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1. Full Text NEK8 Links the ATR-Regulated Replication Stress Response and S Phase CDK Activity to Renal Ciliopathies
by Choi, Hyo Jei Claudia and Lin, Jia-Ren and Vannier, Jean-Baptiste and Slaats, Gisela G and Kile, Andrew C and Paulsen, Renee D and Manning, Danielle K and Beier, David R and Giles, Rachel H and Boulton, Simon J and Cimprich, Karlene A
Molecular Cell, ISSN 1097-2765, 08/2013, Volume 51, Issue 4, pp. 423 - 439
Renal ciliopathies are a leading cause of kidney failure, but their exact etiology is poorly understood. NEK8/NPHP9 is a ciliary kinase associated with two... 
FORK | CHK1 | DNA-DAMAGE RESPONSE | POLYCYSTIC KIDNEY-DISEASE | STABILITY | BIOCHEMISTRY & MOLECULAR BIOLOGY | GENOME INTEGRITY | KINASE | DOUBLE-STRAND BREAKS | MAMMALIAN-CELLS | FAMILY | CELL BIOLOGY | Protein Kinases - metabolism | Genomic Instability | Phosphorylation | Protein Kinases - genetics | Cyclin-Dependent Kinases - metabolism | Humans | Stress, Physiological | Protein Kinases - chemistry | Polycystic Kidney Diseases - pathology | Cell Cycle Proteins - genetics | DNA Damage - genetics | Cell Culture Techniques | Cyclin-Dependent Kinases - genetics | Protein-Serine-Threonine Kinases - metabolism | Polycystic Kidney Diseases - metabolism | Cilia - pathology | Cell Cycle Proteins - metabolism | Protein-Serine-Threonine Kinases - genetics | Ataxia Telangiectasia Mutated Proteins | Mutation - genetics | Cilia - metabolism | Cell Cycle Checkpoints | Animals | DNA Replication - genetics | S Phase - physiology | Mice | NIMA-Related Kinases | Hypertension | Architecture | DNA damage | Genomics | NEK8 | renal ciliopathies | DNA replication | replication stress | cyclin | nephronophthisis | polycystic kidney disease | DNA damage response (DDR) | cyclin-dependent kinase (CDK) | replication fork | ATR | DNA double-strand breaks (DSBs)
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2. Full Text Lethal Skeletal Dysplasia in Mice and Humans Lacking the Golgin GMAP-210
by Smits, Patrick and Bolton, Andrew D and Funari, Vincent and Hong, Minh and Boyden, Eric D and Lu, Lei and Manning, Danielle K and Dwyer, Noelle D and Moran, Jennifer L and Prysak, Mary and Merriman, Barry and Nelson, Stanley F and Bonafé, Luisa and Superti-Furga, Andrea and Ikegawa, Shiro and Krakow, Deborah and Cohn, Daniel H and Kirchhausen, Tom and Warman, Matthew L and Beier, David R
The New England Journal of Medicine, ISSN 0028-4793, 01/2010, Volume 362, Issue 3, pp. 206 - 216
A form of skeletal dysplasia in mice is caused by a mutation in a gene that is critical for the functioning of the Golgi apparatus. A mutation in the... 
