Ординатура / Офтальмология / Английские материалы / Development of the Ocular Lens_Lovicu, Lee Robinson_2004

member of the betagamma-crystallin superfamily, is associated with the control of tumorigenicity in human malignant melanoma. Proc. Natl. Acad. Sci. USA 94, 3229–34.

Redden, J. R. and Dziedzic, D. C. (1982). Insulin-like growth factors, IGF-1, IGF-2 and somatomedin c trigger cell proliferation in mammalian epithelial cells cultured in a serum-free medium. Exp. Cell Res. 142, 293–300.

Redden, J. R. and Wilson-Dziedzic, D. C. (1983). Insulin growth factor and epidermal growth factor trigger mitoses in lenses cultured in a serum-free medium. Invest. Ophthalmol. Vis. Sci. 24, 409–16.

Reddy, S., Smith, D. B. J., Rich, M. M., Leferovich, J. M., Reilly, P., Davis, B. M., Tran, K., Rayburn, H., Bronson, R., Cros, D., et al. (1996). Mice lacking the myotonic dystrophy protein kinase develop a late onset progressive myopathy. Nat. Genet. 13, 325–35.

Reed, N. and Gutmann, D. H. (2001). Tumorigenesis in neurofibromatosis: new insights and potential therapies. Trends Mol. Med. 7, 157–62.

Reed, U. C., Tsanaclis, A. M., Vainzof, M., Marie, S. K., Carvalho, M. S., Roizenblatt, J., Pedreira, C. C., Diament, A. and Levy, J. A. (1999). Merosin-positive congenital muscular dystrophy in two siblings with cataract and slight mental retardation. Brain Dev. 21, 274–8.

Reese, D. H., Puccia, E. and Yamada, T. (1969). Activation of ribosomal RNA synthesis in initiation of Wolffian lens regeneration. J. Exp. Zool. 170, 259–68.

Relaix, F. and Buckingham, M. (1999). From insect eye to vertebrate muscle: redeployment of a regulatory network. Genes Dev. 13, 3171–8.

Ren, Z., Li, A., Shastry, B. S., Padma, T., Ayyagari, R., Scott, M. H., Parks, M. M., Kaiser-Kupfer, M. I. and Hejtmancik, J. F. (2000). A 5-base insertion in the gammaC-crystallin gene is associated with autosomal dominant variable zonular pulverulent cataract. Hum. Genet. 106, 531–7.

Reneker, L. W. and Overbeek, P. A. (1996). Lens-specific expression of PDGF-A alters lens growth and development. Dev. Biol. 180, 554–65.

Renkawek, K., de Jong, W. W., Merck, K. B., Frenken, C. W., van Workum, F. P. and Bosman, G. J. (1992). Alpha B-crystallin is present in reactive glia in Creutzfeldt-Jakob disease. Acta Neuropathol. 83, 324–7.

Resnitsky, D., Hengst, L. and Reed, S. I. (1995). Cyclin A–associated kinase activity is rate limiting for entrance into S phase and is negatively regulated in G1 by p27Kip1. Mol. Cell Biol. 15, 4347–52.

Resnitsky, D. and Reed, S. I. (1995). Different roles for cyclins D1 and E in regulation of the G1-to-S transition. Mol. Cell Biol. 15, 3463–9.

Revel, J. P., Yee, A. G. and Hudspeth, A. J. (1971). Gap junctions between electrotonically coupled cells in tissue culture and in brown fat. Proc. Natl. Acad. Sci., USA 68, 2924–7.

Reyer, R. W. (1962). Differentiation and growth of the embryonic nose, lens and corneal anlagen implanted into the larval eye or dorsal fin in Amblystoma punctatum. J. Exp. Zool. 151, 123–49.

Reyer, R. W. (1948). An experimental study of lens regeneration in Triturus viridescens. I. Regeneration of a lens after lens extirpation in embryos and larvae of different ages. J. Exp. Zool. 107, 217–68.

Reyer, R. W. (1953). Lens regeneration from heteroplastic iris grafts between Triturus viridescens and Amblystoma punctatum. Anat. Rec. 115, 362–3.

Reyer, R. W. (1954). Regeneration of the lens in the amphibian eye. Q. Rev. Biol. 29, 1–46. Reyer, R. W. (1956). Lens regeneration from homoplastic and heteroplastic implants of dorsal iris

into the eye chamber of Triturus viridescens and Amblystoma punctatum. J. Exp. Zool. 133, 145–90.

Reyer, R. W. (1961). Lens regeneration from intra-ocular, iris implants in the presence of the host lens. Anat. Rec. 139, 267.

Reyer, R. W. (1962). Regeneration in the amphibian eye. In Regeneration (20th Growth Symposium), ed. D. Rudnick. New York: Ronald Press, pp. 211–65.

Reyer, R. W. (1966a). DNA synthesis and cell movement during lens regeneration in adult Triturus viridescens. Am. Zool. 6, 329.

Reyer, R. W. (1966b). The influence of neural retina and lens regeneration from dorsal iris implants in Triturus viridescens larvae. Dev. Biol. 14, 214–45.

366 Bibliography

Reyer, R. W. (1971). DNA synthesis and the incorporation of labeled iris cells into the lens during lens regeneration in adult newts. Dev. Biol. 124, 533–58.

Reyer, R. W. (1977). The amphibian eye: development and regeneration. In Handbook of Sensory Physiology. Vol. 2. The Visual System in Vetrebrates, ed. F. Crescitelli. Berlin: Springer-Verlag, pp. 309–90.

Reyer, R. W. (1982). Dedifferentiation of iris epithelium during lens regeneration in newt larvae.

Am. J. Anat. 163, 1–23.

Reyer R. W. (1990a). Macrophage invasion and phagocytic activity during lens regeneration from the iris epithelium in newts. Am. J. Anat. 188, 329–44.

Reyer, R. W. (1990b). Macrophage mobilization and morphology during lens regeneration from the iris epithelium in newts: studies with correlated scanning and transmission electron microscopy. Am. J. Anat. 188, 345–65.

Reyer, R. W., Woolfitt, R. A. and Withersty, L. T. (1973). Stimulation of lens regeneration from the newt dorsal iris when implanted into the blastema of the regenerating limb. Dev. Biol. 32, 258–81.

Reynhout, J. K., Lampe, P. D. and, Johnson, R. G. (1992). An activator of protein kinase C inhibits gap junction communication between cultured bovine lens cells. Exp. Eye Res. 198, 337–42.

