Similar articles for PMID: 8530011

Year	Number of Results
1989	1
1990	2
1991	12
1992	6
1993	13
1994	14
1995	21
1996	8
1997	1
1998	6
1999	1
2000	5
2001	6
2002	2
2003	2
2006	2
2007	1
2024	0

1

A nonsense mutation in the cytochrome P450 CYP2D6 gene identified in a Caucasian with an enzyme deficiency.

Broly F, Marez D, Lo Guidice JM, Sabbagh N, Legrand M, Boone P, Meyer UA. Broly F, et al. Hum Genet. 1995 Nov;96(5):601-3. doi: 10.1007/BF00197419. Hum Genet. 1995. PMID: 8530011

2

An efficient strategy for detection of known and new mutations of the CYP2D6 gene using single strand conformation polymorphism analysis.

Broly F, Marez D, Sabbagh N, Legrand M, Millecamps S, Lo Guidice JM, Boone P, Meyer UA. Broly F, et al. Pharmacogenetics. 1995 Dec;5(6):373-84. doi: 10.1097/00008571-199512000-00006. Pharmacogenetics. 1995. PMID: 8747409

3

A BamHI polymorphism in the human cytochrome P450 gene, CYP2D6.

Morimoto Y, Murayama N, Kuwano A, Yoshimura O, Kondo I. Morimoto Y, et al. Clin Genet. 1995 Feb;47(2):103-4. doi: 10.1111/j.1399-0004.1995.tb03934.x. Clin Genet. 1995. PMID: 7606840 No abstract available.

4

An additional allelic variant of the CYP2D6 gene causing impaired metabolism of sparteine.

Marez D, Legrand M, Sabbagh N, Lo-Guidice JM, Boone P, Broly F. Marez D, et al. Hum Genet. 1996 May;97(5):668-70. doi: 10.1007/BF02281880. Hum Genet. 1996. PMID: 8655150

5

Genetic polymorphism of debrisoquine oxidation: restriction fragment analysis and allele-specific amplification of mutant alleles of CYP2D6.

Heim MH, Meyer UA. Heim MH, et al. Methods Enzymol. 1991;206:173-83. doi: 10.1016/0076-6879(91)06088-k. Methods Enzymol. 1991. PMID: 1686063 No abstract available.

6

Detection of debrisoquine hydroxylation phenotypes.

Wolf CR, Moss JE, Miles JS, Gough AC, Spurr NK. Wolf CR, et al. Lancet. 1990 Dec 8;336(8728):1452-3. doi: 10.1016/0140-6736(90)93163-j. Lancet. 1990. PMID: 1978915 No abstract available.

7

An association study of debrisoquine hydroxylase (CYP2D6) polymorphisms in schizophrenia.

Dawson E, Powell JF, Nöthen MM, Crocq MA, Lanczik M, Körner J, Rietschel M, van Os J, Wright P, Gill M. Dawson E, et al. Psychiatr Genet. 1994 Winter;4(4):215-8. doi: 10.1097/00041444-199400440-00005. Psychiatr Genet. 1994. PMID: 7712118

8

Inherited amplification of an active gene in the cytochrome P450 CYP2D locus as a cause of ultrarapid metabolism of debrisoquine.

Johansson I, Lundqvist E, Bertilsson L, Dahl ML, Sjöqvist F, Ingelman-Sundberg M. Johansson I, et al. Proc Natl Acad Sci U S A. 1993 Dec 15;90(24):11825-9. doi: 10.1073/pnas.90.24.11825. Proc Natl Acad Sci U S A. 1993. PMID: 7903454 Free PMC article.

9

Polymerase chain reaction-single-strand conformation polymorphism based determination of two major genetic defects responsible for a phenotypic polymorphism of cytochrome P450 (CYP) 2C19 in the Japanese population.

Itoh K, Inoue K, Nakao H, Yanagiwara S, Tada H, Suzuki T. Itoh K, et al. Anal Biochem. 2000 Aug 15;284(1):160-2. doi: 10.1006/abio.2000.4671. Anal Biochem. 2000. PMID: 10933870 No abstract available.

10

Identification of the primary gene defect at the cytochrome P450 CYP2D locus.

Gough AC, Miles JS, Spurr NK, Moss JE, Gaedigk A, Eichelbaum M, Wolf CR. Gough AC, et al. Nature. 1990 Oct 25;347(6295):773-6. doi: 10.1038/347773a0. Nature. 1990. PMID: 1978251

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