55 related articles for article (PubMed ID: 14722921)
1. Context of deletions and insertions in human coding sequences.
Kondrashov AS; Rogozin IB
Hum Mutat; 2004 Feb; 23(2):177-185. PubMed ID: 14722921
[TBL] [Abstract][Full Text] [Related]
2. Covariation in frequencies of substitution, deletion, transposition, and recombination during eutherian evolution.
Hardison RC; Roskin KM; Yang S; Diekhans M; Kent WJ; Weber R; Elnitski L; Li J; O'Connor M; Kolbe D; Schwartz S; Furey TS; Whelan S; Goldman N; Smit A; Miller W; Chiaromonte F; Haussler D
Genome Res; 2003 Jan; 13(1):13-26. PubMed ID: 12529302
[TBL] [Abstract][Full Text] [Related]
3. Deletions across the SARS-CoV-2 Genome: Molecular Mechanisms and Putative Functional Consequences of Deletions in Accessory Genes.
Rogozin IB; Saura A; Bykova A; Brover V; Yurchenko V
Microorganisms; 2023 Jan; 11(1):. PubMed ID: 36677521
[TBL] [Abstract][Full Text] [Related]
4. Distinct sequence features underlie microdeletions and gross deletions in the human genome.
Qi M; Stenson PD; Ball EV; Tainer JA; Bacolla A; Kehrer-Sawatzki H; Cooper DN; Zhao H
Hum Mutat; 2022 Mar; 43(3):328-346. PubMed ID: 34918412
[TBL] [Abstract][Full Text] [Related]
5. Template switching and duplications in SARS-CoV-2 genomes give rise to insertion variants that merit monitoring.
Garushyants SK; Rogozin IB; Koonin EV
Commun Biol; 2021 Nov; 4(1):1343. PubMed ID: 34848826
[TBL] [Abstract][Full Text] [Related]
6. Mutational bias in spermatogonia impacts the anatomy of regulatory sites in the human genome.
Kaiser VB; Talmane L; Kumar Y; Semple F; MacLennan M; ; FitzPatrick DR; Taylor MS; Semple CA
Genome Res; 2021 Nov; 31(11):1994-2007. PubMed ID: 34417209
[TBL] [Abstract][Full Text] [Related]
7. Insertions in SARS-CoV-2 genome caused by template switch and duplications give rise to new variants that merit monitoring.
Garushyants SK; Rogozin IB; Koonin EV
bioRxiv; 2021 Aug; ():. PubMed ID: 33907754
[TBL] [Abstract][Full Text] [Related]
8. Analysis of Stop Codons within Prokaryotic Protein-Coding Genes Suggests Frequent Readthrough Events.
Belinky F; Ganguly I; Poliakov E; Yurchenko V; Rogozin IB
Int J Mol Sci; 2021 Feb; 22(4):. PubMed ID: 33672790
[TBL] [Abstract][Full Text] [Related]
9. A recurrent 8 bp frameshifting indel in FOXF1 defines a novel mutation hotspot associated with alveolar capillary dysplasia with misalignment of pulmonary veins.
Karolak JA; Bacolla A; Liu Q; Lantz PE; Petty J; Trapane P; Panzer K; Totapally BR; Niu Z; Xiao R; Xie NG; Wu LR; Szafranski P; Zhang DY; Stankiewicz P
Am J Med Genet A; 2019 Nov; 179(11):2272-2276. PubMed ID: 31436901
[TBL] [Abstract][Full Text] [Related]
10. Stable Intronic Sequences and Exon Skipping Events in the Human RPE65 Gene: Analysis of Expression in Retinal Pigment Epithelium Cells and Cell Culture Models.
Postnikova O; Poliakov E; Golestaneh N; Rogozin IB; Redmond TM
Front Genet; 2019; 10():634. PubMed ID: 31379919
[TBL] [Abstract][Full Text] [Related]
11. Using the Neandertal genome to study the evolution of small insertions and deletions in modern humans.
Chintalapati M; Dannemann M; Prüfer K
BMC Evol Biol; 2017 Aug; 17(1):179. PubMed ID: 28778150
[TBL] [Abstract][Full Text] [Related]
12. Mutational signatures and mutable motifs in cancer genomes.
Rogozin IB; Pavlov YI; Goncearenco A; De S; Lada AG; Poliakov E; Panchenko AR; Cooper DN
Brief Bioinform; 2018 Nov; 19(6):1085-1101. PubMed ID: 28498882
[TBL] [Abstract][Full Text] [Related]
13. EvalMSA: A Program to Evaluate Multiple Sequence Alignments and Detect Outliers.
Chiner-Oms A; González-Candelas F
Evol Bioinform Online; 2016; 12():277-284. PubMed ID: 27920488
[TBL] [Abstract][Full Text] [Related]
14. Spontaneous Chloroplast Mutants Mostly Occur by Replication Slippage and Show a Biased Pattern in the Plastome of Oenothera.
Massouh A; Schubert J; Yaneva-Roder L; Ulbricht-Jones ES; Zupok A; Johnson MT; Wright SI; Pellizzer T; Sobanski J; Bock R; Greiner S
Plant Cell; 2016 Apr; 28(4):911-29. PubMed ID: 27053421
[TBL] [Abstract][Full Text] [Related]
15. Absence of keratins 8 and 18 in rodent epithelial cell lines associates with keratin gene mutation and DNA methylation: Cell line selective effects on cell invasion.
Kwan R; Looi KS; Omary MB
Exp Cell Res; 2015 Jul; 335(1):12-22. PubMed ID: 25882495
[TBL] [Abstract][Full Text] [Related]
16. Single nucleotide polymorphism analysis of Korean native chickens using next generation sequencing data.
Seo DW; Oh JD; Jin S; Song KD; Park HB; Heo KN; Shin Y; Jung M; Park J; Jo C; Lee HK; Lee JH
Mol Biol Rep; 2015 Feb; 42(2):471-7. PubMed ID: 25304812
[TBL] [Abstract][Full Text] [Related]
17. Next-generation sequencing of colorectal cancers in chinese: identification of a recurrent frame-shift and gain-of-function Indel mutation in the TFDP1 gene.
Chen C; Liu J; Zhou F; Sun J; Li L; Jin C; Shao J; Jiang H; Zhao N; Zheng S; Lin B
OMICS; 2014 Oct; 18(10):625-35. PubMed ID: 25133581
[TBL] [Abstract][Full Text] [Related]
18. Genome wide analysis reveals single nucleotide polymorphisms associated with fatness and putative novel copy number variants in three pig breeds.
Fowler KE; Pong-Wong R; Bauer J; Clemente EJ; Reitter CP; Affara NA; Waite S; Walling GA; Griffin DK
BMC Genomics; 2013 Nov; 14():784. PubMed ID: 24225222
[TBL] [Abstract][Full Text] [Related]
19. Strong heterogeneity in mutation rate causes misleading hallmarks of natural selection on indel mutations in the human genome.
Kvikstad EM; Duret L
Mol Biol Evol; 2014 Jan; 31(1):23-36. PubMed ID: 24113537
[TBL] [Abstract][Full Text] [Related]
20. Genetic analysis of West Nile virus isolates from an outbreak in Idaho, United States, 2006-2007.
Grinev A; Chancey C; Añez G; Ball C; Winkelman V; Williamson P; Foster GA; Stramer SL; Rios M
Int J Environ Res Public Health; 2013 Sep; 10(9):4486-506. PubMed ID: 24065039
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]