S81279[Secondary Source ID] - Search Results

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Hereditary and acquired p53 gene mutations in childhood acute lymphoblastic leukemia.

Felix CA, Nau MM, Takahashi T, Mitsudomi T, Chiba I, Poplack DG, Reaman GH, Cole DE, Letterio JJ, Whang-Peng J, et al. Felix CA, et al. J Clin Invest. 1992 Feb;89(2):640-7. doi: 10.1172/JCI115630. J Clin Invest. 1992. PMID: 1737852 Free PMC article.

Molecular cloning of the human Goodpasture antigen demonstrates it to be the alpha 3 chain of type IV collagen.

Turner N, Mason PJ, Brown R, Fox M, Povey S, Rees A, Pusey CD. Turner N, et al. J Clin Invest. 1992 Feb;89(2):592-601. doi: 10.1172/JCI115625. J Clin Invest. 1992. PMID: 1737849 Free PMC article.

Molecular studies on primary lipoprotein lipase (LPL) deficiency. One base deletion (G916) in exon 5 of LPL gene causes no detectable LPL protein due to the absence of LPL mRNA transcript.

Takagi A, Ikeda Y, Tsutsumi Z, Shoji T, Yamamoto A. Takagi A, et al. J Clin Invest. 1992 Feb;89(2):581-91. doi: 10.1172/JCI115624. J Clin Invest. 1992. PMID: 1737848 Free PMC article.

Molecular basis for membrane rigidity of hereditary ovalocytosis. A novel mechanism involving the cytoplasmic domain of band 3.

Mohandas N, Winardi R, Knowles D, Leung A, Parra M, George E, Conboy J, Chasis J. Mohandas N, et al. J Clin Invest. 1992 Feb;89(2):686-92. doi: 10.1172/JCI115636. J Clin Invest. 1992. PMID: 1737855 Free PMC article.

Identification of three mutant alleles of the gene for mitochondrial acetoacetyl-coenzyme A thiolase. A complete analysis of two generations of a family with 3-ketothiolase deficiency.

Fukao T, Yamaguchi S, Orii T, Schutgens RB, Osumi T, Hashimoto T. Fukao T, et al. J Clin Invest. 1992 Feb;89(2):474-9. doi: 10.1172/JCI115608. J Clin Invest. 1992. PMID: 1346617 Free PMC article.

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