-
1
-
-
0033926590
-
Molecular genetics of primary congenital glaucoma
-
[PMID: 11026969]
-
Sarfarazi M, Stoilov I. Molecular genetics of primary congenital glaucoma. Eye (Lond) 2000; 14:422-8. [PMID: 11026969]
-
(2000)
Eye (Lond)
, vol.14
, pp. 422-428
-
-
Sarfarazi, M.1
Stoilov, I.2
-
2
-
-
0019742616
-
The development of the trabecular meshwork and its abnormality in primary infantile glaucoma
-
[PMID: 7342408]
-
Anderson DR. The development of the trabecular meshwork and its abnormality in primary infantile glaucoma. Trans Am Ophthalmol Soc 1981; 79:458-85. [PMID: 7342408]
-
(1981)
Trans Am Ophthalmol Soc
, vol.79
, pp. 458-485
-
-
Anderson, D.R.1
-
3
-
-
0348225298
-
Genetics and biochemistry of primary congenital glaucoma
-
[PMID: 14740995]vi
-
Sarfarazi M, Stoilov I, Schenkman JB. Genetics and biochemistry of primary congenital glaucoma. Ophthalmol Clin North Am 2003; 16:543-54. [PMID: 14740995]vi.
-
(2003)
Ophthalmol Clin North Am
, vol.16
, pp. 543-554
-
-
Sarfarazi, M.1
Stoilov, I.2
Schenkman, J.B.3
-
4
-
-
2442723700
-
Identification of a single ancestral CYP1B1 mutation in Slovak Gypsies (Roms) affected with primary congenital glaucoma
-
[PMID: 10227395]
-
Plásilová M, Stoilov I, Sarfarazi M, Kadasi L, Ferakova E, Ferak V. Identification of a single ancestral CYP1B1 mutation in Slovak Gypsies (Roms) affected with primary congenital glaucoma. J Med Genet 1999; 36:290-4. [PMID: 10227395]
-
(1999)
J Med Genet
, vol.36
, pp. 290-294
-
-
Plásilová, M.1
Stoilov, I.2
Sarfarazi, M.3
Kadasi, L.4
Ferakova, E.5
Ferak, V.6
-
5
-
-
42149113372
-
Contribution of CYP1B1 mutations and founder effect to primary congenital glaucoma in Mexico
-
[PMID: 18414103]
-
Zenteno JC, Hernandez-Merino E, Mejia-Lopez H, Matias-Florentino M, Michel N, Elizondo-Olascoaga C, Korder-Ortega V, Casab-Rueda H, Garcia-Ortiz JE. Contribution of CYP1B1 mutations and founder effect to primary congenital glaucoma in Mexico. J Glaucoma 2008; 17:189-92. [PMID: 18414103]
-
(2008)
J Glaucoma
, vol.17
, pp. 189-192
-
-
Zenteno, J.C.1
Hernandez-Merino, E.2
Mejia-Lopez, H.3
Matias-Florentino, M.4
Michel, N.5
Elizondo-Olascoaga, C.6
Korder-Ortega, V.7
Casab-Rueda, H.8
Garcia-Ortiz, J.E.9
-
6
-
-
0029836678
-
A second locus (GLC3B) for primary congenital glaucoma (Buphthalmos) maps to the 1p36 region
-
[PMID: 8842741]
-
Akarsu AN, Turacli ME, Aktan SG, Barsoum-Homsy M, Chevrette L, Sayli BS, Sarfarazi M. A second locus (GLC3B) for primary congenital glaucoma (Buphthalmos) maps to the 1p36 region. Hum Mol Genet 1996; 5:1199-203. [PMID: 8842741]
-
(1996)
Hum Mol Genet
, vol.5
, pp. 1199-1203
-
-
Akarsu, A.N.1
Turacli, M.E.2
Aktan, S.G.3
Barsoum-Homsy, M.4
Chevrette, L.5
Sayli, B.S.6
Sarfarazi, M.7
-
7
-
-
0036157114
-
Digenic inheritance of early-onset glaucoma: CYP1B1, a potential modifier gene
-
[PMID: 11774072]
