scholarly article | Q13442814 |
P819 | ADS bibcode | 2008Sci...322.1365G |
P356 | DOI | 10.1126/SCIENCE.1163581 |
P932 | PMC publication ID | 2803065 |
P698 | PubMed publication ID | 19039133 |
P5875 | ResearchGate publication ID | 23502903 |
P50 | author | Matthias Futschik | Q37376165 |
Mohan Madan Babu | Q56084741 | ||
Sarah Teichmann | Q19501099 | ||
P2093 | author name string | Jörg Gsponer | |
P2860 | cites work | Ubiquitin- and ATP-independent proteolytic turnover of p21 by the REGgamma-proteasome pathway | Q40115992 |
A homeostatic model of IkappaB metabolism to control constitutive NF-kappaB activity | Q42512304 | ||
alpha-synuclein metabolism and aggregation is linked to ubiquitin-independent degradation by the proteasome | Q43816254 | ||
Proteasomal degradation of tau protein | Q44163168 | ||
Coupled folding and binding with alpha-helix-forming molecular recognition elements | Q48122045 | ||
Cell cycle-dependent caspase-like activity that cleaves p27KIP1 is the β1 subunit of the 20S proteasome | Q61043686 | ||
Prediction and Functional Analysis of Native Disorder in Proteins from the Three Kingdoms of Life | Q22061741 | ||
Cdk-inhibitory activity and stability of p27Kip1 are directly regulated by oncogenic tyrosine kinases | Q24294546 | ||
p27 phosphorylation by Src regulates inhibition of cyclin E-Cdk2 | Q24294568 | ||
Protein misfolding, functional amyloid, and human disease | Q28131732 | ||
Adapting proteostasis for disease intervention | Q28131818 | ||
Intrinsically disordered protein | Q28191444 | ||
Alpha-synuclein and neurodegenerative diseases | Q28204386 | ||
Intrinsic disorder in cell-signaling and cancer-associated proteins | Q28207698 | ||
TC-1 is a novel tumorigenic and natively disordered protein associated with thyroid cancer | Q28256844 | ||
Divorcing ARF and p53: an unsettled case | Q28258356 | ||
NF-kappaB dictates the degradation pathway of IkappaBalpha | Q28588231 | ||
The importance of intrinsic disorder for protein phosphorylation | Q28776125 | ||
Structural studies of p21Waf1/Cip1/Sdi1 in the free and Cdk2-bound state: conformational disorder mediates binding diversity | Q28910326 | ||
Intrinsically unstructured proteins: re-assessing the protein structure-function paradigm | Q29615865 | ||
Control of stochasticity in eukaryotic gene expression | Q29615955 | ||
The interplay between structure and function in intrinsically unstructured proteins. | Q30350853 | ||
Adaptation to ER stress is mediated by differential stabilities of pro-survival and pro-apoptotic mRNAs and proteins | Q33262919 | ||
Interaction of Akt-phosphorylated ataxin-1 with 14-3-3 mediates neurodegeneration in spinocerebellar ataxia type 1. | Q33292483 | ||
20S proteasomes and protein degradation "by default". | Q33998904 | ||
The Cdk inhibitor p27 in human cancer: prognostic potential and relevance to anticancer therapy | Q34763495 | ||
Oncogenic re-wiring of cellular signaling pathways | Q36745360 | ||
Intrinsic disorder in transcription factors | Q36882145 | ||
P433 | issue | 5906 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 1365-1368 | |
P577 | publication date | 2008-11-01 | |
P1433 | published in | Science | Q192864 |
P1476 | title | Tight regulation of unstructured proteins: from transcript synthesis to protein degradation | |
P478 | volume | 322 |
Q37995736 | 14-3-3 protein and ATRAP bind to the soluble class IIB phosphatidylinositol transfer protein RdgBβ at distinct sites. |
Q57169558 | A Methodological Assessment and Characterization of Genetically-Driven Variation in Three Human Phosphoproteomes |
Q28681184 | A decade and a half of protein intrinsic disorder: biology still waits for physics |
Q42939838 | A dehydrin-dehydrin interaction: the case of SK3 from Opuntia streptacantha |
Q35075087 | A disorder-induced domino-like destabilization mechanism governs the folding and functional dynamics of the repeat protein IκBα |
Q39063386 | A majority of the cancer/testis antigens are intrinsically disordered proteins |
Q35560108 | A mass spectrometric strategy for absolute quantification of Plasmodium falciparum proteins of low abundance |
Q33796245 | A multiprotein binding interface in an intrinsically disordered region of the tumor suppressor protein interferon regulatory factor-1 |
Q28484050 | A self-organized model for cell-differentiation based on variations of molecular decay rates |
