Schematic Diagrams and Service Manuals

Electronics Repair Manuals

This website allows you to find the repair manuals for any electronic devices that you could think of. You will also be able to access schematic diagrams and other useful materials for repairing electronics. You will be able to find the documents that you need to repair your TV, your DVD and VCR players, your mobile phones and cameras, and computer monitors, plus more! You will even be able to find the diagrams and repair guides for very old devices, so you don't have to worry if you think that the guide is out of print; chances are that this site will have it! You don't need to freak out now when your TV breaks down; you will be able to find the guide to repair it and have it working again in no time! Most of the guides come in easily downloadable PDF files, so you can read them on your computer, phone, or tablet! Continue reading...

Electronics Repair Manuals Summary

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Highly Recommended

I usually find books written on this category hard to understand and full of jargon. But the author was capable of presenting advanced techniques in an extremely easy to understand language.

All the modules inside this e-book are very detailed and explanatory, there is nothing as comprehensive as this guide.

Setting up the microscope for epifluorescence

The resolution of fluorescence microscopy is limited by light emitted from above and below the focal plane leading to considerable blurring of the image. Confocal microscopy is intended to achieve a high axial resolution, that is structures in the centre of a cell can be distinguished from those at the top or the bottom. Contrary to conventional microscopy, it relies on point illumination, rather than field illumination. A schematic diagram of the corresponding configurations is shown in

Components of the PSD

Fig. 1 Schematic diagram of PSD proteins. Examples of PSD proteins are shown along with their domain structures. PDZ domains are shown as gray ellipses. Other domains are indicated Actl, actin regulatory domain 1 Act2, actin regulatory domain 2 AD, association domain Ank, ankyrin repeats ArfGAP, Arf GTPase-activating protein C2, calcium lipid binding domain 2 CAM kinase, Ca2+ calmodulin-dependent kinase (CAME)-like domain CC, coiled coil domain CRIB, Cdc42 Rac-interactive binding EVH1, ENA VASP homology domain 1 GH1, GKAP homology domain 1 GK, guanylate kinase-like domain GKBD, PSD-95 GK binding domain GRKBD, GRK2 binding domain Kinase, serine threonine kinase domain L27, domain initially found in LIN2 and LIN7 PDZ, PSD-95 Dlg ZO-l domain LRR, leucine rich repeat PH, pleckstrin homology domain RapGAP, Rap GTPase-activating protein RasGAP, Ras GTPase-activating protein RCB, Rac binding domain SAM, sterile a motif SH3, Src homology 3 domain SHD, Spa2 homology domain WW, domain with two...

Targetdirected Pharmacology

A schematic diagram of the high-throughput pharmacology system developed by Axiom Biotechnologies. The open circles (O) represent valves capable of switching between buffer and sample (antagonist or agonist). The closed circles ( ) are mixing chambers for the cells and compound. Cells are preloaded with fluorescent dyes sensitive to physiological endpoints such as intracellular calcium or membrane potential. The length of the pre-incubation and incubation loops dictates the incubation times for the antagonists and agonists prior to entering the fluorescent detector. Figure 3.2. A schematic diagram of the high-throughput pharmacology system developed by Axiom Biotechnologies. The open circles (O) represent valves capable of switching between buffer and sample (antagonist or agonist). The closed circles ( ) are mixing chambers for the cells and compound. Cells are preloaded with fluorescent dyes sensitive to physiological endpoints such as intracellular calcium or membrane...

Patterning with Electrodynamic Instabilities

The generation of well-defined surface topographies on the submicron level by electrodynamic instabilities is simple and free of many harsh chemical processes. Consider the schematic diagram in Fig. 1A, we take a polymer film in a simple capacitive geometry where the thin film is spin coated onto a conducting or semiconducting surface. If a second electrode is placed over the surface of the film with an air gap, then when a voltage is applied to the two electrodes, the dielectric constant of the polymer film and the air between the film and the upper electrode define the electric fields. At the polymer film surface, there is a change in the density from that of the polymer film to air and, as such, there is a small gradient in the dielectric constant at the surface. This gradient in the dielectric constant translates into a gradient in the electric field, which, in turn, defines an

