Results 261 to 270 of about 191,348 (320)
A century of theories of balancing selection
ABSTRACT Traits that affect organismal fitness are often highly genetically variable. This genetic variation is vital for populations to adapt to their environments, but it is also surprising given that nature – after all – ‘selects’ the best genotypes at the expense of those that fall short.
Filip Ruzicka +10 more
wiley +1 more source
<i>DLGAP5</i> mutations Disrupt Normal Chromosome Segregation and Spindle Formation of human Oocyte Meiosis and Lead to Female Infertility. [PDF]
Wang M +8 more
europepmc +1 more source
MASTL drives hepatocellular carcinoma (HCC) progression and paclitaxel resistance by triggering mitotic catastrophe. Depletion of MASTL induces DNA damage and promotes mitotic catastrophe, leading to cell death in HCC. MASTL‐mediated mitotic catastrophe depends on PP2A‐B55α activity, suggesting a novel therapeutic target for overcoming chemotherapy ...
Ke Wang +4 more
wiley +1 more source
Chk2 sustains PLK1 activity in mitosis to ensure proper chromosome segregation. [PDF]
Black EM +7 more
europepmc +1 more source
SPB-associated Atg11 ensures high-fidelity chromosome segregation in budding yeast.
Md. Hashim Reza (18271476) +7 more
openalex +1 more source
Molecular Landscape in Limb Anomalies: Diagnostic Yield and New Candidate Genes
In 132 individuals with limb anomalies, diagnostic yield was 36% (47/132), including 25 novel variants, three cases with new phenotypes, and two candidate loci, HOXA11 and a small 2q31.1 deletion. Mouse data and exome‐wide analysis, key in identifying the candidate loci, represent an important opportunity for gene discovery.
Akram Mokhtari +7 more
wiley +1 more source
Coordination of cell division and chromosome segregation by iron and a sRNA in Escherichia coli. [PDF]
Ng Kwan Lim E +4 more
europepmc +1 more source
MAP1B Variants Disrupt Neuronal Migration: Insights From Three Novel Families
Pathogenic variants in MAP1B have recently emerged as a cause of neurodevelopmental disorders characterized by intellectual disability, epilepsy, and cortical malformations, including periventricular nodular heterotopia (PVNH) and polymicrogyria (PMG).
Jessica Archer +4 more
wiley +1 more source