MEDICINE, GENERAL & INTERNAL | PROTEIN | RIBBON FORMATION | ER STRESS | MOUSE | PHENOTYPE | MECHANISMS | MUTATIONS | THYROID-HORMONE RECEPTOR | APPARATUS | CARTILAGE | Chondrocytes - cytology | Cell Proliferation | Humans | Glycosylation | Codon, Nonsense | Genes, Recessive | Sequence Analysis, DNA | Endoplasmic Reticulum - ultrastructure | Protein Processing, Post-Translational - physiology | Phenotype | Animals | Osteochondrodysplasias - genetics | Mice, Mutant Strains | Nuclear Proteins - deficiency | Cell Differentiation | Mice | Polymorphism, Single Nucleotide | Nuclear Proteins - genetics | Golgi Apparatus - ultrastructure | Aphasia | Lethal mutation | Bones | Genetic aspects | Health aspects | Abnormalities | Neonates | Nonsense mutation | Collagen (type II) | Genes | Perlecan | Genomes | Hybridization | Proteins | Cartilage | Rodents | Fibroblasts | Bone dysplasia | Extracellular matrix | Skeleton | Matrix protein | Golgi cells | Deoxyribonucleic acid--DNA | Thyroid | Phenotypes | Dysplasia | Cloning | Achondrogenesis | Heredity | Lungs | Cell death | Chondrocytes | Mutation | Genetic testing | Aggrecan | Gene mapping | Endoplasmic reticulum | Genetics | Index Medicus | Abridged Index Medicus
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3. Full Text Abstract 3417: Detection and analysis of oncovirus integration sites in FFPE-derived human tumor samples using hybrid capture and massively parallel sequencing
by Slevin, Michael K and Powers, Winslow T and Burns, Robert T and Wollison, Bruce M and Coleman, Haley A and Paskavitz, Amanda L and Nag, Anwesha and Manning, Danielle K and Garcia, Elizabeth and Ducar, Matthew D and Thorner, Aaron R and MacConaill, Laura E
Cancer Research, ISSN 0008-5472, 07/2018, Volume 78, Issue 13 Supplement, pp. 3417 - 3417
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4. Full Text ANKS6 is the critical activator of NEK8 kinase in embryonic situs determination and organ patterning
by Czarnecki, Peter G and Gabriel, George C and Manning, Danielle K and Sergeev, Mikhail and Lemke, Kristi and Klena, Nikolai T and Liu, Xiaoqin and Chen, Yu and Li, You and San Agustin, Jovenal T and Garnaas, Maija K and Francis, Richard J and Tobita, Kimimasa and Goessling, Wolfram and Pazour, Gregory J and Lo, Cecilia W and Beier, David R and Shah, Jagesh V
Nature Communications, ISSN 2041-1723, 01/2015, Volume 6, Issue 1, p. 6023
The ciliary kinase NEK8 plays a critical role in situs determination and cystic kidney disease, yet its exact function remains unknown. In this study, we... 
CILIARY | LOCALIZATION | TRANSITION ZONE | POLYCYSTIC KIDNEY-DISEASE | MULTIDISCIPLINARY SCIENCES | MOUSE | NEPHRONOPHTHISIS | LEFT-RIGHT ASYMMETRY | MUTATIONS | CONGENITAL HEART-DEFECTS | INVERSUS
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5. Full Text Inv acts as a molecular anchor for Nphp3 and Nek8 in the proximal segment of primary cilia
by Shiba, Dai and Manning, Danielle K and Koga, Hisashi and Beier, David R and Yokoyama, Takahiko
Cytoskeleton, ISSN 1949-3584, 02/2010, Volume 67, Issue 2, pp. 112 - 119
A primary cilium is an antenna‐like structure extending from the surface of most vertebrate cells. It is structurally divided along its vertical axis into... 
Inv | Nek8 | Inversin | primary cilia | NPHP | Primary cilia | Nphp | POLYCYSTIN-1 | SITUS-INVERSUS | LOCALIZATION | PROTEIN | CAUSE NEPHRONOPHTHISIS | CELL BIOLOGY | JOUBERT-SYNDROME | NEPHROCYSTIN-4 | GENE | MUTATIONS | CENTROSOMES | Protein Kinases - metabolism | Cell Line | Protein Kinases - genetics | Protein-Serine-Threonine Kinases | Transcription Factors - genetics | Cilia - metabolism | Kinesin - metabolism | Transcription Factors - metabolism | Carrier Proteins - genetics | Animals | Carrier Proteins - metabolism | Kinesin - genetics | Mice | Microscopy, Fluorescence | NIMA-Related Kinases
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6. Full Text Nek8 regulates the expression and localization of polycystin-1 and polycystin-2
by Sohara, Eisei and Luo, Ying and Zhang, Jingjing and Manning, Danielle K and Beier, David R and Zhou, Jing
Journal of the American Society of Nephrology, ISSN 1046-6673, 03/2008, Volume 19, Issue 3, pp. 469 - 476
Nek8 is a serine/threonine kinase that is mutated in the jck (juvenile cystic kidneys) mouse, a model of autosomal recessive juvenile polycystic kidney... 
