Heimann P - Search Results

1

Pathoproteomics of testicular tissue deficient in the GARP component VPS54: the wobbler mouse model of globozoospermia.

Jockusch H, Holland A, Staunton L, Schmitt-John T, Heimann P, Dowling P, Ohlendieck K. Jockusch H, et al. Among authors: heimann p. Proteomics. 2014 Apr;14(7-8):839-52. doi: 10.1002/pmic.201300189. Epub 2013 Nov 13. Proteomics. 2014. PMID: 24115398

2

Mutation of Vps54 causes motor neuron disease and defective spermiogenesis in the wobbler mouse.

Schmitt-John T, Drepper C, Mussmann A, Hahn P, Kuhlmann M, Thiel C, Hafner M, Lengeling A, Heimann P, Jones JM, Meisler MH, Jockusch H. Schmitt-John T, et al. Among authors: heimann p. Nat Genet. 2005 Nov;37(11):1213-5. doi: 10.1038/ng1661. Epub 2005 Oct 23. Nat Genet. 2005. PMID: 16244655

3

Defect of sperm assembly in a neurological mutant of the mouse, wobbler (WR).

Heimann P, Laage S, Jockusch H. Heimann P, et al. Differentiation. 1991 Jul;47(2):77-83. doi: 10.1111/j.1432-0436.1991.tb00225.x. Differentiation. 1991. PMID: 1955109

4

Loss of vps54 function leads to vesicle traffic impairment, protein mis-sorting and embryonic lethality.

Karlsson P, Droce A, Moser JM, Cuhlmann S, Padilla CO, Heimann P, Bartsch JW, Füchtbauer A, Füchtbauer EM, Schmitt-John T. Karlsson P, et al. Among authors: heimann p. Int J Mol Sci. 2013 May 24;14(6):10908-25. doi: 10.3390/ijms140610908. Int J Mol Sci. 2013. PMID: 23708095 Free PMC article.

5

Spinal muscular atrophy gene wobbler of the mouse: evidence from chimeric spinal cord and testis for cell-autonomous function.

Augustin M, Heimann P, Rathke S, Jockusch H. Augustin M, et al. Among authors: heimann p. Dev Dyn. 1997 Jul;209(3):286-95. doi: 10.1002/(SICI)1097-0177(199707)209:3<286::AID-AJA4>3.0.CO;2-E. Dev Dyn. 1997. PMID: 9215643 Free article.

6

Acute pathophysiological effects of muscle-expressed Dp71 transgene on normal and dystrophic mouse muscle.

Wieneke S, Heimann P, Leibovitz S, Nudel U, Jockusch H. Wieneke S, et al. Among authors: heimann p. J Appl Physiol (1985). 2003 Nov;95(5):1861-6. doi: 10.1152/japplphysiol.00326.2003. J Appl Physiol (1985). 2003. PMID: 14555666 Free article.

7

Elimination by necrosis, not apoptosis, of embryonic extraocular muscles in the muscular dysgenesis mutant of the mouse.

Heimann P, Kuschel T, Jockusch H. Heimann P, et al. Cell Tissue Res. 2004 Feb;315(2):243-7. doi: 10.1007/s00441-003-0831-0. Epub 2003 Nov 14. Cell Tissue Res. 2004. PMID: 14618389

8

Progressive loss of striatal neurons causes motor dysfunction in MND2 mutant mice and is not prevented by Bcl-2.

Rathke-Hartlieb S, Schlomann U, Heimann P, Meisler MH, Jockusch H, Bartsch JW. Rathke-Hartlieb S, et al. Among authors: heimann p. Exp Neurol. 2002 May;175(1):87-97. doi: 10.1006/exnr.2002.7868. Exp Neurol. 2002. PMID: 12009762

9

Endosomal accumulation of APP in wobbler motor neurons reflects impaired vesicle trafficking: implications for human motor neuron disease.

Palmisano R, Golfi P, Heimann P, Shaw C, Troakes C, Schmitt-John T, Bartsch JW. Palmisano R, et al. Among authors: heimann p. BMC Neurosci. 2011 Mar 7;12:24. doi: 10.1186/1471-2202-12-24. BMC Neurosci. 2011. PMID: 21385376 Free PMC article.

10

Dolichos biflorus agglutinin receptors in mouse muscle. I. Developmental expression in relation to synaptic acetylcholinesterase and to neuromuscular disease.

Kaupmann K, Heimann P, Jockusch H. Kaupmann K, et al. Among authors: heimann p. Eur J Cell Biol. 1988 Aug;46(3):411-8. Eur J Cell Biol. 1988. PMID: 3181163

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