Backhovens H - Search Results

1

WT1 mutation in malignant mesothelioma and WT1 immunoreactivity in relation to p53 and growth factor receptor expression, cell-type transition, and prognosis.

Kumar-Singh S, Segers K, Rodeck U, Backhovens H, Bogers J, Weyler J, Van Broeckhoven C, Van Marck E. Kumar-Singh S, et al. Among authors: backhovens h. J Pathol. 1997 Jan;181(1):67-74. doi: 10.1002/(SICI)1096-9896(199701)181:1<67::AID-PATH723>3.0.CO;2-Z. J Pathol. 1997. PMID: 9072005

2

Immunoreactivity for p53 and mdm2 and the detection of p53 mutations in human malignant mesothelioma.

Segers K, Backhovens H, Singh SK, De Voecht J, Ramael M, Van Broeckhoven C, Van Marck E. Segers K, et al. Among authors: backhovens h. Virchows Arch. 1995;427(4):431-6. doi: 10.1007/BF00199393. Virchows Arch. 1995. PMID: 8548129

3

Dinucleotide repeat polymorphism at the D21S145 locus.

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

4

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

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

5

Mutation analysis of the connexin 32 (Cx32) gene in Charcot-Marie-Tooth neuropathy type 1: identification of five new mutations.

Nelis E, Simokovic S, Timmerman V, Löfgren A, Backhovens H, De Jonghe P, Martin JJ, Van Broeckhoven C. Nelis E, et al. Among authors: backhovens h. Hum Mutat. 1997;9(1):47-52. doi: 10.1002/(SICI)1098-1004(1997)9:1<47::AID-HUMU8>3.0.CO;2-M. Hum Mutat. 1997. PMID: 8990008 No abstract available.

6

Genetic analysis of the cellular oncogene fos in patients with chromosome 14 encoded Alzheimer's disease.

Cruts M, Backhovens H, Martin JJ, van Broeckhoven C. Cruts M, et al. Among authors: backhovens h. Neurosci Lett. 1994 Jun 6;174(1):97-100. doi: 10.1016/0304-3940(94)90128-7. Neurosci Lett. 1994. PMID: 7970166

7

Genetic variability in the regulatory region of presenilin 1 associated with risk for Alzheimer's disease and variable expression.

Theuns J, Del-Favero J, Dermaut B, van Duijn CM, Backhovens H, Van den Broeck MV, Serneels S, Corsmit E, Van Broeckhoven CV, Cruts M. Theuns J, et al. Among authors: backhovens h. Hum Mol Genet. 2000 Feb 12;9(3):325-31. doi: 10.1093/hmg/9.3.325. Hum Mol Genet. 2000. PMID: 10655540 Free article.

8

Dinucleotide repeat polymorphism at the D21S258 locus.

Wehnert A, Cruts M, Backhovens H, Delabar JM, Thomas G, Van Broeckhoven C. Wehnert A, et al. Among authors: backhovens h. Hum Mol Genet. 1992 Sep;1(6):449. doi: 10.1093/hmg/1.6.449. Hum Mol Genet. 1992. PMID: 1339475 No abstract available.

9

APOE genotype does not modulate age of onset in families with chromosome 14 encoded Alzheimer's disease.

Van Broeckhoven C, Backhovens H, Cruts M, Martin JJ, Crook R, Houlden H, Hardy J. Van Broeckhoven C, et al. Among authors: backhovens h. Neurosci Lett. 1994 Mar 14;169(1-2):179-80. doi: 10.1016/0304-3940(94)90385-9. Neurosci Lett. 1994. PMID: 8047278

10

Nonfibrillar diffuse amyloid deposition due to a gamma(42)-secretase site mutation points to an essential role for N-truncated A beta(42) in Alzheimer's disease.

Kumar-Singh S, De Jonghe C, Cruts M, Kleinert R, Wang R, Mercken M, De Strooper B, Vanderstichele H, Löfgren A, Vanderhoeven I, Backhovens H, Vanmechelen E, Kroisel PM, Van Broeckhoven C. Kumar-Singh S, et al. Among authors: backhovens h. Hum Mol Genet. 2000 Nov 1;9(18):2589-98. doi: 10.1093/hmg/9.18.2589. Hum Mol Genet. 2000. PMID: 11063718

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