Kết quả tìm kiếm - Rahbari, Raheleh

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

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Similarities and differences in patterns of germline mutation between mice and humans Bằng 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 Bằng 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 Bằng 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... Bằng 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 Bằng 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 Bằng 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 Bằng 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 Bằng 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 Bằng 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 Bằng 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 Bằng 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 Bằng 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 Bằng 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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