Q28511898 | A transducible nuclear/nucleolar protein, mLLP, regulates neuronal morphogenesis and synaptic transmission |
Q30358999 | Advantages of proteins being disordered. |
Q35679463 | An N-terminal, 830 residues intrinsically disordered region of the cytoskeleton-regulatory protein supervillin contains Myosin II- and F-actin-binding sites |
Q37958616 | An omics perspective of protein disorder |
Q38454012 | AnGeLi: A Tool for the Analysis of Gene Lists from Fission Yeast |
Q34117231 | Assemblages: functional units formed by cellular phase separation |
Q34320673 | Assembly of the SLIP1-SLBP complex on histone mRNA requires heterodimerization and sequential binding of SLBP followed by SLIP1. |
Q34173951 | Assessing the utility of gene co-expression stability in combination with correlation in the analysis of protein-protein interaction networks |
Q42880692 | Association between intrinsic disorder and serine/threonine phosphorylation in Mycobacterium tuberculosis |
Q27318204 | Association between the intrinsically disordered protein PEX19 and PEX3 |
Q34205647 | Asymmetric mRNA localization contributes to fidelity and sensitivity of spatially localized systems |
Q34215453 | Attributes of short linear motifs. |
Q38019703 | Beyond 'furballs' and 'dumpling soups' - towards a molecular architecture of signaling complexes and networks |
Q37844034 | Bioinformatic approaches for predicting substrates of proteases |
Q34158315 | Bioinformatics study of cancer-related mutations within p53 phosphorylation site motifs |
Q92860552 | Biotin proximity tagging favours unfolded proteins and enables the study of intrinsically disordered regions |
Q30399739 | Bringing order to protein disorder through comparative genomics and genetic interactions |
Q39021870 | Cancer/testis antigen PAGE4, a regulator of c-Jun transactivation, is phosphorylated by homeodomain-interacting protein kinase 1, a component of the stress-response pathway. |
Q38945211 | Cell-wide analysis of protein thermal unfolding reveals determinants of thermostability. |
Q36483608 | Cellular crowding imposes global constraints on the chemistry and evolution of proteomes |
Q36713371 | Cellular strategies for regulating functional and nonfunctional protein aggregation |
Q57027551 | Chaperones, Canalization, and Evolution of Animal Forms |
Q22061736 | Classification of intrinsically disordered regions and proteins |
Q34690914 | Cloning of the cryptochrome-encoding PeCRY1 gene from Populus euphratica and functional analysis in Arabidopsis |
Q37304876 | Comparative proteomics reveal distinct chaperone-client interactions in supporting bacterial acid resistance |
Q58104780 | Computational Studies of Intrinsically Disordered Proteins |
Q42722332 | Conformational B-cell epitopes prediction from sequences using cost-sensitive ensemble classifiers and spatial clustering |
Q47956508 | Constraints and consequences of the emergence of amino acid repeats in eukaryotic proteins |
Q36990763 | Curcumin inhibits HIV-1 by promoting Tat protein degradation |
Q23923181 | Cytochrome c/cardiolipin relations in mitochondria: a kiss of death |
Q36875645 | DNA Replication Stress Phosphoproteome Profiles Reveal Novel Functional Phosphorylation Sites on Xrs2 in Saccharomyces cerevisiae |
Q46607962 | Deciphering the cause of evolutionary variance within intrinsically disordered regions in human proteins |
Q34122227 | Deletion of immunoproteasome subunits imprints on the transcriptome and has a broad impact on peptides presented by major histocompatibility complex I molecules. |
Q30495887 | Dephosphorylation of F-BAR protein Cdc15 modulates its conformation and stimulates its scaffolding activity at the cell division site |
Q33818465 | Describing sequence-ensemble relationships for intrinsically disordered proteins |
Q35006962 | Determinants of translation efficiency and accuracy |
Q33436460 | Development of an accurate classification system of proteins into structured and unstructured regions that uncovers novel structural domains: its application to human transcription factors |
Q22061724 | Digested disorder: Quarterly intrinsic disorder digest (January/February/March, 2013). |
Q27666038 | Directed epitope delivery across the Escherichia coli outer membrane through the porin OmpF |
Q47701746 | Discovery of Cryoprotective Activity in Human Genome-Derived Intrinsically Disordered Proteins |