Riach, R. A., Duncan, G., Williams, M. R. and Webb, S. F. (1995). Histamine and ATP mobilize calcium by activation of H1 and P2U receptors in human epithelial cells. J. Physiol. 486, 273–82.

Richardson, J., Cvekl, A. and Wistow, G. (1995). Pax-6 is essential for lens-specific expression of

ζ -crystallin. Proc. Natl. Acad. Sci. USA 92, 4676–80.

Richardson, N. A. and McAvoy, J. W. (1990). Age-related changes in fibre differentiation of rat lens epithelial explants exposed to fibroblast growth factor. Exp. Eye Res. 50, 203–11.

Richardson, N. A., McAvoy, J. W. and Chamberlain, C. G. (1992). Age of rats affects response of lens epithelial explants to fibroblast growth factor. Exp. Eye Res. 55, 649–56.

Richiert, D. M. and Ireland, M. E. (1999). TGF-beta elicits fibronectin secretion and proliferation in cultured chick lens epithelial cells. Curr. Eye Res. 18, 62–71.

Rieger, D. K., Reichenberger, E., McLean, W., Sidow, A. and Olsen, B. R. (2001). A double-deletion mutation in the Pitx3 gene causes arrested lens development in aphakia mice.

Genomics 72, 61–72.

Ring, B. Z., Cordes, S. P., Overbeek, P. A. and Barsh, G. S. (2000). Regulation of mouse lens fiber cell development and differentiation by the Maf gene. Development 127, 307–17.

Ritz-Laser, B., Estreicher, A., Klages, N., Saule, S. and Philippe, J. (1999). Pax-6 and Cdx-2/3 interact to activate glucagon gene expression on the G1 control element. J. Biol. Chem. 274, 4124–32.

Robanus-Maandag, E., Dekker, M., van der Valk, M., Carrozza, M. L., Jeanny, J. C., Dannenberg, J. H., Berns, A. and te Riele, H. (1998). p107 is a suppressor of retinoblastoma development in pRb-deficient mice. Genes Dev. 12, 1599–609.

Robinson, G. W. and Mahon, K. A. (1994). Differential and overlapping expression domains of Dlx-2 and Dlx-3 suggest distinct roles for Distal-less homeobox genes in craniofacial development. Mech. Dev. 48, 199–215.

Robinson, K. M., Taube, J. R., Reed, N. A. and Duncan, M. K. (2003). Role of betaB2-crystallin in fertility 44, [ARVO E-abstract 2136].

Robinson, K. R. and Patterson, J. W. (1983). Localization of steady-state currents in the lens. Curr. Eye Res. 2, 843–7.

Robinson, M. L., MacMillan-Crow, L. A., Thompson, J. A. and Overbeek, P. A. (1995b). Expression of a truncated FGF receptor results in defective lens development in transgenic mice. Development 121, 3959–67.

Robinson, M. L., Ohtaka-Maruyama, C., Chan, C.-C., Jamieson, S., Dickson, C., Overveek, P. A. and Chepelinsky, A. B. (1998). Disregulation of ocular morphogenesis by lens-specific expression of FGF-3/Int-2 in transgenic mice. Dev. Biol. 198, 13–31.

Robinson, M. L. and Overbeek, P. A. (1996). Differential expression of αA- and αB-crystallin during murine ocular development. Invest. Ophthalmol. Vis. Sci. 37, 2276–84.

Robinson, M. L., Overbeek, P. A., Verran, D. J., Grizzle, W. E., Stockard, C. R., Friesel, R., Maciag, T. and Thompson, J. A. (1995a). Extracellular FGF-1 acts as a lens differentiation factor in transgenic mice. Development 121, 505–14.

Rodokanaki, A., Holmes, R. K. and Borras, T. (1989). Zeta-crystallin, a novel protein from the guinea pig lens is related to alcohol dehydrogenases. Gene 78, 215–24.

Rossant, J., Zirngibl, R., Cado, D., Shago, M. and Giguere, V. (1991). Expression of a retinoic acid response element-hsplacZ transgene defines specific domains of transcriptional activity during mouse embryogenesis. Genes Dev. 5, 1333–44.

Roth, H. J., Das, G. C. and Piatigorsky, J. (1991). Chicken βB1-crystallin gene expression: presence of conserved functional polyomavirus enhancer–like and octamer binding–like promoter elements found in non-lens genes. Mol. Cell. Biol. 11, 1488–99.

Rothstein, H., Van Wyk, J. J., Hayden, J. H., Gordon, S. R. and Weinsieder, A. (1980). Somatomedin C: restoration in vivo of cycle traverse in G0/G1 blocked cells of hypophysectomized animals. Science 208, 410–2.

Rup, D. M., Veenstra, R. D., Wang, H.-Z., Brink, P. R. and Beyer, E. C. (1993). Chick connexin-56, a novel lens gap junction protein: molecular cloning and functional expression. J. Biol. Chem. 268, 706–12.

Russell, P., Qin, C., Garland, D., Tabor, Y. and Zigler, J. S. (1996). RNA and protein synthesis in the primate lens. Exp. Eye Res. 63, 121– 4.

Ryerse, J. S. and Nagel, B. A. (1991). Gap-junction quantification in biological tissues: freeze-fracture replicas versus thin sections. J. Microsc. 163, 65–78.

Saavedra, H. I., Wu, L., De Bruin, A., Timmers, C., Rosol, T. J., Weinstein, M., Robinson, M. L. and Leone, G. (2002). Specificity of E2F1, E2F2, and E2F3 in mediating phenotypes induced by loss of Rb. Cell Growth Diff. 13, 215–25.

Sage, J., Mulligan, G. J., Attardi, L. D., Miller, A., Chen, S., Williams, B., Theodorou, E. and Jacks, T. (2000). Targeted disruption of the three Rb-related genes leads to loss of G1 control and immortalization. Genes Dev. 14, 3037–50.

Saha, M. S., Spann, C. L. and Grainger, R. M. (1989). Embryonic lens induction: more than meets the optic vesicle. Cell Diff. Dev. 28, 153–72.

Saika, S., Kawashima, Y., Miyamoto, T., Tanaka, S., Okada, Y., Yamanaka, O., Katoh, T., Ohnishi, Y., Ohini, S., Ooshima, A., and Yamanaka, A. (1998). Immunolocalization of prolyl 4-hydrolase subunits, alpha-smooth muscle actin, and extracellular matrix components in human lens capsules with lens implants. Exp. Eye Res. 66, 283–94.

Saika, S., Okada, Y., Miyamoto, T., Ohnishi, Y., Ooshima, A. and McAvoy, J. W. (2001). Smad translocation and growth suppression in lens epithelial cells by endogenous TGFbeta2 during wound repair. Exp. Eye Res. 72, 679–86.

