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Fluorescence microscopy is a promising technique for bridging this phase gap.
As a result of the sensitivity and inherent limitations of each spectroscopic approach, several problems are still unaccounted for (e.g. pressure gap, materials gap and phase gap).
The instantaneous phases of the p th and the q th harmonic partials belonging to the same source are approximately proportional with ratio p/q, except an initial phase gap, ϕ0.
The eukaryotic cell cycle can be divided into a gap 1 (G1) phase, DNA synthesis (S) phase, gap 2 (G2) phase and mitotic (M) phase (Fig. 1).
The cycle of eukaryotic cells consists of four phases: G1 phase (gap 1, between mitosis and initiation of DNA replication), S phase while DNA replication begins, and G2 phase (gap 2) during which cell growth is in progress and proteins are synthesized for the next mitosis (M phase) [ 61].
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Layover and shadow distortions were not found along these phase gaps.
Then phase gaps must have not been due to DTM error.
From their facts, obtained phase gaps must be actual surface deformations not noises.
Furthermore, phase gaps were detected in all InSAR pairs that include this area (Additional file 1).
Because there are more slices obtained in the diastole phase, gaps between slices in 2D (3 mm) will increase the measurement error, especially around apical and basal slices.
The Forkhead transcription factor Hcm1 regulates chromosome segregation genes and fills the S-phase gap in the transcriptional circuitry of the cell cycle.
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