Resultats globals: 6 registres trobats en 0.01 segons.
Articles, 6 registres trobats
Articles 6 registres trobats  
1.
11 p, 709.0 KB Histone H3.3 beyond cancer : Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients / Bryant, Laura (Children's Hospital of Philadelphia (Pennsilvània)) ; Li, Dong (Children's Hospital of Philadelphia (Pennsilvània)) ; Cox, Samuel G. (University of Southern California, CA 90033, USA) ; Marchione, Dylan (Epigenetics Institute, Department of Biochemistry and Biophysics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA) ; Joiner, Evan F. (Vagelos College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA) ; Wilson, Khadija (Epigenetics Institute, Department of Biochemistry and Biophysics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA) ; Janssen, Kevin (Epigenetics Institute, Department of Biochemistry and Biophysics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA) ; Lee, Pearl (Abramson Family Cancer Research Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA) ; March, Michael E. (Children's Hospital of Philadelphia (Pennsilvània)) ; Nair, Divya (Children's Hospital of Philadelphia (Pennsilvània)) ; Sherr, Elliott (Department of Neurology, University of California, San Francisco, San Francisco, CA 94158, USA) ; Fregeau, Brieana (Department of Neurology, University of California, San Francisco, San Francisco, CA 94158, USA) ; Wierenga, Klaas J. (Department of Clinical Genomics, Mayo Clinic Florida, Jacksonville, FL 32224, USA) ; Wadley, Alexandrea (Department of Clinical Genomics, Mayo Clinic Florida, Jacksonville, FL 32224, USA) ; Mancini, Grazia M. S. (Department of Clinical Genetics, Erasmus University Medical Center, 3015 CN Rotterdam, Netherlands) ; Powell-Hamilton, Nina (Department of Medical Genetics, Alfred I. duPont Hospital for Children, Wilmington, DE 19810, USA) ; van de Kamp, Jiddeke (Department of Clinical Genetics, VU Medical Center, Amsterdam, Netherlands) ; Grebe, Theresa (Division of Genetics and Metabolism, Phoenix Children's Hospital, Phoenix, AZ 85016, USA) ; Dean, John (Department of Medical Genetics, Aberdeen Royal Infirmary, Aberdeen, Scotland, UK) ; Ross, Alison (Department of Medical Genetics, Aberdeen Royal Infirmary, Aberdeen, Scotland, UK) ; Crawford, Heather P. (Clinical and Metabolic Genetics, Cook Children's Medical Center, Fort Worth, TX 76104, USA) ; Powis, Zoe (Department of Emerging Genetic Medicine, Ambry Genetics, Aliso Viejo, CA 92656, USA) ; Cho, Megan T. (GeneDx, 207 Perry Parkway, Gaithersburg, MD 20877, USA) ; Willing, Marcia C. (Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University in St. Louis, School of Medicine, St. Louis, MO 63110, USA) ; Manwaring, Linda (Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University in St. Louis, School of Medicine, St. Louis, MO 63110, USA) ; Schot, Rachel (Department of Clinical Genetics, Erasmus University Medical Center, 3015 CN Rotterdam, Netherlands) ; Nava, Caroline (AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, F-75013 Paris, France) ; Afenjar, Alexandra (Service de génétique, CRMR des malformations et maladies congénitales du cervelet et CRMR déficience intellectuelle, hôpital Trousseau, AP-HP, France) ; Lessel, Davor (Undiagnosed Disease Program at the University Medical Center Hamburg-Eppendorf (UDP-UKE), Martinistrasse 52, 20246 Hamburg, Germany) ; Wagner, Matias (Institut für Humangenetik, Technische Universität München, Munich, Germany) ; Klopstock, Thomas (Munich Cluster for Systems Neurology, SyNergy, Munich, Germany) ; Winkelmann, Juliane (Klinik und Poliklinik für Neurologie, Klinikum rechts der Isar, Technische Universität München, Munich, Germany) ; Catarino, Claudia B. (Friedrich-Baur-Institute, Department of Neurology, Ludwig-Maximilians University, Ziemssenstr. 