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Items: 1 to 20 of 86

1.

Severe early onset retinitis pigmentosa in a Moroccan patient with Heimler syndrome due to novel homozygous mutation of PEX1 gene.

Ratbi I, Jaouad IC, Elorch H, Al-Sheqaih N, Elalloussi M, Lyahyai J, Berraho A, Newman WG, Sefiani A.

Eur J Med Genet. 2016 Oct;59(10):507-11. doi: 10.1016/j.ejmg.2016.09.004. Epub 2016 Sep 12.

PMID:
27633571
2.

Non-cytotoxic concentrations of acetaminophen induced mitochondrial biogenesis and antioxidant response in HepG2 cells.

Zhang T, Zhang Q, Guo J, Yuan H, Peng H, Cui L, Yin J, Zhang L, Zhao J, Li J, White A, Carmichael PL, Westmoreland C, Peng S.

Environ Toxicol Pharmacol. 2016 Sep;46:71-9. doi: 10.1016/j.etap.2016.06.030. Epub 2016 Jul 1.

PMID:
27438896
3.

Expanding the spectrum of PEX10-related peroxisomal biogenesis disorders: slowly progressive recessive ataxia.

Renaud M, Guissart C, Mallaret M, Ferdinandusse S, Cheillan D, Drouot N, Muller J, Claustres M, Tranchant C, Anheim M, Koenig M.

J Neurol. 2016 Aug;263(8):1552-8. doi: 10.1007/s00415-016-8167-3. Epub 2016 May 26.

PMID:
27230853
4.

Promotion of mitochondrial biogenesis by necdin protects neurons against mitochondrial insults.

Hasegawa K, Yasuda T, Shiraishi C, Fujiwara K, Przedborski S, Mochizuki H, Yoshikawa K.

Nat Commun. 2016 Mar 14;7:10943. doi: 10.1038/ncomms10943.

5.

Sirt1 and the Mitochondria.

Tang BL.

Mol Cells. 2016 Feb;39(2):87-95. doi: 10.14348/molcells.2016.2318. Epub 2016 Feb 2. Review.

6.

First Japanese case of Zellweger syndrome with a mutation in PEX14.

Komatsuzaki S, Ogawa E, Shimozawa N, Sakamoto O, Haginoya K, Uematsu M, Hasegawa Y, Matsubara Y, Ohura T.

Pediatr Int. 2015 Dec;57(6):1189-92. doi: 10.1111/ped.12713. Epub 2015 Dec 2.

PMID:
26627464
7.

PEX6 is Expressed in Photoreceptor Cilia and Mutated in Deafblindness with Enamel Dysplasia and Microcephaly.

Zaki MS, Heller R, Thoenes M, Nürnberg G, Stern-Schneider G, Nürnberg P, Karnati S, Swan D, Fateen E, Nagel-Wolfrum K, Mostafa MI, Thiele H, Wolfrum U, Baumgart-Vogt E, Bolz HJ.

Hum Mutat. 2016 Feb;37(2):170-4. doi: 10.1002/humu.22934. Epub 2015 Dec 14.

PMID:
26593283
8.

Role of AAA(+)-proteins in peroxisome biogenesis and function.

Grimm I, Erdmann R, Girzalsky W.

Biochim Biophys Acta. 2016 May;1863(5):828-37. doi: 10.1016/j.bbamcr.2015.10.001. Epub 2015 Oct 8. Review.

PMID:
26453804
9.

Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6.

Ratbi I, Falkenberg KD, Sommen M, Al-Sheqaih N, Guaoua S, Vandeweyer G, Urquhart JE, Chandler KE, Williams SG, Roberts NA, El Alloussi M, Black GC, Ferdinandusse S, Ramdi H, Heimler A, Fryer A, Lynch SA, Cooper N, Ong KR, Smith CE, Inglehearn CF, Mighell AJ, Elcock C, Poulter JA, Tischkowitz M, Davies SJ, Sefiani A, Mironov AA, Newman WG, Waterham HR, Van Camp G.

Am J Hum Genet. 2015 Oct 1;97(4):535-45. doi: 10.1016/j.ajhg.2015.08.011. Epub 2015 Sep 17.

10.

Epigenetic Modifications in the Biology of Nonalcoholic Fatty Liver Disease: The Role of DNA Hydroxymethylation and TET Proteins.

Pirola CJ, Scian R, Gianotti TF, Dopazo H, Rohr C, Martino JS, Castaño GO, Sookoian S.

