Neesen J - Search Results

1

Asthenozoospermia in mice with targeted deletion of the sperm mitochondrion-associated cysteine-rich protein (Smcp) gene.

Nayernia K, Adham IM, Burkhardt-Göttges E, Neesen J, Rieche M, Wolf S, Sancken U, Kleene K, Engel W. Nayernia K, et al. Among authors: neesen j. Mol Cell Biol. 2002 May;22(9):3046-52. doi: 10.1128/MCB.22.9.3046-3052.2002. Mol Cell Biol. 2002. PMID: 11940662 Free PMC article.

2

Early embryonic lethality in gene trap mice with disruption of the Arfgef2 gene.

Grzmil P, Enkhbaatar Z, Gundsambuu B, Oidovsambuu O, Yalcin S, Wolf S, Engel W, Neesen J. Grzmil P, et al. Among authors: neesen j. Int J Dev Biol. 2010;54(8-9):1259-66. doi: 10.1387/ijdb.092959pg. Int J Dev Biol. 2010. PMID: 20857375 Free article.

3

[Genetic causes of male infertility].

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

4

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. Hum Mol Genet. 2001 May 15;10(11):1117-28. doi: 10.1093/hmg/10.11.1117. Hum Mol Genet. 2001. PMID: 11371505

5

Human cyritestin genes (CYRN1 and CYRN2) are non-functional.

Grzmil P, Kim Y, Shamsadin R, Neesen J, Adham IM, Heinlein UA, Schwarzer UJ, Engel W. Grzmil P, et al. Among authors: neesen j. Biochem J. 2001 Jul 15;357(Pt 2):551-6. doi: 10.1042/0264-6021:3570551. Biochem J. 2001. PMID: 11439107 Free PMC article.

6

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: neesen j. Cytogenet Cell Genet. 2000;91(1-4):171-9. doi: 10.1159/000056840. Cytogenet Cell Genet. 2000. PMID: 11173852

7

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: neesen j. Hum Mutat. 2004 Jan;23(1):98. doi: 10.1002/humu.9205. Hum Mutat. 2004. PMID: 14695538

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. Gene. 1997 Oct 24;200(1-2):193-202. doi: 10.1016/s0378-1119(97)00417-4. Gene. 1997. PMID: 9373155

9

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: neesen j. Hum Mutat. 2002 Aug;20(2):127-32. doi: 10.1002/humu.10105. Hum Mutat. 2002. PMID: 12124993

10

Tep22, a novel testicular expressed gene, is involved in the biogenesis of the acrosome and the midpiece of the sperm tail.

Neesen J, Hartwich T, Brandhorst G, Aumüller G, Gläser B, Burfeind P, Mendoza-Lujambio I. Neesen J, et al. Biochem Biophys Res Commun. 2002 Oct 4;297(4):737-48. doi: 10.1016/s0006-291x(02)02265-9. Biochem Biophys Res Commun. 2002. PMID: 12359214

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