Hasil Pencarian - Saadullah Khan

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  1. 1
    Multisystem Radiologic Manifestations of Erdheim-Chester Disease

    Multisystem Radiologic Manifestations of Erdheim-Chester Disease oleh Umairullah Lodhi, Uzair Sarmast, Saadullah Khan, Kavitha Yaddanapudi

    Diterbitkan 2016-01-01
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  2. 2
    Elucidating Therapeutic and Biological Potential of Berberis baluchistanica Ahrendt Bark, Leaf, and Root Extracts

    Elucidating Therapeutic and Biological Potential of Berberis baluchistanica Ahrendt Bark, Leaf, and Root Extracts oleh Zareen Gul, Zareen Gul, Ali Akbar, Saadullah Khan Leghari

    Diterbitkan 2022-03-01
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  3. 3
    Rainwater Harvesting: A Sustainable Water Management Option for Irrigation of Public Parks

    Rainwater Harvesting: A Sustainable Water Management Option for Irrigation of Public Parks oleh Muhammad Sohail Waqas, Muhammad Jehanzeb Masud Cheema, Saddam Hussain, Muhammad Usman Khalid, Muhammad Saadullah Khan

    Diterbitkan 2022-11-01
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  4. 4
    Hybrid Renewable Energy Sources (Solar and Wind) Potential and Its Application for Sustainable Agriculture in Pakistan: A Case Study of Potohar Plateau

    Hybrid Renewable Energy Sources (Solar and Wind) Potential and Its Application for Sustainable Agriculture in Pakistan: A Case Study of Potohar Plateau oleh Muhammad Saadullah Khan, Saddam Hussain, Muhammad Jehanzeb Masud Cheema, Tahir Iqbal, Shoaib Rashid Saleem, Muhammad Sohail Waqas

    Diterbitkan 2022-12-01
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  5. 5
    A novel mutation in homeobox DNA binding domain of HOXC13 gene underlies pure hair and nail ectodermal dysplasia (ECTD9) in a Pakistani family

    A novel mutation in homeobox DNA binding domain of HOXC13 gene underlies pure hair and nail ectodermal dysplasia (ECTD9) in a Pakistani family oleh Anwar Kamal Khan, Noor Muhammad, Abdul Aziz, Sher Alam Khan, Khadim Shah, Abdul Nasir, Muzammil Ahmad Khan, Saadullah Khan

    Diterbitkan 2017-04-01
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  6. 6
    The molecular genetics of UV-Sensitive syndrome; a rare dermal anomaly

    The molecular genetics of UV-Sensitive syndrome; a rare dermal anomaly oleh Muhammad Muzammal, Muhammad Zeeshan Ali, Safeer Ahmad, Shawana Huma, Rizwan, Sohail Ahmad, Ansar Ahmad Abbasi, Saadullah Khan, Muzammil Ahmad Khan

    Diterbitkan 2021-07-01
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  7. 7
    The Importance of Variable Rate Irrigation in Lowering Greenhouse Gas Emissions in the Agriculture Sector: A Review

    The Importance of Variable Rate Irrigation in Lowering Greenhouse Gas Emissions in the Agriculture Sector: A Review oleh Saddam Hussain, Muhammad Jehanzeb Masud Cheema, Muhammad Sohail Waqas, Shoaib Rashid Saleem, Rameela Rustam, Muhammad Saadullah Khan, Muhammad Habib Ullah

    Diterbitkan 2023-01-01
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  8. 8
    A novel nonsense variant in SLC24A4 causing a rare form of amelogenesis imperfecta in a Pakistani family

    A novel nonsense variant in SLC24A4 causing a rare form of amelogenesis imperfecta in a Pakistani family oleh Sher Alam Khan, Muhammad Adnan Khan, Nazif Muhammad, Hina Bashir, Niamat Khan, Noor Muhammad, Rüstem Yilmaz, Saadullah Khan, Naveed Wasif

    Diterbitkan 2020-05-01
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  9. 9
    Whole Exome Sequencing Confirms Molecular Diagnostics of Three Pakhtun Families With Autosomal Recessive Epidermolysis Bullosa

    Whole Exome Sequencing Confirms Molecular Diagnostics of Three Pakhtun Families With Autosomal Recessive Epidermolysis Bullosa oleh Fozia Fozia, Fozia Fozia, Rubina Nazli, Nousheen Bibi, Sher Alam Khan, Noor Muhammad, Nafila Shakeeb, Saadullah Khan, Musharraf Jelani, Naveed Wasif, Naveed Wasif

    Diterbitkan 2021-08-01
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  10. 10
    A novel pathogenic missense variant in CNNM4 underlying Jalili syndrome: Insights from molecular dynamics simulations

    A novel pathogenic missense variant in CNNM4 underlying Jalili syndrome: Insights from molecular dynamics simulations oleh Asia Parveen, Muhammad U. Mirza, Michiel Vanmeert, Javed Akhtar, Hina Bashir, Saadullah Khan, Saqib Shehzad, Matheus Froeyen, Wasim Ahmed, Muhammad Ansar, Naveed Wasif

