These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

94 related articles for article (PubMed ID: 8499925)

  • 1. DNA sequence abnormalities in human glucose 6-phosphate isomerase deficiency.
    Walker JI; Layton DM; Bellingham AJ; Morgan MJ; Faik P
    Hum Mol Genet; 1993 Mar; 2(3):327-9. PubMed ID: 8499925
    [No Abstract]   [Full Text] [Related]  

  • 2. Molecular characterization of glucose-6-phosphate isomerase deficiency in a mammalian cell mutant.
    Faik P; Redmill AA; Walker JI; Morgan MJ
    Biochem Soc Trans; 1990 Apr; 18(2):259. PubMed ID: 2379702
    [No Abstract]   [Full Text] [Related]  

  • 3. The characterization of gene mutations for human glucose phosphate isomerase deficiency associated with chronic hemolytic anemia.
    Xu W; Beutler E
    J Clin Invest; 1994 Dec; 94(6):2326-9. PubMed ID: 7989588
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Red cell glucose phosphate isomerase (GPI): a molecular study of three novel mutations associated with hereditary nonspherocytic hemolytic anemia.
    Repiso A; Oliva B; Vives-Corrons JL; Beutler E; Carreras J; Climent F
    Hum Mutat; 2006 Nov; 27(11):1159. PubMed ID: 17041899
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hereditary nonspherocytic hemolytic anemia caused by red cell glucose-6-phosphate isomerase (GPI) deficiency in two Portuguese patients: Clinical features and molecular study.
    Manco L; Bento C; Victor BL; Pereira J; Relvas L; Brito RM; Seabra C; Maia TM; Ribeiro ML
    Blood Cells Mol Dis; 2016 Sep; 60():18-23. PubMed ID: 27519939
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Glucose phosphate isomerase deficiency: biochemical and molecular genetic studies on the enzyme variants of two patients with severe haemolytic anaemia.
    Huppke P; Wünsch D; Pekrun A; Kind R; Winkler H; Schröter W; Lakomek M
    Eur J Pediatr; 1997 Aug; 156(8):605-9. PubMed ID: 9266190
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Study of the molecular defects in glucose phosphate isomerase-deficient patients affected by chronic hemolytic anemia.
    Baronciani L; Zanella A; Bianchi P; Zappa M; Alfinito F; Iolascon A; Tannoia N; Beutler E; Sirchia G
    Blood; 1996 Sep; 88(6):2306-10. PubMed ID: 8822952
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Two novel mutations (p.(Ser160Pro) and p.(Arg472Cys)) causing glucose-6-phosphate isomerase deficiency are associated with erythroid dysplasia and inappropriately suppressed hepcidin.
    Mojzikova R; Koralkova P; Holub D; Saxova Z; Pospisilova D; Prochazkova D; Dzubak P; Horvathova M; Divoky V
    Blood Cells Mol Dis; 2018 Mar; 69():23-29. PubMed ID: 28803808
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical, laboratory, and mutational profile of children with glucose phosphate isomerase deficiency: a single centre report.
    Sampagar A; Gosavi M; Kedar P; Patel T; Dongerdiye R; Mahantashetti N
    Int J Hematol; 2022 Feb; 115(2):255-262. PubMed ID: 34704234
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Two cases in a family with new variants of glucose phosphate isomerase deficiency (author's transl)].
    Uga N; Nishina T; Ohyama K; Kitamura M; Tsuchida M; Rin K; Yanagawa Y; Fukushima O; Yoshihara S
    Rinsho Ketsueki; 1980 May; 21(5):633-8. PubMed ID: 7411886
    [No Abstract]   [Full Text] [Related]  

  • 11. Glucose phosphate isomerase deficiency: enzymatic and familial characterization of Arg346His mutation.
    Repiso A; Oliva B; Vives Corrons JL; Carreras J; Climent F
    Biochim Biophys Acta; 2005 Jun; 1740(3):467-71. PubMed ID: 15949716
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Sequence characterization of alleles Gpi1-Sa and Gpi1-Sb at the glucose phosphate isomerase structural locus.
    Pearce SR; Morgan MJ; Ball S; Peters J; Faik P
    Mamm Genome; 1995 Aug; 6(8):537-9. PubMed ID: 8589524
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. [A case of congenital nonspherocytic hemolytic anemia associated with defective glucose phosphate isomerase].
    Soeda A; Yokoi S; Chiba H; Kitani N; Akatsuka J; Nishina T
    Rinsho Ketsueki; 1982 Aug; 23(8):1228-34. PubMed ID: 7143727
    [No Abstract]   [Full Text] [Related]  

  • 15. [Glucose phosphate isomerase deficiency with congenital nonspherocytic hemolytic anemia].
    Shalev O; Leibowitz G; Brok-Simoni F
    Harefuah; 1994 Jun; 126(12):699-702, 764, 763. PubMed ID: 7927011
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hereditary non-spherocytic hemolytic anemia and severe glucose phosphate isomerase deficiency in an Indian patient homozygous for the L487F mutation in the human GPI gene.
    Warang P; Kedar P; Ghosh K; Colah RB
    Int J Hematol; 2012 Aug; 96(2):263-7. PubMed ID: 22782259
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A case of congenital nonspherocytic hemolytic anemia associated with glucosephosphate isomerase (GPI) deficiency-GPI 'Kinki'.
    Takegawa S; Fujii H; Miwa S; Ohba Y; Yamauchi H; Miyata H
    Nihon Ketsueki Gakkai Zasshi; 1983 Feb; 46(1):11-7. PubMed ID: 6858560
    [No Abstract]   [Full Text] [Related]  

  • 18. Genetic and molecular mechanisms of the congenital defects in glucose phosphate isomerase activity: studies of four families.
    Kahn A; Van Biervliet JP; Vives-Corrons JL; Cottreau D; Stall GE
    Pediatr Res; 1977 Nov; 11(11):1123-9. PubMed ID: 411100
    [No Abstract]   [Full Text] [Related]  

  • 19. Identification of a novel tandemly repeated sequence present in an intron of the glucose phosphate isomerase (GPI) gene in mouse and man.
    Faik P; Walker JI; Morgan MJ
    Genomics; 1994 May; 21(1):122-7. PubMed ID: 7545951
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Glucose-6-phosphate isomerase deficiency results in mTOR activation, failed translocation of lipin 1α to the nucleus and hypersensitivity to glucose: Implications for the inherited glycolytic disease.
    Haller JF; Krawczyk SA; Gostilovitch L; Corkey BE; Zoeller RA
    Biochim Biophys Acta; 2011 Nov; 1812(11):1393-402. PubMed ID: 21787864
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.