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APOBEC3A/B-induced mutagenesis is responsible for 20% of heritable mutations in the TpCpW context.
Genome Res. 2017 Feb;27(2):175-184. doi: 10.1101/gr.210336.116. Epub 2016 Dec 9.
Genome Res. 2017.
PMID: 27940951
Free PMC article.
Genomic analysis identifies new drivers and progression pathways in skin basal cell carcinoma.
Bonilla X, Parmentier L, King B, Bezrukov F, Kaya G, Zoete V, Seplyarskiy VB, Sharpe HJ, McKee T, Letourneau A, Ribaux PG, Popadin K, Basset-Seguin N, Ben Chaabene R, Santoni FA, Andrianova MA, Guipponi M, Garieri M, Verdan C, Grosdemange K, Sumara O, Eilers M, Aifantis I, Michielin O, de Sauvage FJ, Antonarakis SE, Nikolaev SI.
Bonilla X, et al. Among authors: andrianova ma.
Nat Genet. 2016 Apr;48(4):398-406. doi: 10.1038/ng.3525. Epub 2016 Mar 7.
Nat Genet. 2016.
PMID: 26950094
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Human mismatch repair system balances mutation rates between strands by removing more mismatches from the lagging strand.
Andrianova MA, Bazykin GA, Nikolaev SI, Seplyarskiy VB.
Andrianova MA, et al.
Genome Res. 2017 Aug;27(8):1336-1343. doi: 10.1101/gr.219915.116. Epub 2017 May 16.
Genome Res. 2017.
PMID: 28512192
Free PMC article.
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Germline PMS2 and somatic POLE exonuclease mutations cause hypermutability of the leading DNA strand in biallelic mismatch repair deficiency syndrome brain tumours.
Andrianova MA, Chetan GK, Sibin MK, Mckee T, Merkler D, Narasinga RK, Ribaux P, Blouin JL, Makrythanasis P, Seplyarskiy VB, Antonarakis SE, Nikolaev SI.
Andrianova MA, et al.
J Pathol. 2017 Nov;243(3):331-341. doi: 10.1002/path.4957. Epub 2017 Sep 28.
J Pathol. 2017.
PMID: 28805995
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Are Nonsense Alleles of Drosophila melanogaster Genes under Any Selection?
Potapova NA, Andrianova MA, Bazykin GA, Kondrashov AS.
Potapova NA, et al. Among authors: andrianova ma.
Genome Biol Evol. 2018 Apr 1;10(4):1012-1018. doi: 10.1093/gbe/evy032.
Genome Biol Evol. 2018.
PMID: 29425311
Free PMC article.
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Error-prone bypass of DNA lesions during lagging-strand replication is a common source of germline and cancer mutations.
Seplyarskiy VB, Akkuratov EE, Akkuratova N, Andrianova MA, Nikolaev SI, Bazykin GA, Adameyko I, Sunyaev SR.
Seplyarskiy VB, et al. Among authors: andrianova ma.
Nat Genet. 2019 Jan;51(1):36-41. doi: 10.1038/s41588-018-0285-7. Epub 2018 Dec 3.
Nat Genet. 2019.
PMID: 30510240
Free PMC article.
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Discovery of recessive effect of human polymerase δ proofreading deficiency through mutational analysis of POLD1-mutated normal and cancer cells.
Andrianova MA, Seplyarskiy VB, Terradas M, Sánchez-Heras AB, Mur P, Soto JL, Aiza G, Borràs E, Kondrashov FA, Kondrashov AS, Bazykin GA, Valle L.
Andrianova MA, et al.
Eur J Hum Genet. 2024 Apr 24. doi: 10.1038/s41431-024-01598-8. Online ahead of print.
Eur J Hum Genet. 2024.
PMID: 38658779
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[Possibilities of pharmacological correction of the arterial hypertension in elderly patients with gout].
Kunitskaia NA, Andrianova MA.
Kunitskaia NA, et al. Among authors: andrianova ma.
Adv Gerontol. 2012;25(2):285-9.
Adv Gerontol. 2012.
PMID: 23130520
Clinical Trial.
Russian.
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