Results 181 to 190 of about 2,836,700 (319)

Adaptive deep clustering integrating DINOv2 embeddings, graph attention, and bio-inspired optimization. [PDF]

Sci Rep
Abdrabo M, Refaat H, Abdallah M, Farouk O.   +3 more
europepmc   +1 more source

Recurrent cancer‐associated ERBB4 mutations are transforming and confer resistance to targeted therapies

Molecular Oncology, EarlyView.
We show that the majority of the 18 analyzed recurrent cancer‐associated ERBB4 mutations are transforming. The most potent mutations are activating, co‐operate with other ERBB receptors, and are sensitive to pan‐ERBB inhibitors. Activating ERBB4 mutations also promote therapy resistance in EGFR‐mutant lung cancer.
Veera K. Ojala, Sini Ahonen, Sara Peltola, Aura Tuohisto‐Kokko, Olaya Esparta, Peppi Suominen, Anne Jokilammi, Iman Farahani, Deepankar Chakroborty, Nikol Dibus, Steffen Boettcher, Tomi T. Airenne, Mark S. Johnson, Lisa D. Eli, Klaus Elenius, Kari J. Kurppa   +15 more
wiley   +1 more source

Four Biomarkers Linked to Activation of Cluster of Differentiation 8–Positive Lymphocytes Predict Clinical Outcomes in Pediatric Acute Liver Failure

, 2020
Mike A. Leonis, Alexander Miethke, Lin Fei, Sean Maynor, Catherine A. Chapin, Jacob J. Bleesing, Estella M. Alonso, Robert H. Squires, for the Pediatric Acute Liver Failure Study Group   +8 more
openalex   +2 more sources

Magnetic mirror structures observed by Cluster in the magnetosheath [PDF]

, 2003
D. Constantinescu, K. Glassmeier, R. A. Treumann, K.‐H. Fornaçon   +3 more
openalex   +1 more source

PyamilySeq: exposing the fragility of conventional gene (re)clustering and prokaryotic pangenomic inference methods. [PDF]

NAR Genom Bioinform
Dimonaco NJ.
europepmc   +1 more source

Crucial parameters for precise copy number variation detection in formalin‐fixed paraffin‐embedded solid cancer samples

Molecular Oncology, EarlyView.
This study shows that copy number variations (CNVs) can be reliably detected in formalin‐fixed paraffin‐embedded (FFPE) solid cancer samples using ultra‐low‐pass whole‐genome sequencing, provided that key (pre)‐analytical parameters are optimized.
Hanne Goris, Vasiliki Siozopoulou, Léon C van Kempen, Anne Sieben, Ella Roelant, Stig Hellemans, Elyne Backx, Laure Sorber, Koen De Winne, Senada Koljenović, Karen Zwaenepoel   +10 more
wiley   +1 more source

A consistent approach to falsifying ΛCDM with rare galaxy clusters [PDF]

, 2013
Ian Harrison, Shaun Hotchkiss
openalex   +1 more source

Robust subspace structure discovery for cell type identification in scRNA-seq data. [PDF]

BMC Bioinformatics
Zhou X, Wei X, Liu C, Shen W, Xuan P, Wu S, Wong HS.   +6 more
europepmc   +1 more source

Phenotypic and genotypic characterization of single circulating tumor cells in the follow‐up of high‐grade serous ovarian cancer

Molecular Oncology, EarlyView.
Single circulating tumor cells (sCTCs) from high‐grade serous ovarian cancer patients were enriched, imaged, and genomically profiled using WGA and NGS at different time points during treatment. sCTCs revealed enrichment of alterations in Chromosomes 2, 7, and 12 as well as persistent or emerging oncogenic CNAs, supporting sCTC identity.
Carolin Salmon, Rui P. L. Neves, Nikolas H. Stoecklein, Sven‐Thorsten Liffers, Jens Siveke, Jan D. Kuhlmann, Pauline Wimberger, Paul Buderath, Rainer Kimmig, Sabine Kasimir‐Bauer   +9 more
wiley   +1 more source

Big Data-Driven Feature Extraction and Clustering Based on Statistical Methods

, 2020
Venkata Rao Maddumala, R. Arunkumar
openalex   +2 more sources