The Cadherin Superfamily

Advances in Molecular and Cell Biology

Volumn 28, Issue C, 1999, Pages 27-63

  Stappert, Jörg ^a   Kemler, Rolf ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

EID: 77956716163     PISSN: 15692558     EISSN: None     Source Type: Book Series    
DOI: 10.1016/S1569-2558(08)60043-0     Document Type: Article

References (235)

1. Butz H., Aberle S., Stappert J., Weissig H., Kemler R., and Hoschuetzky H. Assembly of the cadherin-catenin complex in vitro with recombinant proteins. J. Cell Sci. 107 (1994) 3655-3663
2. Aberle H., Bierkamp C., Torchard D., Serova O., Wagner T., Natt E., Wirsching J., Heidkamper C., Montagna M., Lynch H.T., Lenoir G.M., Scherer G., Feunteun J., and Rentier R. The human plakoglobin gene localizes on chromosome 17q21 and is subjected to loss of heterozygosity in breast and ovarian cancers. Proc. Natl. Acad. Sci. USA. 92 (1995) 6384-6388
3. Aberle H., Schwartz H., Hoschuetzky H., and Kemler R. Single Amino Acid Substitutions In Proteins Of the Armadillo Gene Family Abolish Their Binding to Alpha-Catenin. J. Biol. Chem. 271 (1996) 1520-1526
4. Aberle H., Schwartz H., and Kemler R. Cadherin-catenin complex: protein interactions and their implications for cadherin function. J. Cell Biochem. 61 (1996) 514-523
5. Adams C.L., Nelson W.J., and Smith S.J. Quantitative analysis of cadherin-catenin-actin reorganization during development of. cell-cell adhesion. J. Cell Biol. 135 (1996) 1899-1911
6. Aghib D.F., and McCrea P.D. The E-Cadherin Complex Contains the Src Substrate P120. Exp. Cell Res. 218 (1995) 359-369
7. Amagai M. Adhesion molecules. I: Keratinocyte-keratinocyte interactions; cadherins and pemphigus. J. Invest. Dermatol. 104 (1995) 146-152
8. Angres B., Barth A., and Nelson W.J. Mechanism For Transition From Initial to Stable Cell-Cell Adhesion - Kinetic Analysis Of E-Cadherin-Mediated Adhesion Using a Quantitative Adhesion Assay. J. Cell Biol. 134 (1996) 549-557
9. Behrens J., Vakaet L., Friis R., Winterhager E., Vauroy F., Mareel M.M., and Birchmeier W. Loss Of epithelial differentiation and gain of invasiveness correlates with tyrosine phosphorylation of the E-cadherin beta-catenin complex in cells transformed with a. temperature-sensitive v-src gene. J. Cell Biol. 120 (1993) 757-766
10. Behrens J. Cell contacts, differentiation, and invasiveness of epithelial cells. Invasion Metastasis. 14 (1994) 61-70
11. Behrens J., von Kries J.P., Kuhl M., Bruhn L., Wedlich D., Grosschedl R., and Birchmeier W. Functional interaction of beta-catenin with the transcription factor. LEF-1. Nature. 382 (1996) 638-642
12. 2+-dependent cell adhesion molecule expressed in liver and intestine. J. Cell Biol. 125 (1994) 1353-1369
13. Bierkamp C., McLaughlin K.J., Schwarz H., Huber O., and Kemler R. Embryonic heart and skin defects in mice lacking plakoglobin. Dev. Biol. 180 (1996) 780-785
14. Birchmeier W., Hulsken J., and Behrens J. Adherens junction proteins in tumour progression. Cancer Surveys 24 (1995) 129-140 1995
15. Blaschuk O.W., Pouliot Y., and Holland P.C. Identification of a conserved region common to cadherins and influenza strain A hemagglutinins. J. Mol. Biol. 211 (1990) 679-682
16. Blaschuk O.W., Sullivan R., David S., and Pouliot Y. Identification of a cadherin cell adhesion recognition sequence. Dev. Biol. 139 (1990) 227-229
17. Blum S., Ness W., Petrow W., and Achenbach F. Localization of protein kinase C in primary cultures of human keratinocytes in relation to cell contact proteins. Cell Signal. 6 (1994) 157-165
18. Bornemann A., and Schmalbruch H. Immunocytochemistry of m-cadherin in mature and regenerating rat muscle. Anat. Rec. 239 (1994) 119-125
19. Brady-Kalnay S.M., Rimm D.L., and Tonks N.K. Receptor protein tyrosine phosphatase PTPmu associates with cadherins and catenins in vivo. J. Cell Biol. 130 (1995) 977-986
20. Brieher W.M., Yap A.S., and Gumbiner B.M. Lateral dimerization is required for the homophilic binding activity of C-cadherin. J. Cell Biol. 135 (1996) 487-496
21. Broders F., and Thiery J.P. Contribution of cadherins to directional cell migration and histogenesis in. Xenopus embryos. Cell Adhes. Commun. 3 (1995) 419-440
22. Brunner E., Peter O., Schweizer L., and Basler K. Pangolin Encodes a Lef-1 Homologue That Acts Downstream Of Armadillo to Transduce the Wingless Signal In Drosophila. Nature. 385 (1997) 829-833
23. Bussemakers M.J., and Schalken J.A. The role of cell adhesion molecules and proteases in tumor invasion and metastasis. WorldJ. Urol. 14 (1996) 151-156
24. 2+) -dependent cell-cell adhesion. FEBS Lett. 355 (1994) 195-200
25. Butz S., and Larue L. Expression of catenins during mouse embryonic development and in adult tissues. Cell Adhes. Commun. 3 (1995) 337-352
26. Cepek K.L., Shaw S.K., Parker C.M., Russell G.J., Morrow J.S., Rimm D.L., and Brenner M.B. Adhesion between epithelial cells and t lymphocytes mediated by E-cadherin and the. alpha(E)beta(7) integrin. Nature. 372 (1994) 190-193
27. Cepek K.L., Rimm D.L., and Brenner M.B. Expression of a candidate cadherin int-lymphocytes. Proc. Natl. Acad. Sci. USA. 93 (1996) 6567-6571
28. Chidgey M.A., Clarke J.P., and Garrod D.R. Expression of full-length desmosomol glycoproteins (desmocollins) is not sufficient to confer strong adhesion on transfected. L929 cells. J. Invest. Dermatol. 106 (1996) 689-695
29. Cifuentesdiaz C., Nicolet M., Goudou D., Rieger F., and Mege R.M. N-Cadherin expression in developing, adult and denervated chicken neuromuscular system - accumulations at both the neuromuscular junction and the node of ranvier. Development. 120 (1994) 1-11