Mapping Of Activation And Repolarization

Figure 3 Maps of optical action potentials and methods of analysis. (Left to right, top to bottom) Schematic diagram of anterior epicardium of the guinea pig heart and the imaging field of view. Detection of activation and repolarization time points using first (dF dt) and second (d2F dt2) derivatives of fluorescence, F. Maps of activation and repolarization. Figure 3 Maps of optical action potentials and methods of analysis. (Left to right, top to bottom) Schematic diagram of anterior epicardium of the guinea pig heart and the imaging field of view. Detection of activation and repolarization time points using first (dF dt) and second (d2F dt2) derivatives of fluorescence, F. Maps of activation and repolarization.

Chemokines And Chemokine Receptor Biology

Schematic diagram of a two-dimensional model of a chemokine receptor. The extracellular loops (ECL), the putative helical regions that traverse the cell membrane, and the intracellular loops (ICL) are shown. The GPCR (family A) signature disulfide bridge between Cys residues of ECL1 and ECL2 is also shown. Figure 4.2. Schematic diagram of a two-dimensional model of a chemokine receptor. The extracellular loops (ECL), the putative helical regions that traverse the cell membrane, and the intracellular loops (ICL) are shown. The GPCR (family A) signature disulfide bridge between Cys residues of ECL1 and ECL2 is also shown.

Geothermal Energy Diagram

Figure Options For Storing Co2

Schematic diagram of possible CCS systems showing the sources for which CCS might be relevant, transport of CO2 and storage options (Courtesy of CO2CRC). Figure SPM.1. Schematic diagram of possible CCS systems showing the sources for which CCS might be relevant, transport of CO2 and storage options (Courtesy of CO2CRC).

Chemokine hfcUzHlUr Signaling

Schematic diagram showing the props ed chemokine receptor signaling pathways. This diagram does not represent the complete pathway. Ligand binding induces the exchange of GDP for GTP on the G protein and this causes dissociation of the subunits. Gai decreases the levels of cAMP and GjBy causes the activation of PLC and PI3Ky. PLC, phospholipase C DAG, diacylglycerol IP3, inositol triphosphate PKC, protein kinase C MAPK, mito-gen-activated protein kinase PI3Ky, phosphoinosi-tol 3 kinase y PKB, protein kinase B. Figure 4.3. Schematic diagram showing the props ed chemokine receptor signaling pathways. This diagram does not represent the complete pathway. Ligand binding induces the exchange of GDP for GTP on the G protein and this causes dissociation of the subunits. Gai decreases the levels of cAMP and GjBy causes the activation of PLC and PI3Ky. PLC, phospholipase C DAG, diacylglycerol IP3, inositol triphosphate PKC, protein kinase C MAPK, mito-gen-activated protein kinase...

Cystic Fibrosis ABCC7CFTR

Nherf Dimer

Fig. 3.4 Schematic diagram summarizing ABCC7 (CFTR) interactions in the plasma membrane. CFTR interacts with various proteins in the plasma membrane including syntaxin 1a, CAL (CFTR-associated ligand), and EBP50 NHERF 1 70-175 . Syntaxin 1a contains coiled-coil protein motifs which bind the N-terminal part of CFTR. Syntaxin 1a controls the vesicular trafficking of CFTR through the Golgi to the plasma membrane and thereby inhibits its channel function. CFTR also contains a PSD-95 Disc-large ZO-1 (PDZ)-inter-acting motif at its C-terminus, which binds the PDZ-proteins CAL and EBP50 NHERF (ezrin, radixin, and moesin) binding phospho-protein of 50 kDa Na+ H+ exchanger regula

Pressure autoregulation

Autoregulation Coronary Hypertensive

A schematic diagram of the changes in blood flow to an organ over a wide range of perfusion pressures in the presence or absence of autoregulation is shown in Fig. 6.5. In the absence of autoregulation, pressure-flow relationships are linear, and increases in driving pressure lead to direct increases in perfusion. An autoregulatory curve is characterised by a large range of pressures during which flow remains relatively constant. vasodilation is achieved at lower perfusion pressures by relaxation of smooth muscle, and vascular smooth muscle constriction occurs at higher perfusion pressures to maintain constant flow. The ability to autoregulate assumes that a set point of basal vasomotor tone allows for this dilatation or constriction to occur. Flow varies directly with pressure when the limits of autoregulation are exceeded. In regional beds that are maximally vasodilated, for example by a drug such as dipyridamole, the process of autoregulation is eliminated and flow is directly...

