Engel W - Search Results

1

Novel mutations in the Atlastin gene (SPG3A) in families with autosomal dominant hereditary spastic paraplegia and evidence for late onset forms of HSP linked to the SPG3A locus.

Sauter SM, Engel W, Neumann LM, Kunze J, Neesen J. Sauter SM, et al. Among authors: engel w. Hum Mutat. 2004 Jan;23(1):98. doi: 10.1002/humu.9205. Hum Mutat. 2004. PMID: 14695538

2

Spastin, the most commonly mutated protein in hereditary spastic paraplegia interacts with Reticulon 1 an endoplasmic reticulum protein.

Mannan AU, Boehm J, Sauter SM, Rauber A, Byrne PC, Neesen J, Engel W. Mannan AU, et al. Among authors: engel w. Neurogenetics. 2006 May;7(2):93-103. doi: 10.1007/s10048-006-0034-4. Epub 2006 Apr 7. Neurogenetics. 2006. PMID: 16602018

3

ZFYVE27 (SPG33), a novel spastin-binding protein, is mutated in hereditary spastic paraplegia.

Mannan AU, Krawen P, Sauter SM, Boehm J, Chronowska A, Paulus W, Neesen J, Engel W. Mannan AU, et al. Among authors: engel w. Am J Hum Genet. 2006 Aug;79(2):351-7. doi: 10.1086/504927. Epub 2006 Jun 1. Am J Hum Genet. 2006. PMID: 16826525 Free PMC article.

4

Mutation analysis of the spastin gene (SPG4) in patients in Germany with autosomal dominant hereditary spastic paraplegia.

Sauter S, Miterski B, Klimpe S, Bönsch D, Schöls L, Visbeck A, Papke T, Hopf HC, Engel W, Deufel T, Epplen JT, Neesen J. Sauter S, et al. Among authors: engel w. Hum Mutat. 2002 Aug;20(2):127-32. doi: 10.1002/humu.10105. Hum Mutat. 2002. PMID: 12124993

5

The Hook1 gene is non-functional in the abnormal spermatozoon head shape (azh) mutant mouse.

Mendoza-Lujambio I, Burfeind P, Dixkens C, Meinhardt A, Hoyer-Fender S, Engel W, Neesen J. Mendoza-Lujambio I, et al. Among authors: engel w. Hum Mol Genet. 2002 Jul 1;11(14):1647-58. doi: 10.1093/hmg/11.14.1647. Hum Mol Genet. 2002. PMID: 12075009

6

No correlation between amount of aberrant transcript and severity of phenotype in hereditary spastic paraplegia patients with a c.1242A > G splice mutation in the SPG4 gene.

Sauter SM, Dörwald N, Engel W, Neesen J. Sauter SM, et al. Among authors: engel w. J Neurol. 2006 Jun;253(6):804-5. doi: 10.1007/s00415-005-0074-y. Epub 2005 Dec 13. J Neurol. 2006. PMID: 16362530 No abstract available.

7

Disruption of an inner arm dynein heavy chain gene results in asthenozoospermia and reduced ciliary beat frequency.

Neesen J, Kirschner R, Ochs M, Schmiedl A, Habermann B, Mueller C, Holstein AF, Nuesslein T, Adham I, Engel W. Neesen J, et al. Among authors: engel w. Hum Mol Genet. 2001 May 15;10(11):1117-28. doi: 10.1093/hmg/10.11.1117. Hum Mol Genet. 2001. PMID: 11371505

8

Identification of dynein heavy chain genes expressed in human and mouse testis: chromosomal localization of an axonemal dynein gene.

Neesen J, Koehler MR, Kirschner R, Steinlein C, Kreutzberger J, Engel W, Schmid M. Neesen J, et al. Among authors: engel w. Gene. 1997 Oct 24;200(1-2):193-202. doi: 10.1016/s0378-1119(97)00417-4. Gene. 1997. PMID: 9373155

9

Alternative splicing, chromosome assignment and subcellular localization of the testicular haploid expressed gene (THEG).

Mannan A, Lücke K, Dixkens C, Neesen J, Kämper M, Engel W, Burfeind P. Mannan A, et al. Among authors: engel w. Cytogenet Cell Genet. 2000;91(1-4):171-9. doi: 10.1159/000056840. Cytogenet Cell Genet. 2000. PMID: 11173852

10

[Genetic causes of male infertility].

Engel W, Adham IM, Nayernia K, Neesen J. Engel W, et al. Verh Dtsch Ges Pathol. 2004;88:130-5. Verh Dtsch Ges Pathol. 2004. PMID: 16892543 Review. German.

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