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Items: 1 to 50 of 95

1.

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.

Aging Cell. 2015 Oct;14(5):887-95. doi: 10.1111/acel.12368. Epub 2015 Jun 26.

2.

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.

Hum Mol Genet. 2015 Sep 1;24(17):4829-47. doi: 10.1093/hmg/ddv207. Epub 2015 Jun 3.

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.

Am J Physiol Renal Physiol. 2013 Oct 15;305(8):F1228-38. doi: 10.1152/ajprenal.00143.2013. Epub 2013 Aug 7.

5.

The petrology and geochemistry of a metabasite belt along the southern margin of Alaska.

Bruand E, Gasser D, Bonnand P, Stuewe K.

Lithos. 2011 Nov;127(1-2):282-297.

6.

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.

Mitochondrion. 2012 Mar;12(2):248-57. doi: 10.1016/j.mito.2011.09.011. Epub 2011 Oct 1.

7.

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.

EMBO Mol Med. 2011 Jul;3(7):410-27. doi: 10.1002/emmm.201100149. Epub 2011 Jun 8.

8.

Cross-platform expression microarray performance in a mouse model of mitochondrial disease therapy.

Zhang Z, Gasser DL, Rappaport EF, Falk MJ.

Mol Genet Metab. 2010 Mar;99(3):309-18. doi: 10.1016/j.ymgme.2009.10.179. Epub 2009 Oct 30.

9.

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.

Cell. 2009 Nov 25;139(5):891-906. doi: 10.1016/j.cell.2009.10.027.

10.

Coenzyme Q10 supplementation rescues renal disease in Pdss2kd/kd mice with mutations in prenyl diphosphate synthase subunit 2.

Saiki R, Lunceford AL, Shi Y, Marbois B, King R, Pachuski J, Kawamukai M, Gasser DL, Clarke CF.

Am J Physiol Renal Physiol. 2008 Nov;295(5):F1535-44. doi: 10.1152/ajprenal.90445.2008. Epub 2008 Sep 10.

11.

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.

PLoS Genet. 2008 Apr 25;4(4):e1000061. doi: 10.1371/journal.pgen.1000061.

12.

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.

J Autoimmun. 2006 Feb;26(1):1-6. Epub 2005 Dec 6.

13.

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.

Am J Nephrol. 2005 Nov-Dec;25(6):604-10. Epub 2005 Nov 9.

14.

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

Barisoni L, Madaio MP, Eraso M, Gasser DL, Nelson PJ.

J Am Soc Nephrol. 2005 Oct;16(10):2847-51. Epub 2005 Aug 24.

15.

Sepsis up-regulates the expression of connexin 40 in rat aortic endothelium.

Rignault S, Haefliger JA, Gasser D, Markert M, Nicod P, Liaudet L, Waeber B, Feihl F.

Crit Care Med. 2005 Jun;33(6):1302-10.

PMID:
15942348
16.

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.

Kidney Int. 2004 Jul;66(1):20-8.

17.

Noise control: a nursing team's approach to sleep promotion.

Cmiel CA, Karr DM, Gasser DM, Oliphant LM, Neveau AJ.

Am J Nurs. 2004 Feb;104(2):40-8;quiz 48-9. Review. No abstract available.

PMID:
14767379
18.

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

Hancock WW, Tsai TL, Madaio MP, Gasser DL.

J Immunol. 2003 Sep 15;171(6):2778-81.

19.

Cardiovascular effects of fentanyl in conscious rats.

Baechtold F, Cavadas C, Gasser D, Markert M, Grouzmann E, Peterson KL, Waeber B, Feihl F.

Pflugers Arch. 2001 Oct;443(1):155-62.

PMID:
11692279
20.

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.

Biochem Genet. 2000 Oct;38(9-10):337-40. No abstract available.

PMID:
11129527
21.

Localization of the mouse kidney disease (kd) gene to a YAC/BAC contig on Chromosome 10.

Dell KM, Li YX, Peng M, Neilson EG, Gasser DL.

