Soluble hemojuvelin is released by proprotein convertase-mediated cleavage at a conserved polybasic RNRR site.
暂无分享,去创建一个
T. Ganz | E. Nemeth | J. Goodnough | D. Thapa | Lan Lin | V. Gabayan
[1] L. Silvestri,et al. Defective targeting of hemojuvelin to plasma membrane is a common pathogenetic mechanism in juvenile hemochromatosis. , 2007, Blood.
[2] K. R. Meyers,et al. Evidence That Inhibition of Hemojuvelin Shedding in Response to Iron Is Mediated through Neogenin* , 2007, Journal of Biological Chemistry.
[3] N. Seidah,et al. Proprotein convertases: lessons from knockouts , 2006, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[4] P. Rotwein,et al. Complex biosynthesis of the muscle-enriched iron regulator RGMc , 2006, Journal of Cell Science.
[5] T. Ganz,et al. Regulation of iron acquisition and iron distribution in mammals. , 2006, Biochimica et biophysica acta.
[6] E. Raines,et al. Emerging roles for ectodomain shedding in the regulation of inflammatory responses , 2006, Journal of leukocyte biology.
[7] Raymond T Chung,et al. Bone morphogenetic protein signaling by hemojuvelin regulates hepcidin expression , 2006, Nature Genetics.
[8] Xiaoling Xu,et al. A Role of Smad4 in Iron Metabolism through the Positive Regulation of Hepcidin Expression , 2022 .
[9] N. Andrews,et al. Hemojuvelin Acts as a Bone Morphogenetic Protein Co-Receptor To Regulate Hepcidin Expression. , 2005 .
[10] A. West,et al. Interaction of Hemojuvelin with Neogenin Results in Iron Accumulation in Human Embryonic Kidney 293 Cells* , 2005, Journal of Biological Chemistry.
[11] C. Woolf,et al. Repulsive Guidance Molecule (RGMa), a DRAGON Homologue, Is a Bone Morphogenetic Protein Co-receptor* , 2005, Journal of Biological Chemistry.
[12] P. Thompson,et al. Modulatory effects of sCD14 and LBP on LPS-host cell interactions , 2005, Journal of endotoxin research.
[13] S. Arber,et al. Hemojuvelin is essential for dietary iron sensing, and its mutation leads to severe iron overload. , 2005, The Journal of clinical investigation.
[14] M. Pelto-huikko,et al. Shedding light on ADAM metalloproteinases. , 2005, Trends in biochemical sciences.
[15] A. Brivanlou,et al. DRAGON, a Bone Morphogenetic Protein Co-receptor* , 2005, Journal of Biological Chemistry.
[16] A. Rehemtulla,et al. Furin Directly Cleaves proMMP-2 in the trans-Golgi Network Resulting in a Nonfunctioning Proteinase* , 2005, Journal of Biological Chemistry.
[17] E. Beutler,et al. Regulation of hepcidin transcription by interleukin-1 and interleukin-6. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[18] T. Ganz,et al. Competitive regulation of hepcidin mRNA by soluble and cell-associated hemojuvelin. , 2005, Blood.
[19] A. Lauwers,et al. Limited Redundancy of the Proprotein Convertase Furin in Mouse Liver* , 2004, Journal of Biological Chemistry.
[20] E. Beutler,et al. The IL-6- and lipopolysaccharide-induced transcription of hepcidin in HFE-, transferrin receptor 2-, and beta 2-microglobulin-deficient hepatocytes. , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[21] T. Pihlajaniemi,et al. The shed ectodomain of type XIII collagen affects cell behaviour in a matrix-dependent manner. , 2004, The Biochemical journal.
[22] J. Bartsch,et al. Therapeutic benefits from targeting of ADAM family members. , 2004, Biochemistry.
[23] G. Alvarez-Bolado,et al. Expression pattern of the repulsive guidance molecules RGM A, B and C during mouse development. , 2004, Gene expression patterns : GEP.
