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

Genetic predisposition to porto-sinusoidal vascular disorder: A functional genomic-based, multigenerational family study

门静脉窦血管疾病的遗传易感性:一项基于功能基因组学的多代家族研究

Shan, Jingxuan; Megarbane, André; Chouchane, Aziz; Karthik, Deepak; Temanni, Ramzi; Romero, Atilio Reyes; Hua, Huiying; Pan, Chun; Chen, Xixi; Subramanian, Murugan; Saad, Chadi; Mbarek, Hamdi; Mehawej, Cybel; Chouery, Eliane; Abuaqel, Sirin W; Dömling, Alexander; Remadi, Sami; Yaghi, Cesar; Li, Pu; Chouchane, Lotfi

The QChip1 knowledgebase and microarray for precision medicine in Qatar

卡塔尔精准医疗的 QChip1 知识库和微阵列

Juan L Rodriguez-Flores #, Radja Messai-Badji #, Amal Robay #, Ramzi Temanni, Najeeb Syed, Monika Markovic, Eiman Al-Khayat, Fatima Qafoud, Zafar Nawaz, Ramin Badii, Yasser Al-Sarraj, Hamdi Mbarek, Wadha Al-Muftah, Muhammad Alvi, Mahboubeh R Rostami, Juan Carlos Martinez Cruzado, Jason G Mezey, Alya

Transcriptome Profile Identifies Actin as an Essential Regulator of Cardiac Myosin Binding Protein C3 Hypertrophic Cardiomyopathy in a Zebrafish Model

转录组图谱表明肌动蛋白是斑马鱼模型中心脏肌球蛋白结合蛋白 C3 肥厚性心肌病的重要调节因子

Sahar Isa Da'as, Waseem Hasan, Rola Salem, Nadine Younes, Doua Abdelrahman, Iman A Mohamed, Arwa Aldaalis, Ramzi Temanni, Lisa Sara Mathew, Stephan Lorenz, Magdi Yacoub, Michail Nomikos, Gheyath K Nasrallah, Khalid A Fakhro

Genetic variations influence brain changes in patients with attention-deficit hyperactivity disorder

基因变异会影响注意力缺陷多动障碍患者的大脑变化

Yadav, Santosh K; Bhat, Ajaz A; Hashem, Sheema; Nisar, Sabah; Kamal, Madeeha; Syed, Najeeb; Temanni, Mohamed-Ramzi; Gupta, Rakesh K; Kamran, Saddat; Azeem, Muhammad Waqar; Srivastava, Amit K; Bagga, Puneet; Chawla, Sanjeev; Reddy, Ravinder; Frenneaux, Michael P; Fakhro, Khalid; Haris, Mohammad

Differential responsiveness to BRAF inhibitors of melanoma cell lines BRAF V600E-mutated

BRAF V600E 突变黑色素瘤细胞系对 BRAF 抑制剂的差异反应

Muna Al Hashmi, Konduru S Sastry, Lee Silcock, Lotfi Chouchane, Valentina Mattei, Nicola James, Rebecca Mathew, Davide Bedognetti, Valeria De Giorgi, Daniela Murtas, Wei Liu, Aouatef Chouchane, Ramzi Temanni, Barbara Seliger, Ena Wang, Francesco M Marincola, Sara Tomei

Genome sequencing unveils mutational landscape of the familial Mediterranean fever: Potential implications of IL33/ST2 signalling

基因组测序揭示家族性地中海热的突变图谱:IL33/ST2信号通路的潜在意义

Umar, Meenakshi; Megarbane, Andre; Shan, Jingxuan; Syed, Najeeb; Chouery, Eliane; Aliyev, Elbay; Jithesh, Puthen; Temanni, Ramzi; Mansour, Issam; Chouchane, Lotfi; Ismail Chouchane, Aouatef

Keratinocytes Derived from Patient-Specific Induced Pluripotent Stem Cells Recapitulate the Genetic Signature of Psoriasis Disease

来自患者特异性诱导性多能干细胞的角质形成细胞重现了银屑病的遗传特征

Gowher Ali, Ahmed K Elsayed, Manjula Nandakumar, Mohammed Bashir, Ihab Younis, Yasmin Abu Aqel, Bushra Memon, Ramzi Temanni, Fadhil Abubaker, Shahrad Taheri, Essam M Abdelalim

Monoallelic expression in melanoma

黑色素瘤中的单等位基因表达

Silcock, Lee; Almabrazi, Hakeem; Mokrab, Younes; Jithesh, Puthen; Al-Hashmi, Muna; James, Nicola; Mathew, Rebecca; Mattei, Valentina; Bedognetti, Davide; Lessi, Francesca; Temanni, Ramzi; Seliger, Barbara; Al-Ali, Rashid; Marincola, Francesco M; Wang, Ena; Tomei, Sara

Osteolytic cancer cells induce vascular/axon guidance processes in the bone/bone marrow stroma.

溶骨性癌细胞诱导骨/骨髓基质中的血管/轴突导向过程

Hensel Janine, Wetterwald Antoinette, Temanni Ramzi, Keller Irene, Riether Carsten, van der Pluijm Gabri, Cecchini Marco G, Thalmann George N

Diagnosis implications of the whole genome sequencing in a large Lebanese family with hyaline fibromatosis syndrome

全基因组测序对黎巴嫩一个患有透明纤维瘤病综合征的大家族的诊断意义

Haidar, Zahraa; Temanni, Ramzi; Chouery, Eliane; Jithesh, Puthen; Liu, Wei; Al-Ali, Rashid; Wang, Ena; Marincola, Francesco M; Jalkh, Nadine; Haddad, Soha; Haidar, Wassim; Chouchane, Lotfi; Mégarbané, André