Results 161 to 170 of about 10,288,978 (312)
Human genetics of Whipple's disease. [PDF]
Rosain J, Casanova JL, Bustamante J.
europepmc +1 more source
Nanosecond infrared laser (NIRL) low‐volume sampling combined with shotgun lipidomics uncovers distinct lipidome alterations in oropharyngeal squamous cell carcinoma (OPSCC) of the palatine tonsil. Several lipid species consistently differentiate tumor from healthy tissue, highlighting their potential as diagnostic markers.
Leonard Kerkhoff +11 more
wiley +1 more source
New horizons of human genetics in digestive diseases. [PDF]
Chen L, Lv G.
europepmc +1 more source
Human Genetics of Addiction: New Insights and Future Directions
D. Hancock +3 more
semanticscholar +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
Using human genetics to understand the epidemiological association between child obesity at different ages and MASLD. [PDF]
Ge Q +6 more
europepmc +1 more source
Measuring intolerance to mutation in human genetics
Z. Fuller +4 more
semanticscholar +1 more source
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

