Resultados da pesquisa - (( a small compared case ngs ) OR ((( j nayl clamp j nowe ) OR ( j gram camp can ngsc ))))

Pesquisas alternativas:
nayl » nayla (Expandir a Pesquisa), natl (Expandir a Pesquisa), nail (Expandir a Pesquisa)
nowe » now (Expandir a Pesquisa), none (Expandir a Pesquisa), node (Expandir a Pesquisa)
camp » cam (Expandir a Pesquisa), cap (Expandir a Pesquisa), came (Expandir a Pesquisa)
ngsc » ngoc (Expandir a Pesquisa), ngc (Expandir a Pesquisa), ngsp (Expandir a Pesquisa)

1

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

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)

“... (NGS). This mutation is activating, drives downstream signaling comparable to FLT-3/ITD, and can...”
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2

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

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)

“... efficiently incorporates raw NGS metrics into a statistical discrimination platform to identify functional...”
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3

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

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)

Assuntos: “...Case Report...”
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4

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

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)

“... status of the genes of interest with a more sensitive analysis method to avoid the presence of a small...”
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5

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

Assuntos: “...NGS...”
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6

Phylogeography and hybridization of corvid birds in the Palearctic Region

Phylogeography and hybridization of corvid birds in the Palearctic Region

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

“... the eastern part of the distribution range of the carrion crow. NGS resulted in a clear pattern...”
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7

Clinical feasibility of NGS liquid biopsy analysis in NSCLC patients

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)

“... by the NGS approach in NSCLC patients analyzed at diagnosis. In 36 cases with paired tissue available a high...”
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8

Cost-effectiveness analysis comparing companion diagnostic tests for EGFR, ALK, and ROS1 versus next-generation sequencing (NGS) in advanced adenocarcinoma lung cancer patients

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)

“... cases as well as extra costs attributed to the molecular testing. The ICER comparing NGS with sequential...”
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9

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

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

Assuntos: “...NGS...”
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10

Brigatinib versus other second-generation ALK inhibitors as initial treatment of anaplastic lymphoma kinase positive non-small cell lung cancer with deep phenotyping: study protocol of the ABP trial

Brigatinib versus other second-generation ALK inhibitors as initial treatment of anaplastic lymphoma kinase positive non-small cell lung cancer with deep phenotyping: study protocol of the ABP trial

Por Christopoulos, Petros, Bozorgmehr, Farastuk, Brückner, Lena, Chung, Inn, Krisam, Johannes, Schneider, Marc A., Stenzinger, Albrecht, Eickhoff, Regina, Mueller, Daniel W., Thomas, Michael
Publicado no BMC Cancer (2021)

“... and the perspective of a “chronic disease” will be distinguished from “high-risk” cases, molecular properties of which...”
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11

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

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)

Assuntos: “...Case Reports...”
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12

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

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)

Assuntos: “...Case Report...”
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13

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

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)

“..., for mutations with low allelic frequencies the use of NGS panels with UMI facilitates a more sensitive...”
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14

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

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)

“...) concomitant TP53 mutation at baseline, PFS was significantly shorter compared to six wild-type cases; 8.8 vs...”
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15

KRAS Mutation Detection in Non-small Cell Lung Cancer Using a Peptide Nucleic Acid-Mediated Polymerase Chain Reaction Clamping Method and Comparative Validation with Next-Generation Sequencing

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

“... chemotherapy, so there is now a focus on targeting KRAS-mutated NSCLCs. A feasible mutation detection method...”
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16

Small Cell Lung Cancer Transformation as a Resistance Mechanism to Osimertinib in Epidermal Growth Factor Receptor-Mutated Lung Adenocarcinoma: Case Report and Literature Review

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)

“...Introduction: Small cell lung cancer (SCLC) transformation represents a mechanism of resistance...”
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17

Identification of small segmental translocations in patients with repeated implantation failure and recurrent miscarriage using next generation sequencing after in vitro fertilization/intracytoplasmic sperm injection

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)

Assuntos: “...Case Report...”
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18

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

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)

“... was carried out in a subset of cases. RESULTS: In 127 assessable patients, plasma NGS detected driver...”
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19

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

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

“...-generation sequencing (NGS) because a small percentage of fetal DNA is present in maternal plasma. However...”
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20

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

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)

“... (NGS) and array-comparative genomic hybridization (aCGH). Sixty individuals had a deleterious RASA1...”
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