192 related articles for article (PubMed ID: 29903728)
1. Bioinformatics analysis of
Ou Z; Liu G; Liu W; Deng Y; Zheng L; Zhang S; Feng G
Biosci Rep; 2018 Aug; 38(4):. PubMed ID: 29903728
[TBL] [Abstract][Full Text] [Related]
2. Investigation of CYP1B1 mutations in Chinese patients with primary congenital glaucoma.
Yang M; Guo X; Liu X; Shen H; Jia X; Xiao X; Li S; Fang S; Zhang Q
Mol Vis; 2009; 15():432-7. PubMed ID: 19247456
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. CYP1B1 gene mutations causing primary congenital glaucoma in Tunisia.
Bouyacoub Y; Ben Yahia S; Abroug N; Kahloun R; Kefi R; Khairallah M; Abdelhak S
Ann Hum Genet; 2014 Jul; 78(4):255-63. PubMed ID: 24942078
[TBL] [Abstract][Full Text] [Related]
5. In silico analysis of five missense mutations in CYP1B1 gene in Pakistani families affected with primary congenital glaucoma.
Firasat S; Kaul H; Ashfaq UA; Idrees S
Int Ophthalmol; 2018 Apr; 38(2):807-814. PubMed ID: 28386709
[TBL] [Abstract][Full Text] [Related]
6. Identities and frequencies of variants in
Rashid M; Yousaf S; Sheikh SA; Sajid Z; Shabbir AS; Kausar T; Tariq N; Usman M; Shaikh RS; Ali M; Bukhari SA; Waryah AM; Qasim M; Riazuddin S; Ahmed ZM
Mol Vis; 2019; 25():144-154. PubMed ID: 30820150
[TBL] [Abstract][Full Text] [Related]
7. Investigation of
Jubair S; N Al-Rubae'i SH; M Al-Sharifi AN; Jabbar Suleiman AA
Middle East Afr J Ophthalmol; 2019; 26(4):203-209. PubMed ID: 32153331
[TBL] [Abstract][Full Text] [Related]
8. Disease-causing mutations in proteins: structural analysis of the CYP1B1 mutations causing primary congenital glaucoma in humans.
Achary MS; Reddy AB; Chakrabarti S; Panicker SG; Mandal AK; Ahmed N; Balasubramanian D; Hasnain SE; Nagarajaram HA
Biophys J; 2006 Dec; 91(12):4329-39. PubMed ID: 16963504
[TBL] [Abstract][Full Text] [Related]
9. Functional and Structural Analyses of CYP1B1 Variants Linked to Congenital and Adult-Onset Glaucoma to Investigate the Molecular Basis of These Diseases.
Banerjee A; Chakraborty S; Chakraborty A; Chakrabarti S; Ray K
PLoS One; 2016; 11(5):e0156252. PubMed ID: 27243976
[TBL] [Abstract][Full Text] [Related]
10. Mutational analysis of the CYP1B1 gene in Pakistani primary congenital glaucoma patients: Identification of four known and a novel causative variant at the 3' splice acceptor site of intron 2.
Afzal R; Firasat S; Kaul H; Ahmed B; Siddiqui SN; Zafar SN; Shahzadi M; Afshan K
Congenit Anom (Kyoto); 2019 Sep; 59(5):152-161. PubMed ID: 30270463
[TBL] [Abstract][Full Text] [Related]
11. Screening of CYP1B1 and LTBP2 genes in Saudi families with primary congenital glaucoma: genotype-phenotype correlation.
Abu-Amero KK; Osman EA; Mousa A; Wheeler J; Whigham B; Allingham RR; Hauser MA; Al-Obeidan SA
Mol Vis; 2011; 17():2911-9. PubMed ID: 22128238
[TBL] [Abstract][Full Text] [Related]
12. Genotype/Phenotype Correlation in Primary Congenital Glaucoma Patients in the Lebanese Population: A Pilot Study.
Al-Haddad C; Abdulaal M; Badra R; Barikian A; Noureddine B; Farra C
Ophthalmic Genet; 2016; 37(1):31-6. PubMed ID: 24940937
[TBL] [Abstract][Full Text] [Related]
13. Screening of the LTBP2 gene in 214 Chinese sporadic CYP1B1-negative patients with primary congenital glaucoma.
Chen X; Chen Y; Fan BJ; Xia M; Wang L; Sun X
Mol Vis; 2016; 22():528-35. PubMed ID: 27293371
[TBL] [Abstract][Full Text] [Related]
14. Mutational spectrum of the CYP1B1 gene in Pakistani patients with primary congenital glaucoma: novel variants and genotype-phenotype correlations.
Sheikh SA; Waryah AM; Narsani AK; Shaikh H; Gilal IA; Shah K; Qasim M; Memon AI; Kewalramani P; Shaikh N
Mol Vis; 2014; 20():991-1001. PubMed ID: 25018621
[TBL] [Abstract][Full Text] [Related]
15. CYP1B1 and MYOC mutations in 116 Chinese patients with primary congenital glaucoma.
Chen Y; Jiang D; Yu L; Katz B; Zhang K; Wan B; Sun X
Arch Ophthalmol; 2008 Oct; 126(10):1443-7. PubMed ID: 18852424
[TBL] [Abstract][Full Text] [Related]
16. Candidate Gene Analysis Identifies Mutations in CYP1B1 and LTBP2 in Indian Families with Primary Congenital Glaucoma.
Yang Y; Zhang L; Li S; Zhu X; Sundaresan P
Genet Test Mol Biomarkers; 2017 Apr; 21(4):252-258. PubMed ID: 28384041
[TBL] [Abstract][Full Text] [Related]
17. Molecular analysis of CYP1B1 in Omani patients with primary congenital glaucoma: a pilot study.
El-Gayar S; Ganesh A; Chavarria-Soley G; Al-Zuhaibi S; Al-Mjeni R; Raeburn S; Bialasiewicz AA
Mol Vis; 2009 Jul; 15():1325-31. PubMed ID: 19597567
[TBL] [Abstract][Full Text] [Related]
18. Screening of CYP1B1 and MYOC in Moroccan families with primary congenital glaucoma: three novel mutations in CYP1B1.
Hilal L; Boutayeb S; Serrou A; Refass-Buret L; Shisseh H; Bencherifa F; El Mzibri M; Benazzouz B; Berraho A
Mol Vis; 2010 Jul; 16():1215-26. PubMed ID: 20664688
[TBL] [Abstract][Full Text] [Related]
19. Mutation spectrum of CYP1B1 in North Indian congenital glaucoma patients.
Tanwar M; Dada T; Sihota R; Das TK; Yadav U; Dada R
Mol Vis; 2009 Jun; 15():1200-9. PubMed ID: 19536304
[TBL] [Abstract][Full Text] [Related]
20. Identification of four novel cytochrome P4501B1 mutations (p.I94X, p.H279D, p.Q340H, and p.K433K) in primary congenital glaucoma patients.
Tanwar M; Dada T; Sihota R; Dada R
Mol Vis; 2009 Dec; 15():2926-37. PubMed ID: 20057908
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]