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

Enhanced neurotropism of bovine H5N1 compared to the Vietnam H5N1 isolate in C57BL/6J mice.

与越南 H5N1 分离株相比,牛源 H5N1 对 C57BL/6J 小鼠具有更强的嗜神经性

Goldin Kerry, van Tol Sarah, Johnson Randall C, Mukesh Reshma Koolaparambil, Cooper Kendal G, Gallogly Shane, Schulz Jonathan E, Prado-Smith Jessica, Martens Craig, Saturday Greg, Yinda Kwe Claude, Munster Vincent J, de Wit Emmie, van Doremalen Neeltje

NPHS2 V260E Is a Frequent Cause of Steroid-Resistant Nephrotic Syndrome in Black South African Children

NPHS2 V260E 是南非黑人儿童类固醇抵抗性肾病综合征的常见病因

Asharam, Kareshma; Bhimma, Rajendra; David, Victor A; Coovadia, Hoosen M; Qulu, Wenkosi P; Naicker, Thajasvarie; Gillies, Christopher E; Vega-Warner, Virginia; Johnson, Randall C; Limou, Sophie; Kopp, Jeffrey B; Sampson, Mathew; Nelson, George W; Winkler, Cheryl A

Synthesis and Biological Evaluation of Fluorescent Bryostatin Analogues

荧光布里奥司他汀类似物的合成及生物学评价

Cummins, Thomas J; Kedei, Noemi; Czikora, Agnes; Lewin, Nancy E; Kirk, Sharon; Petersen, Mark E; McGowan, Kevin M; Chen, Jin-Qiu; Luo, Xiaoling; Johnson, Randall C; Ravichandran, Sarangan; Blumberg, Peter M; Keck, Gary E

Common Genetic Variants Found in HLA and KIR Immune Genes in Autism Spectrum Disorder

自闭症谱系障碍中HLA和KIR免疫基因的常见遗传变异

Torres, Anthony R; Sweeten, Thayne L; Johnson, Randall C; Odell, Dennis; Westover, Jonna B; Bray-Ward, Patricia; Ward, David C; Davies, Christopher J; Thomas, Aaron J; Croen, Lisa A; Benson, Michael

ALDsuite: Dense marker MALD using principal components of ancestral linkage disequilibrium

ALDsuite:利用祖先连锁不平衡的主成分进行密集标记MALD分析

Johnson, Randall C; Nelson, George W; Zagury, Jean-Francois; Winkler, Cheryl A

Activating killer-cell immunoglobulin-like receptors (KIR) and their cognate HLA ligands are significantly increased in autism

自闭症患者体内激活型杀伤细胞免疫球蛋白样受体(KIR)及其相应的HLA配体显著增加

Torres, Anthony R; Westover, Jonna B; Gibbons, Cole; Johnson, Randall C; Ward, David C

APOL1 genetic variants in focal segmental glomerulosclerosis and HIV-associated nephropathy

APOL1基因变异与局灶节段性肾小球硬化症和HIV相关肾病有关

Kopp, Jeffrey B; Nelson, George W; Sampath, Karmini; Johnson, Randall C; Genovese, Giulio; An, Ping; Friedman, David; Briggs, William; Dart, Richard; Korbet, Stephen; Mokrzycki, Michele H; Kimmel, Paul L; Limou, Sophie; Ahuja, Tejinder S; Berns, Jeffrey S; Fryc, Justyna; Simon, Eric E; Smith, Michael C; Trachtman, Howard; Michel, Donna M; Schelling, Jeffrey R; Vlahov, David; Pollak, Martin; Winkler, Cheryl A

Differential effects of MYH9 and APOL1 risk variants on FRMD3 Association with Diabetic ESRD in African Americans

MYH9 和 APOL1 风险变异对 FRMD3 与非裔美国人糖尿病终末期肾病关联性的差异性影响

Freedman, Barry I; Langefeld, Carl D; Lu, Lingyi; Divers, Jasmin; Comeau, Mary E; Kopp, Jeffrey B; Winkler, Cheryl A; Nelson, George W; Johnson, Randall C; Palmer, Nicholette D; Hicks, Pamela J; Bostrom, Meredith A; Cooke, Jessica N; McDonough, Caitrin W; Bowden, Donald W

MHC heterozygote advantage in simian immunodeficiency virus-infected Mauritian cynomolgus macaques

感染猴免疫缺陷病毒的毛里求斯食蟹猴中MHC杂合子的优势

O'Connor, Shelby L; Lhost, Jennifer J; Becker, Ericka A; Detmer, Ann M; Johnson, Randall C; Macnair, Caitlin E; Wiseman, Roger W; Karl, Julie A; Greene, Justin M; Burwitz, Benjamin J; Bimber, Benjamin N; Lank, Simon M; Tuscher, Jennifer J; Mee, Edward T; Rose, Nicola J; Desrosiers, Ronald C; Hughes, Austin L; Friedrich, Thomas C; Carrington, Mary; O'Connor, David H

Accounting for multiple comparisons in a genome-wide association study (GWAS)

在全基因组关联研究(GWAS)中考虑多重比较

Johnson, Randall C; Nelson, George W; Troyer, Jennifer L; Lautenberger, James A; Kessing, Bailey D; Winkler, Cheryl A; O'Brien, Stephen J