Q35823574 | Discovery of Small Molecules that Inhibit the Disordered Protein, p27(Kip1). |
Q27025729 | Disease mutations in disordered regions--exception to the rule? |
Q43664090 | Disorderness in Escherichia coli proteome: perception of folding fidelity and protein-protein interactions |
Q34697766 | Distinct types of disorder in the human proteome: functional implications for alternative splicing |
Q46125144 | Do intrinsically disordered proteins possess high specificity in protein-protein interactions? |
Q37588014 | Dynamic interactions of proteins in complex networks: a more structured view. |
Q50472416 | Dynamics of the intrinsically disordered protein CP12 in its association with GAPDH in the green alga Chlamydomonas reinhardtii: a fuzzy complex. |
Q47807596 | Enhanced Sampling of Intrinsic Structural Heterogeneity of the BH3-Only Protein Binding Interface of Bcl-xL. |
Q35739851 | Environmental Pressure May Change the Composition Protein Disorder in Prokaryotes |
Q39005050 | Erythropoietin and co.: intrinsic structure and functional disorder |
Q41769887 | Evaluation and properties of the budding yeast phosphoproteome |
Q35037936 | Evolution and disorder |
Q61798267 | Evolutionary Approach of Intrinsically Disordered CIP/KIP Proteins |
Q34197530 | Expanding the proteome: disordered and alternatively folded proteins |
Q30009321 | Fast and accurate discovery of degenerate linear motifs in protein sequences |
Q39292403 | Fluctuation sensitivity of a transcriptional signaling cascade. |
Q36438743 | From sequence and forces to structure, function, and evolution of intrinsically disordered proteins |
Q42061600 | Functional dissection of an intrinsically disordered protein: understanding the roles of different domains of Knr4 protein in protein-protein interactions |
Q90407754 | Gene Balance Predicts Transcriptional Responses Immediately Following Ploidy Change in Arabidopsis thaliana |
Q67228962 | Genome and transcriptome evolve separately in recently hybridized fungi |
Q33620737 | Genome-wide analysis of rice dehydrin gene family: Its evolutionary conservedness and expression pattern in response to PEG induced dehydration stress |
Q59807755 | Global impacts of chromosomal imbalance on gene expression in and other taxa |
Q33874396 | Global signatures of protein and mRNA expression levels |
Q42272603 | Graphlet kernels for prediction of functional residues in protein structures |
Q41172672 | HIV-1 Rev downregulates Tat expression and viral replication via modulation of NAD(P)H:quinine oxidoreductase 1 (NQO1). |
Q39421348 | Heterogeneity reduces sensitivity of cell death for TNF-stimuli |
Q24337888 | High levels of structural disorder in scaffold proteins as exemplified by a novel neuronal protein, CASK-interactive protein1 |
Q50540318 | How disorder influences order and vice versa--mutual effects in fusion proteins containing an intrinsically disordered and a globular protein. |
Q37756001 | Hub promiscuity in protein-protein interaction networks |
Q30009920 | Human 14-3-3 paralogs differences uncovered by cross-talk of phosphorylation and lysine acetylation |
Q47352295 | HyRes: a coarse-grained model for multi-scale enhanced sampling of disordered protein conformations |
Q47307167 | Hydrophobicity diversity in globular and nonglobular proteins measured with the Gini index |
Q92212142 | Hypothesis: protein and RNA attributes are continuously optimized over time |
Q47227239 | IDPs in macromolecular complexes: the roles of multivalent interactions in diverse assemblies. |
Q38275632 | Identification of intrinsically disordered regions in PTEN and delineation of its function via a network approach |
Q24624622 | Identification, analysis, and prediction of protein ubiquitination sites |
Q37058930 | Influence of crowded cellular environments on protein folding, binding, and oligomerization: biological consequences and potentials of atomistic modeling |
Q47625970 | Insights into human intrinsically disordered proteins from their gene expression profile |
Q33443462 | Insights into the regulation of intrinsically disordered proteins in the human proteome by analyzing sequence and gene expression data. |
Q33813499 | Integrative features of the yeast phosphoproteome and protein-protein interaction map |
Q58621285 | Interaction modulation through arrays of clustered methyl-arginine protein modifications |
Q33811809 | Interplay between chaperones and protein disorder promotes the evolution of protein networks |