-
Vincent AL, Billingsley G, Buys Y, Levin AV, Priston M, Trope G, Williams-Lyn D, Heon E. Digenic inheritance of early-onset glaucoma: CYP1B1, a potential modifier gene. Am J Hum Genet 2002; 70:448-60. [PMID: 11774072]
-
(2002)
Am J Hum Genet
, vol.70
, pp. 448-460
-
-
Vincent, A.L.1
Billingsley, G.2
Buys, Y.3
Levin, A.V.4
Priston, M.5
Trope, G.6
Williams-Lyn, D.7
Heon, E.8
-
8
-
-
15844415263
-
Myocilin gene implicated in primary congenital glaucoma
-
[PMID: 15733270]
-
Kaur K, Reddy AB, Mukhopadhyay A, Mandal AK, Hasnain SE, Ray K, Thomas R, Balasubramanian D, Chakrabarti S. Myocilin gene implicated in primary congenital glaucoma. Clin Genet 2005; 67:335-40. [PMID: 15733270]
-
(2005)
Clin Genet
, vol.67
, pp. 335-340
-
-
Kaur, K.1
Reddy, A.B.2
Mukhopadhyay, A.3
Mandal, A.K.4
Hasnain, S.E.5
Ray, K.6
Thomas, R.7
Balasubramanian, D.8
Chakrabarti, S.9
-
9
-
-
33746349553
-
Analysis of MYOC gene mutation in a Chinese glaucoma family with primary open-angle glaucoma and primary congenital glaucoma
-
[PMID: 16863615]
-
Zhuo YH, Wang M, Wei YT, Huang YL, Ge J. Analysis of MYOC gene mutation in a Chinese glaucoma family with primary open-angle glaucoma and primary congenital glaucoma. Chin Med J (Engl) 2006; 119:1210-4. [PMID: 16863615]
-
(2006)
Chin Med J (Engl)
, vol.119
, pp. 1210-1214
-
-
Zhuo, Y.H.1
Wang, M.2
Wei, Y.T.3
Huang, Y.L.4
Ge, J.5
-
11
-
-
34047256282
-
Association of CYP1B1 germ line mutations with hepatocyte nuclear factor 1alpha-mutated hepatocellular adenoma
-
[PMID: 17363580]
-
Jeannot E, Poussin K, Chiche L, Bacq Y, Sturm N, Scoazec JY, Buffet C, Van Nhieu JT, Bellanne-Chantelot C, de Toma C, Laurent-Puig P, Bioulac-Sage P, Zucman-Rossi J. Association of CYP1B1 germ line mutations with hepatocyte nuclear factor 1alpha-mutated hepatocellular adenoma. Cancer Res 2007; 67:2611-6. [PMID: 17363580]
-
(2007)
Cancer Res
, vol.67
, pp. 2611-2616
-
-
Jeannot, E.1
Poussin, K.2
Chiche, L.3
Bacq, Y.4
Sturm, N.5
Scoazec, J.Y.6
Buffet, C.7
van Nhieu, J.T.8
Bellanne-Chantelot, C.9
de Toma, C.10
Laurent-Puig, P.11
Bioulac-Sage, P.12
Zucman-Rossi, J.13
-
12
-
-
0033623590
-
Novel compound heterozygous mutations in the cytochrome P4501B1 gene (CYP1B1) in a Japanese patient with primary congenital glaucoma
-
[PMID: 11184479]
-
Ohtake Y, Kubota R, Tanino T, Miyata H, Mashima Y. Novel compound heterozygous mutations in the cytochrome P4501B1 gene (CYP1B1) in a Japanese patient with primary congenital glaucoma. Ophthalmic Genet 2000; 21:191-3. [PMID: 11184479]
-
(2000)
Ophthalmic Genet
, vol.21
, pp. 191-193
-
-
Ohtake, Y.1
Kubota, R.2
Tanino, T.3
Miyata, H.4
Mashima, Y.5
-
13
-
-
34548309440
-
Mutational screening of CYP1B1 in Turkish PCG families and functional analyses of newly detected mutations
-
[PMID: 17893647]
-
