Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 25

1.

Genetic and epigenetic regulation of gene expression in fetal and adult human livers.

Bonder MJ, Kasela S, Kals M, Tamm R, Lokk K, Barragan I, Buurman WA, Deelen P, Greve JW, Ivanov M, Rensen SS, van Vliet-Ostaptchouk JV, Wolfs MG, Fu J, Hofker MH, Wijmenga C, Zhernakova A, Ingelman-Sundberg M, Franke L, Milani L.

BMC Genomics. 2014 Oct 4;15:860. doi: 10.1186/1471-2164-15-860.

2.

Epigenetic mechanisms of importance for drug treatment.

Ivanov M, Barragan I, Ingelman-Sundberg M.

Trends Pharmacol Sci. 2014 Aug;35(8):384-96. doi: 10.1016/j.tips.2014.05.004. Epub 2014 Jul 1. Review.

PMID:
24993164
3.

Long-term chronic toxicity testing using human pluripotent stem cell-derived hepatocytes.

Holmgren G, Sjögren AK, Barragan I, Sabirsh A, Sartipy P, Synnergren J, Björquist P, Ingelman-Sundberg M, Andersson TB, Edsbagge J.

Drug Metab Dispos. 2014 Sep;42(9):1401-6. doi: 10.1124/dmd.114.059154. Epub 2014 Jun 30.

PMID:
24980256
4.

CYP2W1 polymorphism: functional aspects and relation to risk for colorectal cancer.

Stenstedt K, Travica S, Guo J, Barragan I, Pors K, Patterson L, Edler D, Mkrtchian S, Johansson I, Ingelman-Sundberg M.

Pharmacogenomics. 2013 Oct;14(13):1615-22. doi: 10.2217/pgs.13.136.

PMID:
24088132
5.

Ontogeny, distribution and potential roles of 5-hydroxymethylcytosine in human liver function.

Ivanov M, Kals M, Kacevska M, Barragan I, Kasuga K, Rane A, Metspalu A, Milani L, Ingelman-Sundberg M.

Genome Biol. 2013 Aug 19;14(8):R83. doi: 10.1186/gb-2013-14-8-r83.

6.

Strong effects of environmental factors on prevalence and course of major depressive disorder are not moderated by 5-HTTLPR polymorphisms in a large Dutch sample.

Peyrot WJ, Middeldorp CM, Jansen R, Smit JH, de Geus EJ, Hottenga JJ, Willemsen G, Vink JM, Virding S, Barragan I, Ingelman-Sundberg M, Sim SC, Boomsma DI, Penninx BW.

J Affect Disord. 2013 Mar 20;146(1):91-9. doi: 10.1016/j.jad.2012.08.044. Epub 2012 Sep 27.

7.

Mutation screening of multiple genes in Spanish patients with autosomal recessive retinitis pigmentosa by targeted resequencing.

González-del Pozo M, Borrego S, Barragán I, Pieras JI, Santoyo J, Matamala N, Naranjo B, Dopazo J, Antiñolo G.

PLoS One. 2011;6(12):e27894. doi: 10.1371/journal.pone.0027894. Epub 2011 Dec 2.

8.

Copy-number variations in EYS: a significant event in the appearance of arRP.

Pieras JI, Barragán I, Borrego S, Audo I, González-Del Pozo M, Bernal S, Baiget M, Zeitz C, Bhattacharya SS, Antiñolo G.

Invest Ophthalmol Vis Sci. 2011 Jul 29;52(8):5625-31. doi: 10.1167/iovs.11-7292.

PMID:
21519034
9.

Mutation spectrum of EYS in Spanish patients with autosomal recessive retinitis pigmentosa.

Barragán I, Borrego S, Pieras JI, González-del Pozo M, Santoyo J, Ayuso C, Baiget M, Millan JM, Mena M, Abd El-Aziz MM, Audo I, Zeitz C, Littink KW, Dopazo J, Bhattacharya SS, Antiñolo G.

Hum Mutat. 2010 Nov;31(11):E1772-800.

10.

EYS is a major gene for rod-cone dystrophies in France.

Audo I, Sahel JA, Mohand-Saïd S, Lancelot ME, Antonio A, Moskova-Doumanova V, Nandrot EF, Doumanov J, Barragan I, Antinolo G, Bhattacharya SS, Zeitz C.

Hum Mutat. 2010 May;31(5):E1406-35. doi: 10.1002/humu.21249.

PMID:
20333770
11.

Identification of novel mutations in the ortholog of Drosophila eyes shut gene (EYS) causing autosomal recessive retinitis pigmentosa.

