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

Biomarker and drug-target discovery using proteomics in a new rat model of sepsis-induced acute renal failure.

利用蛋白质组学在脓毒症诱发急性肾衰竭的大鼠模型中进行生物标志物和药物靶点发现

Holly M K, Dear J W, Hu X, Schechter A N, Gladwin M T, Hewitt S M, Yuen P S T, Star R A

Quantitative analysis of globin gene induction in single human erythroleukemic cells

对单个人类红白血病细胞中珠蛋白基因诱导的定量分析

Smith, R D; Malley, J D; Schechter, A N

Role of circulating nitrite and S-nitrosohemoglobin in the regulation of regional blood flow in humans

循环亚硝酸盐和S-亚硝基血红蛋白在人体区域血流调节中的作用

Gladwin, M T; Shelhamer, J H; Schechter, A N; Pease-Fye, M E; Waclawiw, M A; Panza, J A; Ognibene, F P; Cannon, R O 3rd

Inhaled nitric oxide augments nitric oxide transport on sickle cell hemoglobin without affecting oxygen affinity

吸入一氧化氮可增强镰状细胞血红蛋白上的一氧化氮转运,而不影响氧亲和力。

Gladwin, M T; Schechter, A N; Shelhamer, J H; Pannell, L K; Conway, D A; Hrinczenko, B W; Nichols, J S; Pease-Fye, M E; Noguchi, C T; Rodgers, G P; Ognibene, F P

Modifications of RNA processing modulate the expression of hemoglobin genes

RNA加工过程的改变会调节血红蛋白基因的表达。

Kollia, P; Fibach, E; Najjar, S M; Schechter, A N; Noguchi, C T

Influence of sickle hemoglobin polymerization and membrane properties on deformability of sickle erythrocytes in the microcirculation

镰状血红蛋白聚合和膜特性对微循环中镰状红细胞变形能力的影响

Dong, C; Chadwick, R S; Schechter, A N

Effects of alpha-thalassemia and sickle polymerization tendency on the urine-concentrating defect of individuals with sickle cell trait

α-地中海贫血和镰状细胞聚合倾向对镰状细胞性状携带者尿液浓缩功能障碍的影响

Gupta, A K; Kirchner, K A; Nicholson, R; Adams, J G 3rd; Schechter, A N; Noguchi, C T; Steinberg, M H

Identification of a transcriptional silencer in the 5'-flanking region of the human epsilon-globin gene

人类ε-珠蛋白基因5'侧翼区转录沉默子的鉴定

Cao, S X; Gutman, P D; Dave, H P; Schechter, A N

Alpha thalassemia changes erythrocyte heterogeneity in sickle cell disease

α地中海贫血会改变镰状细胞病中红细胞的异质性

Noguchi, C T; Dover, G J; Rodgers, G P; Serjeant, G R; Antonarakis, S E; Anagnou, N P; Higgs, D R; Weatherall, D J; Schechter, A N

A beta-globin gene, inactive in the K562 leukemic cell, functions normally in a heterologous expression system

在K562白血病细胞中失活的β-珠蛋白基因,在异源表达系统中却能正常发挥功能。

Fordis, C M; Anagnou, N P; Dean, A; Nienhuis, A W; Schechter, A N