Cruts M - Search Results

1

Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21.

Cruts M, Gijselinck I, van der Zee J, Engelborghs S, Wils H, Pirici D, Rademakers R, Vandenberghe R, Dermaut B, Martin JJ, van Duijn C, Peeters K, Sciot R, Santens P, De Pooter T, Mattheijssens M, Van den Broeck M, Cuijt I, Vennekens K, De Deyn PP, Kumar-Singh S, Van Broeckhoven C. Cruts M, et al. Nature. 2006 Aug 24;442(7105):920-4. doi: 10.1038/nature05017. Epub 2006 Jul 16. Nature. 2006. PMID: 16862115

2

Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the beta-amyloid precursor protein gene.

Hendriks L, van Duijn CM, Cras P, Cruts M, Van Hul W, van Harskamp F, Warren A, McInnis MG, Antonarakis SE, Martin JJ, et al. Hendriks L, et al. Among authors: cruts m. Nat Genet. 1992 Jun;1(3):218-21. doi: 10.1038/ng0692-218. Nat Genet. 1992. PMID: 1303239

3

Mapping of a gene predisposing to early-onset Alzheimer's disease to chromosome 14q24.3.

Van Broeckhoven C, Backhovens H, Cruts M, De Winter G, Bruyland M, Cras P, Martin JJ. Van Broeckhoven C, et al. Among authors: cruts m. Nat Genet. 1992 Dec;2(4):335-9. doi: 10.1038/ng1292-335. Nat Genet. 1992. PMID: 1303290

4

Dinucleotide repeat polymorphism at the D21S145 locus.

Cruts M, Backhovens H, Van Broeckhoven C. Cruts M, et al. Nucleic Acids Res. 1992 Mar 11;20(5):1159. Nucleic Acids Res. 1992. PMID: 1549494 Free PMC article.

5

Dinucleotide repeat polymorphism at the D21S16 [correction of D1S16] locus.

Cruts M, Backhovens H, Van Broeckhoven C. Cruts M, et al. Nucleic Acids Res. 1992 Mar 11;20(5):1159. Nucleic Acids Res. 1992. PMID: 1549495 Free PMC article.

6

Identification of chromosome 21 DNA polymorphisms for genetic studies in Alzheimer's disease and Down syndrome.

Van Camp G, Backhovens H, Cruts M, Wehnert A, Van Hul W, Stinissen P, Van Broeckhoven C. Van Camp G, et al. Among authors: cruts m. Hum Genet. 1991 Oct;87(6):649-53. doi: 10.1007/BF00201718. Hum Genet. 1991. PMID: 1682232

7

Unique sequence homology in the pericentromeric regions of the long arms of chromosomes 13 and 21.

Van Camp G, Cruts M, Backhovens H, Wehnert A, Van Broeckhoven C. Van Camp G, et al. Among authors: cruts m. Genomics. 1992 Jan;12(1):158-60. doi: 10.1016/0888-7543(92)90420-w. Genomics. 1992. PMID: 1733854

8

Subregional localization of the chromosome 21 loci D21S24 and D21S26 using physical mapping techniques.

Van Hul W, Backhovens H, Van Camp G, Stinissen P, Cruts M, Wehnert A, Van Broeckhoven C. Van Hul W, et al. Among authors: cruts m. Hum Genet. 1991 Jun;87(2):109-11. doi: 10.1007/BF00204162. Hum Genet. 1991. PMID: 2066096

9

Genetic and physical characterization of the early-onset Alzheimer's disease AD3 locus on chromosome 14q24.3.

Cruts M, Backhovens H, Theuns J, Clark RF, Le Paslier D, Weissenbach J, Goate AM, Martin JJ, Van Broeckhoven C. Cruts M, et al. Hum Mol Genet. 1995 Aug;4(8):1355-64. doi: 10.1093/hmg/4.8.1355. Hum Mol Genet. 1995. PMID: 7581374

10

A population-based study of familial Alzheimer disease: linkage to chromosomes 14, 19, and 21.

van Duijn CM, Hendriks L, Farrer LA, Backhovens H, Cruts M, Wehnert A, Hofman A, Van Broeckhoven C. van Duijn CM, et al. Among authors: cruts m. Am J Hum Genet. 1994 Oct;55(4):714-27. Am J Hum Genet. 1994. PMID: 7942850 Free PMC article.

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