pcg

cytochrome P450 family 1 subfamily B member 1 ; Homo sapiens







69 Article(s)
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51 17718864 Prevalence of CYP1B1 mutations in Australian patients with primary congenital glaucoma. 2007 Sep 2
52 17893647 Mutational screening of CYP1B1 in Turkish PCG families and functional analyses of newly detected mutations. 2007 Aug 27 1
53 18070520 [Analysis of the CYP1B1 gene mutation in primary congenital glaucoma patients of Hubei Han nationality]. 2007 Sep 2
54 16384942 Globally, CYP1B1 mutations in primary congenital glaucoma are strongly structured by geographic and haplotype backgrounds. 2006 Jan 1
55 16490498 Molecular and clinical evaluation of primary congenital glaucoma in Kuwait. 2006 Mar 1
56 15733270 Myocilin gene implicated in primary congenital glaucoma. 2005 Apr 3
57 15255109 Cytochrome P4501B1 mutations cause only part of primary congenital glaucoma in Ecuador. 2004 Mar 1
58 15621878 Molecular basis of Peters anomaly in Saudi Arabia. 2004 Dec 1
59 15666707 [Primary congenital glaucoma]. 2004 Dec 2
60 14635112 Novel cytochrome P450 1B1 (CYP1B1) mutations in patients with primary congenital glaucoma in France. 2003 Dec 1
61 11980847 Identification of novel mutations causing familial primary congenital glaucoma in Indian pedigrees. 2002 May 1
62 12036985 Molecular genetics of primary congenital glaucoma in Brazil. 2002 Jun 1
63 12372064 A novel frameshift founder mutation in the cytochrome P450 1B1 (CYP1B1) gene is associated with primary congenital glaucoma in Morocco. 2002 Oct 1
64 11740343 Effect of two mutations of human CYP1B1, G61E and R469W, on stability and endogenous steroid substrate metabolism. 2001 Dec 1
65 10655546 Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locus. 2000 Feb 12 2
66 11026969 Molecular genetics of primary congenital glaucoma. 2000 Jun 3
67 10227395 Identification of a single ancestral CYP1B1 mutation in Slovak Gypsies (Roms) affected with primary congenital glaucoma. 1999 Apr 1
68 9497261 Sequence analysis and homology modeling suggest that primary congenital glaucoma on 2p21 results from mutations disrupting either the hinge region or the conserved core structures of cytochrome P4501B1. 1998 Mar 1
69 9818478 [Molecular diagnosis of mutations responsible for recurrent and severe forms of primary congenital glaucoma]. 1998 1