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Nuclear envelope

Nuclear Pore A large transporter that spans the nuclear envelope (nuclear membrane). This... [Pg.162]

Breakup of nuclear envelope Nuclear fragmentation Blebbing... [Pg.925]

Nuclear envelope, nuclear pore complex and RNP translocation Phospholipids and lysophospholipids (liposomes, micelles, and lipid polymorphism)... [Pg.3117]

The electron-spm echo envelope modulation (ESEEM) phenomenon [37, 38] is of primary interest in pulsed EPR of solids, where anisotropic hyperfme and nuclear quadnipole interactions persist. The effect can be observed as modulations of the echo intensity in two-pulse and three-pulse experiments in which x or J is varied. In liquids the modulations are averaged to zero by rapid molecular tumbling. The physical origin of ESEEM can be understood in tenns of the four-level spin energy diagram for the S = I = model system... [Pg.1578]

Nuclear power plant systems may be classified as "Frontline" and "Support. . iccurding to their. service in an accident. Frontline systems are the engineered safety systems that deal directly with an accident. Support systems support the frontline systems. Accident initiators are broadly grouped as loss of cooling accidents (LOCAs) or transients. In a LOCA, water cooling the reactor is lost by failure of the cooling envelope. These are typically classified as small-small (SSLOCA), smalt (SLOCA), medium (MLOCA) and large (LLOCA). [Pg.211]

A transient, is a passing event which may upset the reactor operation but does not physically damage the primary cooling envelope. Table 6.1-1 lists PWR transient initiating events that ha c been used in PRA preparation. Typical frontline systems that mitigate LOCAs and transients for a PWR are presented in Table 6.1-2. The frontline systems must be supported by support systems interactions between both are presented in Table 6.1 -3 for ANO-1 (Arkansas Nuclear Unit 1). [Pg.211]

In nuclear magnetic resonance (NMR) spectra the protons of the oxirane ring are usually shifted out of the steroid methylene envelope. Tori et al have tabulated the relationships of the angular methyl proton resonances and the oxirane proton signals with respect to location and configuration of the oxirane group. [Pg.19]

Nucleus The nucleus is separated from the cytosol by a double membrane, the nuclear envelope. The DNA is complexed with basic proteins (histones) to form chromatin fibers, the material from which chromosomes are made. A distinct RNA-rich region, the nucleolus, is the site of ribosome assembly. The nucleus is the repository of genetic information encoded in DNA and organized into chromosomes. During mitosis, the chromosomes are replicated and transmitted to the daughter cells. The genetic information of DNA is transcribed into RNA in the nucleus and passes into the cytosol where it is translated into protein by ribosomes. [Pg.27]

The nucleus, nucleolus, and nuclear envelope of plant cells are like those of animal cells. [Pg.29]

The activated CDKl-cyclin B kinase finally phosphor-ylates a large number of proteins most of which are not well characterized, leading to chromosome condensation, nuclear envelope breakdown, spindle assembly, and chromosome segregation. [Pg.342]

When cells enter mitosis, the interphase array of MTs is dismantled. The centrosome duplicates, and the daughters move to opposite poles of the nucleus. After disassembly of the nuclear envelope, MTs emanat-... [Pg.415]

A system of membrane enclosed cisternae in the cytoplasm. The ER is continuous with the outer membrane of the nuclear envelope. The part of the ER coated with ribosomes is called rough ER, the other part is called smooth-surfaced ER. The rough ER is the first compartment of the secretory pathway. Here, membrane proteins are integrated into and secretory proteins translocated across the ER membrane. Furthermore,... [Pg.469]

The phase of the cell cycle where the sister chromatids are separated and distributed onto two daughter nuclei. First, upon entry into mitosis the chromosomes are condensed followed by the breakdown of the nuclear-envelope (prophase). The two centrosomes are separated and induce the formation of the mitotic spindle. Then, the chromosomes are captures by the spindle and aligned on the metaphase plate (metaphase). The sister-chromatids are separated and pulled to the poles of the spindle (anaphase). In telophase, two new nuclei are formed around the separated chromatids. [Pg.776]

The nuclear pore complex, located in the nuclear envelope, contains more than 50 proteins. It allows diffusion of small proteins between cytoplasm and nucleoplasm. Larger molecules (>50kD) are selectively transported by an energy-dependent mechanism. [Pg.889]