Bagiyeva S, Marfany G, Gonzalez-Angulo O, Gonzalez-Duarte R. Mutational screening of CYP1B1 in Turkish PCG families and functional analyses of newly detected mutations. Mol Vis 2007; 13:1458-68. [PMID: 17893647]
-
(2007)
Mol Vis
, vol.13
, pp. 1458-1468
-
-
Bagiyeva, S.1
Marfany, G.2
Gonzalez-Angulo, O.3
Gonzalez-Duarte, R.4
-
14
-
-
61849142774
-
CYP1B1 mutations in Spanish patients with primary congenital glaucoma: Phenotypic and functional variability
-
[PMID: 19234632]
-
Campos-Mollo E, Lopez-Garrido MP, Blanco-Marchite C, Garcia-Feijoo J, Peralta J, Belmonte-Martinez J, Ayuso C, Escribano J. CYP1B1 mutations in Spanish patients with primary congenital glaucoma: phenotypic and functional variability. Mol Vis 2009; 15:417-31. [PMID: 19234632]
-
(2009)
Mol Vis
, vol.15
, pp. 417-431
-
-
Campos-Mollo, E.1
Lopez-Garrido, M.P.2
Blanco-Marchite, C.3
Garcia-Feijoo, J.4
Peralta, J.5
Belmonte-Martinez, J.6
Ayuso, C.7
Escribano, J.8
-
15
-
-
33646892373
-
Primary congenital glaucoma and Rieger's anomaly: Extended haplotypes reveal founder effects for eight distinct CYP1B1 mutations
-
[PMID: 16735994]
-
Chavarria-Soley G, Michels-Rautenstrauss K, Pasutto F, Flikier D, Flikier P, Cirak S, Bejjani B, Winters DL, Lewis RA, Mardin C, Reis A, Rautenstrauss B. Primary congenital glaucoma and Rieger's anomaly: extended haplotypes reveal founder effects for eight distinct CYP1B1 mutations. Mol Vis 2006; 12:523-31. [PMID: 16735994]
-
(2006)
Mol Vis
, vol.12
, pp. 523-531
-
-
Chavarria-Soley, G.1
Michels-Rautenstrauss, K.2
Pasutto, F.3
Flikier, D.4
Flikier, P.5
Cirak, S.6
Bejjani, B.7
Winters, D.L.8
Lewis, R.A.9
Mardin, C.10
Reis, A.11
Rautenstrauss, B.12
-
16
-
-
1942522732
-
Novel cytochrome P450 1B1 (CYP1B1) mutations in patients with primary congenital glaucoma in France
-
[PMID: 14635112]
-
Colomb E, Kaplan J, Garchon HJ. Novel cytochrome P450 1B1 (CYP1B1) mutations in patients with primary congenital glaucoma in France. Hum Mutat 2003; 22:496. [PMID: 14635112]
-
(2003)
Hum Mutat
, vol.22
, pp. 496
-
-
Colomb, E.1
Kaplan, J.2
Garchon, H.J.3
-
17
-
-
15844383248
-
Mutation spectrum of the CYP1B1 gene in Indian primary congenital glaucoma patients
-
[PMID: 15475877]
-
Reddy AB, Kaur K, Mandal AK, Panicker SG, Thomas R, Hasnain SE, Balasubramanian D, Chakrabarti S. Mutation spectrum of the CYP1B1 gene in Indian primary congenital glaucoma patients. Mol Vis 2004; 10:696-702. [PMID: 15475877]
-
(2004)
Mol Vis
, vol.10
, pp. 696-702
-
-
Reddy, A.B.1
Kaur, K.2
Mandal, A.K.3
Panicker, S.G.4
Thomas, R.5
Hasnain, S.E.6
Balasubramanian, D.7
Chakrabarti, S.8
-
18
-
-
33947711740
-
Genotype and phenotype correlations in congenital glaucoma
-
[PMID: 17471339]
-
Hollander DA, Sarfarazi M, Stoilov I, Wood IS, Fredrick DR, Alvarado JA. Genotype and phenotype correlations in congenital glaucoma. Trans Am Ophthalmol Soc 2006; 104:183-95. [PMID: 17471339]