1a, 80336 Munich, Germany) ; Retterer, Kyle (GeneDx, 207 Perry Parkway, Gaithersburg, MD 20877, USA) ; Schuette, Jane L. (Division of Genetics, Metabolism, and Genomic Medicine, Department of Pediatrics and Communicable Diseases, University of Michigan, Ann Arbor, MI 48109, USA) ; Innis, Jeffrey W. (Division of Genetics, Metabolism, and Genomic Medicine, Department of Pediatrics and Communicable Diseases, University of Michigan, Ann Arbor, MI 48109, USA) ; Pizzino, Amy (Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19103, USA) ; Lüttgen, Sabine (Department of Pediatrics, University Medical Center Eppendorf, 20246 Hamburg, Germany) ; Denecke, Jonas (Department of Pediatrics, University Medical Center Eppendorf, 20246 Hamburg, Germany) ; Strom, Tim M. (Institut für Humangenetik, Technische Universität München, Munich, Germany) ; Monaghan, Kristin G. (GeneDx, 207 Perry Parkway, Gaithersburg, MD 20877, USA) ; Yuan, Zuo-Fei (Epigenetics Institute, Department of Biochemistry and Biophysics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA) ; Dubbs, Holly (Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19103, USA) ; Bend, Renee (Greenwood Genetic Center, Greenwood, SC 29646, USA) ; Lee, Jennifer A. (Greenwood Genetic Center, Greenwood, SC 29646, USA) ; Lyons, Michael J. (Greenwood Genetic Center, Greenwood, SC 29646, USA) ; Hoefele, Julia (Technische Universität München. Institut für Humangenetik) ; Günthner, Roman (Technische Universität München. Institut für Humangenetik) ; Reutter, Heiko (Department of Neonatology and Pediatric Intensive Care, Children's Hospital, University Hospital Bonn & Institute of Human Genetics, University Hospital Bonn, Bonn, Germany) ; Keren, Boris (AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, F-75013 Paris, France) ; Radtke, Kelly (Department of Clinical Genomics, Ambry Genetics, Aliso Viejo, CA 92656, USA) ; Sherbini, Omar (Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19103, USA) ; Mrokse, Cameron (Department of Clinical Genomics, Ambry Genetics, Aliso Viejo, CA 92656, USA) ; Helbig, Katherine L. (Department of Clinical Genomics, Ambry Genetics, Aliso Viejo, CA 92656, USA) ; Odent, Sylvie (CHU Rennes, Service de Génétique Clinique, CNRS UMR6290, University Rennes1, Rennes, France) ; Cogne, Benjamin (Université de Nantes) ; Mercier, Sandra (Université de Nantes) ; Bezieau, Stephane (Université de Nantes) ; Besnard, Thomas (Université de Nantes) ; Kury, Sebastien (Université de Nantes) ; Redon, Richard (Université de Nantes) ; Reinson, Karit (Institute of Clinical Medicine, University of Tartu, Tartu, Estonia) ; Wojcik, Monica H. (Broad Institute, Cambridge, MA 02142, USA) ; Õunap, Katrin (Institute of Clinical Medicine, University of Tartu, Tartu, Estonia) ; Ilves, Pilvi (Tartu University Hospital (Tartu, Estònia)) ; Innes, A. Micheil (Alberta Children's Hospital Research Institute) ; Kernohan, Kristin D. (Newborn Screening Ontario (NSO), Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada) ; Costain, Gregory (Division of Clinical and Metabolic Genetics, Department of Pediatrics, University of Toronto, The Hospital for Sick Children, Toronto, Ontario, Canada) ; Meyn, M. Stephen (The Center for Human Genomics and Precision Medicine, School of Medicine and Public Health, University of Wisconsin - Madison, Madison, Wisconsin 53705, USA) ; Chitayat, David (The Prenatal Diagnosis and Medical Genetics Program, Mount Sinai Hospital, Toronto, Ontario, Canada) ; Zackai, Elaine (Children's Hospital of Philadelphia (Pennsilvània)) ; Lehman, Anna (Department of Medical Genetics, University of British Columbia, Vancouver, Canada) ; Kitson, Hilary (Department of Pediatrics, University of British Columbia, Vancouver, Canada) ; Martin, Martin G. (Eli and Edythe Broad Center of Regenerative Medicine and Stem Cell Research and the David Geffen School of Medicine, UCLA, Los Angeles, CA 90095, USA) ; Martinez-Agosto, Julian A. (Division of Medical Genetics, Department of Pediatrics, David Geffen School of Medicine, UCLA, Los Angeles, CA 90095, USA) ; Nelson, Stan F. (Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, UCLA, Los Angeles, CA 90095, USA) ; Palmer, Christina G. S. (Institute for Society and Genetics, Department of Psychiatry and Biobehavioral Sciences, David Geffen School of Medicine, UCLA, Los Angeles, CA 90095, USA) ; Papp, Jeanette C. (Department of Human Genetics, David Geffen School of Medicine, UCLA, Los Angeles, CA 90095, USA) ; Parker, Neil H. (David Geffen School of Medicine, Los Angeles, CA 90095, USA) ; Sinsheimer, Janet S. (Institute for Society and Genetics, Departments of Human Genetics, Biomathematics, and Biostatistics, David Geffen School of Medicine, UCLA, Los Angeles, CA 90095, USA) ; Vilain, Eric (Center for Genetic Medicine Research, Children's National Medical Center, Washington, DC 20010, USA) ; Wan, Jijun (Department of Human Genetics, David Geffen School of Medicine, UCLA, Los Angeles, CA 90095, USA) ; Yoon, Amanda J. (Department of Human Genetics, David Geffen School of Medicine, UCLA, Los Angeles, CA 90095, USA) ; Zheng, Allison (Department of Human Genetics, David Geffen School of Medicine, UCLA, Los Angeles, CA 90095, USA) ; Brimble, Elise (Department of Neurology and Neurological Sciences, Stanford Medicine, Stanford, CA 94305, USA) ; Ferrero, Giovanni Battista (Department of Public Health and Pediatrics, University of Torino, Turin, Italy) ; Radio, Francesca Clementina (Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, Rome, Italy) ; Carli, Diana (Department of Public Health and Pediatrics, University of Torino, Turin, Italy) ; Barresi, Sabina (Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, Rome, Italy) ; Brusco, Alfredo (Department of Medical Sciences, University of Torino, Turin, Italy) ; Tartaglia, Marco (Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, Rome, Italy) ; Thomas, Jennifer Muncy (Pediatrics and Neurology and Neurotherapeutics, UT Southwestern Medical Center, Dallas, TX 75390, USA) ; Umana, Luis (Genetics and Metabolism, UT Southwestern Medical Center, Dallas, TX 75390, USA) ; Weiss, Marjan M. (Department of Clinical Genetics, VU Medical Center, Amsterdam, Netherlands) ; Gotway, Garrett (Genetics and Metabolism, UT Southwestern Medical Center, Dallas, TX 75390, USA) ; Stuurman, K. E. (Department of Clinical Genetics, Erasmus University Medical Center, 3015 CN Rotterdam, Netherlands) ; Thompson, Michelle L. (HudsonAlpha Institute for Biotechnology, Huntsville, AL 35806, USA) ; McWalter, Kirsty (GeneDx, 207 Perry Parkway, Gaithersburg, MD 20877, USA) ; Stumpel, Constance T. R. M. (Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, Netherlands) ; Stevens, Servi