Sakai, M., Imaki, J., Yoshida, K., Ogata, A., Matsushima-Hibiya, Y., Kuboki, Y., Nishizawa, M. and Nishi, S. (1997). Rat maf related gene: specific expression in chondrocytes, lens and spinal cord. Oncogene 14, 745–50.

Samejima, K. and Earnshaw, W. C. (2000). Differential localization of ICAD-L and ICAD-S in cells due to removal of a C-terminal NLS from ICAD-L by alternative splicing. Exp. Cell Res. 255, 314–20.

Sandilands, A., Hutcheson, A. M., Long, H. A., Prescott, A. R., Vrensen, G., Loster, J., Klopp, N., Lutz, R. B., Graw, J., Masaki, S., et al. (2002). Altered agregation properties of mutant gamma-crystallins cause inherited cataract. Embo. J. 21, 6005–14.

Sandilands, A., Prescott, A. R., Carter, J. M., Hutcheson, A. M., Quinlan, R. A., Richards, J. and FitzGerald, P. G. (1995a). Vimentin and CP49/ filensin form distinct networks in the lens which are independently modulated during lens fibre cell differentiation. J. Cell Sci. 108,

1397–406.

Sandilands, A., Prescott, A. R., Hutcheson, A. M., Quinlan, R. A., Casselman, J. T. and FitzGerald, P. G. (1995b). Filensin is proteolytically processed during lens fiber cell differentiation by multiple independent pathways. Eur. J. Cell Biol. 67, 238–53.

Sandilands, A., Prescott, A. R., Wegener, A., Zoltoski, R. K., Hutcheson, A. M., Masaki, S., Kuszak, J. R. and Quinlan, R. A. (2003). Knockout of the intermediate filament protein CP49 destabilises the lens fibre cell cytoskeleton and decreases lens optical quality, but does not induce cataract. Exp. Eye Res. 76, 385–91.

Sandilands, A., Wang, X., Hutcheson, A. M., James, J., Prescott, A. R., Wegener, A., Pekny, M., Gong, X. and Quinlan, R. A. (2004). Bfsp2 mutation found in mouse 129 strains causes the loss of CP49 and induces vimentin-dependent changes in the lens fibre cell cytoskeleton. Exp. Eye Res. 78, 109–23.

368 Bibliography

Sanyal, S. and Hawkins, R. K. (1979). Dysgenetic lens (dyl): a new gene in the mouse. Invest. Ophthalmol. Vis. Sci. 18, 642–5.

Sardet, C., Vidal, M., Cobrinik, D., Geng, Y., Onufryk, C., Chen, A. and Weinberg, R. A. (1995). E2F-4 and E2F-5, two novel members of the E2F family, are expressed in the early phases of the cell cycle. Proc. Natl. Acad. Sci. USA 92, 2403–7.

Sarkar, P. S., Appukuttan, B., Han, J., Ito, Y., Ai, C. W., Tsai, W. L., Chai, Y., Stout, J. T. and Reddy, S. (2000). Heterozygous loss of Six5 in mice is sufficient to cause ocular cataracts. Nat. Genet. 25, 110–14.

Sas, D. F., Sas, J., Johnson, K. R., Menko, A. S. and Johnson, R. G. (1985). Junctions between lens fiber cells are labeled with a monoclonal antibody shown to be specific for MP26. J. Cell Biol. 100, 216–25.

Sasaki, K., Kojima, M., Nakaizumi, H., Kitagawa, K., Yamada, Y. and Ishizaki, H. (1998). Early lens changes seen in patients with atopic dermatitis applying image analysis processing of Scheimpflug and specular microscopic images. Ophthalmologica 212, 88–94.

Sato, T. (1930). Beitrage zur Analyse der Wolffschen Linssenregeneration. I. Wilhem Roux Arch. Entwickl.-Mech. Org. 122, 451–493.

Sato, T. (1935). Beitrage zur Analyse der Wolffschen Linssenregeneration. Pt. 3. Wilhem Roux Arch. Entwickl.-Mech. Org. 133, 323–48.

Sato, T. (1940). Vergleichende Studien uber die Geschwindigkeit der Wolffschen Linsenregeneration bei Triton taniatus und bei Diemyctylus pyrrhogaster. Wilhem Roux Arch. Entwickl.-Mech. Org. 140, 573–613.

Sato, T. (1961). Uber die Linsen-Regeneration bei den Cobitiden Fischen Misgurnus Anguillicaudatus. Embryologia 6, 251–91.

Saunders J. B. de C. M (John Bertrand de Cusance Morant), and O’Malley, C. D. (1950). The Illustrations from the Works of Andreas Vesalius of Brussels. New York: World Publishing.

Sawhney, R. S. (1995). Identification of SPARC in the anterior lens capsule and its expression by lens epithelial cells. Exp. Eye Res. 61, 645–8.

Sawhney, R. S., Wood, L. S. and Vogeli, G. (1997). Molecular cloning of the bovine 1 (IV) procollagen gene (COL4A1) and its use in investigating the regulation of expression of type IV procollagen by retinoic acid in bovine lens epithelial cells. Cell. Biol. Int. 21, 501–10.

Sax, C. M., Cvekl, A., Kantorow, M., Gopal-Srivastava, R., Ilagan, J. G. Ambulos, N. P., Jr. and Piatigorsky, J. (1995). Lens-specific activity of the mouse alpha A-crystallin promoter in the absence of a TATA box: functional and protein binding analysis of the mouse alpha A-crystallin PE1 region. Nucleic Acids Res. 23, 442–51.

Sax, C. M., Cvekl, A., Kantorow, M., Sommer, B., Chepelinsky, A. B. and Piatigorsky, J. (1994). Identification of negative-acting and protein-binding elements in the mouse alpha A-crystallin −1556/−1165 region. Gene 144, 163–9.

Sax, C. M., Cvekl, A. and Piatigorsky, J. (1997). Transcriptional regulation of the mouse alpha A-crystallin gene: binding of USF to the −7/+5 region. Gene 185, 209–16.

Sax, C. M., Ilagan, J. G. and Haynes, J. I., II. (1996). Lens-preferred activity of the −1809/+46 mouse αA-crystallin promoter in stably integrated chromatin. Biochim. Biophys. Acta 1305, 49–53.

Sax, C. M., Ilagan, J. G. and Piatigorsky, J. (1993). Functional redundancy of the DE-1 and alpha A-CRYBP1 regulatory sites of the mouse alpha A-crystallin promoter. Nucleic Acids Res. 21, 2633–40.