Model of the Fertilization Calcium Wave

Figure 8.2 Schematic diagram of the fertilization Ca2+ wave model. Ca2+ enters the cytosol from the ER via a passive leak and the IP3R, which is activated by both Ca2+ and IP3 on a fast time scale and inhibited by Ca2+ on a slow time scale, all at the cytoplasmic face. The ER is refilled by a SERCA-type Ca2+-ATPase pump. Diffusion of Ca2+ in both the cytosol and ER is accounted for using effective diffusion coefficients (constant) that account for interactions with Ca2+ buffers (not shown) and the volume fractions of both compartments. Reprinted from Jafri and Keizer, 1994 . Figure 8.2 Schematic diagram of the fertilization Ca2+ wave model. Ca2+ enters the cytosol from the ER via a passive leak and the IP3R, which is activated by both Ca2+ and IP3 on a fast time scale and inhibited by Ca2+ on a slow time scale, all at the cytoplasmic face. The ER is refilled by a SERCA-type Ca2+-ATPase pump. Diffusion of Ca2+ in both the cytosol and ER is accounted for using effective diffusion...

Heterochromatic Flicker Photometry

Heterochromatic Flicker Photometry

The most commonly used method to measure macular pigment levels noninvasively in the human eye is the psychophysical technique known as heterochromatic flicker photometry (HFP). This technique was initially described by several investigators in the 1970s, and at that time it usually required rather extensive apparatus utilizing Maxwellian view optics, xenon arc lamps, and fixed optical tables (25,26). In recent years, newer versions using free-view (Newtonian) optics and simpler light sources such as light-emitting diodes or projector lamps have been described that allow for construction of portable flicker devices suitable for clinical studies at multiple sites (27,28). Since the details of the construction of modern HFP devices have been covered in these articles and in a recent review (29), the focus of this section will be on more general principles of the technique. Schematic diagrams of two types of HFP devices are given in Fig. 1.

Biochemical Kinetics and Feedback

In general, a biochemical reaction network is a schematic diagram of boxes and arrows. Each box is a chemical species. Solid arrows represent chemical reactions producing or consuming a molecule. Dashed arrows represent control by one species of a chemical reaction involving other species. Regulatory signals may be activatory (barbed end) or inhibitory (blunt end).

Duplication of Basal Bodies in Chlamydomonas

Chlamydomonas Cytokinesis

Figure 5.8 (A) Schematic diagram of basal body assembly as suggested by Dippell 29 . The first sign of basal body assembly is the appearance of an amorphous disk. This is followed by singlet microtubules that correspond to the A-tubule. These are followed by B- and, finally, C-tubules. Each stage is not completed simultaneously for all nine blades, so it is possible to observe mixtures of singlet, doublet and triplet microtubules within a given cross-section. (B) Schematic diagram of basal body assembly with a traveling cap model of regulation. Proteins (black) destined for fibers at the distal end (such as p210) travel at the tip of elongating microtubule blades. This complex could also serve as a negative regulator to prevent premature elongation of pro-basal bodies. These proteins leave the distal end of the mature basal body and move to various fibers once elongation is complete. Figure 5.8 (A) Schematic diagram of basal body assembly as suggested by Dippell 29 . The first sign of...

Polyanhydride Products Made In Biomedical Field

Schematic diagram describing the flow-limited field-injection electrostatic spraying (FFESS) technology. Shown for comparison is the conventional electrospraying (CES). FIGURE 2.7. Schematic diagram describing the flow-limited field-injection electrostatic spraying (FFESS) technology. Shown for comparison is the conventional electrospraying (CES).

