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1

Teissié, J. "Lateral proton diffusion." Nature 379, no. 6563 (1996): 305–6. http://dx.doi.org/10.1038/379305b0.

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2

Scherrer, Peter. "Lateral proton diffusion." Nature 379, no. 6563 (1996): 306. http://dx.doi.org/10.1038/379306a0.

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3

Gusak, A. M. "Flux-Driven Lateral Grain Growth during Reactive Diffusion." METALLOFIZIKA I NOVEISHIE TEKHNOLOGII 42, no. 10 (2020): 1335–46. http://dx.doi.org/10.15407/mfint.42.10.1335.

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4

Tamm, Lukas K. "Lateral Membrane Diffusion Corralled." Biophysical Journal 104, no. 7 (2013): 1399–400. http://dx.doi.org/10.1016/j.bpj.2013.02.046.

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5

Merchant, S. "Arbitrary lateral diffusion profiles." IEEE Transactions on Electron Devices 42, no. 12 (1995): 2226–30. http://dx.doi.org/10.1109/16.477783.

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6

Saxton, M. J. "Lateral diffusion in an archipelago. Single-particle diffusion." Biophysical Journal 64, no. 6 (1993): 1766–80. http://dx.doi.org/10.1016/s0006-3495(93)81548-0.

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7

Pieruschka, R. "Lateral gas diffusion inside leaves." Journal of Experimental Botany 56, no. 413 (2005): 857–64. http://dx.doi.org/10.1093/jxb/eri072.

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8

Schindler, M., J. F. Holland, and M. Hogan. "Lateral diffusion in nuclear membranes." Journal of Cell Biology 100, no. 5 (1985): 1408–14. http://dx.doi.org/10.1083/jcb.100.5.1408.

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Chemical modification of rat liver nuclei with citraconic anhydride selectively removed outer nuclear membrane. This conclusion was based on (a) transmission electron microscopy, (b) lipid analysis, (c) lamin B as an inner membrane-associated marker, and (d) the demonstration of phospholipid lateral mobility on outer membrane-depleted nuclei as a criteria for inner membrane integrity. Addition of urea or N-ethylmaleimide resulted in the additional disruption of inner membrane. Fluorescence photobleaching was used to determine the long range (greater than 4 microns) lateral transport of lectin
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9

Ramadurai, Sivaramakrishnan, Andrea Holt, Victor Krasnikov, Geert van den Bogaart, J. Antoinette Killian, and Bert Poolman. "Lateral Diffusion of Membrane Proteins." Journal of the American Chemical Society 131, no. 35 (2009): 12650–56. http://dx.doi.org/10.1021/ja902853g.

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10

Adrien, Vladimir, Gamal Rayan, Nicolas Taulier, and Wladimir Urbach. "Correlated Lateral Diffusion of Lipids." Biophysical Journal 106, no. 2 (2014): 84a. http://dx.doi.org/10.1016/j.bpj.2013.11.540.

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11

Boettinger, W. J., G. B. McFadden, S. R. Coriell, R. F. Sekerka, and J. A. Warren. "Lateral deformation of diffusion couples." Acta Materialia 53, no. 7 (2005): 1995–2008. http://dx.doi.org/10.1016/j.actamat.2005.01.011.

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12

Filippov, A. V., M. A. Rudakova, and B. V. Munavirov. "Lateral diffusion in sphingomyelin bilayers." Magnetic Resonance in Chemistry 48, no. 12 (2010): 945–50. http://dx.doi.org/10.1002/mrc.2694.

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13

Pink, David A. "Constraints on protein lateral diffusion." Trends in Biochemical Sciences 10, no. 6 (1985): 230. http://dx.doi.org/10.1016/0968-0004(85)90135-5.

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14

Gogarten, Johan Peter, and Friedrich-Wilhelm Bentrup. "Lateral electrophoresis versus 2D-diffusion." Trends in Biochemical Sciences 10, no. 12 (1985): 471–72. http://dx.doi.org/10.1016/0968-0004(85)90203-8.

