Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2000 | 1 |
2003 | 1 |
2008 | 1 |
2009 | 1 |
2024 | 0 |
Search Results
4 results
Results by year
Filters applied: . Clear all
Page 1
Defective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group G.
Am J Hum Genet. 2000 Oct;67(4):967-75. doi: 10.1086/303071. Epub 2000 Aug 24.
Am J Hum Genet. 2000.
PMID: 10958759
Free PMC article.
The interaction between human PEX3 and PEX19 characterized by fluorescence resonance energy transfer (FRET) analysis.
Muntau AC, Roscher AA, Kunau WH, Dodt G.
Muntau AC, et al.
Eur J Cell Biol. 2003 Jul;82(7):333-42. doi: 10.1078/0171-9335-00325.
Eur J Cell Biol. 2003.
PMID: 12924628
Item in Clipboard
Characterization of the interaction between recombinant human peroxin Pex3p and Pex19p: identification of TRP-104 IN Pex3p as a critical residue for the interaction.
Sato Y, Shibata H, Nakano H, Matsuzono Y, Kashiwayama Y, Kobayashi Y, Fujiki Y, Imanaka T, Kato H.
Sato Y, et al.
J Biol Chem. 2008 Mar 7;283(10):6136-44. doi: 10.1074/jbc.M706139200. Epub 2008 Jan 3.
J Biol Chem. 2008.
PMID: 18174172
Free article.
Item in Clipboard
Pex3p-dependent peroxisomal biogenesis initiates in the endoplasmic reticulum of human fibroblasts.
Toro AA, Araya CA, Córdova GJ, Arredondo CA, Cárdenas HG, Moreno RE, Venegas A, Koenig CS, Cancino J, Gonzalez A, Santos MJ.
Toro AA, et al.
J Cell Biochem. 2009 Aug 15;107(6):1083-96. doi: 10.1002/jcb.22210.
J Cell Biochem. 2009.
PMID: 19479899
Item in Clipboard
Cite
Cite