Ординатура / Офтальмология / Английские материалы / The Retina and its Disorders_Besharse, Bok_2011
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Subject Index |
907 |
arrestin and 587 |
Rodent models, glaucoma 39 |
|
structure 582–4 |
rat 39, 736 |
|
structure 638 |
Rod-isolated ERG response 706 |
|
chromophore binding region 639, 640, 640f |
Rod–OFF pathway, dynamic range and 845 |
|
conserved motifs 639 |
Rod outer segment (ROS) 637, 648 |
|
squid 582–4 |
cytoskeleton 677 |
|
three-dimensional 639, 640f |
development from primary cilia 677 |
|
two-dimensional 638, 639f |
disk membrane proteins 676–7 |
|
vertebrate vs. invertebrate 643–4, 643 |
trafficking 677 |
|
thermal stability 632 |
intraflagellar transport 677 |
|
transport/metabolism |
as modified cilium 680 |
|
retinal degeneration and 731 |
disease associations 680–1 |
|
vertebrate vs. invertebrate 643 |
structure 676 |
|
photoactivation 642 |
Rod photoreceptor(s) 17, 22, 558, 567, 568, 637, 819–24, 854 |
|
regeneration 642 |
biophysical properties 821 |
|
structure 643–4, 643f |
absence of thresholds 615 |
|
Xenopus laevis models 849 |
cones vs. 18, 589 |
|
Rhodopsin targeting/trafficking 676–83 |
monochromacy (achromatopsia) 146 |
|
disease associations 680 |
chromatic function and 102 |
|
Bardet–Biedl syndrome 681 |
degeneration |
|
retinopathy 681–2 |
Xenopus laevis models 849–50 |
|
rhodopsin mutation effects 678 |
zebrafish pde6 mutants 860 |
|
Usher syndrome 682 |
development 568, 569f |
|
membrane trafficking apparatus 677 |
from rod precursor 569f, 570f, 572 |
|
phospholipid co-transport 677 |
signaling molecules 268, 268f, 570f, 572 |
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retinal cell-free assay 677–8 |
distribution 568 |
|
RTCs 677 |
Drosophila photoreceptors vs. 729, 730f |
|
sorting machinery 678 |
electrical coupling 821 |
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rod cell polarity and 676 |
rod–rod 823, 844 |
|
small GTPases and 678, 682f |
evolution 22, 841 |
|
Arfs 679, 680f |
function 841 |
|
Rabs 678 |
goldfish retina 106, 106f |
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SNAREs and their regulators 679, 681f |
light sensitivity 105–6, 596, 610, 611 |
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Rhodopsin transport carriers (RTCs) 677 |
saturation 589–90, 596–7, 597f, 598 |
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Ribbon synapses 661–7 |
Weber’s law and 326–7, 597 |
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amacrine cells 278 |
membrane trafficking 677 |
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bipolar cells 457f, 458 |
mouse retina 568 |
|
calcium and |
pathways |
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Ca2+ channels 664 |
amacrine cells and 280, 281f, 450, 843 |
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Ca2+ currents 664–5, 664f |
critical fusion frequency and 25, 26f |
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intracellular 663, 665 |
definition 105 |
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role in vesicular release 665–6 |
photopigment |
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definition 156, 661, 819, 841–2 |
cones vs. 626 |
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proteins 663 |
stability 626 |
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Ca2+ -binding 663, 665 |
polarized light and 670–1 |
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Ca2+ channel 664, 665 |
retinomotor movements 219, 220, 220f |
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mutations 665, 666 |
function 226 |
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ribbon function 663 |
regulation by cAMP 222–3, 223f, 224f |
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rod photoreceptors 820–1, 820f, 822 |
regulation by light 225 |
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structure 661, 662f |
rod:cone densities 589 |
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vesicles 662, 662f |
structure 637, 638f, 820f |
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numbers 661 |
adherens junctions 677 |
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release mechanism 665 |
axon 819 |
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Ribeye (protein) 663, 664 |
cilia 677, 680 |
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Riluzole 739 |
cytoskeleton 677 |
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Ring perimetry 553, 554f |
gap junctions 821 |
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RLBP1 gene/RLBP1 protein, retinitis pigmentosa 702 |
inner segment 637, 677 |
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RNA helicases, definition 847 |
invagination 821 |
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Rod bipolar cells 25, 285–6, 452, 454f, 455, 820–1, 820f |
ion channels 821 |
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AII amacrine cells and 323 |
morphology/topology 819 |
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definition 284 |
outer limiting membrane 677 |
