Hasil Pencarian - Muhammad Imran Naseer

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  1. 1
    Editorial: Current Trends in Medicinal Plant Research and Neurodegenerative Disorders

    Editorial: Current Trends in Medicinal Plant Research and Neurodegenerative Disorders oleh Muhammad Ayaz, Tahir Ali, Tahir Ali, Abdul Sadiq, Farhat Ullah, Muhammad Imran Naseer, Muhammad Imran Naseer

    Diterbitkan 2022-06-01
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  2. 2
    Identification of Novel Gene Signatures using Next-Generation Sequencing Data from COVID-19 Infection Models: Focus on Neuro-COVID and Potential Therapeutics

    Identification of Novel Gene Signatures using Next-Generation Sequencing Data from COVID-19 Infection Models: Focus on Neuro-COVID and Potential Therapeutics oleh Peter Natesan Pushparaj, Peter Natesan Pushparaj, Angham Abdulrahman Abdulkareem, Angham Abdulrahman Abdulkareem, Muhammad Imran Naseer, Muhammad Imran Naseer

    Diterbitkan 2021-08-01
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  3. 3
    A novel homozygous splice donor variant in the LRPPRC gene causing Leigh syndrome with epilepsy, a French-Canadian disorder in a Saudi family: case report

    A novel homozygous splice donor variant in the LRPPRC gene causing Leigh syndrome with epilepsy, a French-Canadian disorder in a Saudi family: case report oleh Osama Y. Muthaffar, Angham Abdulrhman Abdulkareem, Angham Abdulrhman Abdulkareem, Abrar Ashi, Abrar Ashi, Muhammad Imran Naseer, Muhammad Imran Naseer

    Diterbitkan 2023-11-01
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  4. 4
    Comparative Gene-Expression Analysis of Alzheimer’s Disease Progression with Aging in Transgenic Mouse Model

    Comparative Gene-Expression Analysis of Alzheimer’s Disease Progression with Aging in Transgenic Mouse Model oleh Noman Bin Abid, Muhammad Imran Naseer, Myeong Ok Kim

    Diterbitkan 2019-03-01
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  5. 5
    Whole-Exome Sequencing Reveals a Missense Variant c.1612C>T (p.Arg538Cys) in the BTD Gene Leading to Neuromyelitis Optica Spectrum Disorder in Saudi Families

    Whole-Exome Sequencing Reveals a Missense Variant c.1612C>T (p.Arg538Cys) in the BTD Gene Leading to Neuromyelitis Optica Spectrum Disorder in Saudi Families oleh Muhammad Imran Naseer, Muhammad Imran Naseer, Peter Natesan Pushparaj, Peter Natesan Pushparaj, Peter Natesan Pushparaj, Angham Abdulrahman Abdulkareem, Angham Abdulrahman Abdulkareem, Osama Y. Muthaffar

    Diterbitkan 2022-02-01
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  6. 6
    Whole-Exome Sequencing for Identification of Genetic Variants Involved in Vitamin D Metabolic Pathways in Families With Vitamin D Deficiency in Saudi Arabia

    Whole-Exome Sequencing for Identification of Genetic Variants Involved in Vitamin D Metabolic Pathways in Families With Vitamin D Deficiency in Saudi Arabia oleh Shatha Alharazy, Muhammad Imran Naseer, Muhammad Imran Naseer, Eman Alissa, Margaret Denise Robertson, Susan Lanham-New, Adeel G. Chaudhary, Adeel G. Chaudhary, Adeel G. Chaudhary

    Diterbitkan 2021-06-01
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  7. 7
    Next-Generation Sequencing Reveals Novel Homozygous Missense Variant c.934T > C in POLR1C Gene Causing Leukodystrophy and Hypomyelinating Disease

    Next-Generation Sequencing Reveals Novel Homozygous Missense Variant c.934T > C in POLR1C Gene Causing Leukodystrophy and Hypomyelinating Disease oleh Muhammad Imran Naseer, Muhammad Imran Naseer, Angham Abdulrahman Abdulkareem, Angham Abdulrahman Abdulkareem, Peter Natesan Pushparaj, Peter Natesan Pushparaj, Peter Natesan Pushparaj, Samah Saharti, Osama Y. Muthaffar