Caloric Restriction

FIGURE 8.4 A schematic diagram illustrating age-related changes in excitatory synapses and the effects of IGF-1, estrogen, and caloric restriction on these synapses. Aging is associated with a decrease in synaptic glutamate receptors. Both IGF-1 and estrogen increase glutamate receptor subunit levels and IGF-1 also increases the number of multiple spine bouton synapses. Caloric restriction decreases glutamate receptor subunit levels in young animals, but then maintains those levels across the lifespan. Note the black and white ovals represent AMPA and NMDA glutamate receptor subunits, the open circles represent synaptic vesicles, and the dark gray zone represents the postsynaptic density. FIGURE 8.4 A schematic diagram illustrating age-related changes in excitatory synapses and the effects of IGF-1, estrogen, and caloric restriction on these synapses. Aging is associated with a decrease in synaptic glutamate receptors. Both IGF-1 and estrogen increase glutamate receptor subunit levels...

Laser Scanning Confocal Microscopy

A variety of confocal microscopes are available and include systems manufactured by Leica, Bio-Rad, Zeiss, and Olympus. Herein, a Leica TCS NT confocal microcope (Leica, Heidelberg, Germany) equipped with a multiline 750-mW Omnichrome krypton-argon laser (Chino, USA) was used to image osteoclasts after triple-color immunostaining (6,7). Excitation of the fluorochomes FITC, TRITC, and rhodamine, and CY5 was performed at 488, 568, and 647 nm, respectively, and their optical images were collected, digitised, and displayed in pseudocolors of green, red, and blue, respectively (refer to Fig. 1 for a schematic diagram of LSCM).

Descriptive Examples

Mossbauer spectroscopy along with evidence gathered from EPR and ENDOR have identified the behavior of iron atoms in the M center or FeMo cofactor of the enzyme nitrogenase from Azobacter vinelandii. Figure 6.9 shows a schematic diagram of nitrogenase's M center. At the time of the EPR study, it was known that two M center clusters were contained in each nitrogenase MoFe-protein subunit, that each was of composition MoFe6-8S9 1, and that each cluster contained three unpaired electrons in an S 3 2 system.27 The rhombic EPR signal with g factors g1( gx) 4.32, g2( gy) 3.68 and g3( gz) 2.01 would have the appearance of the rhombic spectrum of Figure 3.13D in Section 3.4.1. (Also see Figure 16 of reference 29.)

Molecular Regulation of Axonal Sprouting

The entorhinal projection to the rat fascia dentata. A) The entorhinal cortex (EC) projects to the hippocampus (H) in a topographically ordered manner. Dorsal portions of the entorhinal cortex project to septal (S) portions of the hippocampus, whereas more ventrally located portions of the entorhinal cortex project to temporal levels of the hippocampus. Thus, the lesion site in the ECL model is far away from the denervated septal portion of the hippocampus. B) Schematic diagram of a slice through the hippocampal formation. Entorhino-hippocampal fibers originate from layer II neurons in the EC. They fasciculate, form the perforant pathway, and terminate in the outer molecular layer (OML) of the dentate gyrus (DG). H, hilus IML, inner molecular layer S, subiculum. C) A typical granule cell of the fascia dentata is illustrated. Afferents terminate on the dendritic arbor of this cell in either a lamina-specific or a diffuse fashion. In the outer molecular layer (OML) fibers of...

Alternative Methods for Applying Strain

Schematic diagram of the custom-built apparatus used for straining cells by subjecting plastic strips to four-point bending. As the eccentric cam rotates it presses the loading platen onto the vertical edges of the plastic strips and causes their deformation (to the dotted position) in an arc around the paired fulcra underlying the strips (white). The platen is returned to the unloaded position by the spring. The rotation of the cam also acts to rock the chamber into which strips to be subjected to flow control are placed. For dose-response experiments, peak strain magnitudes can be altered by vertical displacement of the base unit by using a range of washers (with different thickness, placed between base and upper units see Fig. 4), and frequency altered with rheostat control of cam revolution rate. This unfortunately affects the waveform produced. However, a novel device has recently been designed (yet untried), in which the platen's vertical displacement is governed by a...

