BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

429 related articles for article (PubMed ID: 33279243)

  • 1. Mutation analysis of TMEM family members for early-onset Parkinson's disease in Chinese population.
    Li C; Ou R; Chen Y; Gu X; Wei Q; Cao B; Zhang L; Hou Y; Liu K; Chen X; Song W; Zhao B; Wu Y; Liu Y; Shang H
    Neurobiol Aging; 2021 May; 101():299.e1-299.e6. PubMed ID: 33279243
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic analysis of TRIM family genes for early-onset Parkinson's disease in Chinese population.
    Li C; Ou R; Hou Y; Chen Y; Gu X; Wei Q; Cao B; Zhang L; Liu K; Chen X; Song W; Zhao B; Wu Y; Shang H
    Parkinsonism Relat Disord; 2021 Sep; 90():105-113. PubMed ID: 34419804
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic Analysis of ZNF Protein Family Members for Early-Onset Parkinson's Disease in Chinese Population.
    Li CY; Ou RW; Chen YP; Gu XJ; Wei QQ; Cao B; Zhang LY; Hou YB; Liu KC; Chen XP; Song W; Zhao B; Wu Y; Liu Y; Shang HF
    Mol Neurobiol; 2021 Jul; 58(7):3435-3442. PubMed ID: 33723766
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutation Analysis of DNAJC Family for Early-Onset Parkinson's Disease in a Chinese Cohort.
    Li C; Ou R; Chen Y; Gu X; Wei Q; Cao B; Zhang L; Hou Y; Liu K; Chen X; Song W; Zhao B; Wu Y; Shang H
    Mov Disord; 2020 Nov; 35(11):2068-2076. PubMed ID: 32662538
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutation analysis of seven SLC family transporters for early-onset Parkinson's disease in Chinese population.
    Li C; Ou R; Chen Y; Gu X; Wei Q; Cao B; Zhang L; Hou Y; Liu K; Chen X; Song W; Zhao B; Wu Y; Shang H
    Neurobiol Aging; 2021 Jul; 103():152.e1-152.e6. PubMed ID: 33781609
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The mutation spectrum of Parkinson-disease-related genes in early-onset Parkinson's disease in ethnic Chinese.
    Chen YP; Yu SH; Zhang GH; Hou YB; Gu XJ; Ou RW; Shen Y; Song W; Chen XP; Zhao B; Cao B; Zhang LY; Sun MM; Liu FF; Wei QQ; Liu KC; Lin JY; Yang TM; Yang J; Wu Y; Jiang Z; Liu J; Cheng YF; Xiao Y; Su WM; Feng F; Cai YY; Li SR; Hu T; Yuan XQ; Zhou QQ; Shao N; Ma S; Shang HF
    Eur J Neurol; 2022 Nov; 29(11):3218-3228. PubMed ID: 35861376
    [TBL] [Abstract][Full Text] [Related]  

