Epigenetic mechanisms in neurological disease
Jakovcevski, Mira, Akbarian, Schahram·2012·Nature Medicine
DOI 10.1038/nm.2828
Cited by (454)
Items 401–454 of 454
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- A putative role for genome-wide epigenetic regulatory mechanisms in Huntington’s disease: A computational assessmentEleni Mina, Willeke van Roon‐Mom, Pernette J. Verschure, Peter A.C. ’t Hoen, Mark Thompson, Rajaram Kaliyaperumal, Kristina Maria Hettne, Erik Schultes, Barend Mons, Marco Roos · 2017 · F1000Research
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- АБЕРРАНТНОЕ МЕТИЛИРОВАНИЕ ДНК В ЛИМФОЦИТАХ ДЕТЕЙ С НАРУШЕНИЯМИ РАЗВИТИЯ ЦНС, "Генетика"Oxana Yu. Naumova, С Ю Рычков, В. В. Одинцова, Sergey A. Kornilov, Е. В. Шабалина, D. V. Antsiferova, О. В. Жукова, Elena L. Grigorenko · 2017 · Генетика
- HAB / LAB Mice and Rats: Approaching the Genetics and Epigenetics of Trait AnxietyLudwig Czibere, Rebekka P. Diepold, Alexey E. Umriukhin, Rainer Landgraf, Sergey Sotnikov · 2018
- Pain-Induced Chromatin ModificationsZhizhong Z. Pan, Chenghua Zhou, Yuqing Wu, Zhi Zhang, Youqing Cai · 2018 · Elsevier eBooks
- Epigenetic Dysregulation in the Basocortical Cholinergic Projection System During the Progression of Alzheimer's DiseaseLaura J. Mahady · 2018
- The role for DNA/RNA methylation on neurocognitive dysfunctionsX.Z. Shawn Xu · 2019 · Elsevier eBooks
- Gene regulation during development by chromatin and the Super Elongation ComplexOlle Dahlberg · 2014 · KTH Publication Database DiVA (KTH Royal Institute of Technology)
- Epigenetic Modifications lead towards NeurodegenerationAnna Askari, Shamoon Noushad, Sadaf Ahmed, Faizan Mirza, Syed A. Aziz · 2020 · INTERNATIONAL JOURNAL OF ENDORSING HEALTH SCIENCE RESEARCH (IJEHSR)
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- Loss of Setd1b methyltransferase in the murine forebrain as a novel model for human intellectual disabilityAlexandra Michurina · 2020
- The Human Brain and its EpigenomesAndrew J. Chess, Schahram Akbarian · 2017 · Oxford University Press eBooks
- Redox / methylation signalingMalav Suchin Trivedi · 2013
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- Epigenetics of Brain DisordersAli Jawaid, Eloïse A. Kremer, Nancy V. N. Carullo, Isabelle M. Mansuy · 2022 · Elsevier eBooks
- Disease comorbiditiesHarold I. Zeliger · 2022 · Elsevier eBooks
- Molecular genetic mechanisms of neurodevelopmental and neurodegenerative diseaseDaniel G. Calame, Dana Marafi, James R. Lupski · 2024 · Elsevier eBooks
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- Epigenetic modulation of human neurobiological disorders: Lesch-Nyhan disease as a model disorderKhue Vu Nguyen · 2025 · AIMS neuroscience
- Animal models in epigenetic researchIván Carrera, Vinogran Naidoo, Olaia A. Martínez-Iglesias, Ramón Cacabelos · 2025 · Elsevier eBooks
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- Systems biology approach in the detection of neuronal disordersDhruv Rao, Siddhant Yadav, Nabh Chandra, Tisha Muthamma, Yuvaraj Sivamani, Kiran Sree Pokkuluri, Sumitha Elayaperumal · 2025 · Elsevier eBooks
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- Additional file 7 of Nucleoporin 153 deficiency in adult neural stem cells defines a pathological protein-network signature and defective neurogenesis in a mouse model of ADClaudia Colussi, Alessia Bertozzi, Lucia Leone, Marco Rinaudo, Raimondo Sollazzo, Conte, Federica, Elena Paccosi, Luca Nardella, Giuseppe Aceto, Li Puma, Domenica Donatella et al. · 2024 · Figshare
- Additional file 8 of Nucleoporin 153 deficiency in adult neural stem cells defines a pathological protein-network signature and defective neurogenesis in a mouse model of ADClaudia Colussi, Alessia Bertozzi, Lucia Leone, Marco Rinaudo, Raimondo Sollazzo, Conte, Federica, Elena Paccosi, Luca Nardella, Giuseppe Aceto, Li Puma, Domenica Donatella et al. · 2024 · Figshare