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Rod bipolar pathway, dynamic range 842 |
polarity 676 |
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adaptation to mean background light 845–6 |
synapse 463, 820, 823–4 |
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evolutionary conservation 842 |
terminal 819 |
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RGC sensitivity and 844 |
Rod phototransduction 22, 412, 610, 624–5, 625f, 631–6, 644, 821 |
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scotopic vision sensitivity and 842 |
activation 610–11 |
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signal transfer |
vertebrate rods 631–2, 633f |
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rod bipolar cell to AII amacrine cells 843 |
adaptation 596–604 |
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rod to bipolar cell 842, 843f, 844f |
cyclic guanosine monophosphate (cGMP) role 635 |
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Rod/cone (mixed) bipolar cells 284–5 |
gated channel 635 |
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Rod–cone dystrophy 853–4 |
dark noise 633, 821 |
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bystander effect and 854 |
‘dark thermal events’ 821–2 |
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definition 685, 699 |
elimination mechanisms 842–3 |
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Rod–cone electrical coupling 161, 498, 823, 844 |
sources 821 |
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goldfish retina 106–7, 106f |
synaptic convergence and mitigation 821–2 |
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Rod–cone pathway 105 |
dominant time constant 601 |
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dynamic range and 105–6, 844 |
light-induced changes 602 |
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ERG responses 706 |
electrical coupling and |
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goldfish retina 106, 106f |
starlight 823 |
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Rod dystrophies 853–4 |
twilight 823 |
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Rodent(s) |
G-protein signaling pathway 631 |
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horizontal cell morphology 466–7, 466f |
melatonin effects 503–4 |
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908 |
Subject Index |
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Rod phototransduction (continued) |
Screening, diabetic retinopathy 788 |
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membrane hyperpolarization 631–2 |
Searching nystagmus |
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graded 632 |
definition 333 |
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negative feedback 823 |
recessive optic atrophy 335–6 |
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phosphodiesterase, second amplification step 634 |
Second-order, first slice, definition 506 |
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quantum efficiency of photoactivation 632 |
Second Sight Medical Products Inc. (SSMP) prostheses, clinical |
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refractory period 822 |
trials 356–7 |
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single-photon signal 631, 821, 822 |
Second-site modifier screens, definition 726–7 |
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suction electrode rod recording 631, 632f |
SECORD (severe early childhood-onset retinal dystrophy) 687–9 |
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summation 821 |
Secretory immunoglobulin A (sIgA) 377 |
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synaptic transfer function |
Secretory phospholipid A2 (PLA2), innate immunity 376 |
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high gain and temporal filter 822 |
Sector retinitis pigmentosa 701, 702f |
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nonlinear threshold 822, 842–3 |
Self-signaling |
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vertebrate rods |
definition 360 |
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activation 631–2, 633f |
retinal remodeling 363 |
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single photon detection 631 |
Senior–Loken syndrome, retinitis pigmentosa and 705 |
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vesicle release rate 822, 842 |
Sensory cilia, definition 575 |
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Rod phototransduction inactivation 610–15, 613f |
Sensory receptors |
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lack of action potential and 615 |
Serial competence model |
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light damage and 339–40 |
definition 745 |
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PDE inactivation 612 |
retinal histogenesis 749, 749f |
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restoration of cGMP/Ca2+ levels 612 |
Serotonin (5-HT), fly circadian plasticity and 131 |
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rhodopsin inactivation 611 |
