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 *

117 related articles for article (PubMed ID: 25674135)

  • 1. Contribution of GLC3A locus to Primary Congenital Glaucoma in Pakistani population.
    Bashir R; Sanai M; Azeem A; Altaf I; Saleem F; Naz S
    Pak J Med Sci; 2014; 30(6):1341-5. PubMed ID: 25674135
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Clinical variability of CYP1B1 gene variants in Pakistani primary congenital glaucoma families.
    Bashir R; Yousaf K; Tahir H; Sanai M; Qayyum S; Naz S; Naz S
    J Pak Med Assoc; 2018 Aug; 68(8):1205-1211. PubMed ID: 30108387
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Investigation of the association between the GLC3A locus and normal tension glaucoma in Japanese patients by microsatellite analysis.
    Kamio M; Meguro A; Ota M; Nomura N; Kashiwagi K; Mabuchi F; Iijima H; Kawase K; Yamamoto T; Nakamura M; Negi A; Sagara T; Nishida T; Inatani M; Tanihara H; Aihara M; Araie M; Fukuchi T; Abe H; Higashide T; Sugiyama K; Kanamoto T; Kiuchi Y; Iwase A; Ohno S; Inoko H; Mizuki N
    Clin Ophthalmol; 2009; 3():183-8. PubMed ID: 19668563
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Assignment of a locus (GLC3A) for primary congenital glaucoma (Buphthalmos) to 2p21 and evidence for genetic heterogeneity.
    Sarfarazi M; Akarsu AN; Hossain A; Turacli ME; Aktan SG; Barsoum-Homsy M; Chevrette L; Sayli BS
    Genomics; 1995 Nov; 30(2):171-7. PubMed ID: 8586416
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Linkage of autosomal recessive primary congenital glaucoma to the GLC3A locus in Roms (Gypsies) from Slovakia.
    Plásilová M; Feráková E; Kádasi L; Poláková H; Gerinec A; Ott J; Ferák V
    Hum Hered; 1998; 48(1):30-3. PubMed ID: 9463798
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetics and biochemistry of primary congenital glaucoma.
    Sarfarazi M; Stoilov I; Schenkman JB
    Ophthalmol Clin North Am; 2003 Dec; 16(4):543-54, vi. PubMed ID: 14740995
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic homogeneity for inherited congenital microcoria loci in an Asian Indian pedigree.
    Ramprasad VL; Sripriya S; Ronnie G; Nancarrow D; Saxena S; Hemamalini A; Kumar D; Vijaya L; Kumaramanickavel G
    Mol Vis; 2005 Nov; 11():934-40. PubMed ID: 16288197
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A second locus (GLC3B) for primary congenital glaucoma (Buphthalmos) maps to the 1p36 region.
    Akarsu AN; Turacli ME; Aktan SG; Barsoum-Homsy M; Chevrette L; Sayli BS; Sarfarazi M
    Hum Mol Genet; 1996 Aug; 5(8):1199-203. PubMed ID: 8842741
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. A spectrum of CYP1B1 mutations associated with primary congenital glaucoma in families of Pakistani descent.
    Rauf B; Irum B; Kabir F; Firasat S; Naeem MA; Khan SN; Husnain T; Riazuddin S; Akram J; Riazuddin SA
    Hum Genome Var; 2016; 3():16021. PubMed ID: 27508083
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. A gene for primary congenital glaucoma is not linked to the locus on chromosome 1q for autosomal dominant juvenile-onset open angle glaucoma.
    Anderson KL; Lewis RA; Bejjani BA; Baird L; Otterud B; Tomey KF; Astle WF; Dueker DK; Leppert M; Lupski JR
    J Glaucoma; 1996 Dec; 5(6):416-21. PubMed ID: 8946299
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. Null CYP1B1 genotypes in primary congenital and nondominant juvenile glaucoma.
    López-Garrido MP; Medina-Trillo C; Morales-Fernandez L; Garcia-Feijoo J; Martínez-de-la-Casa JM; García-Antón M; Escribano J
    Ophthalmology; 2013 Apr; 120(4):716-23. PubMed ID: 23218183
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Molecular Genetic Analysis of Pakistani Families With Autosomal Recessive Congenital Cataracts by Homozygosity Screening.
    Chen J; Wang Q; Cabrera PE; Zhong Z; Sun W; Jiao X; Chen Y; Govindarajan G; Naeem MA; Khan SN; Ali MH; Assir MZ; Rahman FU; Qazi ZA; Riazuddin S; Akram J; Riazuddin SA; Hejtmancik JF
    Invest Ophthalmol Vis Sci; 2017 Apr; 58(4):2207-2217. PubMed ID: 28418495
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.