Mahmoud A Pouladi

Scopus Author ID Loop profile ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 20

Top Venues

Cell death & disease

Molecular neurobiology

Science advances

Journal of neurochemistry

This page only lists publications with an associated author ORCID identifier.

Publications

Xuanzhuo Liu, Fang Wang, Xinman Fan, Mingyi Chen, Xiaoxin Xu, Qiuhong Xu, Huili Zhu, Liangxue Lai, Mahmoud A Pouladi, Xiaohong Xu
CHCHD2 up-regulation in Huntington disease mediates a compensatory protective response against oxidative stress. Cell death & disease 15 (2) (2024)
Manisha Yadav, Rachel J Harding, Tiantian Li, Xin Xu, Terence Gall-Duncan, Mahreen Khan, Costanza Ferrari Bardile, Glen Lester Sequiera, Shili Duan, Renu Chandrasekaran, Anni Pan, Jiachuan Bu, Tomohiro Yamazaki, Tetsuro Hirose, Panagiotis Prinos, Lynette Tippett, Clinton Turner, Maurice A Curtis, Richard L M Faull, Mahmoud A Pouladi, Christopher E Pearson, Housheng Hansen He, Cheryl H Arrowsmith
Huntingtin is an RNA binding protein and participates in NEAT1 -mediated paraspeckles. Science advances 10 (29) (2024)
Xuanzhuo Liu, Fang Wang, Xinman Fan, Mingyi Chen, Xiaoxin Xu, Qiuhong Xu, Huili Zhu, Liangxue Lai, Mahmoud A Pouladi, Xiaohong Xu
CHCHD2 up-regulation in Huntington disease mediates a compensatory protective response against oxidative stress. Cell death & disease 15 (2) (2024)
Shaima Hourani, Mahmoud A Pouladi
Oligodendroglia and myelin pathology in fragile X syndrome. Journal of neurochemistry (2024)
Xuanzhuo Liu, Fang Wang, Xinman Fan, Mingyi Chen, Xiaoxin Xu, Qiuhong Xu, Huili Zhu, Liangxue Lai, Mahmoud A Pouladi, Xiaohong Xu
CHCHD2 up-regulation in Huntington disease mediates a compensatory protective response against oxidative stress. Cell death & disease 15 (2) (2024)
Xuanzhuo Liu, Fang Wang, Xinman Fan, Mingyi Chen, Xiaoxin Xu, Qiuhong Xu, Huili Zhu, Liangxue Lai, Mahmoud A Pouladi, Xiaohong Xu
CHCHD2 up-regulation in Huntington disease mediates a compensatory protective response against oxidative stress. Cell death & disease 15 (2) (2024)
Shaima Hourani, Mahmoud A Pouladi
Oligodendroglia and myelin pathology in fragile X syndrome. Journal of neurochemistry (2024)
Xuanzhuo Liu, Fang Wang, Xinman Fan, Mingyi Chen, Xiaoxin Xu, Qiuhong Xu, Huili Zhu, Liangxue Lai, Mahmoud A Pouladi, Xiaohong Xu
CHCHD2 up-regulation in Huntington disease mediates a compensatory protective response against oxidative stress. Cell death & disease 15 (2) (2024)
Manisha Yadav, Rachel J Harding, Tiantian Li, Xin Xu, Terence Gall-Duncan, Mahreen Khan, Costanza Ferrari Bardile, Glen Lester Sequiera, Shili Duan, Renu Chandrasekaran, Anni Pan, Jiachuan Bu, Tomohiro Yamazaki, Tetsuro Hirose, Panagiotis Prinos, Lynette Tippett, Clinton Turner, Maurice A Curtis, Richard L M Faull, Mahmoud A Pouladi, Christopher E Pearson, Housheng Hansen He, Cheryl H Arrowsmith
Huntingtin is an RNA binding protein and participates in NEAT1 -mediated paraspeckles. Science advances 10 (29) (2024)
Carola I Radulescu, Costanza Ferrari Bardile, Marta Garcia-Miralles, Harwin Sidik, Nur Amirah Binte Mohammad Yusof, Mahmoud A Pouladi
Environmental Deprivation Effects on Myelin Ultrastructure in Huntington Disease and Wildtype Mice. Molecular neurobiology (2023)
Amin Ziaei, Marta Garcia-Miralles, Carola I Radulescu, Harwin Sidik, Aymeric Silvin, Han-Gyu Bae, Carine Bonnard, Nur Amirah Binte Mohammad Yusof, Costanza Ferrari Bardile, Liang Juin Tan, Alvin Yu Jin Ng, Sumanty Tohari, Leila Dehghani, Lily Henry, Xin Yi Yeo, Sejin Lee, Byrappa Venkatesh, Sarah R Langley, Vahid Shaygannejad, Bruno Reversade, Sangyong Jung, Florent Ginhoux, Mahmoud A Pouladi
