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Journal Abstract Search

195 related items for PubMed ID: 18452889

  • 21.
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  • 22. Frequencies of Six (Five Novel) STR Markers Linked to TUSC3 (MRT7) or NSUN2 (MRT5) Genes Used for Homozygosity Mapping of Recessive Intellectual Disability.
    Ghadami S, Mohammadi HM, Malbin J, Masoodifard M, Sarhaddi AB, Tavakkoly-Bazzaz J, Zeinali S.
    Clin Lab; 2015; 61(8):925-32. PubMed ID: 26427135
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  • 23. TUSC3: a novel tumour suppressor gene and its functional implications.
    Yu X, Zhai C, Fan Y, Zhang J, Liang N, Liu F, Cao L, Wang J, Du J.
    J Cell Mol Med; 2017 Sep; 21(9):1711-1718. PubMed ID: 28272772
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  • 24. TUSC3 loss alters the ER stress response and accelerates prostate cancer growth in vivo.
    Horak P, Tomasich E, Vaňhara P, Kratochvílová K, Anees M, Marhold M, Lemberger CE, Gerschpacher M, Horvat R, Sibilia M, Pils D, Krainer M.
    Sci Rep; 2014 Jan 17; 4():3739. PubMed ID: 24435307
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  • 29. Next Generation Sequencing and Genome-Wide Genotyping Identify the Genetic Causes of Intellectual Disability in Ten Consanguineous Families from Jordan.
    Froukh TJ.
    Tohoku J Exp Med; 2017 Dec 17; 243(4):297-309. PubMed ID: 29269699
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  • 30. The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardation.
    Basel-Vanagaite L, Attia R, Yahav M, Ferland RJ, Anteki L, Walsh CA, Olender T, Straussberg R, Magal N, Taub E, Drasinover V, Alkelai A, Bercovich D, Rechavi G, Simon AJ, Shohat M.
    J Med Genet; 2006 Mar 17; 43(3):203-10. PubMed ID: 16033914
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  • 31.
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  • 32. A gene for nonsyndromic mental retardation maps to chromosome 3p25-pter.
    Higgins JJ, Rosen DR, Loveless JM, Clyman JC, Grau MJ.
    Neurology; 2000 Aug 08; 55(3):335-40. PubMed ID: 10932263
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  • 36. Next generation sequencing in a family with autosomal recessive Kahrizi syndrome (OMIM 612713) reveals a homozygous frameshift mutation in SRD5A3.
    Kahrizi K, Hu CH, Garshasbi M, Abedini SS, Ghadami S, Kariminejad R, Ullmann R, Chen W, Ropers HH, Kuss AW, Najmabadi H, Tzschach A.
    Eur J Hum Genet; 2011 Jan 08; 19(1):115-7. PubMed ID: 20700148
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  • 37. Mammalian cells lacking either the cotranslational or posttranslocational oligosaccharyltransferase complex display substrate-dependent defects in asparagine linked glycosylation.
    Cherepanova NA, Gilmore R.
    Sci Rep; 2016 Feb 11; 6():20946. PubMed ID: 26864433
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  • 39. [Linkage analysis of six Algerian families with autosomal recessive non specific mental retardation].
    Guessibia N, Sarrai N, Methari N, Ridouh B, Chaabouni Bouhamed H.
    Tunis Med; 2011 May 11; 89(5):466-70. PubMed ID: 21557185
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  • 40. Homozygosity mapping of autosomal recessive intellectual disability loci in 11 consanguineous Pakistani families.
    Ahmed I, Rafiq MA, Vincent JB, Bhatti A, Ayub M, John P.
    Acta Neuropsychiatr; 2015 Feb 11; 27(1):38-47. PubMed ID: 25434728
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