BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

106 related articles for article (PubMed ID: 11112389)

  • 1. A new exon 9 glucose-6-phosphate dehydrogenase mutation (G6PD "Rehovot") in a Jewish Ethiopian family with variable phenotypes.
    Iancovici-Kidon M; Sthoeger D; Abrahamov A; Wolach B; Beutler E; Gelbart T; Barak Y
    Blood Cells Mol Dis; 2000 Dec; 26(6):567-71. PubMed ID: 11112389
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Three new exon 10 glucose-6-phosphate dehydrogenase mutations.
    Beutler E; Westwood B; Melemed A; Dal Borgo P; Margolis D
    Blood Cells Mol Dis; 1995; 21(1):64-72. PubMed ID: 7655862
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Chronic nonspherocytic hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency: report of two families with novel mutations causing G6PD Bangkok and G6PD Bangkok Noi.
    Tanphaichitr VS; Hirono A; Pung-amritt P; Treesucon A; Wanachiwanawin W
    Ann Hematol; 2011 Jul; 90(7):769-75. PubMed ID: 21302115
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Several mutations including two novel mutations of the glucose-6-phosphate dehydrogenase gene in Polish G6PD deficient subjects with chronic nonspherocytic hemolytic anemia, acute hemolytic anemia, and favism.
    Jablonska-Skwiecinska E; Lewandowska I; Plochocka D; Topczewski J; Zimowski JG; Klopocka J; Burzynska B
    Hum Mutat; 1999; 14(6):477-84. PubMed ID: 10571945
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prevalence of beta-thalassemia trait and glucose-6-phosphate dehydrogenase deficiency in Iranian Jews.
    Karimi M; Yavarian M; Afrasiabi A; Dehbozorgian J; Rachmilewitz E
    Arch Med Res; 2008 Feb; 39(2):212-4. PubMed ID: 18164966
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Two new glucose-6-phosphate dehydrogenase mutations causing chronic hemolysis.
    Manco L; Gonçalves P; Macedo-Ribeiro S; Seabra C; Melo P; Ribeiro ML
    Haematologica; 2005 Aug; 90(8):1135-6. PubMed ID: 16079115
    [TBL] [Abstract][Full Text] [Related]  

  • 7. G6PD sumaré: a novel mutation in the G6PD gene (1292 T-->G) associated with chronic nonspherocytic anemia.
    Saad ST; Salles TS; Arruda VR; Sonati MF; Costa FF
    Hum Mutat; 1997; 10(3):245-7. PubMed ID: 9298828
    [No Abstract]   [Full Text] [Related]  

  • 8. G6PD deficiency with hemolytic anemia due to a rare gene deletion--a report of the first case in Malaysia.
    Ainoon O; Boo NY; Yu YH; Cheong SK; Hamidah HN
    Hematology; 2006 Apr; 11(2):113-8. PubMed ID: 16753852
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Glucosephosphate isomerase (GPI) deficiency mutations associated with hereditary nonspherocytic hemolytic anemia (HNSHA).
    Beutler E; West C; Britton HA; Harris J; Forman L
    Blood Cells Mol Dis; 1997 Dec; 23(3):402-9. PubMed ID: 9446754
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [The C1155G mutation of the red blood cell glucose-6-phosphate dehydrogenase gene in a subject with severe hereditary chronic nonspherocytic anaemia].
    Burzyńska B; Adamowicz-Salach A; Płochocka D; Gołaszewska E; Witos I
    Med Wieku Rozwoj; 2009; 13(2):136-9. PubMed ID: 19837994
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Complex mutations of 1311 C-->T in exon 11 and 93 T-->C in intron 11 in G6PD gene].
    Yu GL; Jiang WY; Du CS; Lin QD; Chen LM; Tian QH; Li SG; Zeng JB
    Zhonghua Xue Ye Xue Za Zhi; 2004 Oct; 25(10):610-2. PubMed ID: 15634595
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Glucose-6-phosphate dehydrogenase Guadalajara--a case of chronic non-spherocytic haemolytic anaemia responding to splenectomy and the role of splenectomy in this disorder.
    Hamilton JW; Jones FG; McMullin MF
    Hematology; 2004 Aug; 9(4):307-9. PubMed ID: 15621740
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel missense mutation in glucose-6-phosphate dehydrogenase gene causing chronic nonspherocytic hemolytic anemia in an Indian family.
    Edison ES; Melinkeri SR; Chandy M
    Ann Hematol; 2006 Dec; 85(12):879-80. PubMed ID: 16944148
    [No Abstract]   [Full Text] [Related]  

  • 14. Glucose-6-phosphate dehydrogenase Buenos Aires: a novel de novo missense mutation associated with severe enzyme deficiency.
    Minucci A; Concolino P; Vendittelli F; Giardina B; Zuppi C; Capoluongo E
    Clin Biochem; 2008 Jun; 41(9):742-5. PubMed ID: 18086567
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Linkage analysis of the G6PD gene mutations and its Nla III polymorphic site].
    Xie J; Long G; Tang X
    Zhonghua Xue Ye Xue Za Zhi; 2000 Apr; 21(4):187-9. PubMed ID: 11876978
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Association of glucose-6-phosphate dehydrogenase deficiency and X-linked chronic granulomatous disease in a child with anemia and recurrent infections.
    Agudelo-Flórez P; Costa-Carvalho BT; López JA; Redher J; Newburger PE; Olalla-Saad ST; Condino-Neto A
    Am J Hematol; 2004 Mar; 75(3):151-6. PubMed ID: 14978696
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Glucose-6-phosphate dehydrogenase aveiro: a de novo mutation associated with chronic nonspherocytic hemolytic anemia.
    Costa E; Cabeda JM; Vieira E; Pinto R; Pereira SA; Ferraz L; Santos R; Barbot J
    Blood; 2000 Feb; 95(4):1499-501. PubMed ID: 10666231
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Two new variants of glucose-6-phosphate dehydrogenase associated with hereditary non-spherocytic hemolytic anemia: G6PD Wayne and G6PD Huron.
    Ravindranath Y; Beutler E
    Am J Hematol; 1987 Apr; 24(4):357-63. PubMed ID: 3565372
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Marked decrease in specific activity contributes to disease phenotype in two human glucose 6-phosphate dehydrogenase mutants, G6PD(Union) and G6PD(Andalus).
    Wang XT; Lam VM; Engel PC
    Hum Mutat; 2005 Sep; 26(3):284. PubMed ID: 16088936
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in the Han and Li nationalities in Hainan, China and identification of a new mutation in human G6PD gene].
    Cai W; Filosa S; Martini G; Zhou Y; Zhou D; Cai L; Kuang Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Apr; 18(2):105-9. PubMed ID: 11295127
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.