Allicin inhibits cell polarization, migration and division via its direct effect on microtubules

Structure of the αβ tubulin dimer by electron crystallography

Nogales, E., Wolf, S., & Downing, K. (1998) · Nature · doi:10.1038/34465 · Cited by 1,623 · see citing works

Antimicrobial properties of allicin from garlic

Ankri, S., & Mirelman, D. (1999) · Microbes and Infection · doi:10.1016/s1286-4579(99)80003-3 · Cited by 1,185 · see citing works

Refined structure of αβ-tubulin at 3.5 Å resolution 1 1Edited by I. A. Wilson

Löwe, J., Li, H., Downing, K. H., & Nogales, E. (2001) · Journal of Molecular Biology · doi:10.1006/jmbi.2001.5077 · Cited by 1,139 · see citing works

Allicin, the Antibacterial Principle of Allium sativum. I. Isolation, Physical Properties and Antibacterial Action

Cavallito, C. J., & Bailey, J. H. (1944) · Journal of the American Chemical Society · doi:10.1021/ja01239a048 · Cited by 736 · see citing works

Microtubules and actin filaments: dynamic targets for cancer chemotherapy

Jordan, M. A., & Wilson, L. (1998) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(98)80095-1 · Cited by 613 · see citing works

Targeting Microtubules for Cancer Chemotherapy

Zhou, J., & Giannakakou, P. (2005) · Anti-Cancer Agents in Medicinal Chemistry · doi:10.2174/1568011053352569 · Cited by 473 · see citing works

Cell distribution of stress fibres in response to the geometry of the adhesive environment

Théry, M., Pépin, A., Dressaire, E., Chen, Y., & Bornens, M. (2006) · Cell Motility and the Cytoskeleton · doi:10.1002/cm.20126 · Cited by 452 · see citing works

The mode of action of allicin: trapping of radicals and interaction with thiol containing proteins

Rabinkov, A., Miron, T., Konstantinovski, L., Wilchek, M., Mirelman, D., & Weiner, L. (1998) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/s0304-4165(97)00104-9 · Cited by 426 · see citing works

The effects of methyl (5-(2-thienylcarbonyl)-1H-benzimidazol-2-yl) carbamate, (R 17934; NSC 238159), a new synthetic antitumoral drug interfering with microtubules, on mammalian cells cultured in vitro.

Mj, D. B., de Veire, R. M. V., Fe, A., Borgers, M. J., & Janssen, P. A. (1976) · PubMed · Cited by 426 · see citing works

Involvement of microtubules in the control of adhesion-dependent signal transduction

Bershadsky, A. D., Chausovsky, A., Becker, E., Lyubimova, A., & Geiger, B. (1996) · Current Biology · doi:10.1016/s0960-9822(02)70714-8 · Cited by 379 · see citing works

The mode of action of allicin: Its ready permeability through phospholipid membranes may contribute to its biological activity

Miron, T., Rabinkov, A., Mirelman, D., Wilchek, M., & Weiner, L. (2000) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/s0005-2736(99)00174-1 · Cited by 353 · see citing works

Effect of colcemid on the locomotory behaviour of fibroblasts

Vasiliev, J. M., Gelfand, I. M., Domnina, L. V., Ivanova, O. Y., Sg, K., & Olshevskaja, L. V. (1970) · Development · doi:10.1242/dev.24.3.625 · Cited by 341 · see citing works

Fibroblast contractility and actin organization are stimulated by microtubule inhibitors

Danowski, B. A. (1989) · Journal of Cell Science · doi:10.1242/jcs.93.2.255 · Cited by 308 · see citing works

Allicin, the Antibacterial Principle of Allium sativum. II. Determination of the Chemical Structure

Cavallito, C. J., Buck, J. S., & Suter, C. M. (1944) · Journal of the American Chemical Society · doi:10.1021/ja01239a049 · Cited by 289 · see citing works

Actin-dependent Lamellipodia Formation and Microtubule-dependent Tail Retraction Control-directed Cell Migration

Ballestrem, C., Wehrle‐Haller, B., Hinz, B., et al. (2000) · Molecular Biology of the Cell · doi:10.1091/mbc.11.9.2999 · Cited by 248 · see citing works

Allicin (from garlic) induces caspase-mediated apoptosis in cancer cells

Oommen, S., Anto, R. J., Gopala, S., & Karunagaran, D. (2003) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2003.11.059 · Cited by 237 · see citing works

Diallyl Trisulfide Suppresses the Proliferation and Induces Apoptosis of Human Colon Cancer Cells through Oxidative Modification of β-Tubulin

Hosono, T., Hosono‐Fukao, T., Ogihara, J., et al. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m507127200 · Cited by 237 · see citing works

Allium Vegetables and Organosulfur Compounds: Do They Help Prevent Cancer?