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15

Kaprelyants, A. S. "Lateral non-homogeneity and lateral diffusion of proteins in membranes." Trends in Biochemical Sciences 10, no. 10 (1985): 385–86. http://dx.doi.org/10.1016/0968-0004(85)90062-3.

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16

MYSHLYAVTSEV, A. V., V. P. ZHDANOV, and P. R. NORTON. "SURFACE DIFFUSION AND ANISOTROPIC LATERAL INTERACTIONS." Surface Review and Letters 03, no. 03 (1996): 1417–20. http://dx.doi.org/10.1142/s0218625x96002436.

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Anisotropic lateral interactions between particles on a rectangular lattice result in anisotropy in the coverage dependence of the chemical diffusion coefficient. This effect is studied in the framework of the lattice-gas model taking into account repulsive lateral interactions in the ground state and also lateral interactions in the activated state. To calculate the diffusion coefficient, the transfer-matrix technique is employed.
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17

Busch, R., and Volker Ruth. "Lateral Mass Flows during Binary Diffusion." Defect and Diffusion Forum 66-69 (January 1991): 1287–92. http://dx.doi.org/10.4028/www.scientific.net/ddf.66-69.1287.

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18

Ayton, Gary S., and Gregory A. Voth. "Mesoscopic Lateral Diffusion in Lipid Bilayers." Biophysical Journal 87, no. 5 (2004): 3299–311. http://dx.doi.org/10.1529/biophysj.104.047811.

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19

Palliyil, Biji B., Cong Li, Suzan Owaisat, and David B. Lebo. "Lateral Drug Diffusion in Human Nails." AAPS PharmSciTech 15, no. 6 (2014): 1429–38. http://dx.doi.org/10.1208/s12249-014-0169-9.

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20

Juwono, Tjipto, and Per Arne Rikvold. "Dynamics of desorption with lateral diffusion." Journal of Chemical Physics 139, no. 12 (2013): 124706. http://dx.doi.org/10.1063/1.4821750.

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21

Tocanne, Jean-François, Laurence Dupou-Cézanne, André Lopez, and Jean-François Tournier. "Lipid lateral diffusion and membrane organization." FEBS Letters 257, no. 1 (1989): 10–16. http://dx.doi.org/10.1016/0014-5793(89)81774-0.

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22

Myshlyavtsev, A. V., and V. P. Zhdanov. "Surface diffusion and anisotropic lateral interactions." Surface Science Letters 291, no. 1-2 (1993): A566. http://dx.doi.org/10.1016/0167-2584(93)90296-u.

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23

Lindblom, Göran, and Greger Orädd. "Lipid lateral diffusion and membrane heterogeneity." Biochimica et Biophysica Acta (BBA) - Biomembranes 1788, no. 1 (2009): 234–44. http://dx.doi.org/10.1016/j.bbamem.2008.08.016.

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24

Jacobson, K., A. Ishihara, and R. Inman. "Lateral Diffusion of Proteins in Membranes." Annual Review of Physiology 49, no. 1 (1987): 163–75. http://dx.doi.org/10.1146/annurev.ph.49.030187.001115.

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25

Myshlyavtsev, A. V., and V. P. Zhdanov. "Surface diffusion and anisotropic lateral interactions." Surface Science 291, no. 1-2 (1993): 145–53. http://dx.doi.org/10.1016/0039-6028(93)91486-9.

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26

Weichselbaum, Ewald, Denis Knyazev, and Peter Pohl. "Energetics of Lateral Membrane Proton Diffusion." Biophysical Journal 108, no. 2 (2015): 603a—604a. http://dx.doi.org/10.1016/j.bpj.2014.11.3287.

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27

Gawrisch, Klaus, Holly C. Gaede, Olivier Soubias, and Walter E. Teague. "Phospholipid Structural Features Influence Lateral Diffusion." Biophysical Journal 118, no. 3 (2020): 166a. http://dx.doi.org/10.1016/j.bpj.2019.11.1019.

