Cockayne syndrome pathogenesis: Lessons from mouse models
Author:
Publisher
Elsevier BV
Subject
Developmental Biology,Ageing
Reference161 articles.
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3. An Xpd mouse model for the combined xeroderma pigmentosum/Cockayne syndrome exhibiting both cancer predisposition and segmental progeria;Andressoo;Cancer Cell,2006
4. An Xpb mouse model for combined xeroderma pigmentosum and cockayne syndrome reveals progeroid features upon further attenuation of DNA repair;Andressoo;Molecular and Cellular Biology,2009
5. A ubiquitin-binding domain in Cockayne syndrome B required for transcription-coupled nucleotide excision repair;Anindya;Molecular Cell,2010
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1. HiPSC-derived 3D neural models reveal neurodevelopmental pathomechanisms of the Cockayne Syndrome B;Cellular and Molecular Life Sciences;2024-08-23
2. Cockayne Syndrome Patient iPSC-Derived Brain Organoids and Neurospheres Show Early Transcriptional Dysregulation of Biological Processes Associated with Brain Development and Metabolism;Cells;2024-03-28
3. Premature aging in genetic diseases: what conclusions can be drawn for physiological aging;Frontiers in Aging;2024-02-28
4. Cockayne syndrome patient iPSC-derived brain organoids and neurospheres show early transcriptional dysregulation of biological processes associated with brain development and metabolism;2023-10-17
5. DNA damage and repair: underlying mechanisms leading to microcephaly;Frontiers in Cell and Developmental Biology;2023-10-10
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