Bianchini, F., & Vainio, H. (2001) · Environmental Health Perspectives · doi:10.1289/ehp.01109893 · Cited by 235 · see citing works

G1 and G2 cell-cycle arrest following microtubule depolymerization in human breast cancer cells

Blajeski, A. L., Phan, V., Kottke, T. J., & Kaufmann, S. H. (2002) · Journal of Clinical Investigation · doi:10.1172/jci13275 · Cited by 232 · see citing works

Contraction due to microtubule disruption is associated with increased phosphorylation of myosin regulatory light chain.

Kolodney, M. S., & Elson, E. L. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.22.10252 · Cited by 229 · see citing works

Composition, stability, and bioavailability of garlic products used in a clinical trial

Lawson, L. D., & Gardner, C. D. (2005) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf050536+ · Cited by 227 · see citing works

Colcemid and the mitotic cycle

Rieder, C. L., & Palazzo, R. E. (1992) · Journal of Cell Science · doi:10.1242/jcs.102.3.387 · Cited by 227 · see citing works

Effect of Purified Allicin, the Major Ingredient ofFreshly Crushed Garlic, on Cancer Cell Proliferation

Hirsch, K., Danilenko, M., Giat, J., Miron, T., Rabinkov, A., Wilchek, M., Mirelman, D., Levy, J., & Sharoni, Y. (2000) · Nutrition and Cancer · doi:10.1207/s15327914nc382_14 · Cited by 211 · see citing works

Tubulin sulfhydryl groups as probes and targets for antimitotic and antimicrotubule agents

Ludueña, R. F., & Roach, M. C. (1991) · Pharmacology & Therapeutics · doi:10.1016/0163-7258(91)90027-j · Cited by 208 · see citing works

Microtubule Depolymerization Induces Stress Fibers, Focal Adhesions, and DNA Synthesis via the GTP-Binding Protein Rho

Liu, B. P., Chrzanowska‐Wodnicka, M., & Burridge, K. (1998) · Cell Communication & Adhesion · doi:10.3109/15419069809040295 · Cited by 201 · see citing works

Chemical Investigations on Alliin, the Specific Principle of Garlic

Stoll, A., & Seebeck, E. (1951) · Advances in enzymology and related areas of molecular biology/Advances in enzymology and related subjects · doi:10.1002/9780470122563.ch8 · Cited by 194 · see citing works

Selective, covalent modification of β-tubulin residue Cys-239 by T138067, an antitumor agent with in vivo efficacy against multidrug-resistant tumors

Shan, B., Medina, J. C., Santha, E., et al. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.10.5686 · Cited by 165 · see citing works

Pearling in cells: A clue to understanding cell shape

Bar‐Ziv, R., Tlusty, T., Moses, E., et al. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.18.10140 · Cited by 161 · see citing works

Microtubule-dependent control of cell shape and pseudopodial activity is inhibited by the antibody to kinesin motor domain.

Rodionov, V., Gyoeva, F. K., Tanaka, E. M., Bershadsky, A. D., Vasiliev, J. M., & Gelfand, V. I. (1993) · The Journal of Cell Biology · doi:10.1083/jcb.123.6.1811 · Cited by 156 · see citing works

Caspase-independent cell death by allicin in human epithelial carcinoma cells: involvement of PKA

Park, S., Cho, S.-J., Kwon, H.-C., Lee, K.-R., Rhee, D., & Pyo, S. (2004) · Cancer Letters · doi:10.1016/j.canlet.2004.10.009 · Cited by 151 · see citing works

Induction of apoptosis by the garlic-derived compound S-allylmercaptocysteine (SAMC) is associated with microtubule depolymerization and c-Jun NH(2)-terminal kinase 1 activation.

