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 *

155 related articles for article (PubMed ID: 21507164)

  • 41. Analysis of Glucose-6-Phosphate Dehydrogenase Genetic Polymorphism in the Hakka Population in Southern China.
    Zhong Z; Wu H; Li B; Li C; Liu Z; Yang M; Zhang Q; Zhong W; Zhao P
    Med Sci Monit; 2018 Oct; 24():7316-7321. PubMed ID: 30315739
    [TBL] [Abstract][Full Text] [Related]  

  • 42. [Identification of G6PD gene variants from Hakka population in Guangdong province].
    Yu GL; Jiang WY; DU CS; Chen LM; Lin QD; Tian QH; Zeng JB; Li SG
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Oct; 21(5):448-51. PubMed ID: 15476167
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Prevalence of glucose-6-phosphate dehydrogenase deficiency and the role of the A- variant in a Saudi population.
    Alharbi KK; Khan IA
    J Int Med Res; 2014 Oct; 42(5):1161-7. PubMed ID: 25169987
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Glucose-6-phosphate dehydrogenase (G6PD) mutations in Thailand: G6PD Viangchan (871G>A) is the most common deficiency variant in the Thai population.
    Nuchprayoon I; Sanpavat S; Nuchprayoon S
    Hum Mutat; 2002 Feb; 19(2):185. PubMed ID: 11793482
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Incidence and complete molecular characterization of glucose-6-phosphate dehydrogenase deficiency in the Guangxi Zhuang autonomous region of southern China: description of four novel mutations.
    Yan T; Cai R; Mo O; Zhu D; Ouyang H; Huang L; Zhao M; Huang F; Li L; Liang X; Xu X
    Haematologica; 2006 Oct; 91(10):1321-8. PubMed ID: 17018380
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Genetic heterogeneity of glucose-6-phosphate dehydrogenase deficiency revealed by single-strand conformation and sequence analysis.
    Calabrò V; Mason PJ; Filosa S; Civitelli D; Cittadella R; Tagarelli A; Martini G; Brancati C; Luzzatto L
    Am J Hum Genet; 1993 Mar; 52(3):527-36. PubMed ID: 8447319
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Investigation of the mutation points and effects of some drugs on glucose-6-phosphate dehydrogenase-deficient people in the Erzurum region.
    Ozmen I; Ciftçi M; Küfrevioğlu OI; Cüruk MA
    J Enzyme Inhib Med Chem; 2004 Aug; 19(4):355-60. PubMed ID: 15558953
    [TBL] [Abstract][Full Text] [Related]  

  • 48. 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]  

  • 49. Molecular Heterogeneity of Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency in the Portuguese Population.
    Manco L; Bento C; Relvas L; Maia T; Ribeiro ML
    Acta Med Port; 2023 Feb; 36(2):81-87. PubMed ID: 36150187
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Genetic analysis and molecular basis of G6PD deficiency among malaria patients in Thailand: implications for safe use of 8-aminoquinolines.
    Boonyuen U; Jacob BAC; Wongwigkan J; Chamchoy K; Singha-Art N; Pengsuk N; Songdej D; Adams ER; Edwards T; Chamnanchanunt S; Amran SI; Latif NA; Louis NE; Chandran S
    Malar J; 2024 Feb; 23(1):38. PubMed ID: 38308253
    [TBL] [Abstract][Full Text] [Related]  

  • 51. At least five polymorphic mutants account for the prevalence of glucose-6-phosphate dehydrogenase deficiency in Algeria.
    Nafa K; Reghis A; Osmani N; Baghli L; Aït-Abbes H; Benabadji M; Kaplan JC; Vulliamy T; Luzzatto L
    Hum Genet; 1994 Nov; 94(5):513-7. PubMed ID: 7959686
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Glucose-6-phosphate dehydrogenase deficiency does not result from mutations in the promoter region of the G6PD gene.
    Menounos PG; Garinis GA; Patrinos GP
    J Clin Lab Anal; 2003; 17(3):90-2. PubMed ID: 12696079
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Molecular analysis of eight biochemically unique glucose-6-phosphate dehydrogenase variants found in Japan.
    Hirono A; Fujii H; Takano T; Chiba Y; Azuno Y; Miwa S
    Blood; 1997 Jun; 89(12):4624-7. PubMed ID: 9192788
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Characterization of G6PD genotypes and phenotypes on the northwestern Thailand-Myanmar border.
    Bancone G; Chu CS; Somsakchaicharoen R; Chowwiwat N; Parker DM; Charunwatthana P; White NJ; Nosten FH
    PLoS One; 2014; 9(12):e116063. PubMed ID: 25536053
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Three new mutations account for the prevalence of glucose 6 phosphate deshydrogenase (G6PD) deficiency in Tunisia.
    Bendaoud B; Hosni I; Mosbahi I; Hafsia R; Prehu C; Abbes S
    Pathol Biol (Paris); 2013 Apr; 61(2):64-9. PubMed ID: 22552160
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Hemolysis and Mediterranean G6PD mutation (c.563 C>T) and c.1311 C>T polymorphism among Palestinians at Gaza Strip.
    Sirdah M; Reading NS; Perkins SL; Shubair M; Aboud L; Prchal JT
    Blood Cells Mol Dis; 2012 Apr; 48(4):203-8. PubMed ID: 22364808
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Five different glucose-6-phophate [correction phosphate]dehydrogenase (G6PD) variants found among 11 G6PD-deficient persons in Flores Island, Indonesia.
    Matsuoka H; Arai M; Yoshida S; Tantular IS; Pusarawati S; Kerong H; Kawamoto F
    J Hum Genet; 2003; 48(10):541-544. PubMed ID: 14505231
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Genetic Profiles of Korean Patients With Glucose-6-Phosphate Dehydrogenase Deficiency.
    Lee J; Park J; Choi H; Kim J; Kwon A; Jang W; Chae H; Kim M; Kim Y; Lee JW; Chung NG; Cho B
    Ann Lab Med; 2017 Mar; 37(2):108-116. PubMed ID: 28028996
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Molecular genotyping of G6PD mutations for neonates in Ningbo area.
    Pan J; Zhuang D; Yu Q; Pan X; Bao Y; Pan S; Wang F; Ge L; Li H
    J Clin Lab Anal; 2021 Dec; 35(12):e24104. PubMed ID: 34762759
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Molecular variants of G6PD deficiency among certain tribal communities of Orissa, India.
    Nishank SS; Chhotray GP; Kar SK; Ranjit MR
    Ann Hum Biol; 2008; 35(3):355-61. PubMed ID: 18568599
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.