日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Gene transfer in vivo: sustained expression and regulation of genes introduced into the liver by receptor-targeted uptake

体内基因转移:通过受体靶向摄取将基因导入肝脏后,基因的持续表达和调控

Perales, J C; Ferkol, T; Beegen, H; Ratnoff, O D; Hanson, R W

Inhibition of the activation of Hageman factor (factor XII) by peripheral blood cells

外周血细胞对哈格曼因子(因子XII)活化的抑制

Ratnoff, O D; Emanuelson, M M; Ziats, N P

Inherited incomplete deficiency of the fourth component of complement (C4) determined by a gene not linked to human histocompatibility leukocyte antigens

由与人类组织相容性白细胞抗原无关的基因决定的补体第四成分(C4)遗传性不完全缺乏症

Muir, W A; Hedrick, S; Alper, C A; Ratnoff, O D; Schacter, B; Wisnieski, J J

Activation of the alternative complement pathway by Histoplasma capsulatum

荚膜组织胞浆菌激活替代补体途径

Ratnoff, W D; Pepple, J M; Winkelstein, J A

Interactions among Hageman factor, plasma prekallikrein, high molecular weight kininogen, and plasma thromboplastin antecedent

Hageman因子、血浆前激肽释放酶、高分子量激肽原和血浆凝血活酶前体之间的相互作用

Ratnoff, O D; Saito, H

Amidolytic properties of single-chain activated Hageman factor

单链活化哈格曼因子的酰胺水解特性

Ratnoff, O D; Saito, H

The secondary structure of human Hageman factor (factor XII) and its alteration by activating agents

人哈格曼因子(因子XII)的二级结构及其被激活剂改变的情况

McMillin, C R; Saito, H; Ratnoff, O D; Walton, A G

Studies on the response of patients with classic hemophilia to transfusion with concentrates of antihemophilic factor. A difference in the half-life of antihemophilic factor as measured by procoagulant and immunologic techniques

研究经典型血友病患者对输注浓缩抗血友病因子的反应。采用促凝和免疫学技术测定抗血友病因子半衰期的差异。

Bennett, B; Ratnoff, O D

Immunologic studies in von Willebrand's disease. Evidence that the antihemophilic factor (AHF) produced after transfusions lacks an antigen associated with normal AHF and the inactive material produced by patients with classic hemophilia

血管性血友病免疫学研究。证据表明,输血后产生的抗血友病因子 (AHF) 缺乏与正常 AHF 和经典血友病患者产生的非活性物质相关的抗原。

Bennett, B; Ratnoff, O D; Levin, J

Immunologic differentiation of classic hemophilia (factor 8 deficiency) and von Willebrand's dissase, with observations on combined deficiencies of antihemophilic factor and proaccelerin (factor V) and on an acquired circulating anticoagulant against antihemophilic factor

经典血友病(因子V缺乏症)和血管性血友病的免疫学鉴别,以及抗血友病因子和促凝血因子V(前加速因子)联合缺乏症和获得性循环抗凝血因子的情况的观察

Zimmerman, T S; Ratnoff, O D; Powell, A E