  • 7. ANXA1 and the risk for early-onset Parkinson's disease.
    Li C; Ou R; Gu X; Hou Y; Chen Y; Wei Q; Zhang L; Lin J; Liu K; Huang J; Chen X; Song W; Zhao B; Wu Y; Shang H
    Neurobiol Aging; 2022 Apr; 112():212-214. PubMed ID: 35240489
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Whole-exome sequencing in early-onset Parkinson's disease among ethnic Chinese.
    Li N; Wang L; Zhang J; Tan EK; Li J; Peng J; Duan L; Chen C; Zhou D; He L; Peng R
    Neurobiol Aging; 2020 Jun; 90():150.e5-150.e11. PubMed ID: 32171587
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Whole exome sequencing identified a new compound heterozygous PRKN mutation in a Chinese family with early-onset Parkinson's disease.
    Li T; Kou D; Cui Y; Le W
    Biosci Rep; 2020 May; 40(5):. PubMed ID: 32391545
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Rare variant analysis of essential tremor-associated genes in early-onset Parkinson's disease.
    Liang D; Zhao Y; Pan H; Zhou X; He R; Zhou X; Yang J; Wang Y; Zhou X; Zhou Z; Xu Q; Yan X; Li J; Guo J; Tang B; Sun Q
    Ann Clin Transl Neurol; 2021 Jan; 8(1):119-125. PubMed ID: 33185019
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Screening for TMEM230 mutations in young-onset Parkinson's disease.
    Ma D; Foo JN; Yulin Ng E; Zhao Y; Liu JJ; Tan EK
    Neurobiol Aging; 2017 Oct; 58():239.e9-239.e10. PubMed ID: 28709721
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Rare variant analysis of UQCRC1 in Chinese patients with early-onset Parkinson's disease.
    Wang S; Zheng X; Ou R; Wei Q; Lin J; Yang T; Xiao Y; Jiang Q; Li C; Shang H
    Neurobiol Aging; 2024 Feb; 134():40-42. PubMed ID: 37984314
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Diagnostic exome sequencing in early-onset Parkinson's disease confirms VPS13C as a rare cause of autosomal-recessive Parkinson's disease.
    Schormair B; Kemlink D; Mollenhauer B; Fiala O; Machetanz G; Roth J; Berutti R; Strom TM; Haslinger B; Trenkwalder C; Zahorakova D; Martasek P; Ruzicka E; Winkelmann J
    Clin Genet; 2018 Mar; 93(3):603-612. PubMed ID: 28862745
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic Analysis of Six Transmembrane Protein Family Genes in Parkinson's Disease in a Large Chinese Cohort.
    Zhao Y; Zhang K; Pan H; Wang Y; Zhou X; Xiang Y; Xu Q; Sun Q; Tan J; Yan X; Li J; Guo J; Tang B; Liu Z
    Front Aging Neurosci; 2022; 14():889057. PubMed ID: 35860667
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutation screening and burden analysis of VPS13C in Chinese patients with early-onset Parkinson's disease.
    Gu X; Li C; Chen Y; Ou R; Cao B; Wei Q; Hou Y; Zhang L; Song W; Zhao B; Wu Y; Shang H
    Neurobiol Aging; 2020 Oct; 94():311.e1-311.e4. PubMed ID: 32507414
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of sixteen novel candidate genes for late onset Parkinson's disease.
    Gialluisi A; Reccia MG; Modugno N; Nutile T; Lombardi A; Di Giovannantonio LG; Pietracupa S; Ruggiero D; Scala S; Gambardella S; ; Iacoviello L; Gianfrancesco F; Acampora D; D'Esposito M; Simeone A; Ciullo M; Esposito T
    Mol Neurodegener; 2021 Jun; 16(1):35. PubMed ID: 34148545
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Whole-Exome Sequencing Study of Consanguineous Parkinson's Disease Families and Related Phenotypes: Report of Twelve Novel Variants.
    Soudyab M; Shariati M; Esfehani RJ; Shalaei N; Vafadar S; Nouri V; Zech M; Winkelmann J; Shoeibi A; Sadr-Nabavi A
    J Mol Neurosci; 2022 Dec; 72(12):2486-2496. PubMed ID: 36520381
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Rare missense variants in the PPP2R5D gene associated with Parkinson's disease in the Han Chinese population.
    Ning P; Li K; Ren H; Yang H; Xu Y; Yang X
    Neurosci Lett; 2022 Apr; 776():136564. PubMed ID: 35257824
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutation analysis of PARK2 in a Uyghur family with early-onset Parkinson's disease in Xinjiang, China.
    Li H; Yusufujiang A; Naser S; Zhu Y; Maimaiti M; He X; Bu J; Meng X; Wang M; Li J; Dina B; Yang L; Nayi Z; Dang H; Wang C; Amiti D; Aji A; Yusufu N; Jiao Y; Duan F
    J Neurol Sci; 2014 Jul; 342(1-2):21-4. PubMed ID: 24831986
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Association of three candidate genetic variants in ACMSD/TMEM163, GPNMB and BCKDK /STX1B with sporadic Parkinson's disease in Han Chinese.
    Wang L; Li NN; Lu ZJ; Li JY; Peng JX; Duan LR; Peng R
    Neurosci Lett; 2019 Jun; 703():45-48. PubMed ID: 30880162
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 22.