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28

Goehring, Nathan W., Carsten Hoege, Stephan W. Grill, and Anthony A. Hyman. "PAR proteins diffuse freely across the anterior–posterior boundary in polarized C. elegans embryos." Journal of Cell Biology 193, no. 3 (2011): 583–94. http://dx.doi.org/10.1083/jcb.201011094.

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Polarization of cells by PAR proteins requires the segregation of antagonistic sets of proteins into two mutually exclusive membrane-associated domains. Understanding how nanometer scale interactions between individual PAR proteins allow spatial organization across cellular length scales requires determining the kinetic properties of PAR proteins and how they are modified in space. We find that PAR-2 and PAR-6, which localize to opposing PAR domains, undergo exchange between well mixed cytoplasmic populations and laterally diffusing membrane-associated states. Domain maintenance does not invol
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29

SINTES, T., A. BAUMGÄRTNER, and Y. K. LEVINE. "LATERAL DIFFUSION OF FLEXIBLE LIPID CHAINS: A DYNAMIC MONTE CARLO STUDY." International Journal of Modern Physics C 10, no. 02n03 (1999): 341–54. http://dx.doi.org/10.1142/s0129183199000255.

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A computer simulation study of the lateral diffusion of conformationally-disordered lipid molecules in a monolayer structure is reported. The simulations were carried out with dynamic Monte Carlo methods, employing two different representations of the internal motions of the lipid chains. The results indicate that the dependence of the lateral diffusion coefficients on the density (area-per-molecule) in the monolayer is determined by the conformational behavior of the lipid chains. The classical Cohen–Turnbull theory is found to provide a good description of the simulated lateral diffusion coe
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30

Chen, S. H., C. B. Carter, and C. J. PalmstrΦm. "Lateral diffusion in Ni–GaAs couples investigated by transmission electron microscopy." Journal of Materials Research 3, no. 6 (1988): 1385–96. http://dx.doi.org/10.1557/jmr.1988.1385.

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A method has been devised for preparing lateral Ni–GaAs diffusion couples for transmission electron microscopy investigations. By annealing diffusion couples in situ in a hot stage, the growth of a ternary phase has been observed in the microscope, and shows parabolic time dependence of the growth. In the temperature range of 200–300 °C, Ni is the predominant diffusing species in the ternary phase while Ga and As are essentially immobile. The experimental results are compared with previous investigations of the reactions of Ni thin films with bulk GaAs.
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31

FAN, LEI, and TIAN YOU FAN. "LATERAL DIFFUSION OF MEMBRANE PROTEINS AT CELL MEMBRANE." Modern Physics Letters B 24, no. 14 (2010): 1533–40. http://dx.doi.org/10.1142/s0217984910023311.

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The cell membrane is an important organ of living cells, which has a complex structure influenced by the interaction between membrane proteins and cell membrane. On the basis of fluid motion and diffusion interaction, a simple model is proposed to evaluate quantitatively the effects of the protein size and membrane fluid velocity on the lateral diffusion of membrane proteins at the cell membrane. The study shows that the diffusion coefficient is a dominant factor on the lateral diffusion.
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32

Foley, M., A. N. MacGregor, J. R. Kusel, P. B. Garland, T. Downie, and I. Moore. "The lateral diffusion of lipid probes in the surface membrane of Schistosoma mansoni." Journal of Cell Biology 103, no. 3 (1986): 807–18. http://dx.doi.org/10.1083/jcb.103.3.807.

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The technique of fluorescence recovery after photobleaching was used to measure the lateral diffusion of fluorescent lipid analogues in the surface membrane of Schistosoma mansoni. Our data reveal that although some lipids could diffuse freely others exhibited restricted lateral diffusion. Quenching of lipid fluorescence by a non-permeant quencher, trypan blue, showed that there was an asymmetric distribution of lipids across the double bilayer of mature parasites. Those lipids that diffused freely were found to reside mainly in the external monolayer of the outer membrane whereas lipids with
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33

Wein, Ondřej. "Lateral edge effect in electrodiffusion measurements of wall shear stress." Collection of Czechoslovak Chemical Communications 53, no. 8 (1988): 1678–87. http://dx.doi.org/10.1135/cccc19881678.

