Full Name
Mahmoud Abdul Hossein Pouladi
(not current staff)
Variants
Pouladi M.A.
 
Main Affiliation
 
 
Email
pouladi@nus.edu.sg
 

Publications

Refined By:
Type:  Article
Date Issued:  [2020 TO 2024]

Results 1-7 of 7 (Search time: 0.008 seconds).

Issue DateTitleAuthor(s)
16-Jan-2021A Micropatterned Human-Specific Neuroepithelial Tissue for Modeling Gene and Drug-Induced Neurodevelopmental DefectsSahni, Geetika ; Chang, Shu-Yung ; Meng, Jeremy Teo Choon; Tan, Jerome Zu Yao; Fatien, Jean Jacques Clement; Bonnard, Carine; Utami, Kagistia Hana; Chan, Puck Wee; Tan, Thong Teck; Altunoglu, Umut; Kayserili, Hulya; Pouladi, Mahmoud ; Reversade, Bruno ; Toh, Yi-Chin 
226-Aug-2021Early white matter pathology in the fornix of the limbic system in Huntington diseaseGabery, Sanaz; Kwa, Jing Eugene; Cheong, Rachel Y.; Baldo, Barbara; Ferrari Bardile, C.; Tan, Brendan; McLean, Catriona; Georgiou-Karistianis, Nellie; Poudel, Govinda R.; Halliday, Glenda; Pouladi, Mahmoud A. ; Petersén, Å.
327-May-2020Elevated de novo protein synthesis in FMRP-deficient human neurons and its correction by metformin treatmentUtami, K.H. ; Yusof, N.A.B.M. ; Kwa, J.E.; Peteri, U.-K.; Castrén, M.L.; Pouladi, M.A. 
42020Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathyHengel, H.; Bosso-Lefèvre, C.; Grady, G.; Szenker-Ravi, E.; Li, H.; Pierce, S.; Lebigot, É.; Tan, T.-T.; Eio, M.Y.; Narayanan, G.; Utami, K.H.; Yau, M.; Handal, N.; Deigendesch, W.; Keimer, R.; Marzouqa, H.M.; Gunay-Aygun, M.; Muriello, M.J.; Verhelst, H.; Weckhuysen, S.; Mahida, S.; Naidu, S.; Thomas, T.G.; Lim, J.Y.; Tan, E.S.; Haye, D.; Willemsen, M.A.A.P.; Oegema, R.; Mitchell, W.G.; Pierson, T.M.; Andrews, M.V.; Willing, M.C.; Rodan, L.H.; Barakat, T.S.; van Slegtenhorst, M.; Gavrilova, R.H.; Martinelli, D.; Gilboa, T.; Tamim, A.M.; Hashem, M.O.; AlSayed, M.D.; Abdulrahim, M.M.; Al-Owain, M.; Awaji, A.; Mahmoud, A.A.H.; Faqeih, E.A.; Asmari, A.A.; Algain, S.M.; Jad, L.A.; Aldhalaan, H.M.; Helbig, I.; Koolen, D.A.; Riess, A.; Kraegeloh-Mann, I.; Bauer, P.; Gulsuner, S.; Stamberger, H.; Ng, A.Y.J.; Tang, S.; Tohari, S.; Keren, B.; Schultz-Rogers, L.E.; Klee, E.W.; Barresi, S.; Tartaglia, M.; Mor-Shaked, H.; Maddirevula, S.; Begtrup, A.; Telegrafi, A.; Pfundt, R.; Schüle, R.; Ciruna, B.; Bonnard, C.; Pouladi, M.A. ; Stewart, J.C.; Claridge-Chang, A.; Lefeber, D.J.; Alkuraya, F.S.; Mathuru, A.S.; Venkatesh, B. ; Barycki, J.J.; Simpson, M.A.; Jamuar, S.S.; Schöls, L.; Reversade, B. 
54-Mar-2021Pluripotent stem cell-derived models of neurological diseases reveal early transcriptional heterogeneitySorek, Matan; Oweis, Walaa; Nissim-Rafinia, Malka; Maman, Moria; Simon, Shahar; Hession, Cynthia C.; Adiconis, Xian; Simmons, Sean K.; Sanjana, Neville E.; Shi, Xi; Lu, Congyi; Pan, Jen Q.; Xu, Xiaohong; Pouladi, Mahmoud A. ; Ellerby, Lisa M.; Zhang, Feng; Levin, Joshua Z.; Meshorer, Eran
62020pS421 huntingtin modulates mitochondrial phenotypes and confers neuroprotection in an HD hiPSC modelXu, X.; Ng, B.; Sim, B.; Radulescu, C.I.; Yusof, N.A.B.M.; Goh, W.I.; Lin, S.; Lim, J.S.Y.; Cha, Y.; Kusko, R.; Kay, C.; Ratovitski, T.; Ross, C.; Hayden, M.R.; Wright, G.; Pouladi, M.A. 
724-Aug-2021Urokinase plasminogen activator mediates changes in human astrocytes modeling fragile X syndromePeteri, Ulla-Kaisa; Pitkonen, Juho; de Toma, Ilario; Nieminen, Otso; Utami, Kagistia Hana ; Strandin, Tomas M.; Corcoran, Padraic; Roybon, Laurent; Vaheri, Antti; Ethell, Iryna; Casarotto, Plinio; Pouladi, Mahmoud A. ; Castrén, M.L.