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Biochemical journal, ISSN 1470-8728, 04/2015, Volume 467, Issue 3, pp. 365 - 386
.... The CRLs assemble into functional multisubunit complexes using a repertoire of substrate receptors, adaptors, Cullin scaffolds and RING-box proteins... 
Ubiquitin | Ubiquitination | Small molecule | Structure | Structure-based design | Assembly | Life Sciences & Biomedicine | Biochemistry & Molecular Biology | Science & Technology | Protein Structure, Tertiary | Protein Subunits | Cullin Proteins - antagonists & inhibitors | Proteasome Inhibitors - pharmacology | Humans | Models, Molecular | Proteasome Inhibitors - chemistry | Drug Discovery - methods | Cullin Proteins - chemistry | Cullin Proteins - genetics | Drug Design | Protein Structure, Quaternary | Molecular Structure | Index Medicus | MEL26, maternal effect lethal 26 | small molecule | HECT, homologous with E6-associated protein C-terminus | DCAF, DDB1–Cul4A-associated factor | CPH, conserved within Cul7, PARC and HERC2 | CSA, Cockayne syndrome A | structure-based design | NAE, NEDD8-activating enzyme | Rbx1, RING-box protein 1 | PPI, protein–protein interaction | C, anaphase-promoting complex | SV5, simian virus 5 | Fbxw, F-box | Skp2, S-phase kinase-associated protein 2 | IAA, indole-3-acetic acid | Cpd, compound | Fbw | SMER3, small-molecule enhancer of rapamycin 3 | mTOR, mammalian target of rapamycin | HERC2, HECT domain- and RLD (regulator of chromosome condensation 1 protein-like domain) domain-containing E3 ubiquitin protein ligase 2 | IκB, inhibitor of NF-κB | UPS, ubiquitin–proteasome system | Nrf2, nuclear factor-erythroid 2-related factor 2 | Protac, proteolysis-targeting chimaeric molecule | WD repeat-containing protein | ZIM (zinc finger expressed in inflorescence) domain protein 1 | NF-κB, nuclear factor κB | leucine-rich motif-containing protein | CTD, C-terminal domain | Ub, ubiquitin | Vif, virion infectivity factor | NTD, N-terminal domain | GHR, growth hormone receptor | CRBN, cereblon | HIF-1α, hypoxia-inducible factor 1α | SH2, Src homology 2 | BP, β-propeller | UBL, ubiquitin-like protein | FP, fluorescence polarization | Cks1, cyclin-dependent protein kinase regulatory subunit 1 | CSN, COP9 (constitutive photomorphogenesis 9) signalosome complex | ITC, isothermal titration calorimetry | RING, really interesting new gene | Ubc12, ubiquitin-conjugating enzyme 12 | KLHL, Kelch-like protein | Review | VPRBP, Vpr-binding protein | SCF, Skp1–Cdc53–F-box Cdc4 | POZ, pox virus and zinc finger | JAZ1, jasmonate | Keap1, Kelch-like enoyl-CoA hydratase-associated protein 1 | PARC, p53-associated parkin-like cytoplasmic protein | DDB, damage-specific DNA-binding protein | JA-Ile, jasmonoyl-isoleucine | Fbxl, F-box | MATH, meprin and TRAF (tumour necrosis factor receptor-associated factor) homology | CRL, Cullin–RING E3 ubiquitin ligase | assembly | other domain-containing protein | COI1, coronatine-insensitive protein 1 | EloBC, ElonginB–ElonginC complex | broad complex | VHL, von Hippel–Lindau | Vpr, viral protein R | Aux, auxin | STAT, signal transducer and activator of transcription | CAND1, Cullin-associated NEDD8-dissociated protein 1 | Fbxo, F-box | TIR1, transport inhibitor response 1 | CBFβ, core binding factor β | BCR, BTB–Cul3–Rbx1 | structure | ubiquitin | cyclosome | SOCS, suppressor of cytokine signalling | NEDD, neural-precursor-cell-expressed developmentally down-regulated | BTB, bric-a-brac | APC | ubiquitination | Cdc, cell division cycle | Cul, Cullin | SPOP, speckle-type POZ protein | β-TrCP, β-transducin repeat-containing protein | tramtrack | ASB, ankyrin repeat and SOCS-box
Journal Article
2006, 2nd ed., ISBN 0199212937, x, 352
Amyotrophic lateral sclerosis (or motor neurone disease) is a rare disease but one that can cause profound suffering for both the patient and their family.... 
