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Genetic Variations and mRNA Expression of NRF2 in Parkinson's Disease.
Ran C, Wirdefeldt K, Brodin L, Ramezani M, Westerlund M, Xiang F, Anvret A, Willows T, Sydow O, Johansson A, Galter D, Svenningsson P, Belin AC. Ran C, et al. Among authors: xiang f. Parkinsons Dis. 2017;2017:4020198. doi: 10.1155/2017/4020198. Epub 2017 May 2. Parkinsons Dis. 2017. PMID: 28540099 Free PMC article.
Strong association between glucocerebrosidase mutations and Parkinson's disease in Sweden.
Ran C, Brodin L, Forsgren L, Westerlund M, Ramezani M, Gellhaar S, Xiang F, Fardell C, Nissbrandt H, Söderkvist P, Puschmann A, Ygland E, Olson L, Willows T, Johansson A, Sydow O, Wirdefeldt K, Galter D, Svenningsson P, Belin AC. Ran C, et al. Among authors: xiang f. Neurobiol Aging. 2016 Sep;45:212.e5-212.e11. doi: 10.1016/j.neurobiolaging.2016.04.022. Epub 2016 May 3. Neurobiol Aging. 2016. PMID: 27255555 Free PMC article.
NURR1 mutations in cases of schizophrenia and manic-depressive disorder.
Buervenich S, Carmine A, Arvidsson M, Xiang F, Zhang Z, Sydow O, Jönsson EG, Sedvall GC, Leonard S, Ross RG, Freedman R, Chowdari KV, Nimgaonkar VL, Perlmann T, Anvret M, Olson L. Buervenich S, et al. Among authors: xiang f. Am J Med Genet. 2000 Dec 4;96(6):808-13. doi: 10.1002/1096-8628(20001204)96:6<808::aid-ajmg23>3.0.co;2-e. Am J Med Genet. 2000. PMID: 11121187
Mutation screening in Rett syndrome patients.
Xiang F, Buervenich S, Nicolao P, Bailey ME, Zhang Z, Anvret M. Xiang F, et al. J Med Genet. 2000 Apr;37(4):250-5. doi: 10.1136/jmg.37.4.250. J Med Genet. 2000. PMID: 10745042 Free PMC article.
793 results