Neesen J - Search Results

1

DNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein arm.

Loges NT, Olbrich H, Fenske L, Mussaffi H, Horvath J, Fliegauf M, Kuhl H, Baktai G, Peterffy E, Chodhari R, Chung EM, Rutman A, O'Callaghan C, Blau H, Tiszlavicz L, Voelkel K, Witt M, Zietkiewicz E, Neesen J, Reinhardt R, Mitchison HM, Omran H. Loges NT, et al. Among authors: neesen j. Am J Hum Genet. 2008 Nov;83(5):547-58. doi: 10.1016/j.ajhg.2008.10.001. Epub 2008 Oct 23. Am J Hum Genet. 2008. PMID: 18950741 Free PMC article.

2

Identification and analysis of axonemal dynein light chain 1 in primary ciliary dyskinesia patients.

Horváth J, Fliegauf M, Olbrich H, Kispert A, King SM, Mitchison H, Zariwala MA, Knowles MR, Sudbrak R, Fekete G, Neesen J, Reinhardt R, Omran H. Horváth J, et al. Among authors: neesen j. Am J Respir Cell Mol Biol. 2005 Jul;33(1):41-7. doi: 10.1165/rcmb.2004-0335OC. Epub 2005 Apr 21. Am J Respir Cell Mol Biol. 2005. PMID: 15845866

3

Expansion of mutation spectrum, determination of mutation cluster regions and predictive structural classification of SPAST mutations in hereditary spastic paraplegia.

Shoukier M, Neesen J, Sauter SM, Argyriou L, Doerwald N, Pantakani DV, Mannan AU. Shoukier M, et al. Among authors: neesen j. Eur J Hum Genet. 2009 Feb;17(2):187-94. doi: 10.1038/ejhg.2008.147. Epub 2008 Aug 13. Eur J Hum Genet. 2009. PMID: 18701882 Free PMC article.

4

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: neesen j. Hum Mol Genet. 2002 Jul 1;11(14):1647-58. doi: 10.1093/hmg/11.14.1647. Hum Mol Genet. 2002. PMID: 12075009

5

The murine Dnali1 gene encodes a flagellar protein that interacts with the cytoplasmic dynein heavy chain 1.

Rashid S, Breckle R, Hupe M, Geisler S, Doerwald N, Neesen J. Rashid S, et al. Among authors: neesen j. Mol Reprod Dev. 2006 Jun;73(6):784-94. doi: 10.1002/mrd.20475. Mol Reprod Dev. 2006. PMID: 16496424

6

Ultrastructural changes in the cilia of experimental mice.

Ebsen M, Morgenroth K, Neesen J. Ebsen M, et al. Among authors: neesen j. Bull Exp Biol Med. 2004 Jun;137(6):619-21. doi: 10.1023/b:bebm.0000042727.67636.b3. Bull Exp Biol Med. 2004. PMID: 15455100

7

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: neesen j. 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.

8

Disruption of the murine dynein light chain gene Tcte3-3 results in asthenozoospermia.

Rashid S, Grzmil P, Drenckhahn JD, Meinhardt A, Adham I, Engel W, Neesen J. Rashid S, et al. Among authors: neesen j. Reproduction. 2010 Jan;139(1):99-111. doi: 10.1530/REP-09-0243. Reproduction. 2010. PMID: 19778998

9

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: neesen j. Neurogenetics. 2006 May;7(2):93-103. doi: 10.1007/s10048-006-0034-4. Epub 2006 Apr 7. Neurogenetics. 2006. PMID: 16602018

10

Ccdc181 is a microtubule-binding protein that interacts with Hook1 in haploid male germ cells and localizes to the sperm tail and motile cilia.

Schwarz T, Prieler B, Schmid JA, Grzmil P, Neesen J. Schwarz T, et al. Among authors: neesen j. Eur J Cell Biol. 2017 May;96(3):276-288. doi: 10.1016/j.ejcb.2017.02.003. Epub 2017 Feb 20. Eur J Cell Biol. 2017. PMID: 28283191 Free PMC article.

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