Gasser DL - Search Results

1

The kd/kd mouse is a model of collapsing glomerulopathy.

Barisoni L, Madaio MP, Eraso M, Gasser DL, Nelson PJ. Barisoni L, et al. Among authors: gasser dl. J Am Soc Nephrol. 2005 Oct;16(10):2847-51. doi: 10.1681/ASN.2005050494. Epub 2005 Aug 24. J Am Soc Nephrol. 2005. PMID: 16120817 Free PMC article.

2

Glomerular and tubular epithelial defects in kd/kd mice lead to progressive renal failure.

Madaio MP, Ahima RS, Meade R, Rader DJ, Mendoza A, Peng M, Tomaszewski JE, Hancock WW, Gasser DL. Madaio MP, et al. Among authors: gasser dl. Am J Nephrol. 2005 Nov-Dec;25(6):604-10. doi: 10.1159/000089709. Epub 2005 Nov 9. Am J Nephrol. 2005. PMID: 16282678 Free PMC article.

3

Mutant prenyltransferase-like mitochondrial protein (PLMP) and mitochondrial abnormalities in kd/kd mice.

Peng M, Jarett L, Meade R, Madaio MP, Hancock WW, George AL Jr, Neilson EG, Gasser DL. Peng M, et al. Among authors: gasser dl. Kidney Int. 2004 Jul;66(1):20-8. doi: 10.1111/j.1523-1755.2004.00702.x. Kidney Int. 2004. PMID: 15200409 Free PMC article.

4

The mitochondrial and kidney disease phenotypes of kd/kd mice under germfree conditions.

Hallman TM, Peng M, Meade R, Hancock WW, Madaio MP, Gasser DL. Hallman TM, et al. Among authors: gasser dl. J Autoimmun. 2006 Feb;26(1):1-6. doi: 10.1016/j.jaut.2005.10.006. Epub 2005 Dec 6. J Autoimmun. 2006. PMID: 16337774 Free PMC article.

5

Cutting Edge: Multiple autoimmune pathways in kd/kd mice.

Hancock WW, Tsai TL, Madaio MP, Gasser DL. Hancock WW, et al. Among authors: gasser dl. J Immunol. 2003 Sep 15;171(6):2778-81. doi: 10.4049/jimmunol.171.6.2778. J Immunol. 2003. PMID: 12960297

6

Mapping of mouse alpha 1(XIII) collagen to chromosome 10 and its exclusion as a kd candidate gene.

Mrug M, Stockwin J, Wüthrich RP, Gasser DL, Guay-Woodford LM. Mrug M, et al. Among authors: gasser dl. Biochem Genet. 2000 Oct;38(9-10):337-40. doi: 10.1023/a:1002013218535. Biochem Genet. 2000. PMID: 11129527 No abstract available.

7

Primary coenzyme Q deficiency in Pdss2 mutant mice causes isolated renal disease.

Peng M, Falk MJ, Haase VH, King R, Polyak E, Selak M, Yudkoff M, Hancock WW, Meade R, Saiki R, Lunceford AL, Clarke CF, Gasser DL. Peng M, et al. Among authors: gasser dl. PLoS Genet. 2008 Apr 25;4(4):e1000061. doi: 10.1371/journal.pgen.1000061. PLoS Genet. 2008. PMID: 18437205 Free PMC article.

8

Probucol ameliorates renal and metabolic sequelae of primary CoQ deficiency in Pdss2 mutant mice.

Falk MJ, Polyak E, Zhang Z, Peng M, King R, Maltzman JS, Okwuego E, Horyn O, Nakamaru-Ogiso E, Ostrovsky J, Xie LX, Chen JY, Marbois B, Nissim I, Clarke CF, Gasser DL. Falk MJ, et al. Among authors: gasser dl. EMBO Mol Med. 2011 Jul;3(7):410-27. doi: 10.1002/emmm.201100149. Epub 2011 Jun 8. EMBO Mol Med. 2011. PMID: 21567994 Free PMC article.

9

Focal segmental glomerulosclerosis is associated with a PDSS2 haplotype and, independently, with a decreased content of coenzyme Q10.

Gasser DL, Winkler CA, Peng M, An P, McKenzie LM, Kirk GD, Shi Y, Xie LX, Marbois BN, Clarke CF, Kopp JB. Gasser DL, et al. Am J Physiol Renal Physiol. 2013 Oct 15;305(8):F1228-38. doi: 10.1152/ajprenal.00143.2013. Epub 2013 Aug 7. Am J Physiol Renal Physiol. 2013. PMID: 23926186 Free PMC article.

10

Inhibiting cytosolic translation and autophagy improves health in mitochondrial disease.

Peng M, Ostrovsky J, Kwon YJ, Polyak E, Licata J, Tsukikawa M, Marty E, Thomas J, Felix CA, Xiao R, Zhang Z, Gasser DL, Argon Y, Falk MJ. Peng M, et al. Among authors: gasser dl. Hum Mol Genet. 2015 Sep 1;24(17):4829-47. doi: 10.1093/hmg/ddv207. Epub 2015 Jun 3. Hum Mol Genet. 2015. PMID: 26041819 Free PMC article.

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