Abd El-Aziz MM, O'Driscoll CA, Kaye RS, Barragan I, El-Ashry MF, Borrego S, Antiñolo G, Pang CP, Webster AR, Bhattacharya SS.

Invest Ophthalmol Vis Sci. 2010 Aug;51(8):4266-72. doi: 10.1167/iovs.09-5109. Epub 2010 Mar 17. Erratum in: Invest Ophthalmol Vis Sci. 2014 Dec;55(12):8055.

PMID:
20237254
12.

Microarray-based mutation analysis of 183 Spanish families with Usher syndrome.

Jaijo T, Aller E, García-García G, Aparisi MJ, Bernal S, Avila-Fernández A, Barragán I, Baiget M, Ayuso C, Antiñolo G, Díaz-Llopis M, Külm M, Beneyto M, Nájera C, Millán JM.

Invest Ophthalmol Vis Sci. 2010 Mar;51(3):1311-7. doi: 10.1167/iovs.09-4085. Epub 2009 Aug 13.

PMID:
19683999
13.

EYS, encoding an ortholog of Drosophila spacemaker, is mutated in autosomal recessive retinitis pigmentosa.

Abd El-Aziz MM, Barragan I, O'Driscoll CA, Goodstadt L, Prigmore E, Borrego S, Mena M, Pieras JI, El-Ashry MF, Safieh LA, Shah A, Cheetham ME, Carter NP, Chakarova C, Ponting CP, Bhattacharya SS, Antinolo G.

Nat Genet. 2008 Nov;40(11):1285-7. doi: 10.1038/ng.241. Epub 2008 Oct 5.

14.

Linkage validation of RP25 Using the 10K genechip array and further refinement of the locus by new linked families.

Barragán I, Abd El-Aziz MM, Borrego S, El-Ashry MF, O'Driscoll C, Bhattacharya SS, Antiñolo G.

Ann Hum Genet. 2008 Jul;72(Pt 4):454-62. doi: 10.1111/j.1469-1809.2008.00448.x. Epub 2007 May 29.

PMID:
18510647
15.

Large-scale molecular analysis of a 34 Mb interval on chromosome 6q: major refinement of the RP25 interval.

Abd El-Aziz MM, Barragan I, O'Driscoll C, Borrego S, Abu-Safieh L, Pieras JI, El-Ashry MF, Prigmore E, Carter N, Antinolo G, Bhattacharya SS.

Ann Hum Genet. 2008 Jul;72(Pt 4):463-77. doi: 10.1111/j.1469-1809.2008.00455.x. Epub 2007 May 29. Erratum in: Ann Hum Genet. 2015 Jan;79(1):83.

16.

Genetic analysis of FAM46A in Spanish families with autosomal recessive retinitis pigmentosa: characterisation of novel VNTRs.

Barragán I, Borrego S, Abd El-Aziz MM, El-Ashry MF, Abu-Safieh L, Bhattacharya SS, Antiñolo G.

Ann Hum Genet. 2008 Jan;72(Pt 1):26-34. Epub 2007 Sep 5.

PMID:
17803723
17.

A novel genetic study of Chinese families with autosomal recessive retinitis pigmentosa.

Abd El-Aziz MM, El-Ashry MF, Chan WM, Chong KL, Barragan I, Antiñolo G, Pang CP, Bhattacharya SS.

Ann Hum Genet. 2007 May;71(Pt 3):281-94. Epub 2006 Nov 29.

PMID:
17156103
18.

Effects of incorporated drugs on degradation of novel 2,2'-bis(2-oxazoline) linked poly(lactic acid) films.

Tarvainen T, Malin M, Barragan I, Tuominen J, Seppälä J, Järvinen K.

Int J Pharm. 2006 Mar 9;310(1-2):162-7. Epub 2006 Jan 19.

PMID:
16423475
19.

Molecular genetic analysis of two functional candidate genes in the autosomal recessive retinitis pigmentosa, RP25, locus.

Abd El-Aziz MM, El-Ashry MF, Barragan I, Marcos I, Borrego S, Antiñolo G, Bhattacharya SS.

Curr Eye Res. 2005 Dec;30(12):1081-7.

PMID:
16354621
20.

Mutation screening of three candidate genes, ELOVL5, SMAP1 and GLULD1 in autosomal recessive retinitis pigmentosa.

Barragan I, Marcos I, Borrego S, Antiñolo G.

Int J Mol Med. 2005 Dec;16(6):1163-7.

PMID:
16273301
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Loading ...
Write to the Help Desk