Protection or resection: BOD1L as a novel replication fork protection factor

Bằng Higgs, Martin R., Stewart, Grant S.
Xuất bản năm Nucleus (2016)

Mutational Analysis of the Herpes Simplex Virus Type 1 DNA Packaging Protein UL33

Bằng Beilstein, Frauke, Higgs, Martin R., Stow, Nigel D.
Được phát hành 2009

Downregulation of Gadd45beta expression by hepatitis C virus leads to defective cell cycle arrest

Bằng Higgs, Martin R., Lerat, Hervé, Pawlotsky, Jean-Michel
Được phát hành 2010

The UL15 protein of herpes simplex virus type 1 is necessary for the localization of the UL28 and UL33 proteins to viral DNA replication centres

Bằng Higgs, Martin R., Preston, Valerie G., Stow, Nigel D.
Được phát hành 2008

On your marks, get SET(D1A): the race to protect stalled replication forks

Bằng Begum, Shabana, Goula, Amalia, Bayley, Rachel, Higgs, Martin R.
Xuất bản năm Mol Cell Oncol (2018)

Regulation of Hepatitis C Virus Replication by Nuclear Translocation of Nonstructural 5A Protein and Transcriptional Activation of Host Genes

Bằng Maqbool, Muhammad Ahmad, Imache, Mohamed R., Higgs, Martin R., Carmouse, Sophie, Pawlotsky, Jean-Michel, Lerat, Hervé
Được phát hành 2013

Regulation of Hepatitis C Virus Replication by Nuclear Translocation of Nonstructural 5A Protein and Transcriptional Activation of Host Genes

Bằng Maqbool, Muhammad Ahmad, Imache, Mohamed R., Higgs, Martin R., Carmouse, Sophie, Pawlotsky, Jean-Michel, Lerat, Hervé
Được phát hành 2013

Persistence of RNA transcription during DNA replication delays duplication of transcription start sites until G2/M

Bằng Wang, Jianming, Rojas, Patricia, Mao, Jingwen, Mustè Sadurnì, Martina, Garnier, Olivia, Xiao, Songshu, Higgs, Martin R., Garcia, Paloma, Saponaro, Marco
Xuất bản năm Cell Rep (2021)

Hepatitis C Virus Proteins Induce Lipogenesis and Defective Triglyceride Secretion in Transgenic Mice

Bằng Lerat, Hervé, Kammoun, Hélène L., Hainault, Isabelle, Mérour, Emilie, Higgs, Martin R., Callens, Céline, Lemon, Stanley M., Foufelle, Fabienne, Pawlotsky, Jean-Michel
Được phát hành 2009

PARP1 and PARP2 stabilise replication forks at base excision repair intermediates through Fbh1-dependent Rad51 regulation

Bằng Ronson, George E., Piberger, Ann Liza, Higgs, Martin R., Olsen, Anna L., Stewart, Grant S., McHugh, Peter J., Petermann, Eva, Lakin, Nicholas D.
Xuất bản năm Nat Commun (2018)

Mitotic control of human papillomavirus genome-containing cells is regulated by the function of the PDZ-binding motif of the E6 oncoprotein

Bằng Marsh, Elizabeth K., Delury, Craig P., Davies, Nicholas J., Weston, Christopher J., Miah, Mohammed A.L., Banks, Lawrence, Parish, Joanna L., Higgs, Martin R, Roberts, Sally
Xuất bản năm Oncotarget (2017)

Hepatitis C virus induces a prediabetic state by directly impairing hepatic glucose metabolism in mice

Bằng Lerat, Hervé, Imache, Mohamed Rabah, Polyte, Jacqueline, Gaudin, Aurore, Mercey, Marion, Donati, Flora, Baudesson, Camille, Higgs, Martin R., Picard, Alexandre, Magnan, Christophe, Foufelle, Fabienne, Pawlotsky, Jean-Michel
Xuất bản năm J Biol Chem (2017)

Germline RBBP8 variants associated with early-onset breast cancer compromise replication fork stability

Bằng Zarrizi, Reihaneh, Higgs, Martin R., Voßgröne, Karolin, Rossing, Maria, Bertelsen, Birgitte, Bose, Muthiah, Kousholt, Arne Nedergaard, Rösner, Heike, Network, the COMPLEXO, Ejlertsen, Bent, Stewart, Grant S., Nielsen, Finn Cilius, Sørensen, Claus S.
Xuất bản năm J Clin Invest (2020)

