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And, in cell culture in the laboratory, cells can change shape or may lose specific properties such as protein expression—which processes are also termed dedifferentiation. [ 17 ] Some hypothesize that dedifferentiation is an aberration that likely results in cancers , [ 18 ] but others explain it as a natural part of the immune response that ...
Above is a ball-and-stick model of the inorganic phosphate molecule (H PO 4 2−).Colour coding: P (orange); O (red); H (white). The chemical activity of a protein kinase involves removing a phosphate group from ATP and covalently attaching it to one of three amino acids that have a free hydroxyl group.
The chaperone-mediated autophagy (CMA) protein quality assurance by digesting oxidized and altered proteins under stressful circumstances and supplying amino acids through protein denaturation. [39] Autophagy is the primary intrinsic degradative system for peptides, fats, carbohydrates, and other cellular structures.
Palmitoyl-protein thioesterase 1 (PPT-1), also known as palmitoyl-protein hydrolase 1, is an enzyme that in humans is encoded by the PPT1 gene. [5] [6] [7] Function
3D rendering of centrioles showing the triplets. In cell biology a centriole is a cylindrical organelle composed mainly of a protein called tubulin. [1] Centrioles are found in most eukaryotic cells, but are not present in conifers (), flowering plants (angiosperms) and most fungi, and are only present in the male gametes of charophytes, bryophytes, seedless vascular plants, cycads, and Ginkgo.
Cell synchronization is a process by which cells in a culture at different stages of the cell cycle are brought to the same phase. Cell synchrony is a vital process in the study of cells progressing through the cell cycle as it allows population-wide data to be collected rather than relying solely on single-cell experiments.
Flower differentiation is a plant process by which the shoot apical meristem changes its anatomy to generate a flower or inflorescence in lieu of other structures. Anatomical changes begin at the edge of the meristem, generating first the outer whorls of the flower - the calyx and the corolla, and later the inner whorls of the flower, the androecium and gynoecium.
In 1903, Nikolai K. Koltsov proposed that the shape of cells was determined by a network of tubules that he termed the cytoskeleton. The concept of a protein mosaic that dynamically coordinated cytoplasmic biochemistry was proposed by Rudolph Peters in 1929 [12] while the term (cytosquelette, in French) was first introduced by French embryologist Paul Wintrebert in 1931.