Development of Publicly Available Forensic DNA Sequence Mixture Data. [PDF]
Romsos EL +8 more
europepmc +1 more source
Successful treatment of multifocal pedalPrototheca wickerhamiiinfection in a feline immunodeficiency virus-positive cat with multiple Bowenoid in situ carcinomas containing papillomaviral DNA sequences [PDF]
Allan Kessell +5 more
openalex +1 more source
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 +15 more
wiley +1 more source
The complete mitochondrial DNA sequence of the <i>Pentalagus furnessi</i> (Lagomorpha: Leporidae), an endemic species of Amami Ōshima, Japan. [PDF]
Tsubota M +4 more
europepmc +1 more source
Identification of sequence variants in key vitamin E genes from Elaeis guineensis Jacq. germplasm for development of DNA-based markers [PDF]
Babura Sulaiman Rufa'i
openalex
Peroxidasin enables melanoma immune escape by inhibiting natural killer cell cytotoxicity
Peroxidasin (PXDN) is secreted by melanoma cells and binds the NK cell receptor NKG2D, thereby suppressing NK cell activation and cytotoxicity. PXDN depletion restores NKG2D signaling and enables effective NK cell–mediated melanoma killing. These findings identify PXDN as a previously unrecognized immune evasion factor and a potential target to improve
Hsu‐Min Sung +17 more
wiley +1 more source
A Feature Engineering Method for Whole-Genome DNA Sequence with Nucleotide Resolution. [PDF]
Wang T +8 more
europepmc +1 more source
Fetal Alz-50 Clone 1, a Novel Zinc Finger Protein, Binds a Specific DNA Sequence and Acts as a Transcriptional Regulator [PDF]
Kelly L. Jordan‐Sciutto +3 more
openalex +1 more source
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 +10 more
wiley +1 more source

