Deletions in FLT-3 juxtamembrane domain define a new class of pathogenic mutations: case report and systematic analysis

Por Young, David J., Nguyen, Bao, Zhu, Ruiqi, Seo, Jaesung, Li, Li, Levis, Mark J., Pratz, Keith W., Duffield, Amy S., Small, Donald
Publicado no Blood Adv (2021)

Epigenetic DNA Methylation Profiling with MSRE: A Quantitative NGS Approach Using a Parkinson's Disease Test Case

Por Marsh, Adam G., Cottrell, Matthew T., Goldman, Morton F.
Publicado no Front Genet (2016)

Real-time PCR and targeted next-generation sequencing in the detection of low level EGFR mutations: Instructive case analyses

Por Cheng, Yu-Wei, Stefaniuk, Catherine, Jakubowski, Maureen A.
Publicado no Respir Med Case Rep (2019)

Comparative Study of NGS Platform Ion Torrent Personal Genome Machine and Therascreen Rotor-Gene Q for the Detection of Somatic Variants in Cancer

Por Lombardi, Angela, Russo, Margherita, Luce, Amalia, Morgillo, Floriana, Tirino, Virginia, Misso, Gabriella, Martinelli, Erika, Troiani, Teresa, Desiderio, Vincenzo, Papaccio, Gianpaolo, Iovino, Francesco, Argenziano, Giuseppe, Moscarella, Elvira, Sperlongano, Pasquale, Galizia, Gennaro, Addeo, Raffaele, Necas, Alois, Necasova, Andrea, Ciardiello, Fortunato, Ronchi, Andrea, Caraglia, Michele, Grimaldi, Anna
Publicado no High Throughput (2020)

Molecular Profile of Advanced Non-Small Cell Lung Cancers in Octogenarians: The Door to Precision Medicine in Elderly Patients

Por Caterina Fumagalli, Chiara Catania, Alberto Ranghiero, Carlo Bosi, Giuseppe Viale, Filippo de Marinis, Massimo Barberis, Elena Guerini-Rocco
Publicado em 2019-01-01

Phylogeography and hybridization of corvid birds in the Palearctic Region

Por A. P. Kryukov
Publicado em 2019-03-01

Clinical feasibility of NGS liquid biopsy analysis in NSCLC patients

Por Papadopoulou, Eirini, Tsoulos, Nikolaos, Tsantikidi, Katerina, Metaxa-Mariatou, Vasiliki, Stamou, Pinelopi Eleftheria, Kladi-Skandali, Athina, Kapeni, Evgenia, Tsaousis, Georgios, Pentheroudakis, George, Petrakis, Dimitrios, Lampropoulou, Dimitra Ioanna, Aravantinos, Gerasimos, Varthalitis, Ioannis, Kesisis, George, Boukovinas, Ioannis, Papakotoulas, Pavlos, Katirtzoglou, Nikolaos, Athanasiadis, Elias, Stavridi, Flora, Christodoulou, Christos, Koumarianou, Anna, Eralp, Yeşim, Nasioulas, George
Publicado no PLoS One (2019)

Cost-effectiveness analysis comparing companion diagnostic tests for EGFR, ALK, and ROS1 versus...

Por Schluckebier, Luciene, Caetano, Rosangela, Garay, Osvaldo Ulises, Montenegro, Giuliana T., Custodio, Marcelo, Aran, Veronica, Gil Ferreira, Carlos
Publicado no BMC Cancer (2020)

Simultaneous VENTANA IHC and RT-PCR testing of ALK status in Chinese non-small cell lung cancer patients and response to crizotinib

Por Chun-wei Xu, Wen-xian Wang, Yan-ping Chen, Yu Chen, Wei Liu, Li-hua Zhong, Fang-fang Chen, Wu Zhuang, Zheng-bo Song, Xiao-hui Chen, Yun-jian Huang, Yan-fang Guan, Xin Yi, Tang-feng Lv, Wei-feng Zhu, Jian-ping Lu, Xiao-jiang Wang, Yi Shi, Xian-dong Lin, Gang Chen, Yong Song
Publicado em 2018-04-01

Successful treatment of pyrotinib for bone marrow metastasis induced pancytopenia in a patient with non‐small‐cell lung cancer and ERBB2 mutation

Por Wu, Yanyan, Ni, Jun, Chang, Xiaoyan, Zhang, Xiaotong, Zhang, Li
Publicado no Thorac Cancer (2020)

Fairly rare small-diameter hepatocellular carcinoma with right adrenal gland metastasis having an inferior vena cava tumor thrombus: a case report

