Molecular impacts of Meier–Gorlin syndrome mutations on human origin licensing
Open Access
- 24 December 2025
- journal article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 302 (2) , 111100
Abstract
No abstract availableKeywords
Funding Information
- NIH NCI (F31-CA278331)
- National Institutes of Health
- NIH NIGMS (R01-GM141313)
- NIH NIGMS (R35GM158287)
This publication has 81 references indexed in Scilit:
- Microcephalic primordial dwarfism with predominant Meier–Gorlin phenotype, ichthyosis, and multiple joint deformities—Further expansion of DONSON Cell Cycle‐opathy phenotypic spectrumAmerican Journal of Medical Genetics Part A, 2022
- Biallelic and De Novo Variants in DONSON Reveal a Clinical Spectrum of Cell Cycle‐opathies with Microcephaly, Dwarfism and Skeletal AbnormalitiesAmerican Journal of Medical Genetics Part A, 2019
- Regulation of the initiation of DNA replication in human cellsDNA Repair, 2018
- MacroBac: New Technologies for Robust and Efficient Large-Scale Production of Recombinant Multiprotein Complexes2017
- Mutations in CDC45 , Encoding an Essential Component of the Pre-initiation Complex, Cause Meier-Gorlin Syndrome and CraniosynostosisThe American Journal of Human Genetics, 2016
- Gctf: Real-time CTF determination and correctionJournal of Structural Biology, 2016
- Drosophila model of Meier‐Gorlin syndrome based on the mutation in a conserved C‐Terminal domain of Orc6American Journal of Medical Genetics Part A, 2015
- Concerted Loading of Mcm2–7 Double Hexamers around DNA during DNA Replication Origin LicensingCell, 2009
- Automated electron microscope tomography using robust prediction of specimen movementsJournal of Structural Biology, 2005
- Evolutionary history and higher order classification of AAA+ ATPasesJournal of Structural Biology, 2004