Severe early childhood-onset retinal dystrophy (SECORD) 687–9 |
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transducin inactivation 612, 644 |
Sexual dimorphism, color vision in butterflies 154 |
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Rod spherule, definition 461, 841 |
Shack–Hartmann wavefront sensor 8f |
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Roll back |
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definition 7 |
definition 309 |
Shh (sonic hedgehog) signaling |
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horizontal cells 310, 310f, 316 |
definition 863 |
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Rpe65-isomerase 650 |
in retinal development 864–5 |
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Rpe65 |
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Short posterior ciliary arteries (SPCAs) 179 |
definition 17 |
anastomosis, circle of Zinn 180, 180f, 181f |
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gene therapy in LCA 364–5 |
Short-wavelength automated perimetry 553, 553f |
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light damage role 339–40 |
Signaling pathways |
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in visual cycle 650, 651 |
cell extrinsic, definition 263 |
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RPE-retinal G-protein receptor (RGR) opsin 651 |
cell intrinsic, definition 263 |
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Rubella infection, RP vs. 693, 695f |
Drosophila–human similarities 727–8 |
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retinal neuropeptides 491 |
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Signal transduction, human–Drosophila similarity 727–8 |
S |
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Sign-conserving synapses, definition 276 |
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Sign-inverting synapses, definition 276 |
Saccade(s), suppression and RGCs 307 |
Silent substitution 100–1, 101f |
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Saltatory nerve conduction, definition 506 |
Single nucleotide polymorphism (SNP) |
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SArr (squid arrestin) 584f, 587 |
in AMD 272 |
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Sattler’s layer 30 |
definition 270 |
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Saturation |
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Single photon response, definition 631 |
avoidance, definition 589 |
Six3/Six3 212 |
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definition 589, 596 |
mutations 215–16 |
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Scanning laser ophthalmoscope (SLO) 526 |
structural domains 212, 213f |
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adaptive optics (AO) and 9–10 |
Six6/Six6 212 |
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Schiff base |
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mutations 215–16 |
11-cis-RAL attachment to rhodopsin via 638, 640–1, 640f |
structural domains 212–13, 213f |
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definition 637, 648 |
Skylight, polarization 669–70, 669f |
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Sclera, posterior ciliary artery penetration 180, 180f, 181f |
navigation using 673 |
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Scleral buckle |
Slit/Roundabout4, antiangiogenic activity 549 |
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basic principle 806, 807f |
Small-field amacrine cells 447, 448f |
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rhegmatogenous retinal detachment 806 |
Small GTPases |
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complications 809 |
definition 676 |
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outcomes 808 |
rhodopsin targeting/trafficking 678, 680f, 681f, 682f |
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retinal holes/dialysis 806 |
Smoking, AMD and 766–7, 833 |
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retinal tears 806 |
Smooth endoplasmic reticulum (SER), IP3-mediated Ca2+ release in Limulus |
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S-cones 134, 140, 159 |
phototransduction 620 |
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blue cone bipolar cells 453 |
SNARE proteins |
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clomeleon-labeled 454 |
definition 661, 676 |
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‘genuine’ 452 |
membrane trafficking and 679 |
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L/M cones vs. 145–6 |
protein interactions 680 |
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Parkinson’s disease and 137–8 |
Rab interactions 679 |
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photopigment gene 141, 142f |
rhodopsin targeting/trafficking 679, 681f, 682f |
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species differences in horizontal cell selectivity 467 |
ribbon synapses 663 |
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spectral sensitivity 141f |
structure 680 |