Ductions and Versions

Schematic diagram of motility deficits. The estimates of reduced motility are symbolized by minus signs for each of the diagnostic gaze positions (adduction, abduction, and elevation and depression in abduction and adduction), and over actions are marked by plus signs. In this example, there is a marked deficit of depression in adduction in the right eye and a moderate abduction deficit in the left eye. Additional notes can be helpful, e.g., depression in adduction to midline only

Role Of Ets In Cancer And Disease

Schematic diagram of the human ETS proteins. Uppercase letters (A, B, C and R) define hypothetical ETS domains. The ETS domain is indicated by the black box. The conserved PNT (pointed) domain is shown as a stippled box. Fig. 1. The human ETS gene family. Schematic diagram of the human ETS proteins. Uppercase letters (A, B, C and R) define hypothetical ETS domains. The ETS domain is indicated by the black box. The conserved PNT (pointed) domain is shown as a stippled box.

Basal Bodies Are More than Just Microtubule Organizers The Hitchhikers Guide to the Cytoskeleton

Figure 20.6 A schematic diagram of the tripartite attachment complex in Trypanosomes. Panel (a) illustrates the basal bodies, kinetoplast and the components of the TAC (exclusion zone filaments, differentiated mitochondrial membranes and unilateral filaments) in a trypanosome in G1 of the cell cycle. In this period there is a single flagellum, a basal body and a pro-basal body. Panel (b) shows the organization of the S-phase TAC. When the cell enters S-phase discrete fibrous lobes appear at the poles of the kinetoplast, the pro-basal body matures into a basal body and subtends the new flagellum and two new pro-basal bodies are formed. Two nascent TAC complexes are discernable at this period of the cell cycle. Panel (c) shows the period where movement apart of the flagella basal bodies segregates the replicated kinetoplast DNA. Note that the position and orientation of the basal bodies have been idealized in this two-dimensional diagram (from 58 ) (see Color Plates page XLII). Figure...

Ventricular Pressure Volume Relations and Energetics

FIGURE 11.5 Schematic diagram of left ventricular pressure-volume loops (a) End-systolic pressure-volume relation (ESPVR), end-diastolic pressure volume relation (EDPVR), and stroke work. The three P-V loops show the effects of changes in preload and afterload. (b) Time-varying elastance approximation of ventricular pump function (see text). FIGURE 11.5 Schematic diagram of left ventricular pressure-volume loops (a) End-systolic pressure-volume relation (ESPVR), end-diastolic pressure volume relation (EDPVR), and stroke work. The three P-V loops show the effects of changes in preload and afterload. (b) Time-varying elastance approximation of ventricular pump function (see text).

Central nervous system cardiovascular centres

Fig 6.1 Schematic diagram of the brain stem of a cat demonstrating locations of the depressor (horizontal lines) and pressor (cross hatched) areas. (Reprinted with permission from Alexander.4) Fig 6.1 Schematic diagram of the brain stem of a cat demonstrating locations of the depressor (horizontal lines) and pressor (cross hatched) areas. (Reprinted with permission from Alexander.4)

DNA Damage Checkpoint Genes

P53 Dna Repair

In mammals, the DNA damage checkpoints can be triggered in any phase of the cell cycle, which may lead to a cell cycle block, DNA repair, or apoptosis. Checkpoint activation is required for cells to arrest in Gl, S, and G2 phases, and the substrates include p53, Mdm2, and Chk2 in the Gl checkpoint Nbsl, Brcal, FancDl, and SMCl in the transient IR-induced S phase arrest and Brcal and hRadl7 in the G2 M arrest. A schematic diagram of these pathways is shown in Figs. 7 and 8.