    Diterbitkan 2022-05-01
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  8. 8
    Whole-Exome Sequencing Identifies Novel SCN1A and CACNB4 Genes Mutations in the Cohort of Saudi Patients With Epilepsy

    Whole-Exome Sequencing Identifies Novel SCN1A and CACNB4 Genes Mutations in the Cohort of Saudi Patients With Epilepsy oleh Muhammad Imran Naseer, Muhammad Imran Naseer, Angham Abdulrhman Abdulkareem, Angham Abdulrhman Abdulkareem, Mahmood Rasool, Mahmood Rasool, Hussein Algahtani, Osama Yousef Muthaffar, Peter Natesan Pushparaj, Peter Natesan Pushparaj

    Diterbitkan 2022-06-01
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  9. 9
    Exome Analysis Identified Novel Homozygous Splice Site Donor Alteration in NT5C2 Gene in a Saudi Family Associated With Spastic Diplegia Cerebral Palsy, Developmental Delay, and Intellectual Disability

    Exome Analysis Identified Novel Homozygous Splice Site Donor Alteration in NT5C2 Gene in a Saudi Family Associated With Spastic Diplegia Cerebral Palsy, Developmental Delay, and In... oleh Muhammad Imran Naseer, Muhammad Imran Naseer, Angham Abdulrahman Abdulkareem, Peter Natesan Pushparaj, Peter Natesan Pushparaj, Fehmida Bibi, Fehmida Bibi, Adeel G. Chaudhary, Adeel G. Chaudhary, Adeel G. Chaudhary

    Diterbitkan 2020-02-01
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  10. 10
    Decoding the Impact of Genetic Variants in Gastric Cancer Patients Based on High-Dimensional Copy Number Variation Data Using Next-Generation Knowledge Discovery Methods

    Decoding the Impact of Genetic Variants in Gastric Cancer Patients Based on High-Dimensional Copy Number Variation Data Using Next-Generation Knowledge Discovery Methods oleh Fehmida Bibi, Peter Natesan Pushparaj, Muhammad Imran Naseer, Muhammad Yasir, Esam Ibraheem Azhar

    Diterbitkan 2022-10-01
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  11. 11
    UTILITY OF FUNCTIONALIZED AGAROSE NANOPARTICLES IN HYDROLYZING LACTOSE IN BATCH REACTORS FOR DAIRY INDUSTRIES

    UTILITY OF FUNCTIONALIZED AGAROSE NANOPARTICLES IN HYDROLYZING LACTOSE IN BATCH REACTORS FOR DAIRY INDUSTRIES oleh Shakeel Ahmed Ansari, Syed Ismail Ahmad, Mohammad Alam Jafri, Muhammad Imran Naseer, Rukhsana Satar

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  12. 12
    Whole Exome Sequencing Identifies Three Novel Mutations in the ASPM Gene From Saudi Families Leading to Primary Microcephaly

    Whole Exome Sequencing Identifies Three Novel Mutations in the ASPM Gene From Saudi Families Leading to Primary Microcephaly oleh Muhammad Imran Naseer, Muhammad Imran Naseer, Angham Abdulrahman Abdulkareem, Angham Abdulrahman Abdulkareem, Osama Yousef Muthaffar, Sameera Sogaty, Hiba Alkhatabi, Hiba Alkhatabi, Sarah Almaghrabi, Sarah Almaghrabi, Adeel G. Chaudhary, Adeel G. Chaudhary, Adeel G. Chaudhary

    Diterbitkan 2021-02-01
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  13. 13
    KIF2A regulates the development of dentate granule cells and postnatal hippocampal wiring

    KIF2A regulates the development of dentate granule cells and postnatal hippocampal wiring oleh Noriko Homma, Ruyun Zhou, Muhammad Imran Naseer, Adeel G Chaudhary, Mohammed H Al-Qahtani, Nobutaka Hirokawa

    Diterbitkan 2018-01-01
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  14. 14
    Nicotinamide inhibits alkylating agent-induced apoptotic neurodegeneration in the developing rat brain.

