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ArticlesPeer ReviewedFull Text
Acute and chronic impact of interleukin-33 stimulation on chemokines and growth factors in human cord blood-derived mast cells
Author / Creator:Bakhashab, Sherin ; Banafea, Ghalya H. ; Ahmed, Farid ; Alsolami, Reem ; Schulten, Hans-Juergen ; Gauthaman, Kalamegam ; Naseer, Muhammad Imran ; Pushparaj, Peter Natesan
Publisher:United States: Public Library of Science
Journal title:PloS one, 2024-10, Vol.19 (10), p.e0311981
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Neuroprotection with metformin and thymoquinone against ethanol-induced apoptotic neurodegeneration in prenatal rat cortical neurons
Author / Creator:Ullah, Ikram ; Ullah, Najeeb ; Naseer, Muhammad Imran ; Lee, Hae Young ; Kim, Myeong OK
Publisher:England: BioMed Central Ltd
Journal title:BMC neuroscience, 2012-01, Vol.13 (1), p.11-11, Article 11
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Molecular genetics of human primary microcephaly: an overview
Author / Creator:Faheem, Muhammad ; Naseer, Muhammad Imran ; Rasool, Mahmood ; Chaudhary, Adeel G ; Kumosani, Taha A ; Ilyas, Asad Muhammad ; Pushparaj, Peter Natesan ; Ahmed, Farid ; Algahtani, Hussain A ; Al-Qahtani, Mohammad H ; Saleh Jamal, Hasan
Publisher:England: BioMed Central Ltd
Journal title:BMC medical genomics, 2015-01, Vol.8 (S1), p.S4-S4, Article S4
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The role of epigenetics in personalized medicine: challenges and opportunities
Author / Creator:Rasool, Mahmood ; Malik, Arif ; Naseer, Muhammad Imran ; Manan, Abdul ; Ansari, Shakeel Ahmed ; Begum, Irshad ; Qazi, Mahmood Husain ; Pushparaj, Peter Natesan ; Abuzenadah, Adel M ; Al-Qahtani, Mohammed Hussein ; Kamal, Mohammad Amjad ; Gan, Siew Hua
Publisher:England: BioMed Central Ltd
Journal title:BMC medical genomics, 2015-01, Vol.8 (S1), p.S5-S5, Article S5
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Detection of genetic alterations in gastric cancer patients from Saudi Arabia using comparative genomic hybridization (CGH)
Author / Creator:Bibi, Fehmida ; Ali, Isse ; Naseer, Muhammad Imran ; Ali Mohamoud, Hussein Sheikh ; Yasir, Muhammad ; Alvi, Sana Akhtar ; Jiman-Fatani, Asif Ahmed ; Sawan, Ali ; Azhar, Esam Ibraheem
Publisher:United States: Public Library of Science
Journal title:PloS one, 2018-09, Vol.13 (9), p.e0202576
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Association between vitamin D and glycaemic parameters in a multi-ethnic cohort of postmenopausal women with type 2 diabetes in Saudi Arabia
Author / Creator:Alharazy, Shatha ; Alissa, Eman ; Lanham-New, Susan ; Naseer, Muhammad Imran ; Chaudhary, Adeel G. ; Robertson, M Denise
Publisher:England: BioMed Central Ltd
Journal title:BMC endocrine disorders, 2021-08, Vol.21 (1), p.162-10, Article 162
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Childhood-related neural genotype–phenotype in ATP1A3 mutations: comprehensive analysis
Author / Creator:Muthaffar, Osama Y. ; Alqarni, Asma ; Shafei, Jumana A. ; Bahowarth, Sarah Y. ; Alyazidi, Anas S. ; Naseer, Muhammad Imran
Publisher:Singapore: Springer Nature Singapore
Journal title:Genes & Genomics, 2024, 46(4), , pp.475-487
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Decoding the Impact of Genetic Variants in Gastric Cancer Patients Based on High-Dimensional Copy Number Variation Data Using Next-Generation Knowledge Discovery Methods
Author / Creator:Bibi, Fehmida ; Pushparaj, Peter Natesan ; Naseer, Muhammad Imran ; Yasir, Muhammad ; Azhar, Esam Ibraheem
Publisher:MDPI AG
Journal title:Applied sciences, 2022-10, Vol.12 (19), p.10053
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KIF2A regulates the development of dentate granule cells and postnatal hippocampal wiring
Author / Creator:Homma, Noriko ; Zhou, Ruyun ; Naseer, Muhammad Imran ; Chaudhary, Adeel G ; Al-Qahtani, Mohammed H ; Hirokawa, Nobutaka
Publisher:England: eLife Science Publications, Ltd
Journal title:eLife, 2018-01, Vol.7
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Combinatorial Therapeutic Potential of Stem Cells and Benzimidazol Derivatives for the Reduction of Liver Fibrosis
Author / Creator:Iqbal, Maryam ; Shams, Sulaiman ; Rafiq, Huma ; Khan, Momin ; Khan, Shahid ; Sadique Khattak, Umer ; Afridi, Sahib Gul ; Bibi, Fehmida ; Abdulkareem, Angham Abdulrhman ; Naseer, Muhammad Imran
Publisher:Switzerland: MDPI AG
Journal title:Pharmaceuticals (Basel, Switzerland), 2023-02, Vol.16 (2), p.306
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BAD, a Proapoptotic Protein, Escapes ERK/RSK Phosphorylation in Deguelin and siRNA-Treated HeLa Cells
