Results 191 to 200 of about 1,295,297 (304)

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

open access: yesMolecular 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   +15 more
wiley   +1 more source

Genomic selection and genetic gain for nut yield in an Australian macadamia breeding population. [PDF]

open access: yesBMC Genomics, 2021
O'Connor KM   +5 more
europepmc   +1 more source

Soybean: Genetic Gain × Fertilizer Nitrogen Interaction

open access: yesKansas Agricultural Experiment Station Research Reports, 2017
O. Ortez   +4 more
openaire   +2 more sources

Peroxidasin enables melanoma immune escape by inhibiting natural killer cell cytotoxicity

open access: yesMolecular Oncology, EarlyView.
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

Realized genetic gain for yield and yield attributes in groundnut breeding at ICRISAT from an ERA trial. [PDF]

open access: yesFront Plant Sci
Behera PP   +16 more
europepmc   +1 more source

Heritability and Genetic Gain in Maize

open access: yesANBAR JOURNAL OF AGRICULTURAL SCIENCES, 2010
Benan H. Hadi, Karyma M. Wuhaib
openaire   +1 more source

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

open access: yesMolecular 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   +10 more
wiley   +1 more source

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