Monaco AP - Search Results

1

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: monaco ap. Cell. 1994 Jun 17;77(6):869-80. doi: 10.1016/0092-8674(94)90136-8. Cell. 1994. PMID: 8004674

2

A novel point mutation in the McLeod syndrome gene in neuroacanthocytosis.

Ho MF, Chalmers RM, Davis MB, Harding AE, Monaco AP. Ho MF, et al. Among authors: monaco ap. Ann Neurol. 1996 May;39(5):672-5. doi: 10.1002/ana.410390518. Ann Neurol. 1996. PMID: 8619554

3

Fine mapping of the McLeod locus (XK) to a 150-380-kb region in Xp21.

Ho MF, Monaco AP, Blonden LA, van Ommen GJ, Affara NA, Ferguson-Smith MA, Lehrach H. Ho MF, et al. Among authors: monaco ap. Am J Hum Genet. 1992 Feb;50(2):317-30. Am J Hum Genet. 1992. PMID: 1734714 Free PMC article.

4

Menkes and Wilson diseases.

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

5

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. Among authors: monaco ap. Nat Genet. 1993 Jan;3(1):14-9. doi: 10.1038/ng0193-14. Nat Genet. 1993. PMID: 8490646

6

The chorea of McLeod syndrome.

Danek A, Tison F, Rubio J, Oechsner M, Kalckreuth W, Monaco AP. Danek A, et al. Among authors: monaco ap. Mov Disord. 2001 Sep;16(5):882-9. doi: 10.1002/mds.1188. Mov Disord. 2001. PMID: 11746618

7

McLeod neuroacanthocytosis: genotype and phenotype.

Danek A, Rubio JP, Rampoldi L, Ho M, Dobson-Stone C, Tison F, Symmans WA, Oechsner M, Kalckreuth W, Watt JM, Corbett AJ, Hamdalla HH, Marshall AG, Sutton I, Dotti MT, Malandrini A, Walker RH, Daniels G, Monaco AP. Danek A, et al. Among authors: monaco ap. Ann Neurol. 2001 Dec;50(6):755-64. doi: 10.1002/ana.10035. Ann Neurol. 2001. PMID: 11761473

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: monaco ap. 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

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: monaco ap. Hum Mol Genet. 1992 Oct;1(7):483-9. doi: 10.1093/hmg/1.7.483. Hum Mol Genet. 1992. PMID: 1307248

10

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: monaco ap. Genomics. 1995 Apr 10;26(3):437-42. doi: 10.1016/0888-7543(95)80160-n. Genomics. 1995. PMID: 7607665

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