-
1
-
-
0019956534
-
Spectroscopic studies of lens crystallins. II. Fluorescence probes for polar-apolar nature and sulfhydryl group accessibility
-
Andley, U.P., Liang, J.N., and Chakrabarti, B. 1982. Spectroscopic studies of lens crystallins. II. Fluorescence probes for polar-apolar nature and sulfhydryl group accessibility. Biochemistry 21: 1853-1857.
-
(1982)
Biochemistry
, vol.21
, pp. 1853-1857
-
-
Andley, U.P.1
Liang, J.N.2
Chakrabarti, B.3
-
2
-
-
0029770039
-
Cloning, expression, and chaperone-like activity of human α-crystallin
-
Andley, U.P., Mathur, S., Griest, T.A., and Petrash, J.M. 1996. Cloning, expression, and chaperone-like activity of human α-crystallin. J. Biol. Chem. 271: 31973-31980.
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 31973-31980
-
-
Andley, U.P.1
Mathur, S.2
Griest, T.A.3
Petrash, J.M.4
-
3
-
-
0034765821
-
αB crystallin gene (CRYAB) mutation causes dominant congenital posterior polar cataract in humans
-
Berry, V., Francis, P., Reddy, M.A., Collyer, D., Vithana, E., MacKay, I., Dawson, G., Carey. A.H., Moore, A., Bhattacharya, S.S., et al. 2001. αB crystallin gene (CRYAB) mutation causes dominant congenital posterior polar cataract in humans. Am. J. Hum. Genet. 69: 1141-1145.
-
(2001)
Am. J. Hum. Genet.
, vol.69
, pp. 1141-1145
-
-
Berry, V.1
Francis, P.2
Reddy, M.A.3
Collyer, D.4
Vithana, E.5
MacKay, I.6
Dawson, G.7
Carey, A.H.8
Moore, A.9
Bhattacharya, S.S.10
-
4
-
-
0030613769
-
Subunit exchange of αA-crystallin
-
Bova, M.P., Ding, L.L., Horwitz, J., and Fung, B.K. 1997. Subunit exchange of αA-crystallin. J. Biol. Chem. 272: 29511-29517.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 29511-29517
-
-
Bova, M.P.1
Ding, L.L.2
Horwitz, J.3
Fung, B.K.4
-
5
-
-
15844414479
-
Conformational properties of substrate proteins bound to a molecular chaperone α-crystallin
-
Das, K.P., Petrash, J.M., and Surewicz, W.K. 1996. Conformational properties of substrate proteins bound to a molecular chaperone α-crystallin. J. Biol. Chem. 271: 10449-10452.
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 10449-10452
-
-
Das, K.P.1
Petrash, J.M.2
Surewicz, W.K.3
-
6
-
-
0028988412
-
Interaction of α-crystallin with spin-labeled peptides
-
Farahbakhsh, Z.T., Huang, Q.-L., Ding, L.-L., Altenbach, C., Steinhoff, H.J., Horwitz, J., and Hubbell, W.L. 1995. Interaction of α-crystallin with spin-labeled peptides. Biochemistry 34: 509-516.
-
(1995)
Biochemistry
, vol.34
, pp. 509-516
-
-
Farahbakhsh, Z.T.1
Huang, Q.-L.2
Ding, L.-L.3
Altenbach, C.4
Steinhoff, H.J.5
Horwitz, J.6
Hubbell, W.L.7
-
7
-
-
0037181130
-
Conformational change and destabilization of cataract γC-crystallin T5P mutant
-
Fu, L. and Liang, J.J.N. 2002a. Conformational change and destabilization of cataract γC-crystallin T5P mutant. FEBS Lett. 513: 213-216.
-
(2002)
FEBS Lett.
, vol.513
, pp. 213-216
-
-
Fu, L.1
Liang, J.J.N.2
-
8
-
-
0037336078
-
Alteration of protein-protein interactions of cataract crystallin gene mutants
-
-. 2002b. Alteration of protein-protein interactions of cataract crystallin gene mutants. Invest. Ophthalmol. Vis. Sci. 44: 1155-1159.
-
(2002)
Invest. Ophthalmol. Vis. Sci.
, vol.44
, pp. 1155-1159
-
-
-
9
-
-
0037040277
-
Detection of protein-protein interactions among lens crystallins in a mammalian two-hybrid system assay
-
-. 2002c. Detection of protein-protein interactions among lens crystallins in a mammalian two-hybrid system assay. J. Biol. Chem. III: 4255-4260.
-
(2002)
J. Biol. Chem.
, vol.3
, pp. 4255-4260
-
-
-
10
-
-
0033986327
-
Genetic heterogeneity of the Coppock-like cataract: A mutation in CRYBB2 on chromosome 22q11.2
-
Gill, D., Klose, R., Munier, F.L., McFadden, M., Priston, M., Billingsley, G., Ducrey, N., Schorderet, D.F., and Heon, E. 2000. Genetic heterogeneity of the Coppock-like cataract: A mutation in CRYBB2 on chromosome 22q11.2. Invest. Ophthalmol. Vis. Sci 41: 159-165.
-
(2000)
Invest. Ophthalmol. Vis. Sci.
, vol.41
, pp. 159-165
-
-
Gill, D.1
Klose, R.2
Munier, F.L.3
McFadden, M.4
Priston, M.5
Billingsley, G.6
Ducrey, N.7
Schorderet, D.F.8
Heon, E.9
-
11
-
-
0033358423
-
The γ-crystallins and human cataracts: A puzzle made clearer
-
Heon, E., Priston, M., Schorderet, D.F., Billingsley, G.D., Girard, P.O., Lubsen, N., and Munier, F.L. 1999. The γ-crystallins and human cataracts: A puzzle made clearer. Am J. Hum. Genet. 65: 1261-1267.