Sax, C. M. and Piatigorsky, J. (1994). Expression of the alpha-crystallin/small heat-shock protein/molecular chaperone genes in the lens and other tissues. Adv. Enzymol. Relat. Areas Mol. Biol. 69, 155–201.

Scheffner, M., Werness, B. A., Huibregtse, J. M., Levine, A. J. and Howley, P. M. (1990). The E6 oncoprotein encoded by human papillomavirus types 16 and 18 promotes the degradation of p53. Cell 63, 1129–36.

Scheiner, C. (1619). Oculus hoc est fundamentum opticum Innsbruck, Austria: Agricola. Scherr, M., Morgan, M. A. and Eder, M. (2003). Gene silencing mediated by small interfering

RNAs in mammalian cells. Curr. Med. Chem. 10, 245–56.

Schlotzer-Schrehardt, U. and Dorfler, S. (1993). Immunolocalization of growth factors in the human ciliary body epithelium. Curr. Eye Res. 12, 893–905.

Schmidt, A., Heid, H. W., Schafer, S., Nuber, U. A., Zimbelmann, R. and Franke, W. W. (1994). Desmosomes and cytoskeletal architecture in epithelial differentiation: cell type–specific plaque components and intermediate filament anchorage. Eur. J. Cell Biol. 65, 229–45.

Schmitt, G. A., Pau, H., Spahr, R., Piper, H. M., Skalli, O. and Gabbiani, G. (1990). Appearance of alpha-smooth muscle actin in human eye lens cells of anterior capsular cataract and in cultured bovine lens-forming cells. Differentiation 43, 115–22.

Schorle, H., Meier, P., Buchert, M., Jaenisch, R. and Mitchell, P. J. (1996). Transcription factor AP-2 essential for cranial closure and craniofacial development. Nature 381, 235–8.

Schuetze, S. M. and Goodenough, D. A. (1982). Dye transfer between cells of the embryonic

chick lens becomes less sensitive to CO2 treatment with development. J. Cell Biol. 92, 694–705. Schulz, M. W., Chamberlain, C. G., de Iongh, R. U. and McAvoy, J. W. (1993). Acidic and basic

FGF in ocular media and lens: implications for lens polarity and growth patterns. Development 118, 117–26.

Schulz, M. W., Chamberlain, C. G. and McAvoy, J. W. (1996). Inhibition of TGFB-induced cataractous changes in lens explants by ocular media and a2-macroglobulin. Invest. Ophthalmol. Vis. Sci. 37, 1509–19.

Schulz, M. W., Chamberlain, C. G. and McAvoy, J. W. (1997). Binding of FGF-1 and FGF-2 to heparan sulphate proteoglycans of the mammalian lens capsule. Growth Factors 14, 1–13.

Schulze, E. and Kirschner, M. (1987). Dynamic and stable populations of microtubules in cells. J. Cell Biol. 104, 277–88.

Schwartz, J. S., Lee, D. A. and Isenberg, S. J. (1989). Ocular size and shape. In The Eye in Infancy, ed. S. J. Isenberg. Chicago: Year Book Medical Publishers, pp. 164–84.

Seimiya, M. and Gehring, W. J. (2000). The Drosophila homeobox gene optix is capable of inducing ectopic eyes by an eyeless-independent mechanism. Development 127, 1879–86.

Sekido, R., Murai, K., Funahashi, J., Kamachi, Y., Fujisawa-Sehara, A., Nabeshima, Y. and Kondoh, H. (1994). The delta-crystallin enhancer-binding protein delta EF1 is a repressor of E2-box–mediated gene activation. Mol. Cell. Biol. 14, 5692–700.

Sekido, R., Murai, K., Kamachi, Y. and Kondoh, H. (1997). Two mechanisms in the action of repressor deltaEF1: binding site competition with an activator and active repression. Genes Cells 2, 771–83.

Sellers, W. R., Notvich, B. G., Miyake, S., Heith, A., Otterson, G. A., Kaye, F. J., Lassar, A. B. and Kaelin, W. G., Jr. (1998). Stable binding to E2F is not required for the retinoblastoma protein to activate transcription, promote differentiation, and suppress tumor cell growth. Genes Dev. 12, 95–106.

Semina, E. V., Brownell, I., Mintz-Hittner, H. A., Murray, J. C. and Jamrich, M. (2001). Mutations in the human forkhead transcription factor FOXE3 associated with anterior segment ocular dysgenesis and cataracts. Hum. Mol. Genet. 10, 231–6.

Semina, E. V., Ferrell, R. E., Mintzhittner, H. A., Bitoun, P., Alward, W. L. M., Reiter, R. S., Funkhauser, C., Daackhirsch, S. and Murray, J. C. (1998). A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD. Nat. Genet. 19, 167–70.

Semina, E. V., Murray, J. C., Reiter, R., Hrstka, R. F. and Graw, J. (2000). Deletion in the promoter region and altered expression of Pitx3 homeobox gene in aphakia mice. Hum. Mol. Genet. 9, 1575–85.

Semina, E. V., Reiter, R. S. and Murray, J. C. (1997). Isolation of a new homeobox gene belonging to the Pitx/Rieg family: expression during lens development and mapping to the aphakia region on mouse chromosome 19. Hum. Mol. Genet. 6, 2109–16.

Seo, H. C., Curtiss, J., Mlodzik, M. and Fjose, A. (1999). Six class homeobox genes in Drosophila belong to three distinct families and are involved in head development. Mech. Dev. 83, 127–39.

Seto, Y., Nagawa, H., Mori, M., Tsuruo, T. and Muto, T. (1999). Effect of 5-fluorouracil on gastrointestinal carcinogenesis induced by N-methyl-N -nitro-N-nitrosoguanidine in rats. Dig. Dis. Sci. 44, 75–8.

Servetnick, M., Cook, T. L., Jr. and Grainger, R. M. (1996). Lens induction in axolotls: comparison with inductive signaling mechanisms in Xenopus laevis. Int. J. Dev. Biol. 40, 755–61.

Servetnick, M. and Grainger, R. M. (1991). Changes in neural and lens competence in Xenopus ectoderm: evidence for an autonomous developmental timer. Development 112, 177–88.

370 Bibliography

Shan, B. and Lee, W. H. (1994). Deregulated expression of E2F-1 induces S-phase entry and leads to apoptosis. Mol. Cell Biol. 14, 8166–73.