Author / Creator:Hafeez, Samra ; Urooj, Mahwish ; Saleem, Shamiala ; Gillani, Zeeshan ; Shaheen, Sumaira ; Qazi, Mahmood Husain ; Naseer, Muhammad Imran ; Iqbal, Zafar ; Ansari, Shakeel Ahmed ; Haque, Absarul ; Asif, Muhammad ; Mir, Manzoor Ahmad ; Ali, Ashraf ; Pushparaj, Peter Natesan ; Jamal, Mohammad Sarwar ; Rasool, Mahmood
Publisher:United States: Public Library of Science
Journal title:PloS one, 2016-01, Vol.11 (1), p.e0145780-e0145780
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ArticlesPeer ReviewedFull Text
Phenotypic Classification of Eye Colour and Developmental Validation of the Irisplex System on Population Living in Malakand Division, Pakistan
Author / Creator:Rahat, Murad Ali ; Akbar, Fazal ; Rasool, Akhtar ; Ilyas, Muhammad ; Rakha, Allah ; Shams, Sulaiman ; Jelani, Musharraf ; Bibi, Fehmida ; Shirah, Bader H. ; Abdulkareem, Angham Abdulrhman ; Naseer, Muhammad Imran ; Israr, Muhammad
Publisher:Switzerland: MDPI AG
Journal title:Biomedicines, 2023-04, Vol.11 (4), p.1228
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ArticlesPeer ReviewedFull Text
Nicotinamide Inhibits Alkylating Agent-Induced Apoptotic Neurodegeneration in the Developing Rat Brain
Author / Creator:Ullah, Najeeb ; Lee, Hae Young ; Naseer, Muhammad Imran ; Ullah, Ikram ; Suh, Joo Won ; Kim, Myeong Ok
Publisher:United States: Public Library of Science
Journal title:PloS one, 2011-12, Vol.6 (12), p.e27093
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ArticlesPeer ReviewedFull Text
A novel WDR62 mutation causes primary microcephaly in a large consanguineous Saudi family
Author / Creator:Naseer, Muhammad Imran ; Rasool, Mahmood ; Sogaty, Sameera ; Chaudhary, Rukhaa Adeel ; Mansour, Haifa Mansour ; Chaudhary, Adeel G. ; Abuzenadah, Adel M. ; Al-Qahtani, Mohammad H.
Publisher:Saudi Arabia: KING FAISAL SPECIALIST HOSPITAL & RESEARCH CENTRE
Journal title:Annals of Saudi medicine, 2017-03, Vol.37 (2), p.148-153
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A novel mutation in RDH5 gene causes retinitis pigmentosa in consanguineous Pakistani family
Author / Creator:Sultan, Neelam ; Ali, Irfan ; Bukhari, Shazia Anwer ; Baig, Shahid Mahmood ; Asif, Muhammad ; Qasim, Muhammad ; Naseer, Muhammad Imran ; Rasool, Mahmood
Publisher:Seoul: The Genetics Society of Korea
Journal title:Genes & Genomics, 2018, 40(5), , pp.553-559
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ArticlesPeer ReviewedFull Text
Neuroprotective profile of pyruvate against ethanol-induced neurodegeneration in developing mice brain
Author / Creator:Ullah, Najeeb ; Naseer, Muhammad Imran ; Ullah, Ikram ; Kim, Tae Hyun ; Lee, Hae Young ; Kim, Myeong Ok
Publisher:Milan: Springer Milan
Journal title:Neurological sciences, 2013-12, Vol.34 (12), p.2137-2143
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ArticlesPeer ReviewedFull Text
Microarray based comparative genome hybridization detects genomic imbalances deletions and duplications in different epileptic patients of Saudi Arabia
Author / Creator:Naseer, Muhammad Imran ; Faheem, Muhammad ; Al-Quaiti, Maha Mohsin ; Chaudhary, Adeel G. ; Hirokawa, Nobutaka ; Al-Qahtani, Mohammed H.
Publisher:London: BioMed Central
Journal title:BMC genomics, 2014-04, Vol.15 (S2), p.P49-P49, Article P49
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ArticlesPeer ReviewedFull Text
Use of whole exome sequencing for identification of genetic variants related to Growth Hormone Deficiency and Short Stature: A Family-Based Study
Author / Creator:Alharazy, Shatha ; Naseer, Muhammad Imran
Publisher:Karachi: Knowledge Bylanes
Journal title:Pakistan journal of medical sciences, 2023-10, Vol.39 (5), p.1337-1344
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Genetic studies of autosomal recessive primary microcephaly in 33 Pakistani families: novel sequence variants in ASPM gene
Author / Creator:Gul, Asma ; Hassan, Muhammad Jawad ; Mahmood, Saqib ; Chen, Wenje ; Rahmani, Safa ; Naseer, Muhammad Imran ; Dellefave, Lisa ; Muhammad, Noor ; Rafiq, Muhammad Arshad ; Ansar, Muhammad ; Chishti, Muhammad Salman ; Ali, Ghazanfar ; Siddique, Teepu ; Ahmad, Wasim
Publisher:Berlin: Springer
Journal title:Neurogenetics, 2006-05, Vol.7 (2), p.105-110
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A missense variant in the PACS2 gene cause Epileptic Encephalopathy and seizures in Saudi family
Author / Creator:Naseer, Muhammad Imran ; Absarul Haq
Publisher:Pakistan: Knowledge Bylanes
Journal title:Pakistan journal of medical sciences, 2024-04, Vol.40 (4), p.782-784
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Showing 1 to 20 of 70 results

