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Journal Abstract Search

253 related items for PubMed ID: 8196364

  • 41. Structural analysis of the mouse prosaposin (SGP-1) gene reveals the presence of an exon that is alternatively spliced in transcribed mRNAs.
    Zhao Q, Hay N, Morales CR.
    Mol Reprod Dev; 1997 Sep; 48(1):1-8. PubMed ID: 9266755
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  • 45. A single base mutation in the 5' splice site of intron 7 of the lck gene is responsible for the deletion of exon 7 in lck mRNA of the JCaM1 cell line.
    Rouer E, Brule F, Benarous R.
    Oncogene; 1999 Jul 22; 18(29):4262-8. PubMed ID: 10435639
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  • 47. Alpha 1-antitrypsin deficiency: memorandum from a WHO meeting.
    Bull World Health Organ; 1997 Jul 22; 75(5):397-415. PubMed ID: 9447774
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  • 50. Knockdown of Z Mutant Alpha-1 Antitrypsin In Vivo Using Modified DNA Antisense Oligonucleotides.
    Aghajan M, Guo S, Monia BP.
    Methods Mol Biol; 2017 Jul 22; 1639():127-138. PubMed ID: 28752452
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  • 51. Alpha 1-antitrypsin alleles in patients with pulmonary emphysema, detected by DNA amplification (PCR) and oligonucleotide probes.
    Bruun-Petersen K, Bruun-Petersen G, Dahl R, Larsen B, Kølvraa S, Koch J, Bolund L, Gregersen N.
    Eur Respir J; 1992 May 22; 5(5):531-7. PubMed ID: 1612154
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  • 52. Denaturing gradient gel electrophoresis of the alpha 1-antitrypsin gene: application to prenatal diagnosis.
    Dubel JR, Finwick R, Hejtmancik JF.
    Am J Med Genet; 1991 Oct 01; 41(1):39-43. PubMed ID: 1951462
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  • 56. Modification of gene expression and increase in alpha1-antitrypsin (alpha1-AT) secretion after homologous recombination in alpha1-AT-deficient monocytes.
    McNab GL, Ahmad A, Mistry D, Stockley RA.
    Hum Gene Ther; 2007 Nov 01; 18(11):1171-7. PubMed ID: 17937578
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  • 57. Sustained miRNA-mediated knockdown of mutant AAT with simultaneous augmentation of wild-type AAT has minimal effect on global liver miRNA profiles.
    Mueller C, Tang Q, Gruntman A, Blomenkamp K, Teckman J, Song L, Zamore PD, Flotte TR.
    Mol Ther; 2012 Mar 01; 20(3):590-600. PubMed ID: 22252449
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  • 60. A patient with the rare alpha-1-antitrypsin variant (Z)bristol in compound heterozygosity with the Z mutation.
    Bates KJ, Puxley M, Hill M, Kalsheker N, Barlow A, Clark BE, Sherwood RA.
    Ann Clin Biochem; 2013 Nov 01; 50(Pt 6):618-21. PubMed ID: 23858502
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