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 *

178 related articles for article (PubMed ID: 25978063)

  • 1. 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]  

  • 2. 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]  

  • 3. Genotype and phenotype correlations in congenital glaucoma.
    Hollander DA; Sarfarazi M; Stoilov I; Wood IS; Fredrick DR; Alvarado JA
    Trans Am Ophthalmol Soc; 2006; 104():183-95. PubMed ID: 17471339
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genotype and phenotype correlations in congenital glaucoma: CYP1B1 mutations, goniodysgenesis, and clinical characteristics.
    Hollander DA; Sarfarazi M; Stoilov I; Wood IS; Fredrick DR; Alvarado JA
    Am J Ophthalmol; 2006 Dec; 142(6):993-1004. PubMed ID: 17157584
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. Congenital glaucoma and CYP1B1: an old story revisited.
    Alsaif HS; Khan AO; Patel N; Alkuraya H; Hashem M; Abdulwahab F; Ibrahim N; Aldahmesh MA; Alkuraya FS
    Hum Genet; 2019 Sep; 138(8-9):1043-1049. PubMed ID: 29556725
    [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. Novel compound heterozygous mutations in
    Cai S; Zhang D; Jiao X; Wang T; Fan M; Wang Y; Hejtmancik JF; Liu X
    Mol Med Rep; 2021 Nov; 24(5):. PubMed ID: 34528698
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Angiopoietin receptor TEK interacts with CYP1B1 in primary congenital glaucoma.
    Kabra M; Zhang W; Rathi S; Mandal AK; Senthil S; Pyatla G; Ramappa M; Banerjee S; Shekhar K; Marmamula S; Mettla AL; Kaur I; Khanna RC; Khanna H; Chakrabarti S
    Hum Genet; 2017 Aug; 136(8):941-949. PubMed ID: 28620713
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Survey of familial glaucoma shows a high incidence of cytochrome P450, family 1, subfamily B, polypeptide 1 (CYP1B1) mutations in non-consanguineous congenital forms in a Spanish population.
    Millá E; Mañé B; Duch S; Hernan I; Borràs E; Planas E; Dias Mde S; Carballo M; Gamundi MJ;
    Mol Vis; 2013; 19():1707-22. PubMed ID: 23922489
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 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. 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]  

  • 18. Analysis of
    Reis LM; Tyler RC; Weh E; Hendee KE; Kariminejad A; Abdul-Rahman O; Ben-Omran T; Manning MA; Yesilyurt A; McCarty CA; Kitchner TE; Costakos D; Semina EV
    Mol Vis; 2016; 22():1229-1238. PubMed ID: 27777502
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.