-
(2006)
Trans Am Ophthalmol Soc
, vol.104
, pp. 183-195
-
-
Hollander, D.A.1
Sarfarazi, M.2
Stoilov, I.3
Wood, I.S.4
Fredrick, D.R.5
Alvarado, J.A.6
-
19
-
-
0034854849
-
Novel cytochrome P4501B1 (CYP1B1) gene mutations in Japanese patients with primary congenital glaucoma
-
[PMID: 11527932]
-
Mashima Y, Suzuki Y, Sergeev Y, Ohtake Y, Tanino T, Kimura I, Miyata H, Aihara M, Tanihara H, Inatani M, Azuma N, Iwata T, Araie M. Novel cytochrome P4501B1 (CYP1B1) gene mutations in Japanese patients with primary congenital glaucoma. Invest Ophthalmol Vis Sci 2001; 42:2211-6. [PMID: 11527932]
-
(2001)
Invest Ophthalmol Vis Sci
, vol.42
, pp. 2211-2216
-
-
Mashima, Y.1
Suzuki, Y.2
Sergeev, Y.3
Ohtake, Y.4
Tanino, T.5
Kimura, I.6
Miyata, H.7
Aihara, M.8
Tanihara, H.9
Inatani, M.10
Azuma, N.11
Iwata, T.12
Araie, M.13
-
20
-
-
0036272051
-
Molecular genetics of primary congenital glaucoma in Brazil
-
[PMID: 12036985]
-
Stoilov IR, Costa VP, Vasconcellos JP, Melo MB, Betinjane AJ, Carani JC, Oltrogge EV, Sarfarazi M. Molecular genetics of primary congenital glaucoma in Brazil. Invest Ophthalmol Vis Sci 2002; 43:1820-7. [PMID: 12036985]
-
(2002)
Invest Ophthalmol Vis Sci
, vol.43
, pp. 1820-1827
-
-
Stoilov, I.R.1
Costa, V.P.2
Vasconcellos, J.P.3
Melo, M.B.4
Betinjane, A.J.5
Carani, J.C.6
Oltrogge, E.V.7
Sarfarazi, M.8
-
21
-
-
1942486803
-
Cytochrome P4501B1 mutations cause only part of primary congenital glaucoma in Ecuador
-
[PMID: 15255109]
-
Curry SM, Daou AG, Hermanns P, Molinari A, Lewis RA, Bejjani BA. Cytochrome P4501B1 mutations cause only part of primary congenital glaucoma in Ecuador. Ophthalmic Genet 2004; 25:3-9. [PMID: 15255109]
-
(2004)
Ophthalmic Genet
, vol.25
, pp. 3-9
-
-
Curry, S.M.1
Daou, A.G.2
Hermanns, P.3
Molinari, A.4
Lewis, R.A.5
Bejjani, B.A.6
-
22
-
-
0037340268
-
Phenotype of cytochrome P4501B1 gene (CYP1B1) mutations in Japanese patients with primary congenital glaucoma
-
[PMID: 12598442]
-
Ohtake Y, Tanino T, Suzuki Y, Miyata H, Taomoto M, Azuma N, Tanihara H, Araie M, Mashima Y. Phenotype of cytochrome P4501B1 gene (CYP1B1) mutations in Japanese patients with primary congenital glaucoma. Br J Ophthalmol 2003; 87:302-4. [PMID: 12598442]
-
(2003)
Br J Ophthalmol
, vol.87
, pp. 302-304
-
-
Ohtake, Y.1
Tanino, T.2
Suzuki, Y.3
Miyata, H.4
Taomoto, M.5
Azuma, N.6
Tanihara, H.7
Araie, M.8
Mashima, Y.9
-
23
-
-
25444472655
-
Gln48His is the prevalent myocilin mutation in primary open angle and primary congenital glaucoma phenotypes in India
-
[PMID: 15723004]
-
Chakrabarti S, Kaur K, Komatireddy S, Acharya M, Devi KR, Mukhopadhyay A, Mandal AK, Hasnain SE, Chandrasekhar G, Thomas R, Ray K. Gln48His is the prevalent myocilin mutation in primary open angle and primary congenital glaucoma phenotypes in India. Mol Vis 2005; 11:111-3. [PMID: 15723004]
