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 *

82 related articles for article (PubMed ID: 25625896)

  • 1. Of gypsies and gene flows: CYP1B1.
    Rudkin AK
    Clin Exp Ophthalmol; 2015; 43(1):3-4. PubMed ID: 25625896
    [No Abstract]   [Full Text] [Related]  

  • 2. Identification of novel CYP1B1 gene mutations in patients with primary congenital and primary open-angle glaucoma.
    Micheal S; Ayub H; Zafar SN; Bakker B; Ali M; Akhtar F; Islam F; Khan MI; Qamar R; den Hollander AI
    Clin Exp Ophthalmol; 2015; 43(1):31-9. PubMed ID: 25091052
    [TBL] [Abstract][Full Text] [Related]  

  • 3. CYP1B1 mutational screening in a Portuguese cohort of primary congenital glaucoma patients.
    Simões MJ; Carmona S; Roberts R; Wainwright G; Faro C; Silva E; Egas C
    Ophthalmic Genet; 2017; 38(2):197-199. PubMed ID: 27268095
    [No Abstract]   [Full Text] [Related]  

  • 4. Observations regarding gender and response to initial angle surgery in CYP1B1-related primary congenital glaucoma.
    Al-Shahrani NO; Khan AO
    Ophthalmic Genet; 2017; 38(3):294. PubMed ID: 27438756
    [No Abstract]   [Full Text] [Related]  

  • 5. Functional characterization of eight rare missense CYP1B1 variants involved in congenital glaucoma and their association with null genotypes.
    Medina-Trillo C; Ferre-Fernández JJ; Aroca-Aguilar JD; Bonet-Fernández JM; Escribano J
    Acta Ophthalmol; 2016 Nov; 94(7):e555-e560. PubMed ID: 27060699
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Complete aniridia with central keratopathy and congenital glaucoma is a CYP1B1-related phenotype.
    Khan AO; Aldahmesh MA; Mohamed JY; Hijazi H; Alkuraya FS
    Ophthalmic Genet; 2014 Sep; 35(3):187-9. PubMed ID: 23767995
    [No Abstract]   [Full Text] [Related]  

  • 7. A novel CYP1B1 mutation with congenital glaucoma and total aniridia.
    Alzuhairy S; Abu-Amero KK; Al-Shahwan S; Edward DP
    Ophthalmic Genet; 2015 Mar; 36(1):89-91. PubMed ID: 24001018
    [TBL] [Abstract][Full Text] [Related]  

  • 8. CYP1B1 Mutations are a Major Contributor to Juvenile-Onset Open Angle Glaucoma in Saudi Arabia.
    Abu-Amero KK; Morales J; Aljasim LA; Edward DP
    Ophthalmic Genet; 2015 Jun; 36(2):184-7. PubMed ID: 24099281
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular Karyotyping of a Dysmorphic Girl from Saudi Arabia with CYP1B1-negative Primary Congenital Glaucoma.
    Abu-Amero KK; Kondkar AA; Khan AO
    Ophthalmic Genet; 2016; 37(1):98-101. PubMed ID: 24911043
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genotype-phenotype correlation in Moroccan patients with primary congenital glaucoma.
    Berraho A; Serrou A; Fritez N; El Annas A; Bencherifa F; Gaboun F; Hilal L
    J Glaucoma; 2015; 24(4):297-305. PubMed ID: 25826643
    [TBL] [Abstract][Full Text] [Related]  

  • 11. CYP1B1 gene analysis and phenotypic correlation in Portuguese children with primary congenital glaucoma.
    Cardoso MS; Anjos R; Vieira L; Ferreira C; Xavier A; Brito C
    Eur J Ophthalmol; 2015; 25(6):474-7. PubMed ID: 25952714
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Occurrence of CYP1B1 Mutations in Juvenile Open-Angle Glaucoma With Advanced Visual Field Loss.
    Souzeau E; Hayes M; Zhou T; Siggs OM; Ridge B; Awadalla MS; Smith JE; Ruddle JB; Elder JE; Mackey DA; Hewitt AW; Healey PR; Goldberg I; Morgan WH; Landers J; Dubowsky A; Burdon KP; Craig JE
    JAMA Ophthalmol; 2015 Jul; 133(7):826-33. PubMed ID: 25950505
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Role of CYP1B1, p.E229K and p.R368H mutations among 120 families with sporadic juvenile onset open-angle glaucoma.
    Gupta V; Somarajan BI; Walia GK; Kaur J; Kumar S; Gupta S; Chaurasia AK; Gupta D; Kaushik A; Mehta A; Gupta V; Sharma A
    Graefes Arch Clin Exp Ophthalmol; 2018 Feb; 256(2):355-362. PubMed ID: 29168043
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Homozygous p.G61E mutation in a consanguineous Pakistani family with co-existence of juvenile-onset open angle glaucoma and primary congenital glaucoma.
    Bashir R; Tahir H; Yousaf K; Naz S; Naz S
    Gene; 2015 Oct; 570(2):295-8. PubMed ID: 26164761
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Phenotype and Genotype Correlation in Iranian Primary Congenital Glaucoma Patients.
    Yazdani S; Miraftabi A; Pakravan M; Ghahari E; Tousi BK; Sedigh M; Yaseri M; Elahi E
    J Glaucoma; 2016 Jan; 25(1):33-8. PubMed ID: 25580891
    [TBL] [Abstract][Full Text] [Related]  

  • 16. CYP1B1 Gene and Phenotypic Correlation in Patients From Northeastern Brazil With Primary Congenital Glaucoma.
    Coêlho REA; Sena DR; Santa Cruz F; Moura BCFS; Han CC; Andrade FN; Lira RPC
    J Glaucoma; 2019 Feb; 28(2):161-164. PubMed ID: 30520782
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Overview of Cytochrome P450 1B1 gene mutations in patients with primary congenital glaucoma.
    Li N; Zhou Y; Du L; Wei M; Chen X
    Exp Eye Res; 2011 Nov; 93(5):572-9. PubMed ID: 21854771
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. [Theory of the pathogenetic relation of hydrophthalmia with open-angle glaucoma].
    Eroshevskiĭ TI; Shukunova RP
    Vestn Oftalmol; 1985; 101(3):3-6. PubMed ID: 4035865
    [No Abstract]   [Full Text] [Related]  

  • 20. CYP1B1 analysis of unilateral primary newborn glaucoma in Saudi children.
    Khan AO; Aldahmesh MA; Mohamed JY; Hijazi H; Alkuraya FS
    J AAPOS; 2012 Dec; 16(6):571-2. PubMed ID: 23158549
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.