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    Results: 7

    1.

    Multiple superoxide dismutase 1/splicing factor serine alanine 15 variants are associated with the development and progression of diabetic nephropathy: the Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications Genetics study.

    Al-Kateb H, Boright AP, Mirea L, Xie X, Sutradhar R, Mowjoodi A, Bharaj B, Liu M, Bucksa JM, Arends VL, Steffes MW, Cleary PA, Sun W, Lachin JM, Thorner PS, Ho M, McKnight AJ, Maxwell AP, Savage DA, Kidd KK, Kidd JR, Speed WC, Orchard TJ, Miller RG, Sun L, Bull SB, Paterson AD; Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications Research Group.

    Diabetes. 2008 Jan;57(1):218-28. Epub 2007 Oct 3.PMID: 17914031 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    Polymorphisms within the protein tyrosine phosphatase 1B (PTPN1) gene promoter: functional characterization and association with type 2 diabetes and related metabolic traits.

    Meshkani R, Taghikhani M, Al-Kateb H, Larijani B, Khatami S, Sidiropoulos GK, Hegele RA, Adeli K.

    Clin Chem. 2007 Sep;53(9):1585-92. Epub 2007 Jul 18.PMID: 17634210 [PubMed - indexed for MEDLINE]Related articlesFree article

    3.

    Multiple variants in vascular endothelial growth factor (VEGFA) are risk factors for time to severe retinopathy in type 1 diabetes: the DCCT/EDIC genetics study.

    Al-Kateb H, Mirea L, Xie X, Sun L, Liu M, Chen H, Bull SB, Boright AP, Paterson AD; DCCT/EDIC Research Group.

    Diabetes. 2007 Aug;56(8):2161-8. Epub 2007 May 18.PMID: 17513698 [PubMed - indexed for MEDLINE]Related articlesFree article

    4.

    Efficient two-trait-locus linkage analysis through program optimization and parallelization: application to hypercholesterolemia.

    Dietter J, Spiegel A, an Mey D, Pflug HJ, Al-Kateb H, Hoffmann K, Wienker TF, Strauch K.

    Eur J Hum Genet. 2004 Jul;12(7):542-50.PMID: 15100714 [PubMed - indexed for MEDLINE]Related articlesFree article

    5.

    A splice mutation in a Syrian autosomal recessive hypercholesterolemia family causes a two-nucleotide deletion of mRNA.

    Al-Kateb H, Bautz EK, Luft FC, Bähring S.

    Circ Res. 2003 Sep 5;93(5):e49-50. No abstract available. PMID: 12958143 [PubMed - indexed for MEDLINE]Related articlesFree article

    6.

    Mutation in the ARH gene and a chromosome 13q locus influence cholesterol levels in a new form of digenic-recessive familial hypercholesterolemia.

    Al-Kateb H, Bähring S, Hoffmann K, Strauch K, Busjahn A, Nürnberg G, Jouma M, Bautz EK, Dresel HA, Luft FC.

    Circ Res. 2002 May 17;90(9):951-8.PMID: 12016260 [PubMed - indexed for MEDLINE]Related articlesFree article

    7.

    Coronary risk factors of angiographically assessed patients from Syria.

    al-Kateb H, Zarzzour W, Shameah M, Juoma M.

    J Cardiovasc Risk. 1998 Feb;5(1):31-5.PMID: 9816553 [PubMed - indexed for MEDLINE]Related articles

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