2009 -- Pubmed # 19305391 -- Cho KI, Yi H, Desai R, Hand AR, Haas AL, Ferreira PA. RANBP2 is an allosteric activator of the conventional kinesin-1 motor protein, KIF5B, in a minimal cell-free system.  EMBO Rep.  2009 Mar 20.

2008 -- Pubmed # 18949001 -- Cho KI, Yi H, Yeh A, Tserentsoodol N, Cuadrado L, Searle K, Hao Y, Ferreira PA. Haploinsufficiency of RanBP2 is neuroprotective against light-elicited and age-dependent degeneration of photoreceptor neurons.  Cell Death Differ.  2008 Oct 24.

2007 -- Pubmed # 17470787 -- Moore DF, Gelderman MP, Ferreira PA, Fuhrmann SR, Yi H, Elkahloun A, Lix LM, Brady RO, Schiffmann R, Goldin E. Genomic abnormalities of the murine model of Fabry disease after disease-related perturbation, a systems biology approach. Proc Natl Acad Sci U S A. 2007 May 8;104(19):8065-70.

2007 -- Pubmed # 17887960 -- Cho KI, Cai Y, Yi H, Yeh A, Aslanukov A, Ferreira PA. Association of the Kinesin-Binding Domain of RanBP2 to KIF5B and KIF5C Determines Mitochondria Localization and Function. Traffic. 2007 Sep 20.

2007 -- Pubmed # 17911097 -- Yi H, Friedman J, Ferreira PA. The cyclophilin-like domain of Ran-binding protein-2 modulates selectively the activity of the ubiquitin-proteasome system and protein biogenesis. J Biol Chem. 2007 Oct 2.

2006 -- Pubmed # 17069463 -- Aslanukov A, Bhowmick R, Guruju M, Oswald J, Raz D, Bush RA, Sieving PA, Lu X, Bock CB, Ferreira PA. RanBP2 modulates Cox11 and hexokinase I activities and haploinsufficiency of RanBP2 causes deficits in glucose metabolism. PLoS Genet. 2006 Oct;2(10):e177.

2005 -- Pubmed # 15914599 -- Lu X, Ferreira PA. Identification of novel murine- and human-specific RPGRIP1 splice variants with distinct expression profiles and subcellular localization. Invest Ophthalmol Vis Sci. 2005 Jun;46(6):1882-90.

2005 -- Pubmed # 16339905 -- Roepman R, Letteboer SJ, Arts HH, van Beersum SE, Lu X, Krieger E, Ferreira PA, Cremers FP. Interaction of nephrocystin-4 and RPGRIP1 is disrupted by nephronophthisis or Leber congenital amaurosis-associated mutations. Proc Natl Acad Sci U S A. 2005 Dec 20;102(51):18520-5.

2005 -- Pubmed # 16244324 -- Ferreira PA. Insights into X-linked retinitis pigmentosa type 3, allied diseases and underlying pathomechanisms. Hum Mol Genet. 2005 Oct 15;14 Spec No. 2:R259-67.

2005 -- Pubmed # 15800011 -- Lu X, Guruju M, Oswald J, Ferreira PA. Limited proteolysis differentially modulates the stability and subcellular localization of domains of RPGRIP1 that are distinctly affected by mutations in Leber's congenital amaurosis. Hum Mol Genet. 2005 May 15;14(10):1327-40.

2003 -- Pubmed # 12874105 -- Castagnet P, Mavlyutov T, Cai Y, Zhong F, Ferreira P. RPGRIP1s with distinct neuronal localization and biochemical properties associate selectively with RanBP2 in amacrine neurons. Hum Mol Genet. 2003 Aug 1;12(15):1847-63.