1. ScholarBank@NUS

Mahmoud Abdul Hossein Pouladi

rp01637

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

Publications

Results 1-20 of 21 (Search time: 0.018 seconds).

Issue DateTitleAuthor(s)
12018A homozygous loss-of-function camk2a mutation causes growth delay, frequent seizures and severe intellectual disabilityChia, P.H; Zhong, F.L; Niwa, S; Bonnard, C; Utami, K.H; Zeng, R; Lee, H; Eskin, A; Nelson, S.F; Xie, W.H; Al-Tawalbeh, S; El-Khateeb, M; Shboul, M; Pouladi, M.A ; Al-Raqad, M; Reversade, B 
26-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 
32017A thiol probe for measuring unfolded protein load and proteostasis in cellsChen, M.Z; Moily, N.S; Bridgford, J.L; Wood, R.J; Radwan, M; Smith, T.A; Song, Z; Tang, B.Z; Tilley, L; Xu, X; Reid, G.E; Pouladi, M.A ; Hong, Y; Hatters, D.M
42015Anti-semaphorin 4D immunotherapy ameliorates neuropathology and some cognitive impairment in the YAC128 mouse model of Huntington diseaseSouthwell A.L.; Franciosi S.; Villanueva E.B.; Xie Y.; Winter L.A.; Veeraraghavan J.; Jonason A.; Felczak B.; Zhang W.; Kovalik V.; Waltl S.; Hall G.; Pouladi M.A. ; Smith E.S.; Bowers W.J.; Zauderer M.; Hayden M.R.
526-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.
627-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. 
7Oct-2019Generation of four H1 hESC sublines carrying a hemizygous knock-out/mutant MECP2Zeng, Ruizhu; Sidik, Harwin; Robinson, Kim S; Zhong, Franklin L; Reversade, Bruno ; Pouladi, Mahmoud A 
82016Histone modifications and p53 binding poise the p21 promoter for activation in human embryonic stem cellsItahana Y. ; Zhang J.; Göke J.; Vardy L.A.; Han R. ; Iwamoto K. ; Cukuroglu E.; Robson P.; Pouladi M.A. ; Colman A.; Itahana K. 
92015Inhibition of Excessive Monoamine Oxidase A/B Activity Protects Against Stress-induced Neuronal Death in Huntington DiseaseOoi, J; Hayden, M.R ; Pouladi, M.A 
102016Laquinimod rescues striatal, cortical and white matter pathology and results in modest behavioural improvements in the YAC128 model of Huntington diseaseGarcia-Miralles, M; Hong, X; Tan, L.J; Caron, N.S; Huang, Y; To, X.V; Lin, R.Y; Franciosi, S; Papapetropoulos, S; Hayardeny, L; Hayden, M.R ; Chuang, K.-H; Pouladi, M.A 
112018Large-scale transcriptomic analysis reveals that pridopidine reverses aberrant gene expression and activates neuroprotective pathways in the YAC128 HD mouseKusko R.; Dreymann J.; Ross J.; Cha Y.; Escalante-Chong R.; Garcia-Miralles M. ; Tan L.J.; Burczynski M.E.; Zeskind B.; Laifenfeld D.; Pouladi M. ; Geva M.; Grossman I.; Hayden M.R. 
122020Loss-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. 
132016Modeling Doxorubicin-Induced Cardiotoxicity in Human Pluripotent Stem Cell Derived-CardiomyocytesMaillet, A ; Tan, K; Chai, X ; Sadananda, S.N; Mehta, A ; Ooi, J; Hayden, M.R ; Pouladi, M.A ; Ghosh, S ; Shim, W ; Brunham, L.R 
142017Narciclasine attenuates diet-induced obesity by promoting oxidative metabolism in skeletal muscleJulien S.G.; Kim S.-Y.; Brunmeir R. ; Sinnakannu J.R. ; Ge X.; Li H.; Ma W.; Yaligar J.; Bhanu Prakash K.N.; Velan S.S. ; R�der P.V.; Zhang Q.; Sim C.K.; Wu J.; Garcia-Miralles M. ; Pouladi M.A. ; Xie W.; McFarlane C.; Han W. ; Xu F. 
152019Novel mutation in HTRA1 in a family with diffuse white matter lesions and inflammatory featuresZiaei, A.; Xu, X.; Dehghani, L.; Bonnard, C.; Zellner, A.; Ng, A.Y.J.; Tohari, S.; Venkatesh, B. ; Haffner, C.; Reversade, B.; Shaygannejad, V.; Pouladi, M.A. 
162015Partial rescue of some features of Huntington Disease in the genetic absence of caspase-6 in YAC128 miceWong B.K.Y.; Ehrnhoefer D.E.; Graham R.K.; Martin D.D.O.; Ladha S.; Uribe V.; Stanek L.M.; Franciosi S.; Qiu X.; Deng Y.; Kovalik V.; Zhang W.; Pouladi M.A. ; Shihabuddin L.S.; Hayden M.R.
174-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
182020pS421 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. 
191-Apr-2016Treatment with the MAO-A inhibitor clorgyline elevates monoamine neurotransmitter levels and improves affective phenotypes in a mouse model of Huntington diseaseGarcia-Miralles, Marta ; Ooi, Jolene; Bardile, Costanza Ferrari; Tan, Liang Juin ; George, Maya; Drum, Chester L ; Lin, Rachel Yanping; Hayden, Michael R ; Pouladi, Mahmoud A 
202019Unbiased Profiling of Isogenic Huntington Disease hPSC-Derived CNS and Peripheral Cells Reveals Strong Cell-Type Specificity of CAG Length EffectsOoi, J.; Langley, S.R. ; Xu, X.; Utami, K.H.; Sim, B.; Huang, Y.; Harmston, N.P. ; Tay, Y.L.; Ziaei, A.; Zeng, R.; Low, D.; Aminkeng, F.; Sobota, R.M.; Ginhoux, F.; Petretto, E.; Pouladi, M.A.