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Parkinson’s Disease in Saudi Patients: A Genetic Study
Al-Mubarak, Bashayer R., Bohlega, Saeed A., Alkhairallah, Thamer S., Magrashi, Amna I., AlTurki, Maha I., Khalil, Dania S., AlAbdulaziz, Basma S., Abou Al-Shaar, Hussam, Mustafa, Abeer E., Alyemni, Eman A., Alsaffar, Bashayer A., Tahir, Asma I., Al Tassan, Nada A.
Published in PloS one (14.08.2015)
Published in PloS one (14.08.2015)
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Journal Article
Non-canonical Keap1-independent activation of Nrf2 in astrocytes by mild oxidative stress
Al-Mubarak, Bashayer R., Bell, Karen F.S., Chowdhry, Sudhir, Meakin, Paul J., Baxter, Paul S., McKay, Sean, Dando, Owen, Ashford, Michael L.J., Gazaryan, Irina, Hayes, John D., Hardingham, Giles E.
Published in Redox biology (01.11.2021)
Published in Redox biology (01.11.2021)
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Journal Article
Targeted de-repression of neuronal Nrf2 inhibits α-synuclein accumulation
Baxter, Paul S., Márkus, Nóra M., Dando, Owen, He, Xin, Al-Mubarak, Bashayer R., Qiu, Jing, Hardingham, Giles E.
Published in Cell death & disease (26.02.2021)
Published in Cell death & disease (26.02.2021)
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Journal Article
Estimating transfection efficiency in differentiated and undifferentiated neural cells
Alabdullah, Abeer A., Al-Abdulaziz, Basma, Alsalem, Hanan, Magrashi, Amna, Pulicat, Subramanian M., Almzroua, Amer A., Almohanna, Falah, Assiri, Abdullah Mohamed, Al Tassan, Nada A., Al-Mubarak, Bashayer R.
Published in BMC research notes (15.04.2019)
Published in BMC research notes (15.04.2019)
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Journal Article
Clinical heterogeneity of PLA2G6-related Parkinsonism: analysis of two Saudi families
Bohlega, Saeed A., Al-Mubarak, Bashayer R., Alyemni, Eman A., Abouelhoda, Mohamed, Monies, Dorota, Mustafa, Abeer E., Khalil, Dania S., Al Haibi, Sara, Abou Al-Shaar, Hussam, Faquih, Tariq, El-Kalioby, Mohamed, Tahir, Asma I., Al Tassan, Nada A.
Published in BMC research notes (07.06.2016)
Published in BMC research notes (07.06.2016)
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Journal Article
PTPA variants and the risk for Parkinson’s disease in diverse ancestry populations
Ostrožovičová, Miriam, Mecheri, Yasser, Al-Mubarak, Bashayer R, Al-Tassan, Nada, Makarious, Mary B, Periñan, Maria Teresa, Bandres-Ciga, Sara
Published in Brain (London, England : 1878) (01.12.2023)
Published in Brain (London, England : 1878) (01.12.2023)
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Journal Article
A comprehensive introduction to the genetic basis of non-syndromic hearing loss in the Saudi Arabian population
Imtiaz, Faiqa, Taibah, Khalid, Ramzan, Khushnooda, Bin-Khamis, Ghada, Kennedy, Shelley, Al-Mubarak, Bashayer, Trabzuni, Daniah, Allam, Rabab, Al-Mostafa, Abeer, Sogaty, Sameera, Al-Shaikh, Abdulmoneem H, Bamukhayyar, Saeed S, Meyer, Brian F, Al-Owain, Mohammed
Published in BMC medical genetics (04.07.2011)
Published in BMC medical genetics (04.07.2011)
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Journal Article
The AfrAbia+plus Parkinson's Disease Genomic Consortium
Mohamed, Wael, Eltantawi, Mohamed Abdelhalim, Mecheri, Yasser, Zewde, Yared Zenebe, Kamel, Walaa A, Al-Mubarak, Bashayer R, Alzoubi, Karem H, Kissani, Najib, Alghamdi, Badrah S, Ben Sassi, Samia
Published in Lancet neurology (01.02.2024)
Published in Lancet neurology (01.02.2024)
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Journal Article
Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families
Al-Mubarak, Bashayer, Abouelhoda, Mohamed, Omar, Aisha, AlDhalaan, Hesham, Aldosari, Mohammed, Nester, Michael, Alshamrani, Hussain. A., El-Kalioby, Mohamed, Goljan, Ewa, Albar, Renad, Subhani, Shazia, Tahir, Asma, Asfahani, Sultana, Eskandrani, Alaa, Almusaiab, Ahmed, Magrashi, Amna, Shinwari, Jameela, Monies, Dorota, Al Tassan, Nada
Published in Scientific reports (18.07.2017)
Published in Scientific reports (18.07.2017)
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Journal Article
Whole exome sequencing in ADHD trios from single and multi-incident families implicates new candidate genes and highlights polygenic transmission
Al-Mubarak, Bashayer R., Omar, Aisha, Baz, Batoul, Al-Abdulaziz, Basma, Magrashi, Amna I., Al-Yemni, Eman, Jabaan, Amjad, Monies, Dorota, Abouelhoda, Mohamed, Abebe, Dejene, Ghaziuddin, Mohammad, Al-Tassan, Nada A.
