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Association of a germline copy number polymorphism of APOBEC3A and APOBEC3B with burden of putative APOBEC-dependent mutations in breast cancer.
Published in:
Nature Genetics, 2014, v. 46, n. 5, p. 487, doi. 10.1038/ng.2955
By:
- Nik-Zainal, Serena;
- Wedge, David C;
- Alexandrov, Ludmil B;
- Petljak, Mia;
- Butler, Adam P;
- Bolli, Niccolo;
- Davies, Helen R;
- Knappskog, Stian;
- Martin, Sancha;
- Papaemmanuil, Elli;
- Ramakrishna, Manasa;
- Shlien, Adam;
- Simonic, Ingrid;
- Xue, Yali;
- Tyler-Smith, Chris;
- Campbell, Peter J;
- Stratton, Michael R
Publication type:
Article
POT1 loss-of-function variants predispose to familial melanoma.
Published in:
Nature Genetics, 2014, v. 46, n. 5, p. 478, doi. 10.1038/ng.2947
By:
- Robles-Espinoza, Carla Daniela;
- Harland, Mark;
- Ramsay, Andrew J;
- Aoude, Lauren G;
- Quesada, Víctor;
- Ding, Zhihao;
- Pooley, Karen A;
- Pritchard, Antonia L;
- Tiffen, Jessamy C;
- Petljak, Mia;
- Palmer, Jane M;
- Symmons, Judith;
- Johansson, Peter;
- Stark, Mitchell S;
- Gartside, Michael G;
- Snowden, Helen;
- Montgomery, Grant W;
- Martin, Nicholas G;
- Liu, Jimmy Z;
- Choi, Jiyeon
Publication type:
Article
APOBEC Mutagenesis in Cancer Development and Susceptibility.
Published in:
Cancers, 2024, v. 16, n. 2, p. 374, doi. 10.3390/cancers16020374
By:
- Dananberg, Alexandra;
- Striepen, Josefine;
- Rozowsky, Jacob S.;
- Petljak, Mia
Publication type:
Article
Understanding mutagenesis through delineation of mutational signatures in human cancer.
Published in:
Carcinogenesis, 2016, v. 37, n. 6, p. 531, doi. 10.1093/carcin/bgw055
By:
- Petljak, Mia;
- Alexandrov, Ludmil B.
Publication type:
Article
Germline TERT promoter mutations are rare in familial melanoma.
Published in:
Familial Cancer, 2016, v. 15, n. 1, p. 139, doi. 10.1007/s10689-015-9841-9
By:
- Harland, Mark;
- Petljak, Mia;
- Robles-Espinoza, Carla;
- Ding, Zhihao;
- Gruis, Nelleke;
- Doorn, Remco;
- Pooley, Karen;
- Dunning, Alison;
- Aoude, Lauren;
- Wadt, Karin;
- Gerdes, Anne-Marie;
- Brown, Kevin;
- Hayward, Nicholas;
- Newton-Bishop, Julia;
- Adams, David;
- Bishop, D.
Publication type:
Article
Genome sequencing of normal cells reveals developmental lineages and mutational processes.
Published in:
Nature, 2014, v. 513, n. 7518, p. 422, doi. 10.1038/nature13448
By:
- Behjati, Sam;
- Huch, Meritxell;
- van Boxtel, Ruben;
- Karthaus, Wouter;
- Wedge, David C.;
- Martincorena, Iñigo;
- Petljak, Mia;
- Alexandrov, Ludmil B.;
- Gundem, Gunes;
- Tarpey, Patrick S.;
- Roerink, Sophie;
- Maddison, Mark;
- Mudie, Laura;
- Robinson, Ben;
- Campbell, Peter;
- Stratton, Michael R.;
- Tamuri, Asif U.;
- Goldman, Nick;
- Blokker, Joyce;
- van de Wetering, Marc
Publication type:
Article

Found: 6

Association of a germline copy number polymorphism of APOBEC3A and APOBEC3B with burden of putative APOBEC-dependent mutations in breast cancer.

POT1 loss-of-function variants predispose to familial melanoma.

APOBEC Mutagenesis in Cancer Development and Susceptibility.

Understanding mutagenesis through delineation of mutational signatures in human cancer.

Germline TERT promoter mutations are rare in familial melanoma.

Genome sequencing of normal cells reveals developmental lineages and mutational processes.