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Items: 33

1.

Dynamic changes of DNA methylation and lung disease in cystic fibrosis: lessons from a monogenic disease.

Magalhães M, Tost J, Pineau F, Rivals I, Busato F, Alary N, Mely L, Leroy S, Murris M, Caimmi D, Claustres M, Chiron R, De Sario A.

Epigenomics. 2018 Aug;10(8):1131-1145. doi: 10.2217/epi-2018-0005. Epub 2018 Jul 27.

PMID:
30052057
2.

The HDAC inhibitor SAHA does not rescue CFTR membrane expression in Cystic Fibrosis.

Bergougnoux A, Petit A, Knabe L, Bribes E, Chiron R, De Sario A, Claustres M, Molinari N, Vachier I, Taulan-Cadars M, Bourdin A.

Int J Biochem Cell Biol. 2017 Jul;88:124-132. doi: 10.1016/j.biocel.2017.05.002. Epub 2017 May 3.

PMID:
28478266
3.

DNA methylation at modifier genes of lung disease severity is altered in cystic fibrosis.

Magalhães M, Rivals I, Claustres M, Varilh J, Thomasset M, Bergougnoux A, Mely L, Leroy S, Corvol H, Guillot L, Murris M, Beyne E, Caimmi D, Vachier I, Chiron R, De Sario A.

Clin Epigenetics. 2017 Feb 14;9:19. doi: 10.1186/s13148-016-0300-8. eCollection 2017.

4.

Nasal epithelial cells: a tool to study DNA methylation in airway diseases.

Bergougnoux A, Claustres M, De Sario A.

Epigenomics. 2015;7(1):119-26. doi: 10.2217/epi.14.65. Review.

PMID:
25687471
5.

A balance between activating and repressive histone modifications regulates cystic fibrosis transmembrane conductance regulator (CFTR) expression in vivo.

Bergougnoux A, Rivals I, Liquori A, Raynal C, Varilh J, Magalhães M, Perez MJ, Bigi N, Des Georges M, Chiron R, Squalli-Houssaini AS, Claustres M, De Sario A.

Epigenetics. 2014 Jul;9(7):1007-17. doi: 10.4161/epi.28967. Epub 2014 Apr 29.

6.

DNA replication is altered in Immunodeficiency Centromeric instability Facial anomalies (ICF) cells carrying DNMT3B mutations.

Lana E, Mégarbané A, Tourrière H, Sarda P, Lefranc G, Claustres M, De Sario A.

Eur J Hum Genet. 2012 Oct;20(10):1044-50. doi: 10.1038/ejhg.2012.41. Epub 2012 Feb 29.

7.

Heterochromatic genes undergo epigenetic changes and escape silencing in immunodeficiency, centromeric instability, facial anomalies (ICF) syndrome.

Brun ME, Lana E, Rivals I, Lefranc G, Sarda P, Claustres M, Mégarbané A, De Sario A.

PLoS One. 2011 Apr 29;6(4):e19464. doi: 10.1371/journal.pone.0019464.

8.

Clinical and molecular overview of inherited disorders resulting from epigenomic dysregulation.

De Sario A.

Eur J Med Genet. 2009 Nov-Dec;52(6):363-72. doi: 10.1016/j.ejmg.2009.07.004. Epub 2009 Jul 24. Review.

PMID:
19632366
9.

BAGE Hypomethylation Is an Early Event in Colon Transformation and Is Frequent in Histologically Advanced Adenomas.

Lana E, Brun ME, Rivals I, Selves J, Kirzin S, Lutsyk AP, Gordiyuk VV, Bibeau F, Rynditch A, De Sario A.

Cancers (Basel). 2009 Nov 18;1(1):3-11. doi: 10.3390/cancers1010003.

10.

BAGE hypomethylation, a new epigenetic biomarker for colon cancer detection.

Grunau C, Brun ME, Rivals I, Selves J, Hindermann W, Favre-Mercuret M, Granier G, De Sario A.

Cancer Epidemiol Biomarkers Prev. 2008 Jun;17(6):1374-9. doi: 10.1158/1055-9965.EPI-07-2656. Epub 2008 Jun 9.

11.

Mapping of the juxtacentromeric heterochromatin-euchromatin frontier of human chromosome 21.

Grunau C, Buard J, Brun ME, De Sario A.

Genome Res. 2006 Oct;16(10):1198-207. Epub 2006 Sep 8.

12.

Characterization and expression analysis during embryo development of the mouse ortholog of MLL3.

Brun ME, Gasca S, Girard C, Bouton K, De Massy B, De Sario A.

Gene. 2006 Apr 12;371(1):25-33. Epub 2006 Feb 3.

PMID:
16459028
13.

Frequent DNA hypomethylation of human juxtacentromeric BAGE loci in cancer.

Grunau C, Sanchez C, Ehrlich M, van der Bruggen P, Hindermann W, Rodriguez C, Krieger S, Dubeau L, Fiala E, De Sario A.