Q34201884 | Intrinsic disorder and protein multibinding in domain, terminal, and linker regions |
Q43121399 | Intrinsic disorder in PTEN and its interactome confers structural plasticity and functional versatility |
Q41077744 | Intrinsic disorder: signaling via highly specific but short-lived association |
Q34051941 | Intrinsic protein disorder in human pathways |
Q47171932 | Intrinsic protein disorder reduces small-scale gene duplicability |
Q93060537 | Intrinsically Disordered Proteins in Chronic Diseases |
Q36604641 | Intrinsically disordered proteins and conformational noise: implications in cancer |
Q92697805 | Intrinsically disordered proteins and structured proteins with intrinsically disordered regions have different functional roles in the cell |
Q24633854 | Intrinsically disordered proteins are potential drug targets |
Q30389323 | Intrinsically disordered proteins in bcl-2 regulated apoptosis. |
Q35510300 | Intrinsically disordered proteins in cellular signalling and regulation. |
Q37932415 | Intrinsically disordered regions as affinity tuners in protein-DNA interactions |
Q34438593 | Intrinsically disordered segments affect protein half-life in the cell and during evolution |
Q37893583 | Intrinsically unstructured proteins and neurodegenerative diseases: conformational promiscuity at its best |
Q57080287 | Is there a biological cost of protein disorder? Analysis of cancer-associated mutations |
Q48251022 | Large-scale aggregation analysis of eukaryotic proteins reveals an involvement of intrinsically disordered regions in protein folding |
Q91817045 | Life in Phases: Intra- and Inter- Molecular Phase Transitions in Protein Solutions |
Q33998907 | MIRTFnet: analysis of miRNA regulated transcription factors |
Q26852359 | Mapping and analysis of phosphorylation sites: a quick guide for cell biologists |
Q34688655 | Marked variability in the extent of protein disorder within and between viral families |
Q50993055 | MeCP2, A Modulator of Neuronal Chromatin Organization Involved in Rett Syndrome. |
Q51491940 | Meta-structure correlation in protein space unveils different selection rules for folded and intrinsically disordered proteins. |
Q42206678 | Modelling the structure of full-length Epstein-Barr virus nuclear antigen 1. |
Q64087496 | Modulation of Disordered Proteins with a Focus on Neurodegenerative Diseases and Other Pathologies |
Q42180912 | Molecular principles of human virus protein-protein interactions |
Q37746989 | Molecular simulations of protein disorder |
Q43749902 | MpAsr encodes an intrinsically unstructured protein and enhances osmotic tolerance in transgenic Arabidopsis |
Q27319580 | Mussel adhesion is dictated by time-regulated secretion and molecular conformation of mussel adhesive proteins. |
Q90245881 | Mutations in disordered proteins as early indicators of nucleic acid changes triggering speciation |
Q37919366 | Mutual effects of disorder and order in fusion proteins between intrinsically disordered domains and fluorescent proteins. |
Q37246459 | Mutual synergistic protein folding in split intein |
Q91738942 | Mutually exclusive locales for N-linked glycans and disorder in human glycoproteins |
Q33799817 | N-terminal domains of DELLA proteins are intrinsically unstructured in the absence of interaction with GID1/gibberellic acid receptors. |
Q33999903 | N-termini of fungal CSL transcription factors are disordered, enriched in regulatory motifs and inhibit DNA binding in fission yeast |
Q43206102 | Neurodegeneration and Cancer: Where the Disorder Prevails |
Q36964989 | Non-random distribution of homo-repeats: links with biological functions and human diseases |
Q35094005 | Opposing effects of glutamine and asparagine govern prion formation by intrinsically disordered proteins |
Q26739978 | Order, Disorder, and Everything in Between |
Q64264148 | PEST sequences from a cactus dehydrin regulate its proteolytic degradation |
Q34500105 | PROSPER: an integrated feature-based tool for predicting protease substrate cleavage sites |
Q34410240 | Paradigms of protein degradation by the proteasome |
Q33909288 | Pathological unfoldomics of uncontrolled chaos: intrinsically disordered proteins and human diseases |
Q35397840 | Phosphorylation in intrinsically disordered regions regulates the activity of Neurogenin2. |
