Results 81 to 90 of about 204,536 (259)
Sexual Selection in a Brentid Weevil [PDF]
In most insects, differences between the sexes involve not only primary characters necessary for gamete production, copulation, and oviposition, but also sexual structures and behaviors involved in the acquisition of mates. The most striking of these secondary characters, such as exaggerated size, weaponry, or coloration, tend to occur in males, and ...
openaire +2 more sources
Pair‐wise comparison of the CellSearch and FETCH enrichment technologies for circulating tumor cells (CTCs) from metastatic breast, prostate, and small cell lung cancer patients shows an increased capture of CTCs using FETCH enrichment. The clinical implementation of circulating tumor cells (CTCs) as a predictive tool for therapy efficacy in the ...
Michiel Stevens +6 more
wiley +1 more source
The Handicap Principle in Sexual Selection [PDF]
The theory of the selection of epigamic color, structure and behavior was originally due to Darwin (1874) and was later elaborated by Fisher (1930) and by O'Donald (1962, 1963, 1967). It is well known and is discussed below. An alternative account of this type of sexual selection has been suggested recently by Zahavi (1975).
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The novel styrylquinazolinone‐based molecule W1B effectively suppresses glioblastoma by inhibiting IGF1R and EGFR. In high‐glucose microenvironments driving tumor resistance, W1B acts synergistically with the EGFR inhibitor dacomitinib. This combination safely blocks compensatory survival signaling in zebrafish xenograft models. Showcasing promising in
Patryk Rurka +9 more
wiley +1 more source
Primate brain architecture and selection in relation to sex
Background Social and competitive demands often differ between the sexes in mammals. These differing demands should be expected to produce variation in the relative sizes of various brain structures.
Nunn Charles L +2 more
doaj +1 more source
Circulating microRNAs as biomarkers of cachexia and sex‐specific cancer in senior dogs. In 25 client‐owned dogs, four circulating miRNAs (miR‐15a, miR‐15b, miR‐16, miR‐140) were downregulated in cachexia, with miR‐16 the strongest individual biomarker (AUC = 0.899).
Soon‐Seok Park +6 more
wiley +1 more source
Rapid male plumage evolution drives sexual dichromatism in Ficedula flycatchers
Sexual dichromatism represents a major form of phenotypic differentiation between the sexes in birds, and its evolution is likely shaped by the interplay between sexual and natural selection.
Lijun Gao +3 more
doaj +1 more source
LUNAR is a liver‐specific long noncoding RNA (lncRNA) that is highly expressed in normal liver but becomes epigenetically silenced in hepatocellular carcinoma through promoter hypermethylation. Loss of LUNAR is associated with NOTCH activation, epithelial–mesenchymal transition, and metastasis, whereas restoring LUNAR restrains metastatic progression ...
Se Ha Jang +9 more
wiley +1 more source
Tumour heterogeneity and clonal evolution of metastatic salivary gland cancer were evaluated in two patients with adenoid carcinoma and one patient with myoepithelial carcinoma. Radiology‐guided autopsy enabled multi‐region sampling (total samples n = 149), followed by whole‐genome sequencing and phylogenetic reconstruction (17 tumour samples, 4–7 per ...
Gerben Lassche +10 more
wiley +1 more source
Sexual dimorphism evolves when selection favors different phenotypic optima between the sexes. Such sexually antagonistic selection creates intralocus sexual conflict when traits are genetically correlated between the sexes and have sex‐specific optima ...
Mary C. Duryea +3 more
doaj +1 more source