Ermin deficiency leads to compromised myelin, inflammatory milieu, and susceptibility to demyelinating insult. Brain pathology (Zurich, Switzerland) 32 (5) (2022)
Kagistia Hana Utami, Nur Amirah Binte Mohammad Yusof, Jing Eugene Kwa, Ulla-Kaisa Peteri, Maija L Castrén, Mahmoud A Pouladi
Elevated de novo protein synthesis in FMRP-deficient human neurons and its correction by metformin treatment. Molecular autism 11 (1) (2020)
Xiaohong Xu, Bryan Ng, Bernice Sim, Carola I Radulescu, Nur Amirah Binte Mohammad Yusof, Wah Ing Goh, Shuping Lin, John Soon Yew Lim, Yoonjeong Cha, Rebecca Kusko, Chris Kay, Tamara Ratovitski, Christopher Ross, Michael R Hayden, Graham Daniel Wright, Mahmoud A Pouladi
pS421 huntingtin modulates mitochondrial phenotypes and confers neuroprotection in an HD hiPSC model. Cell death & disease 11 (9) (2020)
Roy Tang Yi Teo, Costanza Ferrari Bardile, Yi Lin Tay, Nur Amirah Binte Mohammad Yusof, Charbel A Kreidy, Liang Juin Tan, Mahmoud A Pouladi
Impaired Remyelination in a Mouse Model of Huntington Disease. Molecular neurobiology 56 (10) (2019)
Costanza Ferrari Bardile, Marta Garcia-Miralles, Nicholas S Caron, Nirmala Arul Rayan, Sarah R Langley, Nathan Harmston, Ana Maria Rondelli, Roy Tang Yi Teo, Sabine Waltl, Lisa M Anderson, Han-Gyu Bae, Sangyong Jung, Anna Williams, Shyam Prabhakar, Enrico Petretto, Michael R Hayden, Mahmoud A Pouladi
Intrinsic mutant HTT-mediated defects in oligodendroglia cause myelination deficits and behavioral abnormalities in Huntington disease. Proceedings of the National Academy of Sciences of the United States of America 116 (19) (2019)
Amin Ziaei, Xiaohong Xu, Leila Dehghani, Carine Bonnard, Andreas Zellner, Alvin Yu Jin Ng, Sumanty Tohari, Byrappa Venkatesh, Christof Haffner, Bruno Reversade, Vahid Shaygannejad, Mahmoud A Pouladi
Novel mutation in HTRA1 in a family with diffuse white matter lesions and inflammatory features. Neurology. Genetics 5 (4) (2019)
Marta Garcia-Miralles, Nur Amirah Binte Mohammad Yusof, Jing Ying Tan, Carola I Radulescu, Harwin Sidik, Liang Juin Tan, Haim Belinson, Neta Zach, Michael R Hayden, Mahmoud A Pouladi
Laquinimod Treatment Improves Myelination Deficits at the Transcriptional and Ultrastructural Levels in the YAC128 Mouse Model of Huntington Disease. Molecular neurobiology 56 (6) (2018)
Poh Hui Chia, Franklin Lei Zhong, Shinsuke Niwa, Carine Bonnard, Kagistia Hana Utami, Ruizhu Zeng, Hane Lee, Ascia Eskin, Stanley F Nelson, William H Xie, Samah Al-Tawalbeh, Mohammad El-Khateeb, Mohammad Shboul, Mahmoud A Pouladi, Mohammed Al-Raqad, Bruno Reversade
A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability. eLife 7 (2018)
Moore Z Chen, Nagaraj S Moily, Jessica L Bridgford, Rebecca J Wood, Mona Radwan, Trevor A Smith, Zhegang Song, Ben-Zhong Tang, Leann Tilley, Xiaohong Xu, Gavin E Reid, Mahmoud A Pouladi, Yuning Hong, Danny M Hatters
A thiol probe for measuring unfolded protein load and proteostasis in cells. Nature communications 8 (1) (2017)
Sofi G Julien, Sun-Yee Kim, Reinhard Brunmeir, Joanna R Sinnakannu, Xiaojia Ge, Hongyu Li, Wei Ma, Jadegoud Yaligar, Bhanu Prakash Kn, Sendhil S Velan, Pia V Röder, Qiongyi Zhang, Choon Kiat Sim, Jingyi Wu, Marta Garcia-Miralles, Mahmoud A Pouladi, Wei Xie, Craig McFarlane, Weiping Han, Feng Xu
Narciclasine attenuates diet-induced obesity by promoting oxidative metabolism in skeletal muscle. PLoS biology 15 (2) (2017)

Mahmoud A Pouladi.css-eqlu8i{font-size:small;padding-left:4px;}

Publication Activity (10 Years)

Top Topics

Top Venues

Mahmoud A Pouladi