Showing 1- [6] of [19] Publications
| Author: | Gr?nborg Sabine S | |
| Pubmed ID: | 20949532 | |
| Journal: | Am J Med Genet A | |
| Title: | Typical cMRI pattern as diagnostic clue for D-bifunctional protein deficiency without apparent biochemical abnormalities in plasma. | |
| Application: | IF | |
| Species: | human | |
| Author: | Thoms Sven S | |
| Pubmed ID: | 21741480 | |
| Journal: | J Struct Biol | |
| Title: | The unusual extended C-terminal helix of the peroxisomal α/β-hydrolase Lpx1 is involved in dimer contacts but dispensable for dimerization. | |
| Application: | IF | |
| Species: | monkey | |
| Author: | Kovacs Werner J WJ | |
| Pubmed ID: | 22441164 | |
| Journal: | Biochim Biophys Acta | |
| Title: | Peroxisome deficiency-induced ER stress and SREBP-2 pathway activation in the liver of newborn PEX2 knock-out mice. | |
| Application: | WB,IF | |
| Species: | mouse | |
| Author: | Huber Nina N | |
| Pubmed ID: | 23628762 | |
| Journal: | EMBO Rep | |
| Title: | Charcot-Marie-Tooth disease-associated mutants of GDAP1 dissociate its roles in peroxisomal and mitochondrial fission. | |
| Application: | IF | |
| Species: | mouse | |
| Author: | Krause Cindy C | |
| Pubmed ID: | 23716570 | |
| Journal: | Hum Mol Genet | |
| Title: | Functional analysis of PEX13 mutation in a Zellweger syndrome spectrum patient reveals novel homooligomerization of PEX13 and its role in human peroxisome biogenesis. | |
| Application: | WB,IF | |
| Species: | human | |
| Author: | Kassmann Celia M CM | |
| Pubmed ID: | 21620837 | |
| Journal: | FEBS Lett | |
| Title: | A role for myelin-associated peroxisomes in maintaining paranodal loops and axonal integrity. | |
| Application: | WB,IHC | |
| Species: | mouse | |