30. Cifuentesdiaz C., Goudou D., Padilla F., Facchinetti P., Nicolet M., Mege R.M., and Rieger F. M-Cadherin distribution in the mouse adult neuromuscular system suggests a role in muscle innervation. Eur. J. Neurosci. 8 (1996) 1666-1676
31. Collins J.E., and Fleming T.P. Epithelial differentiation in the mouse preimplantation embryo: making adhesive cell contacts for the first time. Trends Biochem. Sci. 20 (1995) 307-312
32. Cowin P., Kapprell H.P., Franke W.W., Tamkun J., and Hynes R.O. Plakoglobin: a protein common to different kinds of intercellular adhering junctions. Cell. 46 (1986) 1063-1073
33. Cowin P., and Burke B. Cytoskeleton-membrane interactions. Curr. Opin. Cell Biol. 8 (1996) 56-65
34. Dahl U., Sjodin A., and Semb H. Cadherins regulate aggregation of pancreatic beta-cells in vivo. Development. 122 (1996) 2895-2902
35. Daniel J.M., and Reynolds A.B. The tyrosine kinase substrate p 120cas binds directly to E-cadherin but not to the adenomatous polyposis cold protein or alpha-catenin. Mol. Cell. Biol. 15 (1995) 4819-4824
36. Dantzig A.H., Hoskins J.A., Tabas L.B., Bright S., Shepard R.L., Jenkins I.L., Duckworth D.C., Sportsman J.R., Mackensen D., Rosteck Jr. P.R., et al. Association of intestinal peptide transport with a protein related to the cadherin superfamiiy. Science 264 (1994) 430-433
37. Doherty P., and Walsh F.S. CAM-FGF receptor interactions - a model for axonal growth. Mol. Cell. Neurosci. 8 (1996) 99-111
38. Donalies M., Cramer M., Ringwald M., and Starzinski-Powitz A. Expression of M-cadherin, a member of the cadherin multigene family, correlates with differentiation of skeletal muscle cells. Proc. Natl. Acad. Sci. USA. 88 (1991) 8024-8028
39. Dsouza B., and Taylorpapadimitriou J. Overexpression of erbb2 in human mammary epithelial cells signals inhibition of transcription of the. E-cadherin gene. Proc. Natl. Acad. Sci. U S A. 91 (1994) 7202-7206
40. Dufour S., Saint-Jeannet J.P., Broders F., Wedlich D., and Thiery J.P. Differential perturbations in the morphogenesis of anterior structures induced by overexpression of truncated. XB- and N-cadherins in Xenopus embryos. J. Cell Biol. 127 (1994) 521-535
41. Fannon A.M., Sherman D.L., Brophy G., Ilyina-Gragerova P.J., Friedrich Jr. V.L., and Colman D.R. Novel E-cadherin-mediated adhesion in peripheral nerve: Schwann cell architecture is stabilized by autotypic adherers junctions. J. Cell Biol. 129 (1995) 189-202
42. Franke W.W., Kapprell H.P., and Cowin P. Plakoglobin is a component of the filamentous subplasmalemmal coat of lens cells. Eur. J. Cell Biol. 43 (1987) 301-315
43. Franke W.W., Goldschmidt M.D., Zimbelmann R., Mueller H.M., Schiller D.L., and Cowin P. Molecular cloning and amino acid sequence of human plakoglobin, the common junctional plaque protein. Proc. Natl. Acad. Sci. USA. 86 (1989) 4027-4031
44. Fuchs M., Muller T., Lerch M.M., and Ullrich A. Association of human protein-tyrosine phosphatase kappa with members of the armadillo family. J. Biol. Chem. 271 (1996) 16712-16719
45. Fujimori T., and Takeiehi M. Disruption of epithelial cell-cell adhesion by exogenous expression of a mutated nonfunctional N-cadherin. Mol. Biol. Cell. 4 (1993) 37-47
46. Fukuyama R., and Shimizu N. Detection of epidermal growth factor receptors and E-cadherins in the basolateral membrane of A431 cells by laser scanning fluorescence microscopy. Jpn. J. Cancer Res. 82 (1991) 8-11
47. Funayama N., Fagotto F., McCrea P., and Gumbiner B.M. Embryonic axis induction by the armadillo repeat domain of beta catenin: evidence for intracellular signaling. J. Cell Biol. 128 (1995) 959-968
48. Ganzler S.I., and Redies C. R-cadherin expression during nucleus formation in chicken forebrain neuromeres. J. Neurosci. 15 (1995) 4157-4172
49. Garrod D., Chidgey M., and North A. Desmosomes - differentiation, development, dynamics and disease. Curr. Opin. Cell Biol. 8 (1996) 670-678
50. Geiger B., Yehuda-Levenberg S., and Bershadsky A.D. Molecular interactions in the submembrane plaque of cell-cell and cell-matrix adhesions. Acta Anat. 154 (1995) 46-62
51. Grunwald G.B., Geller R.L., and Lilien J. Enzymatic dissection of embryonic cell adhesive mechanisms. J. Cell Biol. 85 (1980) 766-776
52. Grunwald G.B., Bromberg R.E., Crowley N.J., and Lilien J. Enzymatic dissection of embryonic cell adhesive mechanisms. 11. Developmental regulation of an endogenous adhesive system in the chick neural retina. Dev. Biol. 86 (1981) 327-338
53. Guger K.A., and Gumbiner B.M. Beta- Catenin has Wnt-like activity and mimics the Nieuwkoop signaling center in. Xenopus dorsal-ventral patterning. Dev. Biol. 172 (1995) 115-125
54. Gumbiner B.M. Signal transduction of Beta-catenin. Curr. Opin. Cell Biol. 7 (1995) 634-640
55. Haegel H., Larue L., Ohsugi M., Fedorov L., Herrenknecht K., and Kemler R. Lack of beta-catenin affects mouse development at gastrulation. Development. 121 (1995) 3529-3537
56. Walsh H., Hall F.S., and Doherty P. Review: a role for the FGF receptor in the axonal growth response stimulated by cell adhesion molecules?. Cell Adhes. Commun. 3 (1996) 441-450
57. Hamaguchi M., Matsuyoshi N., Ohnishi Y., Gotoh B., Takeiehi M., and Nagai Y. P60v-src causes tyrosine phosphorylation and inactivation of the N-cadherin-catenin cell adhesion system. EMBOJ. 12 (1993) 307-314
58. Hatta K., Nose A., Nagafuchi A., and Takeiehi M. Cloning and expression of cDNA encoding a neural calcium-dependent cell adhesion molecule: its identity in the cadherin gene family. J. Cell Biol. 106 (1988) 873-881
59. Heasman J., Crawford A., Goldstone K., Garner-Hamriek P., Gumbiner B., MeCrea P., Kintner C., Noro C.Y., and Wylie C. Overexpression of cadherins and underexpression of beta-catenin inhibit dorsal mesoderm induction in early. Xenopus embryos. Cell. 79 (1994) 791-803
