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adult; animals; cos cells; cercopithecus aethiops; child; family; female; genetic predisposition to disease; hela cells; hemiplegia; high-throughput nucleotide sequencing; humans; male; models, biological; pedigree; protein structure, secondary; sodium-potassium-exchanging atpase; mutation; genetics (1) 1
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analysis of variance, base sequence, exome, hemangiosarcoma, human umbilical vein endothelial cells, humans, molecular sequence data, mutation, neovascularization, pathologic, phospholipase c gamma, rna interference, receptor-like protein tyrosine phosphatases, class 3, sequence analysis, rna, vascular endothelial growth factor a (1) 1
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Nature, ISSN 0028-0836, 03/2010, Volume 464, Issue 7287, pp. 405 - 408
Journal Article
NATURE COMMUNICATIONS, ISSN 2041-1723, 07/2019, Volume 10, Issue 1, pp. 2978 - 10
There has been a dramatic increase in the detection of lung nodules, many of which are preneoplasia atypical adenomatous hyperplasia (AAH), adenocarcinoma in... 
NODULES | PATTERN | LANDSCAPE | MULTIDISCIPLINARY SCIENCES | INTRATUMOR HETEROGENEITY | RISK | MUTATIONS | SELECTION | CANCER | Adenocarcinoma | Carcinogens | Transformation | Lung nodules | Invasiveness | Hyperplasia | Evolution | Nucleotides | Mutation | Carcinogenesis | Preneoplasia | Nodules | Index Medicus
Journal Article
Cancer Discovery, ISSN 2159-8274, 10/2017, Volume 7, Issue 10, pp. 1088 - 1097
Journal Article
npj Genomic Medicine, ISSN 2056-7944, 12/2017, Volume 2, Issue 1, pp. 1 - 11
Appreciation for genomic and immune heterogeneity in cancer has grown though the relationship of these factors to treatment response has not been thoroughly... 
CTLA-4 BLOCKADE | EVOLUTION | SIGNATURES | LANDSCAPE | INTRATUMOR HETEROGENEITY | METASTASES | GENETICS & HEREDITY | ACQUIRED-RESISTANCE | RADIOMICS | CANCER | TUMOR HETEROGENEITY | Metastasis | Patients | Melanoma | Tumors
Journal Article
Journal Article
by Heinzen, Erin L and Swoboda, Kathryn J and Hitomi, Yuki and Gurrieri, Fiorella and De Vries, Boukje and Tiziano, F. Danilo and Fontaine, Bertrand and Walley, Nicole M and Heavin, Sinéad and Panagiotakaki, Eleni and Fiori, Stefania and Abiusi, Emanuela and Di Pietro, Lorena and Sweney, Matthew T and Newcomb, Tara M and Viollet, Louis and Huff, Chad and Jorde, Lynn B and Reyna, Sandra P and Murphy, Kelley J and Shianna, Kevin V and Gumbs, Curtis E and Little, Latasha and Silver, Kenneth and Ptáček, Louis J and Haan, Joost and Ferrari, Michel D and Bye, Ann M and Herkes, Geoffrey K and Whitelaw, Charlotte M and Webb, David and Lynch, Bryan J and Uldall, Peter and King, Mary D and Scheffer, Ingrid E and Neri, Giovanni and Arzimanoglou, Alexis and Van Den Maagdenberg, Arn M.J.M and Sisodiya, Sanjay M and Mikati, Mohamad A and Goldstein, David B and Koelewijn, Stephany and Kamphorst, Jessica and Geilenkirchen, Marije and Pelzer, Nadine and Ferrari, Michel and Van Den Maagdenberg, Arn and Zucca, Claudio and Franchini, Filippo and Vavassori, Rosaria and Giannotta, Melania and Gobbi, Giuseppe and Granata, Tiziana and Nardocci, Nardo and De Grandis, Elisa and Veneselli, Edvige and Stagnaro, Michela and Vigevano, Federico and Oechsler, Claudia and Nicole, Sophie and Ninan, Miriam and Neville, Brian and Ebinger, Friedrich and Fons, Carmen and Campistol, Jaume and Kemlink, David and Nevsimalova, Sona and Laan, Laura and Peeters-Scholte, Cacha and Casaer, Paul and Casari, Giorgio and Sange, Guenter and Spiel, Georg and Boneschi, Filippo Martinelli and Bassi, Maria Teresa and Schyns, Tsveta and Crawley, Francis and Poncelin, Dominique and European Alternating Hemiplegia and European Network Res Alternating and Biobanca Registro Clinico and European Network for Research on Alternating Hemiplegia (ENRAH) for Small and Medium-sized Enterpriese (SMEs) Consortium and European Alternating Hemiplegia of Childhood (AHC) Genetics Consortium and Biobanca e Registro Clinico per l'Emiplegia Alternante (I.B.AHC) Consortium
Nature Genetics, ISSN 1061-4036, 09/2012, Volume 44, Issue 9, pp. 1030 - 1034
Journal Article
Nature Genetics, ISSN 1061-4036, 2014, Volume 46, Issue 4, pp. 376 - 379
Journal Article
Nature Communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 2670 - 12
Journal Article
Journal of Clinical Oncology, ISSN 0732-183X, 06/2018, Volume 36, Issue 18, pp. 1788 - 1797
PurposeThe aim of the current study was to determine whether the degree of mutation clearance at remission predicts the risk of relapse in patients with acute... 
CLOFARABINE | THERAPY | ONCOLOGY | CLONAL HEMATOPOIESIS | PERSISTENCE | MONOSOMAL KARYOTYPE | FLOW-CYTOMETRY | DNMT3A MUTATIONS | MINIMAL RESIDUAL DISEASE | CANCER | ADULT | RAPID COMMUNICATION
Journal Article
Blood, ISSN 0006-4971, 11/2018, Volume 132, Issue Supplement 1, pp. 5240 - 5240
Abstract BACKGROUND: AML is a group of clinically heterogeneous diseases. We hypothesized that heterogeneous presentation of AML is a reflection of equally... 
Journal Article
Blood, ISSN 0006-4971, 11/2018, Volume 132, Issue Supplement 1, pp. 88 - 88
Abstract Introduction Increased complexity of sub-clonal architecture has been associated with poor outcome in AML (Papaemmanuil et al. NEJM 2016). Currently,... 
Journal Article