Independent and sequential recruitment of NHEJ and HR factors to DNA damage sites in mammalian cells

Por Kim, Jong-Soo, Krasieva, Tatiana B., Kurumizaka, Hitoshi, Chen, David J., Taylor, A. Malcolm R., Yokomori, Kyoko
Publicado em 2005

Mre11 modulates the fidelity of fusion between short telomeres in human cells

Por Tankimanova, Maira, Capper, Rebecca, Letsolo, Boitelo T., Rowson, Jan, Jones, Rhiannon E., Britt-Compton, Bethan, Taylor, A. Malcolm R., Baird, Duncan M.
Publicado em 2012

A Role for E1B-AP5 in ATR Signaling Pathways during Adenovirus Infection

Por Blackford, Andrew N., Bruton, Rachel K., Dirlik, Orkide, Stewart, Grant S., Taylor, A. Malcolm R., Dobner, Thomas, Grand, Roger J. A., Turnell, Andrew S.
Publicado em 2008

Autosomal Recessive Cerebellar Ataxia with Oculomotor Apraxia (Ataxia-Telangiectasia–Like Syndrome) Is Linked to Chromosome 9q34

Por Németh, Andrea H., Bochukova, Elena, Dunne, Eimear, Huson, Susan M., Elston, John, Hannan, Mohammed A., Jackson, Matthew, Chapman, Cyril J., Taylor, A. Malcolm R.
Publicado em 2000

RIDDLE immunodeficiency syndrome is linked to defects in 53BP1-mediated DNA damage signaling

Por Stewart, Grant S., Stankovic, Tatjana, Byrd, Philip J., Wechsler, Thomas, Miller, Edward S., Huissoon, Aarn, Drayson, Mark T., West, Stephen C., Elledge, Stephen J., Taylor, A. Malcolm R.
Publicado em 2007

Immunostaining of modified histones defines high-level features of the human metaphase epigenome

Por Terrenoire, Edith, McRonald, Fiona, Halsall, John A, Page, Paula, Illingworth, Robert S, Taylor, A Malcolm R, Davison, Val, O'Neill, Laura P, Turner, Bryan M
Publicado em 2010

Adenovirus 12 E4orf6 inhibits ATR activation by promoting TOPBP1 degradation

Por Blackford, Andrew N., Patel, Rakesh N., Forrester, Natalie A., Theil, Kathrin, Groitl, Peter, Stewart, Grant S., Taylor, A. Malcolm R., Morgan, Iain M., Dobner, Thomas, Grand, Roger J. A., Turnell, Andrew S.
Publicado em 2010

A Regulatory Role for NBS1 in Strand-Specific Mutagenesis during Somatic Hypermutation

Por Du, Likun, Dunn-Walters, Deborah K., Chrzanowska, Krystyna H., Stankovic, Tanja, Kotnis, Ashwin, Li, Xin, Lu, Jiayi, Eggertsen, Gösta, Brittain, Claire, Popov, Sergey W., Gennery, Andrew R., Taylor, A. Malcolm R., Pan-Hammarström, Qiang
Publicado em 2008

T-cell number and subtype influence the disease course of primary chronic lymphocytic leukaemia xenografts in alymphoid mice

Por Oldreive, Ceri E., Skowronska, Anna, Davies, Nicholas J., Parry, Helen, Agathanggelou, Angelo, Krysov, Sergey, Packham, Graham, Rudzki, Zbigniew, Cronin, Laura, Vrzalikova, Katerina, Murray, Paul, Odintsova, Elena, Pratt, Guy, Taylor, A. Malcolm R., Moss, Paul, Stankovic, Tatjana
Publicado no Dis Model Mech (2015)

A Hypomorphic PALB2 Allele Gives Rise to an Unusual Form of FA-N Associated with Lymphoid Tumour Development

Por Byrd, Philip J., Stewart, Grant. S., Smith, Anna, Eaton, Charlotte, Taylor, Alexander J., Guy, Chloe, Eringyte, Ieva, Fooks, Peggy, Last, James I., Horsley, Robert, Oliver, Antony W., Janic, Dragana, Dokmanovic, Lidija, Stankovic, Tatjana, Taylor, A. Malcolm R.
Publicado no PLoS Genet (2016)

Variations in ATM Protein Expression During Normal Lymphoid Differentiation and Among B-Cell-Derived Neoplasias

Por Starczynski, Jane, Simmons, William, Flavell, Joanne R., Byrd, Phillip J., Stewart, Grant S., Kullar, Harjit S., Groom, Alix, Crocker, John, Moss, Paul A.H., Reynolds, Gary M., Glavina-Durdov, Meri, Taylor, A. Malcolm R., Fegan, Christopher, Stankovic, Tatjana, Murray, Paul G.
Publicado em 2003

