Gasser DL - Search Results

1

Matrix crosslinking forces tumor progression by enhancing integrin signaling.

Levental KR, Yu H, Kass L, Lakins JN, Egeblad M, Erler JT, Fong SF, Csiszar K, Giaccia A, Weninger W, Yamauchi M, Gasser DL, Weaver VM. Levental KR, et al. Among authors: gasser dl. Cell. 2009 Nov 25;139(5):891-906. doi: 10.1016/j.cell.2009.10.027. Cell. 2009. PMID: 19931152 Free PMC article.

2

Coenzyme Q10 restores oocyte mitochondrial function and fertility during reproductive aging.

Ben-Meir A, Burstein E, Borrego-Alvarez A, Chong J, Wong E, Yavorska T, Naranian T, Chi M, Wang Y, Bentov Y, Alexis J, Meriano J, Sung HK, Gasser DL, Moley KH, Hekimi S, Casper RF, Jurisicova A. Ben-Meir A, et al. Among authors: gasser dl. Aging Cell. 2015 Oct;14(5):887-95. doi: 10.1111/acel.12368. Epub 2015 Jun 26. Aging Cell. 2015. PMID: 26111777 Free PMC article.

3

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.

4

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.

5

Parkinson's disease-like neuromuscular defects occur in prenyl diphosphate synthase subunit 2 (Pdss2) mutant mice.

Ziegler CG, Peng M, Falk MJ, Polyak E, Tsika E, Ischiropoulos H, Bakalar D, Blendy JA, Gasser DL. Ziegler CG, et al. Among authors: gasser dl. Mitochondrion. 2012 Mar;12(2):248-57. doi: 10.1016/j.mito.2011.09.011. Epub 2011 Oct 1. Mitochondrion. 2012. PMID: 21983691 Free PMC article.

6

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.

7

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

8

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.

9

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.

10

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.

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