These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
96 related articles for article (PubMed ID: 25886032)
1. Correction: Pooled sequencing of 531 genes in inflammatory bowel disease identifies an associated rare variant in BTNL2 and implicates other immune related genes. PLOS Genetics Staff PLoS Genet; 2015 Apr; 11(4):e1005172. PubMed ID: 25886032 [TBL] [Abstract][Full Text] [Related]
2. Correction: Exome sequencing in multiple sclerosis families identifies 12 candidate genes and nominates biological pathways for the genesis of disease. PLOS Genetics Editors PLoS Genet; 2020 Apr; 16(4):e1008737. PubMed ID: 32271753 [TBL] [Abstract][Full Text] [Related]
3. Correction: Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease. PLOS Genetics Staff PLoS Genet; 2016 Nov; 12(11):e1006456. PubMed ID: 27893753 [TBL] [Abstract][Full Text] [Related]
4. Correction: A Genetic Screen Identifies a Requirement for Cysteine-Rich-Receptor-Like Kinases in Rice NH1 (OsNPR1)-Mediated Immunity. Chern M; Xu Q; Bart RS; Bai W; Ruan D; Sze-To WH; Canlas PE; Jain R; Chen X; Ronald PC PLoS Genet; 2016 Jul; 12(7):e1006182. PubMed ID: 27385201 [TBL] [Abstract][Full Text] [Related]
5. Correction: Deep Evolutionary Comparison of Gene Expression Identifies Parallel Recruitment of Trans-Factors in Two Independent Origins of C4 Photosynthesis. Aubry S; Kelly S; Kümpers BM; Smith-Unna RD; Hibberd JM PLoS Genet; 2016 May; 12(5):e1006087. PubMed ID: 27220009 [TBL] [Abstract][Full Text] [Related]
6. Correction: shRNA-Based Screen Identifies Endocytic Recycling Pathway Components That Act as Genetic Modifiers of Alpha-Synuclein Aggregation, Secretion and Toxicity. PLOS Genetics Staff PLoS Genet; 2016 Jun; 12(6):e1006148. PubMed ID: 27336682 [TBL] [Abstract][Full Text] [Related]
7. Correction: Experimental evolution of diverse Escherichia coli metabolic mutants identifies genetic loci for convergent adaptation of growth rate. Wytock TP; Fiebig A; Willett JW; Herrou J; Fergin A; Motter AE; Crosson S PLoS Genet; 2018 May; 14(5):e1007411. PubMed ID: 29813063 [TBL] [Abstract][Full Text] [Related]
8. Correction: DNA Sequence Evolution and Rare Homoeologous Conversion in Tetraploid Cotton. Page JT; Liechty ZS; Alexander RH; Clemons K; Hulse-Kemp AM; Ashrafi H; Van Deynze A; Stelly DM; Udall JA PLoS Genet; 2016 Jul; 12(7):e1006206. PubMed ID: 27447832 [TBL] [Abstract][Full Text] [Related]
9. Correction: Morphogenesis of the C. elegans Intestine Involves Axon Guidance Genes. Asan A; Raiders SA; Priess JR PLoS Genet; 2016 May; 12(5):e1006077. PubMed ID: 27192049 [TBL] [Abstract][Full Text] [Related]
10. Correction: A homozygous KAT2B variant modulates the clinical phenotype of ADD3 deficiency in humans and flies. Gonçalves S; Patat J; Guida MC; Lachaussée N; Arrondel C; Helmstädter M; Boyer O; Gribouval O; Gubler MC; Mollet G; Rio M; Charbit M; Bole-Feysot C; Nitschke P; Huber TB; Wheeler PG; Haynes D; Juusola J; de Villemeur TB; Nava C; Afenjar A; Keren B; Bodmer R; Antignac C; Simons M PLoS Genet; 2018 Oct; 14(10):e1007748. PubMed ID: 30365502 [TBL] [Abstract][Full Text] [Related]