60. Hermiston M.L., and Gordon J.I. In vivo analysis of cadherin function in the mouse intestinal epithelium: essential roles in adhesion, maintenance of differentiation, and regulation of programmed cell death. J. Cell Biol. 129 (1995) 489-506
61. Hermiston M.L., and Gordon J.I. Inflammatory bowel disease and adenomas in mice expressing a dominant negative N-cadherin. Science 270 (1995) 1203-1207
62. Herrenknecht K., Ozawa M., Eckerskorn C., Lottspeich F., Lenter M., and Kemler R. The uvomorulin-anchorage protein alpha catenin is a vinculin homologue. Proc. Natl. Acad. Sci. U S A 88 (1991) 9156-9160
63. Hinck L., Nathke I.S., Papkoff J., and Nelson W.J. Dynamics of cadherin/catenin complex formation: novel protein interactions and pathways of complex assembly. J. Cell Biol. 125 (1994) 1327-1340
64. Hirano S., Kimoto N., Shimoyama Y., Hirohashi S., and Takeiehi M. Identification of a neural alpha-catenin as a key regulator of cadherin function and multicellular organization. Cell. 70 (1992) 293-301
65. Hoffmann I., and Balling R. Cloning and expression analysis of a novel mesodermally expressed cadherin. Dev. Biol. 169 (1995) 337-346
66. Holt C.E., Lemaire P., and Gurdon J.B. Cadherin-mediated cell interactions are necessary for the activation of myod in xenopus mesoderm. Proc. Natl. Acad. Sci. U S A. 91 (1994) 10844-10848
67. Hosehuetzky H., Aberle H., and Kemler R. Beta-catenin mediates the interaction of the cadherin-catenin complex with epidermal growth factor receptor. J. Cell Biol. 127 (1994) 1375-1380
68. Huber O., Bierkamp C., and Kemler R. Cadherins and catenins in development. Curr. Opin. Cell Biol. 8 (1996) 685-691
69. Huber O., Korn R., McLaughlin J., Ohsugi M., Herrmann B.G., and Kemler R. Nuclear local ization of beta-catenin by interaction with transcription factor LEF-1. Mech. Dev. 59 (1996) 3-10
70. Hulsken J., Birchmeier W., and Behrens J. E-cadherin and APC compete for the interaction with beta-catenin and the cytoskeleton. J. Cell Biol. 127 (1994) 2061-2069
71. Hynes R.O. Targeted mutations in cell adhesion genes - what have we learned from them. Dev. Biol. 180 (1996) 402-412
72. Hynes R.O., and Lander A.D. Contact and adhesive specificities in the associations, migrations, and targeting of cells and axons. Cell. 68 (1992) 303-322
73. Inuzuka H., Redies C., and Takeichi M. Differential expression of R- and N-cadherin in neural and mesodermal tissues during early chicken development. Development. 113 (1991) 959-967
74. Irintchev A., Zeschnigk M., Starzinskipowitz A., and Wernig A. Expression pattern of M-cadherin in normal, denervated, and regenerating mouse muscles. Dev. Dyn. 199 (1994) 326-337
75. Jiang W.G. E-cadherin and its associated protein catenins, cancer invasion and metastasis. Br. J. Surg. 83 (1996) 437-446
76. Jones E.Y. Three-dimensional structure of cell adhesion molecules. Curr. Opin. Cell Biol. 8 (1996) 602-608
77. Jou T.S., Stewart D.B., Stappert J., Nelson W.J., and Marrs J.A. Genetic and biochemical dissection of protein linkages in the. cadherin-catenin complex. Proc. Natl. Acad. USA. 92 (1995) 5067-5071
78. Kanai Y., Oehiai A., Shibata T., Oyama T., Ushijima S., Akimoto S., and Hirohashi S. C-erbB-2 gene product directly associates with beta-catenin and plakoglobin. Biochem. Biophys. Res. Commun. 208 (1995) 1067-1072
79. Karecla P.I., Bowden S.J., Green S.J., and Kilshaw P.J. Recognition of E-cadherin on epithelial cells by the mucosal T cell integrin alpha M290 beta 7 (alpha E beta 7). Eur. J. Immunol. 25 (1995) 852-856
80. Karecla P.I., Green S.J., Bowden S.J., Coadwell J., and Kilshaw P.J. Identification of a binding site for integrin alphaEbeta7 in the N-terminal domain of. E-cadherin. J. Biol. Chem. 271 (1996) 30909-30915
81. Karnovsky A., and Klymkowsky M.W. Anterior axis duplication in Xenopus induced by the over-expression of the cadherin-binding protein plakoglobin. Proc. Natl. Acad. Sci. USA. 92 (1995) 4522-4526
82. Kelly G.M., Erezyilmaz D.F., and Moon R.T. Induction of a secondary embryonic axis in zebrafish occurs following the overexpression of. Beta-catenin. Mech. Dev. 53 (1995) 261-273
83. Kemler R. Classical cadherins. Semin. Cell Biol. 3 (1992) 149-155
84. Kemler R. From cadherins to catenins: cytoplasmic protein interactions and regulation of cell adhesion. Trends Genet. 9 (1993) 317-321
85. Kemler R., Babinet C., Eisen H., and Jacob F. Surface antigen in early differentiation. Proc. Natl. Acad. Sci. USA. 74 (1977) 4449-4452
86. Kimura Y., Matsunami H., Lnoue T., Shimamura K., Uchida H., Ueno T., Miyazaki T., and Takeichi M. Cadherin-11 expressed in association with mesenchymal morphogenesis in the head, somite, and limb bud of early mouse embryos. Dev. Biol. 169 (1995) 347-358
87. Kinch M.S., Clark G.J., Der C.J., and Burridge K. Tyrosine phosphorylation regulates the adhesions of ras-transformed breast epithelia. J. Cell Biol. 130 (1995) 461-471
88. Kintner C. Regulation of embryonic cell adhesion by the cadherin cytoplasmic domain. Cell. 69 (1992) 225-236
89. Knudsen K.A., Soler A.P., Johnson K.R., and Wheelock M.J. Interaction of alpha-actinin with the cadherin/catenin cell-cell adhesion complex via alpha-catenin. J. Cell Biol. 130 (1995) 67-77
90. Knust E., and Leptin M. Adherens junctions in the drosophila embryo - the role of E-cadherin in their establishment and morphogenetic function. Bioessays. 18 (1996) 609-612
91. Koch P.J., Walsh M.J., Schmelz M., Goldschmidt M.D., Zimbelmann R., and Franke W.W. Identification of desmoglein, a constitutive desmosomal glycoprotein, as a member of the cadherin family of cell adhesion molecules. Eur. J. Cell Biol. 53 (1990) 1-12
