Feil R - Search Results

1

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.

2

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

3

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.

4

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. Among authors: feil r. Am J Hum Genet. 1990 Mar;46(3):459-69. Am J Hum Genet. 1990. PMID: 2309698 Free PMC article.

5

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.

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. Among authors: feil r. 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. Among authors: feil r. Nature. 1993 Feb 25;361(6414):726-30. doi: 10.1038/361726a0. Nature. 1993. PMID: 8441467

8

Chromosomal rearrangement segregating with adrenoleukodystrophy: a molecular analysis.

Sack GH Jr, Alpern M, Webster T, Feil RP, Morrell JC, Chen G, Chen W, Caskey CT, Moser HW. Sack GH Jr, et al. Among authors: feil rp. Proc Natl Acad Sci U S A. 1993 Oct 15;90(20):9489-93. doi: 10.1073/pnas.90.20.9489. Proc Natl Acad Sci U S A. 1993. PMID: 8415728 Free PMC article.

9

Histone methylation is mechanistically linked to DNA methylation at imprinting control regions in mammals.

Henckel A, Nakabayashi K, Sanz LA, Feil R, Hata K, Arnaud P. Henckel A, et al. Among authors: feil r. Hum Mol Genet. 2009 Sep 15;18(18):3375-83. doi: 10.1093/hmg/ddp277. Epub 2009 Jun 10. Hum Mol Genet. 2009. PMID: 19515852

10

The swine steroid 21-hydroxylase gene (CYP21): cloning and mapping within the swine leucocyte antigen complex.

Geffrotin C, Chardon P, de Andres-Cara DF, Feil R, Renard C, Vaiman M. Geffrotin C, et al. Among authors: feil r. Anim Genet. 1990;21(1):1-13. doi: 10.1111/j.1365-2052.1990.tb03202.x. Anim Genet. 1990. PMID: 2109953

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