Dr. Rashid Mehmood

Assistant Professor of Molecular Biology, & Chair of Life Sciences Department

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Bio and Research Interests

Dr. Mehmood completed his PhD from Graduate School of Frontier Biosciences, Osaka University, Japan where he conducted his research on dynamic regulation of proteins transport across the nuclear membrane. During the course of neuronal differentiation from Embryonic stem cells, various helix loop helix transcription factors are expressed. Taking NeuroD1 and E47 as representative molecules, and using proteomic and molecular approaches, Dr. Mehmood showed that their nuclear transport is regulated and heterodimerization plays an important role therein. Moreover, he identified a novel cross talk between two distinct nuclear import pathways, namely importin alpha and beta, for the efficient nuclear import of basic helix loop helix transcription factors.

Dr. Mehmood joined Childrens’ Health Research Institute, Western University, Canada for a postdoc on Epigenetics. While studying the dynamic regulation of epigenetic landscape during pancreatic development and disease, Dr. Mehmood identified unique epigenetic signatures in pancreatitis. Important functional and developmental regulators were identified as direct targets of epigenetic reprogramming that have implications in chronic pancreatic injury and pancreatic cancer progression. He continued his research on Epigenetics at Roswell Park Cancer Institute, USA, where, by utilizing epigenetic approaches he studied the interaction of epigenetic regulators with stem cell factors during cancer progression. Dr. Mehmood joined Alfaisal University in 2018 where his research focusses on the role of epigenetic regulation in cancer and stem cell maintenance. He utilizes bioinformatic and molecular approaches to unravel important epigenetic signalling pathways regulating normal vs. cancer development. Non-coding RNAs, important mediators of gene function, and their interplay with the cellular machinery is another area Dr. Mehmood is interested in.

Dr. Mehmood has won various research and teaching awards and published high impact articles in peer reviewed journals.

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Integrative Molecular Analysis of DNA Methylation Dynamics Unveils Molecules with Prognostic Potential in Breast Cancer

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Integrative Molecular Analysis of DNA Methylation Dynamics Unveils Molecules with Prognostic Potential in Breast Cancer. (2023). Integrative Molecular Analysis of DNA Methylation Dynamics Unveils Molecules with Prognostic Potential in Breast Cancer. Biomedinformatics. Retrieved de https://scholar.google.com/citations?view_op=view_citation&hl=en&user=-EvmiKMAAAAJ&cstart=20&pagesize=80&citation_for_view=-EvmiKMAAAAJ:_kc_bZDykSQC

CRISPR-based epigenome editing: mechanisms and applications

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CRISPR-based epigenome editing: mechanisms and applications. (2023). CRISPR-based epigenome editing: mechanisms and applications. Epigenomics. Retrieved de https://scholar.google.com/citations?view_op=view_citation&hl=en&user=-EvmiKMAAAAJ&cstart=20&pagesize=80&citation_for_view=-EvmiKMAAAAJ%3AqxL8FJ1GzNcC (Original work published 2023)

COVID-19 outbreak and the role of digital twin.

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COVID-19 outbreak and the role of digital twin. (2022). COVID-19 outbreak and the role of digital twin. Retrieved de https://scholar.google.com/citations?view_op=view_citation&hl=en&user=-EvmiKMAAAAJ&citation_for_view=-EvmiKMAAAAJ:KlAtU1dfN6UC

Systems genomics of nucleoporins provides prognostic insights into breast cancer

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Systems genomics of nucleoporins provides prognostic insights into breast cancer. (2022). Systems genomics of nucleoporins provides prognostic insights into breast cancer. Retrieved de https://scholar.google.com/citations?view_op=view_citation&hl=en&user=-EvmiKMAAAAJ&cstart=20&pagesize=80&citation_for_view=-EvmiKMAAAAJ:YOwf2qJgpHMC

Importin α2 association with chromatin: Direct DNA binding via a novel DNA-binding domain.

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Importin α2 association with chromatin: Direct DNA binding via a novel DNA-binding domain. (2021). Importin α2 association with chromatin: Direct DNA binding via a novel DNA-binding domain. Retrieved de https://scholar.google.com/citations?view_op=view_citation&hl=en&user=-EvmiKMAAAAJ&cstart=20&pagesize=80&citation_for_view=-EvmiKMAAAAJ:kNdYIx-mwKoC

Molecular profiling of nucleocytoplasmic transport factor genes in breast cancer

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Molecular profiling of nucleocytoplasmic transport factor genes in breast cancer. (2021). Molecular profiling of nucleocytoplasmic transport factor genes in breast cancer. Retrieved de https://scholar.google.com/citations?view_op=view_citation&hl=en&user=-EvmiKMAAAAJ&citation_for_view=-EvmiKMAAAAJ:5nxA0vEk-isC

Evidence for context-dependent functions of KDM5B in prostate development and prostate cancer.

