Fanconi proteins get histones moving

Por Deans, Andrew J
Publicado em 2012

DNA interstrand crosslink repair and cancer

Por Deans, Andrew J., West, Stephen C.
Publicado em 2011

Cyclin E2 induces genomic instability by mechanisms distinct from cyclin E1

Por Caldon, C. Elizabeth, Sergio, C. Marcelo, Burgess, Andrew, Deans, Andrew J., Sutherland, Robert L., Musgrove, Elizabeth A.
Publicado em 2013

ASCIZ/ATMIN is dispensable for ATM signaling in response to replication stress

Por Liu, Rui, King, Ashleigh, Hoch, Nicolas C., Chang, Catherine, Kelly, Gemma L., Deans, Andrew J., Heierhorst, Jörg
Publicado no DNA Repair (Amst) (2017)

Architecture and DNA Recognition Elements of the Fanconi Anemia FANCM-FAAP24 Complex

Por Coulthard, Rachel, Deans, Andrew J., Swuec, Paolo, Bowles, Maureen, Costa, Alessandro, West, Stephen C., McDonald, Neil Q.
Publicado em 2013

The PTEN phosphatase functions cooperatively with the Fanconi anemia proteins in DNA crosslink repair

Por Vuono, Elizabeth A., Mukherjee, Ananda, Vierra, David A., Adroved, Morganne M., Hodson, Charlotte, Deans, Andrew J., Howlett, Niall G.
Publicado no Sci Rep (2016)

MAD1 and p27(KIP1) Cooperate To Promote Terminal Differentiation of Granulocytes and To Inhibit Myc Expression and Cyclin E-CDK2 Activity

Por McArthur, Grant A., Foley, Kevin P., Fero, Matthew L., Walkley, Carl R., Deans, Andrew J., Roberts, James M., Eisenman, Robert N.
Publicado em 2002

The FA Core Complex Contains a Homo-dimeric Catalytic Module for the Symmetric Mono-ubiquitination of FANCI-FANCD2

Por Swuec, Paolo, Renault, Ludovic, Borg, Aaron, Shah, Fenil, Murphy, Vincent J., van Twest, Sylvie, Snijders, Ambrosius P., Deans, Andrew J., Costa, Alessandro
Publicado no Cell Rep (2016)

The Fanconi Anemia Pathway Maintains Genome Stability by Coordinating Replication and Transcription

Por Schwab, Rebekka A., Nieminuszczy, Jadwiga, Shah, Fenil, Langton, Jamie, Lopez Martinez, David, Liang, Chih-Chao, Cohn, Martin A., Gibbons, Richard J., Deans, Andrew J., Niedzwiedz, Wojciech
Publicado no Mol Cell (2015)

The Rothmund-Thomson syndrome helicase RECQL4 is essential for hematopoiesis

Por Smeets, Monique F., DeLuca, Elisabetta, Wall, Meaghan, Quach, Julie M., Chalk, Alistair M., Deans, Andrew J., Heierhorst, Jörg, Purton, Louise E., Izon, David J., Walkley, Carl R.
Publicado em 2014

Identification of KIAA1018/FAN1, a DNA Repair Nuclease Recruited to DNA Damage by Monoubiquitinated FANCD2

Por MacKay, Craig, Déclais, Anne-Cécile, Lundin, Cecilia, Agostinho, Ana, Deans, Andrew J., MacArtney, Thomas J., Hofmann, Kay, Gartner, Anton, West, Stephen C., Helleday, Thomas, Lilley, David M.J., Rouse, John
Publicado em 2010

Rare variants in Fanconi anemia genes are enriched in acute myeloid leukemia

Por Maung, Kyaw Ze Ya, Leo, Paul J., Bassal, Mahmoud, Casolari, Debora A., Gray, James X, Bray, Sarah C., Pederson, Stephen, Singhal, Deepak, Samaraweera, Saumya E., Nguyen, Tran, Cildir, Gökhan, Marshall, Mhairi, Ewing, Adam, Duncan, Emma L., Brown, Matthew A., Saal, Russell, Tergaonkar, Vinay, To, Luen Bik, Marlton, Paula, Gill, Devinder, Lewis, Ian, Deans, Andrew J, Brown, Anna L, D’Andrea, Richard J, Gonda, Thomas J
Publicado no Blood Cancer J (2018)