Mamm Genome. 2000 Nov;11(11):967-71.

PMID:
11063251
22.

Opitz G/BBB syndrome in Xp22: mutations in the MID1 gene cluster in the carboxy-terminal domain.

Gaudenz K, Roessler E, Quaderi N, Franco B, Feldman G, Gasser DL, Wittwer B, Horst J, Montini E, Opitz JM, Ballabio A, Muenke M.

Am J Hum Genet. 1998 Sep;63(3):703-10. Erratum in: Am J Hum Genet 1998 Nov;63(5):1571.

23.

A gene belonging to the Sm family of snRNP core proteins maps within the mouse MHC.

Bedian V, Adams T, Geiger EA, Bailey LC, Gasser DL.

Immunogenetics. 1997;46(5):427-30. No abstract available.

PMID:
9271633
24.

Nonsyndromic cleft lip with or without cleft palate: erratum.

Amos C, Stein J, Mulliken JB, Stal S, Malcolm S, Winter R, Blanton SH, Seemanova E, Gasser DL, Hecht JT.

Am J Hum Genet. 1996 Sep;59(3):744. No abstract available.

25.

Nonsyndromic cleft lip with or without cleft palate: new BCL3 information.

Amos C, Gasser D, Hecht JT.

Am J Hum Genet. 1996 Sep;59(3):743-4. No abstract available. Erratum in: Am J Hum Genet 1997 Apr;60(4):1012.

26.

[What is your diagnosis? Ebstein Anomaly with additionally hemodynamically relevant left-right shunt in type II atrial septal defect].

Gasser D, Erne P.

Praxis (Bern 1994). 1996 Apr 2;85(14):427-8. German. No abstract available.

PMID:
8657977
27.

Exclusion of linkage between cleft lip with or without cleft palate and markers on chromosomes 4 and 6.

Blanton SH, Crowder E, Malcolm S, Winter R, Gasser DL, Stal S, Mulliken J, Hecht JT.

Am J Hum Genet. 1996 Jan;58(1):239-41. No abstract available.

28.

Genetic polymorphism of the human tumor necrosis factor region in insulin-dependent diabetes mellitus. Linkage disequilibrium of TNFab microsatellite alleles with HLA haplotypes.

Monos DS, Kamoun M, Udalova IA, Csanky E, Cizman B, Turetskaya RL, Smirnova JB, Zharkov VG, Gasser D, Zmijewski CM, et al.

Hum Immunol. 1995 Oct;44(2):70-9.

PMID:
8847231
29.

Nonsyndromic cleft lip with or without cleft palate: evidence of linkage to BCL3 in 17 multigenerational families.

Stein J, Mulliken JB, Stal S, Gasser DL, Malcolm S, Winter R, Blanton SH, Amos C, Seemanova E, Hecht JT.

Am J Hum Genet. 1995 Aug;57(2):257-72. Erratum in: Am J Hum Genet 1996 Sep;59(3):744.

31.

A gene for cleidocranial dysplasia maps to the short arm of chromosome 6.

Feldman GJ, Robin NH, Brueton LA, Robertson E, Thompson EM, Siegel-Bartelt J, Gasser DL, Bailey LC, Zackai EH, Muenke M.

Am J Hum Genet. 1995 Apr;56(4):938-43.

32.

Evidence, from family studies, for linkage disequilibrium between TGFA and a gene for nonsyndromic cleft lip with or without cleft palate.

Feng H, Sassani R, Bartlett SP, Lee A, Hecht JT, Malcolm S, Winter RM, Vintiner GM, Buetow KH, Gasser DL.

Am J Hum Genet. 1994 Nov;55(5):932-6.

33.

P1 and cosmid clones define the organization of 280 kb of the mouse H-2 complex containing the Cps-1 and Hsp70 loci.

Gasser DL, Sternberg NL, Pierce JC, Goldner-Sauve A, Feng H, Haq AK, Spies T, Hunt C, Buetow KH, Chaplin DD.

