The premature ageing syndrome protein, WRN, is a 3′→5′ exonuclease

[1] HOMOLOGOUS RECOMBINATION IS ELEVATED IN SOME WERNER-LIKE SYNDROMES BUT NOT DURING NORMAL INVITRO OR INVIVO SENESCENCE OF MAMMALIAN-CELLS [J]. MUTATION RESEARCH, 1990, 237 (5-6): : 259 - 269

[2] MUTATOR PHENOTYPE OF WERNER SYNDROME IS CHARACTERIZED BY EXTENSIVE DELETIONS [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (15) : 5893 - 5897

[3] BLOOM-SYNDROME - A MENDELIAN PROTOTYPE OF SOMATIC MUTATIONAL DISEASE [J]. MEDICINE, 1993, 72 (06) : 393 - 406

[4] Hierarchical deterioration of body systems in Werner's syndrome: Implications for normal ageing [J]. MECHANISMS OF AGEING AND DEVELOPMENT, 1997, 98 (03) : 239 - 254

[5] The Werner syndrome protein is a DNA helicase [J]. NATURE GENETICS, 1997, 17 (01) : 100 - 103

[6] MAIN IS, 1997, NUCLEIC ACIDS RES, V25, P3187

[7] Martin G M, 1978, Birth Defects Orig Artic Ser, V14, P5

[8] MARTIN GM, 1970, LAB INVEST, V23, P86

[9] Positionally cloned human disease genes: Patterns of evolutionary conservation and functional motifs [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (11) : 5831 - 5836

[10] An apoptosis-inducing genotoxin differentiates heterozygotic carriers for Werner helicase mutations from wild-type and homozygous mutants [J]. HUMAN GENETICS, 1997, 101 (02) : 121 - 125

[1] HOMOLOGOUS RECOMBINATION IS ELEVATED IN SOME WERNER-LIKE SYNDROMES BUT NOT DURING NORMAL INVITRO OR INVIVO SENESCENCE OF MAMMALIAN-CELLS [J]. MUTATION RESEARCH, 1990, 237 (5-6): : 259 - 269

[2] MUTATOR PHENOTYPE OF WERNER SYNDROME IS CHARACTERIZED BY EXTENSIVE DELETIONS [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (15) : 5893 - 5897

[3] BLOOM-SYNDROME - A MENDELIAN PROTOTYPE OF SOMATIC MUTATIONAL DISEASE [J]. MEDICINE, 1993, 72 (06) : 393 - 406

[4] Hierarchical deterioration of body systems in Werner's syndrome: Implications for normal ageing [J]. MECHANISMS OF AGEING AND DEVELOPMENT, 1997, 98 (03) : 239 - 254

[5] The Werner syndrome protein is a DNA helicase [J]. NATURE GENETICS, 1997, 17 (01) : 100 - 103

[6] MAIN IS, 1997, NUCLEIC ACIDS RES, V25, P3187

[7] Martin G M, 1978, Birth Defects Orig Artic Ser, V14, P5

[8] MARTIN GM, 1970, LAB INVEST, V23, P86

[9] Positionally cloned human disease genes: Patterns of evolutionary conservation and functional motifs [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (11) : 5831 - 5836

[10] An apoptosis-inducing genotoxin differentiates heterozygotic carriers for Werner helicase mutations from wild-type and homozygous mutants [J]. HUMAN GENETICS, 1997, 101 (02) : 121 - 125