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The influence of three-dimensional diffusion at lateral edges of an electrodiffusion sensor of friction is analysed by the method of singular perturbations for PeL ≫ 1. It is shown that lateral diffusion at PeL ≫ 1 has a more pronounced effect than longitudinal diffusion at the back edge of the sensor, which has hitherto been exclusively considered.
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34

Lenaz, Giorgio. "Lipid fluidity and membrane protein dynamics." Bioscience Reports 7, no. 11 (1987): 823–37. http://dx.doi.org/10.1007/bf01119473.

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Membrane fluidity plays an important role in cellular functions. Membrane proteins are mobile in the lipid fluid environment; lateral diffusion of membrane proteins is slower than expected by theory, due to both the effect of protein crowding in the membrane and to constraints from the aqueous matrix. A major aspect of diffusion is in macromolecular associations: reduction of dimensionality for membrane diffusion facilitates collisional encounters, as those concerned with receptor-mediated signal transduction and with electron transfer chains. In mitochondrial electron transfer, diffusional co
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35

Liu, Joyce C., and J. W. Mayer. "Aluminum and Ni–silicide lateral reactions." Journal of Materials Research 5, no. 2 (1990): 334–40. http://dx.doi.org/10.1557/jmr.1990.0334.

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The Al–Ni2Si reactions were studied in lateral diffusion couples containing Al islands on Ni–Si multiple layers. The samples were first in situ annealed in a transmission electron microscope at a temperature of 370°C for 5 min to form the Ni2Si phase in the multiple-layer area. Then they were in situ annealed at temperatures ranging from 498–545 °C. During the second-step anneal, a sequential formation of Al3Ni, Al3Ni2, and Ni3Si2 was observed. After the nucleation of the third phase (Ni3Si2), the three phases grew simultaneously with time. The lateral growth of Al3Ni and Al3Ni2 is a result of
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36

Nakajima, Osaake. "Evaluation of Lateral Zn Diffusion in GaAs under a Diffusion Mask." IEEJ Transactions on Electronics, Information and Systems 113, no. 7 (1993): 556–65. http://dx.doi.org/10.1541/ieejeiss1987.113.7_556.

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37

Berezhkovskii, Alexander M., and George H. Weiss. "Diffusion in multilayer media: Transient behavior of the lateral diffusion coefficient." Journal of Chemical Physics 124, no. 15 (2006): 154710. http://dx.doi.org/10.1063/1.2188394.

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38

Mensi, Mounir, Ruslan Ivanov, Tomas K. Uždavinys, et al. "Direct Measurement of Nanoscale Lateral Carrier Diffusion: Toward Scanning Diffusion Microscopy." ACS Photonics 5, no. 2 (2017): 528–34. http://dx.doi.org/10.1021/acsphotonics.7b01061.

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39

Saxton, M. J. "Lateral diffusion in an archipelago. Distance dependence of the diffusion coefficient." Biophysical Journal 56, no. 3 (1989): 615–22. http://dx.doi.org/10.1016/s0006-3495(89)82708-0.

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40

Wu, Wen, Zhouhu Wu, and Zhiwen Song. "Calculation method for steady-state pollutant concentration in mixing zones considering variable lateral diffusion coefficient." Water Science and Technology 76, no. 1 (2017): 201–9. http://dx.doi.org/10.2166/wst.2017.206.

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Prediction of the pollutant mixing zone (PMZ) near the discharge outfall in Huangshaxi shows large error when using the methods based on the constant lateral diffusion assumption. The discrepancy is due to the lack of consideration of the diffusion coefficient variation. The variable lateral diffusion coefficient is proposed to be a function of the longitudinal distance from the outfall. Analytical solution of the two-dimensional advection–diffusion equation of a pollutant is derived and discussed. Formulas to characterize the geometry of the PMZ are derived based on this solution, and a stand
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41

Hayakawa, Katsumi, Koichi Tanda, Akira Nishimura, Daisuke Kinoshita, Zenro Kizaki, and Koji Ohno. "Diffusion Restriction in the Optic Radiation of Term Neonates With Hypoxic-Ischemic Encephalopathy Demonstrated by Magnetic Resonance Imaging (MRI)." Journal of Child Neurology 36, no. 11 (2021): 950–57. http://dx.doi.org/10.1177/08830738211015019.

