Schmitt-John T - 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. 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. Nat Genet. 2005 Nov;37(11):1213-5. doi: 10.1038/ng1661. Epub 2005 Oct 23. Nat Genet. 2005. PMID: 16244655

3

Intricate effects of primary motor neuronopathy on contractile proteins and metabolic muscle enzymes as revealed by label-free mass spectrometry.

Holland A, Schmitt-John T, Dowling P, Meleady P, Henry M, Clynes M, Ohlendieck K. Holland A, et al. Among authors: schmitt john t. Biosci Rep. 2014 Jul 1;34(4):e00119. doi: 10.1042/BSR20140029. Biosci Rep. 2014. PMID: 24895011 Free PMC article.

4

Genetic modifiers that aggravate the neurological phenotype of the wobbler mouse.

Ulbrich M, Schmidt VC, Ronsiek M, Mussmann A, Bartsch JW, Augustin M, Jockusch H, Schmitt-John T. Ulbrich M, et al. Neuroreport. 2002 Mar 25;13(4):535-9. doi: 10.1097/00001756-200203250-00035. Neuroreport. 2002. PMID: 11930176

5

Comparative transcription map of the wobbler critical region on mouse chromosome 11 and the homologous region on human chromosome 2p13-14.

Fuchs S, Resch K, Thiel C, Ulbrich M, Platzer M, Jockusch H, Schmitt-John T. Fuchs S, et al. BMC Genet. 2002 Aug 13;3:14. doi: 10.1186/1471-2156-3-14. Epub 2002 Aug 13. BMC Genet. 2002. PMID: 12174196 Free PMC article.

6

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. 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.

7

Spatiotemporal progression of neurodegeneration and glia activation in the wobbler neuropathy of the mouse.

Rathke-Hartlieb S, Schmidt VC, Jockusch H, Schmitt-John T, Bartsch JW. Rathke-Hartlieb S, et al. Neuroreport. 1999 Nov 8;10(16):3411-6. doi: 10.1097/00001756-199911080-00028. Neuroreport. 1999. PMID: 10599854

8

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. BMC Neurosci. 2011 Mar 7;12:24. doi: 10.1186/1471-2202-12-24. BMC Neurosci. 2011. PMID: 21385376 Free PMC article.

9

Assignment of homologous genes, Peli1/PELI1 and Peli2/PELI2, for the Pelle adaptor protein Pellino to mouse chromosomes 11 and 14 and human chromosomes 2p13.3 and 14q21, respectively, by physical and radiation hybrid mapping.

Resch K, Jockusch H, Schmitt-John T. Resch K, et al. Cytogenet Cell Genet. 2001;92(1-2):172-4. doi: 10.1159/000056895. Cytogenet Cell Genet. 2001. PMID: 11306823 No abstract available.

10

Integrated radiation hybrid map of human chromosome 2p13: possible involvement of dynactin in neuromuscular diseases.

Korthaus D, Wedemeyer N, Lengeling A, Ronsiek M, Jockusch H, Schmitt-John T. Korthaus D, et al. Genomics. 1997 Jul 15;43(2):242-4. doi: 10.1006/geno.1997.4789. Genomics. 1997. PMID: 9244444

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