Výsledky vyhledávání - Khédoudja Nafa

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  1. 1
    Detection of KRAS and BRAF Mutations in Colorectal Carcinoma

    Detection of KRAS and BRAF Mutations in Colorectal Carcinoma Autor Maria E. Arcila, Christopher Lau, Khédoudja Nafa, Marc Ladanyi

    Vydáno 2011
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  2. 2
    Clonal populations of hematopoietic cells with paroxysmal nocturnal hemoglobinuria genotype and phenotype are present in normal individuals

    Clonal populations of hematopoietic cells with paroxysmal nocturnal hemoglobinuria genotype and phenotype are present in normal individuals Autor David J. Araten, Khédoudja Nafa, Kriangsak Pakdeesuwan, Lucio Luzzatto

    Vydáno 1999
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  3. 3
    Mutations in the PIG-A gene causing paroxysmal nocturnal hemoglobinuria are mainly of the frameshift type

    Mutations in the PIG-A gene causing paroxysmal nocturnal hemoglobinuria are mainly of the frameshift type Autor Khédoudja Nafa, PJ Mason, Peter Hillmen, Lucio Luzzatto, Monica Bessler

    Vydáno 1995
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  4. 4
    <i>EWS-CREB1</i>: A Recurrent Variant Fusion in Clear Cell Sarcoma—Association with Gastrointestinal Location and Absence of Melanocytic Differentiation

    <i>EWS-CREB1</i>: A Recurrent Variant Fusion in Clear Cell Sarcoma—Association with Gastrointestinal Location and Absence of Melanocytic Differentiation Autor Cristina R. Antonescu, Khédoudja Nafa, Neil H. Segal, Paola Dal Cin, Marc Ladanyi

    Vydáno 2006
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  5. 5
    Oncogene Mutation Profiling of Pediatric Solid Tumors Reveals Significant Subsets of Embryonal Rhabdomyosarcoma and Neuroblastoma with Mutated Genes in Growth Signaling Pathways

    Oncogene Mutation Profiling of Pediatric Solid Tumors Reveals Significant Subsets of Embryonal Rhabdomyosarcoma and Neuroblastoma with Mutated Genes in Growth Signaling Pathways Autor Neerav Shukla, Nabahet Ameur, İsmail Yılmaz, Khédoudja Nafa, Chyau-Yueh Lau, Angela Marchetti, Laetitia Borsu, Frederic G. Barr, Marc Ladanyi

    Vydáno 2011
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  6. 6
    Additional Primary Malignancies in Patients with Gastrointestinal Stromal Tumor (GIST): A Clinicopathologic Study of 260 Patients with Molecular Analysis and Review of the Literature

    Additional Primary Malignancies in Patients with Gastrointestinal Stromal Tumor (GIST): A Clinicopathologic Study of 260 Patients with Molecular Analysis and Review of the Literatu... Autor Jaclyn F. Hechtman, Ronald P. DeMatteo, Khédoudja Nafa, Ping Chi, Maria E. Arcila, Snjezana Doğan, Alifya Oultache, Wen Chen, Meera Hameed

    Vydáno 2015
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  7. 7
    <i>EGFR</i> Exon 20 Insertion Mutations in Lung Adenocarcinomas: Prevalence, Molecular Heterogeneity, and Clinicopathologic Characteristics

    <i>EGFR</i> Exon 20 Insertion Mutations in Lung Adenocarcinomas: Prevalence, Molecular Heterogeneity, and Clinicopathologic Characteristics Autor Maria E. Arcila, Khédoudja Nafa, Jamie E. Chaft, Natasha Rekhtman, Christopher Lau, Boris Reva, Maureen F. Zakowski, Mark G. Kris, Marc Ladanyi

    Vydáno 2013
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  8. 8
    Loss of the Tumor Suppressor PML in Human Cancers of Multiple Histologic Origins