Medicine (Baltimore). 2015 Sep;94(36):e1480. doi: 10.1097/MD.0000000000001480.

11.

Induced pluripotent stem cell models of Zellweger spectrum disorder show impaired peroxisome assembly and cell type-specific lipid abnormalities.

Wang XM, Yik WY, Zhang P, Lu W, Huang N, Kim BR, Shibata D, Zitting M, Chow RH, Moser AB, Steinberg SJ, Hacia JG.

Stem Cell Res Ther. 2015 Aug 29;6:158. doi: 10.1186/s13287-015-0149-3.

12.

Implications of critical PPARγ2, ADIPOQ and FTO gene polymorphisms in type 2 diabetes and obesity-mediated susceptibility to type 2 diabetes in an Indian population.

Phani NM, Vohra M, Rajesh S, Adhikari P, Nagri SK, D'Souza SC, Satyamoorthy K, Rai PS.

Mol Genet Genomics. 2016 Feb;291(1):193-204. doi: 10.1007/s00438-015-1097-4. Epub 2015 Aug 5.

PMID:
26243686
13.

Cilostazol attenuates murine hepatic ischemia and reperfusion injury via heme oxygenase-dependent activation of mitochondrial biogenesis.

Joe Y, Zheng M, Kim HJ, Uddin MJ, Kim SK, Chen Y, Park J, Cho GJ, Ryter SW, Chung HT.

Am J Physiol Gastrointest Liver Physiol. 2015 Jul 1;309(1):G21-9. doi: 10.1152/ajpgi.00307.2014. Epub 2015 May 7.

14.

Compromised peroxisomes in idiopathic pulmonary fibrosis, a vicious cycle inducing a higher fibrotic response via TGF-β signaling.

Oruqaj G, Karnati S, Vijayan V, Kotarkonda LK, Boateng E, Zhang W, Ruppert C, Günther A, Shi W, Baumgart-Vogt E.

Proc Natl Acad Sci U S A. 2015 Apr 21;112(16):E2048-57. doi: 10.1073/pnas.1415111112. Epub 2015 Apr 6.

15.

Activation of peroxisome proliferator-activated receptor α induces lysosomal biogenesis in brain cells: implications for lysosomal storage disorders.

Ghosh A, Jana M, Modi K, Gonzalez FJ, Sims KB, Berry-Kravis E, Pahan K.

J Biol Chem. 2015 Apr 17;290(16):10309-24. doi: 10.1074/jbc.M114.610659. Epub 2015 Mar 6.

16.

Mutual exacerbation of peroxisome proliferator-activated receptor γ coactivator 1α deregulation and α-synuclein oligomerization.

Eschbach J, von Einem B, Müller K, Bayer H, Scheffold A, Morrison BE, Rudolph KL, Thal DR, Witting A, Weydt P, Otto M, Fauler M, Liss B, McLean PJ, Spada AR, Ludolph AC, Weishaupt JH, Danzer KM.

Ann Neurol. 2015 Jan;77(1):15-32. doi: 10.1002/ana.24294. Epub 2014 Dec 19.

17.

Peripheral nervous system defects in a mouse model for peroxisomal biogenesis disorders.

Hanson MG, Fregoso VL, Vrana JD, Tucker CL, Niswander LA.

Dev Biol. 2014 Nov 1;395(1):84-95. doi: 10.1016/j.ydbio.2014.08.026. Epub 2014 Aug 28.

18.

AAA peroxins and their recruiter Pex26p modulate the interactions of peroxins involved in peroxisomal protein import.

Tamura S, Matsumoto N, Takeba R, Fujiki Y.

J Biol Chem. 2014 Aug 29;289(35):24336-46. doi: 10.1074/jbc.M114.588038. Epub 2014 Jul 11.

19.

Effect of high-intensity exercise on aged mouse brain mitochondria, neurogenesis, and inflammation.

E L, Burns JM, Swerdlow RH.

Neurobiol Aging. 2014 Nov;35(11):2574-83. doi: 10.1016/j.neurobiolaging.2014.05.033. Epub 2014 Jun 10.

20.

The stem cell factor/Kit signalling pathway regulates mitochondrial function and energy expenditure.

Huang Z, Ruan HB, Xian L, Chen W, Jiang S, Song A, Wang Q, Shi P, Gu X, Gao X.

Nat Commun. 2014 Jul 7;5:4282. doi: 10.1038/ncomms5282.

PMID:
24999927

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