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tritan color defects and 144–6 |
Snellen acuity 1–2, 2f |
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Scotoma |
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acuity, definition 717 |
cecocentral, definition 333 |
test–retest variability 3 |
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mfERG results |
Snellen chart, definition 536 |
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bull’s eye retinopathy 510, 512f, 513f |
Snowflake vitreoretinal degeneration 260 |
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central serous retinopathy 510, 511f |
Socs3 gene, retinal regeneration 869–71 |
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small lesions 511, 515f |
SOD-1 (superoxide dismutase 1), in mouse models of AMD 274 |
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Scotopic, definition 558 |
Sodium (Na) RPE transport and 764, 766f |
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Scotopic vision 558, 559–60, 559f, 560f, 631 |
Sodium/bicarbonate co-transporter |
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definition 22, 68, 105, 205, 705, 819, 841, 853 |
RPE and metabolic load reduction 764, 766f |
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sensitivity 596, 842 |
Sodium (Na+) channels, cone photoreceptors 158–9 |
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trade-offs 596 |
Sodium pump, definition 58, 219 |
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910 |
Subject Index |
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Substance P (SP) |
definition 44, 51, 58, 761, 773 |
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retinal |
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diabetic retinopathy pathogenesis and 783 |
excitation of ganglion cells 482, 483f |
Tiling, RGC spatial processing and 302, 303f |
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mRNA localization 488 |
TILLING (targeting-induced local lesions in genomes), zebrafish 855 |
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neurotransmitter release 484 |
timeless (tim) gene/protein 127, 128f |
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peptide immunostaining studies 490 |
Tissue regeneration, retinal |
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radioimmunoassay 487 |
in mammals 872 |
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receptors 478 |
in zebrafish 863–4, 865 |
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Suction-electrode recording 631, 632f |
damage models 867 |
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definition 631 |
genes 869 |
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Superoxide dismutase (SOD) in glaucoma 739, 739f |
Mu¨ller glial cells involved in 867, 868f, 870f, 871–2 |
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Superoxide dismutase 1 (SOD-1), in mouse models of AMD 274 |
process of 870f, 871 |
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Suprachiasmatic nuclei (SCN) |
Toll-like receptors (TLRs) |
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as circadian master pacemaker 112 |
adaptive immune response and 379–80 |
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phase resetting and 112, 114f |
AMD role 273 |
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retinal input 112, 113f |
eye locations 377, 378t |
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Surgery |
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innate–adaptive immunity interactions 379–80 |
PION induction 408 |
innate immune response 377 |
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management 410 |
initiation/amplification 379 |
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Surgical decompression, central retinal vein 83 |
mucin production and 374–5 |
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Swedish interactive threshold algorithm (SITA) 551–2 |
ligand specificity 377, 378t |
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Synapse(s) |
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neovascularization and 352 |
cone photoreceptors 22–3, 158, 462 |
Tonometry, definition 38 |
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definition 105 |
Total deviation plots, perimetry 555 |
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dendrodendritic 276, 277f |
Total internal reflectance (TIRF) microscopy, definition 661 |
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dyads 457f, 458 |
Toxins, acquired color blindness 138 |
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feedback |
|
TRAIL-R, pathogen clearance 379 |
definition 284 |
Transcription factors |
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retinal remodeling 363 |
early patterning 199f, 200–1 |
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rod photoreceptors 463, 820, 823–4 |
light damage injury mechanisms 341, 342 |
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tetrads, fly visual system 126f, 129 |
POU-domain, definition 235 |
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Synaptic ribbon, definition 661 |
