Transcriptional Regulators of Claudins in Epithelial Tight Junctions von Khan, Niamat, Asif, Abdul R.

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Current Analytical Strategies in Studying Chromatin-Associated-Proteome (Chromatome) von Khan, Niamat, Shahid, Sidra, Asif, Abdul R.

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Molecular characterization of plasma virome of hepatocellular carcinoma (HCC) patients von Ullah Khan, Niamat, Sadiq, Asma, Khan, Jadoon, Basharat, Nosheen, Hassan, Zulfiqar Ul, Ali, Ijaz, Shah, Tawaf Ali, Bourhia, Mohammed, Bin Jardan, Yousef A., Wondmie, Gezahign Fentahun

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

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Investigating the genetic basis of hereditary spastic paraplegia and cerebellar Ataxia in Pakistani families von Azeem, Arfa, Ahmed, Asif Naveed, Khan, Niamat, Voutsina, Nikol, Ullah, Irfan, Ubeyratna, Nishanka, Yasin, Muhammad, Baple, Emma L, Crosby, Andrew H, Rawlins, Lettie E, Saleha, Shamim

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

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Genetic heterogeneity in epilepsy and comorbidities: insights from Pakistani families von Yasin, Muhammad, Licchetta, Laura, Khan, Niamat, Ullah, Irfan, Jan, Zakir, Dawood, Muhammad, Ahmed, Asif Naveed, Azeem, Arfa, Minardi, Raffaella, Carelli, Valerio, Saleha, Shamim

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

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Metabolic Proteins Expression Up-Regulated in Blood-Borne Extensively Drug-Resistant Salmonella Typhi Isolates from Pakistan von Yasin, Nusrat, Rahman, Hazir, Qasim, Muhammad, Nisa, Iqbal, Sarwar, Yasra, Khan, Niamat, Alzahrani, Khalid J, Alsuwat, Meshari A, Alzahrani, Fuad M, Aljohani, Abrar

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MPA Modulates Tight Junctions' Permeability via Midkine/PI3K Pathway in Caco-2 Cells: A Possible Mechanism of Leak-Flux Diarrhea in Organ Transplanted Patients von Khan, Niamat, Binder, Lutz, Pantakani, D V Krishna, Asif, Abdul R

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Surface functionalization dependent subcellular localization of Superparamagnetic nanoparticle in plasma membrane and endosome von Thimiri Govinda Raj, Deepak B., Khan, Niamat Ali

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Unravelling the genetic basis of retinal dystrophies in Pakistani consanguineous families von Marwan, Muhammad, Dawood, Muhammad, Ullah, Mukhtar, Shah, Irfan Ullah, Khan, Niamat, Hassan, Muhammad Taimur, Karam, Muhammad, Rawlins, Lettie E, Baple, Emma L, Crosby, Andrew H, Saleha, Shamim

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USH2A gene variants cause Keratoconus and Usher syndrome phenotypes in Pakistani families von Ahmed, Asif Naveed, Tahir, Raheel, Khan, Niamat, Ahmad, Mushtaq, Dawood, Muhammad, Basit, Abdul, Yasin, Muhammad, Nowshid, Maha, Marwan, Muhammad, Sultan, Komal, Saleha, Shamim

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Fragile X premutation carrier screening in Pakistani preconception women in primary care consultation von Meraj, Neelam, Yasin, Muhammad, Rehman, Zia Ur, Tahir, Haleema, Jadoon, Humaira, Khan, Niamat, Shahid, Rabia, Zubair, Maria, Zulfiqar, Irba, Jabeen, Musarrat, Neelam, Shahzadi, Hameed, Abdul, Saleha, Shamim

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Hydroxyquinoline sulfanilamide ameliorates STZ-induced hyperglycemia-mediated amyleoid beta burden and memory impairment in adult mice von Awais, Sajid, Shah, Shahid Ali, Khan, Niamat, Khan, Naeem, Jamila, Nargis, Nishan, Umar, Jan, Muhammad Ishtiaq, Hwang, In Min, Ali, Essam A.

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Synthesis of hybrid AuNPs functionalised superparamagnetic NPs von Thimiri Govinda Raj, Deepak B, Ali Khan, Niamat

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Biochar impact on microbial population and elemental composition of red soil von Ullah, Zabih, Ali, Shafaqat, Muhammad, Niaz, Khan, Naeem, Rizwan, Muhammad, Khan, Muhammad Daud, Khan, Niamat, Khattak, Baharullah, Alhaithloul, Haifa Abdulaziz S., Soliman, Mona H., Ullah, Hamid, Begum, Dilnaz, Ali, Navid, Hashmatullah

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Novel mutations in PDE6A and CDHR1 cause retinitis pigmentosa in Pakistani families von Dawood, Muhammad, Lin, Siying, Din, Taj Ud, Shah, Irfan Ullah, Khan, Niamat, Jan, Abid, Marwan, Muhammad, Sultan, Komal, Nowshid, Maha, Tahir, Raheel, Ahmed, Asif Naveed, Yasin, Muhammad, Baple, Emma L., Crosby, Andrew H., Saleha, Shamim

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Immunosuppressant MPA Modulates Tight Junction through Epigenetic Activation of MLCK/MLC-2 Pathway via p38MAPK von Khan, Niamat, Pantakani, D V Krishna, Binder, Lutz, Qasim, Muhammad, Asif, Abdul R

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Active and Repressive Chromatin-Associated Proteome after MPA Treatment and the Role of Midkine in Epithelial Monolayer Permeability von Khan, Niamat, Lenz, Christof, Binder, Lutz, Pantakani, Dasaradha Venkata Krishna, Asif, Abdul R

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