Microtubule Organizing Centers in Polarized Epithelial Cells

Figure 15.5 Two centrosomal complexes a nucleating and an anchoring complex. Schematic diagram showing the organization of nucleating (y-TURC) and anchoring (ninein) complexes within the centrosome based on recent findings. The possible fates of a microtubule nucleated by a y-TURC and centrosomal anchoring complexes are outlined in 1-4. (1) Microtubule release from the y-TURC following nucleation (2) microtubule minus-end capping by a capping anchoring complex (3) microtubule release from the centrosome or firm anchorage within the PCM closely associated with the mother centriole (4) release of anchoring complexes from the centrosome and their transport along a microtubule (see Color Plates page XXXIV). Figure 15.5 Two centrosomal complexes a nucleating and an anchoring complex. Schematic diagram showing the organization of nucleating (y-TURC) and anchoring (ninein) complexes within the centrosome based on recent findings. The possible fates of a microtubule nucleated by a y-TURC and...

C Rhamm is a Multifunctional Adapter Targeting Protein

Erk Signaling And Genomic Stability

Figure 4 Schematic diagram of RHAMM as an adaptor protein. The identification of multiple protein kinase recognitions sites, its established association with kinases such as src and erk, as well as putative sites for protein-protein interactions including SH2 and SH3 bindings sites, together with its localization to multiple sub-cellular compartments, is consistent with a proposed function of intracellular RHAMM as an adaptor accessory protein that may link and target multiple signaling cascades in a manner resembling the AKAP group of adaptor proteins. Figure 4 Schematic diagram of RHAMM as an adaptor protein. The identification of multiple protein kinase recognitions sites, its established association with kinases such as src and erk, as well as putative sites for protein-protein interactions including SH2 and SH3 bindings sites, together with its localization to multiple sub-cellular compartments, is consistent with a proposed function of intracellular RHAMM as an adaptor accessory...

Specific Labeling Of Rosette

Frequency distributions of the number of gold particles associated with the immune serum containing antibodies to cellulose synthase and the preimmune control serum as a function of the measured distance to the center and the edge of the nearest rosette TC (left). Schematic diagram for the measurement of the distance between gold particles and rosette TC (right) is also shown (green rosette, pink primary antibody to cellulose synthase, blue secondary antibody, red gold particle the 93 kDa antibody-labeled particles. (a) Schematic diagram for the measurement of the distance between gold particles and linear TCs. The distance (double arrowheads) between the edge of gold particles and the linear TCs is indicated by the dotted line. (b) Frequency distribution of the number of gold particles associated with the 93 kDa protein antibody is shown as a function of the measured distance (nanometers) to the linear TC. Total number of gold particles measured was 277, taken from 30...

Masahiko Yoneda

Figure 1 Schematic diagram of horizontal section of the eye indicating each ocular component. A, corneal epithelium B, keratocyte C, corneal endothelium D, aqueous humor E, conjunctiva F, sclera G, trabecular meshwork H, iris I, lens J, ciliary body K, vitreous L, retina M, interphotoreceptor matrix N, retinal pigment epithelium O, Bruch's membrane P, choroid Q, optic nerve. Figure 1 Schematic diagram of horizontal section of the eye indicating each ocular component. A, corneal epithelium B, keratocyte C, corneal endothelium D, aqueous humor E, conjunctiva F, sclera G, trabecular meshwork H, iris I, lens J, ciliary body K, vitreous L, retina M, interphotoreceptor matrix N, retinal pigment epithelium O, Bruch's membrane P, choroid Q, optic nerve.

Analysis of the EEG

Schematic diagram of the method employed in generating topographic brain maps. Power spectra are generated for electrical activity recorded in each of the individual scalp electrodes. (From Lukas, 1997, with permission.) Fig. 5. Schematic diagram of the method employed in generating topographic brain maps. Power spectra are generated for electrical activity recorded in each of the individual scalp electrodes. (From Lukas, 1997, with permission.)

Rb In Cervical Cancr

A variety of highly sensitive and specific laboratory procedures are now available for use as biomarkers to identify individuals exposed to particular chemical carcinogens, to determine individual risk for cancer development, to identify individuals with early-stage clinical disease, and also to use as intermediate endpoints in intervention studies. Figure 1.2 provides a schematic diagram of the sequence of events in the continuum from the initial exposure of an individual to a causative agent(s) to the eventual development of a fully malignant tumor. Several types of biomarkers make it possible to precisely monitor each of these events 40,41 . These biomarkers can be divided into specific categories internal dose, biologically effective dose, early biologic effects (responses), and susceptibility. Biomarkers of internal dose take into account individual differences in absorption or bioaccumulation of the compound in question and indicate the actual level of the compound within the...