92. Koch P.J., and Franke W.W. Desmosomal cadherins: another growing multigene family of adhesion molecules. Curr. Opin. Cell Biol. 6 (1994) 682-687
93. Korinek V., Barker N., Morrn P.J., Vanwichen D., Deweger R., Kinzler K.W., Vogelstein B., and Clevers H. Constitutive transcriptional activation by a beta-catenin-TCF complex in APC(-/-) colon carcinoma. Science. 275 (1997) 1784-1787
94. Kowalczyk A.P., Stappenbeck T.S., Parry D.A., Palka H.L., Virata M.L., Bornslaeger E.A., Nilles L.A., and Green K.J. Structure and function of desmosomal transmembrane core and plaque molecules. Biophys. Chem. 50 (1994) 97-112
95. Kuhl M., Finnemann S., Binder O., and Wedlich D. Dominant negative expression of a cytoplasmically deleted mutant of XB/U-cadherin disturbs mesoderm migration during gastrulation in. Xenopus laevis. Mech. Dev. 54 (1996) 71-82
96. Kuhl M., and Wedlich D. Xenopus cadherins: sorting out types and functions in embryogenesis. Dev. Dyn. 207 (1996) 121-134
97. Kypta R.M., Su H., and Reichardt L.F. Association between a transmembrane protein tyrosine phosphatase and the. cadherin-catenin complex. J. Cell Biol. 134 (1996) 1519-1529
98. Lampugnani M.G., Resnati M., Raiteri M., Pigott R., Pisacane A., Houen G., Ruco L.P., and Dejana E. A novel endothelia -specific membrane protein is a marker of. cell-cell contacts. J. Cell Biol. 118 (1992) 1511-1522
99. Lampugnani M.G., Corada M., Caveda L., Breviario F., Ayalon O., Geiger B., and Dejana E. The molecular organization of endothelial cell to cell junctions: differential association of plakoglobin, beta-catenin, and alpha-catenin with vascular endothelial cadherin (VE-cadherin). J. Cell Biol. 129 (1995) 203-217
100. Larabell C.A., Torres M., Rowning B.A., Yost C., Miller J.R., Wu M., Kimelman D., and Moon R.T. Establishment of the dorso-ventral axis in xenopus embryos is presaged by early asymmetries in beta-catenin that are modulated by the wnt signaling pathway. J. Cell Biol. 136 (1997) 1123-1136
101. Larue L., Ohsugi M., Hirchenhain J., and Kemler R. E-cadherin null mutant embryos fail to form a trophectoderm epithelium. Proc. Natl. Acad. Sci. USA. 91 (1994) 8263-8267
102. Larue L., Antos C., Butz S., Huber O., Delmas V., Dominis M., and Kemler R. A role for cadherins in tissue formation. Development. 122 (1996) 3185-3194
103. Lee C.H., and Gumbiner B.M. Disruption of gastrulation movements in Xenopus by a dominant-negative mutant for. C-cadherin. Dev. Biol. 171 (1995) 363-373
104. Lee S.W. H-cadherin, a novel cadherin with growth inhibitory functions and diminished expression in human breast cancer. Nat. Med. 2 (1996) 776-782
105. Levine E., Lee C.H., Kintner C., and Gumbiner B.M. Selective disruption of E-cadherin function in early Xenopus embryos by a dominant negative mutant. Development. 120 (1994) 901-909
106. Lewis J.E., Jensen P.J., Johnson K.R., and Wheelock M.J. E-cadherin mediates adherers junction organization through protein kinase. C. J. Cell Sci. 107 (1994) 3615-3621
107. Lewis J.E., Wahl J.K., Sass K.M., Jensen P.J., Johnson K.R., and Wheelock M.J. Cross-talk between adherersjunctions and desmosomes depends on plakoglobin. J. Cell Biol. 136 (1997) 919-934
108. Magnani J.L., Thomas W.A., and Steinberg M.S. Two distinct adhesion mechanisms in embryonic neural retina cells. 1. A kinetic analysis. Dev. Biol. 81 (1981) 96-105
109. Mahoney P.A., Weber U., Onofrechuk P., Biessmann H., Bryant P.J., and Goodman C.S. The fat tumor suppressor gene in Drosophila encodes a novel member of the cadherin gene superfamily. Cell. 67 (1991) 853-868
110. Mareel M., Berx G., Vanroy F., and Bracke M. Cadherin/catenin complex - a target for antiinvasive therapy. J. Cell Biochem. 61 (1996) 524-530
111. Marrs J.A., Andersson-Fisone C., Jeong M.C., Zurzolo L., Cohen-Gould C., Nabi I.R., Rodriguez-Boulan E., and Nelson W.J. Plasticity in epithelial cell phenotype: modulation by expression of different cadherin cell adhesion molecules. J. Cell Biol. 129 (1995) 507-519
112. Marrs J.A., and Nelson W.J. Cadherin cell adhesion molecules in differentiation and embryogenesis. Int. Rev. Cytol. 165 (1995) 159-205
113. Mathur M., Goodwin L., and Cowin P. Interactions of the cytoplasmic domain of the desmosomal cadherin Dsgl with plakoglobin. J. Biol. Chem. 269 (1994) 14075-14080
114. Matsunami H., Miyatani S., Inoue T., Copeland N.G., Gilbert D.J., Jenkins N.A., and Takeichi M. Cell binding specificity of mouse R-cadherin and chromosomal mapping of the gene. J. Cell Sci. 106 (1993) 401-409
115. Matsunami H., and Takeichi M. Fetal brain subdivisions defined by R- and E-cadherin expressions; evidence for the role of cadherin activity in region-specific, cell-cell adhesion. Dev. Biol. 172 (1995) 466-478
116. Matsuyoshi N., Hamaguchi M., Taniguchi S., Nagafuchi A., Tsukita S., and Takeichi M. Cadherin-mediated cell-cell adhesion is perturbed by v-src tyrosine phosphorylation in metastatic fibroblasts. J. Cell Biol. 118 (1992) 703-714
117. McNeill H., Ryan T.A., Smith S.J., and Nelson W.J. Spatial and temporal dissection of immediate and early events following cadherin-mediated epithelial cell adhesion. J. Cell Biol. 120 (1993) 1217-1226
118. Miller M. Confocal micrograph of four-cell-stage Xenopus embryo stained with. anti-beta-catenin antibody. Genes Dev. 10 (1996) 3216
119. Molenaar M., Vandewetering M., Oosterwegel M., Petersonmaduro J., Godsave S., Korinek V., Roose J., Destree O., and Clevers H. Xtcf-3 transcription factor mediates beta-catenin-induced axis formation in xenopus embryos. Cell. 86 (1996) 391-399
120. Moore R., and Walsh F.S. The cell adhesion molecule M-cadherin is specifically expressed in developing and regenerating, but not denervated skeletal muscle. Development. 117 (1993) 1409-1420
