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by Scarpa, Aldo and Chang, David K and Nones, Katia and Corbo, Vincenzo and Patch, Ann-Marie and Bailey, Peter and Lawlor, Rita T and Johns, Amber L and Miller, David K and Mafficini, Andrea and Rusev, Borislav and Scardoni, Maria and Antonello, Davide and Barbi, Stefano and Sikora, Katarzyna O and Cingarlini, Sara and Vicentini, Caterina and McKay, Skye and Quinn, Michael C.J and Bruxner, Timothy J.C and Christ, Angelika N and Harliwong, Ivon and Idrisoglu, Senel and McLean, Suzanne and Nourse, Craig and Nourbakhsh, Ehsan and Wilson, Peter J and Anderson, Matthew J and Fink, J. Lynn and Newell, Felicity and Waddell, Nick and Holmes, Oliver and Kazakoff, Stephen H and Leonard, Conrad and Wood, Scott and Xu, Qinying and Nagaraj, Shivashankar Hiriyur and Amato, Eliana and Dalai, Irene and Bersani, Samantha and Cataldo, Ivana and Dei Tos, Angelo P and Capelli, Paola and Davì, Maria Vittoria and Landoni, Luca and Malpaga, Anna and Miotto, Marco and Whitehall, Vicki L.J and Leggett, Barbara A and Harris, Janelle L and Harris, Jonathan and Jones, Marc D and Humphris, Jeremy and Chantrill, Lorraine A and Chin, Venessa and Nagrial, Adnan M and Pajic, Marina and Scarlett, Christopher J and Pinho, Andreia and Rooman, Ilse and Toon, Christopher and Wu, Jianmin and Pinese, Mark and Cowley, Mark and Barbour, Andrew and Mawson, Amanda and Humphrey, Emily S and Colvin, Emily K and Chou, Angela and Lovell, Jessica A and Jamieson, Nigel B and Duthie, Fraser and Gingras, Marie-Claude and Fisher, William E and Dagg, Rebecca A and Lau, Loretta M.S and Lee, Michael and Pickett, Hilda A and Reddel, Roger R and Samra, Jaswinder S and Kench, James G and Merrett, Neil D and Epari, Krishna and Nguyen, Nam Q and Zeps, Nikolajs and Falconi, Massimo and Simbolo, Michele and Butturini, Giovanni and Van Buren, George and Partelli, Stefano and Fassan, Matteo and Khanna, Kum Kum and Gill, Anthony J and Wheeler, David A and Gibbs, Richard A and Musgrove, Elizabeth A and Bassi, Claudio and Tortora, Giampaolo and Pederzoli, Paolo and Pearson, John V and ... and Australian Pancreatic Canc Genome and Australian Pancreatic Cancer Genome Initiative
Nature, ISSN 0028-0836, 03/2017, Volume 543, Issue 7643, pp. 65 - 71
Journal Article
Nature Cell Biology, ISSN 1465-7392, 01/2015, Volume 17, Issue 1, pp. 68 - 80
The contractile actomyosin cytoskeleton and its connection to the plasma membrane are critical for control of cell shape and migration. We identify three... 
