-
1
-
-
0028916193
-
Clinical and histopathologic features of corneal dystrophies in Japan
-
Santo RM, Yamaguchi T, Kanai A, Okisaka S, Nakajima A. Clinical and histopathologic features of corneal dystrophies in Japan. Ophthalmology 1995; 102:557-67.
-
(1995)
Ophthalmology
, vol.102
, pp. 557-567
-
-
Santo, R.M.1
Yamaguchi, T.2
Kanai, A.3
Okisaka, S.4
Nakajima, A.5
-
2
-
-
0002522755
-
Corneal dystrophies and degenerations
-
Smolin G, Tofts RA, editors, 3rd ed. Boston: Little, Brown;
-
Smolin G. Corneal dystrophies and degenerations. In: Smolin G, Tofts RA, editors. The Cornea: Scientific Foundations and Clinical Practice. 3rd ed. Boston: Little, Brown; 1994. p. 499-533.
-
(1994)
The Cornea: Scientific Foundations and Clinical Practice
, pp. 499-533
-
-
Smolin, G.1
-
3
-
-
0032231321
-
Homozygosity mapping of a gene responsible for gelatinous drop-like corneal dystrophy to chromosome 1p
-
Tsujikawa M, Kurahashi H, Tanaka T, Okada M, Yamamoto S, Maeda N, Watanabe H, Inoue Y, Kiridoshi A, Matsumoto K, Ohashi Y, Kinoshita S, Shimomura Y, Nakamura Y, Tano Y. Homozygosity mapping of a gene responsible for gelatinous drop-like corneal dystrophy to chromosome 1p. Am J Hum Genet 1998; 63:1073-7.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 1073-1077
-
-
Tsujikawa, M.1
Kurahashi, H.2
Tanaka, T.3
Okada, M.4
Yamamoto, S.5
Maeda, N.6
Watanabe, H.7
Inoue, Y.8
Kiridoshi, A.9
Matsumoto, K.10
Ohashi, Y.11
Kinoshita, S.12
Shimomura, Y.13
Nakamura, Y.14
Tano, Y.15
-
4
-
-
0032900158
-
Identification of the gene responsible for gelatinous corneal dystrophy
-
Tsujikawa M, Kurahashi H, Tanaka T, Nishida K, Shimomura Y, Tano Y, Nakamura Y. Identification of the gene responsible for gelatinous corneal dystrophy. Nat Genet 1999; 21:420-3.
-
(1999)
Nat Genet
, vol.21
, pp. 420-423
-
-
Tsujikawa, M.1
Kurahashi, H.2
Tanaka, T.3
Nishida, K.4
Shimomura, Y.5
Tano, Y.6
Nakamura, Y.7
-
5
-
-
0035045052
-
Assignment of TACSTD1 (alias TROP1, M4S1) to human chromosome 2p21 and refinement of mapping of TACSTD2 (alias TROP2, M1S1) to human chromosome 1p32 by in situ hybridization
-
Calabrese G, Crescenzi C, Morizio E, Palka G, Guerra E, Alberti S. Assignment of TACSTD1 (alias TROP1, M4S1) to human chromosome 2p21 and refinement of mapping of TACSTD2 (alias TROP2, M1S1) to human chromosome 1p32 by in situ hybridization. Cytogenet Cell Genet 2001; 92:164-5.
-
(2001)
Cytogenet Cell Genet
, vol.92
, pp. 164-165
-
-
Calabrese, G.1
Crescenzi, C.2
Morizio, E.3
Palka, G.4
Guerra, E.5
Alberti, S.6
-
6
-
-
0031800858
-
Human TROP-2 is a tumor-associated calcium signal transducer
-
Ripani E, Sacchetti A, Corda D, Alberti S. Human TROP-2 is a tumor-associated calcium signal transducer. Int J Cancer 1998; 76:671-6.
