These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

228 related articles for article (PubMed ID: 21572728)

  • 1. Primary Congenital Glaucoma and the Involvement of CYP1B1.
    Kaur K; Mandal AK; Chakrabarti S
    Middle East Afr J Ophthalmol; 2011 Jan; 18(1):7-16. PubMed ID: 21572728
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genotyping results of Iranian PCG families suggests one or more PCG locus other than GCL3A, GCL3B, and GCL3C exist.
    Narooie-Nejad M; Chitsazian F; Khoramian Tusi B; Mousavi F; Houshmand M; Rohani MR; Hosseinipour AS; Rismanchian A; Elahi E
    Mol Vis; 2009 Oct; 15():2155-61. PubMed ID: 19898634
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Null mutations in LTBP2 cause primary congenital glaucoma.
    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
    Am J Hum Genet; 2009 May; 84(5):664-71. PubMed ID: 19361779
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. An Insight into Primary Congenital Glaucoma.
    Khan MU; Zia MUQ; Tabassum W
    Crit Rev Eukaryot Gene Expr; 2020; 30(1):39-43. PubMed ID: 32421983
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A polymorphism in the CYP1B1 promoter is functionally associated with primary congenital glaucoma.
    Chakrabarti S; Ghanekar Y; Kaur K; Kaur I; Mandal AK; Rao KN; Parikh RS; Thomas R; Majumder PP
    Hum Mol Genet; 2010 Oct; 19(20):4083-90. PubMed ID: 20660114
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Analysis of copy number variation using whole genome exon-focused array CGH in Korean patients with primary congenital glaucoma.
    Lee JH; Ki CS; Kim HJ; Suh W; Lee ST; Kim JW; Kee C
    Mol Vis; 2011; 17():3583-90. PubMed ID: 22219654
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genotype-Phenotype Correlations in CYP1B1-Associated Primary Congenital Glaucoma Patients Representing Two Large Cohorts from India and Brazil.
    de Melo MB; Mandal AK; Tavares IM; Ali MH; Kabra M; de Vasconcellos JP; Senthil S; Sallum JM; Kaur I; Betinjane AJ; Moura CR; Paula JS; Costa KA; Sarfarazi M; Paolera MD; Finzi S; Ferraz VE; Costa VP; Belfort R; Chakrabarti S
    PLoS One; 2015; 10(5):e0127147. PubMed ID: 25978063
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutations in CYP1B1, the gene for cytochrome P4501B1, are the predominant cause of primary congenital glaucoma in Saudi Arabia.
    Bejjani BA; Lewis RA; Tomey KF; Anderson KL; Dueker DK; Jabak M; Astle WF; Otterud B; Leppert M; Lupski JR
    Am J Hum Genet; 1998 Feb; 62(2):325-33. PubMed ID: 9463332
    [TBL] [Abstract][Full Text] [Related]  

  • 10. LTBP2 gene analysis in the GLC3C-linked family and 94 CYP1B1-negative cases with primary congenital glaucoma.
    Sharafieh R; Child AH; Khaw PT; Fleck B; Sarfarazi M
    Ophthalmic Genet; 2013; 34(1-2):14-20. PubMed ID: 22924778
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of three different truncating mutations in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma (Buphthalmos) in families linked to the GLC3A locus on chromosome 2p21.
    Stoilov I; Akarsu AN; Sarfarazi M
    Hum Mol Genet; 1997 Apr; 6(4):641-7. PubMed ID: 9097971
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Screening of the LTBP2 gene in a north Indian population with primary congenital glaucoma.
    Mohanty K; Tanwar M; Dada R; Dada T
    Mol Vis; 2013; 19():78-84. PubMed ID: 23378721
    [TBL] [Abstract][Full Text] [Related]  

  • 14. LTBP2 and CYP1B1 mutations and associated ocular phenotypes in the Roma/Gypsy founder population.
    Azmanov DN; Dimitrova S; Florez L; Cherninkova S; Draganov D; Morar B; Saat R; Juan M; Arostegui JI; Ganguly S; Soodyall H; Chakrabarti S; Padh H; López-Nevot MA; Chernodrinska V; Anguelov B; Majumder P; Angelova L; Kaneva R; Mackey DA; Tournev I; Kalaydjieva L
    Eur J Hum Genet; 2011 Mar; 19(3):326-33. PubMed ID: 21081970
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locus.
    Bejjani BA; Stockton DW; Lewis RA; Tomey KF; Dueker DK; Jabak M; Astle WF; Lupski JR
    Hum Mol Genet; 2000 Feb; 9(3):367-74. PubMed ID: 10655546
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Update in Genetics and Surgical Management of Primary Congenital Glaucoma.
    Mocan MC; Mehta AA; Aref AA
    Turk J Ophthalmol; 2019 Dec; 49(6):347-355. PubMed ID: 31893591
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. CYP1B1-mediated Pathobiology of Primary Congenital Glaucoma.
    Faiq MA; Dada R; Qadri R; Dada T
    J Curr Glaucoma Pract; 2015; 9(3):77-80. PubMed ID: 26997841
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Analysis of
    Chouiter L; Nadifi S
    J Pediatr Genet; 2017 Dec; 6(4):205-214. PubMed ID: 29142762
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Globally, CYP1B1 mutations in primary congenital glaucoma are strongly structured by geographic and haplotype backgrounds.
    Chakrabarti S; Kaur K; Kaur I; Mandal AK; Parikh RS; Thomas R; Majumder PP
    Invest Ophthalmol Vis Sci; 2006 Jan; 47(1):43-7. PubMed ID: 16384942
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.