121. Morin P.J., Sparks A.B., Korinek V., Barker N., Clevers H., Vogelstein B., and Kinzler K.W. Activation of beta-catenin-Tcf signaling in colon cancer by mutations in Beta-catenin or APC. Science. 275 (1997) 1787-1790
122. Napolitano C., Murphy-Erdosh E.W., and Reichardt L.F. The expression of B-cadherin during embryonic chick development. Dev. Biol. 161 (1994) 107-125
123. Nagafuchi A., Shirayoshi Y., Okazaki K., Yasuda K., and Takeichi M. Transformation of cell adhesion properties by exogenously introduced. E-cadherin cDNA. Nature 329 (1987) 341-343
124. Nagafuchi A., and Takeichi M. Cell binding function of E-cadherin is regulated by the cytoplasmic domain. EMBO J. 7 (1988) 3679-3684
125. Nagafuchi A., and Takeichi M. Transmembrane control of cadherin-mediated cell adhesion: a 94 kDa protein functionally associated with a specific region of the cytoplasmic domain of E-cadherin. Cell Regulation. I (1989) 37-44
126. Nagafuchi A., Takeichi M., and Tsukita S. The 102 kd cadherin-associated protein: similarity to vinculin and posttranscriptional regulation of expression. Cell. 65 (1991) 849-857
127. Nagafuchi A., Ishihara S., and Tsukita S. The roles of catenins in the cadherin-mediated cell adhesion: functional analysis of E-cadherin-a!pha catenin fusion molecules. J. Cell Biol. 127 (1994) 235-245
128. Nagar B., Overduin M., Ikura M., and Rini J.M. Structural basis of calcium-induced E-cadherin rigidification and dimerization. Nature 380 (1996) 360-364
129. Nakagawa S., and Takeichi M. Neural crest cell-cell adhesion controlled by sequential and subpopulation-specific expression of novel cadherins. Development. 121 (1995) 1321-1332
130. Nathke I.S., Hinck L., Swedlow J.R., Papkoff J., and Nelson W.J. Defining interactions and distributions of cadherin and catenin complexes in polarized epithelial cells. J. Cell Biol. 125 (1994) 1341-1352
131. Nelson W.J., and Veshnock P.J. Dynamics of membrane-skeleton (fodrin) organization during development of polarity in Madin-Darby canine kidney epithelial cells. J Cell Biol. 103 (1986) 1751-1765
132. Nelson W.J., and Veshnock P.J. Modulation of fodrin (membrane skeleton) stability by cell-cell contact in Madin-Darby canine kidney epithelial cells. J. Cell Biol. 104 (1987) 1527-1537
133. Nishimura M., Machida K., Imaizumi M., Abe T., Umeda T., Takeshima E., Watanabe T., Ohnishi Y., Takagi K., and Hamaguchi M. Tyrosine phosphorylation of 100-130 KDa proteins in lung cancer correlates with poor prognosis. Br. J. Cancer. 74 (1996) 780-787
134. Nose A., Nagafuchi A., and Takeichi M. Isolation of placental cadherin cDNA: identification of a novel gene family of cell-cell adhesion molecules. EMBO J. 6 (1987) 3655-3661
135. Nose A., Tsuji K., and Takeichi M. Localization of specificity determining sites in cadherin cell adhesion molecules. Cell. 61 (1990) 147-155
136. Obama H., and Ozawa M. Identification of the domain of α-catenin involved in its association with β-catenin and plakoglobin (γ-catenin). J. Biol. Chem. 272 (1997) 11017-11020
137. Obata S., Sago H., Mori N., Rochelle J.M., Seldin M.F., Davidson M., John T.S., Taketani S., and Suzuki S.T. Protocadherin Pcdh2 shows properties similar to, but distinct from, those of classical cadherins. J. Cell Sci. 108 (1995) 3765-3773
138. Ochiai A., Akimoto S., Kanai Y., Shibata T., Oyama T., and Hirohashi S. C-erbB-2 gene product associates with catenins in human cancer cells. Biochem. Biophys. Res. Commun. 205 (1994) 73-78
139. Oda T., Kanai Y., Shimoyama Y., Nagafuchi A., Tsukita S., and Hirohashi S. Cloning of the human α-catenin cDNA and its aberrant mRNA in a human cancer cell line. Biochem. Biophys. Res. Commun. 193 (1993) 897-904
140. Oda H., Uemura T., Shiomi K., Nagafuchi A., Tsukita S., and Takeichi M. Identification of a Drosophila homologue of α-catenin and its association with the armadillo protein. J. Cell Biol. 121 (1993) 1133-1140
141. Oda H., Uemura T., Harada Y., Iwai Y., and Takeichi M. A Drosophila homolog of cadherin associated with armadillo and essential for embryonic. cell-cell adhesion. Dev. Biol. 165 (1994) 716-726
142. Ohsugi M., Hwang S.Y., Butz S., Knowles B.B., Solter D., and Kemler R. Expression and cell membrane localization of catenins during mouse preimplantation development. Dev. Dyn. 206 (1996) 391-402
143. Okazaki M., Takeshita S., Kawai S., Kikuno R., Tsujimura A., Kudo A., and Amann E. Molecular cloning and characterization of OB-cadherin, a new member of cadherin family expressed in osteoblasts. J. Biol. Chem. 269 (1994) 12092-12098
144. Orsulic S., and Peifer M. Cell-cell signalling: Wingless lands at last. Curr. Biol. 6 (1996) 1363-1367
145. Harvey M., Overduin T.S., Bagby S., Tong K.I., Yau P., Takeichi M., and Ikura M. Solution structure of the epithelial cadherin domain responsible for selective cell adhesion [see comments]. Science. 267 (1995) 386-389
146. Oyama T., Kanai Y., Ochiai A., Akimoto S., Oda T., Yanagihara K., Nagafuchi A., Tsukita S., Shibamoto S., Ito F., Takeichi M., Matsuda H., and Hirohashi S. A truncated β-catenin disrupts the interaction between E-cadherin and α-catenin: a cause of loss of intercellular adhesiveness in human cancer cell lines. Cancer Res. 54 (1994) 6282-6287
147. Ozawa M., Baribault H., and Kemler R. The cytoplasmic domain of the cell adhesion molecule uvomorulin associates with three independent proteins structurally related in different Species. EMBO J. 8 (1989) 1711-1717
148. 2+ binding site of uvomorulin abolish the adhesive function. Cell. 63 (1990) 1033-1038
149. Ozawa M., and Kemler R. Correct proteolytic cleavage is required for the cell adhesive function of uvomorulin. J. Cell Biol. Ill (1990) 1645-1650
