280 related articles for article (PubMed ID: 22004014)
41. Molecular analysis of myocilin and optineurin genes in Korean primary glaucoma patients.
Park J; Kim M; Park CK; Chae H; Lee S; Kim Y; Jang W; Chi HY; Park HY; Park SH
Mol Med Rep; 2016 Sep; 14(3):2439-48. PubMed ID: 27485216
[TBL] [Abstract][Full Text] [Related]
42. Screening of common CYP1B1 mutations in Iranian POAG patients using a microarray-based PrASE protocol.
Suri F; Kalhor R; Zargar SJ; Nilforooshan N; Yazdani S; Nezari H; Paylakhi SH; Narooie-Nejhad M; Bayat B; Sedaghati T; Ahmadian A; Elahi E
Mol Vis; 2008; 14():2349-56. PubMed ID: 19096718
[TBL] [Abstract][Full Text] [Related]
43. The role of TIGR and OPTN in Finnish glaucoma families: a clinical and molecular genetic study.
Forsman E; Lemmelä S; Varilo T; Kristo P; Forsius H; Sankila EM; Järvelä I
Mol Vis; 2003 May; 9():217-22. PubMed ID: 12789137
[TBL] [Abstract][Full Text] [Related]
44. Mutation spectrum of CYP1B1 and MYOC genes in Korean patients with primary congenital glaucoma.
Kim HJ; Suh W; Park SC; Kim CY; Park KH; Kook MS; Kim YY; Kim CS; Park CK; Ki CS; Kee C
Mol Vis; 2011; 17():2093-101. PubMed ID: 21850185
[TBL] [Abstract][Full Text] [Related]
45. Nuclear and mitochondrial analysis of patients with primary angle-closure glaucoma.
Abu-Amero KK; Morales J; Osman MN; Bosley TM
Invest Ophthalmol Vis Sci; 2007 Dec; 48(12):5591-6. PubMed ID: 18055808
[TBL] [Abstract][Full Text] [Related]
46. CYP1B1 and MYOC Mutations in Vietnamese Primary Congenital Glaucoma Patients.
Do T; Shei W; Chau PT; Trang DL; Yong VH; Ng XY; Chen YM; Aung T; Vithana EN
J Glaucoma; 2016 May; 25(5):e491-8. PubMed ID: 26550974
[TBL] [Abstract][Full Text] [Related]
47. Correlation between genotype and phenotype in primary open angle glaucoma of Brazilian families with mutations in exon 3 of the TIGR/MYOC gene.
Povoa CA; Malta RF; Rezende Mde M; de Melo KF; Giannella-Neto D
Arq Bras Oftalmol; 2006; 69(3):289-97. PubMed ID: 16936947
[TBL] [Abstract][Full Text] [Related]
48. [Genetic ground of primary open angle glaucoma].
Krawczyński MR
Klin Oczna; 2004; 106(4-5):695-8. PubMed ID: 15646497
[TBL] [Abstract][Full Text] [Related]
49. Mitochondrial abnormalities in patients with primary open-angle glaucoma.
Abu-Amero KK; Morales J; Bosley TM
Invest Ophthalmol Vis Sci; 2006 Jun; 47(6):2533-41. PubMed ID: 16723467
[TBL] [Abstract][Full Text] [Related]
50. Prevalence of myocilin and optineurin sequence variants in German normal tension glaucoma patients.
Weisschuh N; Neumann D; Wolf C; Wissinger B; Gramer E
Mol Vis; 2005 Apr; 11():284-7. PubMed ID: 15851979
[TBL] [Abstract][Full Text] [Related]
51. Clinical and genetic characterization of a large primary open angle glaucoma pedigree.
Kader MA; Namburi P; Ramugade S; Ramakrishnan R; Krishnadas SR; Roos BR; Periasamy S; Robin AL; Fingert JH
Ophthalmic Genet; 2017; 38(3):222-225. PubMed ID: 27355837
[TBL] [Abstract][Full Text] [Related]
52. Glaucoma-associated CYP1B1 mutations share similar haplotype backgrounds in POAG and PACG phenotypes.
Chakrabarti S; Devi KR; Komatireddy S; Kaur K; Parikh RS; Mandal AK; Chandrasekhar G; Thomas R
Invest Ophthalmol Vis Sci; 2007 Dec; 48(12):5439-44. PubMed ID: 18055790
[TBL] [Abstract][Full Text] [Related]
53. Clinical implications of old and new genes for open-angle glaucoma.
Ramdas WD; van Koolwijk LM; Cree AJ; Janssens AC; Amin N; de Jong PT; Wolfs RC; Gibson J; Kirwan JF; Hofman A; Rivadeneira F; Oostra BA; Uitterlinden AG; Ennis S; Lotery AJ; Lemij HG; Klaver CC; Vingerling JR; Jansonius NM; van Duijn CM
Ophthalmology; 2011 Dec; 118(12):2389-97. PubMed ID: 21872936
[TBL] [Abstract][Full Text] [Related]
54. Recurrent Myocilin Asn480Lys glaucoma causative mutation arises de novo in a family of Andean descent.
Guevara-Fujita ML; Perez-Grossmann RA; Estrada-Cuzcano A; Pawar H; Vargas E; Richards JE; Fujita R
J Glaucoma; 2008; 17(1):67-72. PubMed ID: 18303389
[TBL] [Abstract][Full Text] [Related]
55. Sequence analysis of MYOC and CYP1B1 in a Chinese pedigree of juvenile glaucoma with goniodysgenesis.
Chen X; Yan N; Yun H; Sun J; Yu M; Zhou J; Cao G; Yin H; Li M; Liu X
Mol Vis; 2009 Aug; 15():1530-6. PubMed ID: 19668597
[TBL] [Abstract][Full Text] [Related]
56. Genetic variants associated with primary open angle glaucoma in Indian population.
Kumar S; Malik MA; K S; Sihota R; Kaur J
Genomics; 2017 Jan; 109(1):27-35. PubMed ID: 27851990
[TBL] [Abstract][Full Text] [Related]
57. Mutation analysis of seven known glaucoma-associated genes in Chinese patients with glaucoma.
Huang X; Li M; Guo X; Li S; Xiao X; Jia X; Liu X; Zhang Q
Invest Ophthalmol Vis Sci; 2014 May; 55(6):3594-602. PubMed ID: 24825108
[TBL] [Abstract][Full Text] [Related]
58. [Investigation on the mutation of MYOC gene in two family pedigrees with primary open-angle glaucoma in Shanxi].
Qin L; Li J
Yan Ke Xue Bao; 2007 Jun; 23(2):75-8. PubMed ID: 17867509
[TBL] [Abstract][Full Text] [Related]
59. [Study on MYOC/TIGR gene mutations in primary open-angle glaucoma].
Chen JH; Xu L; Li Y; Dong B
Zhonghua Yan Ke Za Zhi; 2011 Feb; 47(2):122-8. PubMed ID: 21426841
[TBL] [Abstract][Full Text] [Related]
60. Functional analysis of CYP1B1 mutations and association of heterozygous hypomorphic alleles with primary open-angle glaucoma.
López-Garrido MP; Blanco-Marchite C; Sánchez-Sánchez F; López-Sánchez E; Chaqués-Alepuz V; Campos-Mollo E; Salinas-Sánchez AS; Escribano J
Clin Genet; 2010 Jan; 77(1):70-8. PubMed ID: 19793111
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