In terms of evolutionary biology, the complex mitotic process of higher animals and plants has evolved through a progression of steps from simple prokaryotic fission sequences. In prokaryotic cells, the two copies of replicated chromosomes become attached to specialized regions of the cell membrane and are separated by the slow intrusion of the membrane between them. In many primitive eukaryotes, the nuclear membrane participates in a similar process and remains intact the spindle microtubules are extranuclear but may indent the nuclear membrane to form parallel channels. In yeasts and diatoms, the nuclear membrane also remains intact, an intranuclear polar spindle forms and attaches at each pole to the nuclear envelope, and a single kinetochore microtubule moves each chromosome to a pole. In the cells of higher animals and plants, the mitotic spindle starts to form outside of the nucleus, the nuclear envelope breaks down, and the spindle microtubules are captured by chromosomes (Kubai, 1975 Heath, 1980 Alberts et al., 1989). [Pg.20]

Lazo ND, Meine JG, Downing DT (1995) Lipids are covalently attached to rigid corneocyte protein envelope existing predominantly as beta-sheets a solid state nuclear magnetic resonance study. J Invest Dermatol 105 296-300... [Pg.29]

A question of practical interest is the amount of electrolyte adsorbed into nanostructures and how this depends on various surface and solution parameters. The equilibrium concentration of ions inside porous structures will affect the applications, such as ion exchange resins and membranes, containment of nuclear wastes [67], and battery materials [68]. Experimental studies of electrosorption studies on a single planar electrode were reported [69]. Studies on porous structures are difficult, since most structures are ill defined with a wide distribution of pore sizes and surface charges. Only rough estimates of the average number of fixed charges and pore sizes were reported [70-73]. Molecular simulations of nonelectrolyte adsorption into nanopores were widely reported [58]. The confinement effect can lead to abnormalities of lowered critical points and compressed two-phase envelope [74]. [Pg.632]

Riedel A, S Fetzner, M Rampp, F Lingens, U Liebl, J-L Zrmmermann, W Nitschke (1995) EPR, electron spin echo envelope modulation, and electron nuclear double resonance studies of the 2Ee-2S centers of the 2-halobenzoate 1,2-dioxygenase from Burkholderia (Pseudomonas) cepacia 2CBS. J Biol Chem 270 30869-30873. [Pg.293]

NFS spectra recorded at 300 K for -cut and c-cut crystals are shown in Fig. 9.17 [48]. The/factors for the two orientations were derived from the speed-up of the nuclear decay (i.e., from the slope of the time-dependent intensity in Fig. 9.17a and from the slope of the envelope in Fig. 9.17b). The factors obtained f ( P = 0.122 (10) and f = 0.206(10) exhibit significant anisotropic vibrational behavior of iron in GNP. This anisotropy in f is the reason for the observed asymmetry in the line intensity of the quadrupole doublet (in a conventional Mossbauer spectrum in the energy domain) of a powder sample of GNP caused by the Goldanskii-Karyagin effect [49]. [Pg.495]

Hunt Normally cyclin A goes away very early in mitosis—almost as soon as the nuclear envelope breaks down. If it doesn t go away, what seems to happen is that the spindle doesn t organize itself properly, yet it goes through anaphase. It is peculiar the spindles look horrible. These are spindles with both cyclin A and cyclin B. The cyclin A seems to be necessary to get it up to that point, but then you need to get rid of it in order for the cyclin B to take over. [Pg.153]


See other pages where Nuclear envelope is mentioned: [Pg.24]    [Pg.350]    [Pg.162]    [Pg.53]    [Pg.807]    [Pg.24]    [Pg.350]    [Pg.162]    [Pg.53]    [Pg.807]    [Pg.219]    [Pg.235]    [Pg.27]    [Pg.582]    [Pg.686]    [Pg.686]    [Pg.1164]    [Pg.160]    [Pg.151]    [Pg.110]    [Pg.338]    [Pg.99]    [Pg.236]    [Pg.238]    [Pg.9]    [Pg.13]    [Pg.30]    [Pg.60]    [Pg.64]    [Pg.86]    [Pg.218]   
See also in sourсe #XX -- [ Pg.6 ]

See also in sourсe #XX -- [ Pg.346 ]




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