NIMA-RELATED KINASE | FAMILY KINASE | GENE HOMOLOG | IN-VIVO | MOUSE | SUBCELLULAR-LOCALIZATION | UROLOGY & NEPHROLOGY | C-ELEGANS | MURINE MODELS | KIDNEY-DISEASE PROTEINS | PRIMARY CILIA | Protein Kinases - metabolism | Up-Regulation | Phosphorylation | Cilia - pathology | Protein-Serine-Threonine Kinases | Cilia - metabolism | Animals | Mice | Kidney Tubules - pathology | Mutation | Kidney Tubules - metabolism | NIMA-Related Kinases | TRPP Cation Channels - metabolism | Basic Research
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7. Full Text Loss of the ciliary kinase Nek8 causes left-right asymmetry defects
by Manning, Danielle K and Sergeev, Mikhail and Van Heesbeen, Roy G and Wong, Michael D and Oh, Jin-Hee and Liu, Yan and Henkelman, R. Mark and Drummond, Iain and Shah, Jagesh V and Beier, David R
Journal of the American Society of Nephrology, ISSN 1046-6673, 12/2013, Volume 24, Issue 1, pp. 100 - 112
A missense mutation in mouse Nek8, which encodes a ciliary kinase, produces the juvenile cystic kidneys (jck) model of polycystic kidney disease, but the... 
SITUS-INVERSUS | NODAL EXPRESSION | POLYCYSTIC KIDNEY-DISEASE | PROTEIN-KINASE | CAUSE NEPHRONOPHTHISIS | CATION CHANNEL | MOUSE MODEL | NEURAL ACTIVITY | UROLOGY & NEPHROLOGY | RIGHT AXIS DETERMINATION | MICE | Biomarkers - metabolism | Cilia - physiology | Polycystic Kidney Diseases - genetics | Heart Defects, Congenital - embryology | Mice, Inbred C57BL | Protein-Serine-Threonine Kinases - genetics | Male | Zebrafish | Homozygote | Phenotype | Animals | Body Patterning | Female | Heterozygote | Mice | Protein-Serine-Threonine Kinases - metabolism | Disease Models, Animal | NIMA-Related Kinases | TRPP Cation Channels - metabolism | Basic Research
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8. Full Text Loss of the Ciliary KinaseNek8Causes Left-Right Asymmetry Defects
by Manning, Danielle K and Sergeev, Mikhail and van Heesbeen, Roy G and Wong, Michael D and Oh, Jin-Hee and Liu, Yan and Henkelman, R. Mark and Drummond, Iain and Shah, Jagesh V and Beier, David R
Journal of the American Society of Nephrology, ISSN 1046-6673, 01/2013, Volume 24, Issue 1, pp. 100 - 112
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9. Full Text Utilization of a whole genome SNP panel for efficient genetic mapping in the mouse
by Moran, Jennifer L and Bolton, Andrew D and Tran, Pamela V and Brown, Alison and Dwyer, Noelle D and Manning, Danielle K and Bjork, Bryan C and Li, Cheng and Montgomery, Kate and Siepka, Sandra M and Vitaterna, Martha Hotz and Takahashi, Joseph S and Wiltshire, Tim and Kwiatkowski, David J and Kucherlapati, Raju and Beier, David R
Genome Research, ISSN 1088-9051, 03/2006, Volume 16, Issue 3, pp. 436 - 440
Phenotype-driven genetics can be used to create mouse models of human disease and birth defects. However, the utility of these mutant models is limited without... 
POLYMORPHISMS | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | BIOCHEMISTRY & MOLECULAR BIOLOGY | DISEASE | GENETICS & HEREDITY | MICE | MUTATIONS | EXPRESSION | Mice - genetics | Animals | Cloning, Organism | Chromosome Mapping - methods | Humans | Mice, Inbred C57BL | Genotype | Polymorphism, Single Nucleotide | Mutation | Genome | Mice, Inbred Strains | Chromosome mapping | Birth defects | Genetic aspects | Single nucleotide polymorphisms | Research | Resources
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10. Full Text A forward genetic screen with a thalamocortical axon reporter mouse yields novel neurodevelopment mutants and a distinct emx2 mutant phenotype
by Dwyer, Noelle D and Manning, Danielle K and Moran, Jennifer L and Mudbhary, Raksha and Fleming, Michael S and Favero, Carlita B and Vock, Vita M and O'Leary, Dennis D.M and Walsh, Christopher A and Beier, David R
Neural Development, ISSN 1749-8104, 01/2011, Volume 6, Issue 1, pp. 3 - 3
Background: The dorsal thalamus acts as a gateway and modulator for information going to and from the cerebral cortex. This activity requires the formation of... 
