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

Progressive Elevation of Store-Operated Calcium Entry-Associated Regulatory Factor (SARAF) and Calcium Pathway Dysregulation in Multiple Sclerosis

多发性硬化症中储存操纵性钙内流相关调节因子(SARAF)的进行性升高和钙通路失调

Taha, Safa; Aljishi, Muna; Sultan, Ameera; Al-Nashmi, Moudi E; Bakhiet, Moiz; Spicuglia, Salvatore; Belhocine, Mohamed

Calcium Homeostasis Disrupted-How Store-Operated Calcium Entry Factor SARAF Silencing Impacts HepG2 Liver Cancer Cells

钙稳态紊乱——SARAF基因沉默如何影响HepG2肝癌细胞

Taha, Safa; Aljishi, Muna; Sultan, Ameera; Bakhiet, Moiz

The Whole Blood Transcriptomic Analysis in Sickle Cell Disease Reveals RUNX3 as a Potential Marker for Vaso-Occlusive Crises

镰状细胞病全血转录组分析揭示RUNX3是血管阻塞危象的潜在标志物

Taha, Safa; Abdulwahab, Hawra; Aljishi, Muna; Sultan, Ameera; Bakhiet, Moiz; Spicuglia, Salvatore; Belhocine, Mohamed

Enhanced Cytotoxicity and Receptor Modulation by SMA-WIN 55,212-2 Micelles in Glioblastoma Cells.

SMA-WIN 55,212-2 胶束增强胶质母细胞瘤细胞的细胞毒性和受体调节作用

Taha Safa, Aljishi Muna, Sultan Ameera, Sridharan Kannan, Taurin Sebastien, Greish Khaled, Bakhiet Moiz

Molecular insights into T cell development, activation and signal transduction (Review)

T细胞发育、激活和信号转导的分子机制研究(综述)

Omar, Isra; Alakhras, Ahmed; Mutwali, Samahir; Bakhiet, Moiz

Plasminogen activator inhibitor-2 and impaired fibrinolysis in pregnancy and sickle cell anemia

妊娠期和镰状细胞贫血症中的纤溶酶原激活物抑制剂-2和纤溶功能障碍

Shome, Durjoy; Al-Jamea, Lamiaa; Woodman, Alexander; Salem, Abdel Halim; Bakhiet, Moiz; Taha, Safa; Sandhu, Amarjit Kaur; Al-Yami, Fatimah S; Waheed, Khawaja Bilal; Elnagi, Elmoeiz Ali; Almish, Mohammed; Quiambao, Jenifer Vecina

A Rare 46,X,t(Y;10)(q12;p14) Balanced Translocation in Non-Obstructive Azoospermic Patient with Elevated FSH and LH Levels

一例罕见的46,X,t(Y;10)(q12;p14)平衡易位,发生于非梗阻性无精子症患者,伴有FSH和LH水平升高

Jahan Syeeda Khursheed, Kousar; Rahman Kaleemullah, Mohammed; Joseph, Annu; Hasan Al Durazi, Mohammed; Bakhiet, Moiz

Mitochondrial DNA haplogroup analysis in Saudi Arab patients with multiple sclerosis

沙特阿拉伯多发性硬化症患者的线粒体DNA单倍群分析

Al-Kafaji, Ghada; Alwehaidah, Materah Salem; Alsabbagh, Manahel Mahmood; Alharbi, Maram A; Bakhiet, Moiz

Next-generation sequencing of the whole mitochondrial genome identifies functionally deleterious mutations in patients with multiple sclerosis

对整个线粒体基因组进行新一代测序,可识别多发性硬化症患者体内功能有害的突变

Al-Kafaji, Ghada; Bakheit, Halla F; AlAli, Faisal; Fattah, Mina; Alhajeri, Saad; Alharbi, Maram A; Daif, Abdulqader; Alsabbagh, Manahel Mahmood; Alwehaidah, Materah Salem; Bakhiet, Moiz

Clinical delineation of myasthenia gravis in the Kingdom of Bahrain

巴林王国重症肌无力的临床描述

Binfalah, Mohamed F; Alhafnawi, Hussein H; Jaradat, Ahmed A; Shosha, Eslam; Alhilly, Ali J; Al Nidawi, Firas K; Alhammadi, Mariam M; Bakhiet, Moiz O; Abdulla, Fatema M