Xiao, D., Pinto, J. T., Soh, J., Deguchi, A., Gundersen, G. G., Palazzo, A. F., Yoon, J.-T., Shirin, H., & Weinstein, I. B. (2003) · PubMed · Cited by 140 · see citing works

Microtubule Dynamics during the Cell Cycle: The Effects of Taxol and Nocodazole on the Microtubule System of Pt K2 Cells at Different Stages of the Mitotic Cycle

Brabander, M. D., Geuens, G., Nuydens, R., Willebrords, R., Aerts, F., Mey, J. D., & McIntosh, J. R. (1986) · International review of cytology · doi:10.1016/s0074-7696(08)60250-8 · Cited by 139 · see citing works

S-Allylmercaptoglutathione: the reaction product of allicin with glutathione possesses SH-modifying and antioxidant properties

Rabinkov, A., Miron, T., Mirelman, D., Wilchek, M., Glozman, S., Yavin, E., & Weiner, L. M. (2000) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/s0167-4889(00)00119-1 · Cited by 137 · see citing works

Bcl-2 phosphorylation and apoptosis activated by damaged microtubules require mTOR and are regulated by Akt

Asnaghi, L., Calastretti, A., Bevilacqua, A., D’Agnano, I., Gatti, G., Canti, G. L., Delia, D., Capaccioli, S., & Nicolin, A. (2004) · Oncogene · doi:10.1038/sj.onc.1207698 · Cited by 132 · see citing works

An overview of the antifungal properties of allicin and its breakdown products-the possibility of a safe and effective antifungal prophylactic

Davis, S. R. (2005) · Mycoses · doi:10.1111/j.1439-0507.2004.01076.x · Cited by 119 · see citing works

The Antiatherogenic Effect of Allicin: Possible Mode of Action

Gonen, A., Harats, D., Rabinkov, A., Miron, T., Mirelman, D., Wilchek, M., Weiner, L. M., Ulman, E., Levkovitz, H., Ben‐Shushan, D., et al. (2005) · Pathobiology · doi:10.1159/000091330 · Cited by 119 · see citing works

Spreading of non-transformed and transformed cells

Vasiliev, J. M. (1984) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/0304-419x(84)90006-4 · Cited by 117 · see citing works

Antitumor activity of Z-ajoene, a natural compound purified from garlic: antimitotic and microtubule-interaction properties

Li, M. (2002) · Carcinogenesis · doi:10.1093/carcin/23.4.573 · Cited by 114 · see citing works

Effects of a series of organosulfur compounds on mitotic arrest and induction of apoptosis in colon cancer cells

Xiao, D., Pinto, J. T., Gundersen, G. G., et al. (2005) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-05-0152 · Cited by 110 · see citing works

The Local Electrostatic Environment Determines Cysteine Reactivity of Tubulin

Britto, P. J., Knipling, L., & Wolff, J. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m204263200 · Cited by 108 · see citing works

The pharmacological effects of allicin, a constituent of garlic oil

Mayeux, P. R., AGRAWAL, K. C., Tou, J., King, B. T., Lippton, H. L., Hyman, A. L., Kadowitz, P. J., & McNamara, D. B. (1988) · Inflammation Research · doi:10.1007/bf01969110 · Cited by 96 · see citing works

Alliin Lyase (Alliinase) from Garlic (Allium sativum)

Rabimkov, A., Zhu, X.-Z., Grafi, G., Galili, G., & Mirelman, D. (1994) · Applied Biochemistry and Biotechnology · doi:10.1007/bf02788739 · Cited by 94 · see citing works

A Spectrophotometric Assay for Allicin and Alliinase (Alliin lyase) Activity: Reaction of 2-Nitro-5-thiobenzoate with Thiosulfinates

Miron, T., Rabinkov, A., Mirelman, D., Weiner, L. M., & Wilchek, M. (1998) · Analytical Biochemistry · doi:10.1006/abio.1998.2924 · Cited by 92 · see citing works

Differential Inhibition of Human Platelet Aggregation by Selected Allium Thiosulfinates

Briggs, W. H., Xiao, H., Parkin, K. L., Shen, C., & Goldman, I. L. (2000) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf0004412 · Cited by 92 · see citing works