Q34095295 | Phosphorylation in protein-protein binding: effect on stability and function. |
Q38910392 | Phosphorylation-induced conformational dynamics in an intrinsically disordered protein and potential role in phenotypic heterogeneity |
Q26823798 | Physicochemical properties of cells and their effects on intrinsically disordered proteins (IDPs) |
Q30420946 | Post-translational modifications induce significant yet not extreme changes to protein structure |
Q33734025 | Posttranslational regulation impacts the fate of duplicated genes |
Q41660989 | Potential Roles of Intrinsic Disorder in Maternal-Effect Proteins Involved in the Maintenance of DNA Methylation |
Q35906471 | PredRSA: a gradient boosted regression trees approach for predicting protein solvent accessibility |
Q37549950 | Predicting intrinsic disorder in proteins: an overview |
Q28476679 | Prediction and analysis of protein hydroxyproline and hydroxylysine |
Q30378436 | Prediction of Functionally Important Phospho-Regulatory Events in Xenopus laevis Oocytes. |
Q34460299 | Prediction of protein phosphorylation sites by using the composition of k-spaced amino acid pairs |
Q30380439 | Prediction of protein solvent accessibility using PSO-SVR with multiple sequence-derived features and weighted sliding window scheme |
Q42714012 | Proceedings of the 12th Annual UT-ORNL-KBRIN Bioinformatics Summit 2013 |
Q38132466 | Promiscuity as a functional trait: intrinsically disordered regions as central players of interactomes |
Q34448124 | Prostate-associated gene 4 (PAGE4) protects cells against stress by elevating p21 and suppressing reactive oxygen species production |
Q26748530 | Prostate-associated gene 4 (PAGE4), an intrinsically disordered cancer/testis antigen, is a novel therapeutic target for prostate cancer |
Q59813486 | Proteasomal Degradation Machinery: Favorite Target of HIV-1 Proteins |
Q92818075 | Protein Abundance Biases the Amino Acid Composition of Disordered Regions to Minimize Non-functional Interactions |
Q31039692 | Protein Ensembles: How Does Nature Harness Thermodynamic Fluctuations for Life? The Diverse Functional Roles of Conformational Ensembles in the Cell |
Q36153874 | Protein abundance is key to distinguish promiscuous from functional phosphorylation based on evolutionary information |
Q28485920 | Protein complex formation: computational clarification of the sequential versus probabilistic recruitment puzzle |
Q35610649 | Protein expression regulation under oxidative stress |
Q36320524 | Protein folding and the order/disorder paradox |
Q37241586 | Protein intrinsic disorder and influenza virulence: the 1918 H1N1 and H5N1 viruses |
Q37541123 | Protein intrinsic disorder and network connectivity. The case of 14-3-3 proteins |
Q54985031 | Protein plasticity driven by disorder and collapse governs the heterogeneous binding of CytR to DNA. |
Q39094533 | Protein synthesis rate is the predominant regulator of protein expression during differentiation |
Q21999552 | Quantifying the mechanisms of domain gain in animal proteins |
Q36455398 | Quantitative nature of overexpression experiments |
Q30387256 | Reciprocal regulation of metabolic and signaling pathways |
Q27488434 | Regulating highly dynamic unstructured proteins and their coding mRNAs |
Q36152760 | Regulation of HBEGF by Micro-RNA for Survival of Developing Human Trophoblast Cells. |
Q37040613 | Regulation of Proteasomal Degradation by Modulating Proteasomal Initiation Regions |
Q34567970 | Regulation of protein-protein binding by coupling between phosphorylation and intrinsic disorder: analysis of human protein complexes |
Q27010644 | Relating sequence encoded information to form and function of intrinsically disordered proteins |
Q35806093 | Roles of long and short replication initiation proteins in the fate of IncP-1 plasmids. |
Q39743125 | SCFFbl12 Increases p21Waf1/Cip1 Expression Level through Atypical Ubiquitin Chain Synthesis |
Q34133238 | Sequence signatures and mRNA concentration can explain two-thirds of protein abundance variation in a human cell line |
Q27021549 | Signal activation and inactivation by the Gα helical domain: a long-neglected partner in G protein signaling |
Q42151102 | Specificity and affinity quantification of flexible recognition from underlying energy landscape topography |
Q52666816 | Stoichiometric balance of protein copy numbers is measurable and functionally significant in a protein-protein interaction network for yeast endocytosis. |