150. Ozawa M., and Kemler R. Molecular organization of the uvomorulin-catenin complex. J. Cell Biol. 116 (1992) 989-996
151. Ozawa M., Nuruki K., Toyoyama H., and Ohi Y. Cloning of an alternative form of plakoglobin (γ-catenin) lacking the fourth armadillo repeat. J. Biochem. 118 (1995) 836-840
152. Ozawa M., Terada H., and Pedraza C. The fourth armadillo repeat of plakoglobin (γ-catenin) is required for its high affinity binding to the cytoplasmic domains of E-cadherin and desmosomal cadherin Dsg2, and the tumor suppressor APC protein. J Biochem. 118 (1995) 1077-1082
153. Kirkpatrick L.M., Pai C., Blanton J., Oda H., Takeichi M., and Peifer M. Drosophila α-catenin and E-cadherin bind to distinct regions of. Drosophila armadillo. J. Biol. Chem. 271 (1996) 32411-32420
154. Paradies N.E., and Grunwald G.B. Purification and characterization of NCAD90, a soluble endogenous form of N-cadherin, which is generated by proteolysis during retinal development and retains adhesive and. neurite-promoting function. J. Neurosci. Res. 36 (1993) 33-45
155. Peifer M., and Wieschaus E. The segment polarity gene armadillo encodes a functionally modular protein that is the Drosophila homolog of human plakoglobin. Cell. 63 (1990) 1167-1176
156. Peifer M., Berg S., and Reynolds A.B. A repeating amino acid motif shared by proteins with diverse cellular roles. [letter]. Cell. 76 (1994) 789-791
157. Peifer M. Cell adhesion and signal transduction-The armadillo connection. Trends Cell. Biol. 5 (1995) 224-229
158. Pokutta S., Herrenknecht K., Kemler R., and Engel J. Conformational changes of the recombinant extracellular domain of E-cadherin upon calcium binding. Eur. J. Biochem. 223 (1994) 1019-1026
159. Radice G.L., Rayburn H., Matsunami H., Knudsen K.A., Takeichi M., and Hynes R.O. Developmental defects in mouse embryos lacking. N-cadherin. Dev. Biol. 181 (1997) 64-78
160. Rajasekaran A.K., Hojo M., Huima T., and Rodriguez-Boulan E. Catenins and zonula occludens-1 form a complex during early stages in the assembly of tight junctions. J. Cell Biol. 132 (1996) 451-463
161. Ranscht B., and Dours-Zimmermann M.T. T-cadherin, a novel cadherin cell adhesion molecule in the nervous system lacks the conserved cytoplasmic region. Neuron. 7 (1991) 391-402
162. Ranscht B. Cadherins and catenins: Interactions and functions in embryonic development. Curr. Opin. Cell Biol. 6 (1994) 740-746
163. Redies C., Engelhart K., and Takeichi M. Differential expression of N- and R-cadherin in functional neuronal systems and other structures of the developing chicken brain. J. Comp. Neurol. 333 (1993) 398-416
164. Redies C. Cadherin expression in the developing vertebrate CNS: from neuromeres to brain nuclei and neural circuits. Exp. Cell Res. 220 (1995) 243-256
165. Redies C., and Takeichi M. Cadherins in the developing central nervous system: An adhesive code for segmental and functional subdivisions. Dev. Biol. 180 (1996) 413-423
166. Reynolds A.B., Herbert L., Cleveland J.L., Berg S.T., and Gaut J.R. Pl20, anovel substrate of protein tyrosine kinase receptors and of p60v-src, is related to cadherin-binding factors β-catenin, plakoglobin and armadillo. Oncogene. 7 (1992) 2439-2445
167. Reynolds A.B., Daniel J., McCrea P.D., Wheelock M.J., Wu J., and Zhang Z. Identification of a new catenin: The tyrosine kinase substrate pl20cas associates with. E-cadherin complexes. Mol. Cell. Biol. 14 (1994) 8333-8342
168. Rimm D.L., Koslov E.R., Kebriaei P., Cianci C.D., and Morrow J.S. α 1(E)-catenin is an actin-binding and -bundling protein mediating the attachment of F-actin to the membrane adhesion complex. Proc. Natl. Acad. Sci. USA 92 (1995) 8813-8817
169. +-dependent cell adhesion. EMBO J. 6 (1987) 3647-3653
170. Roh J.Y., and Stanley J.R. Intracellular domain of desmoglein 3 (Pemphigus vulgaris antigen) confers adhesive function on the extracellular domain of E-cadherin without binding catenins. J. Cell Biol. 128 (1995) 939-947
171. Roh J.Y., and Stanley J.R. Plakoglobin binding by human Dsg3 (Pemphigus vulgaris antigen) in keratmocytes requires the cadherin-like intracytoplasmic segment. J. Invest. Dermatol. 104 (1995) 720-724
172. Rose O., Grund C., Remhardt S., Starzinski-Powitz A., and Franke W.W. Contactus adherens, a special type of plaque-bearing adheringjunction containing M-cadherin, in the granule cell layer of the cerebellar glomerulus. Proc. Natl. Acad. Sci. USA 92 (1995) 6022-6026
173. Rubinfeld B., Souza B., Albert I., Muller O., Chamberlain S.H., Masiarz F.R., Munemitsu S., and Polakis P. Association of the APC gene product with β-catenin. Science 262 (1993) 1731-1734
174. Rubinfeld B., Albert I., Porfiri E., Fiol C., Munemitsu S., and Polakis P. Binding of gGSK3-β to the APC-β-catenin complex and regulation of complex assembly. Science. 272 (1996) 1023-1026
175. Rubinfeld B., Robbins P., Elgamil M., Albert I., Porfiri E., and Polakis P. Stabilization of β-catenin by genetic defects in melanoma cell lines. Science. 275 (1997) 1790-1792
176. Ruiz P., Brinkmann V., Ledermann B., Behrend M., Grund C., Thalhammer C., Vogel F., Birchmeier C., Gunthert U., Franke W.W., and Birchmeier W. Targeted mutation of plakoglobin in mice reveals essential functions of desmosomes in the embryonic heart. J. Cell Biol. 135 (1996) 215-225
177. Sacco P.A., McGranahan T.M., Wheelock M.J., and Johnson K.R. Identification of plakoglobin domains required for association with. N-cadherin and α-catenin. J. Biol. Chem. 270 (1995) 20201-20206
178. Sago H., Kitagawa M., Obata S., Mori N., Taketani S., Rochelle J.M., Seldin M.F., Davidson M., John T.St., and Suzuki S.T. Cloning, expression, and chromosomal localization of a novel Cadherin-related protein, protocadherin-3. Genomics. 29 (1995) 631-640
