Overexpressed TTC3 Protein Tends to be Cleaved into Fragments and Form Aggregates in the Nucleus
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Fei Dou | Kun Wang | Y. Shang | Yueqing Gong | S. Xiao | Panying Mi | Wanjie Li
[1] Fei Dou,et al. Tetratricopeptide repeat domain 3 overexpression tends to form aggregates and inhibit ubiquitination and degradation of DNA polymerase γ , 2017, Oncotarget.
[2] Margaret A. Pericak-Vance,et al. Segregation of a rare TTC3 variant in an extended family with late-onset Alzheimer disease , 2016, Neurology: Genetics.
[3] A. Amon,et al. Aneuploidy: implications for protein homeostasis and disease , 2014, Disease Models & Mechanisms.
[4] David Haussler,et al. Current status and new features of the Consensus Coding Sequence database , 2013, Nucleic Acids Res..
[5] P. Capkova,et al. Partial trisomy and tetrasomy of chromosome 21 without Down Syndrome phenotype and short overview of genotype-phenotype correlation. A case report. , 2013, Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia.
[6] Adriana B Ferreira,et al. Calpain Dysregulation in Alzheimer's Disease , 2012, ISRN biochemistry.
[7] M. Mann,et al. Global analysis of genome, transcriptome and proteome reveals the response to aneuploidy in human cells , 2012, Molecular Systems Biology.
[8] Jane Loveland,et al. Tracking and coordinating an international curation effort for the CCDS Project , 2012, Database J. Biol. Databases Curation.
[9] Toshiyuki Obata,et al. The E3 ligase TTC3 facilitates ubiquitination and degradation of phosphorylated Akt. , 2009, Developmental cell.
[10] Jonathan M. Mudge,et al. The consensus coding sequence (CCDS) project: Identifying a common protein-coding gene set for the human and mouse genomes. , 2009, Genome research.
[11] M. Tomita,et al. Systematic identification of cell cycle-dependent yeast nucleocytoplasmic shuttling proteins by prediction of composite motifs , 2009, Proceedings of the National Academy of Sciences.
[12] F. Di Cunto,et al. The Down syndrome critical region protein TTC3 inhibits neuronal differentiation via RhoA and Citron kinase , 2007, Journal of Cell Science.
[13] Markus Brameier,et al. BIOINFORMATICS APPLICATIONS NOTE doi:10.1093/bioinformatics/btm066 Sequence analysis NucPred—Predicting nuclear localization of proteins , 2007 .
[14] E. Sinforiani,et al. Peripheral proteasome and caspase activity in Parkinson disease and Alzheimer disease , 2006, Neurology.
[15] Stylianos E. Antonarakis,et al. Chromosome 21 and Down syndrome: from genomics to pathophysiology , 2004, Nature Reviews Genetics.
[16] R. Berry,et al. Caspase cleavage of tau: Linking amyloid and neurofibrillary tangles in Alzheimer's disease , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[17] C. Pickart,et al. Inhibition of the ubiquitin-proteasome system in Alzheimer's disease. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[18] J. Delabar,et al. Regional and cellular specificity of the expression of TPRD, the tetratricopeptide Down syndrome gene, during human embryonic development , 2000, Mechanisms of Development.
[19] J. Delabar,et al. Developmentally regulated expression of mtprd, the murine ortholog of tprd, a gene from the Down syndrome chromosomal region 1 , 1999, Mechanisms of Development.
[20] M. Hattori,et al. Molecular characterization of the mouse mtprd gene, a homologue of human TPRD: unique gene expression suggesting its critical role in the pathophysiology of Down syndrome. , 1998, Journal of Biochemistry (Tokyo).
[21] S. Antonarakis,et al. Transcriptional map of the 2.5-Mb CBR-ERG region of chromosome 21 involved in Down syndrome. , 1998, Genomics.
[22] M. Hattori,et al. Identification and cloning of a novel cDNA belonging to tetratricopeptide repeat gene family from Down syndrome-critical region 21q22.2. , 1996, Journal of biochemistry.
[23] C. Disteche,et al. Down syndrome phenotypes: the consequences of chromosomal imbalance. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[24] K. Blomgren,et al. Calpain and calpastatin in normal and Alzheimer-degenerated human brain tissue , 1990, Neurobiology of Aging.
[25] D. Mann. Alzheimer's disease and Down's syndrome , 1988, Histopathology.
[26] B. Hyman. Caspase activation without apoptosis: insight into Aβ initiation of neurodegeneration , 2010, Nature Neuroscience.
[27] N. Nomura,et al. Identification of a novel human gene containing the tetratricopeptide repeat domain from the Down syndrome region of chromosome 21. , 1996, DNA research : an international journal for rapid publication of reports on genes and genomes.
[28] J. Delabar,et al. Molecular Mapping of Twenty-Four Features of Down Syndrome on Chromosome 21 , 1993, European journal of human genetics : EJHG.