Effects of allicin on both telomerase activity and apoptosis in gastric cancer SGC-7901 cells

Sun, L. (2003) · World Journal of Gastroenterology · doi:10.3748/wjg.v9.i9.1930 · Cited by 89 · see citing works

Induction of Histone Acetylation and Inhibition of Growth of Mouse Erythroleukemia Cells by S-Allylmercaptocysteine

Lea, M. A., Rasheed, M., Randolph, V. M., Khan, F., Shareef, A., & desBordes, C. (2002) · Nutrition and Cancer · doi:10.1207/s15327914nc431_11 · Cited by 88 · see citing works

Efficacy of allicin, the reactive molecule of garlic, in inhibiting Aspergillus spp. in vitro, and in a murine model of disseminated aspergillosis

Shadkchan, Y. (2004) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkh174 · Cited by 80 · see citing works

Polarization of pseudopodial activities: cytoskeletal mechanisms

Vasiliev, J. M. (1991) · Journal of Cell Science · doi:10.1242/jcs.98.1.1 · Cited by 77 · see citing works

Apoptotic killing of B-chronic lymphocytic leukemia tumor cells by allicin generated in situ using a rituximab-alliinase conjugate

Arditti, F. D., Rabinkov, A., Miron, T., Reisner, Y., Berrébi, A., Wilchek, M., & Mirelman, D. (2005) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.325.4.2 · Cited by 76 · see citing works

Allicin-induced decrease in formation of fatty streaks (atherosclerosis) in mice fed a cholesterol-rich diet

Abramovitz, D., Gavri, S., Harats, D., et al. (1999) · Coronary Artery Disease · doi:10.1097/00019501-199910000-00012 · Cited by 76 · see citing works

Inhibition of tumor growth by a novel approach: in situ allicin generation using targeted alliinase delivery.

Miron, T., Mironchik, M., Mirelman, D., Wilchek, M., & Rabinkov, A. (2003) · PubMed · Cited by 76 · see citing works

Microtubule disassembly delays the G2–M transition in vertebrates

Rieder, C. L., & Cole, R. W. (2000) · Current Biology · doi:10.1016/s0960-9822(00)00678-3 · Cited by 73 · see citing works

Mechanisms of polarization of the shape of fibroblasts and epitheliocytes: Separation of the roles of microtubules and Rho-dependent actin–myosin contractility

Omelchenko, T., Vasiliev, J. M., Gelfand, I. M., Feder, H. H., & Bonder, E. M. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.152339899 · Cited by 71 · see citing works

Peroxynitrite Oxidation of Tubulin Sulfhydryls Inhibits Microtubule Polymerization

Landino, L. M., Hasan, R., McGaw, A., Cooley, S., Smith, A. W., Masselam, K., & Kim, G. J. (2002) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.2001.2729 · Cited by 70 · see citing works

Effect of Microtubule Inhibitors on Malignant Invasion In Vitro 2

Mareel, M. M. K., & Brabander, M. J. D. (1978) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/61.3.787 · Cited by 70 · see citing works

A Multidisciplinary Approach to the Study of T Cell Migration

Long, A., Mitchell, S. B., Kashanin, D., Williams, V., Prina‐Mello, A., Shvets, I. V., Kelleher, D. P., & Volkov, Y. (2004) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1322.035 · Cited by 69 · see citing works

Quantitative analysis of cytoskeletal organization by digital fluorescent microscopy

Lichtenstein, N., Geiger, B., & Kam, Z. (2003) · Cytometry Part A · doi:10.1002/cyto.a.10053 · Cited by 69 · see citing works

Platelets and Microtubules

Menche, D., Israel, A. L., & Karpatkin, S. (1980) · Journal of Clinical Investigation · doi:10.1172/jci109855 · Cited by 64 · see citing works

Allicin inhibits SDF-1α-induced T cell interactions with fibronectin and endothelial cells by down-regulating cytoskeleton rearrangement, Pyk-2 phosphorylation and VLA-4 expression

Sela, U., Ganor, S., Hecht, I., Brill, A., Miron, T., Rabinkov, A., Wilchek, M., Mirelman, D., Lider, O., & Hershkoviz, R. (2004) · Immunology · doi:10.1111/j.0019-2805.2004.01841.x · Cited by 63 · see citing works

