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

Strategies to improve pharmacogenomic-guided treatment options for patients with β-hemoglobinopathies

改善β-血红蛋白病患者药物基因组学指导治疗方案的策略

Patrinos, George P; Chui, David H K; Hardison, Ross C; Steinberg, Martin H

A phased SNP-based classification of sickle cell anemia HBB haplotypes

基于SNP的镰状细胞贫血HBB单倍型分期分类

Shaikho, Elmutaz M; Farrell, John J; Alsultan, Abdulrahman; Qutub, Hatem; Al-Ali, Amein K; Figueiredo, Maria Stella; Chui, David H K; Farrer, Lindsay A; Murphy, George J; Mostoslavsky, Gustavo; Sebastiani, Paola; Steinberg, Martin H

The clinical severity of hemoglobin S/Black ((A) γδβ)(0) -thalassemia

血红蛋白S/黑((A)γδβ)(0)-地中海贫血的临床严重程度

Cancio, Maria I; Aygun, Banu; Chui, David H K; Rothman, Jennifer A; Scott, J Paul; Estepp, Jeremie H; Hankins, Jane S

A candidate transacting modulator of fetal hemoglobin gene expression in the Arab-Indian haplotype of sickle cell anemia

镰状细胞贫血症阿拉伯-印度单倍型中胎儿血红蛋白基因表达的候选转录调节因子

Vathipadiekal, Vinod; Farrell, John J; Wang, Shuai; Edward, Heather L; Shappell, Heather; Al-Rubaish, A M; Al-Muhanna, Fahad; Naserullah, Z; Alsuliman, A; Qutub, Hatem Othman; Simkin, Irene; Farrer, Lindsay A; Jiang, Zhihua; Luo, Hong-Yuan; Huang, Shengwen; Mostoslavsky, Gustavo; Murphy, George J; Patra, Pradeep K; Chui, David H K; Alsultan, Abdulrahman; Al-Ali, Amein K; Sebastiani, Paola; Steinberg, Martin H

Homozygosity for a haplotype in the HBG2-OR51B4 region is exclusive to Arab-Indian haplotype sickle cell anemia

HBG2-OR51B4 区域单倍型的纯合性是阿拉伯-印度单倍型镰状细胞贫血症所特有的。

Vathipadiekal, Vinod; Alsultan, Abdulrahman; Baltrusaitis, Kristin; Farrell, John J; Al-Rubaish, Abdullah M; Al-Muhanna, Fahad; Naserullah, Zaki; Suliman, Ahmed; Patra, P K; Milton, Jacqueline N; Farrer, Lindsay A; Chui, David H K; Al-Ali, Amein K; Sebastiani, Paola; Steinberg, Martin H

The genetics of hemoglobin A2 regulation in sickle cell anemia

镰状细胞贫血症中血红蛋白A2调控的遗传学

Griffin, Paula J; Sebastiani, Paola; Edward, Heather; Baldwin, Clinton T; Gladwin, Mark T; Gordeuk, Victor R; Chui, David H K; Steinberg, Martin H

A phase 2 study of HQK-1001, an oral fetal haemoglobin inducer, in β-thalassaemia intermedia

一项针对中间型β-地中海贫血患者的II期临床研究,评估口服胎儿血红蛋白诱导剂HQK-1001的疗效。

Inati, Adlette; Kahale, Mario; Perrine, Susan P; Chui, David H K; Taher, Ali T; Koussa, Suzanne; Abi Nasr, Therese; Abbas, Hussein A; Ghalie, Richard G

Sickle cell disease in Saudi Arabia: the phenotype in adults with the Arab-Indian haplotype is not benign

沙特阿拉伯的镰状细胞病:携带阿拉伯-印度单倍型的成年人表型并非良性

Alsultan, Abdulrahman; Alabdulaali, Mohammed K; Griffin, Paula J; Alsuliman, Ahmed M; Ghabbour, Hazem A; Sebastiani, Paola; Albuali, Waleed H; Al-Ali, Amein K; Chui, David H K; Steinberg, Martin H

The aryl hydrocarbon receptor directs hematopoietic progenitor cell expansion and differentiation.

芳烃受体指导造血祖细胞的扩增和分化

Smith Brenden W, Rozelle Sarah S, Leung Amy, Ubellacker Jessalyn, Parks Ashley, Nah Shirley K, French Deborah, Gadue Paul, Monti Stefano, Chui David H K, Steinberg Martin H, Frelinger Andrew L, Michelson Alan D, Theberge Roger, McComb Mark E, Costello Catherine E, Kotton Darrell N, Mostoslavsky Gustavo, Sherr David H, Murphy George J

Fetal hemoglobin in sickle cell anemia: genetic studies of the Arab-Indian haplotype

镰状细胞贫血症中的胎儿血红蛋白:阿拉伯-印度单倍型的遗传学研究

Ngo, Duyen; Bae, Harold; Steinberg, Martin H; Sebastiani, Paola; Solovieff, Nadia; Baldwin, Clinton T; Melista, Efthymia; Safaya, Surinder; Farrer, Lindsay A; Al-Suliman, Ahmed M; Albuali, Waleed H; Al Bagshi, Muneer H; Naserullah, Zaki; Akinsheye, Idowu; Gallagher, Patrick; Luo, Hong-yuan; Chui, David H K; Farrell, John J; Al-Ali, Amein K; Alsultan, Abdulrahman