Amyotrophic lateral sclerosis | Palliative Care | Palliative treatment | therapy | Patient Care and End-of-Life Decision Making | Palliative Medicine Research | neurology team | als | psychosocial care | amyotrophic lateral sclerosis | palliative care | motor neurone disease
Book
Nature (London), ISSN 1476-4687, 08/2012, Volume 489, Issue 7415, pp. 313 - 317
Cornelia de Lange syndrome (CdLS) is a dominantly inherited congenital malformation disorder, caused by mutations in the cohesin-loading protein NIPBL1,2 for nearly 60... 
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Chromatin - metabolism | Chondroitin Sulfate Proteoglycans - chemistry | Humans | Crystallography, X-Ray | Male | Phosphoproteins - metabolism | Cell Cycle Proteins - chemistry | Chromatin Immunoprecipitation | Repressor Proteins - deficiency | De Lange Syndrome - metabolism | Fibroblasts | Female | Transcription, Genetic | Acetylation | Binding Sites | Repressor Proteins - metabolism | De Lange Syndrome - genetics | Repressor Proteins - chemistry | Chromosomal Proteins, Non-Histone - metabolism | Histone Deacetylases - genetics | Cell Cycle Proteins - metabolism | Chondroitin Sulfate Proteoglycans - metabolism | Histone Deacetylases - chemistry | Histone Deacetylases - deficiency | Mutant Proteins - genetics | Prophase | Models, Molecular | Repressor Proteins - genetics | Histone Deacetylases - metabolism | Mutant Proteins - metabolism | Nuclear Proteins - metabolism | Mutation - genetics | Proteins - genetics | Mutant Proteins - chemistry | Protein Conformation | HeLa Cells | Adaptor Proteins, Signal Transducing - metabolism | Anaphase | Chromatin - genetics | Chromosomal Proteins, Non-Histone - chemistry | Genetics | De Lange syndrome | Genetic aspects | Research | Mutation (Biology) | Proteins | Cell culture | Genes | Cell cycle | Mutation | Females | Chromosomes | Crystal structure | Index Medicus | Chromatin | Repressor Proteins | Life Sciences | Phosphoproteins | Chromosomal Proteins, Non-Histone | Histone Deacetylases | De Lange Syndrome | Chondroitin Sulfate Proteoglycans | Nuclear Proteins | Mutant Proteins | Adaptor Proteins, Signal Transducing | Development Biology | Cell Cycle Proteins
Journal Article
Cell (Cambridge), ISSN 0092-8674, 11/2001, Volume 107, Issue 4, pp. 513 - 523
In humans, low peak bone mass is a significant risk factor for osteoporosis. We report that LRP5, encoding the low-density lipoprotein receptor-related protein 5, affects bone mass accrual during growth... 
Biochemistry & Molecular Biology | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Wnt2 Protein | Humans | Child, Preschool | Male | Bone Density - genetics | Wnt Proteins | Mesoderm - cytology | Wnt-5a Protein | Eye - embryology | Osteoporosis - genetics | Animals, Outbred Strains | Dishevelled Proteins | Bone Morphogenetic Proteins - pharmacology | Child | Organ Culture Techniques | Transforming Growth Factor beta | Signal Transduction | Chromosomes, Human, Pair 11 - genetics | Adaptor Proteins, Signal Transducing | Skull - cytology | Wnt3 Protein | Mice | Receptors, LDL - physiology | COS Cells | Species Specificity | LDL-Receptor Related Proteins | DNA, Complementary - genetics | Recombinant Fusion Proteins - physiology | Cercopithecus aethiops | Culture Media, Conditioned - pharmacology | Recombinant Proteins | Transfection | Receptors, LDL - deficiency | Stromal Cells - drug effects | Adult | Female | Phosphoproteins - physiology | Proteins - physiology | Receptors, LDL - genetics | Bone Morphogenetic Protein 2 | Low Density Lipoprotein Receptor-Related Protein-5 | Mice, Inbred C57BL | Zebrafish Proteins | Proto-Oncogene Proteins - genetics | Phosphoproteins - genetics | Eye Abnormalities - genetics | Genes, Recessive | Syndrome | Proteins - genetics | Animals | Proto-Oncogene Proteins - physiology | Heterozygote | Osteoblasts - metabolism | Stromal Cells - cytology | Wnt4 Protein | Osteoporosis | Bones | Density | Low density lipoproteins | Proteins | Cell research | Lipoproteins | Growth | Analysis | Physiological aspects | LDL receptor-related protein 5 | LRP5 protein | low density lipoprotein receptor-related protein 5 | osteoporosis-pseudoglioma syndrome | Index Medicus | Receptors, LDL | Mesoderm | Osteoblasts | Recombinant Fusion Proteins | Eye | Life Sciences | Stromal Cells | Eye Abnormalities | Phosphoproteins | Proto-Oncogene Proteins | Bone Density | Biochemistry, Molecular Biology | Culture Media, Conditioned | Skull | Chromosomes, Human, Pair 11 | Bone Morphogenetic Proteins | DNA, Complementary
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 02/2008, Volume 283, Issue 9, pp. 5598 - 5610
Spinal muscular atrophy (SMA) is caused by reduced levels of the survival of motor neuron (SMN) protein... 
