BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

78 related articles for article (PubMed ID: 932535)

  • 1. Chromosomal breakage and scleroderma: studies in family members.
    Emerit I; Housset E; Feingold J
    J Lab Clin Med; 1976 Jul; 88(1):81-6. PubMed ID: 932535
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Chromosomal alterations in scleroderma.
    Constantin M; Leucuţia M; Purice S
    Med Interne; 1987; 25(4):245-9. PubMed ID: 3423700
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Spontaneous and clastogen induced chromosomal breakage in scleroderma.
    Wolff DJ; Needleman BW; Wasserman SS; Schwartz S
    J Rheumatol; 1991 Jun; 18(6):837-40. PubMed ID: 1716681
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Chromosome changes in lymphocytes of patients with scleroderma.
    Casalone R; Granata P; Minelli E; Righi R; Meroni E; Mazzola D; Sammarelli G; Baratelli E; Broggini M
    Ann Genet; 1995; 38(3):145-50. PubMed ID: 8540685
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Chromosome studies in scleroderma with consideration of anticentromere antibody status and assessment of possible in vitro clastogenic activity.
    Powell FC; Schroeter AL; Winkelmann RK; Dewald GW
    Acta Derm Venereol; 1986; 66(5):414-8. PubMed ID: 2431579
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Cytogenetic findings in acute myelogenous leukemias (FAB M 1 to M 6)].
    Prösch U; Stobbe H
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1985; 112(4):481-94. PubMed ID: 2414178
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Familial scleroderma with Sjogren's syndrome and lymphocyte and chromosome abnormalities].
    Camus JP; Emerit I; Reinert P; Guillien P; Crouzet J; Fourot J
    Ann Med Interne (Paris); 1970 Feb; 121(2):149-61. PubMed ID: 5491196
    [No Abstract]   [Full Text] [Related]  

  • 8. [Chromosome abnormalities in systemic scleroderma].
    Emerit I; Camus JP
    Rev Rhum Mal Osteoartic; 1972 Nov; 39(11):731-4. PubMed ID: 4654971
    [No Abstract]   [Full Text] [Related]  

  • 9. [Generalized scleroderma and chromosome breakage. Demonstration of a breaking factor in patients serum].
    Emerit I; Levy A; Housset E
    Ann Genet; 1973 Jun; 16(2):135-8. PubMed ID: 4541907
    [No Abstract]   [Full Text] [Related]  

  • 10. Spontaneous chromosome damage (micronuclei) in systemic sclerosis and Raynaud's phenomenon.
    Porciello G; Scarpato R; Ferri C; Storino F; Cagetti F; Morozzi G; Bellisai F; Migliore L; Marcolongo R; Galeazzi M
    J Rheumatol; 2003 Jun; 30(6):1244-7. PubMed ID: 12784397
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Chromosomal breakage in systemic sclerosis and related disorders.
    Emerit I
    Dermatologica; 1976; 153(3):145-56. PubMed ID: 14037
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Chromosomal breakage in diffuse scleroderma. A study of 27 patients.
    Emerit I; Housset E; de Grouchy J; Camus JP
    Rev Eur Etud Clin Biol; 1971; 16(7):684-94. PubMed ID: 5125548
    [No Abstract]   [Full Text] [Related]  

  • 13. Chromosome instability in human and murine autoimmune disease: anticlastogenic effect of superoxide dismutase.
    Emerit I; Michelson AM
    Acta Physiol Scand Suppl; 1980; 492():59-65. PubMed ID: 6939306
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A cytogenetic analysis of twenty cases of systemic scleroderma.
    Romani F; Viguie F; Siffroi JP; Fiessenger JN
    Ann Genet; 1986; 29(4):240-5. PubMed ID: 3495226
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Family studies in scleroderma (systemic sclerosis) demonstrating an HLA-linked increased chromosomal breakage rate in cultured lymphocytes.
    Rittner G; Schwanitz G; Baur MP; Black CM; Welsh KI; Kühnl P; Rittner C
    Hum Genet; 1988 Dec; 81(1):64-70. PubMed ID: 3198128
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Deficient DNA repair capacity: a predisposing factor and high risk predictive marker in familial colorectal cancer.
    Ankathil R; Jyothish B; Madhavan J; Nair MK
    J Exp Clin Cancer Res; 1999 Mar; 18(1):33-7. PubMed ID: 10374674
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Chromosome aberrations in Raynaud's phenomenon.
    Porciello G; Scarpato R; Storino F; Migliore L; Ferri C; Cagetti F; Morozzi G; Bellisai F; Marcolongo R; Galeazzi M
    Eur J Dermatol; 2004; 14(5):327-31. PubMed ID: 15358572
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Analysis of naturally occurring and radiation-induced breakpoint locations in human chromosomes 1, 2 and 4.
    Tucker JD; Senft JR
    Radiat Res; 1994 Oct; 140(1):31-6. PubMed ID: 7938452
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prevalence of anticentromere antibody in blood relatives of anticentromere positive patients.
    Ruffatti A; Artifoni L; Glorioso S; Calligaro A; Doria A; Gambari P; Todesco S
    J Rheumatol; 1985 Oct; 12(5):940-3. PubMed ID: 3878881
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Chromosomal aberrations in peripheral blood lymphocytes from patients with dermatomyositis and their first-degree relatives.
    Severin E
    Rom J Morphol Embryol; 1995; 41(1-2):49-53. PubMed ID: 8680025
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.