PMC Links for GEO Profiles (Select 29329668) - PMC

Select item 33284321.

Molecular Requirements for Peroxisomal Targeting of Alanine-Glyoxylate Aminotransferase as an Essential Determinant in Primary Hyperoxaluria Type 1

Krisztián Fodor, Janina Wolf, Ralf Erdmann, Wolfgang Schliebs, Matthias Wilmanns

PLoS Biol. 2012 Apr; 10(4): e1001309. Published online 2012 Apr 17. doi: 10.1371/journal.pbio.1001309

PMCID:: PMC3328432

Abstract Article PDF–696K

Select item 31780592.

Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium

Pascale Gaudet, Michael S. Livstone, Suzanna E. Lewis, Paul D. Thomas

Brief Bioinform. 2011 Sep; 12(5): 449–462. Published online 2011 Aug 27. doi: 10.1093/bib/bbr042

PMCID:: PMC3178059

Abstract Article PDF–1.0M

Select item 28403503.

Molecular defects of the glycine 41 variants of alanine glyoxylate aminotransferase associated with primary hyperoxaluria type I

Barbara Cellini, Riccardo Montioli, Alessandro Paiardini, Antonio Lorenzetto, Fabio Maset, Tiziana Bellini, Elisa Oppici, Carla Borri Voltattorni

Proc Natl Acad Sci U S A. 2010 Feb 16; 107(7): 2896–2901. Published online 2010 Feb 1. doi: 10.1073/pnas.0908565107

PMCID:: PMC2840350

Abstract Article PDF–711K

Select item 21164064.

Identification of mutations associated with peroxisome-to-mitochondrion mistargeting of alanine/glyoxylate aminotransferase in primary hyperoxaluria type 1

J Cell Biol. 1990 Dec 1; 111(6): 2341–2351. doi: 10.1083/jcb.111.6.2341

PMCID:: PMC2116406

Summary PDF–2.3M

Select item 20490845.

Human wild-type alanine:glyoxylate aminotransferase and its naturally occurring G82E variant: functional properties and physiological implications

Barbara Cellini, Mariarita Bertoldi, Riccardo Montioli, Alessandro Paiardini, Carla Borri Voltattorni

Biochem J. 2007 Nov 15; 408(Pt 1): 39–50. Prepublished online 2007 Aug 13. Published online 2007 Oct 29. doi: 10.1042/BJ20070637

PMCID:: PMC2049084

Abstract Article PDF–316K

Select item 18387386.

Alanine–glyoxylate aminotransferase-deficient mice, a model for primary hyperoxaluria that responds to adenoviral gene transfer

Eduardo C. Salido, Xiao M. Li, Yang Lu, Xia Wang, Alfredo Santana, Namita Roy-Chowdhury, Armando Torres, Larry J. Shapiro, Jayanta Roy-Chowdhury

Proc Natl Acad Sci U S A. 2006 Nov 28; 103(48): 18249–18254. Published online 2006 Nov 16. doi: 10.1073/pnas.0607218103

PMCID:: PMC1838738

Abstract Article PDF–572K

Select item 16823527.

Enzymological and mutational analysis of a complex primary hyperoxaluria type 1 phenotype involving alanine:Glyoxylate aminotransferase peroxisome-to-mitochondrion mistargeting and intraperoxisomal aggregation

C. J. Danpure, P. E. Purdue, P. Fryer, S. Griffiths, J. Allsop, M. J. Lumb, K. M. Guttridge, P. R. Jennings, J. I. Scheinman, S. M. Mauer, N. O. Davidson

Am J Hum Genet. 1993 Aug; 53(2): 417–432.

PMCID:: PMC1682352

Summary Page Browse PDF–4.9M

Select item 1392418.

Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences

Mammalian Gene Collection (MGC) Program Team

Proc Natl Acad Sci U S A. 2002 Dec 24; 99(26): 16899–16903. Published online 2002 Dec 11. doi: 10.1073/pnas.242603899

PMCID:: PMC139241

Abstract Article PDF–118K

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