179. Sano K., Tanihara H., Heimark R.L., Obata S., Davidson M., John T.St., Taketani S., and Suzuki S. Protocadherins: A large family of cadherin-related molecules in central nervous system. EMBO J. 12 (1993) 2249-2256
180. Schmelz M., and Franke W.W. Complexus adhaerentes, a new group of desmoplakin-containing junctions in endothelial cells: The syndesmos connecting retothelial cells of lymph nodes. Eur. J. Cell Biol. 61 (1993) 274-289
181. Schmidt A., Heid H.W., Schafer S., Nuber U.A., Zimbelmann R., and Franke W.W. Desmosomes and cytoskeletal architecture in epithelial differentiation: Cell type-specific plaque components and intermediate filament anchorage. Eur. J. Cell Biol. 65 (1994) 229-245
182. Schneider S., Steinbeisser H., Warga R.M., and Hausen P. β-Catenin translocation into nuclei demarcates the dorsalizing centers in frog and fish embryos. Mech. Dev. 57 (1996) 191-198
183. Sefton M., Johnson M.H., Clayton L., and McConnell J.M.L. Experimental manipulations of compaction and their effects on the phosphorylation of uvomorulin. Mol. Reprod. Dev. 44 (1996) 77-87
184. Shapiro L., Fannon A.M., Kwong P.D., Thompson A., Lehmann M.S., Grubel G., Legrand J.F., Colman J., Als-Nielsen D.R., and Hendrickson W.A. Structural basis of cell-cell adhesion by cadherins (see comments). Nature 374 (1995) 327-337
185. Shapiro L., Kwong P.D., Fannon A.M., Colman D.R., and Hendrickson W.A. Considerations on the folding topology and evolutionary origin of cadherin domains. Proc. Natl. Acad. Sci. USA. 92 (1995) 6793-6797
186. Shibamoto S., Hayakawa M., Takeuchi K., Hori T., Oku N., Miyazawa K., Kitamura N., Takeichi M., and Ito F. Tyrosine phosphorylation of β-catenin and plakoglobin enhanced by hepatocyte growth factor and epidermal growth factor in human carcinoma cells. Cell Adhes. Commun. 1 (1994) 295-305
187. Shibamoto S., Hayakawa M., Takeuchi K., Hori T., Miyazawa K., Kitamura N., Johnson K.R., Wheelock M.J., Matsuyoshi N., Takeichi M., and Ito F. Association of p120, a tyrosine kinase. substrate, with E-cadherin/catenin complexes. J. Cell Biol. 128 (1995) 949-957
188. Shibata T., Gotoh M., Ochiai A., and Hirohashi S. Association of plakoglobin with APC, a tumor suppressor gene product, and its regulation by tyrosine phosphorylation. Biochem. Biophys. Res. Commun. 203 (1994) 519-522
189. Shimamura K., and Takeichi M. Local and transient expression of E-cadherin involved in mouse embryonic brain morphogenesis. Development. 116 (1992) 1011-1019
190. Shimoyama Y., Nagafuchi A., Fujita S., Gotoh M., Takeichi M., Tsukita S., and Hirohashi S. Cadherin dysfunction in a human cancer cell line: Possible involvement of loss of α-catenin expression in reduced. cell-cell adhesiveness. Cancer Res. 52 (1992) 5770-5774
191. Shiozaki H., Oka H., Inoue M., Tamura S., and Monden M. E-cadherin mediated adhesion system in cancer cells. Cancer. 77 (1996) 1605-1613
192. Simonneau L., Kitagawa M., Suzuki S., and Thiery J.P. Cadherin 11 expression marks the mesenchymal phenotype: Towards new functions for cadherins?. Cell Adhes. Commun. 3 (1995) 115-130
193. Soler A.P., and Knudsen K.A. N-cadherin involvement in cardiac myocyte interaction and myofibrillogenesis. Dev. Biol. 162 (1994) 9-17
194. Sommers C.L., Gelmann E.P., Kemler R., Cowin P., and Byers S.W. Alterations in β-catenin phosphorylation and plakoglobin expression in human breast cancer cells. Cancer Res. 54 (1994) 3544-3552
195. Stanley J.R. Defective cell-cell adhesion in the epidermis. Ciba Foundation Symposium 189 (1995) 107-120
196. Stappert J., and Kemler R. A short core region of E-cadherin is essential for catenin binding and is highly phosphorylated. Cell Adhes. Commun. 2 (1994) 319-327
197. Su L.K., Vogelstein B., and Kinzler K.W. Association of the APC tumor suppressor protein with catenins. Science. 262 (1993) 1734-1737
198. Suzuki S.T. Structural and functional diversity of cadherin superfamily-are new members of cadherin superfamily involved in signal transduction pathway. J. Cell Biochem. 61 (1996) 531-542
199. Takeda H., Nagafuchi A., Yonemura S., Tsukita S., Behrens J., Birchmeier W., and Tsukita S. V-src kinase shifts the cadherin-based cell adhesion from the strong to the weak state and β catenin is not required for the shift. J. Cell Biol. 131 (1995) 1839-1847
200. Takeichi M. Functional correlation between cell adhesive properties and some cell surface proteins. J. Cell Biol. 75 (1977) 464-474
201. Takeichi M., Ozaki H.S., Tokunaga K., and Okada T.S. Experimental manipulation of cell surface to affect cellular recognition mechanisms. Dev. Biol. 70 (1979) 195-205
202. Takeichi M. The cadherins: Cell-cell adhesion molecules controlling animal morphogenesis. Development. 102 (1988) 639-655
203. +-dependent sites. Dev. Biol. 87 (1981) 340-350
204. Takeichi M. Morphogenetic roles of classic cadherins. Curr. Opin. Cell Biol. 7 (1995) 619-627
205. Tanihara H., Kido M., Obata S., Heimark R.L., Davidson M., John T.St., and Suzuki S. Characterization of cadherin-4 and cadherin-5 reveals new aspects of cadherins. J. Cell Sci. 107 (1994) 1697-1704
206. Tanihara H., Sano K., Heimark R.L., John T.St., and Suzuki S. Cloning of five human cadherins clarifies characteristic features of cadherin extracellular domain and provides further evidence for two structurally different types of cadherin. Cell Adhes. Commun. 2 (1994) 15-26
207. Tepass U., Haag E., Gruszynski-DeFeo T.A., Omatyar L., Torok T., and Hartenstein V. Shotgun encodes Drosophila E-cadherin and is preferentially required during cell rearrangement in the neurectoderm and other morphogenetically active epithelia. Genes Dev. 10 (1996) 672-685
