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

Replication and Functional Prediction of Two GWAS-Reported SNPs Located on RAD50 Gene Associated with Asthma in Pakistani Children

对巴基斯坦儿童哮喘相关的位于RAD50基因上的两个GWAS报告的SNP进行复制和功能预测

Ghani, Muhammad Usman; Sabar, Muhammad Farooq; Bano, Iqbal; Ain, Qurat-Ul; Shahid, Mariam; Mehdi, Zohair; Khan, Muhammad Umer

Ethnogenetic analysis reveals the Bronze Age genetic affiliation of Yashkuns with West Eurasians.

民族遗传学分析揭示了青铜时代亚什昆人与西欧亚人的遗传联系

Khan Muhammad Umer, Zahid Tazeen, Sabar Muhammad Farooq, Masood Tayyaba, Ali Qurban, Han Shiming, Ahmad Ajaz

Genetic Variations on Chromosome 6p21 Are Associated with Asthma Risk and Disease Severity: A Case-Control Study from Pakistan

巴基斯坦一项病例对照研究表明,6p21染色体上的基因变异与哮喘风险和疾病严重程度相关。

Aslam, Aqsa; Vijverberg, Susanne J H; Zee, Anke-Hilse Maitland-van der; Sabar, Muhammad Farooq

Dilemmas in the Diagnosis and Management of CML in Pakistan

巴基斯坦慢性粒细胞白血病诊断和治疗中的困境

Khan, Sahrish; Sabar, Muhammad Farooq; Akbar, Mariyam; Waris, Abdul

Role of Vascular Endothelial Growth Factor as a Potential Biomarker in Congenital Heart Defects: A Systematic Review

血管内皮生长因子作为先天性心脏缺陷潜在生物标志物的作用:系统评价

Ashiq, Sana; Hyder, Syed Najam; Ashiq, Kanwal; Sabar, Muhammad Farooq

The role of NKX2-5 gene polymorphisms in congenital heart disease (CHD): a systematic review and meta-analysis

NKX2-5基因多态性在先天性心脏病(CHD)中的作用:系统评价和荟萃分析

Ashiq, Sana; Ashiq, Kanwal; Sabar, Muhammad Farooq

Detection of Exon 12 and 14 Mutations in Janus Kinase 2 Gene Including a Novel Mutant in V617F Negative Polycythemia Vera Patients from Pakistan

在巴基斯坦真性红细胞增多症V617F阴性患者中检测到Janus激酶2基因第12和14外显子突变,包括一种新的突变体

Akram, Afia Muhammad; Kausar, Humera; Chaudhary, Asma; Khalid, Ahmad Mukhtar; Shahzad, Muhammad Mudassar; Akhtar, Muhammad Waheed; Sabar, Muhammad Farooq; Sajid, Nadia; Anazi, Nawaf Al; Aleem, Aamer; Iqbal, Zafar

Presence of novel compound BCR-ABL mutations in late chronic and advanced phase imatinib sensitive CML patients indicates their possible role in CML progression

在晚期慢性期和进展期伊马替尼敏感的慢性粒细胞白血病(CML)患者中发现新的复合型BCR-ABL突变,表明这些突变可能在CML进展中发挥作用。

Akram, Afia Muhammad; Iqbal, Zafar; Akhtar, Tanveer; Khalid, Ahmed Mukhtar; Sabar, Muhammad Farooq; Qazi, Mahmood Hussain; Aziz, Zeba; Sajid, Nadia; Aleem, Aamer; Rasool, Mahmood; Asif, Muhammad; Aloraibi, Saleh; Aljamaan, Khaled; Iqbal, Mudassar