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Comparison of Eight Technologies to Determine Genotype at the UGT1A1 (TA)n Repeat Polymorphism: Potential Clinical Consequences of Genotyping Errors?
Sissung TM, Barbier RH, Price DK, Plona TM, Pike KM, Mellott SD, Baugher RN, Whiteley GR, Soppet DR, Venzon D, Berman A, Rajan A, Giaccone G, Meltzer P, Figg WD. Sissung TM, et al. Among authors: mellott sd. Int J Mol Sci. 2020 Jan 30;21(3):896. doi: 10.3390/ijms21030896. Int J Mol Sci. 2020. PMID: 32019188 Free PMC article.
A novel mouse model of PMS2 founder mutation that causes mismatch repair defect due to aberrant splicing.
Biswas K, Couillard M, Cavallone L, Burkett S, Stauffer S, Martin BK, Southon E, Reid S, Plona TM, Baugher RN, Mellott SD, Pike KM, Albaugh ME, Maedler-Kron C, Hamel N, Tessarollo L, Marcus V, Foulkes WD, Sharan SK. Biswas K, et al. Among authors: mellott sd. Cell Death Dis. 2021 Sep 6;12(9):838. doi: 10.1038/s41419-021-04130-8. Cell Death Dis. 2021. PMID: 34489406 Free PMC article.
Organoids and metastatic orthotopic mouse model for mismatch repair-deficient colorectal cancer.
Song Y, Kerr TD, Sanders C, Dai L, Baxter SS, Somerville B, Baugher RN, Mellott SD, Young TB, Lawhorn HE, Plona TM, Xu B, Wei L, Hu Q, Liu S, Hutson A, Karim B, Burkett S, Difilippantonio S, Pinto L, Gebert J, Kloor M, Lipkin SM, Sei S, Shoemaker RH. Song Y, et al. Among authors: mellott sd. Front Oncol. 2023 Sep 8;13:1223915. doi: 10.3389/fonc.2023.1223915. eCollection 2023. Front Oncol. 2023. PMID: 37746286 Free PMC article.
Frameshift mutations in peripheral blood as a biomarker for surveillance of lynch syndrome.
Song Y, Loomans-Kropp H, Baugher RN, Somerville B, Baxter SS, Kerr TD, Plona TM, Mellott SD, Young TB, Lawhorn HE, Wei L, Hu Q, Liu S, Hutson A, Pinto L, Potter JD, Sei S, Gelincik O, Lipkin SM, Gebert J, Kloor M, Shoemaker RH. Song Y, et al. Among authors: mellott sd. J Natl Cancer Inst. 2024 Mar 11:djae060. doi: 10.1093/jnci/djae060. Online ahead of print. J Natl Cancer Inst. 2024. PMID: 38466935