Resultats de la cerca - Rahbari, Raheleh

IAP Display: A Simple Method to Identify Mouse Strain Specific IAP Insertions per Ray, Akshay, Rahbari, Raheleh, Badge, Richard M.

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Similarities and differences in patterns of germline mutation between mice and humans per Lindsay, Sarah J., Rahbari, Raheleh, Kaplanis, Joanna, Keane, Thomas, Hurles, Matthew E.

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A novel L1 retrotransposon marker for HeLa cell line identification per Rahbari, Raheleh, Sheahan, Tom, Modes, Vasileios, Collier, Pam, Macfarlane, Catriona, Badge, Richard M.

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Transduction-Specific ATLAS (TS-ATLAS) reveals a cohort of highly active L1 retrotransposons in human populations per Macfarlane, Catriona M., Collier, Pamela, Rahbari, Raheleh, Beck, Christine R., Wagstaff, John F., Igoe, Samantha, Moran, John V., Badge, Richard M.

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Understanding the Genomic Structure of Copy‐Number Variation of the Low‐Affinity Fcγ Receptor Region Allows Confirmation of the Association of FCGR3B Deletion with Rheumatoid Arthr... per Rahbari, Raheleh, Zuccherato, Luciana W, Tischler, German, Chihota, Belinda, Ozturk, Hasret, Saleem, Sara, Tarazona‐Santos, Eduardo, Machado, Lee R, Hollox, Edward J

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Detection of structural mosaicism from targeted and whole-genome sequencing data per King, Daniel A., Sifrim, Alejandro, Fitzgerald, Tomas W., Rahbari, Raheleh, Hobson, Emma, Homfray, Tessa, Mansour, Sahar, Mehta, Sarju G., Shehla, Mohammed, Tomkins, Susan E., Vasudevan, Pradeep C., Hurles, Matthew E.

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Somatic Mutations Detected in Parkinson Disease Could Affect Genes With a Role in Synaptic and Neuronal Processes per Lobon, Irene, Solís-Moruno, Manuel, Juan, David, Muhaisen, Ashraf, Abascal, Federico, Esteller-Cucala, Paula, García-Pérez, Raquel, Martí, Maria Josep, Tolosa, Eduardo, Ávila, Jesús, Rahbari, Raheleh, Marques-Bonet, Tomas, Casals, Ferran, Soriano, Eduardo

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Genetic and chemotherapeutic influences on germline hypermutation per Kaplanis, Joanna, Ide, Benjamin, Sanghvi, Rashesh, Neville, Matthew, Danecek, Petr, Coorens, Tim, Prigmore, Elena, Short, Patrick, Gallone, Giuseppe, McRae, Jeremy, Carmichael, Jenny, Barnicoat, Angela, Firth, Helen, O’Brien, Patrick, Rahbari, Raheleh, Hurles, Matthew

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Estimating the human mutation rate from autozygous segments reveals population differences in human mutational processes per Narasimhan, Vagheesh M., Rahbari, Raheleh, Scally, Aylwyn, Wuster, Arthur, Mason, Dan, Xue, Yali, Wright, John, Trembath, Richard C., Maher, Eamonn R., van Heel, David A., Auton, Adam, Hurles, Matthew E., Tyler-Smith, Chris, Durbin, Richard

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Inherent mosaicism and extensive mutation of human placentas per Coorens, Tim H. H., Oliver, Thomas R. W., Sanghvi, Rashesh, Sovio, Ulla, Cook, Emma, Vento-Tormo, Roser, Haniffa, Muzlifah, Young, Matthew D., Rahbari, Raheleh, Sebire, Neil, Campbell, Peter J., Charnock-Jones, D. Stephen, Smith, Gordon C. S., Behjati, Sam

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Meiosis and beyond – understanding the mechanistic and evolutionary processes shaping the germline genome per Bergero, Roberta, Ellis, Peter, Haerty, Wilfried, Larcombe, Lee, Macaulay, Iain, Mehta, Tarang, Mogensen, Mette, Murray, David, Nash, Will, Neale, Matthew J., O'Connor, Rebecca, Ottolini, Christian, Peel, Ned, Ramsey, Luke, Skinner, Ben, Suh, Alexander, Summers, Michael, Sun, Yu, Tidy, Alison, Rahbari, Raheleh, Rathje, Claudia, Immler, Simone

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Common clonal origin of conventional T cells and induced regulatory T cells in breast cancer patients per Xydia, Maria, Rahbari, Raheleh, Ruggiero, Eliana, Macaulay, Iain, Tarabichi, Maxime, Lohmayer, Robert, Wilkening, Stefan, Michels, Tillmann, Brown, Daniel, Vanuytven, Sebastiaan, Mastitskaya, Svetlana, Laidlaw, Sean, Grabe, Niels, Pritsch, Maria, Fronza, Raffaele, Hexel, Klaus, Schmitt, Steffen, Müller-Steinhardt, Michael, Halama, Niels, Domschke, Christoph, Schmidt, Manfred, von Kalle, Christof, Schütz, Florian, Voet, Thierry, Beckhove, Philipp

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Increased somatic mutation burdens in normal human cells due to defective DNA polymerases per Robinson, Philip S., Coorens, Tim H. H., Palles, Claire, Mitchell, Emily, Abascal, Federico, Olafsson, Sigurgeir, Lee, Bernard C. H., Lawson, Andrew R. J., Lee-Six, Henry, Moore, Luiza, Sanders, Mathijs A., Hewinson, James, Martin, Lynn, Pinna, Claudia M. A., Galavotti, Sara, Rahbari, Raheleh, Campbell, Peter J., Martincorena, Iñigo, Tomlinson, Ian, Stratton, Michael R.

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Somatic mutations reveal asymmetric cellular dynamics in the early human embryo per Ju, Young Seok, Martincorena, Inigo, Gerstung, Moritz, Petljak, Mia, Alexandrov, Ludmil B, Rahbari, Raheleh, Wedge, David C, Davies, Helen R, Ramakrishna, Manasa, Fullam, Anthony, Martin, Sancha, Alder, Christopher, Patel, Nikita, Gamble, Steve, O’Meara, Sarah, Giri, Dilip D, Sauer, Torril, Pinder, Sarah E, Purdie, Colin A, Borg, Åke, Stunnenberg, Henk, van de Vijver, Marc, Tan, Benita K.T., Caldas, Carlos, Tutt, Andrew, Ueno, Naoto T, van’t Veer, Laura J, Martens, John W. M., Sotiriou, Christos, Knappskog, Stian, Span, Paul N., Lakhani, Sunil R., Eyfjörd, Jórunn Erla, Børresen-Dale, Anne-Lise, Richardson, Andrea, Thompson, Alastair M., Viari, Alain, Hurles, Matthew E, Nik-Zainal, Serena, Campbell, Peter J, Stratton, Michael R

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