BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

121 related articles for article (PubMed ID: 1323345)

  • 1. Molecular characterization of glucose-6-phosphate dehydrogenase (G6PD) deficiency by natural and amplification created restriction sites: five mutations account for most G6PD deficiency cases in Taiwan.
    Chang JG; Chiou SS; Perng LI; Chen TC; Liu TC; Lee LS; Chen PH; Tang TK
    Blood; 1992 Aug; 80(4):1079-82. PubMed ID: 1323345
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Diagnosis of glucose-6-phosphate dehydrogenase (G6PD) mutations by DNA amplification and allele-specific oligonucleotide probes.
    Huang CS; Tang CJ; Huang MJ; Tang TK
    Acta Haematol; 1992; 88(2-3):92-5. PubMed ID: 1466205
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Neonatal jaundice and molecular mutations in glucose-6-phosphate dehydrogenase deficient newborn infants.
    Huang CS; Hung KL; Huang MJ; Li YC; Liu TH; Tang TK
    Am J Hematol; 1996 Jan; 51(1):19-25. PubMed ID: 8571933
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular characterisation of red cell glucose-6-phosphate dehydrogenase deficiency in Singapore Chinese.
    Saha S; Saha N; Tay JS; Jeyaseelan K; Basair JB; Chew SE
    Am J Hematol; 1994 Dec; 47(4):273-7. PubMed ID: 7977299
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Diverse point mutations result in glucose-6-phosphate dehydrogenase (G6PD) polymorphism in Taiwan.
    Tang TK; Huang CS; Huang MJ; Tam KB; Yeh CH; Tang CJ
    Blood; 1992 Apr; 79(8):2135-40. PubMed ID: 1562739
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Two novel glucose 6-phosphate dehydrogenase deficiency mutations and association of such mutations with F8C/G6PD haplotype in Chinese.
    Chen HL; Huang MJ; Huang CS; Tang TK
    J Formos Med Assoc; 1997 Dec; 96(12):948-54. PubMed ID: 9444913
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in Chinese infants with or without severe neonatal hyperbilirubinaemia.
    Lo YS; Lu CC; Chiou SS; Chen BH; Chang TT; Chang JG
    Br J Haematol; 1994 Apr; 86(4):858-62. PubMed ID: 7918083
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular characterization of Chinese G6PD deficiency by using polymerase chain reaction/single strand conformation polymorphism.
    Chen BH; Lin SR; Chiang CH; Chao MC
    Kaohsiung J Med Sci; 1998 Apr; 14(4):197-202. PubMed ID: 9589612
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular characterisation of red cell glucose-6-phosphate dehydrogenase deficiency in north-west Pakistan.
    Saha N; Ramzan M; Tay JS; Low PS; Basair JB; Khan FM
    Hum Hered; 1994; 44(2):85-9. PubMed ID: 8188314
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular characterization of glucose-6-phosphate dehydrogenase (G6PD) deficiency in patients of Chinese descent and identification of new base substitutions in the human G6PD gene.
    Chiu DT; Zuo L; Chao L; Chen E; Louie E; Lubin B; Liu TZ; Du CS
    Blood; 1993 Apr; 81(8):2150-4. PubMed ID: 8471773
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular basis of glucose-6-phosphate dehydrogenase (G6PD) deficiency in three Taiwan aboriginal tribes.
    Tang TK; Huang WY; Tang CJ; Hsu M; Cheng TA; Chen KH
    Hum Genet; 1995 Jun; 95(6):630-2. PubMed ID: 7789945
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Detection of the most common G6PD gene mutations in Chinese using amplification refractory mutation system.
    Du CS; Ren X; Chen L; Jiang W; He Y; Yang M
    Hum Hered; 1999 Jun; 49(3):133-8. PubMed ID: 10364676
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Identification of molecular variants of the enzyme glucose-6-phosphate dehydrogenase by the polymerase chain reaction technique].
    Rovira A; Vives Corrons JL; Estrada M; GutiƩrrez A; Pujades MA; Colomer D; Corbella M; Aymerich M
    Med Clin (Barc); 1994 Mar; 102(8):281-4. PubMed ID: 8170224
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Nucleotide 1376 G-->T mutation in G6PD-deficient Chinese in Malaysia.
    Ainoon O; Joyce J; Boo NY; Cheong SK; Hamidah NH
    Malays J Pathol; 1995 Dec; 17(2):61-5. PubMed ID: 8935127
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Definition of the mutations of G6PD Wayne, G6PD Viangchan, G6PD Jammu, and G6PD 'LeJeune'.
    Beutler E; Westwood B; Kuhl W
    Acta Haematol; 1991; 86(4):179-82. PubMed ID: 1805484
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Glucose-6-phosphate dehydrogenase deficiency in Portugal: biochemical and mutational profiles, heterogeneity, and haplotype association.
    Rodrigues MO; Freire AP; Martins G; Pereira J; Martins MD; Monteiro C
    Blood Cells Mol Dis; 2002; 28(2):249-59. PubMed ID: 12064920
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in Pakistani population.
    Moiz B; Nasir A; Moatter T; Naqvi ZA; Khurshid M
    Int J Lab Hematol; 2011 Dec; 33(6):570-8. PubMed ID: 21507207
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in Brazil.
    Saad ST; Salles TS; Carvalho MH; Costa FF
    Hum Hered; 1997; 47(1):17-21. PubMed ID: 9017974
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular variants of red cell glucose-6-phosphate dehydrogenase deficiency in Central Java, Indonesia.
    Soemantri AG; Saha S; Saha N; Tay JS
    Hum Hered; 1995; 45(6):346-50. PubMed ID: 8537082
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Rapid diagnosis of beta-thalassemia mutations in Chinese by naturally and amplified created restriction sites.
    Chang JG; Chen PH; Chiou SS; Lee LS; Perng LI; Liu TC
    Blood; 1992 Oct; 80(8):2092-6. PubMed ID: 1391961
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.