Sharma, Y., Rao, C. M., Narasu, M. L., Rao, S. C., Somasundaram, T., Gopalakrishna, A. and Balasubramanian, D. (1989). Calcium ion binding to δ- and to β-crystallins: the presence of the EF-hand motif in δ-crystallin that aids in calcium ion binding. J. Biol. Chem. 264, 12794–9.

Sharon-Friling, R., Richardson, J., Sperbeck, S., Lee, D., Rauchman, M., Maas, R., Swaroop, A. and Wistow, G. (1998). Lens-specific gene recruitment of zeta-crystallin through Pax6, Nrl-Maf, and brain suppressor sites. Mol. Cell. Biol. 18, 2067–76.

Shaw, L. M., Lotz, M. M. and Mercurio, A. M. (1993). Inside-out integrin signaling in macrophages: analysis of the role of the alpha 6A beta 1 and alpha 6B beta 1 integrin variants in laminin adhesion by cDNA expression in an alpha 6 integrin–deficient macrophage cell line.

J. Biol. Chem. 268, 11401–8.

Shaw, L. M., Messier, J. M. and Mercurio, A. M. (1990). The activation dependent adhesion of macrophages to laminin involves cytoskeletal anchoring and phosphorylation of the alpha 6 beta 1 integrin. J. Cell Biol. 110, 2167–74.

Shen, L., Shrager, P., Girsch, S. J. and Peracchia, C. (1991). Channel reconstitution in liposomes and planar lipid bilayers with HPLC-purified MIP26 of bovine lens. J. Membr. Biol. 124, 21–32.

Shen, W. and Mardon, G. (1997). Ectopic eye development in Drosophila induced by directed dachshund expression. Development 124, 45–52.

Sheng, G., Harris, E., Bertuccioli, C. and Desplan, C. (1997a). Modular organization of Pax/homeodomain proteins in transcriptional regulation. Biol. Chem. 378, 863–72.

Sheng, G., Thouvenot, E., Schmucker, D., Wilson, D. S. and Desplan, C. (1997b). Direct regulation of rhodopsin 1 by Pax-6/eyeless in Drosophila: evidence for a conserved function in photoreceptors. Genes Dev. 11, 1122–31.

Shepard, A. R. and Rae, J. L. (1998). Ion transporters and receptors in cDNA libraries from lens and cornea epithelia. Curr. Eye Res. 17, 708–19.

Shepard, A. R. and Rae, J. L. (1999). Electrically silent potassium channel subunits from human lens epithelium. Am. J. Physiol. 46, C412–24.

Sherr, C. J. (1993). Mammalian G1 cyclins. Cell 73, 1059–65.

Sherr, C. J. (1994). G1 phase progression: cycling on cue. Cell 79, 551–5. Sherr, C. J. (1996). Cancer cell cycles. Science 274, 1672–7.

Sherr, C. J. and Roberts, J. M. (1995). Inhibitors of mammalian G1 cyclin–dependent kinases.

Genes Dev. 9, 1149–63.

Shestopalov, V. I. and Bassnett, S. (1999). Exogenous gene expression and protein targeting in lens

fiber cells. Invest. Ophthalmol. Vis. Sci. 40, 1435–43.

Shestopalov, V. I. and Bassnett, S. (2000a). Expression of autofluorescent proteins reveals a novel protein permeable pathway between cells in the lens core. J. Cell Sci. 113, 1913–21.

Shestopalov, V. I. and Bassnett, S. (2000b). Three-dimensional organization of primary lens fiber cells. Invest. Ophthalmol. Vis. Sci. 41, 859–63.

Sheterline, P., Clayton, J. and Sparrow, J. (1995). Actin. Protein Profile 2, 1–103.

Shiels, A. and Bassnett, S. (1996). Mutations in the founder of the MIP gene family underlie cataract development in the mouse. Nat. Genet. 12, 212–15.

Shiels, A., Mackay, D., Ionides, A., Berry, V., Moore, A. and Bhattacharya, S. (1998). A missense mutation in the human connexin50 gene (GJA8) underlies autosomal dominant “zonular pulverent” cataract, on chromosome 1q. Am. J. Hum. Genet. 62, 526–32.

Shiloh, Y., Donlon, T., Bruns, G., Breitman, M. L. and Tsui, L. C. (1986). Assignment of the human gamma-crystallin gene cluster (CRYG) to the long arm of chromosome 2, region q33–36. Hum. Genet. 73, 17–9.

Shimada, N., Aya-Murata, T., Reza, H. M. and Yasuda, K. (2003). Coorperative action between L-Maf and Sox2 on delta-crystallin gene expression during chick lens development. Mech. Dev. 120, 455–65.

Shinohara, T. and Piatigorsky, J. (1976). Quantitation of delta-crystallin messenger RNA during lens induction in chick embryos. Proc. Natl. Acad. Sci. USA 73, 2808–12.

Shinohara, T., Singh, D. P. and Fatma, N. (2002). LEDGF, a survival factor, activates stress-related genes. Prog. Retin. Eye Res. 21, 341–58.

Shirke, S., Faber, S. C., Hallem, E., Makarenkova, H. P., Robinson, M. L., Overbeek, P. A. and

Lang, R. A. (2001). Misexpression of IGF-I in the mouse lens expands the transitional zone and perturbs lens polarization. Mech. Dev. 101, 167–74.

Shirodkar, S., Ewen, M., DeCaprio, J. A., Morgan, J. and Livingston, D. M. (1992). The transcription factor E2F interacts with the retinoblastoma product and a p107–cyclin A complex in a cell cycle-regulated manner. Cell 68, 157–66.

Shroff, N. P., Cherian-Shaw, M., Bera, S. and Abraham, E. C. (2000). Mutation of R116C results in highly oligomerized alpha A-crystallin with modified structure and defective chaperone-like function. Biochemistry 39, 1420–6.

Siegner, A., May, C. A., Welge-Lussen, U. W., Bloemendal, H. and Lutjen-Drecoll, E. (1996). Alpha B-crystallin in the primate ciliary muscle and trabecular meshwork. Eur. J. Cell Biol. 71, 165–9.

Siezen, R. J., Bindels, J. G. and Hoenders, H. J. (1978). The quaternary structure of bovine alpha-crystallin: size and charge microheterogeneity: more than 1000 different hybrids? Eur. J. Biochem. 91, 387–96.

Siezen, R. J. and Shaw, D. C. (1982). Physicochemical characterization of lens proteins of the squid Nototodarus gouldi and comparison with vertebrate crystallins. Biochim. Biophys. Acta 704, 304–20.

