Genetic advances in skeletal disorders: an overview by Safdar Abbas, Hammal Khan, Qamre Alam, Arif Mahmood, Muhammad Umair

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MDR1 Gene Polymorphisms and Its Association With Expression as a Clinical Relevance in Terms of Response to Chemotherapy and Prognosis in Ovarian Cancer by Absarul Haque, Absarul Haque, Khalid Hussain Wali Sait, Qamre Alam, Qamre Alam, Mohammad Zubair Alam, Mohammad Zubair Alam, Nisreen Anfinan, Abdul Wahab Noor Wali, Abdul Wahab Noor Wali, Mahmood Rasool, Mahmood Rasool

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Dimethoate Induces DNA Damage and Mitochondrial Dysfunction Triggering Apoptosis in Rat Bone-Marrow and Peripheral Blood Cells by Nazia Nazam, Mohammad Iqbal Lone, Abid Hamid, Talal Qadah, Alaa Banjar, Qamre Alam, Mohd Saeed, Waseem Ahmad

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Novel homozygous pathogenic mitochondrial DNAJC19 variant in a patient with dilated cardiomyopathy and global developmental delay by Abeer Al Tuwaijri, Yusra Alyafee, Mashael Alharbi, Maryam Ballow, Mohammed Aldrees, Qamre Alam, Rola A. Sleiman, Muhammad Umair, Majid Alfadhel

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Next-Generation Sequencing-Based Pre-Implantation Genetic Testing for Aneuploidy (PGT-A): First Report from Saudi Arabia by Yusra Alyafee, Qamre Alam, Abeer Al Tuwaijri, Muhammad Umair, Shahad Haddad, Meshael Alharbi, Hayat Alrabiah, Maha Al-Ghuraibi, Sahar Al-Showaier, Majid Alfadhel

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Microneedles Drug Delivery Systems for Treatment of Cancer: A Recent Update by Aravindram Attiguppe Seetharam, Hani Choudhry, Muhammed A. Bakhrebah, Wesam H. Abdulaal, Maram Suresh Gupta, Syed Mohd Danish Rizvi, Qamre Alam, Siddaramaiah, Devegowda Vishakante Gowda, Afrasim Moin

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Congenital disorder of glycosylation with defective fucosylation 2 (FCSK gene defect): The third report in the literature with a mild phenotype by Abeer Al Tuwaijri, Yusra Alyafee, Muhammad Umair, Arwa Alsubait, Mashael Alharbi, Hamad AlEidi, Mariam Ballow, Mohammed Aldrees, Qamre Alam, Abdulkareem Al Abdulrahman, Muhammad Talal Alrifai, Majid Alfadhel

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Next Generation Sequencing Based Non-invasive Prenatal Testing (NIPT): First Report From Saudi Arabia by Yusra Alyafee, Abeer Al Tuwaijri, Qamre Alam, Muhammad Umair, Shahad Haddad, Mashael Alharbi, Maryam Ballow, Mohammed Al Drees, Abdulkareem AlAbdulrahman, Aziza Al Khaldi, Majid Alfadhel, Majid Alfadhel

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Case report: A novel de novo loss of function variant in the DNA-binding domain of TBX2 causes severe osteochondrodysplasia by Misbahuddin M. Rafeeq, Hussam Aly Sayed Murad, Najumuddin, Samee Ullah, Zaheer Ahmed, Qamre Alam, Muhammad Bilal, Alaa Hamed Habib, Ziaullah M. Sain, Muhammad Jawad Khan, Muhammad Umair, Muhammad Umair

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Loss-of-function variant in the LRR domain of SLITRK2 implicated in a neurodevelopmental disorder by Tayyaba Afsar, Tayyaba Afsar, Hongxia Fu, Hammal Khan, Zain Ali, Zamrud Zehri, Gohar Zaman, Safdar Abbas, Arif Mahmood, Qamre Alam, Junjian Hu, Suhail Razak, Suhail Razak, Muhammad Umair, Muhammad Umair

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Targeting Kaposi’s sarcoma associated herpesvirus encoded protease (ORF17) by a lysophosphatidic acid molecule for treating KSHV associated diseases by Misbahuddin M Rafeeq, Alaa Hamed Habib, Alaa F. Nahhas, Najat Binothman, Majidah Aljadani, Jawaher Almulhim, Ziaullah M Sain, Mohammad Zubair Alam, Mohammad Zubair Alam, Norah A Alturki, Qamre Alam, Manish Manish, Rajnish Kumar Singh

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Biocomputational Prediction Approach Targeting FimH by Natural SGLT2 Inhibitors: A Possible Way to Overcome the Uropathogenic Effect of SGLT2 Inhibitor Drugs by Mutaib M. Mashraqi, Navaneet Chaturvedi, Qamre Alam, Saleh Alshamrani, Mosa M. Bahnass, Khurshid Ahmad, Amany I. Alqosaibi, Mashael M. Alnamshan, Syed Sayeed Ahmad, Mirza Masroor Ali Beg, Abha Mishra, Sibhghatulla Shaikh, Syed Mohd Danish Rizvi

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Non-invasive prenatal testing for autosomal recessive disorders: A new promising approach by Yusra Alyafee, Abeer Al Tuwaijri, Abeer Al Tuwaijri, Muhammad Umair, Mashael Alharbi, Shahad Haddad, Maryam Ballow, Latifah Alayyar, Qamre Alam, Saleh Althenayyan, Nadia Al Ghilan, Aziza Al Khaldi, Majid S. Faden, Hamad Al Sufyan, Majid Alfadhel, Majid Alfadhel

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Case Report: Biallelic Variant in the tRNA Methyltransferase Domain of the AlkB Homolog 8 Causes Syndromic Intellectual Disability by Ahmed Waqas, Anam Nayab, Shabnam Shaheen, Safdar Abbas, Muhammad Latif, Misbahuddin M. Rafeeq, Ibtesam S. Al-Dhuayan, Amany I. Alqosaibi, Mashael M. Alnamshan, Ziaullah M. Sain, Alaa Hamed Habib, Qamre Alam, Muhammad Umair, Muhammad Umair, Muhammad Arif Nadeem Saqib

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Biallelic Variants in Seven Different Genes Associated with Clinically Suspected Bardet–Biedl Syndrome by Hamed Nawaz, Mujahid, Sher Alam Khan, Farhana Bibi, Ahmed Waqas, Abdul Bari, Fardous, Niamatullah Khan, Nazif Muhammad, Amjad Khan, Sohail Aziz Paracha, Qamre Alam, Mohammad Azhar Kamal, Misbahuddin M. Rafeeq, Noor Muhammad, Fayaz Ul Haq, Shazia Khan, Arif Mahmood, Saadullah Khan, Muhammad Umair

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