J. C. (Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, Netherlands) ; Stegmann, Alexander P. A. (Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, Netherlands) ; Tveten, Kristian (Department of Medical Genetics, Telemark Hospital Trust, 3710 Skien, Norway) ; Vøllo, Arve (Department of Pediatrics, Hospital of Østfold, 1714 Grålum, Norway) ; Prescott, Trine (Department of Medical Genetics, Telemark Hospital Trust, 3710 Skien, Norway) ; Fagerberg, Christina (Odense University Hospital (Dinamarca)) ; Laulund, Lone Walentin (Odense University Hospital (Dinamarca)) ; Larsen, Martin J. (Odense University Hospital (Dinamarca)) ; Byler, Melissa (SUNY Upstate Medical University, Syracuse, NY 13210, USA) ; Lebel, Robert Roger (SUNY Upstate Medical University, Syracuse, NY 13210, USA) ; Hurst, Anna C. (University of Alabama at Birmingham, Birmingham, AL 35294, USA) ; Dean, Joy (University of Alabama at Birmingham, Birmingham, AL 35294, USA) ; Schrier Vergano, Samantha A. (Division of Medical Genetics and Metabolism, Children's Hospital of The King's Daughters, Norfolk VA 23507, USA) ; Norman, Jennifer (INTEGRIS Pediatric Neurology, Oklahoma City, OK 73112, USA) ; Mercimek-Andrews, Saadet (Division of Clinical and Metabolic Genetics, Department of Pediatrics, University of Toronto, The Hospital for Sick Children, Toronto, Ontario, Canada) ; Neira, Juanita (Department of Human Genetics, Emory University, Atlanta, GA 30322, USA) ; Van Allen, Margot I. (Medical Genetics Programs, Provincial Health Shared Services BC and Vancouver Island Health Shared Services BC, Canada) ; Longo, Nicola (Division of Medical Genetics, Department of Pediatrics, University of Utah, Salt Lake City, UT 84112, USA) ; Sellars, Elizabeth (University of Arkansas for Medical Sciences, Little Rock, AR 72701, USA) ; Louie, Raymond J. (Greenwood Genetic Center, Greenwood, SC 29646, USA) ; Cathey, Sara S. (Greenwood Genetic Center, Greenwood, SC 29646, USA) ; Brokamp, Elly (Vanderbilt University, Nashville, TN 37203, USA) ; Heron, Delphine (AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, F-75013 Paris, France) ; Snyder, Molly (Child Neurology, UT Southwestern Medical Center, Dallas, TX 75390, USA) ; Vanderver, Adeline (Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19103, USA) ; Simon, Celeste (Vagelos College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA) ; de la Cruz, Xavier (Institució Catalana de Recerca i Estudis Avançats) ; Padilla Sirera, Natàlia (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Crump, J. Gage (Department of Stem Cell Biology and Regenerative Medicine, Keck School of Medicine, University of Southern California, CA 90033, USA) ; Chung, Wendy (Departments of Pediatrics and Medicine, Columbia University Irving Medical Center, New York, NY 10032, USA) ; Garcia, Benjamin (Epigenetics Institute, Department of Biochemistry and Biophysics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA) ; Hakonarson, Hakon (Children's Hospital of Philadelphia (Pennsilvània)) ; Bhoj, Elizabeth J. (Children's Hospital of Philadelphia (Pennsilvània)) ; Universitat Autònoma de Barcelona
Germ line mutations in H3F3A and H3F3B cause a previously unidentified neurodevelopmental syndrome. Although somatic mutations in Histone 3. 3 (H3. 3) are well-studied drivers of oncogenesis, the role of germline mutations remains unreported. [...]
2020 - 10.1126/sciadv.abc9207
Science advances, Vol. 6 (december 2020)  
2.
