BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

179 related articles for article (PubMed ID: 17568986)

  • 1. OCA2 481Thr, a hypofunctional allele in pigmentation, is characteristic of northeastern Asian populations.
    Yuasa I; Umetsu K; Harihara S; Miyoshi A; Saitou N; Park KS; Dashnyam B; Jin F; Lucotte G; Chattopadhyay PK; Henke L; Henke J
    J Hum Genet; 2007; 52(8):690-693. PubMed ID: 17568986
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Distribution of OCA2∗481Thr and OCA2∗615Arg, associated with hypopigmentation, in several additional populations.
    Yuasa I; Harihara S; Jin F; Nishimukai H; Fujihara J; Fukumori Y; Takeshita H; Umetsu K; Saitou N
    Leg Med (Tokyo); 2011 Jul; 13(4):215-7. PubMed ID: 21565543
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Distribution of two Asian-related coding SNPs in the MC1R and OCA2 genes.
    Yuasa I; Umetsu K; Harihara S; Kido A; Miyoshi A; Saitou N; Dashnyam B; Jin F; Lucotte G; Chattopadhyay PK; Henke L; Henke J
    Biochem Genet; 2007 Aug; 45(7-8):535-42. PubMed ID: 17570052
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Association study confirms the role of two OCA2 polymorphisms in normal skin pigmentation variation in East Asian populations.
    Eaton K; Edwards M; Krithika S; Cook G; Norton H; Parra EJ
    Am J Hum Biol; 2015; 27(4):520-5. PubMed ID: 25809079
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Association of the OCA2 polymorphism His615Arg with melanin content in east Asian populations: further evidence of convergent evolution of skin pigmentation.
    Edwards M; Bigham A; Tan J; Li S; Gozdzik A; Ross K; Jin L; Parra EJ
    PLoS Genet; 2010 Mar; 6(3):e1000867. PubMed ID: 20221248
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A Genetic Mechanism for Convergent Skin Lightening during Recent Human Evolution.
    Yang Z; Zhong H; Chen J; Zhang X; Zhang H; Luo X; Xu S; Chen H; Lu D; Han Y; Li J; Fu L; Qi X; Peng Y; Xiang K; Lin Q; Guo Y; Li M; Cao X; Zhang Y; Liao S; Peng Y; Zhang L; Guo X; Dong S; Liang F; Wang J; Willden A; Seang Aun H; Serey B; Sovannary T; Bunnath L; Samnom H; Mardon G; Li Q; Meng A; Shi H; Su B
    Mol Biol Evol; 2016 May; 33(5):1177-87. PubMed ID: 26744415
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Variants in melanogenesis-related genes associate with skin cancer risk among Japanese populations.
    Yoshizawa J; Abe Y; Oiso N; Fukai K; Hozumi Y; Nakamura T; Narita T; Motokawa T; Wakamatsu K; Ito S; Kawada A; Tamiya G; Suzuki T
    J Dermatol; 2014 Apr; 41(4):296-302. PubMed ID: 24617981
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A global view of the OCA2-HERC2 region and pigmentation.
    Donnelly MP; Paschou P; Grigorenko E; Gurwitz D; Barta C; Lu RB; Zhukova OV; Kim JJ; Siniscalco M; New M; Li H; Kajuna SL; Manolopoulos VG; Speed WC; Pakstis AJ; Kidd JR; Kidd KK
    Hum Genet; 2012 May; 131(5):683-96. PubMed ID: 22065085
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic evidence for the convergent evolution of light skin in Europeans and East Asians.
    Norton HL; Kittles RA; Parra E; McKeigue P; Mao X; Cheng K; Canfield VA; Bradley DG; McEvoy B; Shriver MD
    Mol Biol Evol; 2007 Mar; 24(3):710-22. PubMed ID: 17182896
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Association of melanogenesis genes with skin color variation among Japanese females.
    Abe Y; Tamiya G; Nakamura T; Hozumi Y; Suzuki T