Genes Chromosomes Cancer. 2005 May;43(1):11-24.

PMID:
15704127
14.

Centromeres and neocentromeres.

Roizés G, Grunau C, Buard J, De Sario A, Puechberty J.

Methods Mol Biol. 2004;240:77-104. No abstract available.

PMID:
14970406
15.

Juxtacentromeric region of human chromosome 21: a boundary between centromeric heterochromatin and euchromatic chromosome arms.

Brun ME, Ruault M, Ventura M, Roizès G, De Sario A.

Gene. 2003 Jul 17;312:41-50.

PMID:
12909339
16.

BAGE genes generated by juxtacentromeric reshuffling in the Hominidae lineage are under selective pressure.

Ruault M, Ventura M, Galtier N, Brun ME, Archidiacono N, Roizès G, De Sario A.

Genomics. 2003 Apr;81(4):391-9.

PMID:
12676563
17.

New BAGE (B melanoma antigen) genes mapping to the juxtacentromeric regions of human chromosomes 13 and 21 have a cancer/testis expression profile.

Ruault M, van der Bruggen P, Brun ME, Boyle S, Roizès G, De Sario A.

Eur J Hum Genet. 2002 Dec;10(12):833-40.

18.

MLL3, a new human member of the TRX/MLL gene family, maps to 7q36, a chromosome region frequently deleted in myeloid leukaemia.

Ruault M, Brun ME, Ventura M, Roizès G, De Sario A.

Gene. 2002 Feb 6;284(1-2):73-81.

PMID:
11891048
19.

Characterization of the human tubulin tyrosine ligase-like 1 gene (TTLL1) mapping to 22q13.1.

Trichet V, Ruault M, Roizès G, De Sario A.

Gene. 2000 Oct 17;257(1):109-17.

PMID:
11054573
20.

Genomic structure of a copy of the human TPTE gene which encompasses 87 kb on the short arm of chromosome 21.

Guipponi M, Yaspo ML, Riesselman L, Chen H, De Sario A, Roizès G, Antonarakis SE.

Hum Genet. 2000 Aug;107(2):127-31.

PMID:
11030409
21.

Juxta-centromeric region of human chromosome 21 is enriched for pseudogenes and gene fragments.

Ruault M, Trichet V, Gimenez S, Boyle S, Gardiner K, Rolland M, Roizès G, De Sario A.

Gene. 1999 Oct 18;239(1):55-64.

PMID:
10571034
22.

Molecular cloning of a human cDNA IGSF3 encoding an immunoglobulin-like membrane protein: expression and mapping to chromosome band 1p13.

Saupe S, Roizès G, Peter M, Boyle S, Gardiner K, De Sario A.

Genomics. 1998 Sep 15;52(3):305-11.

PMID:
9790749
23.

A compositional map of the cen-q21 region of human chromosome 21.

De Sario A, Roizes G, Allegre N, Bernardi G.

Gene. 1997 Jul 18;194(1):107-13.

PMID:
9266679
24.

A compositional map of human chromosome band Xq28.

De Sario A, Geigl EM, Palmieri G, D'Urso M, Bernardi G.

Proc Natl Acad Sci U S A. 1996 Feb 6;93(3):1298-302.

25.

A rapid procedure for the compositional analysis of yeast artificial chromosomes.

De Sario A, Geigl EM, Bernardi G.

Nucleic Acids Res. 1995 Oct 11;23(19):4013-4. No abstract available.

26.

Correlations between isochores and chromosomal bands in the human genome.

Saccone S, De Sario A, Wiegant J, Raap AK, Della Valle G, Bernardi G.

Proc Natl Acad Sci U S A. 1993 Dec 15;90(24):11929-33.

27.

The highest gene concentrations in the human genome are in telomeric bands of metaphase chromosomes.

Saccone S, De Sario A, Della Valle G, Bernardi G.

Proc Natl Acad Sci U S A. 1992 Jun 1;89(11):4913-7.

28.

Compositional properties of telomeric regions from human chromosomes.

De Sario A, Aïssani B, Bernardi G.

FEBS Lett. 1991 Dec 16;295(1-3):22-6.

29.
30.

Aneuploidy induced by chloral hydrate detected in human lymphocytes with the Y97 probe.

Vagnarelli P, De Sario A, De Carli L.

Mutagenesis. 1990 Nov;5(6):591-2.

PMID:
2263216
31.
32.

Aneuploidy assays on interphase nuclei by means of in situ hybridization with DNA probes.

Raimondi E, Scariolo S, De Sario A, De Carli L.

Mutagenesis. 1989 May;4(3):165-9.

PMID:
2659934
33.

Detection of chromosome variation in interphase by in situ hybridization with repetitive DNA probes: potential applications to cytogenetic analysis and mutagenicity testing.

Raimondi E, Scariolo S, Vagnarelli P, De Sario A, De Carli L.

Cytotechnology. 1987 Oct;1(1):13-7. doi: 10.1007/BF00351116.

PMID:
22358434

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