-
(2005)
Mol Vis
, vol.11
, pp. 111-113
-
-
Chakrabarti, S.1
Kaur, K.2
Komatireddy, S.3
Acharya, M.4
Devi, K.R.5
Mukhopadhyay, A.6
Mandal, A.K.7
Hasnain, S.E.8
Chandrasekhar, G.9
Thomas, R.10
Ray, K.11
-
24
-
-
65149084930
-
Null mutations in LTBP2 cause primary congenital glaucoma
-
[PMID: 19361779]
-
Ali M, McKibbin M, Booth A, Parry DA, Jain P, Riazuddin SA, Hejtmancik JF, Khan SN, Firasat S, Shires M, Gilmour DF, Towns K, Murphy AL, Azmanov D, Tournev I, Cherninkova S, Jafri H, Raashid Y, Toomes C, Craig J, Mackey DA, Kalaydjieva L, Riazuddin S, Inglehearn CF. Null mutations in LTBP2 cause primary congenital glaucoma. Am J Hum Genet 2009; 84:664-71. [PMID: 19361779]
-
(2009)
Am J Hum Genet
, vol.84
, pp. 664-671
-
-
Ali, M.1
McKibbin, M.2
Booth, A.3
Parry, D.A.4
Jain, P.5
Riazuddin, S.A.6
Hejtmancik, J.F.7
Khan, S.N.8
Firasat, S.9
Shires, M.10
Gilmour, D.F.11
Towns, K.12
Murphy, A.L.13
Azmanov, D.14
Tournev, I.15
Cherninkova, S.16
Jafri, H.17
Raashid, Y.18
Toomes, C.19
Craig, J.20
Mackey, D.A.21
Kalaydjieva, L.22
Riazuddin, S.23
Inglehearn, C.F.24
more..
-
25
-
-
70349578331
-
Loss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucoma
-
[PMID: 19656777]
-
Narooie-Nejad M, Paylakhi SH, Shojaee S, Fazlali Z, Rezaei Kanavi M, Nilforushan N, Yazdani S, Babrzadeh F, Suri F, Ronaghi M, Elahi E, Paisan-Ruiz C. Loss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucoma. Hum Mol Genet 2009; 18:3969-77. [PMID: 19656777]
-
(2009)
Hum Mol Genet
, vol.18
, pp. 3969-3977
-
-
Narooie-Nejad, M.1
Paylakhi, S.H.2
Shojaee, S.3
Fazlali, Z.4
Rezaei Kanavi, M.5
Nilforushan, N.6
Yazdani, S.7
Babrzadeh, F.8
Suri, F.9
Ronaghi, M.10
Elahi, E.11
Paisan-Ruiz, C.12
-
26
-
-
34548368522
-
The third genetic locus (GLC3C) for primary congenital glaucoma (PCG) maps to chromosome 14q24.3
-
May 5-10; Ft. Lauderdale, FL
-
Stoilov I, Sarfarazi M. The third genetic locus (GLC3C) for primary congenital glaucoma (PCG) maps to chromosome 14q24.3. ARVO Annual Meeting; 2002 May 5-10; Ft. Lauderdale, FL.
-
(2002)
ARVO Annual Meeting
-
-
Stoilov, I.1
Sarfarazi, M.2
-
27
-
-
18344398251
-
CYP1B1 gene analysis in primary congenital glaucoma in Indonesian and European patients
-
[PMID: 12525557]
-
Sitorus R, Ardjo SM, Lorenz B, Preising M. CYP1B1 gene analysis in primary congenital glaucoma in Indonesian and European patients. J Med Genet 2003; 40:e9. [PMID: 12525557]
-
(2003)
J Med Genet
, vol.40
-
-
Sitorus, R.1
Ardjo, S.M.2
Lorenz, B.3
Preising, M.4
-
28
-
-
34548138898
-
Prevalence of CYP1B1 mutations in Australian patients with primary congenital glaucoma
-
[PMID: 17718864]
-
Dimasi DP, Hewitt AW, Straga T, Pater J, MacKinnon JR, Elder JE, Casey T, Mackey DA, Craig JE. Prevalence of CYP1B1 mutations in Australian patients with primary congenital glaucoma. Clin Genet 2007; 72:255-60. [PMID: 17718864]