- Additional file 6 of Nucleoporin 153 deficiency in adult neural stem cells defines a pathological protein-network signature and defective neurogenesis in a mouse model of ADClaudia Colussi, Alessia Bertozzi, Lucia Leone, Marco Rinaudo, Raimondo Sollazzo, Conte, Federica, Elena Paccosi, Luca Nardella, Giuseppe Aceto, Domenica Donatella Li Puma et al. · 2024 · Figshare
- Additional file 5 of Nucleoporin 153 deficiency in adult neural stem cells defines a pathological protein-network signature and defective neurogenesis in a mouse model of ADClaudia Colussi, Alessia Bertozzi, Lucia Leone, Marco Rinaudo, Raimondo Sollazzo, Conte, Federica, Elena Paccosi, Luca Nardella, Aceto, Giuseppe, Domenica Donatella Li Puma et al. · 2024 · Figshare
- Additional file 4 of Nucleoporin 153 deficiency in adult neural stem cells defines a pathological protein-network signature and defective neurogenesis in a mouse model of ADClaudia Colussi, Alessia Bertozzi, Lucia Leone, Marco Rinaudo, Raimondo Sollazzo, Conte, Federica, Elena Paccosi, Luca Nardella, Aceto, Giuseppe, Li Puma, Domenica Donatella et al. · 2024 · Figshare
- Additional file 2 of Nucleoporin 153 deficiency in adult neural stem cells defines a pathological protein-network signature and defective neurogenesis in a mouse model of ADClaudia Colussi, Alessia Bertozzi, Lucia Leone, Marco Rinaudo, Raimondo Sollazzo, Conte, Federica, Elena Paccosi, Luca Nardella, Giuseppe Aceto, Li Puma, Domenica Donatella et al. · 2024 · Figshare
- Additional file 1 of Nucleoporin 153 deficiency in adult neural stem cells defines a pathological protein-network signature and defective neurogenesis in a mouse model of ADClaudia Colussi, Alessia Bertozzi, Lucia Leone, Marco Rinaudo, Raimondo Sollazzo, Conte, Federica, Elena Paccosi, Luca Nardella, Aceto, Giuseppe, Domenica Donatella Li Puma et al. · 2024 · Figshare
- Additional file 3 of Nucleoporin 153 deficiency in adult neural stem cells defines a pathological protein-network signature and defective neurogenesis in a mouse model of ADClaudia Colussi, Alessia Bertozzi, Lucia Leone, Marco Rinaudo, Raimondo Sollazzo, Conte, Federica, Elena Paccosi, Luca Nardella, Aceto, Giuseppe, Li Puma, Domenica Donatella et al. · 2024 · Figshare
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- Interaction mechanisms of epigenetic integrator UHRF1 with TIP60 acetyltransferaseWaseem Ashraf · 2018 · theses.fr (ABES)
- Inhibition of UHRF1 protein by epigenetic partners and epi-drugsTanveer Ahmad · 2019 · theses.fr (ABES)
- Histone acetylation and methylation in rare diseases: from molecular mechanisms to clinical presentationsBurcu Akman, Semra Gürsoy, Pınar Gençpınar, Ayşe Polat, Ayşe Semra Hız, Yavuz Oktay, Tahsin Stefan Barakat, Uğur Özbek, Serap Erkek · 2026 · Frontiers in Cell and Developmental Biology
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- A Dnmt3a-Mediated Epigenetic Mechanism for Chronic-Pain-Induced Behaviors of Negative Emotion in MiceJianlong Ge, Youqing Cai, Zhizhong Z. Pan · 2026 · Cells
- Infection-driven gut dysbiosis and epigenetic programming of microglia: toward a systems level framework linking microbial metabolites, neuroinflammation, synaptic dysfunction, and probiotic modulationDelin Han, Chunyu Yang · 2026 · Frontiers in Cellular and Infection Microbiology
- Epigenetic Pathways to Giftedness: Bridging Biology and Talent DevelopmentHasan Akdeniz · 2026 · Gifted Child Quarterly
- Treating neurological diseases through epigenetic inhibition: A neuroepigenetic therapy hypothesisDoodipala Samba Reddy, Lauren Franklin, Victoria M. Golub, Hetvi Desai, Sreevidhya Ramakrishnan · 2026 · Journal of Pharmacology and Experimental Therapeutics
- Epigenetic and Transcriptomic Regulations in Brain DisordersAjay Pal, Jaishriram Rathored · 2026 · Royal Society of Chemistry eBooks
- S-Adenosylmethionine Depletion as Potential Rate-Limiting Nexus of Redox–Epigenetic Crosstalk in Neural Tube Defects: A Mechanistic Theory and Experimental HypothesisBoniface Ezenwata Echefu, Maria Becker, Asher Ornoy · 2026 · Cells