    Loss of the Tumor Suppressor PML in Human Cancers of Multiple Histologic Origins Autor Carmela Gurrieri, Paola Capodieci, Rosa Bernardi, Pier Paolo Scaglioni, Khédoudja Nafa, Laura J. Rush, David Verbel, Carlos Cordón-Cardo, Pier Paolo Pandolfi

    Vydáno 2004
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  9. 9
    Epidermal growth factor receptor exon 20 insertions in advanced lung adenocarcinomas: Clinical outcomes and response to erlotinib

    Epidermal growth factor receptor exon 20 insertions in advanced lung adenocarcinomas: Clinical outcomes and response to erlotinib Autor Jarushka Naidoo, Camelia S. Sima, Katherine Rodríguez, Natalie Busby, Khédoudja Nafa, Marc Ladanyi, Gregory J. Riely, Mark G. Kris, Maria E. Arcila, Helena A. Yu

    Vydáno 2015
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  10. 10
    Prevalence, Clinicopathologic Associations, and Molecular Spectrum of <i>ERBB2</i> (<i>HER2</i>) Tyrosine Kinase Mutations in Lung Adenocarcinomas

    Prevalence, Clinicopathologic Associations, and Molecular Spectrum of <i>ERBB2</i> (<i>HER2</i>) Tyrosine Kinase Mutations in Lung Adenocarcinomas Autor Maria E. Arcila, Jamie E. Chaft, Khédoudja Nafa, Sinchita Roy‐Chowdhuri, Christopher Lau, Michael Zaidinski, Paul K. Paik, Maureen F. Zakowski, Mark G. Kris, Marc Ladanyi

    Vydáno 2012
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  11. 11
    Reliable Clinical MLH1 Promoter Hypermethylation Assessment Using a High-Throughput Genome-Wide Methylation Array Platform

    Reliable Clinical MLH1 Promoter Hypermethylation Assessment Using a High-Throughput Genome-Wide Methylation Array Platform Autor Jamal Benhamida, Jaclyn F. Hechtman, Khédoudja Nafa, Liliana Villafania, Justyna Sadowska, Jiajing Wang, Donna Wong, Ahmet Zehir, Liying Zhang, Tejus Bale, Maria E. Arcila, Marc Ladanyi

    Vydáno 2019
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  12. 12
    Rebiopsy of Lung Cancer Patients with Acquired Resistance to EGFR Inhibitors and Enhanced Detection of the T790M Mutation Using a Locked Nucleic Acid-Based Assay

    Rebiopsy of Lung Cancer Patients with Acquired Resistance to EGFR Inhibitors and Enhanced Detection of the T790M Mutation Using a Locked Nucleic Acid-Based Assay Autor Maria E. Arcila, Geoffrey R. Oxnard, Khédoudja Nafa, Gregory J. Riely, Stephen B. Solomon, Maureen F. Zakowski, Mark G. Kris, William Pao, Vincent A. Miller, Marc Ladanyi

    Vydáno 2011
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  13. 13
    Incidence of non-founder BRCA1 and BRCA2 mutations in high risk Ashkenazi breast and ovarian cancer families

    Incidence of non-founder BRCA1 and BRCA2 mutations in high risk Ashkenazi breast and ovarian cancer families Autor Noah D. Kauff, Pedro Pérez‐Segura, Mark E. Robson, Lauren Scheuer, Beth Siegel, Alice E. Schluger, Bernardo Rapaport, T. Frank, Khédoudja Nafa, Nathan A. Ellis, Giovanni Parmigiani, Kenneth Offit

    Vydáno 2002
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  14. 14
    Diagnosis of known sarcoma fusions and novel fusion partners by targeted RNA sequencing with identification of a recurrent ACTB-FOSB fusion in pseudomyogenic hemangioendothelioma

    Diagnosis of known sarcoma fusions and novel fusion partners by targeted RNA sequencing with identification of a recurrent ACTB-FOSB fusion in pseudomyogenic hemangioendothelioma Autor Guo Zhu, Ryma Benayed, Caleb Ho, Kerry Mullaney, Purvil Sukhadia, Kelly Rios, R. Stephen Berry, Brian P. Rubin, Khédoudja Nafa, Lu Wang, David S. Klimstra, Marc Ladanyi, Meera Hameed