Published in European journal of human genetics : EJHG (01.08.2020)
Published in European journal of human genetics : EJHG (01.08.2020)
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Journal Article
The Subtype of GluN2 C-terminal Domain Determines the Response to Excitotoxic Insults
Martel, Marc-André, Ryan, Tomás J., Bell, Karen F.S., Fowler, Jill H., McMahon, Aoife, Al-Mubarak, Bashayer, Komiyama, Noboru H., Horsburgh, Karen, Kind, Peter C., Grant, Seth G.N., Wyllie, David J.A., Hardingham, Giles E.
Published in Neuron (Cambridge, Mass.) (10.05.2012)
Published in Neuron (Cambridge, Mass.) (10.05.2012)
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Journal Article
Mild oxidative stress activates Nrf2 in astrocytes, which contributes to neuroprotective ischemic preconditioning
Bell, Karen F, Al-Mubarak, Bashayer, Fowler, Jill H, Baxter, Paul S, Gupta, Kunal, Tsujita, Tadayuki, Chowdhry, Sudhir, Patani, Rickie, Chandran, Siddharthan, Horsburgh, Karen, Hayes, John D, Hardingham, Giles E
Published in Proceedings of the National Academy of Sciences - PNAS (04.01.2011)
Published in Proceedings of the National Academy of Sciences - PNAS (04.01.2011)
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Journal Article
Homeostatic Presynaptic Plasticity Is Specifically Regulated by P/Q-type Ca2+ Channels at Mammalian Hippocampal Synapses
Jeans, Alexander F., van Heusden, Fran C., Al-Mubarak, Bashayer, Padamsey, Zahid, Emptage, Nigel J.
Published in Cell reports (Cambridge) (10.10.2017)
Published in Cell reports (Cambridge) (10.10.2017)
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Journal Article
The Genetic Architecture of Parkinson's Disease in the AfrAbia Population: Current State and Future Perspectives
Mohamed, Wael, Eltantawi, Mohamed Abdelhalim, Agarwal, Vidhu, Bandres-Ciga, Sara, Makarious, Mary B, Mecheri, Yasser, Zewde, Yared Zenebe, Kamel, Walaa A., Al-Mubarak, Bashayer, Alzoubi, Karem H., Kissani, Najib, Alghamdi, Badrah S, Sassi, Samia Ben, AA-PD-GC, on behalf of
Published in Journal of integrative neuroscience (01.01.2024)
Published in Journal of integrative neuroscience (01.01.2024)
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Journal Article
Nrf2 target genes can be controlled by neuronal activity in the absence of Nrf2 and astrocytes
Deighton, Ruth F., Márkus, Nóra M., Al-Mubarak, Bashayer, Bell, Karen F. S., Papadia, Sofia, Meakin, Paul J., Chowdhry, Sudhir, Hayes, John D., Hardingham, Giles E.
Published in Proceedings of the National Academy of Sciences - PNAS (06.05.2014)
Published in Proceedings of the National Academy of Sciences - PNAS (06.05.2014)
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Journal Article
Validation of Ion TorrentTM Inherited Disease Panel with the PGMTM Sequencing Platform for Rapid and Comprehensive Mutation Detection
Mustafa, Abeer E., Faquih, Tariq, Baz, Batoul, Kattan, Rana, Al-Issa, Abdulelah, Tahir, Asma I., Imtiaz, Faiqa, Ramzan, Khushnooda, Al-Sayed, Moeenaldeen, Alowain, Mohammed, Al-Hassnan, Zuhair, Al-Zaidan, Hamad, Abouelhoda, Mohamed, Al-Mubarak, Bashayer R., Al Tassan, Nada A.
Published in Genes (22.05.2018)
Published in Genes (22.05.2018)
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Journal Article
Identification of mutations causing hereditary tyrosinemia type I in patients of Middle Eastern origin
Imtiaz, Faiqa, Rashed, Mohamed S., Al-Mubarak, Bashayer, Allam, Rabab, El-Karaksy, Hanaa, Al-Hassnan, Zuhair, Al-Owain, Mohammed, Al-Zaidan, Hamad, Rahbeeni, Zuhair, Qari, Alya, Meyer, Brian F., Al-Sayed, Moeen
Published in Molecular genetics and metabolism (01.12.2011)
Published in Molecular genetics and metabolism (01.12.2011)
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Journal Article