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Stimulation of either nucleus by electrode or serotonin agonist yields equivalent effects on circadian rhythmicity.
Tract tracer studies revealed cells in the DR that project to the MnR, as well as cells in the MnR that project to the DR. Double label immunofluorescence methods demonstrated that some of the cells projecting from either nucleus to the other contain serotonin immunoreactivity.
Since both YFP positive and negative neurons were added to the vagal and pectoral motoneuron pool from 2 to 20 dpf (Table S4), recruitment to either nucleus was not hoxb4a dependent.
This low occurrence of the hues, and the different hue in either nucleus and membrane of the cell, made analysis of the random expression of these 12 fluorophores sufficient to discriminate clonal relationships.
Nub immunostaining was not restricted in its subcellular localization to either nucleus or cytoplasm, instead its nuclear-cytoplasmic localization varied in different regions of these tissues, possibly reflecting alternative states of transcriptional regulation.
There is controversy regarding the localization of BRCA1 and BRCA2 proteins to either nucleus or cytoplasm and whether the expression is present in premeiotic germ cells or can still be expressed in mitotic spermatogonia.
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Mitochondrial transcription is controlled by nucleus-encoded transcription regulators that localize to either the nucleus or the mitochondrion.
Mitotic SA, kar9Δ and dyn1Δ cells exhibited abnormal features with either a nucleus improperly located (20 %, 41 %, 13 respectively) or two nuclei in the mother cell (16%, 10% and 47%, respectively).
In our conclusion, we raised two possible explanations: either the nucleus is active or the mRNAs are imported into the nucleus at stage 9.
Inspection of 4-nucleate asci revealed that, whereas in the wild type, 96% (n = 104) contained four nuclei of equal sizes, in the mutant only 71% (n = 179) had normal nuclei and the remainder featured either four nuclei of different sizes (20%), 1 3 nuclei (4%) or a completely abnormal distribution of DNA masses.
Participants: One hundred consecutive patients with either herniated nucleus pulposus (HNP) or lumbar spinal stenosis (LSS).
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