BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

151 related articles for article (PubMed ID: 27538669)

  • 1. Mutational analysis of CHCHD2 in Chinese patients with multiple system atrophy and amyotrophic lateral sclerosis.
    Yang X; An R; Zhao Q; Zheng J; Tian S; Chen Y; Xu Y
    J Neurol Sci; 2016 Sep; 368():389-91. PubMed ID: 27538669
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutational scanning of the CHCHD2 gene in Han Chinese patients with Parkinson's disease and meta-analysis of the literature.
    Yang X; Zhao Q; An R; Zheng J; Tian S; Chen Y; Xu Y
    Parkinsonism Relat Disord; 2016 Aug; 29():42-6. PubMed ID: 27269965
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Identification of CHCHD2 mutations in patients with Alzheimer's disease, amyotrophic lateral sclerosis and frontotemporal dementia in China.
    Liu X; Jiao B; Zhang W; Xiao T; Hou L; Pan C; Tang B; Shen L
    Mol Med Rep; 2018 Jul; 18(1):461-466. PubMed ID: 29749507
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic analysis of CHCHD2 gene in Chinese Parkinson's disease.
    Li NN; Wang L; Tan EK; Cheng L; Sun XY; Lu ZJ; Li JY; Zhang JH; Peng R
    Am J Med Genet B Neuropsychiatr Genet; 2016 Dec; 171(8):1148-1152. PubMed ID: 27626775
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Association analysis of SNP rs11868035 in SREBF1 with sporadic Parkinson's disease, sporadic amyotrophic lateral sclerosis and multiple system atrophy in a Chinese population.
    Yuan X; Cao B; Wu Y; Chen Y; Wei Q; Ou R; Yang J; Chen X; Zhao B; Song W; Shang H
    Neurosci Lett; 2018 Jan; 664():128-132. PubMed ID: 29128630
    [TBL] [Abstract][Full Text] [Related]  

  • 6. SLC1A2 rs3794087 are associated with susceptibility to Parkinson's disease, but not essential tremor, amyotrophic lateral sclerosis or multiple system atrophy in a Chinese population.
    Xu Y; Cao B; Chen Y; Ou R; Wei Q; Yang J; Zhao B; Song W; Shang HF
    J Neurol Sci; 2016 Jun; 365():96-100. PubMed ID: 27206883
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic Variants of SNCA Are Associated with Susceptibility to Parkinson's Disease but Not Amyotrophic Lateral Sclerosis or Multiple System Atrophy in a Chinese Population.
    Chen Y; Wei QQ; Ou R; Cao B; Chen X; Zhao B; Guo X; Yang Y; Chen K; Wu Y; Song W; Shang HF
    PLoS One; 2015; 10(7):e0133776. PubMed ID: 26208350
    [TBL] [Abstract][Full Text] [Related]  

  • 8. SNCA variants rs2736990 and rs356220 as risk factors for Parkinson's disease but not for amyotrophic lateral sclerosis and multiple system atrophy in a Chinese population.
    Guo XY; Chen YP; Song W; Zhao B; Cao B; Wei QQ; Ou RW; Yang Y; Yuan LX; Shang HF
    Neurobiol Aging; 2014 Dec; 35(12):2882.e1-2882.e6. PubMed ID: 25129240
    [TBL] [Abstract][Full Text] [Related]  

