Synaptic NMDAR activity suppresses FOXO1 expression via a cis-acting FOXO binding site: FOXO1 is a FOXO target gene

由 Al-Mubarak, Bashayer, Soriano, Francesc X., Hardingham, Giles E.
出版 2009

Activation of Nrf2-Regulated Glutathione Pathway Genes by Ischemic Preconditioning

由 Bell, Karen F. S., Fowler, Jill H., Al-Mubarak, Bashayer, Horsburgh, Karen, Hardingham, Giles E.
出版 2011

Homeostatic Presynaptic Plasticity Is Specifically Regulated by P/Q-type Ca(2+) Channels at Mammalian Hippocampal Synapses

由 Jeans, Alexander F., van Heusden, Fran C., Al-Mubarak, Bashayer, Padamsey, Zahid, Emptage, Nigel J.
發表在 Cell Rep (2017)

Targeted de-repression of neuronal Nrf2 inhibits α-synuclein accumulation

由 Baxter, Paul S., Márkus, Nóra M., Dando, Owen, He, Xin, Al-Mubarak, Bashayer R., Qiu, Jing, Hardingham, Giles E.
發表在 Cell Death Dis (2021)

Nrf2 target genes can be controlled by neuronal activity in the absence of Nrf2 and astrocytes

由 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.
出版 2014

Analysis of shared homozygosity regions in Saudi siblings with attention deficit hyperactivity disorder

由 Shinwari, Jameela M.A., Al Yemni, Eman A.A., Alnaemi, Faten M., Abebe, Dejene, Al-Abdulaziz, Basma S., Al Mubarak, Bashayer R., Ghaziuddin, Mohammad, Al Tassan, Nada A.
發表在 Psychiatr Genet (2017)

Mild oxidative stress activates Nrf2 in astrocytes, which contributes to neuroprotective ischemic preconditioning

由 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.
出版 2010

Estimating transfection efficiency in differentiated and undifferentiated neural cells

由 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.
發表在 BMC Res Notes (2019)

Whole exome sequencing in ADHD trios from single and multi-incident families implicates new candidate genes and highlights polygenic transmission

由 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.
發表在 Eur J Hum Genet (2020)

A comprehensive introduction to the genetic basis of non-syndromic hearing loss in the Saudi Arabian population

由 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
出版 2011

The Subtype of GluN2 C-terminal Domain Determines the Response to Excitotoxic Insults

由 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.
出版 2012

Clinical heterogeneity of PLA2G6-related Parkinsonism: analysis of two Saudi families

由 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.
發表在 BMC Res Notes (2016)

Parkinson’s Disease in Saudi Patients: A Genetic Study

由 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.
發表在 PLoS One (2015)

Validation of Ion Torrent(TM) Inherited Disease Panel with the PGM(TM) Sequencing Platform for Rapid and Comprehensive Mutation Detection

由 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.
發表在 Genes (Basel) (2018)

Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families

由 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
發表在 Sci Rep (2017)

Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson’s Disease

由 Yemni, Eman Al, Monies, Dorota, Alkhairallah, Thamer, Bohlega, Saeed, Abouelhoda, Mohamed, Magrashi, Amna, Mustafa, Abeer, AlAbdulaziz, Basma, Alhamed, Mohamed, Baz, Batoul, Goljan, Ewa, Albar, Renad, Jabaan, Amjad, Faquih, Tariq, Subhani, Shazia, Ali, Wafa, Shinwari, Jameela, Al-Mubarak, Bashayer, Al-Tassan, Nada
發表在 Sci Rep (2019)

Spectrum of Mutations in 60 Saudi Patients with Mut Methylmalonic Acidemia

由 Imtiaz, Faiqa, Al-Mubarak, Bashayer M., Al-Mostafa, Abeer, Al-Hamed, Mohamed, Allam, Rabab, Al-Hassnan, Zuhair, Al-Owain, Mohammed, Al-Zaidan, Hamad, Rahbeeni, Zuhair, Qari, Alya, Faqeih, Eissa Ali, Alasmari, Ali, Al-Mutairi, Fuad, Alfadhel, Majid, Eyaid, Wafaa M., Rashed, Mohamed S., Al-Sayed, Moeenaldeen
發表在 JIMD Rep (2015)

Neuronal development is promoted by weakened intrinsic antioxidant defences due to epigenetic repression of Nrf2

由 Bell, Karen F.S., Al-Mubarak, Bashayer, Martel, Marc-André, McKay, Sean, Wheelan, Nicola, Hasel, Philip, Márkus, Nóra M., Baxter, Paul, Deighton, Ruth F., Serio, Andrea, Bilican, Bilada, Chowdhry, Sudhir, Meakin, Paul J., Ashford, Michael L.J., Wyllie, David J.A., Scannevin, Robert H., Chandran, Siddharthan, Hayes, John D., Hardingham, Giles E.
發表在 Nat Commun (2015)