Por Igarashi, Takamichi, Harimoto, Norifumi, Matsumura, Nozomi, Sugiyama, Masaya, Araki, Kenichiro, Yokobori, Takehiko, Kosone, Takashi, Takagi, Hitoshi, Aishima, Shinichi, Yokoo, Hideaki, Shirabe, Ken
Publicado no Surg Case Rep (2019)

Validation and comparison of two NGS assays for the detection of EGFR T790M resistance mutation in liquid biopsies of NSCLC patients

Por Vollbrecht, Claudia, Lehmann, Annika, Lenze, Dido, Hummel, Michael
Publicado no Oncotarget (2018)

Plasma Predictive Features in Treating EGFR-Mutated Non-Small Cell Lung Cancer

Por Steendam, Christi M. J., Veerman, G. D. Marijn, Pruis, Melinda A., Atmodimedjo, Peggy, Paats, Marthe S., van der Leest, Cor, von der Thüsen, Jan H., Yick, David C. Y., Oomen-de Hoop, Esther, Koolen, Stijn L. W., Dinjens, Winand N. M., van Schaik, Ron H. N., Mathijssen, Ron H. J., Aerts, Joachim G. J. V., Dubbink, Hendrikus Jan, Dingemans, Anne-Marie C.
Publicado no Cancers (Basel) (2020)

KRAS Mutation Detection in Non-small Cell Lung Cancer Using a Peptide Nucleic Acid-Mediated...

Por Lee, Boram, Lee, Boin, Han, Gangmin, Kwon, Mi Jung, Han, Joungho, Choi, Yoon-La
Publicado em 2014

Small Cell Lung Cancer Transformation as a Resistance Mechanism to Osimertinib in Epidermal Growth...

Por Leonetti, Alessandro, Minari, Roberta, Mazzaschi, Giulia, Gnetti, Letizia, La Monica, Silvia, Alfieri, Roberta, Campanini, Nicoletta, Verzè, Michela, Olivani, Andrea, Ventura, Luigi, Tiseo, Marcello
Publicado no Front Oncol (2021)

Identification of small segmental translocations in patients with repeated implantation failure...

Por Ou, Jian, Wang, Wei, Feng, Tao, Liao, Lianming, Meng, Qingxia, Zou, Qinyan, Ding, Jie, Zheng, Aiyan, Duan, Chengying, Li, Peipei, Liu, Qiang, Lin, Chunhua, Li, Hong
Publicado no Mol Cytogenet (2015)

Ultra-deep next-generation sequencing of plasma cell-free DNA in patients with advanced lung cancers: results from the Actionable Genome Consortium

Por Li, B T, Janku, F, Jung, B, Hou, C, Madwani, K, Alden, R, Razavi, P, Reis-Filho, J S, Shen, R, Isbell, J M, Blocker, A W, Eattock, N, Gnerre, S, Satya, R V, Xu, H, Zhao, C, Hall, M P, Hu, Y, Sehnert, A J, Brown, D, Ladanyi, M, Rudin, C M, Hunkapiller, N, Feeney, N, Mills, G B, Paweletz, C P, Janne, P A, Solit, D B, Riely, G J, Aravanis, A, Oxnard, G R
Publicado no Ann Oncol (2019)

WISECONDOR: detection of fetal aberrations from shallow sequencing maternal plasma based on a within-sample comparison scheme

Por Straver, Roy, Sistermans, Erik A., Holstege, Henne, Visser, Allerdien, Oudejans, Cees B. M., Reinders, Marcel J. T.
Publicado em 2014

Expanding the clinical and molecular findings in RASA1 capillary malformation-arteriovenous malformation

Por Wooderchak-Donahue, Whitney L., Johnson, Peter, McDonald, Jamie, Blei, Francine, Berenstein, Alejandro, Sorscher, Michelle, Mayer, Jennifer, Scheuerle, Angela E., Lewis, Tracey, Grimmer, J. Fredrik, Richter, Gresham T., Steeves, Marcie A., Lin, Angela E., Stevenson, David A., Bayrak-Toydemir, Pinar
Publicado no Eur J Hum Genet (2018)

Genomic profiling in ovarian cancer retreated with platinum based chemotherapy presented homologous recombination deficiency and copy number imbalances of CCNE1 and RB1 genes

Por da Costa, Alexandre A. B. A., do Canto, Luisa M., Larsen, Simon Jonas, Ribeiro, Adriana Regina Gonçalves, Stecca, Carlos Eduardo, Petersen, Annabeth Høgh, Aagaard, Mads M., de Brot, Louise, Baumbach, Jan, Baiocchi, Glauco, Achatz, Maria Isabel, Rogatto, Silvia Regina
Publicado no BMC Cancer (2019)