Siezen, R. J., Wu, E., Kaplan, E. D., Thomson, J. A. and Benedek, G. B. (1988). Rat lens γ -crystallin: characterization of the six gene products and their spatial and temporal distribution resulting from differential synthesis. J. Mol. Bio. 199, 475–90.

Simeone, A., Acampora, D., Gulisano, M., Stornaiuolo, A. and Boncinelli, E. (1992). Nested expression domains of four homeobox genes in developing rostral brain. Nature 358, 687–90.

Simeone, A., Acampora, D., Mallamaci, A., Stornaiuolo, A., D’Apice, M. R., Nigro, V. and Boncinelli, E. (1993). A vertebrate gene related to orthodenticle contains a homeodomain of the bicoid class and demarcates anterior neuroectoderm in the gastrulating mouse embryo. EMBO J. 12, 2735–47.

Singer, C. (1921). Steps leading to the invention of first optical apparatus. In C. Singer, ed., Studies in the History and Method of Science. Oxford: Clarendon, pp. 385–413.

Singer, B. and Grunberger, D. (1983). Molecular Biology of Mutagens and Carcinogens. New York: Plenum, pp. 55–78.

Sinha, D., Esumi, N., Jaworski, C., Kozak, C. A., Pierce, E. and Wistow, G. (1998). Cloning and mapping the mouse Crygs gene and non-lens expression of [gamma]S-crystallin. Mol. Vis. 4, 8.

Sirotkin, A. M., Edelmann, W., Cheng, G., Klein-Szanto, A., Kucherlapati, R. and Skoultchi, A. I. (1995). Mice develop normally without the H1(0) linker histone. Proc. Natl. Acad. Sci. USA 92, 6434–8.

Sivak, J. G., Gershon, D., Dovrat, A. and Weerheim, J. (1986). Computer assisted scanning laser monitor of optical quality of the excised crystalline lens. Vision Res. 26, 1873–9.

Sivak, J. G., Herbert, K. L., Peterson, K. L. and Kuszak, J. R. (1994). The inter-relationship of lens anatomy and optical quality. I. Non-primate lenses. Exp. Eye Res. 59, 505–20.

Skow, L. C., Donner, M. E., Huang, S. M., Gardner, J. M., Taylor, B. A., Beamer, W. G. and Lalley, P. A. (1988). Mapping of mouse gamma crystallin genes on chromosome 1. Biochem. Genet. 26, 557–70.

Slack, J. M., Isaacs, H. V., Song, J., Durbin, L. and Pownall, M. E. (1996). The role of fibroblast growth factors in early Xenopus development. Biochem. Soc. Symp. 62, 1–12.

Slee, E. A., Adrain, C. and Martin, S. J. (2000). Executioner caspase-3, -6 and -7 perform distinct, non-redundant roles during the demolition phase of apoptosis. J. Biol. Chem. 276, 7320–6.

Slingsby, C. and Bateman, O. A. (1990). Rapid separation of bovine beta-crystallin subunits βA3 and βA4. Exp. Eye Res. 51, 21–6.

Smith, B. S. (1989). Histochemical analysis of extracellular matrix material in embryonic trisomy 1 mouse eye. Dev. Genet. 10, 287–91.

Smith, F. J., Eady, R. A., Leigh, I. M., McMillan, J. R., Rugg, E. L., Kelsell, D. P., Bryant, S. P., Spurr, N. K., Geddes, J. F., Kirtschig, G., et al. (1996). Plectin deficiency results in muscular dystrophy with epidermolysis bullosa. Nat. Genet. 13, 450–7.

Smith, R. S., Hawes, N. L., Chang, B., Roderick, T. H., Akeson, E. C., Heckenlively, J. R., Gong, X., Wang, X. and Davisson, M. T. (2000). Lop12, a mutation in mouse Crygd causing lens opacity similar to human Coppock cataract. Genomics 63, 314–20.

372 Bibliography

Smolich, B. D., Tarkington, S. K., Saha, M. S. and Grainger, R. M. (1994). Xenopus g-crystallin gene expression: evidence that the g-crystallin gene family is transcribed in lens and non-lens tissues. Mol. Cell. Biol. 14, 1355–63.

Smulders, R. H., van Boekel, M. A. and de Jong, W. W. (1998). Mutations and modifications support a “pitted-flexiball” model for alpha-crystallin. Int. J. Biol. Macromol. 22, 187–96.

Somasundaram, T. and Bhat, S. P. (2000). Canonical heat shock element in the alpha B-crystallin gene shows tissue-specific and developmentally controlled interactions with heat shock factor.

J. Biol. Chem. 275, 17154–9.

Song, S., Pitot, H. C. and Lambert, P. F. (1999). The human papillomavirus type 16 E6 gene alone is sufficient to induce carcinomas in transgenic animals. J. Virol. 73, 5887–93.

Soriano, P. (1997). The PDGF alpha receptor is required for neural crest cell development and for normal patterning of the somites. Development 124, 2691–700.

Spector, A., Chiesa, R., Sredy, J. and Garner, W. (1985). cAMP-dependent phosphorylation of bovine lens alpha-crystallin. Proc. Natl. Acad. Sci. USA 82, 4712–6.

Spemann, H. (1901). Ueber Corelationen in der Entwicklung des Auges. Verh. Anat. Ges. 15, 61–79. Spemann, H. (1907). Neue Tatsachen zum Linsenproblem. Zool. Anz. 31, 379–86.

Spemann, H. (1912). Zur Entwicklung des Wirbeltierauges. Zool. Jahrb. 32, 1–98. Spemann, H. (1938). Embryonic Development and Induction. New York: Hafner.

Spiewak Rinaudo, J. A. and Zelenka, P. S. (1992). Expression of c-fos and c-jun mRNA in the developing chicken lens: relationship to cell proliferation, quiescence, and differentiation. Exp. Cell Res. 199, 147–53.

Spivak-Kroizman, T., Lemmon, M. A., Dikic, I., Ladbury, J. E., Pinchasi, D., Huang, J., Jaye, M., Crumley, G., Schlessinger, J. and Lax I. (1994). Heparin-induced oligomerization of FGF molecules is responsible for FGF receptor dimerization, activation, and cell proliferation. Cell 79, 1015–24.

Srinivasan, Y., Lovicu, F. J. and Overbeek, P. A. (1998). Lens-specific expression of transforming growth factor beta1 in transgenic mice causes anterior subcapsular cataracts. J. Clin. Invest. 101, 625–34.

Stamer, W. D., Snyder, R. W., Smith, B. L., Agre, P. and Regan, J. W. (1994). Localization of aquaporin CHIP in the human eye: implications in the pathogenesis of glaucoma and other disorders of ocular fluid balance. Invest. Ophthalmol. Vis. Sci. 35, 3867–72.