‘stemness’ 368 |
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Synaptogenesis |
Transducin(s) |
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inner plexiform layer 393–4, 393f, 394f, 395 |
achromatopsia and 146 |
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outer plexiform layer 393–4, 393f, 394f, 396 |
activation during phototransduction |
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retinal remodeling 363 |
cones 627 |
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vertical pathway 393, 393f, 394f, 395f |
rods (rhodopsin interaction) 610–11, 631–2, 633, 644, 645f |
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Synaptotagmin 663 |
definition 412, 605, 610 |
|
Synchronous neural activity, RGC spatial processing and 302–4 |
guanosine diphosphate (GDP)-bound inactive state 634 |
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Synechia, definition 38 |
guanosine triphosphate (GTP)-bound active state 634 |
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Systemic disease, central retinal vein occlusion and 75–6 |
inactivation after phototransduction |
|
|
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cones 607, 628 |
|
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rods 612, 613f, 644 |
T |
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light-driven translocation in photoreceptors 412, 413f, 614–15 |
|
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active transport vs. diffusion 413–14 |
Tachykinin(s), retina |
mechanisms 414, 414f |
|
immunostaining studies 490 |
possible functions 413 |
|
receptor autoradiography 491 |
return to dark-adapted locations 415 |
|
receptor mRNA expression 491 |
threshold light intensity 412–13 |
|
Tamponade |
rod vs. cone 627 |
|
definition 801 |
subunit dissociation 414, 414f |
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PVR management 714–15, 715f |
Transepithelial electrical potential (TEP), assessment of RPE barrier function 60 |
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Tapetal-like reflex/sheen, retinitis pigmentosa 701, 703f |
Transepithelial electrical resistance (TER) |
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Tapetoretinal, definition 333 |
assessment of RPE barrier function 60 |
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Targeting-induced local lesions in genomes (TILLING), zebrafish 855 |
definition 773 |
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Tbx3 213, 213f |
RPE tight junctions 778–9 |
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T-cell(s) |
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Transfer function |
AMD role 272 |
definition 276 |
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optic neuritis 536–7 |
nonlinear in cone phototransduction 159, 160f |
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proliferative vitreoretinopathy and 711 |
Transgenic animals |
|
T-cell receptor (TCR), T-cell activation and 126f |
bipolar cell morphology 456f, 457, 459 |
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Tear film/tears structure 374–5, 376f |
retinal peptide localization and 488 |
|
Tear film, defensive role 374 |
Transgenic mouse, definition 567 |
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Telangiectatic, definition 87 |
trans-Golgi network (TGN), definition 676 |
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Telodendria, definition 156, 819 |
Transient receptor potential (TRP), definition 438 |
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Temporal frequency, definition 163 |
Transient tritanopia 331–2 |
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Temporal processing |
Transitional cell, definition 235 |
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contrast sensitivity 166–8, 168f, 291 |
Transplantation, autologous RPE grafts, RP treatment 697 |
|
horizontal cells and 316 |
Transporter proteins, cone photoreceptors 158–9 |
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Tetrachromatic vision, definition 205 |
Transretinal waves, starburst amacrine cells 451 |
|
D9-Tetrahydrocannabinol (THC) 717 |
Trauma |
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TGFb |
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head injury and acquired color blindness 137 |
choroidal neovascularization role 91 |
inflammation and, RP vs. 692–3 |
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choroidal neovascularization 91 |
Tree shrew (Tupaia belangeri ), horizontal cells 465–6, 466f |
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signaling pathway 266, 267f |
Triad synapse(s) 309 |
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retinal histogenesis 266–7 |
cone photoreceptors 158 |
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Threshold, definition 290, 325 |
definition 156, 461 |
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Thrombospondin-1, CNV role 91 |
horizontal cells 461, 462f |
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Tight junctions (TJs) |
photoreceptors 309 |
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blood–retinal barrier 51, 52f |