-
(1999)
Am J. Hum. Genet.
, vol.65
, pp. 1261-1267
-
-
Heon, E.1
Priston, M.2
Schorderet, D.F.3
Billingsley, G.D.4
Girard, P.O.5
Lubsen, N.6
Munier, F.L.7
-
12
-
-
0026483279
-
α-Crystallin can function as a molecular chaperone
-
Horwitz, J. 1992. α-Crystallin can function as a molecular chaperone. Proc. NaTL. Acad. Sci. 89: 10449-10453.
-
(1992)
Proc. Natl. Acad. Sci.
, vol.89
, pp. 10449-10453
-
-
Horwitz, J.1
-
14
-
-
0030914095
-
Autosomal dominant cerulean cataract is associated with a chain termination mutation in the human β-crystallin gene CRYBB2
-
Litt, M., Carrero-Valenzuela, R., LaMorticella, D.M., Schultz, D.W., Mitchell, T.N., Kramer, P., and Maumenee, I.H. 1997. Autosomal dominant cerulean cataract is associated with a chain termination mutation in the human β-crystallin gene CRYBB2. Hum. Mol. Genet. 6: 665-668.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 665-668
-
-
Litt, M.1
Carrero-Valenzuela, R.2
LaMorticella, D.M.3
Schultz, D.W.4
Mitchell, T.N.5
Kramer, P.6
Maumenee, I.H.7
-
15
-
-
0031934121
-
Autosomal dominant congenital cataract associated with a missense mutation in the human α-crystallin gene CRYAA
-
Litt, M., Kramer, P., LaMorticella, D.M., Murphey, W., Lovrien, E.W., and Weleber, R.G. 1998. Autosomal dominant congenital cataract associated with a missense mutation in the human α-crystallin gene CRYAA. Hum. Mol. Genet. 7: 471-474.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 471-474
-
-
Litt, M.1
Kramer, P.2
LaMorticella, D.M.3
Murphey, W.4
Lovrien, E.W.5
Weleber, R.G.6
-
16
-
-
0026585599
-
Statistical determination of the average values of the extinction coefficients of tryptophan and tyrosine in native proteins
-
Mach, H., Middaugh, C.R., and Lewis, R. V. 1992. Statistical determination of the average values of the extinction coefficients of tryptophan and tyrosine in native proteins. Anal. Biochem. 200: 74-80.
-
(1992)
Anal. Biochem.
, vol.200
, pp. 74-80
-
-
Mach, H.1
Middaugh, C.R.2
Lewis, R.V.3
-
17
-
-
0036093256
-
Novel mutations in the γ-crystallin genes cause autosomal dominant congenital cataracts
-
Santhiya, S.T, Shyam Manohar, M., Rawlley, D., Vijayalakshmi, P., Namperumalsamy, P., Gopinath, P.M., Loster, J., and Graw, J. 2002. Novel mutations in the γ-crystallin genes cause autosomal dominant congenital cataracts. J. Med. Genet. 39: 352-358.
-
(2002)
J. Med. Genet.
, vol.39
, pp. 352-358
-
-
Santhiya, S.T.1
Shyam Manohar, M.2
Rawlley, D.3
Vijayalakshmi, P.4
Namperumalsamy, P.5
Gopinath, P.M.6
Loster, J.7
Graw, J.8
-
18
-
-
0031962334
-
Intermolecular exchange and stabilization of human lens recombinant αA- and αB-crystallins
-
Sun, T.-X. and Liang, J.J.N. 1998. Intermolecular exchange and stabilization of human lens recombinant αA- and αB-crystallins. J. Biol. Chem. 273: 286-290.
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 286-290
-
-
Sun, T.-X.1
Liang, J.J.N.2
-
19
-
-
0030933472
-
Conformational and functional differences between recombinant human lens αA- and αB-crystallin
-
Sun, T.-X., Das, B.K., and Liang, J.J.N. 1997. Conformational and functional differences between recombinant human lens αA- and αB-crystallin. J. Biol. Chem. 272: 6220-6225.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 6220-6225
-
-
Sun, T.-X.1
Das, B.K.2
Liang, J.J.N.3
-
20
-
-
0032479355
-
Subunit exchange of lens α-crystallin: A fluorescence energy transfer study with the fluorescent labeled α-crystallin mutant W9F as a probe
-
Sun, T.-X., Akhtar, N.J., and Liang, J.J.N. 1998. Subunit exchange of lens α-crystallin: A fluorescence energy transfer study with the fluorescent labeled α-crystallin mutant W9F as a probe. FEBS Lett. 430: 401-404.
-
(1998)
FEBS Lett.
, vol.430
, pp. 401-404
-
-
Sun, T.-X.1
Akhtar, N.J.2
Liang, J.J.N.3
-
21
-
-
17344361902
-
A missense mutation in the αB-crystallin chaperone gene causes a desmin-related myopathy
-
Vicart, P., Caron, A., Guicheney, P., Li, Z., Prevost, M.C., Faure, A., Chateau, D., Chapon, F., Tome. F., Dupret, J.M., et al. 1998. A missense mutation in the αB-crystallin chaperone gene causes a desmin-related myopathy. Nat. Genet. 20: 92-95.
-
(1998)
Nat. Genet.
, vol.20
, pp. 92-95
-
-
Vicart, P.1
Caron, A.2
Guicheney, P.3
Li, Z.4
Prevost, M.C.5
Faure, A.6
Chateau, D.7
Chapon, F.8
Tome, F.9
Dupret, J.M.10
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