Venovenous Bypass

Cannulas For Venoveno Bypass

Systemic blood is actively drained from the femoral vein via a centrifugal pump to the central venous system. Portal decompression may be achieved via the inferior mesenteric vein. Fig. 3.5. Schematic diagram of VVB. Systemic blood is actively drained from the femoral vein via a centrifugal pump to the central venous system. Portal decompression may be achieved via the inferior mesenteric vein.

Periodontitis Drugs

I he U.S. food arid l> rug Administration recently granted marketing approval for doxycycline hyclate (IVriostat) for the adjunctive treatment of periodontitis. IVriostat, available as a 20-mg capsule ol doxycycline hyclate, is prescribed lor use by patients twice daily. I he mechanism of action is by suppression of the activity of collage-nase, particularly that produced by polymorphonuclear leukocytes. A schematic diagram of the role of matrix mctalloproteinascs in the progression of periodontal

Symptom Of Pelopsia

Allesthesia

Schematic diagram of the most common (pseudo) hallucinations. Upside down inverted objects. Macropsia microp-sia objects seen as too large or small. Telopsia pelopsia objects seen as too far or near. Palinopsia objects seen in correct relation to others (e.g., exclusively situated on horizontal planes) and thus in multiple locations (a subtype of polyopsia). Metamorphopsia objects misshapen. Polyopsia multiple images of a single object (a failure of the extinguishing center). Platyopsia loss of spatial perception in which all objects appear flat. Allesthesia objects appear to be floating Fig. 13.3. Schematic diagram of the most common (pseudo) hallucinations. Upside down inverted objects. Macropsia microp-sia objects seen as too large or small. Telopsia pelopsia objects seen as too far or near. Palinopsia objects seen in correct relation to others (e.g., exclusively situated on horizontal planes) and thus in multiple locations (a subtype of polyopsia). Metamorphopsia...

B Rhamm as a TACC

Rhamm Structure

Figure 3 Comparison of RHAMM with the TACC and Klp family of proteins. (A) Schematic diagram of putative structure of RHAMM with the TACC family of proteins. The TACC proteins all contain significant sequence identity in the TACC domain located at their extreme carboxyl-terminus, though they contain little sequence identity in other regions of the proteins. RHAMM, which has been reported to be a member of the TACC family does not contain a carboxyl terminal TACC domain and otherwise has little sequence identity (7-10 ) with TACC family members. Any observed identity is located primarily within the amino acids responsible for the coiled-coil structure. (B) The region of RHAMM reported to be required for its centrosomal targeting overlaps with the two B(X)7B motifs required for hyaluronan binding. This region more closely resembles the centrosomal targeting domain of the Klp (kinesin) family of proteins than that of TACC proteins. However, RHAMM does not contain the highly conserved...

Campylobacter LOS

Schematic diagram of nuclear magnetic resonance (NMR) spectroscopy tubes. (A) For high-resolution (HR)-NMR, a 5-mm NMR tube with 500 L of soluble sample is typically used. (B) For HR-MAS NMR using a nanoprobe, the 40- L sample is contained in a cylindrical rotor whose axis is inclined at an angle of 54.7 relative to the magnetic field (Ho). The sample is rotated about the rotor's axis at rates typically exceeding 2000 Hz. The tubes are drawn to scale relative to each other. Fig. 7. Schematic diagram of nuclear magnetic resonance (NMR) spectroscopy tubes. (A) For high-resolution (HR)-NMR, a 5-mm NMR tube with 500 L of soluble sample is typically used. (B) For HR-MAS NMR using a nanoprobe, the 40- L sample is contained in a cylindrical rotor whose axis is inclined at an angle of 54.7 relative to the magnetic field (Ho). The sample is rotated about the rotor's axis at rates typically exceeding 2000 Hz. The tubes are drawn to scale relative to each other.

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