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1. Full Text TDP-43 binds heterogeneous nuclear ribonucleoprotein A/B through its C-terminal tail: An important region for the inhibition of cystic fibrosis transmembrane conductance regulator exon 9 splicing
by Buratti, Emanuele and Brindisi, Antonia and Giombi, Maurizio and Tisminetzky, Sergio and Ayala, Youhna M and Baralle, Francisco E
The Journal of biological chemistry, ISSN 0021-9258, 11/2005, Volume 280, Issue 45, pp. 37572 - 37584
Life Sciences & Biomedicine | Biochemistry & Molecular Biology | Science & Technology | DNA-Binding Proteins - metabolism | Multigene Family | Alternative Splicing - genetics | Humans | RNA Splicing - genetics | Protein Binding | Cystic Fibrosis Transmembrane Conductance Regulator - genetics | Exons - genetics | Heterogeneous-Nuclear Ribonucleoprotein Group A-B - metabolism | Cystic Fibrosis Transmembrane Conductance Regulator - metabolism | HeLa Cells | DNA-Binding Proteins - chemistry | Index Medicus
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2. Full Text Formation and Maturation of Phase-Separated Liquid Droplets by RNA-Binding Proteins
by Lin, Yuan and Protter, David S.W and Rosen, Michael K and Parker, Roy
Molecular cell, ISSN 1097-2765, 10/2015, Volume 60, Issue 2, pp. 208 - 219
Biochemistry & Molecular Biology | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Organelles - chemistry | Fluorescence Recovery After Photobleaching | Humans | Polyethylene Glycols - chemistry | Amyloid - chemistry | Cytoplasmic Granules - chemistry | Molecular Mimicry | Amyloid - metabolism | Protein Aggregation, Pathological - pathology | Solutions | Cytoplasmic Granules - metabolism | Escherichia coli - metabolism | Heterogeneous-Nuclear Ribonucleoprotein Group A-B - genetics | Protein Aggregation, Pathological - genetics | RNA - metabolism | Sodium Chloride - chemistry | Protein Structure, Tertiary | Recombinant Proteins - metabolism | Amyloid - genetics | Gene Expression | Recombinant Proteins - chemistry | Heterogeneous-Nuclear Ribonucleoprotein Group A-B - metabolism | Recombinant Proteins - genetics | RNA - chemistry | Intrinsically Disordered Proteins - genetics | Heterogeneous Nuclear Ribonucleoprotein A1 | Heterogeneous-Nuclear Ribonucleoprotein Group A-B - chemistry | Escherichia coli - genetics | Intrinsically Disordered Proteins - chemistry | Protein Binding | Organelles - metabolism | Protein Aggregation, Pathological - metabolism | Intrinsically Disordered Proteins - metabolism | Fluorescence | Marine biology | Chemical properties | RNA | Binding proteins | Protein binding | Yuan (China) | Index Medicus
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3. Full Text A Crohn's disease-associated NOD2 mutation suppresses transcription of human IL10 by inhibiting activity of the nuclear ribonucleoprotein hnRNP-A1
by Noguchi, E and Homma, Y and Kang, X and Netea, M.G and Ma, X
Nature immunology, ISSN 1529-2908, 2009, Volume 10, Issue 5, pp. 471 - 479
Life Sciences & Biomedicine | Immunology | Science & Technology | Crohn Disease - genetics | Genetic Predisposition to Disease | Humans | Gene Expression Regulation | Crohn Disease - metabolism | Heterogeneous-Nuclear Ribonucleoprotein Group A-B - metabolism | Male | Monocytes - metabolism | Nod2 Signaling Adaptor Protein - genetics | Monocytes - immunology | Crohn Disease - immunology | Heterogeneous Nuclear Ribonucleoprotein A1 | Mice, Knockout | Macrophages - metabolism | Animals | Interleukin-10 - genetics | Adult | Female | Interleukin-10 - biosynthesis | Transcription, Genetic | Mice | Mutation | Heterogeneous-Nuclear Ribonucleoprotein Group A-B - genetics | Macrophages - immunology | Care and treatment | Nucleoproteins | Physiological aspects | Crohn's disease | Genetic aspects | Research | Risk factors | Index Medicus
