These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

138 related articles for article (PubMed ID: 26016408)

  • 1. Evaluation of PARKIN gene variants in West Bengal Parkinson's disease patients.
    Sanyal J; Jana A; Ghosh E; Banerjee TK; Chakraborty DP; Rao VR
    J Hum Genet; 2015 Sep; 60(9):485-92. PubMed ID: 26016408
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular pathogenesis of Parkinson's disease: identification of mutations in the Parkin gene in Indian patients.
    Biswas A; Gupta A; Naiya T; Das G; Neogi R; Datta S; Mukherjee S; Das SK; Ray K; Ray J
    Parkinsonism Relat Disord; 2006 Oct; 12(7):420-6. PubMed ID: 16793319
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prevalence of parkin gene mutations and variations in idiopathic Parkinson's disease.
    Sinha R; Racette B; Perlmutter JS; Parsian A
    Parkinsonism Relat Disord; 2005 Sep; 11(6):341-7. PubMed ID: 16019250
    [TBL] [Abstract][Full Text] [Related]  

  • 4. PARKIN-coding polymorphisms are not associated with Parkinson's disease in a population from northeastern Mexico.
    Martínez HR; González-González H; Cantú-Martínez L; Rangel-Guerra R; Hernández-Castillo CD; Vergara-Saavedra JJ; Ramos-Gonzalez MR; Cerda-Flores RM; Morales-Garza MA; Guerrero-Muñoz MJ; Montes-de-Oca-Luna R; Saucedo-Cárdenas O
    Neurosci Lett; 2010 Jan; 468(3):264-6. PubMed ID: 19909784
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Coding polymorphisms in the parkin gene and susceptibility to Parkinson disease.
    Lücking CB; Chesneau V; Lohmann E; Verpillat P; Dulac C; Bonnet AM; Gasparini F; Agid Y; Dürr A; Brice A
    Arch Neurol; 2003 Sep; 60(9):1253-6. PubMed ID: 12975291
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutation screening and association analysis of the parkin gene in Parkinson's disease patients from South-West China.
    Peng R; Gou Y; Yuan Q; Li T; Latsoudis H; Yuan G; Luo D; Liu X; Collier DA
    Eur Neurol; 2003; 49(2):85-9. PubMed ID: 12584415
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Heterozygous parkin point mutations are as common in control subjects as in Parkinson's patients.
    Kay DM; Moran D; Moses L; Poorkaj P; Zabetian CP; Nutt J; Factor SA; Yu CE; Montimurro JS; Keefe RG; Schellenberg GD; Payami H
    Ann Neurol; 2007 Jan; 61(1):47-54. PubMed ID: 17187375
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Evaluating intra-genetic variants of DJ-1 among Parkinson's disease patients of eastern India.
    Sanyal J; Sarkar B; Banerjee TK; Mukherjee SC; Ray BC; Raghavendra Rao V
    Neurol Res; 2011 May; 33(4):349-53. PubMed ID: 21535932
    [TBL] [Abstract][Full Text] [Related]  

  • 9. PARK2 and PARK7 Gene Polymorphisms as Risk Factors Associated with Serum Element Concentrations and Clinical Symptoms of Parkinson's Disease.
    Sanyal J; Anirudhan A; Banerjee TK; Guha G; Ramakrishnan Veerabathiran ; Murugesan R; Ahmed SSJS; Rao VR
    Cell Mol Neurobiol; 2020 Apr; 40(3):357-367. PubMed ID: 31512170
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutational screening of the parkin gene among South Indians with early onset Parkinson's disease.
    Madegowda RH; Kishore A; Anand A
    J Neurol Neurosurg Psychiatry; 2005 Nov; 76(11):1588-90. PubMed ID: 16227559
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Parkin polymorphisms and environmental exposure: decrease in age at onset of Parkinson's disease.
    Ghione I; Di Fonzo A; Saladino F; Del Bo R; Bresolin N; Comi GP; Rango M
    Neurotoxicology; 2007 May; 28(3):698-701. PubMed ID: 17335904
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Case-control study of the parkin gene in early-onset Parkinson disease.
    Clark LN; Afridi S; Karlins E; Wang Y; Mejia-Santana H; Harris J; Louis ED; Cote LJ; Andrews H; Fahn S; Waters C; Ford B; Frucht S; Ottman R; Marder K
    Arch Neurol; 2006 Apr; 63(4):548-52. PubMed ID: 16606767
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Parkin mutations in familial and sporadic Parkinson's disease among Indians.
    Chaudhary S; Behari M; Dihana M; Swaminath PV; Govindappa ST; Jayaram S; Goyal V; Maitra A; Muthane UB; Juyal RC; Thelma BK
    Parkinsonism Relat Disord; 2006 May; 12(4):239-45. PubMed ID: 16500134
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Parkin variants in North American Parkinson's disease: cases and controls.
    Lincoln SJ; Maraganore DM; Lesnick TG; Bounds R; de Andrade M; Bower JH; Hardy JA; Farrer MJ
    Mov Disord; 2003 Nov; 18(11):1306-11. PubMed ID: 14639672
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular analysis of the parkin gene in South African patients diagnosed with Parkinson's disease.
    Bardien S; Keyser R; Yako Y; Lombard D; Carr J
    Parkinsonism Relat Disord; 2009 Feb; 15(2):116-21. PubMed ID: 18514563
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Parkin polymorphisms: risk for Parkinson's disease in Indian population.
    Biswas A; Maulik M; Das SK; ; Ray K; Ray J
    Clin Genet; 2007 Nov; 72(5):484-6. PubMed ID: 17935510
    [No Abstract]   [Full Text] [Related]  

  • 17. Mutations in the parkin gene are a minor cause of Parkinson's disease in the South African population.
    Haylett WL; Keyser RJ; du Plessis MC; van der Merwe C; Blanckenberg J; Lombard D; Carr J; Bardien S
    Parkinsonism Relat Disord; 2012 Jan; 18(1):89-92. PubMed ID: 21996382
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Association study of Parkin gene polymorphisms with idiopathic Parkinson disease.
    Oliveira SA; Scott WK; Nance MA; Watts RL; Hubble JP; Koller WC; Lyons KE; Pahwa R; Stern MB; Hiner BC; Jankovic J; Ondo WG; Allen FH; Scott BL; Goetz CG; Small GW; Mastaglia FL; Stajich JM; Zhang F; Booze MW; Reaves JA; Middleton LT; Haines JL; Pericak-Vance MA; Vance JM; Martin ER
    Arch Neurol; 2003 Jul; 60(7):975-80. PubMed ID: 12873854
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Etiology and pathogenesis of Parkinson's disease: from mitochondrial dysfunctions to familial Parkinson's disease].
    Hattori N
    Rinsho Shinkeigaku; 2004; 44(4-5):241-62. PubMed ID: 15287506
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Evaluation of PINK1 variants in Indian Parkinson's disease patients.
    Biswas A; Sadhukhan T; Majumder S; Misra AK; Das SK; Variation Consortium IG; Ray K; Ray J
    Parkinsonism Relat Disord; 2010 Mar; 16(3):167-71. PubMed ID: 19889566
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.