Found: 21
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A droplet digital PCR detection method for rare L1 insertions in tumors.
- Published in:
- Mobile DNA, 2014, v. 5, n. 1, p. 1, doi. 10.1186/s13100-014-0030-4
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- Article
LINE-1 and Alu retrotransposition exhibit clonal variation.
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- Mobile DNA, 2013, v. 4, n. 1, p. 1, doi. 10.1186/1759-8753-4-16
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- Article
Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function.
- Published in:
- Nature Genetics, 2002, v. 30, n. 3, p. 277, doi. 10.1038/ng842
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- Article
Repeat sequence families derived from mammalian tRNA genes.
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- Nature, 1985, v. 317, n. 6040, p. 819, doi. 10.1038/317819a0
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- Article
ALU REPEATS AND HUMAN GENOMIC DIVERSITY.
- Published in:
- Nature Reviews Genetics, 2002, v. 3, n. 5, p. 370, doi. 10.1038/nrg798
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- Article
The USH1C 216G→A mutation and the 9-repeat VNTR(t,t) allele are in complete linkage disequilibrium in the Acadian population.
- Published in:
- Human Genetics, 2002, v. 110, n. 1, p. 95, doi. 10.1007/s00439-001-0653-7
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- Article
Insertion of Retrotransposons at Chromosome Ends: Adaptive Response to Chromosome Maintenance.
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- Frontiers in Genetics, 2016, p. 1, doi. 10.3389/fgene.2015.00358
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- Article
Polymorphic human specific Alu insertions as markers for human identification.
- Published in:
- Electrophoresis, 1995, v. 16, n. 1, p. 1596, doi. 10.1002/elps.11501601263
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- Article
Cis-acting influences on Alu RNA levels.
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- Nucleic Acids Research, 2000, v. 28, n. 23, p. 4755, doi. 10.1093/nar/28.23.4755
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- Article
BC1 RNA, the Transcript from A Master Gene for ID Element Amplification, Is Able to Prime Its Own Reverse Transcription.
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- Nucleic Acids Research, 1997, v. 25, n. 8, p. 1641, doi. 10.1093/nar/25.8.1641
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- Article
Transcription coupled repair and biased insertion of human retrotransposon L1 in transcribed genes.
- Published in:
- Mobile DNA, 2017, v. 8, p. 1, doi. 10.1186/s13100-017-0100-5
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- Publication type:
- Article
Predicting Mammalian SINE Subfamily Activity from A-tail Length.
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- Molecular Biology & Evolution, 2004, v. 21, n. 11, p. 2140, doi. 10.1093/molbev/msh225
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- Article
Heavy Metal Exposure Influences Double Strand Break DNA Repair Outcomes.
- Published in:
- PLoS ONE, 2016, v. 11, n. 3, p. 1, doi. 10.1371/journal.pone.0151367
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- Article
Alu Insertion Polymorphism: A New Type of Marker for Human Population Studies.
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- Human Biology, 1992, v. 64, n. 5, p. 641
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- Article
The Nucleotide Excision Repair Pathway Limits L1 Retrotransposition.
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- Genetics, 2017, v. 205, n. 1, p. 139, doi. 10.1534/genetics.116.188680
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- Article
The Contribution of Alu Elements to Mutagenic DNA Double-Strand Break Repair.
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- PLoS Genetics, 2015, v. 11, n. 3, p. 1, doi. 10.1371/journal.pgen.1005016
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- Article
Rare mutations of FGFR2 causing apert syndrome: identification of the first partial gene deletion, and an Alu element insertion from a new subfamily.
- Published in:
- Human Mutation, 2009, v. 30, n. 2, p. 204, doi. 10.1002/humu.20825
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- Article
Sequencing, identification and mapping of primed L1 elements (SIMPLE) reveals significant variation in full length L1 elements between individuals.
- Published in:
- BMC Genomics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12864-015-1374-y
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- Article
Potential for Retroposition by Old Alu Subfamilies.
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- Journal of Molecular Evolution, 2003, v. 56, n. 6, p. 658, doi. 10.1007/s00239-002-2433-y
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- Article
Phylogenetic Analysis of the Friedreich Ataxia GAA Trinucleotide Repeat.
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- Journal of Molecular Evolution, 2001, v. 52, n. 3, p. 232, doi. 10.1007/s002390010151
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- Article
Analysis of CAG Repeat of the Machado-Joseph Gene in Human, Chimpanzee and Monkey Populations: A Variant Nucleotide is Associated with the Number of CAG Repeats.
- Published in:
- Human Molecular Genetics, 1996, v. 5, n. 2, p. 207, doi. 10.1093/hmg/5.2.207
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- Article