Van Agtmael T - Search Results

1

Parametric and nonparametric genome scan analyses for human handedness.

Van Agtmael T, Forrest SM, Del-Favero J, Van Broeckhoven C, Williamson R. Van Agtmael T, et al. Among authors: van broeckhoven c. Eur J Hum Genet. 2003 Oct;11(10):779-83. doi: 10.1038/sj.ejhg.5201048. Eur J Hum Genet. 2003. PMID: 14512968

2

Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome.

Alamowitch S, Plaisier E, Favrole P, Prost C, Chen Z, Van Agtmael T, Marro B, Ronco P. Alamowitch S, et al. Among authors: van agtmael t. Neurology. 2009 Dec 1;73(22):1873-82. doi: 10.1212/WNL.0b013e3181c3fd12. Neurology. 2009. PMID: 19949034 Free PMC article.

3

COL4A1 mutations and hereditary angiopathy, nephropathy, aneurysms, and muscle cramps.

Plaisier E, Gribouval O, Alamowitch S, Mougenot B, Prost C, Verpont MC, Marro B, Desmettre T, Cohen SY, Roullet E, Dracon M, Fardeau M, Van Agtmael T, Kerjaschki D, Antignac C, Ronco P. Plaisier E, et al. Among authors: van agtmael t. N Engl J Med. 2007 Dec 27;357(26):2687-95. doi: 10.1056/NEJMoa071906. N Engl J Med. 2007. PMID: 18160688 Free article.

4

A novel human iPSC model of COL4A1/A2 small vessel disease unveils a key pathogenic role of matrix metalloproteinases.

Al-Thani M, Goodwin-Trotman M, Bell S, Patel K, Fleming LK, Vilain C, Abramowicz M, Allan SM, Wang T, Cader MZ, Horsburgh K, Van Agtmael T, Sinha S, Markus HS, Granata A. Al-Thani M, et al. Among authors: van agtmael t. Stem Cell Reports. 2023 Dec 12;18(12):2386-2399. doi: 10.1016/j.stemcr.2023.10.014. Epub 2023 Nov 16. Stem Cell Reports. 2023. PMID: 37977146 Free PMC article.

5

Parametric and non-parametric linkage analysis of several candidate regions for genes for human handedness.

Van Agtmael T, Forrest SM, Williamson R. Van Agtmael T, et al. Eur J Hum Genet. 2002 Oct;10(10):623-30. doi: 10.1038/sj.ejhg.5200851. Eur J Hum Genet. 2002. PMID: 12357333

6

Genes for left-handedness: how to search for the needle in the haystack?

Van Agtmael T, Forrest SM, Williamson R. Van Agtmael T, et al. Laterality. 2001 Apr;6(2):149-64. doi: 10.1080/713754403. Laterality. 2001. PMID: 15513167

7

Dominant mutations of Col4a1 result in basement membrane defects which lead to anterior segment dysgenesis and glomerulopathy.

Van Agtmael T, Schlötzer-Schrehardt U, McKie L, Brownstein DG, Lee AW, Cross SH, Sado Y, Mullins JJ, Pöschl E, Jackson IJ. Van Agtmael T, et al. Hum Mol Genet. 2005 Nov 1;14(21):3161-8. doi: 10.1093/hmg/ddi348. Epub 2005 Sep 13. Hum Mol Genet. 2005. PMID: 16159887

8

Col4a1 mutation in mice causes defects in vascular function and low blood pressure associated with reduced red blood cell volume.

Van Agtmael T, Bailey MA, Schlötzer-Schrehardt U, Craigie E, Jackson IJ, Brownstein DG, Megson IL, Mullins JJ. Van Agtmael T, et al. Hum Mol Genet. 2010 Mar 15;19(6):1119-28. doi: 10.1093/hmg/ddp584. Epub 2010 Jan 7. Hum Mol Genet. 2010. PMID: 20056676 Free PMC article.

9

Identification and characterization of a novel member of the EXT gene family, EXTL2.

Wuyts W, Van Hul W, Hendrickx J, Speleman F, Wauters J, De Boulle K, Van Roy N, Van Agtmael T, Bossuyt P, Willems PJ. Wuyts W, et al. Among authors: van agtmael t, van roy n, van hul w. Eur J Hum Genet. 1997 Nov-Dec;5(6):382-9. Eur J Hum Genet. 1997. PMID: 9450183

10

17th International Mouse Genome Conference.

Smyth I, Van Agtmael T, Jackson IJ. Smyth I, et al. Among authors: van agtmael t. Mamm Genome. 2004 Jul;15(7):509-14. doi: 10.1007/s00335-004-4001-9. Mamm Genome. 2004. PMID: 15366370 No abstract available.

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