Histone Methylation by SETD1A Protects Nascent DNA through the Nucleosome Chaperone Activity of FANCD2

Bằng Higgs, Martin R., Sato, Koichi, Reynolds, John J., Begum, Shabana, Bayley, Rachel, Goula, Amalia, Vernet, Audrey, Paquin, Karissa L., Skalnik, David G., Kobayashi, Wataru, Takata, Minoru, Howlett, Niall G., Kurumizaka, Hitoshi, Kimura, Hiroshi, Stewart, Grant S.
Xuất bản năm Mol Cell (2018)

TRAIP promotes DNA damage response during genome replication and is mutated in primordial dwarfism

Bằng Harley, Margaret E., Murina, Olga, Leitch, Andrea, Higgs, Martin R., Bicknell, Louise S., Yigit, Gökhan, Blackford, Andrew N., Zlatanou, Anastasia, Mackenzie, Karen J., Reddy, Kaalak, Halachev, Mihail, McGlasson, Sarah, Reijns, Martin A. M., Fluteau, Adeline, Martin, Carol-Anne, Sabbioneda, Simone, Elcioglu, Nursel H., Altmüller, Janine, Thiele, Holger, Greenhalgh, Lynn, Chessa, Luciana, Maghnie, Mohamad, Salim, Mahmoud, Bober, Michael B., Nürnberg, Peter, Jackson, Stephen P., Hurles, Matthew E., Wollnik, Bernd, Stewart, Grant S., Jackson, Andrew P.
Xuất bản năm Nat Genet (2015)

Hypomorphic Mutations in TONSL Cause SPONASTRIME Dysplasia

Bằng Chang, Hae Ryung, Cho, Sung Yoon, Lee, Jae Hoon, Lee, Eunkyung, Seo, Jieun, Lee, Hye Ran, Cavalcanti, Denise P., Mäkitie, Outi, Valta, Helena, Girisha, Katta M., Lee, Chung, Neethukrishna, Kausthubham, Bhavani, Gandham S., Shukla, Anju, Nampoothiri, Sheela, Phadke, Shubha R., Park, Mi Jung, Ikegawa, Shiro, Wang, Zheng, Higgs, Martin R., Stewart, Grant S., Jung, Eunyoung, Lee, Myeong-Sok, Park, Jong Hoon, Lee, Eun A., Kim, Hongtae, Myung, Kyungjae, Jeon, Woosung, Lee, Kyoungyeul, Kim, Dongsup, Kim, Ok-Hwa, Choi, Murim, Lee, Han-Woong, Kim, Yonghwan, Cho, Tae-Joon
Xuất bản năm Am J Hum Genet (2019)

Mutations in DONSON disrupt replication fork stability and cause microcephalic dwarfism

Bằng 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
Xuất bản năm Nat Genet (2017)

Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes

Bằng Burrage, Lindsay C., Reynolds, John J., Baratang, Nissan Vida, Phillips, Jennifer B., Wegner, Jeremy, McFarquhar, Ashley, Higgs, Martin R., Christiansen, Audrey E., Lanza, Denise G., Seavitt, John R., Jain, Mahim, Li, Xiaohui, Parry, David A., Raman, Vandana, Chitayat, David, Chinn, Ivan K., Bertuch, Alison A., Karaviti, Lefkothea, Schlesinger, Alan E., Earl, Dawn, Bamshad, Michael, Savarirayan, Ravi, Doddapaneni, Harsha, Muzny, Donna, Jhangiani, Shalini N., Eng, Christine M., Gibbs, Richard A., Bi, Weimin, Emrick, Lisa, Rosenfeld, Jill A., Postlethwait, John, Westerfield, Monte, Dickinson, Mary E., Beaudet, Arthur L., Ranza, Emmanuelle, Huber, Celine, Cormier-Daire, Valérie, Shen, Wei, Mao, Rong, Heaney, Jason D., Orange, Jordan S., Bertola, Débora, Yamamoto, Guilherme L., Baratela, Wagner A.R., Butler, Merlin G., Ali, Asim, Adeli, Mehdi, Cohn, Daniel H., Krakow, Deborah, Jackson, Andrew P., Lees, Melissa, Offiah, Amaka C., Carlston, Colleen M., Carey, John C., Stewart, Grant S., Bacino, Carlos A., Campeau, Philippe M., Lee, Brendan
Xuất bản năm Am J Hum Genet (2019)