-
(1998)
Int J Cancer
, vol.76
, pp. 671-676
-
-
Ripani, E.1
Sacchetti, A.2
Corda, D.3
Alberti, S.4
-
7
-
-
34347268821
-
Two novel mutations identified in two Chinese gelatinous drop-like corneal dystrophy families
-
Zhang B, Yao YF, Zhou P. Two novel mutations identified in two Chinese gelatinous drop-like corneal dystrophy families. Mol Vis 2007; 13:988-92.
-
(2007)
Mol Vis
, vol.13
, pp. 988-992
-
-
Zhang, B.1
Yao, Y.F.2
Zhou, P.3
-
8
-
-
34548122892
-
Four mutations (three novel, one founder) in TACSTD2 among Iranian GDLD patients
-
Alavi A, Elahi E, Tehrani MH, Amoli FA, Javadi MA, Rafati N, Chiani M, Banihosseini SS, Bayat B, Kalhor R, Amini SS. Four mutations (three novel, one founder) in TACSTD2 among Iranian GDLD patients. Invest Ophthalmol Vis Sci 2007; 48:4490-7.
-
(2007)
Invest Ophthalmol Vis Sci
, vol.48
, pp. 4490-4497
-
-
Alavi, A.1
Elahi, E.2
Tehrani, M.H.3
Amoli, F.A.4
Javadi, M.A.5
Rafati, N.6
Chiani, M.7
Banihosseini, S.S.8
Bayat, B.9
Kalhor, R.10
Amini, S.S.11
-
9
-
-
14644398011
-
Gelatinous drop-like corneal dystrophy in a child with developmental delay: Clinicopathological features and exclusion of the M1S1 gene
-
Akhtar S, Bron AJ, Qin X, Creer RC, Guggenheim JA, Meek KM. Gelatinous drop-like corneal dystrophy in a child with developmental delay: Clinicopathological features and exclusion of the M1S1 gene. Eye 2005; 19:198-204.
-
(2005)
Eye
, vol.19
, pp. 198-204
-
-
Akhtar, S.1
Bron, A.J.2
Qin, X.3
Creer, R.C.4
Guggenheim, J.A.5
Meek, K.M.6
-
10
-
-
11844280378
-
A novel missense mutation in a Japanese patient with gelatinous droplike corneal dystrophy
-
Taniguchi Y, Tsujikawa M, Hibino S, Tsujikawa K, Tanaka T, Kiridoushi A, Tano Y. A novel missense mutation in a Japanese patient with gelatinous droplike corneal dystrophy. Am J Ophthalmol 2005; 139:186-8.
-
(2005)
Am J Ophthalmol
, vol.139
, pp. 186-188
-
-
Taniguchi, Y.1
Tsujikawa, M.2
Hibino, S.3
Tsujikawa, K.4
Tanaka, T.5
Kiridoushi, A.6
Tano, Y.7
-
11
-
-
0036626520
-
Allelic and locus heterogeneity in autosomal recessive gelatinous drop-like corneal dystrophy
-
Ren Z, Lin PY, Klintworth GK, Iwata F, Munier FL, Schorderet DF, El Matri L, Theendakara V, Basti S, Reddy M, Hejtmancik JF. Allelic and locus heterogeneity in autosomal recessive gelatinous drop-like corneal dystrophy. Hum Genet 2002; 110:568-77.
-
(2002)
Hum Genet
, vol.110
, pp. 568-577
-
-
Ren, Z.1
Lin, P.Y.2
Klintworth, G.K.3
Iwata, F.4
Munier, F.L.5
Schorderet, D.F.6
El Matri, L.7
Theendakara, V.8
Basti, S.9
Reddy, M.10
Hejtmancik, J.F.11
-
12
-
-
33845738288
-
A novel TACSTD2 gene mutation in a Turkish family with a gelatinous drop-like corneal dystrophy
-
Markoff A, Bogdanova N, Uhlig CE, Groppe M, Horst J, Kennerknecht I. A novel TACSTD2 gene mutation in a Turkish family with a gelatinous drop-like corneal dystrophy. Mol Vis 2006; 12:1473-6.