Steele, E. C., Kerscher, S., Lyon, M., Glenister, P. H., Favor, J., Wang, J. H. and Church, R. L. (1997). Identification of a mutation in the MP19 gene, Lim2, in the cataractous mouse mutant To3. Mol. Vis. 3, 5. Available at http://www.molvis.org/molvis/v3/steele.

Steele, E. C., Lyon, M. F., Favor, J., Guillot, P. V., Boyd, Y. and Church, R. L. (1998). A mutation in the connexin50 (Cx50) gene is a candidate for the No2 mouse cataract. Curr. Eye Res. 17, 883–9.

Steinert, P. M., Chou, Y. H., Prahlad, V., Parry, D. A., Marekov, L. N., Wu, K. C., Jang, S. I. and Goldman, R. D. (1999). A high molecular weight intermediate filament–associated protein in BHK-21 cells is nestin, a type VI intermediate filament protein: limited co-assembly in vitro to form heteropolymers with type III vimentin and type IV alpha-internexin. J. Biol. Chem. 274, 9881–90.

Steno, N. (1910). Opera Philosophica. Copenhagen: Christian Christensen.

Stephan, D. A., Gillanders, E., Vanderveen, D., Freas-Lutz, D., Wistow, G., Baxevanis, A. D., Robbins, C. M., VanAuken, A., Quesenberry, M. I., Bailey-Wilson, J., et al. (1999). Progressive juvenile-onset punctate cataracts caused by mutation of the gammaD-crystallin gene. Proc. Natl. Acad. Sci. USA 96, 1008–12.

Stillman, B. (1996). Cell cycle control of DNA replication. Science 274, 1659–64.

Stolen, C. M. and Griep, A. E. (2000). Disruption of lens fiber cell differentiation and survival at multiple stages by region-specific expression of truncated FGF receptors. Dev. Biol. 217, 205–20.

Stolen, C. M., Jackson, M. W. and Griep, A. E. (1997). Overexpression of FGF-2 modulates fiber cell differentiation and survival in the mouse lens. Development 124, 4009–17.

Stone, L. S. (1943). Factors controlling lens regeneration from the dorsal iris in de adult Triturus viridescens eye. Proc. Soc. Exp. Biol. Med. 54, 102–03.

Stone, L. S. (1952). An experimental study of the inhibition and release of lens regeneration in adults eyes of Triturus viridescens. J. Exp. Zool. 121, 181–23.

Stone, L. S. (1953). An experimental analysis of lens regeneration. Am. J. Ophthalmol. 36, 31–9. Stone, L. S. (1954a). Further experiments on lens regeneration in eyes of the adult newt Triturus v.

viridescens. Anat. Rec. 120, 599–624.

Stone, L. S. (1954b). Lens regeneration in secondary pupils experimentally produced in eyes of the adult newt Triturus v. viridescens. J. Exp. Zool. 127, 463–92.

Stone, L. S. (1958a). Lens regeneration in adult newt eyes related to retina pigment cells and the neural retina factor. J. Exp. Zool. 139, 69–84.

Stone, L. S. (1958b). Inhibition of lens regeneration in newt eyes by isolating the dorsal iris from the neural retina. Anat. Rec. 131, 151–72.

Stone, L. S. (1966). Experiments dealing with the inhibition and release of lens regeneration in eyes of adult newts. J. Exp. Zool. 161, 83–93.

Stone, L. S. (1967). An investigation recording all salamanders which can and cannot regenerate a lens from the dorsal iris. J. Exp. Zool. 164, 87–103.

Stone, L. S. and Steinitz, H. (1953). The regeneration of lenses in eyes with intact and regenerating retina in adult Triturus v. viridescens. J. Exp. Zool. 124, 435–67.

Stone, L. S. and Vultee, J. H. (1949). Inhibition and release of lens regenaration in the dorsal iris of

Triturus v. viridescens. Anat. Rec. 103, 560.

St-Onge, L., Sosa-Pineda, B., Chowdhury, K., Mansouri, A. and Gruss, P. (1997). Pax6 is required for differentiation of glucagon-producing α-cells in mouse pancreas. Nature 387, 406–9.

Straub, B. K., Boda, J., Kuhn, C., Schnoelzer, M., Korf, U., Kempf, T., Spring, H., Hatzfeld, M. and Franke, W. W. (2003). A novel cell-cell junction system: the cortex adhaerens mosaic of lens fiber cells. J. Cell Sci. 116, 4985–95.

Streeten, B. W. and Eshaghian, J. (1978). Human posterior subcapsular cataract: a gross and flat preparation study. Arch. Ophthalmol. 96, 1653–8.

Streuli, C. H., Bailey, N. and Bissell, M. J. (1991). Control of mammary epithelial differentiation: basement membrane induces tissue-specific gene expression in the absence of cell-cell interaction and morphological polarity. J. Cell Biol. 115, 1383–95.

Stump, R. J., Ang, S., Chen, Y., van Bahr, T., Lovicu, F. J., Pinson, K., de Iongh, R. U., Yamaguchi, T. P., Sassoon, D. A., and McAvoy, J. W. (2003). A role for Wnt/beta-catenin signaling in lens epithelial differentiation. Dev. Biol. 259, 48–61.

Sugimura, T., Fujimura, S. and Baba, T. (1970). Tumor production in the glandular stomach and alimentary tract of the rat by N-methyl-N -nitro-N-nitrosoguanidine. Cancer Res. 30, 455–65.

Sullivan, C. H., Marker, P. C., Thorn, J. M. and Brown, J. D. (1998). Reliability of delta-crystallin as a marker for studies of chick lens induction. Differentiation 64, 1–9.

Sullivan, C. H., Norman, J. T., Borras, T. and Grainger, R. M. (1989). Developmental regulation of hypomethylation of delta-crystallin genes in chicken embryo lens cells. Mol. Cell. Biol. 9, 3132–5.

Sullivan, C. H., O’Farrell, S. and Grainger, R. M. (1991). Delta-crystallin gene expression and patterns of hypomethylation demonstrate two levels of regulation for the delta-crystallin genes in embryonic chick tissues. Dev. Biol. 145, 40–50.

Sveinsson, O. (1993). The ultrastructure of Elschnig’s pearls in a pseudophakic eye. Acta Ophthalmol. (Copenhagen) 71, 95–8.

Svennevik, E. and Linser, P. J. (1993). The inhibitory effects of integrin antibodies and the RGD tripeptide on early eye development. Invest. Ophthalmol. Vis. Sci. 34, 1774–84.