    Vydáno 2018
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  15. 15
    Frequency and Distinctive Spectrum of <i>KRAS</i> Mutations in Never Smokers with Lung Adenocarcinoma

    Frequency and Distinctive Spectrum of <i>KRAS</i> Mutations in Never Smokers with Lung Adenocarcinoma Autor Gregory J. Riely, Mark G. Kris, Daniel G. Rosenbaum, Jenifer L. Marks, Allan Li, Dhananjay Chitale, Khédoudja Nafa, Elyn Riedel, Meier Hsu, William Pao, Vincent A. Miller, Marc Ladanyi

    Vydáno 2008
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  16. 16
    Functional and genomic approaches reveal an ancient CHEK2 allele associated with breast cancer in the Ashkenazi Jewish population

    Functional and genomic approaches reveal an ancient CHEK2 allele associated with breast cancer in the Ashkenazi Jewish population Autor Avraham Shaag, Tom Walsh, Paul Renbaum, Tomas Kirchhoff, Khédoudja Nafa, Stacey Shiovitz, Jessica B. Mandell, Piri Welcsh, Ming K. Lee, Nathan A. Ellis, Kenneth Offit, Ephrat Levy‐Lahad, Mary‐Claire King

    Vydáno 2005
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  17. 17
    Dedifferentiation in Gastrointestinal Stromal Tumor to an Anaplastic KIT-negative Phenotype

    Dedifferentiation in Gastrointestinal Stromal Tumor to an Anaplastic KIT-negative Phenotype Autor Cristina R. Antonescu, Salvatore Romeo, Lei Zhang, Khédoudja Nafa, Jason L. Hornick, G. Petur Nielsen, Mari Mino‐Kenudson, Hsuan-Ying Huang, Juan‐Miguel Mosquera, Angelo Paolo Dei Tos, Christopher D.�M. Fletcher

    Vydáno 2013
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  18. 18
    Genomic aberrations frequently alter chromatin regulatory genes in chordoma

    Genomic aberrations frequently alter chromatin regulatory genes in chordoma Autor Lu Wang, Ahmet Zehir, Khédoudja Nafa, Nengyi Zhou, Michael F. Berger, Jacklyn Casanova, Justyna Sadowska, Chao Lü, C. David Allis, Mrinal M. Gounder, Chandhanarat Chandhanayingyong, Marc Ladanyi, Patrick J. Boland, Meera Hameed

    Vydáno 2016
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  19. 19
    Ultrarapid EGFR Mutation Screening Followed by Comprehensive Next-Generation Sequencing: A Feasible, Informative Approach for Lung Carcinoma Cytology Specimens With a High Success Rate

    Ultrarapid EGFR Mutation Screening Followed by Comprehensive Next-Generation Sequencing: A Feasible, Informative Approach for Lung Carcinoma Cytology Specimens With a High Success... Autor Maria E. Arcila, Soo‐Ryum Yang, Amir Momeni, Douglas A. Mata, Paulo Salazar, Roger Chan, Daniela Elezovic, Ryma Benayed, Ahmet Zehir, Darren J. Buonocore, Natasha Rekhtman, Oscar Lin, Marc Ladanyi, Khédoudja Nafa

    Vydáno 2020
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  20. 20
    <i>EGFR</i> Exon 19 Insertions: A New Family of Sensitizing <i>EGFR</i> Mutations in Lung Adenocarcinoma

    <i>EGFR</i> Exon 19 Insertions: A New Family of Sensitizing <i>EGFR</i> Mutations in Lung Adenocarcinoma Autor Mai He, Marzia Capelletti, Khédoudja Nafa, Cai‐Hong Yun, Maria E. Arcila, Vincent A. Miller, Michelle S. Ginsberg, Binsheng Zhao, Mark G. Kris, Michael J. Eck, Pasi A. Jänne, Marc Ladanyi, Geoffrey R. Oxnard

    Vydáno 2011
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