-
(2007)
Clin Genet
, vol.72
, pp. 255-260
-
-
Dimasi, D.P.1
Hewitt, A.W.2
Straga, T.3
Pater, J.4
McKinnon, J.R.5
Elder, J.E.6
Casey, T.7
Mackey, D.A.8
Craig, J.E.9
-
29
-
-
54049126558
-
CYP1B1 and MYOC mutations in 116 Chinese patients with primary congenital glaucoma
-
[PMID: 18852424]
-
Chen Y, Jiang D, Yu L, Katz B, Zhang K, Wan B, Sun X. CYP1B1 and MYOC mutations in 116 Chinese patients with primary congenital glaucoma. Arch Ophthalmol 2008; 126:1443-7. [PMID: 18852424]
-
(2008)
Arch Ophthalmol
, vol.126
, pp. 1443-1447
-
-
Chen, Y.1
Jiang, D.2
Yu, L.3
Katz, B.4
Zhang, K.5
Wan, B.6
Sun, X.7
-
30
-
-
17344362827
-
Mutations in CYP1B1, the gene for cytochrome P4501B1, are the predominant cause of primary congenital glaucoma in Saudi Arabia
-
[PMID: 9463332]
-
Bejjani BA, Lewis RA, Tomey KF, Anderson KL, Dueker DK, Jabak M, Astle WF, Otterud B, Leppert M, Lupski JR. Mutations in CYP1B1, the gene for cytochrome P4501B1, are the predominant cause of primary congenital glaucoma in Saudi Arabia. Am J Hum Genet 1998; 62:325-33. [PMID: 9463332]
-
(1998)
Am J Hum Genet
, vol.62
, pp. 325-333
-
-
Bejjani, B.A.1
Lewis, R.A.2
Tomey, K.F.3
Anderson, K.L.4
Dueker, D.K.5
Jabak, M.6
Astle, W.F.7
Otterud, B.8
Leppert, M.9
Lupski, J.R.10
-
31
-
-
58449127816
-
Multiple gene polymorphisms analysis revealed a different profile of genetic polymorphisms of primary open-angle glaucoma in northern Chinese
-
[PMID: 19145250]
-
Jia LY, Tam PO, Chiang SW, Ding N, Chen LJ, Yam GH, Pang CP, Wang NL. Multiple gene polymorphisms analysis revealed a different profile of genetic polymorphisms of primary open-angle glaucoma in northern Chinese. Mol Vis 2009; 15:89-98. [PMID: 19145250]
-
(2009)
Mol Vis
, vol.15
, pp. 89-98
-
-
Jia, L.Y.1
Tam, P.O.2
Chiang, S.W.3
Ding, N.4
Chen, L.J.5
Yam, G.H.6
Pang, C.P.7
Wang, N.L.8
-
32
-
-
0034020149
-
Truncations in the TIGR gene in individuals with and without primary open-angle glaucoma
-
[PMID: 10798654]
-
Lam DS, Leung YF, Chua JK, Baum L, Fan DS, Choy KW, Pang CP. Truncations in the TIGR gene in individuals with and without primary open-angle glaucoma. Invest Ophthalmol Vis Sci 2000; 41:1386-91. [PMID: 10798654]
-
(2000)
Invest Ophthalmol Vis Sci
, vol.41
, pp. 1386-1391
-
-
Lam, D.S.1
Leung, Y.F.2
Chua, J.K.3
Baum, L.4
Fan, D.S.5
Choy, K.W.6
Pang, C.P.7
-
33
-
-
0036784796
-
TIGR/MYOC gene sequence alterations in individuals with and without primary openangle glaucoma
-
[PMID: 12356829]
-
Pang CP, Leung YF, Fan B, Baum L, Tong WC, Lee WS, Chua JK, Fan DS, Liu Y, Lam DS. TIGR/MYOC gene sequence alterations in individuals with and without primary openangle glaucoma. Invest Ophthalmol Vis Sci 2002; 43:3231-5. [PMID: 12356829]
-
(2002)
Invest Ophthalmol Vis Sci
, vol.43
, pp. 3231-3235
-
-
Pang, C.P.1
Leung, Y.F.2
Fan, B.3
Baum, L.4
Tong, W.C.5
Lee, W.S.6
