Lysosomal processing of progranulin
暂无分享,去创建一个
[1] Fenghua Hu,et al. Frontotemporal lobar degeneration (FTLD) is the most prevalent early-onset dementia after Alzheimer’s disease (AD) and accounts for 20–25% of pre-senile dementias , 2017 .
[2] L. Petrucelli,et al. The lysosomal protein cathepsin L is a progranulin protease , 2017, Molecular Neurodegeneration.
[3] Tuancheng Feng,et al. Regulation of cathepsin D activity by the FTLD protein progranulin , 2017, Acta Neuropathologica.
[4] T. Reinheckel,et al. Inherited diseases caused by mutations in cathepsin protease genes , 2017, The FEBS journal.
[5] W. Robberecht,et al. Progranulin functions as a cathepsin D chaperone to stimulate axonal outgrowth in vivo , 2017, Human molecular genetics.
[6] V. Turk,et al. Lysosomal cathepsins and their regulation in aging and neurodegeneration , 2016, Ageing Research Reviews.
[7] I. Santana,et al. Portuguese family with the co-occurrence of frontotemporal lobar degeneration and neuronal ceroid lipofuscinosis phenotypes due to progranulin gene mutation , 2016, Neurobiology of Aging.
[8] Ying Sun,et al. Prosaposin facilitates sortilin-independent lysosomal trafficking of progranulin , 2015, The Journal of cell biology.
[9] C. Sephton,et al. Progranulin: A Proteolytically Processed Protein at the Crossroads of Inflammation and Neurodegeneration* , 2012, The Journal of Biological Chemistry.
[10] Katherine R. Smith,et al. Strikingly different clinicopathological phenotypes determined by progranulin-mutation dosage. , 2012, American journal of human genetics.
[11] Sunhee C. Lee,et al. Regulation of Progranulin Expression in Human Microglia and Proteolysis of Progranulin by Matrix Metalloproteinase-12 (MMP-12) , 2012, PloS one.
[12] L. Petrucelli,et al. Progranulin axis and recent developments in frontotemporal lobar degeneration , 2012, Alzheimer's Research & Therapy.
[13] D. di Bernardo,et al. Transcriptional gene network inference from a massive dataset elucidates transcriptome organization and gene function , 2011, Nucleic acids research.
[14] H. Feldman,et al. Sortilin-Mediated Endocytosis Determines Levels of the Frontotemporal Dementia Protein, Progranulin , 2010, Neuron.
[15] O. Vasiljeva,et al. Synergistic antitumor effects of combined cathepsin B and cathepsin Z deficiencies on breast cancer progression and metastasis in mice , 2010, Proceedings of the National Academy of Sciences.
[16] A. Bateman,et al. The granulin gene family: from cancer to dementia , 2009, BioEssays : news and reviews in molecular, cellular and developmental biology.
[17] J. Matsuda,et al. The function of sphingolipids in the nervous system: lessons learnt from mouse models of specific sphingolipid activator protein deficiencies , 2007, Journal of neurochemistry.
[18] D. Dickson,et al. Journal of Neuroinflammation BioMed Central Review , 2006 .
[19] L. Pennacchio,et al. Human cathepsin L rescues the neurodegeneration and lethality in cathepsin B/L double-deficient mice , 2006, Biological chemistry.
[20] Maribel González-García,et al. Use of polyethyleneimine polymer in cell culture as attachment factor and lipofection enhancer , 2004, BMC biotechnology.
[21] H. Erdjument-Bromage,et al. Conversion of Proepithelin to Epithelins Roles of SLPI and Elastase in Host Defense and Wound Repair , 2002, Cell.
[22] X. Qi,et al. Molecular and cell biology of acid beta-glucosidase and prosaposin. , 2001, Progress in nucleic acid research and molecular biology.
[23] J. Deussing,et al. Cathepsin L deficiency as molecular defect of furless: hyperproliferation of keratinocytes and pertubation of hair follicle cycling , 2000, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[24] H Lippert,et al. Role of cathepsin B in intracellular trypsinogen activation and the onset of acute pancreatitis. , 2000, The Journal of clinical investigation.
[25] R. Faber,et al. Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria. , 1999, Neurology.
[26] Sheila J. Jones,et al. Impaired osteoclastic bone resorption leads to osteopetrosis in cathepsin-K-deficient mice. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[27] C. Peters,et al. Mice deficient for the lysosomal proteinase cathepsin D exhibit progressive atrophy of the intestinal mucosa and profound destruction of lymphoid cells. , 1995, The EMBO journal.
[28] Y. Kishimoto,et al. Saposin proteins: structure, function, and role in human lysosomal storage disorders , 1991, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.