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Journal Abstract Search

189 related items for PubMed ID: 24897126

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  • 3. Genetic variants in RET and risk of Hirschsprung's disease in Southeastern Chinese: a haplotype-based analysis.
    Tou J, Wang L, Liu L, Wang Y, Zhong R, Duan S, Liu W, Xiong Q, Gu Q, Yang H, Li H.
    BMC Med Genet; 2011 Feb 25; 12():32. PubMed ID: 21349203
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  • 4. Association analysis of the RET proto-oncogene with Hirschsprung disease in the Han Chinese population of southeastern China.
    Liu CP, Tang QQ, Lou JT, Luo CF, Zhou XW, Li DM, Chen F, Li X, Li JC.
    Biochem Genet; 2010 Jun 25; 48(5-6):496-503. PubMed ID: 20454948
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  • 5. Cumulative Risk Impact of RET, SEMA3, and NRG1 Polymorphisms Associated With Hirschsprung Disease in Han Chinese.
    Li Q, Zhang Z, Diao M, Gan L, Cheng W, Xiao P, Su L, Shangguan S, Jiang Q, Li L.
    J Pediatr Gastroenterol Nutr; 2017 Mar 25; 64(3):385-390. PubMed ID: 27203398
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  • 6. RET genotypes comprising specific haplotypes of polymorphic variants predispose to isolated Hirschsprung disease.
    Borrego S, Ruiz A, Saez ME, Gimm O, Gao X, López-Alonso M, Hernández A, Wright FA, Antiñolo G, Eng C.
    J Med Genet; 2000 Aug 25; 37(8):572-8. PubMed ID: 10922382
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  • 8. Genotyping analysis of 3 RET polymorphisms demonstrates low somatic mutation rate in Chinese Hirschsprung disease patients.
    Zhang Z, Jiang Q, Li Q, Cheng W, Qiao G, Xiao P, Gan L, Su L, Miao C, Li L.
    Int J Clin Exp Pathol; 2015 Aug 25; 8(5):5528-34. PubMed ID: 26191260
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  • 9. Association of genetic polymorphisms in the RET-protooncogene and NRG1 with Hirschsprung disease in Thai patients.
    Phusantisampan T, Sangkhathat S, Phongdara A, Chiengkriwate P, Patrapinyokul S, Mahasirimongkol S.
    J Hum Genet; 2012 May 25; 57(5):286-93. PubMed ID: 22377709
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  • 10. Effects of RET, NRG1 and NRG3 Polymorphisms in a Chinese Population with Hirschsprung Disease.
    Yang D, Yang J, Li S, Jiang M, Cao G, Yang L, Zhang X, Zhou Y, Li K, Tang ST.
    Sci Rep; 2017 Mar 03; 7():43222. PubMed ID: 28256518
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  • 11. A founding locus within the RET proto-oncogene may account for a large proportion of apparently sporadic Hirschsprung disease and a subset of cases of sporadic medullary thyroid carcinoma.
    Borrego S, Wright FA, Fernández RM, Williams N, López-Alonso M, Davuluri R, Antiñolo G, Eng C.
    Am J Hum Genet; 2003 Jan 03; 72(1):88-100. PubMed ID: 12474140
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  • 16. RET mutational spectrum in Hirschsprung disease: evaluation of 601 Chinese patients.
    So MT, Leon TY, Cheng G, Tang CS, Miao XP, Cornes BK, Diem NN, Cui L, Ngan ES, Lui VC, Wu XZ, Wang B, Wang H, Yuan ZW, Huang LM, Li L, Xia H, Zhu D, Liu J, Nguyen TL, Chan IH, Chung PH, Liu XL, Zhang R, Wong KK, Sham PC, Cherny SS, Tam PK, Garcia-Barcelo MM.
    PLoS One; 2011 Jan 03; 6(12):e28986. PubMed ID: 22174939
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  • 19. A rare haplotype of the RET proto-oncogene is a risk-modifying allele in hirschsprung disease.
    Griseri P, Pesce B, Patrone G, Osinga J, Puppo F, Sancandi M, Hofstra R, Romeo G, Ravazzolo R, Devoto M, Ceccherini I.
    Am J Hum Genet; 2002 Oct 03; 71(4):969-74. PubMed ID: 12214285
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