-
(2006)
Mol Vis
, vol.12
, pp. 1473-1476
-
-
Markoff, A.1
Bogdanova, N.2
Uhlig, C.E.3
Groppe, M.4
Horst, J.5
Kennerknecht, I.6
-
13
-
-
0037373685
-
A novel mutation of M1S1 gene found in a Vietnamese patient with gelatinous droplike corneal dystrophy
-
Ha NT, Chau HM, Cung LX, Thanh TK, Fujiki K, Murakami A, Kanai A. A novel mutation of M1S1 gene found in a Vietnamese patient with gelatinous droplike corneal dystrophy. Am J Ophthalmol 2003; 135:390-3.
-
(2003)
Am J Ophthalmol
, vol.135
, pp. 390-393
-
-
Ha, N.T.1
Chau, H.M.2
Cung, L.X.3
Thanh, T.K.4
Fujiki, K.5
Murakami, A.6
Kanai, A.7
-
14
-
-
1542297331
-
Compound heterozygous mutations of M1S1 gene in gelatinous droplike corneal dystrophy
-
Tian X, Fujiki K, Li Q, Murakami A, Xie P, Kanai A, Wang W, Liu Z. Compound heterozygous mutations of M1S1 gene in gelatinous droplike corneal dystrophy. Am J Ophthalmol 2004; 137:567-9.
-
(2004)
Am J Ophthalmol
, vol.137
, pp. 567-569
-
-
Tian, X.1
Fujiki, K.2
Li, Q.3
Murakami, A.4
Xie, P.5
Kanai, A.6
Wang, W.7
Liu, Z.8
-
15
-
-
0026682657
-
Transcription factors: Structural families and principle of DNA recognition
-
Pabo CO, Sauer RT. Transcription factors: structural families and principle of DNA recognition. Annu Rev Biochem 1992; 61:1053-95.
-
(1992)
Annu Rev Biochem
, vol.61
, pp. 1053-1095
-
-
Pabo, C.O.1
Sauer, R.T.2
-
16
-
-
0347445017
-
Structural similarity in the DNA-binding domains of catabolite gene activator and cro repressor protein
-
Steitz TA, Ohlendorf DH, McKay DB, Anderson WF, Matthews BW. Structural similarity in the DNA-binding domains of catabolite gene activator and cro repressor protein. Proc Natl Acad Sci USA 1982; 79:3097-100.
-
(1982)
Proc Natl Acad Sci USA
, vol.79
, pp. 3097-3100
-
-
Steitz, T.A.1
Ohlendorf, D.H.2
McKay, D.B.3
Anderson, W.F.4
Matthews, B.W.5
-
17
-
-
0002345176
-
DNA recognition by the helix-turn-helix motif
-
Brennan RG. DNA recognition by the helix-turn-helix motif. Curr Opin Struct Biol 1992; 2:100-8.
-
(1992)
Curr Opin Struct Biol
, vol.2
, pp. 100-108
-
-
Brennan, R.G.1
-
18
-
-
0040736139
-
Thyroglobulin type-1 domains in equistatin inhibit both papain-like cysteine proteinases and cathespsin D
-
Lenarcic B, Turk V. Thyroglobulin type-1 domains in equistatin inhibit both papain-like cysteine proteinases and cathespsin D. J Biol Chem 1999; 274:563-6.
-
(1999)
J Biol Chem
, vol.274
, pp. 563-566
-
-
Lenarcic, B.1
Turk, V.2
-
19
-
-
0033939852
-
Epithelial barrier function and ultrastructure of gelatinous drop-like corneal dystrophy
-
Kinoshita S, Nishida K, Dota A, Inatomi T, Koizumi N, Elliott A, Lewis D, Quantock A, Fullwood N. Epithelial barrier function and ultrastructure of gelatinous drop-like corneal dystrophy. Cornea 2000; 19:551-5.
-
(2000)
Cornea
, vol.19
, pp. 551-555
-
-
Kinoshita, S.1
Nishida, K.2
Dota, A.3
Inatomi, T.4
Koizumi, N.5
Elliott, A.6
Lewis, D.7
Quantock, A.8
Fullwood, N.9
|