Q38130678 | Structural disorder and the loss of RNA homeostasis in aging and neurodegenerative disease. |
Q37588016 | Structural disorder in amyloid fibrils: its implication in dynamic interactions of proteins |
Q47562775 | Structural disorder: a tool for housekeeping proteins performing tissue-specific interactions |
Q42541552 | Structural role of RKS motifs in chromatin interactions: a molecular dynamics study of HP1 bound to a variably modified histone tail |
Q97092532 | Survival of the cheapest: how proteome cost minimization drives evolution |
Q42680947 | Susceptibility of p53 unstructured N terminus to 20 S proteasomal degradation programs the stress response. |
Q42595942 | System-wide analysis reveals intrinsically disordered proteins are prone to ubiquitylation after misfolding stress. |
Q34154562 | TANGLE: two-level support vector regression approach for protein backbone torsion angle prediction from primary sequences |
Q42582536 | Tau-er of Power |
Q59137449 | Ten Years of Tau-Targeted Immunotherapy: The Path Walked and the Roads Ahead |
Q92411725 | The Balancing Act of Intrinsically Disordered Proteins: Enabling Functional Diversity while Minimizing Promiscuity |
Q38268329 | The Bcl-2 family: structures, interactions and targets for drug discovery |
Q35161827 | The Cryptochrome Blue Light Receptors |
Q64266529 | The Evolutionary History and Functional Divergence of Trehalase () Genes in Insects |
Q36114159 | The Loss and Gain of Functional Amino Acid Residues Is a Common Mechanism Causing Human Inherited Disease |
Q35684410 | The Role of Interferon Regulatory Factor-1 (IRF1) in Overcoming Antiestrogen Resistance in the Treatment of Breast Cancer. |
Q41768887 | The SCHOOL of nature: II. Protein order, disorder and oligomericity in transmembrane signaling |
Q38779767 | The alphabet of intrinsic disorder: I. Act like a Pro: On the abundance and roles of proline residues in intrinsically disordered proteins |
Q28080017 | The contribution of intrinsically disordered regions to protein function, cellular complexity, and human disease |
Q92458761 | The host cell ubiquitin ligase protein CHIP is a potent suppressor of HIV-1 replication |
Q26863623 | The interface of protein structure, protein biophysics, and molecular evolution |
Q43258539 | The nanny model for IDPs. |
Q56700805 | The phosphatidylinositol transfer protein RdgBβ binds 14-3-3 via its unstructured C-terminus, whereas its lipid-binding domain interacts with the integral membrane protein ATRAP (angiotensin II type I receptor-associated protein) |
Q34046537 | The protein kingdom extended: ordered and intrinsically disordered proteins, their folding, supramolecular complex formation, and aggregation. |
Q39155657 | The protein level of PGC-1α, a key metabolic regulator, is controlled by NADH-NQO1. |
Q35185458 | The relationships among microRNA regulation, intrinsically disordered regions, and other indicators of protein evolutionary rate |
Q36019033 | The role of protein intrinsic disorder in major psychiatric disorders |
Q30501250 | The role of proteosome-mediated proteolysis in modulating potentially harmful transcription factor activity in Saccharomyces cerevisiae. |
Q41969384 | The role of structural disorder in the rewiring of protein interactions through evolution. |
Q47693846 | The roles of intrinsic disorder-based liquid-liquid phase transitions in the "Dr. Jekyll-Mr. Hyde" behavior of proteins involved in amyotrophic lateral sclerosis and frontotemporal lobar degeneration |
Q30569787 | The rust transferred proteins-a new family of effector proteins exhibiting protease inhibitor function |
Q42663688 | The structural and functional signatures of proteins that undergo multiple events of post-translational modification |
Q34355349 | Therapeutic strategies to inhibit MYC |
Q30398082 | Time, space, and disorder in the expanding proteome universe |
Q88030587 | Translational Control by Prion-like Proteins |
Q51060526 | Tuning the precision of predictors to reduce overestimation of protein disorder over large datasets. |
Q50919522 | Under-folded proteins: Conformational ensembles and their roles in protein folding, function, and pathogenesis. |
Q30385084 | Understanding protein non-folding. |
Q27000495 | Wrecked regulation of intrinsically disordered proteins in diseases: pathogenicity of deregulated regulators |
Search more.