Immunogenetics. 1994;39(1):48-55.

PMID:
7993390
34.

Chromosomal localization of five murine HSP70 gene family members: Hsp70-1, Hsp70-2, Hsp70-3, Hsc70t, and Grp78.

Hunt CR, Gasser DL, Chaplin DD, Pierce JC, Kozak CA.

Genomics. 1993 Apr;16(1):193-8.

PMID:
8486356
35.

Association between alleles of the transforming growth factor-alpha locus and the occurrence of cleft lip.

Sassani R, Bartlett SP, Feng H, Goldner-Sauve A, Haq AK, Buetow KH, Gasser DL.

Am J Med Genet. 1993 Mar 1;45(5):565-9.

PMID:
8096116
36.

Palate teratogenicity and embryotoxicity of cyclosporin A in mice.

Gasser DL, Yang P, Buetow KH.

J Craniofac Genet Dev Biol. 1992 Jul-Sep;12(3):155-8.

PMID:
1517394
37.
38.

Chromosome assignments of the genes for glucocorticoid receptor, myelin basic protein, leukocyte common antigen, and TRPM2 in the rat.

Goldner-Sauvé A, Szpirer C, Szpirer J, Levan G, Gasser DL.

Biochem Genet. 1991 Jun;29(5-6):275-86.

PMID:
1722973
39.

Alloreactive lymphocytes from T cell receptor (beta-chain) transgenic mice do not mediate a graft-versus-host reaction.

Rimm IJ, Ghayur T, Gasser DL, Rosenkrantz K, Burakoff SJ, Seidman JG, Ferrara JL.

J Immunol. 1991 Feb 15;146(4):1130-3.

PMID:
1825104
40.

Genetic control of resistance to clinical EAE accompanied by histological symptoms.

Gasser DL, Goldner-Sauvé A, Hickey WF.

Immunogenetics. 1990;31(5-6):377-82.

PMID:
2370083
42.
43.

DNA polymorphisms defined by the Tu108 probe map to the Tla region of mouse chromosome 17.

Gasser DL, Yadvish K, Feinstein P, Passmore HC.

Biochem Genet. 1988 Aug;26(7-8):475-80. No abstract available.

PMID:
2906539
44.

A monoclonal antibody specific for the Yc subunit of rat liver glutathione S-transferase B.

Matsumoto K, Matsuhashi A, Gasser DL, Litwack G.

Cancer Res. 1986 Oct;46(10):5259-63.

45.

Detection of a serum class I molecule in rat with anti-rat liver beta-2-microglobulin.

Matsumoto K, Natori T, Agui T, Tsutimoto S, Matsuhashi A, Gasser DL.

Biochem Genet. 1986 Feb;24(1-2):93-102.

PMID:
3516141
46.

Polymorphous endocytotic organelles in the receptor-mediated endocytosis of gold-labelled alpha 2-macroglobulin complexes by human fibroblasts.

Van der Schueren B, Gasser D, Marynen P, Van Leuven F, David G, Cassiman JJ, Van den Berghe H.

J Cell Sci. 1985 Apr;75:411-21.

47.

A new beta-2 microglobulin allele in mice defined by DNA sequencing.

Gasser DL, Klein KA, Choi E, Seidman JG.

Immunogenetics. 1985;22(4):413-6. No abstract available.

PMID:
3902633
48.

Characterization of a monoclonal antibody to ligandin.

Oxenham EA, Matsumoto K, Gasser DL, Litwack G.

Cancer Res. 1984 Feb;44(2):772-6.

49.

Mapping of the genes for tubular basement membrane antigen and a submaxillary gland protease in the rat.

Matsumoto K, McCafferty E, Neilson EG, Gasser DL.

Immunogenetics. 1984;20(2):117-23.

PMID:
6381295
50.

Characterization of RT1gv1: a new rat MHC haplotype isolated from the wild.

Begovich AB, Ziebur J, Gasser DL.

Immunogenetics. 1984;20(2):205-9. No abstract available.

PMID:
6236148

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