Non-B DNA conformations, genomic rearrangements, and human disease

[1] Flexible DNA: Genetically unstable CTG center dot CAG and CGG center dot CCG from human hereditary neuromuscular disease genes [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (27) : 16783 - 16792

[2] Breakpoints of gross deletions coincide with non-B DNA conformations [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (39) : 14162 - 14167

[3] PKD1 unusual DNA conformations are recognized by nucleotide excision repair [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (21) : 18597 - 18604

[4] The breakpoint region of the most common isochromosome, i(17q), in human neoplasia is characterized by a complex genomic architecture with large, palindromic, low-copy repeats [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2004, 74 (01) : 1 - 10

[5] Mutational mechanisms of Williams-Beuren syndrome deletions [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (01) : 131 - 151

[6] Reciprocal crossovers and a positional preference for strand exchange in recombination events resulting in deletion or duplication of chromosome 17p11.2 [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (06) : 1302 - 1315

[7] Bissler John J., 1998, Frontiers in Bioscience, V3, pD408

[8] Bowater RP, 2001, PROG NUCLEIC ACID RE, V66, P159

[9] Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy [J]. NATURE GENETICS, 1998, 18 (02) : 164 - 167

[10] Transcription-targeted DNA deamination by the AID antibody diversification enzyme [J]. NATURE, 2003, 422 (6933) : 726 - 730

[1] Flexible DNA: Genetically unstable CTG center dot CAG and CGG center dot CCG from human hereditary neuromuscular disease genes [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (27) : 16783 - 16792

[2] Breakpoints of gross deletions coincide with non-B DNA conformations [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (39) : 14162 - 14167

[3] PKD1 unusual DNA conformations are recognized by nucleotide excision repair [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (21) : 18597 - 18604

[4] The breakpoint region of the most common isochromosome, i(17q), in human neoplasia is characterized by a complex genomic architecture with large, palindromic, low-copy repeats [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2004, 74 (01) : 1 - 10

[5] Mutational mechanisms of Williams-Beuren syndrome deletions [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (01) : 131 - 151

[6] Reciprocal crossovers and a positional preference for strand exchange in recombination events resulting in deletion or duplication of chromosome 17p11.2 [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (06) : 1302 - 1315

[7] Bissler John J., 1998, Frontiers in Bioscience, V3, pD408

[8] Bowater RP, 2001, PROG NUCLEIC ACID RE, V66, P159

[9] Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy [J]. NATURE GENETICS, 1998, 18 (02) : 164 - 167

[10] Transcription-targeted DNA deamination by the AID antibody diversification enzyme [J]. NATURE, 2003, 422 (6933) : 726 - 730