155 related articles for article (PubMed ID: 24916375)
1. Human skin color is influenced by an intergenic DNA polymorphism regulating transcription of the nearby BNC2 pigmentation gene.
Visser M; Palstra RJ; Kayser M
Hum Mol Genet; 2014 Nov; 23(21):5750-62. PubMed ID: 24916375
[TBL] [Abstract][Full Text] [Related]
2. Allele-specific transcriptional regulation of IRF4 in melanocytes is mediated by chromatin looping of the intronic rs12203592 enhancer to the IRF4 promoter.
Visser M; Palstra RJ; Kayser M
Hum Mol Genet; 2015 May; 24(9):2649-61. PubMed ID: 25631878
[TBL] [Abstract][Full Text] [Related]
3. HERC2 rs12913832 modulates human pigmentation by attenuating chromatin-loop formation between a long-range enhancer and the OCA2 promoter.
Visser M; Kayser M; Palstra RJ
Genome Res; 2012 Mar; 22(3):446-55. PubMed ID: 22234890
[TBL] [Abstract][Full Text] [Related]
4. Molecular genetics of human pigmentation diversity.
Sturm RA
Hum Mol Genet; 2009 Apr; 18(R1):R9-17. PubMed ID: 19297406
[TBL] [Abstract][Full Text] [Related]
5. A conserved transcriptional enhancer that specifies Tyrp1 expression to melanocytes.
Murisier F; Guichard S; Beermann F
Dev Biol; 2006 Oct; 298(2):644-55. PubMed ID: 16934245
[TBL] [Abstract][Full Text] [Related]
6. Comprehensive candidate gene study highlights UGT1A and BNC2 as new genes determining continuous skin color variation in Europeans.
Jacobs LC; Wollstein A; Lao O; Hofman A; Klaver CC; Uitterlinden AG; Nijsten T; Kayser M; Liu F
Hum Genet; 2013 Feb; 132(2):147-58. PubMed ID: 23052946
[TBL] [Abstract][Full Text] [Related]
7. A Functional SNP in BNC2 Is Associated with Adolescent Idiopathic Scoliosis.
Ogura Y; Kou I; Miura S; Takahashi A; Xu L; Takeda K; Takahashi Y; Kono K; Kawakami N; Uno K; Ito M; Minami S; Yonezawa I; Yanagida H; Taneichi H; Zhu Z; Tsuji T; Suzuki T; Sudo H; Kotani T; Watanabe K; Hosogane N; Okada E; Iida A; Nakajima M; Sudo A; Chiba K; Hiraki Y; Toyama Y; Qiu Y; Shukunami C; Kamatani Y; Kubo M; Matsumoto M; Ikegawa S
Am J Hum Genet; 2015 Aug; 97(2):337-42. PubMed ID: 26211971
[TBL] [Abstract][Full Text] [Related]
8. A common atopy-associated variant in the Th2 cytokine locus control region impacts transcriptional regulation and alters SMAD3 and SP1 binding.
Kretschmer A; Möller G; Lee H; Laumen H; von Toerne C; Schramm K; Prokisch H; Eyerich S; Wahl S; Baurecht H; Franke A; Claussnitzer M; Eyerich K; Teumer A; Milani L; Klopp N; Hauck SM; Illig T; Peters A; Waldenberger M; Adamski J; Reischl E; Weidinger S
Allergy; 2014 May; 69(5):632-42. PubMed ID: 24661001
[TBL] [Abstract][Full Text] [Related]
9. BNC2 is a putative tumor suppressor gene in high-grade serous ovarian carcinoma and impacts cell survival after oxidative stress.
Cesaratto L; Grisard E; Coan M; Zandonà L; De Mattia E; Poletto E; Cecchin E; Puglisi F; Canzonieri V; Mucignat MT; Zucchetto A; Stocco G; Colombatti A; Nicoloso MS; Spizzo R
Cell Death Dis; 2016 Sep; 7(9):e2374. PubMed ID: 27899818
[TBL] [Abstract][Full Text] [Related]
10. A Genome-Wide Association Study Identifies the Skin Color Genes IRF4, MC1R, ASIP, and BNC2 Influencing Facial Pigmented Spots.
Jacobs LC; Hamer MA; Gunn DA; Deelen J; Lall JS; van Heemst D; Uh HW; Hofman A; Uitterlinden AG; Griffiths CEM; Beekman M; Slagboom PE; Kayser M; Liu F; Nijsten T
J Invest Dermatol; 2015 Jul; 135(7):1735-1742. PubMed ID: 25705849
[TBL] [Abstract][Full Text] [Related]
11. Ovarian cancer-associated polymorphisms in the BNC2 gene among women with endometriosis.
Sundqvist J; Falconer H; Seddighzadeh M; Vodolazkaia A; Fassbender A; Kyama C; Bokor A; Stephansson O; Gemzell-Danielsson K; D'Hooghe TM
Hum Reprod; 2011 Aug; 26(8):2253-7. PubMed ID: 21642636
[TBL] [Abstract][Full Text] [Related]
12. Complex patterns of cis-regulatory polymorphisms in ebony underlie standing pigmentation variation in Drosophila melanogaster.
