Dbl3 drives Cdc42 signaling at the apical margin to regulate junction position and apical differentiation

Por Zihni, Ceniz, Munro, Peter M.G., Elbediwy, Ahmed, Keep, Nicholas H., Terry, Stephen J., Harris, John, Balda, Maria S., Matter, Karl
Publicado em 2014

Basement membrane changes in capillaries of the ageing human retina

Por Powner, Michael B, Scott, Andrew, Zhu, Meidong, Munro, Peter M G, Foss, Alexander J E, Hageman, Gregory S, Gillies, Mark C, Fruttiger, Marcus
Publicado no Br J Ophthalmol (2011)

Real-Time In Vivo Imaging of Retinal Cell Apoptosis after Laser Exposure

Por Schmitz-Valckenberg, Steffen, Guo, Li, Maass, Annelie, Cheung, William, Vugler, Anthony, Moss, Stephen E., Munro, Peter M. G., Fitzke, Frederick W., Cordeiro, M. Francesca
Publicado em 2008

Ccl2, Cx3cr1 and Ccl2/Cx3cr1 chemokine deficiencies are not sufficient to cause age-related retinal degeneration

Por Luhmann, Ulrich F.O., Carvalho, Livia S., Robbie, Scott J., Cowing, Jill A., Duran, Yanai, Munro, Peter M.G., Bainbridge, James W.B., Ali, Robin R.
Publicado em 2013

WASp-dependent actin cytoskeleton stability at the dendritic cell immunological synapse is required for extensive, functional T cell contacts

Por Malinova, Dessislava, Fritzsche, Marco, Nowosad, Carla R., Armer, Hannah, Munro, Peter M. G., Blundell, Michael P., Charras, Guillaume, Tolar, Pavel, Bouma, Gerben, Thrasher, Adrian J.
Publicado no J Leukoc Biol (2016)

The Tight Junction Associated Signalling Proteins ZO-1 and ZONAB Regulate Retinal Pigment Epithelium Homeostasis in Mice

Por Georgiadis, Anastasios, Tschernutter, Marion, Bainbridge, James W. B., Balaggan, Kamaljit S., Mowat, Freya, West, Emma L., Munro, Peter M. G., Thrasher, Adrian J., Matter, Karl, Balda, Maria S., Ali, Robin R.
Publicado em 2010

The drusen-like phenotype in aging Ccl2 knockout mice is caused by an accelerated accumulation of swollen autofluorescent subretinal macrophages

Por Luhmann, Ulrich F.O., Robbie, Scott, Munro, Peter M.G., Barker, Susie E., Duran, Yanai, Luong, Vy, Fitzke, Frederick W., Bainbridge, James W.B., Ali, Robin R., MacLaren, Robert E.
Publicado em 2009

The severity of retinal pathology in homozygous Crb1(rd8/rd8) mice is dependent on additional genetic factors

Por Luhmann, Ulrich F.O., Carvalho, Livia S., Holthaus, Sophia-Martha kleine, Cowing, Jill A., Greenaway, Simon, Chu, Colin J., Herrmann, Philipp, Smith, Alexander J., Munro, Peter M.G., Potter, Paul, Bainbridge, James W.B., Ali, Robin R.
Publicado no Hum Mol Genet (2015)

Differential Modulation of Retinal Degeneration by Ccl2 and Cx3cr1 Chemokine Signalling

Por Luhmann, Ulrich F. O., Lange, Clemens A., Robbie, Scott, Munro, Peter M. G., Cowing, Jill A., Armer, Hannah E. J., Luong, Vy, Carvalho, Livia S., MacLaren, Robert E., Fitzke, Frederick W., Bainbridge, James W. B., Ali, Robin R.
Publicado em 2012

Identification and Correction of Mechanisms Underlying Inherited Blindness in Human iPSC-Derived Optic Cups

Por Parfitt, David A., Lane, Amelia, Ramsden, Conor M., Carr, Amanda-Jayne F., Munro, Peter M., Jovanovic, Katarina, Schwarz, Nele, Kanuga, Naheed, Muthiah, Manickam N., Hull, Sarah, Gallo, Jean-Marc, da Cruz, Lyndon, Moore, Anthony T., Hardcastle, Alison J., Coffey, Peter J., Cheetham, Michael E.
Publicado no Cell Stem Cell (2016)

Rescue of mutant rhodopsin traffic by metformin-induced AMPK activation accelerates photoreceptor degeneration

Por Athanasiou, Dimitra, Aguila, Monica, Opefi, Chikwado A., South, Kieron, Bellingham, James, Bevilacqua, Dalila, Munro, Peter M., Kanuga, Naheed, Mackenzie, Francesca E., Dubis, Adam M., Georgiadis, Anastasios, Graca, Anna B., Pearson, Rachael A., Ali, Robin R., Sakami, Sanae, Palczewski, Krzysztof, Sherman, Michael Y., Reeves, Philip J., Cheetham, Michael E.
Publicado no Hum Mol Genet (2017)

Mutations in TOPORS Cause Autosomal Dominant Retinitis Pigmentosa with Perivascular Retinal Pigment Epithelium Atrophy

Por Chakarova, Christina F. , Papaioannou, Myrto G. , Khanna, Hemant , Lopez, Irma , Waseem, Naushin , Shah, Amna , Theis, Torsten , Friedman, James , Maubaret, Cecilia , Bujakowska, Kinga , Veraitch, Brotati , El-Aziz, Mai M. Abd , Prescott, De Quincy , Parapuram, Sunil K. , Bickmore, Wendy A. , Munro, Peter M. G. , Gal, Andreas , Hamel, Christian P. , Marigo, Valeria , Ponting, Chris P. , Wissinger, Bernd , Zrenner, Eberhart , Matter, Karl , Swaroop, Anand , Koenekoop, Robert K. , Bhattacharya, Shomi S. 
Publicado em 2007

Mutations in REEP6 Cause Autosomal-Recessive Retinitis Pigmentosa

Por Arno, Gavin, Agrawal, Smriti A., Eblimit, Aiden, Bellingham, James, Xu, Mingchu, Wang, Feng, Chakarova, Christina, Parfitt, David A., Lane, Amelia, Burgoyne, Thomas, Hull, Sarah, Carss, Keren J., Fiorentino, Alessia, Hayes, Matthew J., Munro, Peter M., Nicols, Ralph, Pontikos, Nikolas, Holder, Graham E., Asomugha, Chinwe, Raymond, F. Lucy, Moore, Anthony T., Plagnol, Vincent, Michaelides, Michel, Hardcastle, Alison J., Li, Yumei, Cukras, Catherine, Webster, Andrew R., Cheetham, Michael E., Chen, Rui
Publicado no Am J Hum Genet (2016)