Feil RP - Search Results

1

A probe from an X-Y homology region detects RFLPs in Xq13-q22.

Feil RP, Gillard E, Affara NA, Ferguson-Smith MA, Mandel JL. Feil RP, et al. Nucleic Acids Res. 1989 Feb 11;17(3):1279. doi: 10.1093/nar/17.3.1279. Nucleic Acids Res. 1989. PMID: 2564188 Free PMC article. No abstract available.

2

Adrenoleukodystrophy: a complex chromosomal rearrangement in the Xq28 red/green-color-pigment gene region indicates two possible gene localizations.

Feil R, Aubourg P, Mosser J, Douar AM, Le Paslier D, Philippe C, Mandel JL. Feil R, et al. Am J Hum Genet. 1991 Dec;49(6):1361-71. Am J Hum Genet. 1991. PMID: 1746561 Free PMC article.

3

A 195-kb cosmid walk encompassing the human Xq28 color vision pigment genes.

Feil R, Aubourg P, Heilig R, Mandel JL. Feil R, et al. Genomics. 1990 Feb;6(2):367-73. doi: 10.1016/0888-7543(90)90578-i. Genomics. 1990. PMID: 1968424

4

Physical and genetic mapping of polymorphic loci in Xq28 (DXS15, DXS52, and DXS134): analysis of a cosmid clone and a yeast artificial chromosome.

Feil R, Palmieri G, d'Urso M, Heilig R, Oberlé I, Mandel JL. Feil R, et al. Am J Hum Genet. 1990 Apr;46(4):720-8. Am J Hum Genet. 1990. PMID: 1969226 Free PMC article.

5

The red-green visual pigment gene region in adrenoleukodystrophy.

Aubourg P, Feil R, Guidoux S, Kaplan JC, Moser H, Kahn A, Mandel JL. Aubourg P, et al. Am J Hum Genet. 1990 Mar;46(3):459-69. Am J Hum Genet. 1990. PMID: 2309698 Free PMC article.

6

[The progeny of the two protan and deutan families described by Franceschetti and Klein (1949, 1956), one generation later. Genealogy, color vision and genomic DNA].

Roth A, Klein D, Paccolat F, Hermès D, Pelizzone M, Mandel JL, Feil R. Roth A, et al. Ophtalmologie. 1989 Sep-Dec;3(4):275-8. Ophtalmologie. 1989. PMID: 2641134 French.

7

Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters.

Mosser J, Douar AM, Sarde CO, Kioschis P, Feil R, Moser H, Poustka AM, Mandel JL, Aubourg P. Mosser J, et al. Nature. 1993 Feb 25;361(6414):726-30. doi: 10.1038/361726a0. Nature. 1993. PMID: 8441467

8

The long non-coding RNA Meg3 mediates imprinted gene expression during stem cell differentiation.

Farhadova S, Ghousein A, Charon F, Surcis C, Gomez-Velazques M, Roidor C, Di Michele F, Borensztein M, De Sario A, Esnault C, Noordermeer D, Moindrot B, Feil R. Farhadova S, et al. Nucleic Acids Res. 2024 Jun 24;52(11):6183-6200. doi: 10.1093/nar/gkae247. Nucleic Acids Res. 2024. PMID: 38613389 Free PMC article.

9

Analysis of chromatin in limited numbers of cells: a PCR-SSCP based assay of allele-specific nuclease sensitivity.

Gregory RI, Feil R. Gregory RI, et al. Nucleic Acids Res. 1999 Nov 15;27(22):e32. doi: 10.1093/nar/27.22.e32. Nucleic Acids Res. 1999. PMID: 10536165 Free PMC article.

10

PRMT5-mediated histone H4 arginine-3 symmetrical dimethylation marks chromatin at G + C-rich regions of the mouse genome.

Girardot M, Hirasawa R, Kacem S, Fritsch L, Pontis J, Kota SK, Filipponi D, Fabbrizio E, Sardet C, Lohmann F, Kadam S, Ait-Si-Ali S, Feil R. Girardot M, et al. Nucleic Acids Res. 2014 Jan;42(1):235-48. doi: 10.1093/nar/gkt884. Epub 2013 Oct 3. Nucleic Acids Res. 2014. PMID: 24097435 Free PMC article.

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