Biology Reference
In-Depth Information
occludens-1 causes embryonic lethal phenotype associated with defected yolk sac angio-
genesis and apoptosis of embryonic cells. Mol. Biol. Cell 19, 2465-2475.
Kaz, A.M., Luo, Y., Dzieciatkowski, S., Chak, A., Willis, J.E., Upton, M.P., Leidner, R.S.,
Grady, W.M., 2012. Aberrantly methylated PKP1 in the progression of Barrett's esoph-
agus to esophageal adenocarcinoma. Genes Chromosomes Cancer 51, 384-393.
Kelsell, D.P., Dunlop, J., Stevens, H.P., Lench, N.J., Liang, J.N., Parry, G., Mueller, R.F.,
Leigh, I.M., 1997. Connexin 26 mutations in hereditary non-syndromic sensorineural
deafness. Nature 387, 80-83.
Kidder, G.M., Winterhager, E., 2001. Intercellular communication in preimplantation
development: the role of gap junctions. Front. Biosci. 6, D731-D736.
Kim, J., Gye, M.C., Kim, M.K., 2004. Role of occludin, a tight junction protein, in blas-
tocoel formation, and in the paracellular permeability and differentiation of
trophectoderm in preimplantation mouse embryos. Mol. Cells 17, 248-254.
Kimber, S.J., Surani, M.A., Barton, S.C., 1982. Interactions of blastomeres suggest changes in
cell surface adhesiveness during the formation of inner cell mass and trophectoderm in
the preimplantation mouse embryo. J. Embryol. Exp. Morphol. 70, 133-152.
Kjaer, K.W., Hansen, L., Schwabe, G.C., Marques-de-Faria, A.P., Eiberg, H., Mundlos, S.,
Tommerup, N., Rosenberg, T., 2005. Distinct CDH3 mutations cause ectodermal dys-
plasia, ectrodactyly, macular dystrophy (EEM syndrome). J. Med. Genet. 42, 292-298.
Kobielak, A., Fuchs, E., 2006. Links between alpha-catenin, NF-kappaB, and squamous cell
carcinoma in skin. Proc. Natl. Acad. Sci. U.S.A. 103, 2322-2327.
Kofron, M., Heasman, J., Lang, S.A., Wylie, C.C., 2002. Plakoglobin is required for main-
tenance of the cortical actin skeleton in early Xenopus embryos and for cdc42-mediated
wound healing. J. Cell Biol. 158, 695-708.
Kottke, M.D., Delva, E., Kowalczyk, A.P., 2006. The desmosome: cell science lessons from
human diseases. J. Cell Sci. 119, 797-806.
Krishnan, R., Klumpers, D.D., Park, C.Y., Rajendran, K., Trepat, X., van Bezu, J., van
Hinsbergh, V.W., Carman, C.V., Brain, J.D., Fredberg, J.J., Butler, J.P., van Nieuw
Amerongen, G.P., 2011. Substrate stiffening promotes endothelial monolayer disrup-
tion through enhanced physical
forces. Am.
J. Physiol. Cell Physiol. 300,
C146-C154.
Kuner, R., Muley, T., Meister, M., Ruschhaupt, M., Buness, A., Xu, E.C., Schnabel, P.,
Warth, A., Poustka, A., Sultmann, H., Hoffmann, H., 2009. Global gene expression
analysis reveals specific patterns of cell junctions in non-small cell lung cancer subtypes.
Lung Cancer 63, 32-38.
Kuphal, F., Behrens, J., 2006. E-cadherin modulates Wnt-dependent transcription in colo-
rectal cancer cells but does not alter Wnt-independent gene expression in fibroblasts.
Exp. Cell Res. 312, 457-467.
Kurzen, H., Munzing, I., Hartschuh, W., 2003. Expression of desmosomal proteins in squa-
mous cell carcinomas of the skin. J. Cutan. Pathol. 30, 621-630.
Lai-Cheong, J.E., Arita, K., McGrath, J.A., 2007. Genetic diseases of junctions. J. Invest.
Dermatol. 127, 2713-2725.
Larue, L., Ohsugi, M., Hirchenhain, J., Kemler, R., 1994. E-cadherin null mutant embryos
fail to form a trophectoderm epithelium. Proc. Natl. Acad. Sci. U.S.A. 91, 8263-8267.
Lecuit, T., Lenne, P.F., 2007. Cell surface mechanics and the control of cell shape, tissue
patterns and morphogenesis. Nat. Rev. Mol. Cell Biol. 8, 633-644.
Lie, D.C., Colamarino, S.A., Song, H.J., Desire, L., Mira, H., Consiglio, A., Lein, E.S.,
Jessberger, S., Lansford, H., Dearie, A.R., Gage, F.H., 2005. Wnt signalling regulates
adult hippocampal neurogenesis. Nature 437, 1370-1375.
Liu, Z., Tan, J.L., Cohen, D.M., Yang, M.T., Sniadecki, N.J., Ruiz, S.A., Nelson, C.M.,
Chen, C.S., 2010. Mechanical tugging force regulates the size of cell-cell junctions. Proc.
Natl. Acad. Sci. U.S.A. 107, 9944-9949.
 
Search WWH ::




Custom Search