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 *

129 related articles for article (PubMed ID: 16565383)

  • 1. Of mice and men: tyrosinase modification of congenital glaucoma in mice but not in humans.
    Bidinost C; Hernandez N; Edward DP; Al-Rajhi A; Lewis RA; Lupski JR; Stockton DW; Bejjani BA
    Invest Ophthalmol Vis Sci; 2006 Apr; 47(4):1486-90. PubMed ID: 16565383
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Modification of ocular defects in mouse developmental glaucoma models by tyrosinase.
    Libby RT; Smith RS; Savinova OV; Zabaleta A; Martin JE; Gonzalez FJ; John SW
    Science; 2003 Mar; 299(5612):1578-81. PubMed ID: 12624268
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. A clinical and molecular genetic study of Egyptian and Saudi Arabian patients with primary congenital glaucoma (PCG).
    El-Ashry MF; Abd El-Aziz MM; Bhattacharya SS
    J Glaucoma; 2007 Jan; 16(1):104-11. PubMed ID: 17224759
    [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. Molecular basis of Peters anomaly in Saudi Arabia.
    Edward D; Al Rajhi A; Lewis RA; Curry S; Wang Z; Bejjani B
    Ophthalmic Genet; 2004 Dec; 25(4):257-70. PubMed ID: 15621878
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Variable expressivity and high penetrance of CYP1B1 mutations associated with primary congenital glaucoma.
    Suri F; Yazdani S; Narooie-Nejhad M; Zargar SJ; Paylakhi SH; Zeinali S; Pakravan M; Elahi E
    Ophthalmology; 2009 Nov; 116(11):2101-9. PubMed ID: 19744731
    [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. Mutational screening of CYP1B1 in Turkish PCG families and functional analyses of newly detected mutations.
    Bagiyeva S; Marfany G; Gonzalez-Angulo O; Gonzalez-Duarte R
    Mol Vis; 2007 Aug; 13():1458-68. PubMed ID: 17893647
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular analysis of the CYP1B1 gene: identification of novel truncating mutations in patients with primary congenital glaucoma.
    Messina-Baas OM; González-Huerta LM; Chima-Galán C; Kofman-Alfaro SH; Rivera-Vega MR; Babayán-Mena I; Cuevas-Covarrubias SA
    Ophthalmic Res; 2007; 39(1):17-23. PubMed ID: 17164573
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular and clinical evaluation of primary congenital glaucoma in Kuwait.
    Alfadhli S; Behbehani A; Elshafey A; Abdelmoaty S; Al-Awadi S
    Am J Ophthalmol; 2006 Mar; 141(3):512-6. PubMed ID: 16490498
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Identification of novel mutations causing familial primary congenital glaucoma in Indian pedigrees.
    Panicker SG; Reddy AB; Mandal AK; Ahmed N; Nagarajaram HA; Hasnain SE; Balasubramanian D
    Invest Ophthalmol Vis Sci; 2002 May; 43(5):1358-66. PubMed ID: 11980847
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutation spectrum of the CYP1B1 gene in Indian primary congenital glaucoma patients.
    Reddy AB; Kaur K; Mandal AK; Panicker SG; Thomas R; Hasnain SE; Balasubramanian D; Chakrabarti S
    Mol Vis; 2004 Sep; 10():696-702. PubMed ID: 15475877
    [TBL] [Abstract][Full Text] [Related]  

  • 16. CYP1B1 mutations in patients with primary congenital glaucoma from Saudi Arabia.
    Badeeb OM; Micheal S; Koenekoop RK; den Hollander AI; Hedrawi MT
    BMC Med Genet; 2014 Sep; 15():109. PubMed ID: 25261878
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cytochrome P4501B1 mutations cause only part of primary congenital glaucoma in Ecuador.
    Curry SM; Daou AG; Hermanns P; Molinari A; Lewis RA; Bejjani BA
    Ophthalmic Genet; 2004 Mar; 25(1):3-9. PubMed ID: 15255109
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular genetics of primary congenital glaucoma in Brazil.
    Stoilov IR; Costa VP; Vasconcellos JP; Melo MB; Betinjane AJ; Carani JC; Oltrogge EV; Sarfarazi M
    Invest Ophthalmol Vis Sci; 2002 Jun; 43(6):1820-7. PubMed ID: 12036985
    [TBL] [Abstract][Full Text] [Related]  

  • 19. CYP1B1 genotype influences the phenotype in primary congenital glaucoma and surgical treatment.
    Chen X; Chen Y; Wang L; Jiang D; Wang W; Xia M; Yu L; Sun X
    Br J Ophthalmol; 2014 Feb; 98(2):246-51. PubMed ID: 24227805
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 7.