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Mahmoud A. Pouladi

British Columbia Children's Hospital Research Institute

44H指数
164论文数
8.0K被引数
收录论文 86
发表时间
Convergent and Divergent Molecular Pathways in FMR1-, TSC2- and FMR1/TSC2 Knockout NeuronsFMR1-、TSC2-和FMR1/TSC2基因敲除神经元中的汇聚与发散分子通路
err2026-09-08
err0
PREAI
errKagistia Hana Utami; Nur Amirah Binte Muhammed Yusof; Yazhini Ramaswamy; Stacey Kiat Hong Tay; Ramkumar Aishworiya; Nevin Tham; Sarah R. Langley; Mahmoud A. Pouladi; Velda X. Han
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TSC2 GAP Domain V1646Cfs*7 Variant Alters Protein Stability and Interaction Networks in Tuberous Sclerosis ComplexTSC2 GTP酶激活蛋白结构域V1646Cfs*7变异改变结节性硬化症的蛋白质稳定性和相互作用网络
err2026-04-01
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PREAI
errUtami, Kagistia Hana; Han, Velda X.; Mohammad Yusof, Nur Amirah Bte; Ramaswamy, Yazhini; Feng, Jia; Tay, Stacey Kiat Hong; Langley, Sarah R.; Pouladi, Mahmoud A.
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Molecular and imaging biomarker responses to brain mutant HTT lowering in a mouse model of Huntington disease分子和成像生物标志物对亨廷顿病小鼠模型中脑突变HTT降低的反应
err2025-09-06
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errOAAI
errNicholas S. Caron; Jianjia Fan; Da Ma; Andrew Yung; Seunghyun Ko; Kirsten Bale; Christine Anderson; Piotr Kozlowski; Mahmoud A. Pouladi; Cheryl L. Wellington; Michael R. Hayden
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A potential role for NADPH oxidase (NOX1/2) in mutant huntingtin-induced anomalous neurite outgrowthNADPH氧化酶(NOX1/2)在突变亨廷蛋白诱导的异常神经突起生长中的潜在作用
err2025-05-22
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PREAI
errLuisana Duque Villegas; Alberte Vad Mathiesen; Izabela Rasmussen; Maria von Broich; Filippa Liliendahl Qvist; Niels Skotte; Costanza Ferrari Bardile; Esben Budtz-Jørgensen; Kristine Freude; Benjamin Schmid; Mahmoud A. Pouladi; Anne Nørremølle; Frederik Vilhardt
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PRMT5 promotes full-length HTT expression by repressing multiple proximal intronic polyadenylation sitesPRMT5通过抑制多个近端内含子多聚腺苷酸化位点来促进全长HTT的表达。
err2025-04-30
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errOAAI
errYadav, Manisha; AlQazzaz, Mona A.; Ciamponi, Felipe E.; Ho, Jolene C.; Maron, Maxim, I; Sababi, Aiden M.; MacLeod, Graham; Ahmadi, Moloud; Bullivant, Garrett; Tano, Vincent; Langley, Sarah R.; Sanchez-Osuna, Maria; Sachamitr, Patty; Kushida, Michelle; Bardile, Costanza Ferrari; Pouladi, Mahmoud A.; Kurtz, Rebecca; Richards, Laura; Pugh, Trevor; Tyers, Mike; Angers, Stephane; Dirks, Peter B.; Bader, Gary D.; Truant, Ray; Massirer, Katlin B.; Barsyte-Lovejoy, Dalia; Shechter, David; Harding, Rachel J.; Arrowsmith, Cheryl H.; Prinos, Panagiotis
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Huntingtin is an RNA binding protein and participates in NEAT1-mediated paraspeckles
err2024-07-19
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errOAAI
errYadav, Manisha; Harding, Rachel J.; Li, Tiantian; Xu, Xin; Gall-Duncan, Terence; Khan, Mahreen; Bardile, Costanza Ferrari; Sequiera, Glen L.; Duan, Shili; Chandrasekaran, Renu; Pan, Anni; Bu, Jiachuan; Yamazaki, Tomohiro; Hirose, Tetsuro; Prinos, Panagiotis; Tippett, Lynette; Turner, Clinton; Curtis, Maurice A.; Faull, Richard L. M.; Pouladi, Mahmoud A.; Pearson, Christopher E.; He, Housheng Hansen; Arrowsmith, Cheryl H.
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CHCHD2 up-regulation in Huntington disease mediates a compensatory protective response against oxidative stress
err2024-02-10
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errOAAI
errLiu, Xuanzhuo; Wang, Fang; Fan, Xinman; Chen, Mingyi; Xu, Xiaoxin; Xu, Qiuhong; Zhu, Huili; Xu, Anding; Pouladi, Mahmoud A.; Xu, Xiaohong
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Claudin-11 in health and disease: implications for myelin disorders, hearing, and fertility
err2024-01-17
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errOAAI
errGjervan, Sophia C.; Ozgoren, Oguz K.; Gow, Alexander; Stockler-Ipsiroglu, Sylvia; Pouladi, Mahmoud A.
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Oligodendrocyte pathology in Huntington's disease: from mechanisms to therapeutics
err2023-10-01
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PREAI
errBardile, Costanza Ferrari; Radulescu, Carola I.; Pouladi, Mahmoud A.