  • 9. No association of GPNMB rs156429 polymorphism with Parkinson's disease, amyotrophic lateral sclerosis and multiple system atrophy in Chinese population.
    Xu Y; Chen Y; Ou R; Wei QQ; Cao B; Chen K; Shang HF
    Neurosci Lett; 2016 May; 622():113-7. PubMed ID: 27132081
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Lack of CHCHD2 mutations in Parkinson's disease in a Taiwanese population.
    Fan TS; Lin HI; Lin CH; Wu RM
    Neurobiol Aging; 2016 Feb; 38():218.e1-218.e2. PubMed ID: 26725463
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Association analysis of polymorphisms in VMAT2 and TMEM106B genes for Parkinson's disease, amyotrophic lateral sclerosis and multiple system atrophy.
    Hu T; Chen Y; Ou R; Wei Q; Cao B; Zhao B; Wu Y; Song W; Chen X; Shang HF
    J Neurol Sci; 2017 Jun; 377():65-71. PubMed ID: 28477711
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Aberrant CHCHD2-associated mitochondriopathy in Kii ALS/PDC astrocytes.
    Leventoux N; Morimoto S; Ishikawa M; Nakamura S; Ozawa F; Kobayashi R; Watanabe H; Supakul S; Okamoto S; Zhou Z; Kobayashi H; Kato C; Hirokawa Y; Aiba I; Takahashi S; Shibata S; Takao M; Yoshida M; Endo F; Yamanaka K; Kokubo Y; Okano H
    Acta Neuropathol; 2024 May; 147(1):84. PubMed ID: 38750212
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutation Screening of the CHCHD2 Gene for Alzheimer's Disease and Frontotemporal Dementia in Chinese Mainland Population.
    Che XQ; Zhao QH; Huang Y; Li X; Ren RJ; Chen SD; Guo QH; Wang G
    J Alzheimers Dis; 2018; 61(4):1283-1288. PubMed ID: 29376860
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutation analysis of CHCHD2 gene in Chinese Han familial essential tremor patients and familial Parkinson's disease patients.
    Gao C; Chen YM; Sun Q; He YC; Huang P; Wang T; Li DH; Liang L; Liu J; Xiao Q; Chen SD
    Neurobiol Aging; 2017 Jan; 49():218.e9-218.e11. PubMed ID: 27814991
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The relationship between four GWAS-identified loci in Alzheimer's disease and the risk of Parkinson's disease, amyotrophic lateral sclerosis, and multiple system atrophy.
    Chen Y; Cao B; Chen X; Ou R; Wei Q; Zhao B; Wu Y; Yuan L; Shang HF
    Neurosci Lett; 2018 Nov; 686():205-210. PubMed ID: 30144538
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutation analysis of CHCHD2 in Canadian patients with familial Parkinson's disease.
    Zhang M; Xi Z; Fang S; Ghani M; Sato C; Moreno D; Liang Y; Lang AE; Rogaeva E
    Neurobiol Aging; 2016 Feb; 38():217.e7-217.e8. PubMed ID: 26639156
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A new CHCHD2 mutation identified in a southern italy patient with multiple system atrophy.
    Nicoletti G; Gagliardi M; Procopio R; Iannello G; Morelli M; Annesi G; Quattrone A
    Parkinsonism Relat Disord; 2018 Feb; 47():91-93. PubMed ID: 29248339
    [No Abstract]   [Full Text] [Related]  

  • 18. An association analysis of the rs1572931 polymorphism of the RAB7L1 gene in Parkinson's disease, amyotrophic lateral sclerosis and multiple system atrophy in China.
    Guo XY; Chen YP; Song W; Zhao B; Cao B; Wei QQ; Ou RW; Yang Y; Yuan LX; Shang HF
    Eur J Neurol; 2014 Oct; 21(10):1337-43. PubMed ID: 25040112
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Determining the Effect of the HNMT, STK39, and NMD3 Polymorphisms on the Incidence of Parkinson's Disease, Amyotrophic Lateral Sclerosis, and Multiple System Atrophy in Chinese Populations.
    Chen Y; Cao B; Ou R; Wei Q; Chen X; Zhao B; Wu Y; Song W; Shang HF
    J Mol Neurosci; 2018 Apr; 64(4):574-580. PubMed ID: 29564728
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutation Screening of the CHCHD10 Gene in Chinese Patients with Amyotrophic Lateral Sclerosis.
    Zhou Q; Chen Y; Wei Q; Cao B; Wu Y; Zhao B; Ou R; Yang J; Chen X; Hadano S; Shang HF
    Mol Neurobiol; 2017 Jul; 54(5):3189-3194. PubMed ID: 27056076
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.