1
Execution of apoptosis in higher eukaryotes is apparently more complicated than in nematodes.
2
Cyclin-dependent kinases regulate the cell cycle and transcription in higher eukaryotes.
3
Chromosome organization in higher eukaryotes controls gene expression, DNA replication, and DNA repair.
4
The mechanisms that couple translation and protein processing are poorly understood in higher eukaryotes.
5
Our findings suggest that physiological ER load regulates a developmental decision in higher eukaryotes.
6
In higher eukaryotes, replication program specification in different cell types remains to be fully understood.
7
DNA replication in higher eukaryotes initiates at thousands of origins according to a spatio-temporal program.
8
Our results show that TMEM70 is involved in mitochondrial ATP synthase biogenesis in higher eukaryotes.
9
These approaches could be adapted to identify TFs and cis regulatory elements in higher eukaryotes.
10
These findings suggest that BuGZ has evolved to facilitate Bub3 activity and chromosome congression in higher eukaryotes.
11
In higher eukaryotes, non-homologous end-joining (NHEJ) DNA is the primary pathway that repairs these breaks.
12
Enzymes belonging to this group are widely distributed in bacteria, fungi, and plants but not in higher eukaryotes.
13
Gene activation in higher eukaryotes is often under the control of regulatory elements quite distant from their target promoters.
14
The results are discussed within the context of the current understanding of NE structure and function in higher eukaryotes.
15
Long non-coding RNAs (lncRNAs) are emerging as important players in regulation of gene expression in higher eukaryotes.
16
The regulatory light chain, in contrast to regulatory light chains of higher eukaryotes, is unable to bind divalent cations.