DEFECTS | TOPOGRAPHY | MICE | DEVELOPMENTAL BIOLOGY | MUTATIONS | CONNECTIONS | LOCUS TEST | PROJECTIONS | MAMMALIAN FOREBRAIN | EXPRESSION | NEUROSCIENCES | CEREBRAL-CORTEX | Body Patterning - drug effects | Thalamus - metabolism | Embryo, Mammalian | Alkylating Agents - pharmacology | Gene Expression Regulation, Developmental - genetics | Lac Operon - genetics | Male | Axons - physiology | Genetic Testing - methods | Cerebral Cortex - metabolism | Serine Endopeptidases - genetics | beta-Galactosidase - metabolism | Female | Cell Adhesion Molecules, Neuronal - metabolism | Neural Pathways - embryology | Extracellular Matrix Proteins - metabolism | Extracellular Matrix Proteins - genetics | Mice, Inbred C57BL | Neural Pathways - growth & development | Gene Expression Regulation, Developmental - drug effects | Mice, Transgenic | Transcription Factors - genetics | Mutation - genetics | Nerve Tissue Proteins - genetics | Cell Adhesion Molecules, Neuronal - genetics | Homeodomain Proteins - genetics | Ethylnitrosourea - pharmacology | Nerve Tissue Proteins - metabolism | Thalamus - embryology | Phenotype | Thalamus - growth & development | Animals | Cerebral Cortex - embryology | Neural Pathways - abnormalities | Cerebral Cortex - growth & development | Mice | Mice, Inbred BALB C | Serine Endopeptidases - metabolism | Body Patterning - genetics | Usage | Genetic aspects | Research | Gene mutations | Neurogenesis | Genetic screening | Brain | Neurosciences | Histology | Rodents
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11. Full Text Defects in ciliary localization of Nek8 is associated with cystogenesis
by Trapp, Melissa L and Trapp, Melissa L and Galtseva, Alevtina and Galtseva, Alevtina and Manning, Danielle K and Manning, Danielle K and Beier, David R and Beier, David R and Rosenblum, Norman D and Rosenblum, Norman D and Quarmby, Lynne M and Quarmby, Lynne M
Pediatric Nephrology, ISSN 0931-041X, 3/2008, Volume 23, Issue 3, pp. 377 - 387
Mutations in the human NIMA (Never in Mitosis gene A)-related kinase 8 (Nek8) are associated with a rare form of the juvenile renal cystic disease,... 
Pediatrics | Nephronophthisis | Medicine & Public Health | Kinases | Polycystic kidney disease | Cilia | nephronophthisis | POLYCYSTIC KIDNEY-DISEASE | MOUSE | PKD1 | CHLAMYDOMONAS | NIMA-RELATED KINASE | kinases | polycystic kidney disease | UROLOGY & NEPHROLOGY | PEDIATRICS | cilia | MICE | CENTROSOMES | GENE-PRODUCT | Polycystic Kidney Diseases - genetics | Protein Kinases - genetics | Animals | Kidney - embryology | Protein-Serine-Threonine Kinases | Mice | Mutation | Kidney Tubules - metabolism | Protein Kinases - biosynthesis | Cilia - metabolism | Cilia - genetics | NIMA-Related Kinases
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12. Full Text ANKS6 is the critical activator of NEK8 kinase in embryonic situs determination and organ patterning
by Czarnecki, Peter G and Gabriel, George C and Manning, Danielle K and Sergeev, Mikhail and Lemke, Kristi and Klena, Nikolai T and Liu, Xiaoqin and Chen, Yu and Li, You and San Agustin, Jovenal T and Garnaas, Maija K and Francis, Richard J and Tobita, Kimimasa and Goessling, Wolfram and Pazour, Gregory J and Lo, Cecilia W and Beier, David R and Shah, Jagesh V
Nature communications, 01/2015, Volume 6, p. 6023
The ciliary kinase NEK8 plays a critical role in situs determination and cystic kidney disease, yet its exact function remains unknown. In this study, we... 
