Chelly J - Search Results

1

Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein.

Chelly J, Tümer Z, Tønnesen T, Petterson A, Ishikawa-Brush Y, Tommerup N, Horn N, Monaco AP. Chelly J, et al. Nat Genet. 1993 Jan;3(1):14-9. doi: 10.1038/ng0193-14. Nat Genet. 1993. PMID: 8490646

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

Menkes and Wilson diseases.

Monaco AP, Chelly J. Monaco AP, et al. Among authors: chelly j. Adv Genet. 1995;33:233-53. doi: 10.1016/s0065-2660(08)60335-1. Adv Genet. 1995. PMID: 7484454 Review. No abstract available.

4

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

5

Cloning the Wilson disease gene.

Chelly J, Monaco AP. Chelly J, et al. Nat Genet. 1993 Dec;5(4):317-8. doi: 10.1038/ng1293-317. Nat Genet. 1993. PMID: 8298634 No abstract available.

6

A Golgi localization signal identified in the Menkes recombinant protein.

Francis MJ, Jones EE, Levy ER, Ponnambalam S, Chelly J, Monaco AP. Francis MJ, et al. Among authors: chelly j. Hum Mol Genet. 1998 Aug;7(8):1245-52. doi: 10.1093/hmg/7.8.1245. Hum Mol Genet. 1998. PMID: 9668166

7

Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein.

Ho M, Chelly J, Carter N, Danek A, Crocker P, Monaco AP. Ho M, et al. Among authors: chelly j. Cell. 1994 Jun 17;77(6):869-80. doi: 10.1016/0092-8674(94)90136-8. Cell. 1994. PMID: 8004674

8

Dinucleotide repeat polymorphisms from DXS106 and DXS227 YACs using a two stage approach.

Fairweather N, Chelly J, Monaco AP. Fairweather N, et al. Among authors: chelly j. Hum Mol Genet. 1993 May;2(5):607-8. doi: 10.1093/hmg/2.5.607. Hum Mol Genet. 1993. PMID: 8518803 No abstract available.

9

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

10

Mutations in the connexin 32 gene in X-linked dominant Charcot-Marie-Tooth disease (CMTX1).

Fairweather N, Bell C, Cochrane S, Chelly J, Wang S, Mostacciuolo ML, Monaco AP, Haites NE. Fairweather N, et al. Among authors: chelly j. Hum Mol Genet. 1994 Jan;3(1):29-34. doi: 10.1093/hmg/3.1.29. Hum Mol Genet. 1994. PMID: 8162049

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