Chemoprevention by naturally occurring and synthetic agents in oral, liver, and large bowel carcinogenesis

Mori, H., Tanaka, T., Sugie, S., Yoshimi, N., Kawamori, T., Hirose, Y., & Ohnishi, M. (1997) · Journal of Cellular Biochemistry · doi:10.1002/(sici)1097-4644(1997)27+ · Cited by 58 · see citing works

Nocodazole, a microtubule depolymerising agent, induces apoptosis of chronic lymphocytic leukaemia cells associated with changes in Bcl-2 phosphorylation and expression

Beswick, R. W., Ambrose, H. E., & Wagner, S. D. (2005) · Leukemia Research · doi:10.1016/j.leukres.2005.08.009 · Cited by 57 · see citing works

Thiol–disulphide interchange in tubulin: kinetics and the effect on polymerization

Britto, P. J., Knipling, L., McPhie, P., et al. (2005) · Biochemical Journal · doi:10.1042/bj20042118 · Cited by 55 · see citing works

Effect of colcemid on the spreading of fibroblasts in culture

Ivanova, O. Y., Margolis, L. B., Vasiliev, J. M., et al. (1976) · Experimental Cell Research · doi:10.1016/0014-4827(76)90431-6 · Cited by 51 · see citing works

Sulfhydryls of tubulin

Roychowdhury, M., Sarkar, N., Manna, T. K., et al. (2000) · European Journal of Biochemistry · doi:10.1046/j.1432-1327.2000.01369.x · Cited by 47 · see citing works

Detection of Disulfide Bonds in Bovine Brain Tubulin and Their Role in Protein Folding and Microtubule Assembly in Vitro: A Novel Disulfide Detection Approach

Chaudhuri, A. R., KHAN, I. A., & Ludueña, R. F. (2001) · Biochemistry · doi:10.1021/bi0101603 · Cited by 46 · see citing works

What structures, besides adhesions, prevent spread cells from rounding up?

Zand, M. S., & Albrecht‐Buehler, G. (1989) · Cell Motility and the Cytoskeleton · doi:10.1002/cm.970130307 · Cited by 43 · see citing works

The polarization of fibroblasts in early primary cultures is independent of microtubule integrity

Middleton, C. A., Brown, A. F., Brown, R. M., et al. (1989) · Journal of Cell Science · doi:10.1242/jcs.94.1.25 · Cited by 38 · see citing works

Spreading and locomotion of tissue cells: factors controlling the distribution of pseudopodia

Vasiliev, J. M. (1982) · Philosophical transactions of the Royal Society of London. Series B, Biological sciences · doi:10.1098/rstb.1982.0122 · Cited by 36 · see citing works

Stabilization of a metastable state of <i>Torpedo californica</i> acetylcholinesterase by chemical chaperones

Millard, C. B., Shnyrov, V. L., Newstead, S., Shin, I., Roth, E., Silman, I., & Weiner, L. (2003) · Protein Science · doi:10.1110/ps.03110703 · Cited by 30 · see citing works

Rapid completion of mitosis and cytokinesis in PtK cells following release from nocodazole arrest.

Hamilton, B. T., & Snyder, J. A. (1982) · PubMed · Cited by 29 · see citing works

A method for continuous production of allicin using immobilized alliinase

Miron, T., Sivaraman, H., Rabinkov, A., et al. (2006) · Analytical Biochemistry · doi:10.1016/j.ab.2006.01.030 · Cited by 27 · see citing works

The action of cytochalasin A on the in vitro polymerization of brain tubulin and muscle G‐actin

Himes, R. H., & Houston, L. L. (1976) · Journal of Supramolecular Structure · doi:10.1002/jss.400050109 · Cited by 26 · see citing works

Ethacrynic acid inhibition of microtubule assembly in Vitro

Xu, S., Roychowdhury, S., Gaskin, F., et al. (1992) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(92)90598-q · Cited by 20 · see citing works

A dozen questions about how tissue cells crawl.

Harris, A. K. (1999) · PubMed · Cited by 17 · see citing works

[Allicin induced cell cycle arrest in human gastric cancer cell lines].