MATRIX | BORDER CELLS | INVASION | COMPLEX | IN-VIVO | PROTEIN PHOSPHATASE 2A | POLARIZATION | MYOSIN PHOSPHATASE | MICROARRAY DATA | DROSOPHILA | CELL BIOLOGY | Phosphorylation | Autoantigens - metabolism | Humans | Phosphoprotein Phosphatases - metabolism | Autoantigens - genetics | Cell Movement - genetics | Neoplasm Metastasis | RNA Interference | rho-Associated Kinases - metabolism | Apoptosis Regulatory Proteins - genetics | Cytoskeletal Proteins - metabolism | Female | Membrane Proteins - metabolism | Microfilament Proteins - metabolism | Calmodulin-Binding Proteins - genetics | Actin Cytoskeleton - metabolism | Signal Transduction | Membrane Proteins - genetics | Computational Biology | Protein-Serine-Threonine Kinases - genetics | Proto-Oncogene Proteins - genetics | Calmodulin-Binding Proteins - metabolism | Actomyosin - metabolism | Protein-Serine-Threonine Kinases - biosynthesis | Carrier Proteins - genetics | Protein Phosphatase 1 - metabolism | Animals | Breast Neoplasms - genetics | Carrier Proteins - metabolism | Breast Neoplasms - pathology | Protein Phosphatase 2 - metabolism | Cell Line, Tumor | RNA, Small Interfering | Drosophila melanogaster | Metastasis | Muscle proteins | Health aspects | Phosphotransferases | Analysis | Cancer cells | Index Medicus | Cytoskeletal Proteins | Medical and Health Sciences | Medicin och hälsovetenskap | Protein-Serine-Threonine Kinases | Breast Neoplasms | Klinisk medicin | Calmodulin-Binding Proteins | Journal Article | rho-Associated Kinases | Proto-Oncogene Proteins | Protein Phosphatase 2 | Protein Phosphatase 1 | Carrier Proteins | Phosphoprotein Phosphatases | Actin Cytoskeleton | Actomyosin | Autoantigens | Membrane Proteins | Clinical Medicine | Apoptosis Regulatory Proteins | Microfilament Proteins | Research Support, Non-U.S. Gov't | Cancer and Oncology | Cell Movement | Cancer och onkologi
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 07/2011, Volume 286, Issue 28, pp. 25065 - 25075
Cerebral cavernous malformations (CCMs) are alterations in brain capillary architecture that can result in neurological deficits, seizures, or stroke. We... 
CEREBRAL CAVERNOUS MALFORMATIONS | STRIATIN FAMILY | PHOSPHATASE 2A | PATHWAY | BIOCHEMISTRY & MOLECULAR BIOLOGY | VASCULAR INTEGRITY | KINASE | RHO GTPASES | CELL-GROWTH | SACCHAROMYCES-CEREVISIAE | GENOME-SCALE | Protein Phosphatase 2 - chemistry | Humans | Multiprotein Complexes - genetics | Proto-Oncogene Proteins - chemistry | Structure-Activity Relationship | Multiprotein Complexes - metabolism | Nerve Tissue Proteins - chemistry | HEK293 Cells | Apoptosis Regulatory Proteins - genetics | Membrane Proteins - metabolism | Golgi Apparatus - chemistry | Protein-Serine-Threonine Kinases - metabolism | Calmodulin-Binding Proteins - genetics | Proto-Oncogene Proteins - metabolism | Membrane Proteins - genetics | Apoptosis Regulatory Proteins - chemistry | Protein Phosphatase 2 - genetics | Protein-Serine-Threonine Kinases - genetics | Proto-Oncogene Proteins - genetics | Calmodulin-Binding Proteins - chemistry | Calmodulin-Binding Proteins - metabolism | Nerve Tissue Proteins - genetics | Apoptosis Regulatory Proteins - metabolism | Nerve Tissue Proteins - metabolism | Multiprotein Complexes - chemistry | Animals | Membrane Proteins - chemistry | Protein Phosphatase 2 - metabolism | Golgi Apparatus - metabolism | Mice | Protein-Serine-Threonine Kinases - chemistry | HeLa Cells | Golgi Apparatus - genetics | Index Medicus | MST4 | Striatin | Signal Transduction | Mass Spectrometry (MS) | Golgi | PP2A | Serine Threonine Protein Phosphatase | Serine Threonine Protein Kinase | Cerebral Cavernous Malformations | Protein-Protein Interactions
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 03/2010, Volume 120, Issue 3, pp. 744 - 755
Wolfram syndrome is an autosomal-recessive disorder characterized by insulin-dependent diabetes mellitus, caused by nonautoimmune loss of beta cells, and... 