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Evidence for context-dependent functions of KDM5B in prostate development and prostate cancer. (2020). Evidence for context-dependent functions of KDM5B in prostate development and prostate cancer. Retrieved de https://scholar.google.com/citations?view_op=view_citation&hl=en&user=-EvmiKMAAAAJ&citation_for_view=-EvmiKMAAAAJ:0EnyYjriUFMC

Impact of lockdowns on the spread of COVID-19 in Saudi Arabia.

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Impact of lockdowns on the spread of COVID-19 in Saudi Arabia. (2020). Impact of lockdowns on the spread of COVID-19 in Saudi Arabia. Retrieved de https://scholar.google.com/citations?view_op=view_citation&hl=en&user=-EvmiKMAAAAJ&citation_for_view=-EvmiKMAAAAJ:hqOjcs7Dif8C

LRIG1 is a pleiotropic androgen receptor-regulated feedback tumor suppressor in prostate cancer.

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LRIG1 is a pleiotropic androgen receptor-regulated feedback tumor suppressor in prostate cancer. (2019). LRIG1 is a pleiotropic androgen receptor-regulated feedback tumor suppressor in prostate cancer. Retrieved de https://scholar.google.com/citations?view_op=view_citation&hl=en&user=-EvmiKMAAAAJ&citation_for_view=-EvmiKMAAAAJ:u5HHmVD_uO8C

MicroRNA Regulation Along the Course of Cellular Reprogramming to Pluripotency

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MicroRNA Regulation Along the Course of Cellular Reprogramming to Pluripotency. (2018). MicroRNA Regulation Along the Course of Cellular Reprogramming to Pluripotency. Retrieved de https://scholar.google.com/citations?view_op=view_citation&hl=en&user=-EvmiKMAAAAJ&cstart=20&pagesize=80&citation_for_view=-EvmiKMAAAAJ:Se3iqnhoufwC

Transgenic overexpression of NanogP8 in the mouse prostate is insufficient to initiate tumorigenesis but weakly promotes tumor development in the Hi-Myc mouse model

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Transgenic overexpression of NanogP8 in the mouse prostate is insufficient to initiate tumorigenesis but weakly promotes tumor development in the Hi-Myc mouse model. (2017). Transgenic overexpression of NanogP8 in the mouse prostate is insufficient to initiate tumorigenesis but weakly promotes tumor development in the Hi-Myc mouse model. Retrieved de https://scholar.google.com/citations?view_op=view_citation&hl=en&user=-EvmiKMAAAAJ&cstart=20&pagesize=80&citation_for_view=-EvmiKMAAAAJ:u-x6o8ySG0sC

Activating Transcription Factor 3 promotes loss of the acinar cell phenotype in response to ceruelin-induced pancreatitis in mice

Journal ,
://scholar.google.com/citations?view_op=view_citation&hl=en&user=-EvmiKMAAAAJ&citation_for_view=-EvmiKMAAAAJ:W7OEmFMy1HYC, https. (2017). Activating Transcription Factor 3 promotes loss of the acinar cell phenotype in response to ceruelin-induced pancreatitis in mice.

Epigenetic mechanisms regulating development of Hepatocellular Carcinoma and their promise for therapeutics

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Epigenetic mechanisms regulating development of Hepatocellular Carcinoma and their promise for therapeutics. (2017). Epigenetic mechanisms regulating development of Hepatocellular Carcinoma and their promise for therapeutics. Retrieved de https://scholar.google.com/citations?view_op=view_citation&hl=en&user=-EvmiKMAAAAJ&citation_for_view=-EvmiKMAAAAJ:roLk4NBRz8UC

Atp2c2 is transcribed from a unique transcriptional start site in mouse pancreatic acinar cells

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Atp2c2 is transcribed from a unique transcriptional start site in mouse pancreatic acinar cells. (2016). Atp2c2 is transcribed from a unique transcriptional start site in mouse pancreatic acinar cells. Retrieved de https://scholar.google.com/citations?view_op=view_citation&hl=en&user=-EvmiKMAAAAJ&citation_for_view=-EvmiKMAAAAJ:_FxGoFyzp5QC

Acinar cell reprogramming: a clinical important target in pancreatic disease.

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Acinar cell reprogramming: a clinical important target in pancreatic disease. (2015). Acinar cell reprogramming: a clinical important target in pancreatic disease. Retrieved de https://scholar.google.com/citations?view_op=view_citation&hl=en&user=-EvmiKMAAAAJ&citation_for_view=-EvmiKMAAAAJ:Y0pCki6q_DkC

Targeting the bHLH transcriptional networks by mutated E proteins in experimental glioma.

