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Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea.

Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea. Research Abstract Details 

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  • Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea. Abstract Text:

    q maQ Ma,d f wyszynskiD F Wyszynski,j j farrellJ J Farrell,a kutlarA Kutlar,l a farrerL A Farrer,c t baldwinC T Baldwin,m h steinbergM H Steinberg,q maQ Ma,d f wyszynskiD F Wyszynski,j j farrellJ J Farrell,a kutlarA Kutlar,l a farrerL A Farrer,c t baldwinC T Baldwin,m h steinbergM H Steinberg,q maQ Ma,d f wyszynskiD F Wyszynski,j j farrellJ J Farrell,a kutlarA Kutlar,l a farrerL A Farrer,c t baldwinC T Baldwin,m h steinbergM H Steinberg,

    The increase in fetal hemoglobin (HbF) in response to hydroxyurea (HU) varies among patients with sickle cell anemia. Twenty-nine candidate genes within loci previously reported to be linked to HbF level (6q22.3-q23.2, 8q11-q12 and Xp22.2-p22.3), involved in metabolism of HU and related to erythroid progenitor proliferation were studied in 137 sickle cell anemia patients treated with HU. Three-hundred and twenty tagging single nucleotide polymorphisms (SNPs) for genotyping were selected based on HapMap data. Multiple linear regression and the nonlinear regression Random Forest method were used to investigate the association between SNPs and the change in HbF level after 2 years of treatment with HU. Both methods revealed that SNPs in genes within the 6q22.3-23.2 and 8q11-q12 linkage peaks, and also the ARG2, FLT1, HAO2 and NOS1 genes were associated with the HbF response to HU. Polymorphisms in genes regulating HbF expression, HU metabolism and erythroid progenitor proliferation might modulate the patient response to HU.The Pharmacogenomics Journal (2007) 7, 386-394; doi:10.1038/sj.tpj.6500433; published online 13 February 2007.

    Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea. Publishing Authors By Initials

    q maQ Ma,df wyszynskiDF Wyszynski,jj farrellJJ Farrell,a kutlarA Kutlar,la farrerLA Farrer,ct baldwinCT Baldwin,mh steinbergMH Steinberg,q maQ Ma,df wyszynskiDF Wyszynski,jj farrellJJ Farrell,a kutlarA Kutlar,la farrerLA Farrer,ct baldwinCT Baldwin,mh steinbergMH Steinberg,q maQ Ma,df wyszynskiDF Wyszynski,jj farrellJJ Farrell,a kutlarA Kutlar,la farrerLA Farrer,ct baldwinCT Baldwin,mh steinbergMH Steinberg,

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    Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: The pharmacogenomics journal

    VOLUME: 7

    Page Numbers: 386-94

    Journal Abbreviation: Pharmacogenomics J.

    ISSN: 1470-269X

    DAY: 13

    MONTH: 02

    YEAR: 2007

    Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea. Information

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    LANGUAGE: eng

    NlmUniqueID: 101083949

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    Grant and Affiliation Information for Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea.

    AFFILIATION: 1Department of Medicine, Boston University School of Medicine, Boston, MA, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: Pharmacogenomics J

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