|1.||Ghaedi, Kamran: 3 articles (04/2013 - 03/2002)|
|2.||Nasr-Esfahani, Mohammad Hossein: 2 articles (04/2013 - 01/2013)|
|3.||Mohamadynejad, Parisa: 2 articles (04/2013 - 01/2013)|
|4.||Salamian, Ahmad: 2 articles (04/2013 - 01/2013)|
|5.||Shafeghati, Yousef: 2 articles (04/2013 - 01/2013)|
|6.||Baharvand, Hossein: 2 articles (04/2013 - 01/2013)|
|7.||Tanhaie, Somayeh: 1 article (04/2013)|
|8.||Rabiee, Farzaneh: 1 article (04/2013)|
|9.||Karamali, Fereshteh: 1 article (04/2013)|
|10.||Parivar, Kazem: 1 article (04/2013)|
|1.||Rhizomelic Chondrodysplasia Punctata
01/01/2013 - "C86Y: as a destructive homozygous mutation deteriorating Pex7p function causing rhizomelic chondrodysplasia punctata type I."
03/15/2002 - "We investigated the molecular dysfunction of Pex7p variants in mammals, including Pex7p-W221ter and Pex7p with one site mutation at G217R, A218V, or L292ter, which frequently occurs in the human fatal genetic peroxisomal disease rhizomelic chondrodysplasia punctata, showing a cell phenotype of PTS2 import defect. "
04/01/1999 - "Rhizomelic chondrodysplasia punctata, a peroxisomal biogenesis disorder caused by defects in Pex7p, a peroxisomal protein import receptor: a minireview."
02/23/1998 - "In addition, we used PpPex7p as a model protein to understand the effect of the Pex7p mutations found in human patients with rhizomelic chondrodysplasia punctata. "
04/01/1997 - "Rhizomelic chondrodysplasia punctata is caused by deficiency of human PEX7, a homologue of the yeast PTS2 receptor."
|2.||Refsum Disease (Refsum's Disease)
|3.||Chondrodysplasia Punctata (Stippled Epiphyses)
|1.||peroxisomal targeting signal 2 receptor
|2.||Proteins (Proteins, Gene)
|3.||phytanoyl-coenzyme A (phytanoyl CoA)