13 p, 6.8 MB Genomic Analyses across Six Cancer Types Identify Basal-like Breast Cancer as a Unique Molecular Entity / Prat, Aleix (Vall d'Hebron Institut d'Oncologia) ; Adamo, Barbara (Vall d'Hebron Institut d'Oncologia) ; Fan, Cheng (Lineberger Comprehensive Cancer Center, University of North Carolina) ; Peg, Vicente (Hospital Universitari Vall d'Hebron) ; Vidal Losada, Maria (Vall d'Hebron Institut d'Oncologia) ; Galván, Patricia (Vall d'Hebron Institut d'Oncologia) ; Vivancos, Ana (Vall d'Hebron Institut d'Oncologia) ; Palmer, Héctor G. ; Nuciforo, Paolo (Vall d'Hebron Institut d'Oncologia) ; Dawood, Shaheenah (Department of Medical Oncology, Dubai Hospital) ; Rodón, Jordi (Vall d'Hebron Institut d'Oncologia) ; Ramón y Cajal, Santiago (Hospital Universitari Vall d'Hebron) ; Campo, Josep Maria Del (Vall d'Hebron Institut d'Oncologia) ; Felip, Enriqueta (Vall d'Hebron Institut d'Oncologia) ; Tabernero, Josep (Vall d'Hebron Institut d'Oncologia) ; Cortés, Javier (Vall d'Hebron Institut d'Oncologia) ; Universitat Autònoma de Barcelona
To improve our understanding of the biological relationships among different types of cancer, we have characterized variation in gene expression patterns in a set of 1,707 samples representing 6 human cancer types (breast, ovarian, brain, colorectal, lung adenocarcinoma and squamous cell lung cancer). [...]
2013 - 10.1038/srep03544
Scientific reports, Vol. 3 (december 2013)  
3.
7 p, 740.6 KB Dual MET and ERBB inhibition overcomes intratumor plasticity in osimertinib-resistant-advanced non-small-cell lung cancer (NSCLC) / Martinez-Marti, Alex (Universitat Autònoma de Barcelona) ; Felip, Enriqueta (Universitat Autònoma de Barcelona) ; Matito, Judit (Vall d'Hebron Institut d'Oncologia) ; Mereu, Elisabetta (Universitat Pompeu Fabra) ; Navarro, Alejandro (Vall d'Hebron Institut d'Oncologia) ; Cedrés, Susana (Vall d'Hebron Institut d'Oncologia) ; Pardo Aranda, Nuria (Universitat Autònoma de Barcelona) ; Martinez de Castro, Ana (Vall d'Hebron Institut d'Oncologia) ; Remon, Jordin (Vall d'Hebron Institut d'Oncologia) ; Miquel, J. M. (Vall d'Hebron Institut d'Oncologia) ; Guillaumet-Adkins, A. (Universitat Pompeu Fabra) ; Nadal, Ernest (Institut Català d'Oncologia) ; Rodriguez Esteban, Gustavo (Universitat Pompeu Fabra) ; Arqués, O. (Stem Cells and Cancer Group) ; Fasani, R. (Vall d'Hebron Institut d'Oncologia) ; Nuciforo, Paolo (Vall d'Hebron Institut d'Oncologia) ; Heyn, Holger (Universitat Pompeu Fabra) ; Villanueva Garatachea, Alberto (Institut Català d'Oncologia) ; Palmer, Héctor G (Stem Cells and Cancer Group) ; Vivancos, Ana (Vall d'Hebron Institut d'Oncologia)
Third-generation epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) such as osimertinib are the last line of targeted treatment of metastatic non-small-cell lung cancer (NSCLC) EGFR -mutant harboring T790M. [...]
2017 - 10.1093/annonc/mdx396
Annals of oncology, Vol. 28 (july 2017) , p. 2451-2457  
4.
