Ingelman-Sundberg M - Search Results

1

Heterozygous loss-of-function variants in CYP1B1 predispose to primary open-angle glaucoma.

Pasutto F, Chavarria-Soley G, Mardin CY, Michels-Rautenstrauss K, Ingelman-Sundberg M, Fernández-Martínez L, Weber BH, Rautenstrauss B, Reis A. Pasutto F, et al. Invest Ophthalmol Vis Sci. 2010 Jan;51(1):249-54. doi: 10.1167/iovs.09-3880. Epub 2009 Jul 30. Invest Ophthalmol Vis Sci. 2010. PMID: 19643970 Free article.

2

Mutations in CYP1B1 cause primary congenital glaucoma by reduction of either activity or abundance of the enzyme.

Chavarria-Soley G, Sticht H, Aklillu E, Ingelman-Sundberg M, Pasutto F, Reis A, Rautenstrauss B. Chavarria-Soley G, et al. Hum Mutat. 2008 Sep;29(9):1147-53. doi: 10.1002/humu.20786. Hum Mutat. 2008. PMID: 18470941

3

Functional analysis of six different polymorphic CYP1B1 enzyme variants found in an Ethiopian population.

Aklillu E, Oscarson M, Hidestrand M, Leidvik B, Otter C, Ingelman-Sundberg M. Aklillu E, et al. Mol Pharmacol. 2002 Mar;61(3):586-94. doi: 10.1124/mol.61.3.586. Mol Pharmacol. 2002. PMID: 11854439

4

Characterization of common CYP1B1 variants with different capacity for benzo[a]pyrene-7,8-dihydrodiol epoxide formation from benzo[a]pyrene.

Aklillu E, Øvrebø S, Botnen IV, Otter C, Ingelman-Sundberg M. Aklillu E, et al. Cancer Res. 2005 Jun 15;65(12):5105-11. doi: 10.1158/0008-5472.CAN-05-0113. Cancer Res. 2005. PMID: 15958554

5

Characterization and functional analysis of two common human cytochrome P450 1B1 variants.

McLellan RA, Oscarson M, Hidestrand M, Leidvik B, Jonsson E, Otter C, Ingelman-Sundberg M. McLellan RA, et al. Arch Biochem Biophys. 2000 Jun 1;378(1):175-81. doi: 10.1006/abbi.2000.1808. Arch Biochem Biophys. 2000. PMID: 10871058

6

Molecular genetics and epigenetics of the cytochrome P450 gene family and its relevance for cancer risk and treatment.

Rodriguez-Antona C, Gomez A, Karlgren M, Sim SC, Ingelman-Sundberg M. Rodriguez-Antona C, et al. Hum Genet. 2010 Jan;127(1):1-17. doi: 10.1007/s00439-009-0748-0. Epub 2009 Oct 8. Hum Genet. 2010. PMID: 19823875 Review.

7

The clinically relevant CYP2C8*3 and CYP2C9*2 haplotype is inherited from Neandertals.

Haeggström S, Ingelman-Sundberg M, Pääbo S, Zeberg H. Haeggström S, et al. Pharmacogenomics J. 2022 Jul;22(4):247-249. doi: 10.1038/s41397-022-00284-6. Epub 2022 Jul 2. Pharmacogenomics J. 2022. PMID: 35780191 Free PMC article.

8

Characterization of a human glutathione S-transferase mu cluster containing a duplicated GSTM1 gene that causes ultrarapid enzyme activity.

McLellan RA, Oscarson M, Alexandrie AK, Seidegård J, Evans DA, Rannug A, Ingelman-Sundberg M. McLellan RA, et al. Mol Pharmacol. 1997 Dec;52(6):958-65. doi: 10.1124/mol.52.6.958. Mol Pharmacol. 1997. PMID: 9415705

9

Identification of sequences responsible for intracellular targeting and membrane binding of rat CYP2E1 in yeast.

Neve EP, Hidestrand M, Ingelman-Sundberg M. Neve EP, et al. Biochemistry. 2003 Dec 16;42(49):14566-75. doi: 10.1021/bi035193s. Biochemistry. 2003. PMID: 14661969

10

Frequent occurrence of CYP2D6 gene duplication in Saudi Arabians.

McLellan RA, Oscarson M, Seidegård J, Evans DA, Ingelman-Sundberg M. McLellan RA, et al. Pharmacogenetics. 1997 Jun;7(3):187-91. doi: 10.1097/00008571-199706000-00003. Pharmacogenetics. 1997. PMID: 9241658

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