Ha, M.-W., & Yuan, Y. (2004) · PubMed · Cited by 15 · see citing works

Interaction of ethacrynic acid with bovine brain tubulin

Ludueña, R. F., Roach, M. C., & Epstein, D. L. (1994) · Biochemical Pharmacology · doi:10.1016/0006-2952(94)90547-9 · Cited by 15 · see citing works

Mechanisms of regulation of pseudopodial activity by the microtubule system.

Bershadsky, A. D., & Vasiliev, J. M. (1993) · PubMed · Cited by 13 · see citing works

Die Synthese des natürlichen Alliins

Stoll, A., & Seebeck, E. (1950) · Cellular and Molecular Life Sciences · doi:10.1007/bf02152860 · Cited by 9 · see citing works

Antimicrotubular effect of calvatic acid and of some related compounds

Gadoni, E., Gabriel, L., Olivero, A., et al. (1995) · Cell Biochemistry and Function · doi:10.1002/cbf.290130403 · Cited by 8 · see citing works

Proteasome inhibitors abolish cell death downstream of caspase activation during anti-microtubule drug-induced apoptosis in leukemia cells.

Nagy, K., Peták, I., Imre, G., et al. (2005) · PubMed · Cited by 5 · see citing works

Stepwise Modulation of ATPase Activity, Nucleotide Trapping, and Sliding Motility of Myosin S1 by Modification of the Thiol Region with Residues of Increasing Size

Tiepold, M., Kliche, W., Pfannstiel, J., et al. (2000) · Biochemistry · doi:10.1021/bi991199z · Cited by 4 · see citing works

Chemical Constituents and Pharmacological Activities of Garlic (Allium sativum L.): A Review

El-Saber Batiha, G., Magdy Beshbishy, A., G. Wasef, L., Elewa, Y. H. A., A. Al-Sagan, A., Abd El-Hack, M. E., Taha, A. E., M. Abd-Elhakim, Y., & Prasad Devkota, H. (2020) · Nutrients · doi:10.3390/nu12030872 · Cited by 931 · see citing works

Allicin: Chemistry and biological properties

Borlinghaus, J., Albrecht, F., Gruhlke, M., Nwachukwu, I., & Slusarenko, A. (2014) · Molecules · doi:10.3390/molecules190812591 · Cited by 893 · see citing works

The Effects of Allicin, a Reactive Sulfur Species from Garlic, on a Selection of Mammalian Cell Lines

Gruhlke, M., Nicco, C., Batteux, F., & Slusarenko, A. (2016) · Antioxidants · doi:10.3390/antiox6010001 · Cited by 165 · see citing works

Biological evaluation of synthesized allicin and its transformation products obtained by microwaves in methanol: Antioxidant activity and effect on cell growth

Ilić, D. P., Stojanović, S., Najman, S., Nikolić, V. D., Stanojević, L. P., Tačić, A., & Nikolić, L. B. (2015) · Biotechnology &amp; Biotechnological Equipment · doi:10.1080/13102818.2014.994267 · Cited by 20 · see citing works

Low Allicin Release from Garlic Supplements: a Major Problem Due to the Sensitivities of Alliinase Activity

Lawson, L. D., & Wang, Z. J. (2001) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf001287m · Cited by 115 · see citing works

Equine platelets contain an anisotropic array of microtubules which reorganise upon activation

Tablin, F., & Castro, M. D. (1992) · Comparative Clinical Pathology · doi:10.1007/bf00426165 · Cited by 7 · see citing works

Distribution of acetylated α‐tubulin in retina and in in vitro—assembled microtubules

Sale, W. S., Besharse, J. C., & Piperno, G. (1988) · Cell Motility and the Cytoskeleton · doi:10.1002/cm.970090306 · Cited by 94 · see citing works

Interactions of a new antimitotic agent, NSC-181928, with purified tubulin

Hamel, E., & Lin, C. M. (1982) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(82)91338-9 · Cited by 17 · see citing works

Cardiostimulatory and antiarrhythmic activity of tubulin-binding agents.

Lampidis, T. J., Kolonias, D. S., Savaraj, N., & Rubin, R. W. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.4.1256 · Cited by 48 · see citing works