[24] S. Arber,et al. Repulsive Guidance Molecule (RGM) Gene Function Is Required for Neural Tube Closure But Not Retinal Topography in the Mouse Visual System , 2004, The Journal of Neuroscience.
[25] D. Engelkamp,et al. Isolation and expression pattern of three mouse homologues of chick Rgm. , 2004, Gene expression patterns : GEP.
[26] Marie-Pierre Dubé,et al. Mutations in HFE2 cause iron overload in chromosome 1q–linked juvenile hemochromatosis , 2004, Nature Genetics.
[27] I. Hampson,et al. GPI-specific phospholipase D mRNA expression in tumor cells of different malignancy , 2004, Clinical & Experimental Metastasis.
[28] W. V. D. Van de Ven,et al. Curbing activation: proprotein convertases in homeostasis and pathology , 2003, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[29] G. Thomas,et al. Furin at the cutting edge: From protein traffic to embryogenesis and disease , 2002, Nature Reviews Molecular Cell Biology.
[30] Matthias Mann,et al. RGM is a repulsive guidance molecule for retinal axons , 2002, Nature.
[31] A. Beaudet,et al. Altered processing of the neurotensin/neuromedin N precursor in PC2 knock down mice: a biochemical and immunohistochemical study , 2002, Journal of neurochemistry.
[32] T. Howell,et al. Alterations in membrane-associated CD14 expression and the simultaneous liberation of soluble CD14 fragment in adherent macrophages mediated by a leukocyte carboxyl/aspartate protease , 2002, Journal of endotoxin research.
[33] J. Fowlkes,et al. Exploring the interface between metallo-proteinase activity and growth factor and cytokine bioavailability. , 2002, Cytokine & growth factor reviews.
[34] M. Pfaffl,et al. A new mathematical model for relative quantification in real-time RT-PCR. , 2001, Nucleic acids research.
[35] K. Mann,et al. 1,10-Phenanthroline inhibits glycosylphosphatidylinositol anchoring by preventing phosphoethanolamine addition to glycosylphosphatidylinositol anchor precursors. , 2001, Biochemistry.
[36] J G Flanagan,et al. Regulated cleavage of a contact-mediated axon repellent. , 2000, Science.
[37] M. Chignard,et al. Proteolysis of monocyte CD14 by human leukocyte elastase inhibits lipopolysaccharide-mediated cell activation. , 1999, The Journal of clinical investigation.
[38] G. Thomas,et al. BMP‐4 is proteolytically activated by furin and/or PC6 during vertebrate embryonic development , 1998, The EMBO journal.
[39] K Nakayama,et al. Furin: a mammalian subtilisin/Kex2p-like endoprotease involved in processing of a wide variety of precursor proteins. , 1997, The Biochemical journal.
[40] N. Hooper,et al. Membrane protein secretases. , 1997, The Biochemical journal.
[41] J. Massagué,et al. Diverse Cell Surface Protein Ectodomains Are Shed by a System Sensitive to Metalloprotease Inhibitors (*) , 1996, The Journal of Biological Chemistry.
[42] K. Nakayama,et al. Localization of Furin to the trans-Golgi Network and Recycling from the Cell Surface Involves Ser and Tyr Residues within the Cytoplasmic Domain (*) , 1995, The Journal of Biological Chemistry.
[43] C. Eckerskorn,et al. Soluble lipopolysaccharide receptor (CD14) is released via two different mechanisms from human monocytes and CD14 transfectants , 1995, European journal of immunology.
[44] H. Klenk,et al. Maturation of the trans-Golgi network protease furin: compartmentalization of propeptide removal, substrate cleavage, and COOH-terminal truncation , 1994, The Journal of cell biology.
[45] M. G. Low,et al. Factors affecting the ability of glycosylphosphatidylinositol-specific phospholipase D to degrade the membrane anchors of cell surface proteins. , 1991, The Biochemical journal.
[46] J. Strominger,et al. Shedding as a mechanism of down-modulation of CD14 on stimulated human monocytes. , 1991, Journal of immunology.
[47] H. Lodish. Molecular Cell Biology , 1986 .