DK19394/DK/NIDDK NIH HHS/United States[Grant Number] - Search Results

Year	Number of Results
1988	1
1994	1
1995	3
1996	4
1997	1
1998	1
1999	1
2000	1
2001	2
2003	1
2021	0

1

Peroxisome biogenesis.

Purdue PE, Lazarow PB. Purdue PE, et al. Annu Rev Cell Dev Biol. 2001;17:701-52. doi: 10.1146/annurev.cellbio.17.1.701. Annu Rev Cell Dev Biol. 2001. PMID: 11687502 Review.

2

Peroxisome biogenesis: advances and conundrums.

Lazarow PB. Lazarow PB. Curr Opin Cell Biol. 2003 Aug;15(4):489-97. doi: 10.1016/s0955-0674(03)00082-6. Curr Opin Cell Biol. 2003. PMID: 12892791 Review.

3

Peroxisome structure, function, and biogenesis--human patients and yeast mutants show strikingly similar defects in peroxisome biogenesis.

Lazarow PB. Lazarow PB. J Neuropathol Exp Neurol. 1995 Sep;54(5):720-5. doi: 10.1097/00005072-199509000-00015. J Neuropathol Exp Neurol. 1995. PMID: 7666062 Review.

4

Rhizomelic chondrodysplasia punctata, a peroxisomal biogenesis disorder caused by defects in Pex7p, a peroxisomal protein import receptor: a minireview.

Purdue PE, Skoneczny M, Yang X, Zhang JW, Lazarow PB. Purdue PE, et al. Neurochem Res. 1999 Apr;24(4):581-6. doi: 10.1023/a:1023957110171. Neurochem Res. 1999. PMID: 10227689 Review.

5

Peroxisomal biogenesis: multiple pathways of protein import.

Purdue PE, Lazarow PB. Purdue PE, et al. J Biol Chem. 1994 Dec 2;269(48):30065-8. J Biol Chem. 1994. PMID: 7982905 Review. No abstract available.

6

Eci1p uses a PTS1 to enter peroxisomes: either its own or that of a partner, Dci1p.

Yang X, Purdue PE, Lazarow PB. Yang X, et al. Eur J Cell Biol. 2001 Feb;80(2):126-38. doi: 10.1078/0171-9335-00144. Eur J Cell Biol. 2001. PMID: 11302517

7

Rhizomelic chondrodysplasia punctata is caused by deficiency of human PEX7, a homologue of the yeast PTS2 receptor.

Purdue PE, Zhang JW, Skoneczny M, Lazarow PB. Purdue PE, et al. Nat Genet. 1997 Apr;15(4):381-4. doi: 10.1038/ng0497-381. Nat Genet. 1997. PMID: 9090383

8

Pex18p and Pex21p, a novel pair of related peroxins essential for peroxisomal targeting by the PTS2 pathway.

Purdue PE, Yang X, Lazarow PB. Purdue PE, et al. J Cell Biol. 1998 Dec 28;143(7):1859-69. doi: 10.1083/jcb.143.7.1859. J Cell Biol. 1998. PMID: 9864360 Free PMC article.

9

Peroxisomal ghosts are intracellular structures distinct from lysosomal compartments in Zellweger syndrome: a confocal laser scanning microscopy study.

Santos MJ, Henderson SC, Moser AB, Moser HW, Lazarow PB. Santos MJ, et al. Biol Cell. 2000 Apr;92(2):85-94. doi: 10.1016/s0248-4900(00)89016-4. Biol Cell. 2000. PMID: 10879629

10

Identification of peroxisomal membrane ghosts with an epitope-tagged integral membrane protein in yeast mutants lacking peroxisomes.

Purdue PE, Lazarow PB. Purdue PE, et al. Yeast. 1995 Sep 15;11(11):1045-60. doi: 10.1002/yea.320111106. Yeast. 1995. PMID: 7502580

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