檢索結果 - Robles-Espinoza, Carla Daniela

Beating tumour drug resistance: “Lamarckian” induction in the spotlight 由 Robles‐Espinoza, Carla Daniela

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Melanoma predisposition—A limited role for germline BRCA1 and BRCA2 variants 由 Adams, David J., Bishop, David Timothy, Robles‐Espinoza, Carla Daniela

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Allele-specific expression: applications in cancer and technical considerations 由 Robles-Espinoza, Carla Daniela, Mohammadi, Pejman, Bonilla, Ximena, Gutierrez-Arcelus, Maria

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Cake: a bioinformatics pipeline for the integrated analysis of somatic variants in cancer genomes 由 Rashid, Mamunur, Robles-Espinoza, Carla Daniela, Rust, Alistair G., Adams, David J.

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Telomere-regulating Genes and the Telomere Interactome in Familial Cancers 由 Robles-Espinoza, Carla Daniela, del Castillo Velasco-Herrera, Martin, Hayward, Nicholas K., Adams, David J.

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An Overview of Strategies for Detecting Genotype-Phenotype Associations Across Ancestrally Diverse Populations 由 Simonin-Wilmer, Irving, Orozco-del-Pino, Pedro, Bishop, D. Timothy, Iles, Mark M., Robles-Espinoza, Carla Daniela

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Respiratory syncytial virus A genotype classification based on systematic intergenotypic and intragenotypic sequence analysis 由 Muñoz-Escalante, Juan Carlos, Comas-García, Andreu, Bernal-Silva, Sofía, Robles-Espinoza, Carla Daniela, Gómez-Leal, Guillermo, Noyola, Daniel E.

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Somatic drivers of B-ALL in a model of ETV6-RUNX1; Pax5(+/−) leukemia 由 van der Weyden, Louise, Giotopoulos, George, Wong, Kim, Rust, Alistair G., Robles-Espinoza, Carla Daniela, Osaki, Hikari, Huntly, Brian J., Adams, David J.

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VCF/Plotein: visualization and prioritization of genomic variants from human exome sequencing projects 由 Ossio, Raul, Garcia-Salinas, O Isaac, Anaya-Mancilla, Diego Said, Garcia-Sotelo, Jair S, Aguilar, Luis A, Adams, David J, Robles-Espinoza, Carla Daniela

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More than just acral melanoma: the controversies of defining the disease 由 Bernardes, Sara S, Ferreira, Ingrid, Elder, David E, Nobre, Aretha B, Martínez‐Said, Héctor, Adams, David J, Robles‐Espinoza, Carla Daniela, Possik, Patricia A

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Germline MC1R status influences somatic mutation burden in melanoma 由 Robles-Espinoza, Carla Daniela, Roberts, Nicola D., Chen, Shuyang, Leacy, Finbarr P., Alexandrov, Ludmil B., Pornputtapong, Natapol, Halaban, Ruth, Krauthammer, Michael, Cui, Rutao, Timothy Bishop, D., Adams, David J.

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BRAF/NRAS wild-type melanoma, NF1 status and sensitivity to trametinib 由 Ranzani, Marco, Alifrangis, Constantine, Perna, Daniele, Dutton-Regester, Ken, Pritchard, Antonia, Wong, Kim, Rashid, Mamunur, Robles-Espinoza, Carla Daniela, Hayward, Nicholas K, McDermott, Ultan, Garnett, Mathew, Adams, David J

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A Genome-Wide Association Study for Regulators of Micronucleus Formation in Mice 由 McIntyre, Rebecca E., Nicod, Jérôme, Robles-Espinoza, Carla Daniela, Maciejowski, John, Cai, Na, Hill, Jennifer, Verstraten, Ruth, Iyer, Vivek, Rust, Alistair G., Balmus, Gabriel, Mott, Richard, Flint, Jonathan, Adams, David J.

