BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

100 related articles for article (PubMed ID: 32253809)

  • 1. Comment on: "Investigation of intermediate CAG alleles of the HTT in the general population of Rio de Janeiro, Brazil, in comparison with a sample of Huntington disease-affected families.".
    Franklin GL; Meira AT; Camargo CHF; Teive HAG
    Mol Genet Genomic Med; 2020 Jun; 8(6):e1243. PubMed ID: 32253809
    [No Abstract]   [Full Text] [Related]  

  • 2. Investigation of intermediate CAG alleles of the HTT in the general population of Rio de Janeiro, Brazil, in comparison with a sample of Huntington disease-affected families.
    Apolinário TA; da Silva IDS; Agostinho LA; Paiva CLA
    Mol Genet Genomic Med; 2020 Apr; 8(4):e1181. PubMed ID: 32067426
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Huntington disease and Huntington disease-like in a case series from Brazil.
    Castilhos RM; Souza AF; Furtado GV; Gheno TC; Silva AL; Vargas FR; Lima MA; Barsottini O; Pedroso JL; Godeiro C; Salarini D; Pereira ET; Lin K; Toralles MB; Saute JA; Rieder CR; Quintas M; Sequeiros J; Alonso I; Saraiva-Pereira ML; Jardim LB
    Clin Genet; 2014 Oct; 86(4):373-7. PubMed ID: 24102565
    [TBL] [Abstract][Full Text] [Related]  

  • 4. REVIEW-ARTICLE Intermediate alleles of Huntington's disease HTT gene in different populations worldwide: a systematic review.
    Apolinário TA; Paiva CL; Agostinho LA
    Genet Mol Res; 2017 Apr; 16(2):. PubMed ID: 28387881
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A new mutation for Huntington disease following maternal transmission of an intermediate allele.
    Semaka A; Kay C; Belfroid RD; Bijlsma EK; Losekoot M; van Langen IM; van Maarle MC; Oosterloo M; Hayden MR; van Belzen MJ
    Eur J Med Genet; 2015 Jan; 58(1):28-30. PubMed ID: 25464109
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The CAG repeat at the Huntington disease gene in the Portuguese population: insights into its dynamics and to the origin of the mutation.
    Costa MDC; Magalhães P; Guimarães L; Maciel P; Sequeiros J; Sousa A
    J Hum Genet; 2006; 51(3):189-195. PubMed ID: 16372132
    [TBL] [Abstract][Full Text] [Related]  

  • 7. CAG size-specific risk estimates for intermediate allele repeat instability in Huntington disease.
    Semaka A; Kay C; Doty C; Collins JA; Bijlsma EK; Richards F; Goldberg YP; Hayden MR
    J Med Genet; 2013 Oct; 50(10):696-703. PubMed ID: 23896435
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Enhanced Detection and Sizing of the HTT CAG Repeat Expansion in Huntington Disease Using an Improved Triplet-Primed PCR Assay.
    Zhao M; Lee CG; Law HY; Chong SS
    Neurodegener Dis; 2016; 16(5-6):348-51. PubMed ID: 27207688
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Predictive testing for Huntington disease: interpretation and significance of intermediate alleles.
    Semaka A; Creighton S; Warby S; Hayden MR
    Clin Genet; 2006 Oct; 70(4):283-94. PubMed ID: 16965319
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic features of Huntington disease in Cuban population: implications for phenotype, epidemiology and predictive testing.
    Vázquez-Mojena Y; Laguna-Salvia L; Laffita-Mesa JM; González-Zaldívar Y; Almaguer-Mederos LE; Rodríguez-Labrada R; Almaguer-Gotay D; Zayas-Feria P; Velázquez-Pérez L
    J Neurol Sci; 2013 Dec; 335(1-2):101-4. PubMed ID: 24054538
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular diagnosis of Huntington disease in Brazilian patients.
    Lima E Silva TC; Serra HG; Bertuzzo CS; Lopes-Cendes I
    Arq Neuropsiquiatr; 2000 Mar; 58(1):11-7. PubMed ID: 10770860
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Contribution of DNA sequence and CAG size to mutation frequencies of intermediate alleles for Huntington disease: evidence from single sperm analyses.
    Chong SS; Almqvist E; Telenius H; LaTray L; Nichol K; Bourdelat-Parks B; Goldberg YP; Haddad BR; Richards F; Sillence D; Greenberg CR; Ives E; Van den Engh G; Hughes MR; Hayden MR
    Hum Mol Genet; 1997 Feb; 6(2):301-9. PubMed ID: 9063751
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Huntington disease reduced penetrance alleles occur at high frequency in the general population.
    Kay C; Collins JA; Miedzybrodzka Z; Madore SJ; Gordon ES; Gerry N; Davidson M; Slama RA; Hayden MR
    Neurology; 2016 Jul; 87(3):282-8. PubMed ID: 27335115
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Increased instability of intermediate alleles in families with sporadic Huntington disease compared to similar sized intermediate alleles in the general population.
    Goldberg YP; McMurray CT; Zeisler J; Almqvist E; Sillence D; Richards F; Gacy AM; Buchanan J; Telenius H; Hayden MR
    Hum Mol Genet; 1995 Oct; 4(10):1911-8. PubMed ID: 8595415
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical phenotype in carriers of intermediate alleles in the huntingtin gene.
    Savitt D; Jankovic J
    J Neurol Sci; 2019 Jul; 402():57-61. PubMed ID: 31103960
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Allelic frequency distribution for three VNTR markers--D6S132, D7S467, D17S26--in Rio de Janeiro population, Brazil.
    Silva R; Moura-Neto RS
    Forensic Sci Int; 1998 Jun; 94(1-2):33-8. PubMed ID: 9670481
    [TBL] [Abstract][Full Text] [Related]  

  • 17. HTT gene intermediate alleles in neurodegeneration: evidence for association with Alzheimer's disease.
    Menéndez-González M; Clarimón J; Rosas-Allende I; Blázquez M; San Martín ES; García-Fernández C; Lleó A; Dols-Icardo O; Illán-Gala I; Morís G; Ribacoba R; Álvarez V; Martínez C
    Neurobiol Aging; 2019 Apr; 76():215.e9-215.e14. PubMed ID: 30583877
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Haplotype analysis of the CAG and CCG repeats in 21 Brazilian families with Huntington's disease.
    Agostinho Lde A; Rocha CF; Medina-Acosta E; Barboza HN; da Silva AF; Pereira SP; da Silva Idos S; Paradela ER; Figueiredo AL; Nogueira Ede M; Alvarenga RM; Hernan Cabello P; dos Santos SR; Paiva CL
    J Hum Genet; 2012 Dec; 57(12):796-803. PubMed ID: 23051704
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Large normal and reduced penetrance alleles in Huntington disease: instability in families and frequency at the laboratory, at the clinic and in the population.
    Sequeiros J; Ramos EM; Cerqueira J; Costa MC; Sousa A; Pinto-Basto J; Alonso I
    Clin Genet; 2010 Oct; 78(4):381-7. PubMed ID: 20236117
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic polymorphism of MJD1 alleles and molecular analysis of SCA3 patients from Rio de Janeiro, Brazil.
    Gestinari RS; Duarte SF; Pimentel MM; Lima MA
    Genet Test; 2004; 8(3):281-5. PubMed ID: 15727252
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.