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Acute and chronic impact of interleukin-33 stimulation on chemokines and growth factors in human cord blood-derived mast cells

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Neuroprotection with metformin and thymoquinone against ethanol-induced apoptotic neurodegeneration in prenatal rat cortical neurons

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Molecular genetics of human primary microcephaly: an overview

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The role of epigenetics in personalized medicine: challenges and opportunities

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Detection of genetic alterations in gastric cancer patients from Saudi Arabia using comparative genomic hybridization (CGH)

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

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Childhood-related neural genotype–phenotype in ATP1A3 mutations: comprehensive analysis

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

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KIF2A regulates the development of dentate granule cells and postnatal hippocampal wiring

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Combinatorial Therapeutic Potential of Stem Cells and Benzimidazol Derivatives for the Reduction of Liver Fibrosis

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BAD, a Proapoptotic Protein, Escapes ERK/RSK Phosphorylation in Deguelin and siRNA-Treated HeLa Cells

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Phenotypic Classification of Eye Colour and Developmental Validation of the Irisplex System on Population Living in Malakand Division, Pakistan

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Nicotinamide Inhibits Alkylating Agent-Induced Apoptotic Neurodegeneration in the Developing Rat Brain

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A novel WDR62 mutation causes primary microcephaly in a large consanguineous Saudi family

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A novel mutation in RDH5 gene causes retinitis pigmentosa in consanguineous Pakistani family

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Neuroprotective profile of pyruvate against ethanol-induced neurodegeneration in developing mice brain

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Microarray based comparative genome hybridization detects genomic imbalances deletions and duplications in different epileptic patients of Saudi Arabia

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Use of whole exome sequencing for identification of genetic variants related to Growth Hormone Deficiency and Short Stature: A Family-Based Study

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Genetic studies of autosomal recessive primary microcephaly in 33 Pakistani families: novel sequence variants in ASPM gene

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A missense variant in the PACS2 gene cause Epileptic Encephalopathy and seizures in Saudi family

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