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A population-based analysis of germline BAP1 mutations in melanoma 由 O’Shea, Sally J., Robles-Espinoza, Carla Daniela, McLellan, Lauren, Harrigan, Jeanine, Jacq, Xavier, Hewinson, James, Iyer, Vivek, Merchant, Will, Elliott, Faye, Harland, Mark, Bishop, D. Timothy, Newton-Bishop, Julia A., Adams, David J.

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Acral lentiginous melanoma: Basic facts, biological characteristics and research perspectives of an understudied disease 由 Basurto‐Lozada, Patricia, Molina‐Aguilar, Christian, Castaneda‐Garcia, Carolina, Vázquez‐Cruz, Martha Estefania, Garcia‐Salinas, Omar Isaac, Álvarez‐Cano, Alethia, Martínez‐Said, Héctor, Roldán‐Marín, Rodrigo, Adams, David J., Possik, Patricia A., Robles‐Espinoza, Carla Daniela

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RSAT 2018: regulatory sequence analysis tools 20th anniversary 由 Nguyen, Nga Thi Thuy, Contreras-Moreira, Bruno, Castro-Mondragon, Jaime A, Santana-Garcia, Walter, Ossio, Raul, Robles-Espinoza, Carla Daniela, Bahin, Mathieu, Collombet, Samuel, Vincens, Pierre, Thieffry, Denis, van Helden, Jacques, Medina-Rivera, Alejandra, Thomas-Chollier, Morgane

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Clinical Exome Sequencing Enables Congenital Sialidosis Type II Diagnosis in Two Siblings Presenting with Unreported Clinical Features from a Rare Homozygous Sequence Variant p.(Ty... 由 Flores-Contreras, Elda Ariadna, García-Ortiz, José Elías, Robles-Espinoza, Carla Daniela, Zomosa-Signoret, Viviana, Becerra-Solano, Luis Eduardo, Vidaltamayo, Román, Castaneda-García, Carolina, Esparza-García, Eduardo, Molina-Aguilar, Christian, Hernández-Orozco, Angélica Alejandra, Córdova-Fletes, Carlos

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Genomic analysis and clinical management of adolescent cutaneous melanoma 由 Rabbie, Roy, Rashid, Mamunur, Arance, Ana M., Sánchez, Marcelo, Tell‐Marti, Gemma, Potrony, Miriam, Conill, Carles, van Doorn, Remco, Dentro, Stefan, Gruis, Nelleke A., Corrie, Pippa, Iyer, Vivek, Robles‐Espinoza, Carla Daniela, Puig‐Butille, Joan A., Puig, Susana, Adams, David J.

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BRN2 suppresses apoptosis, reprograms DNA damage repair, and is associated with a high somatic mutation burden in melanoma 由 Herbert, Katharine, Binet, Romuald, Lambert, Jean-Philippe, Louphrasitthiphol, Pakavarin, Kalkavan, Halime, Sesma-Sanz, Laura, Robles-Espinoza, Carla Daniela, Sarkar, Sovan, Suer, Eda, Andrews, Sarah, Chauhan, Jagat, Roberts, Nicola D., Middleton, Mark R., Gingras, Anne-Claude, Masson, Jean-Yves, Larue, Lionel, Falletta, Paola, Goding, Colin R.

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Genome-wide chemical mutagenesis screens allow unbiased saturation of the cancer genome and identification of drug resistance mutations 由 Brammeld, Jonathan S., Petljak, Mia, Martincorena, Inigo, Williams, Steven P., Alonso, Luz Garcia, Dalmases, Alba, Bellosillo, Beatriz, Robles-Espinoza, Carla Daniela, Price, Stacey, Barthorpe, Syd, Tarpey, Patrick, Alifrangis, Constantine, Bignell, Graham, Vidal, Joana, Young, Jamie, Stebbings, Lucy, Beal, Kathryn, Stratton, Michael R., Saez-Rodriguez, Julio, Garnett, Mathew, Montagut, Clara, Iorio, Francesco, McDermott, Ultan

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