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

Truncated Variants in FAM20A and WDR72 Genes Underlie Autosomal Recessive Amelogenesis Imperfecta in Four Pakistani Families

巴基斯坦四个家族中,FAM20A 和 WDR72 基因的截短变异是常染色体隐性遗传性牙釉质发育不全的病因

Ullah, Sadaqat; Khan, Sher Alam; Jan, Samin; Din, Salah Ud; Muhammad, Nazif; Rehman, Zia Ur; Jan, Abid; Tariq, Muhammad; Muhammad, Noor; Ghani, Abdul; Wasif, Naveed; Khan, Saadullah

Work-Related Stress, Professional Respect, and Psychological Counseling Among Nurses: A Cross-Sectional Study

护士的工作压力、职业尊重和心理咨询:一项横断面研究

Ullah, Hanif; Arbab, Safia; Khan, Sher Alam; Liu, Chang-Qing; Fayaz, Muhammad; Tian, Yali; Li, Ka

An integrated approach to predict genetic risk for Mosquito-Borne diseases in the local Population of Tehsil Haripur, Khyber Pakhtunkhwa, Pakistan

采用综合方法预测巴基斯坦开伯尔-普赫图赫瓦省哈里普尔县当地居民罹患蚊媒疾病的遗传风险

Basri, Rabea; Aqeel, Muslim Bin; Awan, Faryal Mehwish; Khan, Sadiq Noor; Obaid, Ayesha; Parveen, Rubina; Mohsin, Muhammad; Akhtar, Wajeeha; Shah, Abdal Hussain; Afghan, Tahira Sher; Alam, Amir; Khan, Saira; Naz, Anam

Potential therapeutic use of Indian medicinal plants for preeclampsia management

印度药用植物在先兆子痫治疗中的潜在应用

Wazib, Sheema; Ambardar, Yashesvi; Quasimi, Huma; Alam, Sushmita; Afghan, Sher; Alam, Md Iqbal

Professional Quality of Life and Psychological Impact on Frontline Healthcare Worker during the Fourth Wave of COVID-19

新冠疫情第四波期间一线医护人员的职业生活质量和心理影响

Ullah, Hanif; Arbab, Safia; Liu, Chang-Qing; Khan, Sher Alam; Shahzad, Sohail; Li, Ka

Brachyolmia, dental anomalies and short stature (DASS): Phenotype and genotype analyses of Egyptian and Pakistani patients

短身畸形、牙齿异常和矮小症(DASS):埃及和巴基斯坦患者的表型和基因型分析

Nawaz, Hamed; Parveen, Asia; Khan, Sher Alam; Zalan, Abul Khair; Khan, Muhammad Adnan; Muhammad, Noor; Hassib, Nehal F; Mostafa, Mostafa I; Elhossini, Rasha M; Roshdy, Nehal Nabil; Ullah, Asmat; Arif, Amina; Khan, Saadullah; Ammerpohl, Ole; Wasif, Naveed

Variants in HCFC1 and MN1 genes causing intellectual disability in two Pakistani families

巴基斯坦两个家庭的智力障碍是由HCFC1和MN1基因变异引起的

Hussain, Syeda Iqra; Muhammad, Nazif; Shah, Shahbaz Ali; Rehman, Adil U; Khan, Sher Alam; Saleha, Shamim; Khan, Yar Muhammad; Muhammad, Noor; Khan, Saadullah; Wasif, Naveed

Autosomal recessive variants c.953A>C and c.97-1G>C in NSUN2 causing intellectual disability: a molecular dynamics simulation study of loss-of-function mechanisms

NSUN2基因中的常染色体隐性变异c.953A>C和c.97-1G>C导致智力障碍:功能丧失机制的分子动力学模拟研究

Muhammad, Nazif; Hussain, Syeda Iqra; Rehman, Zia Ur; Khan, Sher Alam; Jan, Samin; Khan, Niamatullah; Muzammal, Muhammad; Abbasi, Sumra Wajid; Kakar, Naseebullah; Rehman, Zia Ur; Khan, Muzammil Ahmad; Mirza, Muhammad Usman; Muhammad, Noor; Khan, Saadullah; Wasif, Naveed

Biallelic Variants in Seven Different Genes Associated with Clinically Suspected Bardet-Biedl Syndrome

与临床疑似巴德-比德尔综合征相关的七个不同基因的双等位基因变异

Nawaz, Hamed; Mujahid; Khan, Sher Alam; Bibi, Farhana; Waqas, Ahmed; Bari, Abdul; Fardous; Khan, Niamatullah; Muhammad, Nazif; Khan, Amjad; Paracha, Sohail Aziz; Alam, Qamre; Kamal, Mohammad Azhar; Rafeeq, Misbahuddin M; Muhammad, Noor; Haq, Fayaz Ul; Khan, Shazia; Mahmood, Arif; Khan, Saadullah; Umair, Muhammad

Structural and functional implications of SLC13A3 and SLC9A6 mutations: an in silico approach to understanding intellectual disability

SLC13A3 和 SLC9A6 基因突变的结构和功能影响:利用计算机模拟方法理解智力障碍

Hussain, Syeda Iqra; Muhammad, Nazif; Shah, Salah Ud Din; Fardous, Fardous; Khan, Sher Alam; Khan, Niamatullah; Rehman, Adil U; Siddique, Mehwish; Wasan, Shoukat Ali; Niaz, Rooh; Ullah, Hafiz; Khan, Niamat; Muhammad, Noor; Mirza, Muhammad Usman; Wasif, Naveed; Khan, Saadullah