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

What could be the role of genetic tests and machine learning of AXIN2 variant dominance in non-syndromic hypodontia? A case-control study in orthodontically treated patients

基因检测和机器学习在非综合征性牙齿缺失中对 AXIN2 变异显性有何作用?一项针对接受正畸治疗患者的病例对照研究

Nora Alhazmi, Ali Alaqla, Bader Almuzzaini, Mohammed Aldrees, Ghaida Alnaqa, Farah Almasoud, Omar Aldibasi, Hala Alshamlan

Pharmacological p38 MAPK inhibitor SB203580 enhances AML stem cell line KG1a chemosensitivity to daunorubicin by promoting late apoptosis, cell growth arrest in S-phase, and miR-328-3p upregulation

药理学p38 MAPK抑制剂SB203580通过促进晚期细胞凋亡、S期细胞生长停滞和miR-328-3p上调,增强AML干细胞系KG1a对柔红霉素的化疗敏感性。

Sara Bahattab ,Ali Assiri ,Yazeid Alhaidan ,Thadeo Trivilegio ,Rehab AlRoshody ,Sarah Huwaizi ,Bader Almuzzaini ,Abir Alamro ,Manal Abudawood ,Zeyad Alehaideb ,Sabine Matou-Nasri

Blockade of p38 MAPK overcomes AML stem cell line KG1a resistance to 5-Fluorouridine and the impact on miRNA profiling

阻断 p38 MAPK 可克服 AML 干细胞系 KG1a 对 5-氟尿苷的抗性以及对 miRNA 分析的影响

Sabine Matou-Nasri, Maria Najdi, Nouran Abu AlSaud, Yazeid Alhaidan, Hamad Al-Eidi, Ghada Alatar, Deemah AlWadaani, Thadeo Trivilegio, Arwa AlSubait, Abeer AlTuwaijri, Manal Abudawood, Bader Almuzzaini

Interferon-induced transmembrane protein-3 genetic variant rs12252 is associated with COVID-19 mortality

干扰素诱导的跨膜蛋白 3 基因变异 rs12252 与 COVID-19 死亡率相关

Jahad Alghamdi, Manal Alaamery, Tlili Barhoumi, Mamoon Rashid, Hala Alajmi, Nasser Aljasser, Yaseen Alhendi, Hind Alkhalaf, Hanadi Alqahtani, Omer Algablan, Abdulraham I Alshaya, Nabiha Tashkandi, Salam Massadeh, Bader Almuzzaini, Salleh N Ehaideb, Mohammad Bosaeed, Kamal Ayoub, Saber Yezli, Anas Kh

Biallelic variant in DACH1, encoding Dachshund Homolog 1, defines a novel candidate locus for recessive postaxial polydactyly type A

DACH1 中的双等位基因变体(编码腊肠犬同源物 1)定义了 A 型隐性轴后多指畸形的新型候选基因座

Muhammad Umair, Oliva Palander, Muhammad Bilal, Bader Almuzzaini, Qamre Alam, Farooq Ahmad, Muhammad Younus, Amjad Khan, Ahmed Waqas, Misbahuddin M Rafeeq, Majid Alfadhel

Discovery of a novel potentially transforming somatic mutation in CSF2RB gene in breast cancer

发现乳腺癌 CSF2RB 基因中一种新型潜在转化体细胞突变

Mamoon Rashid, Rizwan Ali, Bader Almuzzaini, Hao Song, Alshaimaa AlHallaj, Al Abdulrahman Abdulkarim, Omar Mohamed Baz, Hajar Al Zahrani, Muhammed Mustafa Sabeena, Wardah Alharbi, Mohamed Hussein, Mohamed Boudjelal

Herbal melanin induces interleukin-1β secretion and production by human THP-1 monocytes via Toll-like receptor 2 and p38 MAPK activation

草本黑色素通过激活 Toll 样受体 2 和 p38 MAPK 诱导人 THP-1 单核细胞分泌和产生白细胞介素-1β。

Adila El-Obeid ,Wesam Bin Yahya ,Bader Almuzzaini ,Abeer Al Tuwaijri ,Maria Najdi ,Adil Hassib ,Sabine Matou-Nasri

β-Actin-dependent global chromatin organization and gene expression programs control cellular identity

β-肌动蛋白依赖性整体染色质组织和基因表达程序控制细胞身份

Xin Xie, Bader Almuzzaini, Nizar Drou, Stephan Kremb, Ayman Yousif, Ann-Kristin Östlund Farrants, Kristin Gunsalus, Piergiorgio Percipalle

Nuclear Wiskott-Aldrich syndrome protein co-regulates T cell factor 1-mediated transcription in T cells

核 Wiskott-Aldrich 综合征蛋白共同调节 T 细胞因子 1 介导的 T 细胞转录

Nikolai V Kuznetsov, Bader Almuzzaini, Joanna S Kritikou, Marisa A P Baptista, Mariana M S Oliveira, Marton Keszei, Scott B Snapper, Piergiorgio Percipalle, Lisa S Westerberg

In β-actin knockouts, epigenetic reprogramming and rDNA transcription inactivation lead to growth and proliferation defects

在 β-肌动蛋白敲除中,表观遗传重编程和 rDNA 转录失活导致生长和增殖缺陷

Bader Almuzzaini, Aishe A Sarshad, Aldwin S Rahmanto, Magnus L Hansson, Anne Von Euler, Olle Sangfelt, Neus Visa, Ann-Kristin Östlund Farrants, Piergiorgio Percipalle