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Dysregulated COMT Expression in Fragile X Syndrome
err2023-09-08
err1
PREAI
errUtami, Kagistia Hana; Yusof, Nur Amirah Binte Muhammed; Garcia-Miralles, Marta; Skotte, Niels Henning; Nama, Srikanth; Sampath, Prabha; Langley, Sarah R.; Pouladi, Mahmoud A.
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Widespread dysregulation of mRNA splicing implicates RNA processing in the development and progression of disease
err2023-08-01
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errOAAI
errTano, Vincent; Utami, Kagistia Hana; Yusof, Nur Amirah Binte Mohammad; Begin, Jocelyn; Tan, Willy Wei Li; Pouladi, Mahmoud A.; Langley, Sarah R.
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Evidences for Mutant Huntingtin Inducing Musculoskeletal and Brain Growth Impairments via Disturbing Testosterone Biosynthesis in Male Huntington Disease Animals
errCELLS
IF5.2
err2022-11-25
err4
errOAAI
errYu-Taeger, Libo; Novati, Arianna; Weber, Jonasz Jeremiasz; Singer-Mikosch, Elisabeth; Pabst, Ann-Sophie; Cheng, Fubo; Saft, Carsten; Koenig, Jennifer; Ellrichmann, Gisa; Heikkinen, Taneli; Pouladi, Mahmoud A.; Riess, Olaf; Nguyen, Huu Phuc
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MUTANT HUNTINGTIN IMPAIRS MUSCULOSKELETAL AND BRAIN GROWTH VIA DISTURBING TESTOSTERONE BIOSYNTHESIS IN MALE HUNTINGTON DISEASE ANIMALS
err2022-09-12
err0
PREAI
errYu-Taeger, Libo; Novati, Arianna; Weber, Jonasz Jeremiasz; Singer-Mikosch, Elisabeth; Pabst, Ann-Sophie; Saft, Carsten; Koenig, Jennifer; Ellrichmann, Gisa; Heikkinen, Taneli; Pouladi, Mahmoud A.; Riess, Olaf; Nguyen, Huu Phuc
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Maturation Delay of Human GABAergic Neurogenesis in Fragile X Syndrome Pluripotent Stem Cells
err2022-05-12
err11
errOAAI
errZhang, Ai; Sokolova, Irina; Domissy, Alain; Davis, Joshua; Rao, Lee; Utami, Kagistia Hana; Wang, Yanling; Hagerman, Randi J.; Pouladi, Mahmoud A.; Sanna, Pietro; Boland, Michael J.; Loring, Jeanne F.
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Ermin deficiency leads to compromised myelin, inflammatory milieu, and susceptibility to demyelinating insult
err2022-03-13
err8
errOAAI
errZiaei, Amin; Garcia-Miralles, Marta; Radulescu, Carola, I; Sidik, Harwin; Silvin, Aymeric; Bae, Han-Gyu; Bonnard, Carine; Yusof, Nur Amirah Binte Mohammad; Bardile, Costanza Ferrari; Tan, Liang Juin; Ng, Alvin Yu Jin; Tohari, Sumanty; Dehghani, Leila; Henry, Lily; Yeo, Xin Yi; Lee, Sejin; Venkatesh, Byrappa; Langley, Sarah R.; Shaygannejad, Vahid; Reversade, Bruno; Jung, Sangyong; Ginhoux, Florent; Pouladi, Mahmoud A.
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Rescue of aberrant huntingtin palmitoylation ameliorates mutant huntingtin-induced toxicity异常亨廷顿棕榈酰化的拯救改善突变亨廷顿诱导的毒性
err2021-10-01
err21
errOAAI
errLemarie, Fanny L.; Caron, Nicholas S.; Sanders, Shaun S.; Schmidt, Mandi E.; Nguyen, Yen T. N.; Ko, Seunghyun; Xu, Xiaohong; Pouladi, Mahmoud A.; Martin, Dale D. O.; Hayden, Michael R.
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ABNORMAL SPINAL CORD MYELINATION DUE TO OLIGODENDROCYTE DYSFUNCTION IN A MODEL OF HUNTINGTON DISEASE
err2021-09-05
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PREAI
errBardile, Costanza Ferrari; Sidik, Harwin; Quek, Reynard; Yusof, Nur Amirah Binte Mohammad; Garcia-Miralles, Marta; Pouladi, Mahmoud A.
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Early white matter pathology in the fornix of the limbic system in Huntington disease亨廷顿病边缘系统的the骨的早期白质病理学
err2021-08-26
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errOAAI
errGabery, Sanaz; Kwa, Jing Eugene; Cheong, Rachel Y.; Baldo, Barbara; Bardile, Costanza Ferrari; Tan, Brendan; McLean, Catriona; Georgiou-Karistianis, Nellie; Poudel, Govinda R.; Halliday, Glenda; Pouladi, Mahmoud A.; Petersen, Asa
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Urokinase plasminogen activator mediates changes in human astrocytes modeling fragile X syndrome
errGLIA
IF5.1
err2021-08-24
err12
errOAAI
errPeteri, 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.; Castren, Maija L.
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A Micropatterned Human-Specific Neuroepithelial Tissue for Modeling Gene and Drug-Induced Neurodevelopmental Defects (vol 8, 2001100, 2021)
err2021-07-07
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errOAAI
errSahni, Geetika; Chang, Shu-Yung; Teo, Jeremy Choon Meng; 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
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