Life Sciences & Biomedicine | Biochemistry & Molecular Biology | Science & Technology | RNA-Binding Proteins - genetics | Humans | Fragile X Syndrome - pathology | Fragile X Mental Retardation Protein - metabolism | Recombinant Fusion Proteins - metabolism | Motor Neurons - pathology | Muscular Atrophy, Spinal - genetics | Fragile X Syndrome - genetics | Muscular Atrophy, Spinal - metabolism | Survival of Motor Neuron 1 Protein | Fragile X Syndrome - metabolism | Hypothalamus - pathology | SMN Complex Proteins | Muscular Atrophy, Spinal - pathology | Nerve Tissue Proteins - genetics | Exons - physiology | Motor Neurons - metabolism | Nerve Tissue Proteins - metabolism | Cyclic AMP Response Element-Binding Protein - genetics | Animals | Hypothalamus - metabolism | Cyclic AMP Response Element-Binding Protein - metabolism | Cell Line, Tumor | Recombinant Fusion Proteins - genetics | Fragile X Mental Retardation Protein - genetics | Mice | RNA-Binding Proteins - metabolism | Protein Structure, Tertiary - physiology | Index Medicus | Protein Structure, Tertiary | Exons | Fragile X Syndrome | Biochemistry, Molecular Biology | Nerve Tissue Proteins | RNA-Binding Proteins | Hypothalamus | Recombinant Fusion Proteins | Fragile X Mental Retardation Protein | Life Sciences | Muscular Atrophy, Spinal | Motor Neurons | Cyclic AMP Response Element-Binding Protein | Molecular biology
Journal Article
Development (Cambridge), ISSN 1477-9129, 11/2006, Volume 133, Issue 23, pp. 4619 - 4630
sox10 is necessary for development of neural and pigment cell derivatives of the neural crest (NC). However, whereas a direct role for Sox10 activity has been... 
Fate specification | Waardenburg-shah syndrome | Zebrafish | Determination | Neural crest | Transgene | Dorsal roots ganglion | Sox10 | Neurogenin | Life Sciences & Biomedicine | Developmental Biology | Science & Technology | Ganglia, Spinal - cytology | Green Fluorescent Proteins - genetics | Stem Cells - cytology | Zebrafish - embryology | Recombinant Fusion Proteins - metabolism | Gene Expression Regulation, Developmental | Base Sequence | SOXE Transcription Factors | Carrier Proteins - physiology | Green Fluorescent Proteins - metabolism | Neurons, Afferent - cytology | Promoter Regions, Genetic | Basic Helix-Loop-Helix Transcription Factors - physiology | Nerve Tissue Proteins - physiology | Neural Crest - cytology | Basic Helix-Loop-Helix Transcription Factors - genetics | Animals, Genetically Modified | Cell Survival | Ganglia, Spinal - embryology | Nerve Tissue Proteins - genetics | Zebrafish - genetics | Zebrafish Proteins - physiology | DNA - genetics | Carrier Proteins - genetics | Phenotype | Animals | Neural Crest - embryology | Alleles | Recombinant Fusion Proteins - genetics | High Mobility Group Proteins - physiology | Models, Neurological | Mutation | Zebrafish Proteins - genetics | High Mobility Group Proteins - genetics | Index Medicus | High Mobility Group Proteins | Green Fluorescent Proteins | Neural Crest | Recombinant Fusion Proteins | Stem Cells | Life Sciences | Neurons, Afferent | Ganglia, Spinal | Basic Helix-Loop-Helix Transcription Factors | Carrier Proteins | Promoter Regions (Genetics) | Biochemistry, Molecular Biology | Zebrafish Proteins | Nerve Tissue Proteins | DNA
Journal Article