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

Comparative characterisation of human and ovine non-aureus staphylococci isolated in Sardinia (Italy) for antimicrobial susceptibility profiles and resistance genes

对意大利撒丁岛分离的人类和绵羊非金黄色葡萄球菌进行抗菌药物敏感性谱和耐药基因的比较表征

Longheu, C M; Azara, E; Attene, S; Sanna, S; Sale, M; Addis, M F; Tola, S

Circulating cellular adhesion molecules and risk of diabetes: the Multi-Ethnic Study of Atherosclerosis (MESA).

循环细胞粘附分子与糖尿病风险:动脉粥样硬化多民族研究(MESA)

Pankow J S, Decker P A, Berardi C, Hanson N Q, Sale M, Tang W, Kanaya A M, Larson N B, Tsai M Y, Wassel C L, Bielinski S J

The N-DRC forms a conserved biochemical complex that maintains outer doublet alignment and limits microtubule sliding in motile axonemes

N-DRC 形成保守的生化复合物,维持外部双链排列并限制运动轴丝中的微管滑动

Raqual Bower, Douglas Tritschler, Kristyn Vanderwaal, Catherine A Perrone, Joshua Mueller, Laura Fox, Winfield S Sale, M E Porter

Genetic admixture is associated with plasma hemostatic factor levels in self-identified African Americans and Hispanics: the Multi-Ethnic Study of Atherosclerosis

基因混合与自我认同为非裔美国人和西班牙裔人群的血浆止血因子水平相关:动脉粥样硬化多民族研究

Lutsey, P L; Wassel, C L; Cushman, M; Sale, M M; Divers, J; Folsom, A R

Transcobalamin 2 variant associated with poststroke homocysteine modifies recurrent stroke risk

与卒中后同型半胱氨酸相关的转钴胺素2变异体可改变复发性卒中风险

Hsu, F-C; Sides, E G; Mychaleckyj, J C; Worrall, B B; Elias, G A; Liu, Y; Chen, W-M; Coull, B M; Toole, J F; Rich, S S; Furie, K L; Sale, M M

Variants in intron 13 of the ELMO1 gene are associated with diabetic nephropathy in African Americans

ELMO1基因第13号内含子的变异与非裔美国人的糖尿病肾病相关

Leak, T S; Perlegas, P S; Smith, S G; Keene, K L; Hicks, P J; Langefeld, C D; Mychaleckyj, J C; Rich, S S; Kirk, J K; Freedman, B I; Bowden, D W; Sale, M M

A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetrance

连接蛋白46基因的一种新突变导致常染色体显性遗传性先天性白内障,且外显率不完全。

Burdon, K P; Wirth, M G; Mackey, D A; Russell-Eggitt, I M; Craig, J E; Elder, J E; Dickinson, J L; Sale, M M

Investigation of crystallin genes in familial cataract, and report of two disease associated mutations

对家族性白内障中晶状体蛋白基因的研究,并报告了两种与疾病相关的突变

Burdon, K P; Wirth, M G; Mackey, D A; Russell-Eggitt, I M; Craig, J E; Elder, J E; Dickinson, J L; Sale, M M

Investigation of chromosome 2q in osteoarthritis of the hand: no significant linkage in a Tasmanian population

对2q染色体与手部骨关节炎的研究:在塔斯马尼亚人群中未发现显著连锁关系

Stankovich, J; Sale, M M; Cooley, H M; Bahlo, M; Reilly, A; Dickinson, J L; Jones, G

Retinopathy of prematurity: recent advances in our understanding

早产儿视网膜病变:我们认识的最新进展

Wheatley, C M; Dickinson, J L; Mackey, D A; Craig, J E; Sale, M M