Hasil Pencarian - Qamre Alam

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  1. 1
    Genetic advances in skeletal disorders: an overview

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

    Diterbitkan 2023-06-01
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  2. 2
    MDR1 Gene Polymorphisms and Its Association With Expression as a Clinical Relevance in Terms of Response to Chemotherapy and Prognosis in Ovarian Cancer

    MDR1 Gene Polymorphisms and Its Association With Expression as a Clinical Relevance in Terms of Response to Chemotherapy and Prognosis in Ovarian Cancer oleh 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

    Diterbitkan 2020-05-01
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  3. 3
    Dimethoate Induces DNA Damage and Mitochondrial Dysfunction Triggering Apoptosis in Rat Bone-Marrow and Peripheral Blood Cells

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

    Diterbitkan 2020-10-01
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  4. 4
    Novel homozygous pathogenic mitochondrial DNAJC19 variant in a patient with dilated cardiomyopathy and global developmental delay

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

    Diterbitkan 2022-08-01
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  5. 5
    Microneedles Drug Delivery Systems for Treatment of Cancer: A Recent Update

    Microneedles Drug Delivery Systems for Treatment of Cancer: A Recent Update oleh 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

    Diterbitkan 2020-11-01
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  6. 6
    Congenital disorder of glycosylation with defective fucosylation 2 (FCSK gene defect): The third report in the literature with a mild phenotype

    Congenital disorder of glycosylation with defective fucosylation 2 (FCSK gene defect): The third report in the literature with a mild phenotype oleh 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

    Diterbitkan 2023-04-01
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  7. 7
    Next Generation Sequencing Based Non-invasive Prenatal Testing (NIPT): First Report From Saudi Arabia

    Next Generation Sequencing Based Non-invasive Prenatal Testing (NIPT): First Report From Saudi Arabia oleh 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

    Diterbitkan 2021-02-01
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  8. 8
    Case report: A novel de novo loss of function variant in the DNA-binding domain of TBX2 causes severe osteochondrodysplasia

    Case report: A novel de novo loss of function variant in the DNA-binding domain of TBX2 causes severe osteochondrodysplasia oleh 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

    Diterbitkan 2023-01-01
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  9. 9
    Loss-of-function variant in the LRR domain of SLITRK2 implicated in a neurodevelopmental disorder

    Loss-of-function variant in the LRR domain of SLITRK2 implicated in a neurodevelopmental disorder oleh 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

    Diterbitkan 2024-01-01
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  10. 10
    A Novel Homozygous Missense Mutation in the Zinc Finger DNA Binding Domain of GLI1 Causes Recessive Post-Axial Polydactyly

    A Novel Homozygous Missense Mutation in the Zinc Finger DNA Binding Domain of GLI1 Causes Recessive Post-Axial Polydactyly oleh Muhammad Umair, Farooq Ahmad, Saeed Ahmad, Qamre Alam, Mohd Rehan, Mohd Rehan, Amany I. Alqosaibi, Mashael M. Alnamshan, Misbahuddin M Rafeeq, Shahnaz Haque, Ziaullah M Sain, Muhammad Ismail, Majid Alfadhel, Majid Alfadhel

    Diterbitkan 2021-10-01
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  11. 11
    Targeting Kaposi’s sarcoma associated herpesvirus encoded protease (ORF17) by a lysophosphatidic acid molecule for treating KSHV associated diseases

    Targeting Kaposi’s sarcoma associated herpesvirus encoded protease (ORF17) by a lysophosphatidic acid molecule for treating KSHV associated diseases oleh 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

    Diterbitkan 2023-01-01
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  12. 12
    Biocomputational Prediction Approach Targeting FimH by Natural SGLT2 Inhibitors: A Possible Way to Overcome the Uropathogenic Effect of SGLT2 Inhibitor Drugs

    Biocomputational Prediction Approach Targeting FimH by Natural SGLT2 Inhibitors: A Possible Way to Overcome the Uropathogenic Effect of SGLT2 Inhibitor Drugs oleh 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

    Diterbitkan 2021-01-01
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  13. 13
    Non-invasive prenatal testing for autosomal recessive disorders: A new promising approach

    Non-invasive prenatal testing for autosomal recessive disorders: A new promising approach oleh 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

    Diterbitkan 2022-11-01
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  14. 14
    Case Report: Biallelic Variant in the tRNA Methyltransferase Domain of the AlkB Homolog 8 Causes Syndromic Intellectual Disability

    Case Report: Biallelic Variant in the tRNA Methyltransferase Domain of the AlkB Homolog 8 Causes Syndromic Intellectual Disability oleh 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

    Diterbitkan 2022-04-01
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  15. 15
    The genetic cause of neurodevelopmental disorders in 30 consanguineous families

    The genetic cause of neurodevelopmental disorders in 30 consanguineous families oleh Sohail Aziz Paracha, Shoaib Nawaz, Muhammad Tahir Sarwar, Asmat Shaheen, Gohar Zaman, Jawad Ahmed, Fahim Shah, Sundus Khwaja, Abid Jan, Nida Khan, Mohammad Azhar Kamal, Qamre Alam, Safdar Abbas, Saman Farman, Ahmed Waqas, Afnan Alkathiri, Abdullah Hamadi, Federico Santoni, Federico Santoni, Federico Santoni, Naseeb Ullah, Bisma Khalid, Stylianos E. Antonarakis, Khalid A Fakhro, Khalid A Fakhro, Khalid A Fakhro, Muhammad Umair, Muhammad Umair, Muhammad Ansar, Muhammad Ansar

    Diterbitkan 2024-08-01
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