Chua, J.K.7
Fan, D.S.8
Liu, Y.9
Lam, D.S.10
-
34
-
-
0033358533
-
Mutations of the TIGR/MYOC gene in primary open-angle glaucoma in Korea
-
[PMID: 10330365]
-
Yoon SJ, Kim HS, Moon JI, Lim JM, Joo CK. Mutations of the TIGR/MYOC gene in primary open-angle glaucoma in Korea. Am J Hum Genet 1999; 64:1775-8. [PMID: 10330365]
-
(1999)
Am J Hum Genet
, vol.64
, pp. 1775-1778
-
-
Yoon, S.J.1
Kim, H.S.2
Moon, J.I.3
Lim, J.M.4
Joo, C.K.5
-
35
-
-
0344889215
-
Analysis of myocilin mutations in 1703 glaucoma patients from five different populations
-
[PMID: 10196380]
-
Fingert JH, Heon E, Liebmann JM, Yamamoto T, Craig JE, Rait J, Kawase K, Hoh ST, Buys YM, Dickinson J, Hockey RR, Williams-Lyn D, Trope G, Kitazawa Y, Ritch R, Mackey DA, Alward WL, Sheffield VC, Stone EM. Analysis of myocilin mutations in 1703 glaucoma patients from five different populations. Hum Mol Genet 1999; 8:899-905. [PMID: 10196380]
-
(1999)
Hum Mol Genet
, vol.8
, pp. 899-905
-
-
Fingert, J.H.1
Heon, E.2
Liebmann, J.M.3
Yamamoto, T.4
Craig, J.E.5
Rait, J.6
Kawase, K.7
Hoh, S.T.8
Buys, Y.M.9
Dickinson, J.10
Hockey, R.R.11
Williams-Lyn, D.12
Trope, G.13
Kitazawa, Y.14
Ritch, R.15
Mackey, D.A.16
Alward, W.L.17
Sheffield, V.C.18
Stone, E.M.19
-
36
-
-
26244460821
-
SNPs and interaction analyses of myocilin, optineurin, and apolipoprotein E in primary open angle glaucoma patients
-
[PMID: 16148883]
-
Fan BJ, Wang DY, Fan DS, Tam PO, Lam DS, Tham CC, Lam CY, Lau TC, Pang CP. SNPs and interaction analyses of myocilin, optineurin, and apolipoprotein E in primary open angle glaucoma patients. Mol Vis 2005; 11:625-31. [PMID: 16148883]
-
(2005)
Mol Vis
, vol.11
, pp. 625-631
-
-
Fan, B.J.1
Wang, D.Y.2
Fan, D.S.3
Tam, P.O.4
Lam, D.S.5
Tham, C.C.6
Lam, C.Y.7
Lau, T.C.8
Pang, C.P.9
-
37
-
-
34250316971
-
Myocilin variants in Indian patients with open-angle glaucoma
-
[PMID: 17562996]
-
Bhattacharjee A, Acharya M, Mukhopadhyay A, Mookherjee S, Banerjee D, Bandopadhyay AK, Thakur SK, Sen A, Ray K. Myocilin variants in Indian patients with open-angle glaucoma. Arch Ophthalmol 2007; 125:823-9. [PMID: 17562996]
-
(2007)
Arch Ophthalmol
, vol.125
, pp. 823-829
-
-
Bhattacharjee, A.1
Acharya, M.2
Mukhopadhyay, A.3
Mookherjee, S.4
Banerjee, D.5
Bandopadhyay, A.K.6
Thakur, S.K.7
Sen, A.8
Ray, K.9
-
38
-
-
18244369509
-
Molecular analysis of the myocilin gene in Chinese subjects with chronic primary-angle closure glaucoma
-
[PMID: 15790895]
-
Aung T, Yong VH, Chew PT, Seah SK, Gazzard G, Foster PJ, Vithana EN. Molecular analysis of the myocilin gene in Chinese subjects with chronic primary-angle closure glaucoma. Invest Ophthalmol Vis Sci 2005; 46:1303-6. [PMID: 15790895]
-
(2005)
Invest Ophthalmol Vis Sci
, vol.46
, pp. 1303-1306
-
-
Aung, T.1
Yong, V.H.2
Chew, P.T.3
Seah, S.K.4
Gazzard, G.5
Foster, P.J.6
Vithana, E.N.7
|