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Human lecithin-cholesterol acyltransferase gene: complete gene sequence and sites of expression.
Nucleic Acids Res. 1986 Dec 9;14(23):9397-406
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Amplification dynamics of human-specific (HS) Alu family members.
Nucleic Acids Res. 1991 Jul 11;19(13):3619-23
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Alu-Alu recombination deletes splice acceptor sites and produces secreted low density lipoprotein receptor in a subject with familial hypercholesterolemia.
J Biol Chem. 1987 Mar 5;262(7):3354-61
PMID: 3818645
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Unequal crossing-over between two alu-repetitive DNA sequences in the low-density-lipoprotein-receptor gene. A possible mechanism for the defect in a patient with familial hypercholesterolaemia.
Eur J Biochem. 1987 Apr 1;164(1):77-81
PMID: 3549308
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Recombination at the human alpha-globin gene cluster: sequence features and topological constraints.
Cell. 1987 May 8;49(3):369-78
PMID: 3032452
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DNA sequencing with chain-terminating inhibitors.
Proc Natl Acad Sci U S A. 1977 Dec;74(12):5463-7
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SINEs and LINEs: highly repeated short and long interspersed sequences in mammalian genomes.
Cell. 1982 Mar;28(3):433-4
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Molecular drive: a cohesive mode of species evolution.
Nature. 1982 Sep 9;299(5879):111-7
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The human LDL receptor: a cysteine-rich protein with multiple Alu sequences in its mRNA.
Cell. 1984 Nov;39(1):27-38
PMID: 6091915
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The origin and evolution of retroposons.
Int Rev Cytol. 1985;93:187-279
PMID: 2409043
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Integration site preferences of the Alu family and similar repetitive DNA sequences.
Nucleic Acids Res. 1985 Dec 20;13(24):8939-54
PMID: 3001654
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Primate eta-globin DNA sequences and man's place among the great apes.
Nature. 1986 Jan 16-22;319(6050):234-8
PMID: 3945312
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A sex chromosome rearrangement in a human XX male caused by Alu-Alu recombination.
Cell. 1987 Nov 6;51(3):417-25
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Clustering and subfamily relationships of the Alu family in the human genome.
Mol Biol Evol. 1987 Jan;4(1):19-29
PMID: 3128713
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Existence of at least three distinct Alu subfamilies.
J Mol Evol. 1987;26(3):180-6
PMID: 3129565
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Sources and evolution of human Alu repeated sequences.
Proc Natl Acad Sci U S A. 1988 Jul;85(13):4770-4
PMID: 3387437
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A fundamental division in the Alu family of repeated sequences.
Proc Natl Acad Sci U S A. 1988 Jul;85(13):4775-8
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The Alu family developed through successive waves of fixation closely connected with primate lineage history.
J Mol Evol. 1988;27(3):194-202
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Molecular systematics of higher primates: genealogical relations and classification.
Proc Natl Acad Sci U S A. 1988 Oct;85(20):7627-31
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In vivo transcription of a cloned prosimian primate SINE sequence.
Nucleic Acids Res. 1989 Nov 11;17(21):8669-82
PMID: 2479909
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Genetic exchange between endogenous and exogenous LINE-1 repetitive elements in mouse cells.
Nucleic Acids Res. 1990 Nov 11;18(21):6385-91
PMID: 1978749
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Structure and variability of recently inserted Alu family members.
Nucleic Acids Res. 1990 Dec 11;18(23):6793-8
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Reconstruction and analysis of human Alu genes.
J Mol Evol. 1991 Feb;32(2):105-21
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A human-specific subfamily of Alu sequences.
Genomics. 1991 Mar;9(3):481-7
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DNA deletions in the low density lipoprotein (LDL) receptor gene in Danish families with familial hypercholesterolemia.
Clin Genet. 1991 Jun;39(6):451-62
PMID: 1863993
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Recombinational biases in the rearranged C1-inhibitor genes of hereditary angioedema patients.
Am J Hum Genet. 1991 Nov;49(5):1055-62
PMID: 1656734
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A de novo Alu insertion results in neurofibromatosis type 1.
Nature. 1991 Oct 31;353(6347):864-6
PMID: 1719426
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Inactivation of the cholinesterase gene by Alu insertion: possible mechanism for human gene transposition.
Proc Natl Acad Sci U S A. 1991 Dec 15;88(24):11315-9
PMID: 1662391
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Evolution of the master Alu gene(s).
J Mol Evol. 1991 Oct;33(4):311-20
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Involvement of cDNA in homologous recombination between Ty elements in Saccharomyces cerevisiae.
Mol Cell Biol. 1992 Apr;12(4):1613-20
PMID: 1372387
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Phylogenetic evidence for multiple Alu source genes.
J Mol Evol. 1992 Jul;35(1):7-16
PMID: 1325566
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Alu insertion polymorphism: a new type of marker for human population studies.
Hum Biol. 1992 Oct;64(5):641-8
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Identification of an Alu retrotransposition event in close proximity to a strong candidate gene for Huntington's disease.
Nature. 1993 Mar 25;362(6418):370-3
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A new subfamily of recently retroposed human Alu repeats.
Nucleic Acids Res. 1993 May 11;21(9):2252
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An Alu element retroposition in two families with Huntington disease defines a new active Alu subfamily.
Nucleic Acids Res. 1993 Jul 25;21(15):3379-83
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Evolutionary analyses of repetitive DNA sequences.
Methods Enzymol. 1993;224:213-32
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BC200 RNA: a neural RNA polymerase III product encoded by a monomeric Alu element.
Proc Natl Acad Sci U S A. 1993 Dec 15;90(24):11563-7
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Phylogenetic isolation of a human Alu founder gene: drift to new subfamily identity [corrected].
J Mol Evol. 1993 Dec;37(6):559-65
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Mobility of short interspersed repeats within the chimpanzee lineage.
J Mol Evol. 1993 Dec;37(6):566-72
PMID: 8114109
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Haemophilia B due to a de novo insertion of a human-specific Alu subfamily member within the coding region of the factor IX gene.
Eur J Hum Genet. 1993;1(1):30-6
PMID: 8069649
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Duplication of seven exons in LDL receptor gene caused by Alu-Alu recombination in a subject with familial hypercholesterolemia.
Cell. 1987 Mar 13;48(5):827-35
PMID: 3815525
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Master genes in mammalian repetitive DNA amplification.
Trends Genet. 1992 Sep;8(9):307-11
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