DIABETES-MELLITUS | MEDICINE, RESEARCH & EXPERIMENTAL | WFS1 GENE | UNFOLDED PROTEIN RESPONSE | HUMAN HRD1 | PANCREATIC BETA-CELLS | PSYCHIATRIC-ILLNESS | ENDOPLASMIC-RETICULUM STRESS | OPTIC ATROPHY | ATF6 | TRANSMEMBRANE PROTEIN | Humans | Ubiquitin - metabolism | Cercopithecus aethiops | Endoplasmic Reticulum - metabolism | Wolfram Syndrome - genetics | Activating Transcription Factor 6 - genetics | Wolfram Syndrome - pathology | Endoplasmic Reticulum - pathology | Insulin-Secreting Cells - metabolism | Trans-Activators - genetics | Membrane Proteins - metabolism | Calmodulin-Binding Proteins - genetics | Endoplasmic Reticulum - genetics | Signal Transduction | Gene Expression Regulation - genetics | Membrane Proteins - genetics | Ubiquitin-Protein Ligases - metabolism | Rats | Wolfram Syndrome - metabolism | Calmodulin-Binding Proteins - metabolism | Ubiquitin - genetics | Unfolded Protein Response | Proteasome Endopeptidase Complex - genetics | Activating Transcription Factor 6 - metabolism | Animals | Cell Line, Tumor | Trans-Activators - metabolism | Mice | Insulin-Secreting Cells - pathology | Proteasome Endopeptidase Complex - metabolism | Ubiquitin-Protein Ligases - genetics | COS Cells | Ubiquitination - genetics | Ubiquitin | Care and treatment | Pancreatic beta cells | Genetic disorders | Physiological aspects | Genetic aspects | Research | Gene expression | Risk factors | Index Medicus | Abridged Index Medicus
Journal Article
The Plant Journal, ISSN 0960-7412, 09/2008, Volume 55, Issue 5, pp. 760 - 773
Based on our previous findings, we proposed a pathway for the participation of Ca 2+ /calmodulin (CaM) in heat‐shock (HS) signal transduction. The specific... 
calmodulin‐binding protein kinase | thermotolerance | calmodulin | phosphorylation of HSF | Arabidopsis | signal transduction | Signal transduction | Phosphorylation of HSF | Thermotolerance | Calmodulin | Calmodulin-binding protein kinase | DNA-BINDING | PHOSPHORYLATION | MOLECULAR CHAPERONES | STRESS TRANSCRIPTION FACTORS | ACQUIRED THERMOTOLERANCE | PLANT SCIENCES | IN-VITRO | calmodulin-binding protein kinase | CALCIUM | BINDING PROTEIN-KINASE | ENERGY-TRANSFER | Phosphorylation | Arabidopsis - enzymology | Genes, Plant | Genetic Complementation Test | Heat Shock Transcription Factors | Arabidopsis Proteins - metabolism | DNA-Binding Proteins - metabolism | Heat-Shock Proteins - genetics | Gene Expression Regulation, Plant | Fluorescence Resonance Energy Transfer | Transcription, Genetic | Plant Proteins - metabolism | Arabidopsis Proteins - genetics | Calcium-Calmodulin-Dependent Protein Kinases - genetics | Plants, Genetically Modified - genetics | Signal Transduction | Heat-Shock Proteins - metabolism | Plants, Genetically Modified - enzymology | Hot Temperature | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Reverse Transcriptase Polymerase Chain Reaction | Arabidopsis - genetics | Transcription Factors - metabolism | Heat-Shock Response | Plant Proteins - genetics | Two-Hybrid System Techniques | DNA, Bacterial - genetics | Protein Binding | Mutagenesis, Insertional | Calcium-Calmodulin-Dependent Protein Kinases - metabolism | Arabidopsis thaliana | Proteins | Heat shock proteins | Physiological aspects | Protein kinases | Fluorescence | Kinases | Genetic recombination | Botany | Index Medicus
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 06/2009, Volume 84, Issue 6, pp. 718 - 727
Journal Article
Genes Chromosomes and Cancer, ISSN 1045-2257, 2009, Volume 49, Issue 12, pp. 1114 - 1124
The diagnosis of myoepithelial (ME) tumors outside salivary glands remains challenging, especially in unusual clinical presentations, such as bone or visceral... 
