic systemsS Wakabayashi, H Yoshida, T Shigekiyo, et al.
Journal of Thrombosis and Haemostasis : JTH|July 23, 2003
Prekallikrein (PK) Tokushima: PK deficiency caused by a Gly401-->Glu mutationT Shigekiyo, O Fujino, Y Kanagawa, et al.
Thrombosis Research|April 1, 1996
Increase in plasma thrombomodulin level in patients with vibration syndromeM Kanazuka, T Shigekiyo, N Toibana, et al.
Thrombosis and Haemostasis|January 1, 1996
A novel missense mutation in two families with congenital plasminogen deficiency: identification of an Ala675 to Thr675 substitutionN Mima, H Azuma, T Shigekiyo, et al.
Pageof 5

Showing results (1-10 of 49) with videos related to

Sort By:
Pageof 5
Ryoikibetsu Shokogun Shirizu|December 2, 1998
[Congenital histidine-rich glycoprotein deficiency]T Shigekiyo
International Journal of Hematology|August 1, 1992
Replacement therapy in a patient with congenital prekallikrein deficiency undergoing surgeryT Shigekiyo, O Fujino
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|April 1, 1993
[Gammaglobulin infusion therapy in a patient with antiphospholipid syndrome]M Takagi, T Shigekiyo
Ryoikibetsu Shokogun Shirizu|December 16, 1998
[Congenital hypoplasminogenemia and dysplasminogenemia (type I and type II congenital plasminogen deficiency)]T Shigekiyo, H Azuma
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|March 1, 1990
[Congenital plasminogen deficiency in a Japanese family]Y Uno, T Shigekiyo, S Saito
Central European Journal of Public Health|January 1, 1995
High level of plasma thrombomodulin (TM) concentration and correlation with endothelin (ET)-1 in vibration-exposed patientsN Toibana, M Kanazuka, T Shigekiyo
Journal of Biochemistry|August 2, 2000
Intracellular degradation of histidine-rich glycoprotein mutants: tokushima-1 and 2 mutants are degraded by different proteolytic systemsS Wakabayashi, H Yoshida, T Shigekiyo, et al.
Journal of Thrombosis and Haemostasis : JTH|July 23, 2003
Prekallikrein (PK) Tokushima: PK deficiency caused by a Gly401-->Glu mutationT Shigekiyo, O Fujino, Y Kanagawa, et al.
Thrombosis Research|April 1, 1996
Increase in plasma thrombomodulin level in patients with vibration syndromeM Kanazuka, T Shigekiyo, N Toibana, et al.
Thrombosis and Haemostasis|January 1, 1996
A novel missense mutation in two families with congenital plasminogen deficiency: identification of an Ala675 to Thr675 substitutionN Mima, H Azuma, T Shigekiyo, et al.
Pageof 5