11. Correction: Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth. Huusko JM; Karjalainen MK; Graham BE; Zhang G; Farrow EG; Miller NA; Jacobsson B; Eidem HR; Murray JC; Bedell B; Breheny P; Brown NW; Bødker FL; Litterman NK; Jiang PP; Russell L; Hinds DA; Hu Y; ; Rokas A; Teramo K; Christensen K; Williams SM; Rämet M; Kingsmore SF; Ryckman KK; Hallman M; Muglia LJ PLoS Genet; 2018 Sep; 14(9):e1007673. PubMed ID: 30212495 [TBL] [Abstract][Full Text] [Related]
12. Correction: Penetration of the Stigma and Style Elicits a Novel Transcriptome in Pollen Tubes, Pointing to Genes Critical for Growth in a Pistil. Qin Y; Leydon AR; Manziello A; Pandey R; Mount D; Denic S; Vasic B; Johnson MA; Palanivelu R PLoS Genet; 2016 Jul; 12(7):e1006210. PubMed ID: 27434655 [TBL] [Abstract][Full Text] [Related]
13. Correction: 3'UTR Shortening Potentiates MicroRNA-Based Repression of Pro-differentiation Genes in Proliferating Human Cells. PLOS Genetics Staff PLoS Genet; 2016 Aug; 12(8):e1006254. PubMed ID: 27494143 [TBL] [Abstract][Full Text] [Related]
14. Correction: Functional significance of rare neuroligin 1 variants found in autism. Nakanishi M; Nomura J; Ji X; Tamada K; Arai T; Takahashi E; Bućan M; Takumi T PLoS Genet; 2017 Oct; 13(10):e1007035. PubMed ID: 28972980 [TBL] [Abstract][Full Text] [Related]
15. Correction: Epistatic control of intrinsic resistance by virulence genes in Listeria. Scortti M; Han L; Alvarez S; Leclercq A; Moura A; Lecuit M; Vazquez-Boland J PLoS Genet; 2018 Oct; 14(10):e1007727. PubMed ID: 30321174 [TBL] [Abstract][Full Text] [Related]
16. Correction: A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease. Emdin CA; Haas ME; Khera AV; Aragam K; Chaffin M; Klarin D; Hindy G; Jiang L; Wei WQ; Feng Q; Karjalainen J; Havulinna A; Kiiskinen T; Bick A; Ardissino D; Wilson JG; Schunkert H; McPherson R; Watkins H; Elosua R; Bown MJ; Samani NJ; Baber U; Erdmann J; Gupta N; Danesh J; Saleheen D; Chang KM; Vujkovic M; Voight B; Damrauer S; Lynch J; Kaplan D; Serper M; Tsao P; Program MV; Mercader J; Hanis C; Daly M; Denny J; Gabriel S; Kathiresan S PLoS Genet; 2021 Apr; 17(4):e1009503. PubMed ID: 33822779 [TBL] [Abstract][Full Text] [Related]
17. Correction: An AP endonuclease functions in active DNA demethylation and gene imprinting in Arabidopsis. PLOS Genetics Staff PLoS Genet; 2015 Apr; 11(4):e1005198. PubMed ID: 25915657 [TBL] [Abstract][Full Text] [Related]
18. Correction: Drosophila TIM binds importin α1, and acts as an adapter to transport PER to the nucleus. PLOS Genetics Staff PLoS Genet; 2015 Apr; 11(4):e1005205. PubMed ID: 25915778 [TBL] [Abstract][Full Text] [Related]
19. Correction: Highly dynamic and sex-specific expression of microRNAs during early ES cell differentiation. PLOS Genetics Staff PLoS Genet; 2015 Mar; 11(3):e1005077. PubMed ID: 25807357 [TBL] [Abstract][Full Text] [Related]
20. Correction: Unified inference of missense variant effects and gene constraints in the human genome. PLOS Genetics Staff PLoS Genet; 2021 Jan; 17(1):e1009348. PubMed ID: 33507918 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]