    Nicotinamide inhibits alkylating agent-induced apoptotic neurodegeneration in the developing rat brain. oleh Najeeb Ullah, Hae Young Lee, Muhammad Imran Naseer, Ikram Ullah, Joo Won Suh, Myeong Ok Kim

    Diterbitkan 2011-01-01
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  15. 15
    Autosomal recessive cerebellar ataxia with spasticity due to a rare mutation in GBA2 gene in a large consanguineous Saudi family

    Autosomal recessive cerebellar ataxia with spasticity due to a rare mutation in GBA2 gene in a large consanguineous Saudi family oleh Hussein Algahtani, Bader Shirah, Ikram Ullah, Mohammad H. Al-Qahtani, Angham Abdulrahman Abdulkareem, Muhammad Imran Naseer

    Diterbitkan 2021-01-01
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  16. 16
    Association between vitamin D and glycaemic parameters in a multi-ethnic cohort of postmenopausal women with type 2 diabetes in Saudi Arabia

    Association between vitamin D and glycaemic parameters in a multi-ethnic cohort of postmenopausal women with type 2 diabetes in Saudi Arabia oleh Shatha Alharazy, Eman Alissa, Susan Lanham-New, Muhammad Imran Naseer, Adeel G. Chaudhary, M Denise Robertson

    Diterbitkan 2021-08-01
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  17. 17
    Directly measured free and total 25-hydroxyvitamin D levels in relation to metabolic health in multi-ethnic postmenopausal females in Saudi Arabia

    Directly measured free and total 25-hydroxyvitamin D levels in relation to metabolic health in multi-ethnic postmenopausal females in Saudi Arabia oleh Shatha Alharazy, M Denise Robertson, Susan Lanham-New, Muhammad Imran Naseer, Adeel G Chaudhary, Eman Alissa

    Diterbitkan 2021-12-01
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  18. 18
    Whole exome sequencing identified five novel variants in CNTN2, CARS2, ARSA, and CLCN4 leading to epilepsy in consanguineous families

    Whole exome sequencing identified five novel variants in CNTN2, CARS2, ARSA, and CLCN4 leading to epilepsy in consanguineous families oleh Angham Abdulrhman Abdulkareem, Angham Abdulrhman Abdulkareem, Qaiser Zaman, Qaiser Zaman, Qaiser Zaman, Hamza Khan, Sabar Khan, Gauhar Rehman, Nabeel Tariq, Mashal Ahmad, Muhammad Owais, Najumuddin, Osama Yousef Muthaffar, Fehmida Bibi, Fehmida Bibi, Rin Khang, Seung Woo Ryu, Muhammad Imran Naseer, Muhammad Imran Naseer, Musharraf Jelani

    Diterbitkan 2023-06-01
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  19. 19
    Novel Missense Variant in Heterozygous State in the BRPF1 Gene Leading to Intellectual Developmental Disorder With Dysmorphic Facies and Ptosis

    Novel Missense Variant in Heterozygous State in the BRPF1 Gene Leading to Intellectual Developmental Disorder With Dysmorphic Facies and Ptosis oleh Muhammad Imran Naseer, Muhammad Imran Naseer, Angham Abdulrahman Abdulkareem, Francisco J. Guzmán-Vega, Francisco J. Guzmán-Vega, Stefan T. Arold, Stefan T. Arold, Peter Natesan Pushparaj, Peter Natesan Pushparaj, Adeel G. Chaudhary, Adeel G. Chaudhary, Adeel G. Chaudhary, Mohammad H. AlQahtani, Mohammad H. AlQahtani

    Diterbitkan 2020-05-01
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  20. 20
    Deciphering the Association of Cytokines, Chemokines, and Growth Factors in Chondrogenic Differentiation of Human Bone Marrow Mesenchymal Stem Cells Using an ex vivo Osteochondral Culture System

    Deciphering the Association of Cytokines, Chemokines, and Growth Factors in Chondrogenic Differentiation of Human Bone Marrow Mesenchymal Stem Cells Using an ex vivo Osteochondral... oleh Mohammad Alam Jafri, Mohammad Alam Jafri, Gauthaman Kalamegam, Gauthaman Kalamegam, Gauthaman Kalamegam, Gauthaman Kalamegam, Mohammed Abbas, Mohammed Abbas, Mohammed Al-Kaff, Mohammed Al-Kaff, Farid Ahmed, Sherin Bakhashab, Mahmood Rasool, Mahmood Rasool, Muhammad Imran Naseer, Muhammad Imran Naseer, Vasan Sinnadurai, Peter Natesan Pushparaj, Peter Natesan Pushparaj

    Diterbitkan 2020-01-01
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