    Diterbitkan 2019-09-01
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  11. 11
    Novel mutations in ALDH1A3 associated with autosomal recessive anophthalmia/microphthalmia, and review of the literature

    Novel mutations in ALDH1A3 associated with autosomal recessive anophthalmia/microphthalmia, and review of the literature oleh Siying Lin, Gaurav V. Harlalka, Abdul Hameed, Hadia Moattar Reham, Muhammad Yasin, Noor Muhammad, Saadullah Khan, Emma L. Baple, Andrew H. Crosby, Shamim Saleha

    Diterbitkan 2018-09-01
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  12. 12
    Variants in HCFC1 and MN1 genes causing intellectual disability in two Pakistani families

    Variants in HCFC1 and MN1 genes causing intellectual disability in two Pakistani families oleh Syeda Iqra Hussain, Nazif Muhammad, Shahbaz Ali Shah, Adil u Rehman, Sher Alam Khan, Shamim Saleha, Yar Muhammad Khan, Noor Muhammad, Saadullah Khan, Naveed Wasif

    Diterbitkan 2024-07-01
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  13. 13
    Expanding the genetic spectrum of hereditary motor sensory neuropathies in Pakistan

    Expanding the genetic spectrum of hereditary motor sensory neuropathies in Pakistan oleh Asif Naveed Ahmed, Lettie E. Rawlins, Niamat Khan, Zakir Jan, Nishanka Ubeyratna, Nikol Voutsina, Arfa Azeem, Saadullah Khan, Emma L. Baple, Andrew H. Crosby, Shamim Saleha

    Diterbitkan 2024-10-01
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  14. 14
    The First Report of a Missense Variant in RFX2 Causing Non-Syndromic Tooth Agenesis in a Consanguineous Pakistani Family

    The First Report of a Missense Variant in RFX2 Causing Non-Syndromic Tooth Agenesis in a Consanguineous Pakistani Family oleh Sher Alam Khan, Saadullah Khan, Noor Muhammad, Zia Ur Rehman, Muhammad Adnan Khan, Abdul Nasir, Umm-e- Kalsoom, Anwar Kamal Khan, Hassan Khan, Naveed Wasif, Naveed Wasif

    Diterbitkan 2022-01-01
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  15. 15
    Brachyolmia, dental anomalies and short stature (DASS): Phenotype and genotype analyses of Egyptian and Pakistani patients

    Brachyolmia, dental anomalies and short stature (DASS): Phenotype and genotype analyses of Egyptian and Pakistani patients oleh Hamed Nawaz, Asia Parveen, Sher Alam Khan, Abul Khair Zalan, Muhammad Adnan Khan, Noor Muhammad, Nehal F. Hassib, Mostafa I. Mostafa, Rasha M. Elhossini, Nehal Nabil Roshdy, Asmat Ullah, Amina Arif, Saadullah Khan, Ole Ammerpohl, Naveed Wasif

    Diterbitkan 2024-01-01
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  16. 16
    Structural and functional implications of SLC13A3 and SLC9A6 mutations: an in silico approach to understanding intellectual disability

    Structural and functional implications of SLC13A3 and SLC9A6 mutations: an in silico approach to understanding intellectual disability oleh Syeda Iqra Hussain, Nazif Muhammad, Salah Ud Din Shah, Fardous Fardous, Sher Alam Khan, Niamatullah Khan, Adil U Rehman, Mehwish Siddique, Shoukat Ali Wasan, Rooh Niaz, Hafiz Ullah, Niamat Khan, Noor Muhammad, Muhammad Usman Mirza, Naveed Wasif, Saadullah Khan

    Diterbitkan 2023-10-01
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  17. 17
    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

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

    Diterbitkan 2023-05-01
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  18. 18
    Deleterious Variants in <i>WNT10A</i>, <i>EDAR,</i> and <i>EDA</i> Causing Isolated and Syndromic Tooth Agenesis: A Structural Perspective from Molecular Dynamics Simulations

    Deleterious Variants in <i>WNT10A</i>, <i>EDAR,</i> and <i>EDA</i> Causing Isolated and Syndromic Tooth Agenesis: A Structural Perspective from Molecular Dynamics Simulations oleh Asia Parveen, Sher Alam Khan, Muhammad Usman Mirza, Hina Bashir, Fatima Arshad, Maria Iqbal, Waseem Ahmad, Ahsan Wahab, Amal Fiaz, Sidra Naz, Fareeha Ashraf, Tayyaba Mobeen, Salman Aziz, Syed Shoaib Ahmed, Noor Muhammad, Nehal F. Hassib, Mostafa I. Mostafa, Nagwa E. Gaboon, Roquyya Gul, Saadullah Khan, Matheus Froeyen, Muhammad Shoaib, Naveed Wasif

    Diterbitkan 2019-10-01
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