10 p, 506.2 KB Analysis of mutant allele fractions in driver genes in colorectal cancer - biological and clinical insights / Dienstmann, Rodrigo (Vall d'Hebron Institut d'Oncologia) ; Elez, Elena (Hospital Universitari Vall d'Hebron) ; Argilés Martínez, Guillem (Vall d'Hebron Institut d'Oncologia) ; Matos, Ignacio (Vall d'Hebron Institut d'Oncologia) ; Sanz García, Enrique (Vall d'Hebron Institut d'Oncologia) ; Ortiz, Carolina (Vall d'Hebron Institut d'Oncologia) ; Macarulla Mercadé, Teresa (Vall d'Hebron Institut d'Oncologia) ; Capdevila Castillón, Jaume (Vall d'Hebron Institut d'Oncologia) ; Alsina, Maria (Vall d'Hebron Institut d'Oncologia) ; Saurí Nadal, Tamara (Vall d'Hebron Institut d'Oncologia) ; Verdaguer, Helena (Vall d'Hebron Institut d'Oncologia) ; Vilaró, Marta (Vall d'Hebron Institut d'Oncologia) ; Ruiz-Pace, Fiorella (Vall d'Hebron Institut d'Oncologia) ; Viaplana, Cristina (Vall d'Hebron Institut d'Oncologia) ; García Rodríguez, Ariadna (Vall d'Hebron Institut d'Oncologia) ; Landolfi, Stefania (Universitat Autònoma de Barcelona) ; Palmer, Héctor G (Vall d'Hebron Institut d'Oncologia) ; Nuciforo, Paolo (Vall d'Hebron Institut d'Oncologia) ; Rodón Ahnert, Jordi (Vall d'Hebron Institut d'Oncologia) ; Vivancos, Ana (Vall d'Hebron Institut d'Oncologia) ; Tabernero, Josep (Vall d'Hebron Institut d'Oncologia)
Sequencing of tumors is now routine and guides personalized cancer therapy. Mutant allele fractions (s, or the 'mutation dose') of a driver gene may reveal the genomic structure of tumors and influence response to targeted therapies. [...]
2017 - 10.1002/1878-0261.12099
Molecular Oncology, Vol. 11, Issue 9 (September 2017) , p. 1263-1272  
5.
14 p, 4.6 MB A simplified interventional mapping system (SIMS) for the selection of combinations of targeted treatments in non-small cell lung cancer / Lazar, Vladimir (Gustave-Roussy Cancer Center (France)) ; Rubin, Eitan (Ben-Gurion University of the Negev (Israel)) ; Depil, Stephane (Leon Berard Cancer Center (France)) ; Pawitan, Yudi (Karolinska Institutet (Estocolm, Suècia)) ; Martini, Jean-François (Pfizer Oncology Research (USA)) ; Gomez-Navarro, Jesus (Takeda Pharmaceuticals International Co.(USA)) ; Yver, Antoine (AstraZeneca Pharmaceuticals LP (USA)) ; Kan, Zhengyin (Pfizer Oncology Research (USA)) ; Dry, Jonathan R. (AstraZeneca Pharmaceuticals LP (USA)) ; Kehren, Jeanne (Sanofi (France)) ; Validire, Pierre (Institut Mutualiste Montsouris (France)) ; Rodón Ahnert, Jordi (Vall d'Hebron Institut d'Oncologia) ; Vielh, Philippe (Gustave-Roussy Cancer Center (France)) ; Ducreux, Michel (Gustave-Roussy Cancer Center (France)) ; Galbraith, Susan (AstraZeneca Pharmaceuticals LP (USA)) ; Lehnert, Manfred (Takeda Pharmaceuticals International Co. (USA)) ; Onn, Amir (Chaim Sheba Medical Center (Israel)) ; Berger, Raanan (Chaim Sheba Medical Center (Israel)) ; Pierotti, Marco A. (Fondazione IRCCS Istituto Nazionale dei Tumori (Italy)) ; Porgador, Angel (Ben-Gurion University of the Negev (Israel)) ; Pramesh, C. S. (Tata Memorial Centre (India)) ; Ye, Ding-wei (Fudan University Shanghai Cancer Center (China)) ; Carvalho, Andre L. (Barretos Cancer Hospital. Fundacao Pio XII (Brazil)) ; Batist, Gerald (Jewish General Hospita. Segal Cancer Centre (Canada)) ; Le Chevalier, Thierry (Gustave-Roussy Cancer Center (France)) ; Morice, Philippe (Gustave-Roussy Cancer