Bejjani BA - Search Results

1

Single amino acid mutations, but not common polymorphisms, decrease the activity of CYP1B1 against (-)benzo[a]pyrene-7R-trans-7,8-dihydrodiol.

Mammen JS, Pittman GS, Li Y, Abou-Zahr F, Bejjani BA, Bell DA, Strickland PT, Sutter TR. Mammen JS, et al. Among authors: bejjani ba. Carcinogenesis. 2003 Jul;24(7):1247-55. doi: 10.1093/carcin/bgg088. Epub 2003 Jun 5. Carcinogenesis. 2003. PMID: 12807732

2

Normal expression of the Fanconi anemia proteins FAA and FAC and sensitivity to mitomycin C in two patients with Seckel syndrome.

Abou-Zahr F, Bejjani B, Kruyt FA, Kurg R, Bacino C, Shapira SK, Youssoufian H. Abou-Zahr F, et al. Am J Med Genet. 1999 Apr 23;83(5):388-91. doi: 10.1002/(sici)1096-8628(19990423)83:5<388::aid-ajmg9>3.0.co;2-1. Am J Med Genet. 1999. PMID: 10232749

3

Primary congenital glaucoma and Rieger's anomaly: extended haplotypes reveal founder effects for eight distinct CYP1B1 mutations.

Chavarria-Soley G, Michels-Rautenstrauss K, Pasutto F, Flikier D, Flikier P, Cirak S, Bejjani B, Winters DL, Lewis RA, Mardin C, Reis A, Rautenstrauss B. Chavarria-Soley G, et al. Mol Vis. 2006 May 22;12:523-31. Mol Vis. 2006. PMID: 16735994 Free article.

4

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. Bejjani BA, et al. Hum Mol Genet. 2000 Feb 12;9(3):367-74. doi: 10.1093/hmg/9.3.367. Hum Mol Genet. 2000. PMID: 10655546

5

Cytochrome P4501B1 mutations cause only part of primary congenital glaucoma in Ecuador.

Curry SM, Daou AG, Hermanns P, Molinari A, Lewis RA, Bejjani BA. Curry SM, et al. Among authors: bejjani ba. Ophthalmic Genet. 2004 Mar;25(1):3-9. doi: 10.1076/opge.25.1.3.28999. Ophthalmic Genet. 2004. PMID: 15255109

6

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. Bejjani BA, et al. Am J Hum Genet. 1998 Feb;62(2):325-33. doi: 10.1086/301725. Am J Hum Genet. 1998. PMID: 9463332 Free PMC article.

7

Genetic disorders that masquerade as multiple sclerosis.

Natowicz MR, Bejjani B. Natowicz MR, et al. Am J Med Genet. 1994 Jan 15;49(2):149-69. doi: 10.1002/ajmg.1320490202. Am J Med Genet. 1994. PMID: 8116663 Review.

8

Identification of novel suggestive loci for high-grade myopia in Polish families.

Rydzanicz M, Nath SK, Sun C, Podfigurna-Musielak M, Frajdenberg A, Mrugacz M, Winters D, Ratnamala U, Radhakrishna U, Bejjani BA, Gajecka M. Rydzanicz M, et al. Among authors: bejjani ba. Mol Vis. 2011;17:2028-39. Epub 2011 Jul 22. Mol Vis. 2011. PMID: 21850178 Free PMC article.

9

Molecular basis of Peters anomaly in Saudi Arabia.

Edward D, Al Rajhi A, Lewis RA, Curry S, Wang Z, Bejjani B. Edward D, et al. Ophthalmic Genet. 2004 Dec;25(4):257-70. doi: 10.1080/13816810490902648. Ophthalmic Genet. 2004. PMID: 15621878

10

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. Bidinost C, et al. Among authors: bejjani ba. Invest Ophthalmol Vis Sci. 2006 Apr;47(4):1486-90. doi: 10.1167/iovs.05-0763. Invest Ophthalmol Vis Sci. 2006. PMID: 16565383

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