321 related articles for article (PubMed ID: 34351705)
1. The biochemical basis of mitochondrial dysfunction in Zellweger Spectrum Disorder.
Nuebel E; Morgan JT; Fogarty S; Winter JM; Lettlova S; Berg JA; Chen YC; Kidwell CU; Maschek JA; Clowers KJ; Argyriou C; Chen L; Wittig I; Cox JE; Roh-Johnson M; Braverman N; Bonkowsky J; Gygi SP; Rutter J
EMBO Rep; 2021 Oct; 22(10):e51991. PubMed ID: 34351705
[TBL] [Abstract][Full Text] [Related]
2. Mitochondria as emergency landing for abandoned peroxins.
Vögtle FN; Meisinger C
EMBO Rep; 2021 Oct; 22(10):e53790. PubMed ID: 34414648
[TBL] [Abstract][Full Text] [Related]
3. Hypomorphic mutation of PEX3 with peroxisomal mosaicism reveals the oscillating nature of peroxisome biogenesis coupled with differential metabolic activities.
Takashima S; Fujita H; Toyoshi K; Ohba A; Hirata Y; Shimozawa N; Oh-Hashi K
Mol Genet Metab; 2022; 137(1-2):68-80. PubMed ID: 35932552
[TBL] [Abstract][Full Text] [Related]
4. Drosophila carrying pex3 or pex16 mutations are models of Zellweger syndrome that reflect its symptoms associated with the absence of peroxisomes.
Nakayama M; Sato H; Okuda T; Fujisawa N; Kono N; Arai H; Suzuki E; Umeda M; Ishikawa HO; Matsuno K
PLoS One; 2011; 6(8):e22984. PubMed ID: 21826223
[TBL] [Abstract][Full Text] [Related]
5. Peroxisome biogenesis disorders: molecular basis for impaired peroxisomal membrane assembly: in metabolic functions and biogenesis of peroxisomes in health and disease.
Fujiki Y; Yagita Y; Matsuzaki T
Biochim Biophys Acta; 2012 Sep; 1822(9):1337-42. PubMed ID: 22705440
[TBL] [Abstract][Full Text] [Related]
6. Peroxisome Biogenesis Disorders.
Honsho M; Okumoto K; Tamura S; Fujiki Y
Adv Exp Med Biol; 2020; 1299():45-54. PubMed ID: 33417206
[TBL] [Abstract][Full Text] [Related]
7. Cellular and molecular aspects of Zellweger syndrome and other peroxisome biogenesis disorders.
Brosius U; Gärtner J
Cell Mol Life Sci; 2002 Jun; 59(6):1058-69. PubMed ID: 12169017
[TBL] [Abstract][Full Text] [Related]
8. Molecular basis of peroxisomal biogenesis disorders caused by defects in peroxisomal matrix protein import.
Nagotu S; Kalel VC; Erdmann R; Platta HW
Biochim Biophys Acta; 2012 Sep; 1822(9):1326-36. PubMed ID: 22617146
[TBL] [Abstract][Full Text] [Related]
9. Failure of microtubule-mediated peroxisome division and trafficking in disorders with reduced peroxisome abundance.
Nguyen T; Bjorkman J; Paton BC; Crane DI
J Cell Sci; 2006 Feb; 119(Pt 4):636-45. PubMed ID: 16449325
[TBL] [Abstract][Full Text] [Related]
10. 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; 6():158. PubMed ID: 26319495
[TBL] [Abstract][Full Text] [Related]
11. The peroxisomal AAA ATPase complex prevents pexophagy and development of peroxisome biogenesis disorders.
Law KB; Bronte-Tinkew D; Di Pietro E; Snowden A; Jones RO; Moser A; Brumell JH; Braverman N; Kim PK
Autophagy; 2017 May; 13(5):868-884. PubMed ID: 28521612
[TBL] [Abstract][Full Text] [Related]
12. Identification of novel mutations and sequence variation in the Zellweger syndrome spectrum of peroxisome biogenesis disorders.
Yik WY; Steinberg SJ; Moser AB; Moser HW; Hacia JG
Hum Mutat; 2009 Mar; 30(3):E467-80. PubMed ID: 19105186
[TBL] [Abstract][Full Text] [Related]
13. Peroxisome biogenesis disorders: the role of peroxisomes and metabolic dysfunction in developing brain.
Faust PL; Banka D; Siriratsivawong R; Ng VG; Wikander TM
J Inherit Metab Dis; 2005; 28(3):369-83. PubMed ID: 15868469
[TBL] [Abstract][Full Text] [Related]
14. Recent insights into peroxisome biogenesis and associated diseases.
Fujiki Y; Abe Y; Imoto Y; Tanaka AJ; Okumoto K; Honsho M; Tamura S; Miyata N; Yamashita T; Chung WK; Kuroiwa T
J Cell Sci; 2020 May; 133(9):. PubMed ID: 32393673
[TBL] [Abstract][Full Text] [Related]
15. Liver disease predominates in a mouse model for mild human Zellweger spectrum disorder.
Berendse K; Boek M; Gijbels M; Van der Wel NN; Klouwer FC; van den Bergh-Weerman MA; Shinde AB; Ofman R; Poll-The BT; Houten SM; Baes M; Wanders RJA; Waterham HR
Biochim Biophys Acta Mol Basis Dis; 2019 Oct; 1865(10):2774-2787. PubMed ID: 31207289
[TBL] [Abstract][Full Text] [Related]
16. A Drosophila model for the Zellweger spectrum of peroxisome biogenesis disorders.
Mast FD; Li J; Virk MK; Hughes SC; Simmonds AJ; Rachubinski RA
Dis Model Mech; 2011 Sep; 4(5):659-72. PubMed ID: 21669930
[TBL] [Abstract][Full Text] [Related]
17. Defective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group G.
Muntau AC; Mayerhofer PU; Paton BC; Kammerer S; Roscher AA
Am J Hum Genet; 2000 Oct; 67(4):967-75. PubMed ID: 10958759
[TBL] [Abstract][Full Text] [Related]
18. Accurate and live peroxisome biogenesis evaluation achieved by lentiviral expression of a green fluorescent protein fused to a peroxisome targeting signal 1.
Demaret T; Courtoy GE; Ravau J; Van Der Smissen P; Najimi M; Sokal EM
Histochem Cell Biol; 2020 May; 153(5):295-306. PubMed ID: 32124009
[TBL] [Abstract][Full Text] [Related]
19. Phenotypic variability (heterogeneity) of peroxisomal disorders.
Mandel H; Korman SH
Adv Exp Med Biol; 2003; 544():9-30. PubMed ID: 14713208
[TBL] [Abstract][Full Text] [Related]
20. Autosomal dominant Zellweger spectrum disorder caused by de novo variants in PEX14 gene.
Waterham HR; Koster J; Ebberink MS; Ješina P; Zeman J; Nosková L; Kmoch S; Devic P; Cheillan D; Wanders RJA; Ferdinandusse S
Genet Med; 2023 Nov; 25(11):100944. PubMed ID: 37493040
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