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Targeting the bHLH transcriptional networks by mutated E proteins in experimental glioma. (2014). Targeting the bHLH transcriptional networks by mutated E proteins in experimental glioma. Retrieved de https://scholar.google.com/citations?view_op=view_citation&hl=en&user=-EvmiKMAAAAJ&citation_for_view=-EvmiKMAAAAJ:IjCSPb-OGe4C

Silencing of the Fibroblast growth factor 21 gene is an underlying cause of acinar cell injury in mice lacking MIST1

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Silencing of the Fibroblast growth factor 21 gene is an underlying cause of acinar cell injury in mice lacking MIST1. (2014). Silencing of the Fibroblast growth factor 21 gene is an underlying cause of acinar cell injury in mice lacking MIST1. Retrieved de https://scholar.google.com/citations?view_op=view_citation&hl=en&user=-EvmiKMAAAAJ&citation_for_view=-EvmiKMAAAAJ:ufrVoPGSRksC

Epigenetic reprogramming in Mist1-/- mice predicts the molecular response to cerulein-induced pancreatitis

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Epigenetic reprogramming in Mist1-/- mice predicts the molecular response to cerulein-induced pancreatitis. (2014). Epigenetic reprogramming in Mist1-/- mice predicts the molecular response to cerulein-induced pancreatitis. Retrieved de https://scholar.google.com/citations?view_op=view_citation&hl=en&user=-EvmiKMAAAAJ&citation_for_view=-EvmiKMAAAAJ:Tyk-4Ss8FVUC

Importin Alpha Subtypes Determine Differential Transcription Factor Localization in Embryonic Stem Cells Maintenance.

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Importin Alpha Subtypes Determine Differential Transcription Factor Localization in Embryonic Stem Cells Maintenance. (2013). Importin Alpha Subtypes Determine Differential Transcription Factor Localization in Embryonic Stem Cells Maintenance. Retrieved de https://scholar.google.com/citations?view_op=view_citation&hl=en&user=-EvmiKMAAAAJ&citation_for_view=-EvmiKMAAAAJ:2osOgNQ5qMEC

The Absence of MIST1 Leads to Increased Ethanol Sensitivity and Decreased Activity of the Unfolded Protein Response in Mouse Pancreatic Acinar Cells

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The Absence of MIST1 Leads to Increased Ethanol Sensitivity and Decreased Activity of the Unfolded Protein Response in Mouse Pancreatic Acinar Cells. (2011). The Absence of MIST1 Leads to Increased Ethanol Sensitivity and Decreased Activity of the Unfolded Protein Response in Mouse Pancreatic Acinar Cells. Retrieved de https://scholar.google.com/citations?view_op=view_citation&hl=en&user=-EvmiKMAAAAJ&citation_for_view=-EvmiKMAAAAJ:LkGwnXOMwfcC

Cross-talk between distinct nuclear import pathways enables efficient nuclear import of E47 in conjunction with its partner transcription factors

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Cross-talk between distinct nuclear import pathways enables efficient nuclear import of E47 in conjunction with its partner transcription factors. (2011). Cross-talk between distinct nuclear import pathways enables efficient nuclear import of E47 in conjunction with its partner transcription factors. Retrieved de https://scholar.google.com/citations?view_op=view_citation&hl=en&user=-EvmiKMAAAAJ&citation_for_view=-EvmiKMAAAAJ:d1gkVwhDpl0C

Mice lacking Ran binding protein 1 are viable and show male infertility.

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Mice lacking Ran binding protein 1 are viable and show male infertility. (2011). Mice lacking Ran binding protein 1 are viable and show male infertility. Retrieved de https://scholar.google.com/citations?view_op=view_citation&hl=en&user=-EvmiKMAAAAJ&citation_for_view=-EvmiKMAAAAJ:Zph67rFs4hoC

Axotomy induces axonogenesis in hippocampal neurons by a mechanism dependent on importin β.

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Axotomy induces axonogenesis in hippocampal neurons by a mechanism dependent on importin β. (2011). Axotomy induces axonogenesis in hippocampal neurons by a mechanism dependent on importin β. Retrieved de https://scholar.google.com/citations?view_op=view_citation&hl=en&user=-EvmiKMAAAAJ&citation_for_view=-EvmiKMAAAAJ:qjMakFHDy7sC

Synergistic Nuclear Import of NeuroD1 and its partner transcription factor, E47, via heterodimerization.

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Synergistic Nuclear Import of NeuroD1 and its partner transcription factor, E47, via heterodimerization. (2009). Synergistic Nuclear Import of NeuroD1 and its partner transcription factor, E47, via heterodimerization. Retrieved de https://scholar.google.com/citations?view_op=view_citation&hl=en&user=-EvmiKMAAAAJ&citation_for_view=-EvmiKMAAAAJ:9yKSN-GCB0IC

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