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Objective: There has been no previous report of diffusion restriction in the optic radiation of term neonates with hypoxic-ischemic encephalopathy. Here, using diffusion-weighted magnetic resonance imaging (MRI), we assessed diffusion restriction in the optic radiation within the first 2 weeks of life and estimated signal changes and the apparent diffusion coefficient in the optic radiation and lateral geniculate body using T1-weighted MRI. Materials and Methods: Forty-five term neonates with hypoxic-ischemic encephalopathy underwent MRI twice during the first 2 weeks of life. Diffusion-weight
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42

Susfalk, R. B., W. X. Cheng, D. W. Johnson, R. F. Walker, P. Verburg, and S. Fu. "Lateral diffusion and atmospheric CO2 mixing compromise estimates of rhizosphere respiration in a forest soil." Canadian Journal of Forest Research 32, no. 6 (2002): 1005–15. http://dx.doi.org/10.1139/x02-028.

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Measurements of rhizosphere carbon efflux are critical to the determination of soil carbon balance by CO2 flux measurements. We attempted to measure rhizosphere respiration in a forest ecosystem by transplanting 13C-enriched soils from a tallgrass prairie into a mixed-conifer forest soil but found that atmospheric air mixing and lateral diffusion confounded delta13C-CO2 measurements. Surface CO2 efflux (delta13C [Formula: see text] –20‰) was enriched 6‰ relative to soil CO2 measured at depth because of the presence of atmospheric-derived CO2 (–8‰) near the soil surface. The delta13C-CO2 value
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43

Ohta, Takao, and Shigeyuki Komura. "Lateral diffusion on a frozen random surface." EPL (Europhysics Letters) 132, no. 5 (2020): 50007. http://dx.doi.org/10.1209/0295-5075/132/50007.

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44

Musagalieva, G. B., L. A. Dzhigola, K. V. Kargina, and A. S. Resnyanskaya. "The study lateral diffusion of oil sludge." NATURAL SCIENCES 57, no. 4 (2016): 095–99. http://dx.doi.org/10.21672/1818-507x-2016-57-4-095-099.

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45

Liu, Joyce C., J. W. Mayer, and J. C. Barbour. "Phase formation of NiAl3on lateral diffusion couples." Journal of Applied Physics 64, no. 2 (1988): 651–55. http://dx.doi.org/10.1063/1.341956.

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46

MORISON, JAMES I. L., and TRACY LAWSON. "Does lateral gas diffusion in leaves matter?" Plant, Cell & Environment 30, no. 9 (2007): 1072–85. http://dx.doi.org/10.1111/j.1365-3040.2007.01685.x.

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47

Lalchev, Z. I., and A. R. Mackie. "Molecular lateral diffusion in model membrane systems." Colloids and Surfaces B: Biointerfaces 15, no. 2 (1999): 147–60. http://dx.doi.org/10.1016/s0927-7765(99)00054-5.

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48

Budiarto, E., M. Segovia, P. Borden, and S. Felch. "Carrier illumination measurement of dopant lateral diffusion." Nuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms 237, no. 1-2 (2005): 324–29. http://dx.doi.org/10.1016/j.nimb.2005.05.008.

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49

Šonský, J., H. Valk, J. Huizenga, R. W. Hollander, C. W. E. van Eijk, and P. M. Sarro. "Silicon drift detector with reduced lateral diffusion:." Nuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment 439, no. 2-3 (2000): 513–18. http://dx.doi.org/10.1016/s0168-9002(99)00939-0.

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50

Soubias, Olivier, Walter E. Teague, and Klaus Gawrisch. "Lipid Lateral Diffusion and Hydrocarbon Chain Order." Biophysical Journal 100, no. 3 (2011): 331a. http://dx.doi.org/10.1016/j.bpj.2010.12.2008.

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