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4. Full Text RNA-binding proteins with prion-like domains in health and disease
by Harrison, Alice Ford and Shorter, James
Biochemical journal, ISSN 0264-6021, 04/2017, Volume 474, Issue 8, pp. 1417 - 1438
Life Sciences & Biomedicine | Biochemistry & Molecular Biology | Science & Technology | Proteostasis Deficiencies - metabolism | RNA-Binding Proteins - genetics | TATA-Binding Protein Associated Factors - metabolism | Humans | Prion Proteins - metabolism | DNA-Binding Proteins - metabolism | Frontotemporal Dementia - metabolism | RNA-Binding Protein FUS - chemistry | TDP-43 Proteinopathies - genetics | Protein Domains | TDP-43 Proteinopathies - pathology | Prion Proteins - chemistry | Prion Proteins - genetics | Heterogeneous-Nuclear Ribonucleoprotein Group A-B - genetics | Frontotemporal Dementia - pathology | Calmodulin-Binding Proteins - genetics | Frontotemporal Dementia - genetics | Cytoplasmic Granules | Neurodegenerative Diseases - pathology | Amyotrophic Lateral Sclerosis - genetics | RNA-Binding Proteins - chemistry | TDP-43 Proteinopathies - metabolism | Proteostasis Deficiencies - pathology | RNA-Binding Protein FUS - genetics | Heterogeneous-Nuclear Ribonucleoprotein Group A-B - metabolism | Neurodegenerative Diseases - genetics | Calmodulin-Binding Proteins - chemistry | Calmodulin-Binding Proteins - metabolism | RNA-Binding Protein FUS - metabolism | Neurodegenerative Diseases - metabolism | TATA-Binding Protein Associated Factors - chemistry | DNA-Binding Proteins - genetics | TATA-Binding Protein Associated Factors - genetics | DNA-Binding Proteins - chemistry | Heterogeneous Nuclear Ribonucleoprotein A1 | Proteostasis Deficiencies - genetics | Amyotrophic Lateral Sclerosis - pathology | Heterogeneous-Nuclear Ribonucleoprotein Group A-B - chemistry | Amyotrophic Lateral Sclerosis - metabolism | Mutation | RNA-Binding Proteins - metabolism | RNA-Binding Protein EWS | Index Medicus
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5. Full Text HnRNP proteins controlled by c-Myc deregulate pyruvate kinase mRNA splicing in cancer
by Manley, James L and David, Charles J and Chen, Mo and Canoll, Peter and Assanah, Marcela
Nature (London), ISSN 0028-0836, 01/2010, Volume 463, Issue 7279, pp. 364 - 368
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Biological and medical sciences | Multiple tumors. Solid tumors. Tumors in childhood (general aspects) | Medical sciences | Tumors | Neoplasms - metabolism | NIH 3T3 Cells | Pyruvate Kinase - metabolism | Alternative Splicing - genetics | Humans | RNA, Messenger - genetics | Oxidative Phosphorylation | Neoplasms - enzymology | Exons - genetics | Heterogeneous-Nuclear Ribonucleoprotein Group A-B - metabolism | Polypyrimidine Tract-Binding Protein - metabolism | Genes, myc | RNA, Messenger - metabolism | Proto-Oncogene Proteins c-myc - metabolism | Animals | Neoplasms - genetics | Cell Line, Tumor | Glycolysis | Protein Binding | Mice | Proto-Oncogene Proteins c-myc - genetics | Neoplasms - pathology | Pyruvate Kinase - genetics | Cell proliferation | Cancer cells | Ribonucleoproteins | Physiological aspects | Genetic aspects | Research | RNA splicing | Proteins | Kinases | Mass spectrometry | Binding sites | Cancer | Index Medicus
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6. Full Text Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS
by Kim, Hong Joo and Kim, Nam Chul and Wang, Yong-Dong and Scarborough, Emily A and Moore, Jennifer and Diaz, Zamia and MacLea, Kyle S and Freibaum, Brian and Li, Songqing and Molliex, Amandine and Kanagaraj, Anderson P and Carter, Robert and Boylan, Kevin B and Wojtas, Aleksandra M and Rademakers, Rosa and Pinkus, Jack L and Greenberg, Steven A and Trojanowski, John Q and Traynor, Bryan J and Smith, Bradley N and Topp, Simon and Gkazi, Athina-Soragia and Miller, Jack and Shaw, Christopher E and Kottlors, Michael and Kirschner, Janbernd and Pestronk, Alan and Li, Yun R and Ford, Alice Flynn and Gitler, Aaron D and Benatar, Michael and King, Oliver D and Kimonis, Virginia E and Ross, Eric D and Weihl, Conrad C and Shorter, James and Taylor, J. Paul
Nature (London), ISSN 0028-0836, 03/2013, Volume 495, Issue 7442, pp. 467 - 473
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Prions - genetics | Humans | Molecular Sequence Data | Osteitis Deformans - metabolism | Male | Drosophila melanogaster - genetics | Osteitis Deformans - genetics | Drosophila melanogaster - metabolism | Frontotemporal Dementia - metabolism | Muscular Dystrophies, Limb-Girdle - genetics | Myositis, Inclusion Body - pathology | Female | Inclusion Bodies - metabolism | Muscular Dystrophies, Limb-Girdle - pathology | Heterogeneous-Nuclear Ribonucleoprotein Group A-B - genetics | Frontotemporal Dementia - pathology | RNA - metabolism | Frontotemporal Dementia - genetics | Amino Acid Sequence | Prions - metabolism | Peptide Termination Factors - genetics | Amyotrophic Lateral Sclerosis - genetics | Drosophila melanogaster - cytology | Mutant Proteins - genetics | Heterogeneous-Nuclear Ribonucleoprotein Group A-B - metabolism | Mutant Proteins - metabolism | Protein Structure, Tertiary - genetics | Prions - chemistry | Saccharomyces cerevisiae Proteins - genetics | Mutation - genetics | Myositis, Inclusion Body - genetics | Peptide Termination Factors - metabolism | Amyotrophic Lateral Sclerosis - pathology | Inclusion Bodies - genetics | Osteitis Deformans - pathology | Animals | Heterogeneous-Nuclear Ribonucleoprotein Group A-B - chemistry | Muscular Dystrophies, Limb-Girdle - metabolism | Mutant Proteins - chemistry | Amyotrophic Lateral Sclerosis - metabolism | Saccharomyces cerevisiae Proteins - metabolism | Inclusion Bodies - pathology | Myositis, Inclusion Body - metabolism | Mice | Peptide Termination Factors - chemistry | HeLa Cells | Saccharomyces cerevisiae Proteins - chemistry | Pathology | Insects | Genomics | Genetics | Software | Genomes | Mutation | Genetic testing | Patients | Index Medicus
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7. Full Text TDP-43 functions within a network of hnRNP proteins to inhibit the production of a truncated human SORT1 receptor
by Mohagheghi, Fatemeh and Prudencio, Mercedes and Stuani, Cristiana and Cook, Casey and Jansen-West, Karen and Dickson, Dennis W and Petrucelli, Leonard and Buratti, Emanuele
Human molecular genetics, ISSN 0964-6906, 02/2016, Volume 25, Issue 3, pp. 534 - 545
Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Frontotemporal Lobar Degeneration - pathology | Neurons - pathology | Alternative Splicing | Exons | Humans | Adaptor Proteins, Vesicular Transport - genetics | Molecular Sequence Data | Heterogeneous-Nuclear Ribonucleoprotein Group C - metabolism | Adaptor Proteins, Vesicular Transport - metabolism | DNA-Binding Proteins - metabolism | Frontotemporal Lobar Degeneration - metabolism | Base Sequence | Neurons - metabolism | Heterogeneous-Nuclear Ribonucleoprotein Group A-B - genetics | Heterogeneous-Nuclear Ribonucleoprotein Group C - genetics | Signal Transduction | Introns | Heterogeneous-Nuclear Ribonucleoprotein Group A-B - metabolism | DNA-Binding Proteins - genetics | Heterogeneous-Nuclear Ribonucleoprotein Group F-H - genetics | Heterogeneous Nuclear Ribonucleoprotein A1 | Heterogeneous-Nuclear Ribonucleoprotein Group F-H - metabolism | Animals | Cell Line, Tumor | Mice | Frontotemporal Lobar Degeneration - genetics | Mutation | Index Medicus
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