Triamcinolone, intravitreal, macular edema treatment 82 |
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breach of 51–2, 52f |
Trichromacy/trichromatic vision |
|
inner blood–retinal barrier (iBRB) 44–5, 46 |
cone subtypes and 140, 141f |
|
912 |
Subject Index |
|
Visual loss, transient in GCA 405 |
Weber’s law 326–7, 591–2 |
|
Vitamin(s), protective against AMD 833 |
cone adaptation and 591, 591f |
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Vitamin A |
|
definition 589, 596 |
deficiency |
rod adaptation and 597 |
|
acquired color blindness 139 |
Weissenbacher–Zweymuller syndrome 253 |
|
Xenopus laevis model 849 |
White mutants 727, 728f |
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retinitis pigmentosa treatment 696 |
Wide-field three-dimensional choroidal OCT 527, 528f |
|
Vitamin E deficiency, retinitis pigmentosa and 704 |
Wnt/calcium pathway 264, 265f |
|
treatment 696 |
Wnt signaling pathway |
|
Vitrectomy |
|
familial exudative vitreoretinopathy 261 |
basic principle 806, 808f |
noncanonical 264, 265f |
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rhegmatogenous retinal detachment 806 |
retinal histogenesis 264, 265f |
|
complications 809 |
retinopathy of prematurity and 795 |
|
due to retinal holes/dialysis 807 |
Wolfram’s syndrome 336 |
|
due to retinal tears 806 |
|
|
outcomes 808 |
|
|
small-gauge sutureless 809 |
X |
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Vitreochoroidopathy, autosomal dominant (ADVIRC) 259 |
|
|
Vitreoretinal interface |
Xanthopsia 137 |
|
macular holes 825, 826, 827f, 828f |
Xenopus 500 |
|
Vitreoretinopathies, hereditary 252–62 |
Xenopus laevis |
|
abnormal retinal vasculature and 253t, 254t, 258 |
eye development 851 |
|
autosomal dominant vitreochoroidopathy 259 |
retinal regeneration and 848, 852 |
|
familial exudative vitreoretinopathy 259, 261, 261f |
utility as model organism 847–8 |
|
classification 252, 253t |
Xenopus laevis models of retinal disease 847–52 |
|
clinical features 252, 254t |
advantages 847–8, 848f, 852 |
|
corneal changes 253t, 254t |
developmental disorders 851 |
|
snowflake vitreoretinal degeneration 260 |
disadvantages 852 |
|
molecular genetics 260, 262t |
drug-inducible degeneration 851 |
|
collagen genes 260 |
electrophysiology and 848 |
|
fibrillin 261 |
expression of cone opsins in rod cells 851 |
|
inheritance patterns 261–2 |
glaucoma 849 |
|
phenotypic relationship 261 |
historical aspects 848 |
|
versican 261 |
retinitis pigmentosa |
|
Wnt signaling pathway 261 |
rhodopsin P23H mutation 850 |
|
progressive retinal dysfunction and 253t, 254t, 257 |
rhodopsin Q348ter mutation 850 |
|
Goldmann–Favre syndrome 258, 261 |
rhodopsin transport and 849 |
|
Wagner syndrome 257, 259f, 260f, 261, 261f |
transgenic animals 850 |
|
skeletal abnormalities and 252, 253t, 254t |
rhodopsin transport/metabolism and 849 |
|
Kniest dysplasia 253, 258f, 260 |
Stargardt’s disease 851 |
|
Knobloch syndrome 256 |
vitamin A deficiency 849 |
|
Marfan syndrome 256–7, 258f, 259f, 261 |
X-linked disorders, juvenile retinoschisis, mfERG results 510, 514f |
|
Marshall syndrome 253–4 |
|
|
spondyloepiphyseal dysplasia 253, 258f, 260 |
|
|
Vitreoschisis, definition 825 |
Z |
|
Vitreous |
|
|
anatomy, 825 |
Zebrafish (Danio rerio) 853 |
|
biochemistry 825 |
cone outer segment axonemes 579f |
|
definition 801 |
persistent neurogenesis of retina 865, 867f, 870f, 871 |
|
development 182 |
phototransduction in 856, 856f |
|
persistent hyperplastic primary vitreous 183 |
visual system 854–5 |
|
traction 825 |
embryogenesis 854–5, 864, 864f |
|
Vitreous fluorometry |
retina 864 |
|
blood–retinal barrier (BRB) assessment 54–5, 61 |
humans vs. 862 |
|
definition 44 |
regenerative potential 860, 862 |
|
Vitreous hemorrhage, in CRVO 80, 80f, 81f |
Zebrafish models 863, 867 |
|
Voltage-gated calcium channels |
glaucoma 42 |
|
cone photoreceptors 158–9 |
Zebrafish models of retinal disease 853–62 |
|
rod photoreceptors 821 |
advantages 854–6, 858, 862 |
|
Voltage-gated currents |
high-throughput drug screening 856, 862 |
|
horizontal cells and 311, 311f |
molecular techniques used 854 |
|
retinal cannabinoids and photoreceptor modulation 721 |
chimera production 856 |
|
von Kries scaling 99 |
DSBs 855–6 |
|
Vortex veins 179, 180–2, 180f |
morpholinos 855 |
|
|
|
mutagenesis 855 |
|
|
observation of cells in intact animals 855, 855f |
W |
|
TILLING 855 |
|
|
Pde6 mutants 857 |
Wagner syndrome 257–8, 259f, 260f, 261, 261f |
bipolar cells 860 |
|
Wallerian degeneration 386 |
cone photoreceptors 860–1 |
|
Water |
|
missense mutant (els) 858 |
animal behavior relating to 673–4 |
Mu¨ller cells 860 |
|
generation of polarization 669–70, 670f |
null mutant (pde6cw59) 858, 859f |
|
Wavefront sensor, Shack-Hartmann 8f |
rod photoreceptors 860 |
|
definition 7 |
structural effects 861, 861f |
|
Wavelets 164–5, 165f |
vision evaluation in 856 |
|
definition 163 |
Zeitgeber time, definition 68, 124 |
|
Wavenumber, definition 96 |
Zinc ions (Zn2+), GABA receptor modulation in retina 232–3 |
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