Chelly J - Search Results

1

Construction of a YAC contig spanning the Xq13.3 subband.

Villard L, Gecz J, Colleaux L, Lossi AM, Chelly J, Ishikawa-Brush Y, Monaco AP, Fontes M. Villard L, et al. Among authors: chelly j. Genomics. 1995 Mar 1;26(1):115-22. doi: 10.1016/0888-7543(95)80089-5. Genomics. 1995. PMID: 7782069

2

Characterization of a 1.0 Mb YAC contig spanning two chromosome breakpoints related to Menkes disease.

Tümer Z, Chelly J, Tommerup N, Ishikawa-Brush Y, Tønnesen T, Monaco AP, Horn N. Tümer Z, et al. Among authors: chelly j. Hum Mol Genet. 1992 Oct;1(7):483-9. doi: 10.1093/hmg/1.7.483. Hum Mol Genet. 1992. PMID: 1307248

3

Analysis of Mnk, the murine homologue of the locus for Menkes disease, in normal and mottled (Mo) mice.

George AM, Reed V, Glenister P, Chelly J, Tümer Z, Horn N, Monaco AP, Boyd Y. George AM, et al. Among authors: chelly j. Genomics. 1994 Jul 1;22(1):27-35. doi: 10.1006/geno.1994.1341. Genomics. 1994. PMID: 7959788

4

Characterization of a highly complex region in Xq13 and mapping of three isodicentric breakpoints associated with preleukemia.

McDonell N, Ramser J, Francis F, Vinet MC, Rider S, Sudbrak R, Riesselman L, Yaspo ML, Reinhardt R, Monaco AP, Ross F, Kahn A, Kearney L, Buckle V, Chelly J. McDonell N, et al. Among authors: chelly j. Genomics. 2000 Mar 15;64(3):221-9. doi: 10.1006/geno.2000.6128. Genomics. 2000. PMID: 10756090

5

Characterization of the exon structure of the Menkes disease gene using vectorette PCR.

Tümer Z, Vural B, Tønnesen T, Chelly J, Monaco AP, Horn N. Tümer Z, et al. Among authors: chelly j. Genomics. 1995 Apr 10;26(3):437-42. doi: 10.1016/0888-7543(95)80160-n. Genomics. 1995. PMID: 7607665

6

Assignment of the dystonia-parkinsonism syndrome locus, DYT3, to a small region within a 1.8-Mb YAC contig of Xq13.1.

Haberhausen G, Schmitt I, Köhler A, Peters U, Rider S, Chelly J, Terwilliger JD, Monaco AP, Müller U. Haberhausen G, et al. Among authors: chelly j. Am J Hum Genet. 1995 Sep;57(3):644-50. Am J Hum Genet. 1995. PMID: 7668293 Free PMC article.

7

Assignment of the gene (EPLG2) encoding a high-affinity binding protein for the receptor tyrosine kinase elk to a 200-kilobasepair region in human chromosome Xq12.

Fletcher FA, Huebner K, Shaffer LG, Fairweather ND, Monaco AP, Müller U, Druck T, Simoneaux DK, Chelly J, Belmont JW, et al. Fletcher FA, et al. Among authors: chelly j. Genomics. 1995 Jan 1;25(1):334-5. doi: 10.1016/0888-7543(95)80156-g. Genomics. 1995. PMID: 7774950 No abstract available.

8

DXS106 and DXS559 flank the X-linked dystonia-parkinsonism syndrome locus (DYT3).

Müller U, Haberhausen G, Wagner T, Fairweather ND, Chelly J, Monaco AP. Müller U, et al. Among authors: chelly j. Genomics. 1994 Sep 1;23(1):114-7. doi: 10.1006/geno.1994.1465. Genomics. 1994. PMID: 7829058

9

2.6 Mb YAC contig of the human X inactivation center region in Xq13: physical linkage of the RPS4X, PHKA1, XIST and DXS128E genes.

Lafrenière RG, Brown CJ, Rider S, Chelly J, Taillon-Miller P, Chinault AC, Monaco AP, Willard HF. Lafrenière RG, et al. Among authors: chelly j. Hum Mol Genet. 1993 Aug;2(8):1105-15. doi: 10.1093/hmg/2.8.1105. Hum Mol Genet. 1993. PMID: 8401491

10

Linkage of X-linked myopathy with excessive autophagy (XMEA) to Xq28.

Villard L, des Portes V, Levy N, Louboutin JP, Recan D, Coquet M, Chabrol B, Figarella-Branger D, Chelly J, Pellissier JF, Fontes M. Villard L, et al. Among authors: chelly j. Eur J Hum Genet. 2000 Feb;8(2):125-9. doi: 10.1038/sj.ejhg.5200432. Eur J Hum Genet. 2000. PMID: 10757644

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