208. Thomas W.A., and Steinberg M.S. Two distinct adhesion mechanisms in embryonic neural retina cells. II. An immunological analysis. Dev. Biol. 81 (1981) 106-114
209. Thomas W.A., Thomson J., Magnani J.L., and Steinberg M.S. Two distinct adhesion mechanisms in embryonic neural retinacells III. Functional specificity. Dev. Biol. 81 (1981) 379-385
210. Thomson R.B., Igarashi P., Biemesderfer D., Kim R., Soleimani A., Abu-Alfa M., and Aronson P.S. Isolation and cDNA cloning of Ksp-cadherin, a novel kidney-specific member of the cadherin multigene family. J. Biol. Chem. 270 (1995) 17594-17601
211. Tomschy A., Fauser C., Landwehr R., and Engel J. Homophilic adhesion of E-cadherin occurs by a co-operative two-step interaction of. N-terminal domains. EMBO J. 15 (1996) 3507-3514
212. Townes P.L., and Holtfreter J. Directed movements and selective adhesion of embryonic amphibian cells. J. Exp. Zool. 128 (1955) 53-120
213. Troyanovsky S.M., Eshkind L.G., Troyanovsky R.B., Leube R.E., and Franke W.W. Contributions of cytoplasmic domains of desmosomal cadherins to desmosome assembly and intermediate filament anchorage. Cell. 72 (1993) 561-574
214. Troyanovsky S.M., Troyanovsky R.B., Eshkind L.G., Krutovskikh V.A., Leube R.E., and Franke W.W. Identification of the plakoglobin-binding domain in desmoglein and its role in plaque assembly and intermediate filament anchorage. J. Cell Biol. 127 (1994) 151-160
215. Troyanovsky S.M., Troyanovsky R.B., Eshkind L.G., Leube R.E., and Franke W.W. Identification of amino acid sequence motifs in desmocollin, a desmosomal glycoprotein, that are required for plakoglobin binding and plaque formation. Proc. Natl. Acad. Sci. USA 91 (1994) 10790-10794
216. Troyanovsky R.B., Chitaev N.A., and Troyanovsky S.M. Cadherin binding sites of plakoglobin-localization, specificity and role in targeting to adhering junctions. J. Cell Sci. 109 (1996) 3069-3078
217. Tsukita S., Oishi K., Akiyama T., Yamanashi Y., Yamamoto T., and Tsukita S. Specific proto-oncogenic tyrosine kinases of src family are enriched in cell-to-cell adherens junctions where the level of tyrosine phosphorylation is elevated. J. Cell Biol. 113 (1991) 867-879
218. Tsukita S., Tsukita S., Nagafuchi A., and Yonemura S. Molecular linkage between cadherins and actin filaments in cell-cell adherens junctions. Curr. Opin. Cell Biol. 4 (1992) 834-839
219. Tsukita S., Yonemura S., and Tsukita S. Erm (Ezrin/Radixin/Moesin) family-from cytoskeleton to signal transduction. Curr. Opin. Cell Biol. 9 (1997) 70-75
220. Uchiyama N., Hasegawa M., Yamashima T., Yamashita J., Shimamura K., and Takeichi M. Immunoelectron microscopic localization of E-cadherin in dorsal root ganglia, dorsal root, and dorsal horn of postnatal mice. J. Neurocytol. 23 (1994) 460-468
221. Uemura T., Oda H., Kraut R., Hayashi S., Kotaoka Y., and Takeichi M. Zygotic Drosophila E-cadherin expression is required for processes of dynamic epithelial cell rearrangement in the. Drosophila embryo. Genes Dev. 10 (1996) 659-671
222. Urushihara H., Ozaki H.S., and Takeichi M. Immunological detection of cell surface components related with aggregation of Chinese hamster and chick embryonic cells. Dev. Biol. 70 (1979) 206-216
223. Vandewetering M., Cavallo R., Dooijes D., Vanbeest M., Vanes J., Loureiro J., Ypma A., Hursh D., Jones T., Bejsovec A., Peifer M., Mortin M., and Clevers H. Armadillo coactivates transcription driven by the product of the Drosophila segment polarity gene. Dtcf. Cell. 88 (1997) 789-799
224. Vestal D.J., and Ranscht B. Glycosyl phosphatidylinositol-anchored T-cadherin mediates calcium-dependent, homophilic cell adhesion. J. Cell Biol. 119 (1992) 451-461
225. Vleminckx K., Vakaet Jr. L., Mareel M., Fiers W., and van Roy F. Genetic manipulation of E-cadherin expression by epithelial tumor cells reveals an invasion suppressor role. Cell. 66 (1991) 107-119
226. Volberg T., Geiger B., Dror R., and Zick Y. Modulation of intercellular adherens-type junctions and tyrosine phosphorylation of their components in RSV-transformed cultured chick lens cells. Cell Regulation. 2 (1991) 105-120
227. Volberg T., Zick Y., Dror R., Sabanay I., Gilon C., Levitzki A., and Geiger B. The effect of tyrosine-specific protein phosphorylation on the assembly of adherens-type junctions. EMBO J. 11 (1992) 1733-1742
228. Volk T., Cohen O., and Geiger B. Formation of heterotypic adherens-type junctions between L-CAM-containing liver cells and A-CAM-containing lens cells. Cell. 50 (1987) 987-994
229. Weis W.I. Cadherin structure: A revealing zipper. Structure 3 (1995) 425-427
230. Whitehead I., Kirk H., and Kay R. Expression cloning of oncogenes by retroviral transfer of. cDNA libraries. Mol. Cell. Biol. 15 (1995) 704-710
231. Williams C.L., Hayes V.Y., Hummel A.M., Tarara J.E., and Halsey T.J. Regulation of E-cadherin mediated adhesion by muscarinic acetylcholine receptors in small cell lung carcinoma. J. Cell Biol. 121 (1993) 643-654
232. Winkel G.K., Ferguson J.E., Takeichi M., and Nuccitelli R. Activation of protein kinase C triggers premature compaction in the four-cell stage mouse embryo. Dev. Biol. 138 (1990) 1-15
233. Witcher L.L., Collins R., Puttagunta S., Mechanic S.E., Munson M., Gumbiner B., and Cowin P. Desmosomal cadherin binding domains of plakoglobin. J. Biol. Chem. 271 (1996) 10904-10909
234. Yamada K.M., and Geiger B. Molecular interactions in cell adhesion complexes. Curr. Opin. Cell Biol. 9 (1997) 76-85
235. Yoshida-Noro C., Suzuki N., and Takeichi M. Molecular nature of the calcium-dependent cell-cell adhesion system in mouse teratocarcinoma and embryonic cells studied with a monoclonal antibody. Dev. Biol. 101 (1984) 19-27