Svitkina, T. M., Verkhovsky, A. B. and Borisy, G. G. (1996). Plectin sidearms mediate interaction of intermediate filaments with microtubules and other components of the cytoskeleton. J. Cell Biol. 135, 991–1007.

Swamynathan, S. K., and Piatigorsky, J. (2002). Orientation-dependent influence of an intergenic enhancer on the promoter activity of the divergently transcribed mouse Shsp/alpha B-crystallin and Mkbp/HspB2 genes. J. Biol. Chem. 277, 49700–6.

Swenson, K. I., Jordan, J. R., Beyer, E. C. and Paul, D. L. (1989). Formation of gap junctions by expression of connexins in Xenopus oocyte pairs. Cell 57, 145–55.

Takagi, T., Moribe, H., Kondoh, H. and Higashi, Y. (1998). DeltaEF1, a zinc finger and homeodomain transcription factor, is required for skeleton patterning in multiple lineages.

Development 125, 21–31.

Takahashi, Y., Hanaoka, K., Goto, K. and Kondoh, H. (1994). Lens-specific activity of the chicken delta 1-crystallin enhancer in the mouse. Int. J. Dev. Biol. 38, 365–8.

374 Bibliography

Takano, K., Yamanaka, G. and Mikami, Y. (1958). Wolffian lens-regeneration in the eye containing a full brown lens in Triturus pyrrhogaster. Mie Med. J. 8, 177–82.

Takata, C., Albright, J. F. and Yamada, T. (1964). Lens antigens in the lens-regenerating system studied by immunofluorescent technique. Dev. Biol. 9, 385–97.

Takata, C., Albright, J. F. and Yamada, T. (1966). Gamma-crystallins in Wolffian lens regeneration demonstrated by immunofluorescence. Dev. Biol. 14, 382–400.

Takeda, H., Nagafuchi, A., Yonemura, S., Tsukita, S., Behrens, J. and Birchmeier, W. (1995). V-src kinase shifts the cadherin-based cell adhesion from the strong to the weak state and beta catenin is not required for the shift. J. Cell Biol. 131, 1839–47.

Takei, K., Furuya, A., Hommura, S. and Yamaguchi, N. (2001). Ultrastructural fragility and type iv collagen abnormality of the anterior lens capsules in a patient with Alport syndrome. Jpn. J. Ophthalmol. 45, 103–4.

Takeichi, M. (1991). Cadherin cell adhesion receptors as a morphogenetic regulator [review].

Science 251, 1451–5.

Takeichi, M. (1995). Morphogenetic roles of classical cadherins. Curr. Opin. Cell Biol. 5, 806–11. Tamm, E. R., Russell, P., Johnson, D. H. and Piatigorsky, J. (1996). Human and monkey trabecular meshwork accumulate alpha B-crystallin in response to heat shock and oxidative stress. Invest.

Ophthalmol. Vis. Sci. 37, 2402–13.

Tamura, R. N., Cooper, H. M., Collo, G. and Quaranta, V. (1991). Cell type specific integrin variants with alternative alpha chain cytoplasmic domains. Proc Nat. Acad. Sci. USA 88, 10183–7.

Tanaka, T., Tsujimura, T., Takeda, K., Sugihara, A., Maekawa, A., Terada, N., Yoshida, N. and Akira, S. (1998). Targeted disruption of ATF4 discloses its essential role in the formation of eye lens fibres. Genes Cells 3, 801–10.

Tang, S.-S., Lin, C.-C. and Chang, G.-G. (1994). Isolation and characterization of octopus hepatopancreatic glutathione S-transferase: comparison of digestive gland enzyme with lens S-crystallin. J. Prot. Chem. 13, 609–18.

Tao, Q. F., Hollenberg, N. K. and Graves, S. W. (1999). Sodium pump inhibition and regional expression of sodium pump α-isoforms in the lens. Hypertension 34, 1168–74.

Tardieu, A. and Delaye, M. (1988). Eye lens proteins and transparency: from light transmission theory to solution X-ray structural analysis. Ann. Rev. Biophys. Biochem. 17, 47–70.

Tardieu, A., Veretout, F., Krop, B. and Slingsby, C. (1992). Protein interactions in the calf eye lens: interactions between beta-crystallins are repulsive whereas in gamma-crystallins they are attractive. Eur. Biophys. J. 21, 1–12.

Taube, J. R., Gao, C. Y., Ueda, Y., Zelenka, P. S., David, L. L. and Duncan, M. K. (2002). General utility of the chicken betaB1-crystallin promoter to drive protein expression in lens fiber cells of transgenic mice. Transgenic Res. 11, 397–410.

Taylor, V., Welcher, A. A., Program, A. E. and Suter, U. (1995). Epithelial membrane protein-1, peripheral myelin protein 22, and lens membrane protein 20 define a novel gene family. J. Biol. Chem. 270, 28824–33.

Taylor, V. L., Al-Ghoul, K. J., Lane, C. W., Davis, V. A., Kuszak, J. R. and Costello, M. J. (1996). Morphology of the normal human lens. Invest. Ophthalmol. Visual Sci. 37, 1396–410.

Taylor, V. L. and Costello, M. J. (1999). Fourier analysis of textural variations in human normal and cataractous lens nuclear fiber cell cytoplasm. Exp. Eye Res. 69, 163–74.

Tebar, M., Destree, O., de Vree, W. J. and Ten Have-Opbroek, A. A. (2001). Expression of Tcf/Lef and sFrp and localization of beta-catenin in the developing mouse lung. Mech. Dev. 109, 437–40.

TenBroek, E. M., Louis, C. F. and Johnson, R. (1997). The differential effects of 12-O-tetradecanoylphorbol-13-acetate on the gap junctions and connexins of the developing mammalian lens. Dev. Biol. 191, 88–102.

Thiery, J. P., Delouvee, A., Gallin, W. J., Cunningham, B. A. and Edelman, G. M. (1984). Ontogenetic expression of cell adhesion molecules: L-CAM is found in epithelia derived from the three primary germ layers. Dev. Biol. 102, 61–78.

Thomas, G., Zelenka, P. S., Cuthbertson, R. A., Norman, B. L. and Piatigorsky, J. (1990). Differential expression of the two delta-crystallin/argininosuccinate lyase genes in lens, heart, and brain of chicken embryos. New Biol. 2, 903–14.

Thomas, G. R., Duncan, G. and Sanderson, J. (1998). Acetylcholine-induced membrane potential oscillations in the intact lens. Invest. Ophthalmol. Vis. Sci. 39, 111–19.