Center (France)) ; Besse, Benjamin (Gustave-Roussy Cancer Center (France)) ; Vassal, Gilles (Gustave-Roussy Cancer Center (France)) ; Mortlock, Andrew (AstraZeneca Pharmaceuticals LP (USA)) ; Hansson, Johan (Karolinska Institutet (Estocolm, Suècia)) ; Berindan Neagoe, Ioana (Universitatea de Medicină şi Farmacie Iuliu Haţieganu Cluj-Napoca (Romania)) ; Dann, Robert (General Electric Healthcare (USA)) ; Haspel, Joel (Oracle Corporation (UK)) ; Irimie, Alexandru (Universitatea de Medicină şi Farmacie Iuliu Haţieganu Cluj-Napoca (Romania)) ; Laderman, Steve (Agilent Technologies (USA)) ; Nechushtan, Hovav (Hadassah Hebrew University Medical Center (Israel)) ; Al Omari, Amal S. (King Hussein Cancer Center (Jordan)) ; Haywood, Trent (Blue Cross Blue Shield Association (USA)) ; Bresson, Catherine (WIN Consortium (France)) ; Soo, Khee Chee (National Cancer Centre (Singapore)) ; Osman, Iman (New York University Langone Medical Center (USA)) ; Mata, Hilario (MD Anderson Cancer Center (USA)) ; Lee, Jack J. (MD Anderson Cancer Center (USA)) ; Jhaveri, Komal (New York University Langone Medical Center (USA)) ; Meurice, Guillaume (Gustave-Roussy Cancer Center (France)) ; Palmer, Gary (Foundation Medicine Inc. (USA)) ; Lacroix, Ludovic (Gustave-Roussy Cancer Center (France)) ; Koscielny, Serge (Gustave-Roussy Cancer Center (France)) ; Eterovic, Karina Agda (MD Anderson Cancer Center (USA)) ; Blay, Jean-Yves (Leon Berard Cancer Center (France)) ; Buller, Richard (Pfizer Oncology Research (USA)) ; Eggermont, Alexander (Gustave-Roussy Cancer Center (France)) ; Schilsky, Richard L. (American Society of Clinical Oncology (USA)) ; Mendelsohn, John (MD Anderson Cancer Center (USA)) ; Soria, Jean-Charles (Gustave-Roussy Cancer Center (France)) ; Rothenberg, Mace (Pfizer Oncology Research (USA)) ; Scoazec, Jean-Yves (Gustave-Roussy Cancer Center (France)) ; Ki Hong, Waun (MD Anderson Cancer Center (USA)) ; Kurzrock, Razelle (Moores Cancer Center (USA)) ; Universitat Autònoma de Barcelona
Non-small cell lung cancer (NSCLC) is a leading cause of death worldwide. Targeted monotherapies produce high regression rates, albeit for limited patient subgroups, who inevitably succumb. We present a novel strategy for identifying customized combinations of triplets of targeted agents, utilizing a simplified interventional mapping system (SIMS) that merges knowledge about existent drugs and their impact on the hallmarks of cancer. [...]
2015 - 10.18632/oncotarget.3741
Oncotarget, Vol. 6, no. 16 (June 2015) , p. 14139-14152  
6.
6 p, 2.0 MB Síndrome mieloproliferativo canino de curso agudo / Palmer, G. (Clínica Veterinaria Dr. Palmer (Portals Nous, Mallorca))
Debido a un caso clínico compatible con una leucemia, hemos llegado a la conclusión de que se trata de un síndrome mieloproliferativo según diferentes hemogramas seriados y tinciones citoquímicas de médula ósea.
While studying a clinical case leading to leukemia, we have come the conclusion that its best description is that of myeloproliferative syndrome according to the different studies carried out through blood testing and cytochemical staining of bone marrow sample.

1996
Clínica veterinaria de pequeños animales, Vol. 16, Núm. 1 (Enero-Marzo 1996) , p. 52-57  

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1 Palmer, Gary
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