BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

99 related articles for article (PubMed ID: 302667)

  • 1. [Possible localization of the glutathione reductase (EC 1.6.4.2) on the 8p21 band].
    Sinet PM; Bresson JL; Couturier J; Laurent C; Prieur M; Rethoré MO; Taillemite JL; Toudic D; Jérome H; Lejeune J
    Ann Genet; 1977 Mar; 20(1):13-7. PubMed ID: 302667
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mapping of the gene for glutathione reductase on chromosome 8.
    de la Chapelle A; Icen A; Aula P; Leisti J; Turleau C; de Grouchy J
    Ann Genet; 1976 Dec; 19(4):253-6. PubMed ID: 1087855
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The red cell glutathione reductase in trisomy of the chromosome 8.
    Jabłońska-Skwiecińska E; Rogoỳski A; Babel M; Tronowska TD
    Biomed Biochim Acta; 1984; 43(6):S101-2. PubMed ID: 6487283
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Inverted tandem ("mirror") duplications in human chromosomes: -nv dup 8p, 4q, 22q.
    Taylor KM; Francke U; Brown MG; George DL; Kaufhold M
    Am J Med Genet; 1977; 1(1):3-19. PubMed ID: 610424
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Inverted tandem duplication of the short arm of chromosome 8: a non-random de novo structural aberration in man. Localization of the gene for glutathione reductase in subband 8p21.1.
    Jensen PK; Junien C; Despoisse S; Bernsen A; Thelle T; Friedrich U; de la Chapelle A
    Ann Genet; 1982; 25(4):207-11. PubMed ID: 6985008
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Duplication 2p and monosomy 8p in mosaicism: clinical, molecular cytogenetic and molecular markers of a unique case.
    Martínez A; Ramos S; González-del Angel A; Alcántara MA; Molina B; Carnevale A
    Rev Invest Clin; 2007; 59(6):444-8. PubMed ID: 18402336
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Deficiency of chromosome 8p21.1----8pter: case report and review of the literature.
    Dobyns WB; Dewald GW; Carlson RO; Mair DD; Michels VV
    Am J Med Genet; 1985 Sep; 22(1):125-34. PubMed ID: 3901750
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Red cell glutathione reductase activity in patients with bone-marrow trisomy 8.
    De la Chapelle A; Vuopio P; Icén A
    Birth Defects Orig Artic Ser; 1976; 12(7):277-9. PubMed ID: 1024625
    [No Abstract]   [Full Text] [Related]  

  • 9. Evidence of gene dosage effect for HK 1 in the red cells of a patient with trisomy 10pter leads to p13.
    Dallapiccola B; Serena Lungarotti M; Magnani M; Dacha M
    Ann Genet; 1981; 24(1):45-7. PubMed ID: 6971618
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Duplication 8p syndrome: studies in a family with a reciprocal translocation between chromosomes 8 and 12.
    Moreno Fuenmayor HM; Meilinger KL; Rucknagel DL; Mohrenweiser HL; Chu EH
    Am J Med Genet; 1980; 7(3):361-8. PubMed ID: 7468661
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Enzyme activity of red blood cells in a child with chromosome 8 trisomy].
    Rogóyski A; Jabłońska-Skwiecińska E; Tronowska TD
    Pediatr Pol; 1982; 57(10):799-801. PubMed ID: 7182765
    [No Abstract]   [Full Text] [Related]  

  • 12. Glutathione, glutathione S-transferase and glutathione reductase in human erythrocytes and lymphocytes as a function of sex.
    al-Turk WA; Stohs SJ; el-Rashidy FH; Othman S; Shaheen O
    Drug Des Deliv; 1987 Feb; 1(3):237-43. PubMed ID: 3509337
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Interstitial deletion 8p21.3----p23.1 in a 6-year-old girl.
    Morrison PJ; Jones J; Nevin NC
    Am J Med Genet; 1992 Mar; 42(5):678-80. PubMed ID: 1632437
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Trisomy 7p due to a mosaic normal/dir dup(7)(p13----p22). Syndrome delineation, critical segment assignment, and a comment on duplications.
    Cantú JM; Rivas F; Ruiz C; Barajas LO; Moller M; Rivera H
    Ann Genet; 1985; 28(4):254-7. PubMed ID: 3879442
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Trisomy 8 in the bone marrow associated with high red cell glutathione reductase activity.
    de la Chapelle A; Vuopio P; Icén A
    Blood; 1976 May; 47(5):815-26. PubMed ID: 1063047
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Localization of the gene of the glyceraldehyde 3 phosphate dehydrogenase on the distal segment of the short arm of the chromosome 12].
    Rethoré MO; Junien C; Malpuech G; Baccichetti C; Tenconi R; Kaplan JC; de Romeuf J; Lejeune J
    Ann Genet; 1976 Jun; 19(2):140-2. PubMed ID: 1085604
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Effect of gene dose in human cells].
    Annenkov GA
    Tsitol Genet; 1978; 12(4):362-70. PubMed ID: 151956
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Deletion of the long arm of chromosome 8 resulting from a de novo translocation t(4;8) (q13;q213).
    Dallapiccola B; Santoro L; Trabace S; Ramenghi M; Mastroiacovo P; Gandini E
    Hum Genet; 1977 Sep; 38(2):125-30. PubMed ID: 908558
    [TBL] [Abstract][Full Text] [Related]  

  • 19. t(15;21)(q15;q22.1) pat resulting in partial trisomy and partial monosomy of chromosomes 15 and 21 in two offspring.
    Abeliovich D; Dagan J; Lerer I; Silberstein S; Katznelson MB; Frydman M
    Am J Med Genet; 1996 Dec; 66(1):45-51. PubMed ID: 8957510
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Red cell glutathione reductase activity in patients with bone-marrow trisomy 8.
    De La Chapelle A; Vuopio P; Icén A
    Cytogenet Cell Genet; 1976; 16(1-5):277-9. PubMed ID: 975890
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.