    J Dermatol Sci; 2013 Feb; 69(2):167-72. PubMed ID: 23165166
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutational Analysis of the TYR and OCA2 Genes in Four Chinese Families with Oculocutaneous Albinism.
    Wang Y; Wang Z; Chen M; Fan N; Yang J; Liu L; Wang Y; Liu X
    PLoS One; 2015; 10(4):e0125651. PubMed ID: 25919014
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic analyses of oculocutaneous albinism types 1 and 2 with four novel mutations.
    Yang Q; Yi S; Li M; Xie B; Luo J; Wang J; Rong X; Zhang Q; Qin Z; Hang L; Feng S; Fan X
    BMC Med Genet; 2019 Jun; 20(1):106. PubMed ID: 31196117
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A decreasing gradient of 374F allele frequencies in the skin pigmentation gene SLC45A2, from the north of West Europe to North Africa.
    Lucotte G; Mercier G; Diéterlen F; Yuasa I
    Biochem Genet; 2010 Feb; 48(1-2):26-33. PubMed ID: 19916045
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The light skin allele of SLC24A5 in South Asians and Europeans shares identity by descent.
    Basu Mallick C; Iliescu FM; Möls M; Hill S; Tamang R; Chaubey G; Goto R; Ho SY; Gallego Romero I; Crivellaro F; Hudjashov G; Rai N; Metspalu M; Mascie-Taylor CG; Pitchappan R; Singh L; Mirazon-Lahr M; Thangaraj K; Villems R; Kivisild T
    PLoS Genet; 2013 Nov; 9(11):e1003912. PubMed ID: 24244186
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Inheritance of a novel mutated allele of the OCA2 gene associated with high incidence of oculocutaneous albinism in a Polynesian community.
    Johanson HC; Chen W; Wicking C; Sturm RA
    J Hum Genet; 2010 Feb; 55(2):103-11. PubMed ID: 20019752
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of P gene mutations in individuals with oculocutaneous albinism in sub-Saharan Africa.
    Kerr R; Stevens G; Manga P; Salm S; John P; Haw T; Ramsay M
    Hum Mutat; 2000; 15(2):166-72. PubMed ID: 10649493
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel compound heterozygous mutations in OCA2 gene associated with non-syndromic oculocutaneous albinism in a Chinese Han patient: a case report.
    Wang H; Wan Y; Yang Y; Li H; Mao L; Gao S; Xu J; Wang J
    BMC Med Genet; 2019 Jul; 20(1):130. PubMed ID: 31345173
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A GWAS in Latin Americans highlights the convergent evolution of lighter skin pigmentation in Eurasia.
    Adhikari K; Mendoza-Revilla J; Sohail A; Fuentes-Guajardo M; Lampert J; Chacón-Duque JC; Hurtado M; Villegas V; Granja V; Acuña-Alonzo V; Jaramillo C; Arias W; Lozano RB; Everardo P; Gómez-Valdés J; Villamil-Ramírez H; Silva de Cerqueira CC; Hunemeier T; Ramallo V; Schuler-Faccini L; Salzano FM; Gonzalez-José R; Bortolini MC; Canizales-Quinteros S; Gallo C; Poletti G; Bedoya G; Rothhammer F; Tobin DJ; Fumagalli M; Balding D; Ruiz-Linares A
    Nat Commun; 2019 Jan; 10(1):358. PubMed ID: 30664655
    [TBL] [Abstract][Full Text] [Related]  

  • 19. NGS-based targeted sequencing identified two novel variants in Southwestern Chinese families with oculocutaneous albinism.
    Xiao Y; Zhou C; Xie H; Huang S; Wang J; Liu S
    BMC Genomics; 2022 Apr; 23(1):332. PubMed ID: 35488210
    [TBL] [Abstract][Full Text] [Related]  

  • 20. P gene mutations associated with oculocutaneous albinism type II (OCA2).
    Oetting WS; Garrett SS; Brott M; King RA
    Hum Mutat; 2005 Mar; 25(3):323. PubMed ID: 15712365
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.