Regulation of DNA-end resection by hnRNPU-like proteins promotes DNA double-strand break signaling and repair

Por Polo, Sophie E., Blackford, Andrew N., Chapman, J. Ross, Baskcomb, Linda, Gravel, Serge, Rusch, Andre, Thomas, Anoushka, Blundred, Rachel, Smith, Philippa, Kzhyshkowska, Julia, Dobner, Thomas, Taylor, A. Malcolm R., Turnell, Andrew S., Stewart, Grant S., Grand, Roger J., Jackson, Stephen P.
Publicado em 2012

Identification of the First ATRIP–Deficient Patient and Novel Mutations in ATR Define a Clinical Spectrum for ATR–ATRIP Seckel Syndrome

Por Ogi, Tomoo, Walker, Sarah, Stiff, Tom, Hobson, Emma, Limsirichaikul, Siripan, Carpenter, Gillian, Prescott, Katrina, Suri, Mohnish, Byrd, Philip J., Matsuse, Michiko, Mitsutake, Norisato, Nakazawa, Yuka, Vasudevan, Pradeep, Barrow, Margaret, Stewart, Grant S., Taylor, A. Malcolm R., O'Driscoll, Mark, Jeggo, Penny A.
Publicado em 2012

Targeting the Ataxia Telangiectasia Mutated-null phenotype in chronic lymphocytic leukemia with pro-oxidants

Por Agathanggelou, Angelo, Weston, Victoria J., Perry, Tracey, Davies, Nicholas J., Skowronska, Anna, Payne, Daniel T., Fossey, John S., Oldreive, Ceri E., Wei, Wenbin, Pratt, Guy, Parry, Helen, Oscier, David, Coles, Steve J., Hole, Paul S., Darley, Richard L., McMahon, Michael, Hayes, John D., Moss, Paul, Stewart, Grant S., Taylor, A. Malcolm R., Stankovic, Tatjana
Publicado no Haematologica (2015)

Hypomorphic PCNA mutation underlies a human DNA repair disorder

Por Baple, Emma L., Chambers, Helen, Cross, Harold E., Fawcett, Heather, Nakazawa, Yuka, Chioza, Barry A., Harlalka, Gaurav V., Mansour, Sahar, Sreekantan-Nair, Ajith, Patton, Michael A., Muggenthaler, Martina, Rich, Phillip, Wagner, Karin, Coblentz, Roselyn, Stein, Constance K., Last, James I., Taylor, A. Malcolm R., Jackson, Andrew P., Ogi, Tomoo, Lehmann, Alan R., Green, Catherine M., Crosby, Andrew H.
Publicado em 2014

Mutations in DONSON disrupt replication fork stability and cause microcephalic dwarfism

Por Reynolds, John J, Bicknell, Louise S, Carroll, Paula, Higgs, Martin R, Shaheen, Ranad, Murray, Jennie E, Papadopoulos, Dimitrios K, Leitch, Andrea, Murina, Olga, Tarnauskaitė, Žygimantė, Wessel, Sarah R, Zlatanou, Anastasia, Vernet, Audrey, von Kriegsheim, Alex, Mottram, Rachel MA, Logan, Clare V, Bye, Hannah, Li, Yun, Brean, Alexander, Maddirevula, Sateesh, Challis, Rachel C, Skouloudaki, Kassiani, Almoisheer, Agaadir, Alsaif, Hessa S, Amar, Ariella, Prescott, Natalie J, Bober, Michael B, Duker, Angela, Faqeih, Eissa, Seidahmed, Mohammed Zain, Al Tala, Saeed, Alswaid, Abdulrahman, Ahmed, Saleem, Al-Aama, Jumana Yousuf, Altmüller, Janine, Al Balwi, Mohammed, Brady, Angela F, Chessa, Luciana, Cox, Helen, Fischetto, Rita, Heller, Raoul, Henderson, Bertram D, Hobson, Emma, Nürnberg, Peter, Percin, E Ferda, Peron, Angela, Spaccini, Luigina, Quigley, Alan J, Thakur, Seema, Wise, Carol A, Yoon, Grace, Alnemer, Maha, Tomancak, Pavel, Yigit, Gökhan, Taylor, A Malcolm R, Reijns, Martin AM, Simpson, Michael A, Cortez, David, Alkuraya, Fowzan S, Mathew, Christopher G, Jackson, Andrew P, Stewart, Grant S
Publicado no Nat Genet (2017)