ONCOLOGY | CHORDOMA | GENETICS & HEREDITY | IN-SITU HYBRIDIZATION | DEFINES | SALIVARY-GLANDS | MUCOEPIDERMOID CARCINOMA | EXPRESSION | ADENOMAS | POU5F1 | RNA-Binding Proteins - genetics | Salivary Gland Neoplasms - genetics | Soft Tissue Neoplasms - diagnosis | Humans | Middle Aged | Biomarkers, Tumor | Octamer Transcription Factor-3 - genetics | Young Adult | Molecular Diagnostic Techniques | Oncogene Fusion | Skin Neoplasms - diagnosis | Adult | Bone Neoplasms - genetics | Cytogenetic Analysis | Pre-B-Cell Leukemia Transcription Factor 1 | Child | Soft Tissue Neoplasms - genetics | Calmodulin-Binding Proteins - genetics | Myoepithelioma - diagnosis | Gene Expression | Zinc Fingers | Bone Neoplasms - diagnosis | RNA-Binding Protein FUS - genetics | Immunophenotyping | In Situ Hybridization, Fluorescence | Proto-Oncogene Proteins - genetics | DNA-Binding Proteins - genetics | Myoepithelioma - genetics | Salivary Gland Neoplasms - diagnosis | Oncogene Proteins, Fusion - genetics | Gene Rearrangement | Skin Neoplasms - genetics | Adolescent | Aged | RNA-Binding Protein EWS | Pediatrics | Lung | Benign | Cytology | FUS gene | Salivary gland | Bone tumors | EWSR1 gene | FLI-1 protein | Soft tissues | Clear cells | FUS protein | Fluorescence in situ hybridization | Skin | Children | gene rearrangement | Differentiation | Tumors | Index Medicus
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 09/2018, Volume 103, Issue 3, pp. 413 - 420
Journal Article
Scientific Reports, ISSN 2045-2322, 03/2016, Volume 6, Issue 1, pp. 23685 - 23685
Journal Article
Clinical Journal of the American Society of Nephrology, ISSN 1555-9041, 12/2017, Volume 12, Issue 12, pp. 1974 - 1983
Background and objectives Genetic heterogeneity and phenotypic variability are major challenges in familial nephronophthisis and related ciliopathies. To date,... 
Prevalence | Nephronophthisis related ciliopathy | Ciliopathies | Joubert-like syndromes | NEPHREG registry | Bardet-Biedl syndrome | Senior-Løken syndrome | Congenital oculomotor apraxia | Genetic heterogeneity | Kidney diseases, cystic | Homozygote | Kidney failure, chronic | Nephronophthisis (NPH) | Adolescent | Mainzer-Saldino syndrome | Registries | Mutation | COACH syndrome | Nephronophthisis, familial juvenile | Cross-Sectional studies | ADOLESCENT NEPHRONOPHTHISIS | JOUBERT-SYNDROME | FAMILIAL JUVENILE NEPHRONOPHTHISIS | SENIOR-LOKEN SYNDROME | CYSTIC KIDNEY-DISEASE | GENE | RENAL-FAILURE | UROLOGY & NEPHROLOGY | NPHP3 | MUTATIONS | DOMAIN PROTEIN | Polyuria - genetics | Humans | Kidney Diseases, Cystic - diagnostic imaging | Male | Ciliopathies - complications | Nervous System Diseases - genetics | Young Adult | Ciliopathies - genetics | Anemia - genetics | Kidney - diagnostic imaging | Ultrasonography | Kidney Diseases, Cystic - genetics | Kinesin - genetics | Female | Glomerular Filtration Rate - genetics | Neoplasm Proteins - genetics | Child | Calmodulin-Binding Proteins - genetics | Kidney Failure, Chronic - physiopathology | Antigens, Neoplasm - genetics | Cross-Sectional Studies | Membrane Proteins - genetics | Kidney Failure, Chronic - genetics | Proteins - genetics | Carrier Proteins - genetics | Phenotype | Adaptor Proteins, Signal Transducing - genetics | Kidney Diseases, Cystic - complications | Kidney Diseases, Cystic - congenital | Longitudinal Studies | Index Medicus | Genetic Heterogeneity | Kidney Diseases, Cystic | Kidney Failure, Chronic | Original
Journal Article