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American Journal of Medical Genetics. Part A|May 11, 2019
Alveolar capillary dysplasia with misalignment of the pulmonary veins and hypoplastic left heart sequence caused by an in frame deletion within FOXF1Danielle K Bourque, Inara Chacon Fonseca, Andrea Staines, et al.
Frontiers in Genetics|December 5, 2022
Fragile sites, chromosomal lesions, tandem repeats, and diseaseMila Mirceta, Natalie Shum, Monika H M Schmidt, et al.
Epigenetics|March 3, 2011
Identification of restriction endonucleases sensitive to 5-cytosine methylation at non-CpG sites, including expanded (CAG)n/(CTG)n repeatsArturo López Castel, Masayuki Nakamori, Charles A Thornton, et al.
Nucleic Acids Research|January 19, 2019
CtIP-BRCA1 complex and MRE11 maintain replication forks in the presence of chain terminating nucleoside analogsMohiuddin Mohiuddin, Md Maminur Rahman, Julian E Sale, et al.
Nature Genetics|April 23, 2002
Evidence of cis-acting factors in replication-mediated trinucleotide repeat instability in primate cellsJohn D Cleary, Kerrie Nichol, Yuh-Hwa Wang, et al.
Biochemical and Biophysical Research Communications|December 24, 2017
Thermodynamic and spectroscopic investigations of TMPyP4 association with guanine- and cytosine-rich DNA and RNA repeats of C9orf72Hasan Alniss, Bita Zamiri, Melisa Khalaj, et al.
The Journal of Biological Chemistry|September 3, 2023
Pathogenic CANVAS-causing but not nonpathogenic RFC1 DNA/RNA repeat motifs form quadruplex or triplex structuresMohammad Hossein Abdi, Bita Zamiri, Gholamreza Pazuki, et al.
DNA Repair|May 20, 2008
Mutagenic roles of DNA "repair" proteins in antibody diversity and disease-associated trinucleotide repeat instabilityMeghan M Slean, Gagan B Panigrahi, Laura P Ranum, et al.
Nucleic Acids Research|October 4, 2015
Quadruplex formation by both G-rich and C-rich DNA strands of the C9orf72 (GGGGCC)8•(GGCCCC)8 repeat: effect of CpG methylationBita Zamiri, Mila Mirceta, Karol Bomsztyk, et al.
American Journal of Human Genetics|October 24, 2003
Replication inhibitors modulate instability of an expanded trinucleotide repeat at the myotonic dystrophy type 1 disease locus in human cellsZhi Yang, Rachel Lau, Julien L Marcadier, et al.
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