Miyagi R; Akiyama N; Osada N; Takahashi A
Mol Ecol; 2015 Dec; 24(23):5829-41. PubMed ID: 26503353
[TBL] [Abstract][Full Text] [Related]
13. Meta-analysis of GWA studies provides new insights on the genetic architecture of skin pigmentation in recently admixed populations.
Lona-Durazo F; Hernandez-Pacheco N; Fan S; Zhang T; Choi J; Kovacs MA; Loftus SK; Le P; Edwards M; Fortes-Lima CA; Eng C; Huntsman S; Hu D; Gómez-Cabezas EJ; Marín-Padrón LC; Grauholm J; Mors O; Burchard EG; Norton HL; Pavan WJ; Brown KM; Tishkoff S; Pino-Yanes M; Beleza S; Marcheco-Teruel B; Parra EJ
BMC Genet; 2019 Jul; 20(1):59. PubMed ID: 31315583
[TBL] [Abstract][Full Text] [Related]
14. Assessment of polymorphic variants in the melanocortin-1 receptor gene with cutaneous pigmentation using an evolutionary approach.
Kanetsky PA; Ge F; Najarian D; Swoyer J; Panossian S; Schuchter L; Holmes R; Guerry D; Rebbeck TR
Cancer Epidemiol Biomarkers Prev; 2004 May; 13(5):808-19. PubMed ID: 15159314
[TBL] [Abstract][Full Text] [Related]
15. Polymorphisms upstream of the melanocortin-1 receptor coding region are associated with human pigmentation variation in a Brazilian population.
Neitzke-Montinelli V; Urmenyi TP; Rondinelli E; Cabello PH; Silva R; Moura-Neto RS
Am J Hum Biol; 2012; 24(6):853-5. PubMed ID: 22961816
[TBL] [Abstract][Full Text] [Related]
16. Genetic variation in the MITF promoter affects skin colour and transcriptional activity in black-boned chickens.
Wang G; Liao J; Tang M; Yu S
Br Poult Sci; 2018 Feb; 59(1):21-27. PubMed ID: 28891677
[TBL] [Abstract][Full Text] [Related]
17. A polymorphism in IRF4 affects human pigmentation through a tyrosinase-dependent MITF/TFAP2A pathway.
Praetorius C; Grill C; Stacey SN; Metcalf AM; Gorkin DU; Robinson KC; Van Otterloo E; Kim RS; Bergsteinsdottir K; Ogmundsdottir MH; Magnusdottir E; Mishra PJ; Davis SR; Guo T; Zaidi MR; Helgason AS; Sigurdsson MI; Meltzer PS; Merlino G; Petit V; Larue L; Loftus SK; Adams DR; Sobhiafshar U; Emre NC; Pavan WJ; Cornell R; Smith AG; McCallion AS; Fisher DE; Stefansson K; Sturm RA; Steingrimsson E
Cell; 2013 Nov; 155(5):1022-33. PubMed ID: 24267888
[TBL] [Abstract][Full Text] [Related]
18. A Common Type 2 Diabetes Risk Variant Potentiates Activity of an Evolutionarily Conserved Islet Stretch Enhancer and Increases C2CD4A and C2CD4B Expression.
Kycia I; Wolford BN; Huyghe JR; Fuchsberger C; Vadlamudi S; Kursawe R; Welch RP; Albanus RD; Uyar A; Khetan S; Lawlor N; Bolisetty M; Mathur A; Kuusisto J; Laakso M; Ucar D; Mohlke KL; Boehnke M; Collins FS; Parker SCJ; Stitzel ML
Am J Hum Genet; 2018 Apr; 102(4):620-635. PubMed ID: 29625024
[TBL] [Abstract][Full Text] [Related]
19. Identification of a regulatory variant that binds FOXA1 and FOXA2 at the CDC123/CAMK1D type 2 diabetes GWAS locus.
Fogarty MP; Cannon ME; Vadlamudi S; Gaulton KJ; Mohlke KL
PLoS Genet; 2014 Sep; 10(9):e1004633. PubMed ID: 25211022
[TBL] [Abstract][Full Text] [Related]
20. Promoter polymorphisms in the MATP (SLC45A2) gene are associated with normal human skin color variation.
Graf J; Voisey J; Hughes I; van Daal A
Hum Mutat; 2007 Jul; 28(7):710-7. PubMed ID: 17358008
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]