Cell Line | Morphogenesis - genetics | Humans | Protein-Serine-Threonine Kinases - genetics | Rats | Male | Nuclear Proteins - metabolism | Transcription Factors - genetics | Blotting, Western | Body Patterning - physiology | Kinesin - metabolism | Transcription Factors - metabolism | Carrier Proteins - genetics | Animals | Carrier Proteins - metabolism | Kinesin - genetics | Female | Mice | Mutation | Nuclear Proteins - genetics | Body Patterning - genetics | Morphogenesis - physiology | Protein-Serine-Threonine Kinases - metabolism | NIMA-Related Kinases
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13. Utilization of a whole genome SNP panel for efficient genetic mapping in the mouse
by Moran, Jennifer L and Bolton, Andrew D and Tran, Pamela V and Brown, Alison and Dwyer, Noelle D and Manning, Danielle K and Bjork, Bryan C and Li, Cheng and Montgomery, Kate and Siepka, Sandra M and Vitaterna, Martha Hotz and Takahashi, Joseph S and Wiltshire, Tim and Kwiatkowski, David J and Kucherlapati, Raju and Beier, David R
Genome Research, ISSN 1088-9051, 03/2006, Volume 16, Issue 3, pp. 436 - 440
Phenotype-driven genetics can be used to create mouse models of human disease and birth defects. However, the utility of these mutant models is limited without... 
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14. Full Text Rare and low-frequency coding variants alter human adult height
by Marouli, Eirini and Graff, Mariaelisa and Medina-Gomez, Carolina and Lo, Ken Sin and Wood, Anew R and Kjaer, Troels R and Fine, Rebecca S and Lu, Yingchang and Schurmann, Claudia and Highland, Heather M and Rüeger, Sina and Thorleifsson, Gudmar and Justice, Anne E and Lamparter, David and Stirrups, Kathleen E and Turcot, Valérie and Young, Kristin L and Winkler, Thomas W and Esko, Tõnu and Karaderi, Tugce and Locke, Adam E and Masca, Nicholas G. D and Ng, Maggie C. Y and Mudgal, Poorva and Rivas, Manuel A and Vedantam, Sailaja and Mahajan, Anubha and Guo, Xiuqing and Abecasis, Goncalo and Aben, Katja K and Adair, Linda S and Alam, Dewan S and Albrecht, Eva and Allin, Kristine H and Allison, Matthew and Amouyel, Philippe and Appel, Emil V and Arveiler, Dominique and Asselbergs, Folkert W and Auer, Paul L and Balkau, Beverley and Banas, Bernhard and Bang, Lia E and Benn, Marianne and Bergmann, Sven and Bielak, Lawrence F and Blüher, Matthias and Boeing, Heiner and Boerwinkle, Eric and Böger, Carsten A and Bonnycastle, Lori L and Bork-Jensen, Jette and Bots, Michiel L and Bottinger, Erwin P and Bowden, Donald W and Brandslund, Ivan and Breen, Gerome and Brilliant, Murray H and Broer, Linda and Burt, Amber A and Butterworth, Adam S and Carey, David J and Caulfield, Mark J and Chambers, John C and Chasman, Daniel I and Chen, Yii-Der Ida and Chowdhury, Rajiv and Christensen, Cramer and Chu, Auey Y and Cocca, Massimiliano and Collins, Francis S and Cook, James P and Corley, Janie and Galbany, Jordi Corominas and Cox, Amanda J and Cuellar-Partida, Gabriel and Danesh, John and Davies, Gail and de Bakker, Paul I. W and de Borst, Gert J and de Denus, Simon and de Groot, Mark C. H and de Mutsert, Renée and Deary, Ian J and Dedoussis, George and Demerath, Ellen W and den Hollander, Anneke I and Dennis, Joe G and Di Angelantonio, Emanuele and nos, Fotios and Du, Mengmeng and Dunning, Alison M and Easton, Douglas F and Ebeling, Tapani and Edwards, Todd L and Ellinor, Patrick T and Elliott, Paul and Evangelou, Evangelos and Farmaki, Aliki-Eleni and Faul, Jessica D and ... and EPIC-CVD Consortium and GoT2D Genes Consortium and MAGIC Investigators and Global Lipids Genetics Consortium and EPIC-InterAct Consortium and ReproGen Consortium and ExomeBP Consortium and CHD Exome Consortium and T2D-Genes Consortium and The EPIC-InterAct Consortium and CHD Exome+ Consortium and Medicinska fakulteten and Institutionen för folkhälsa och klinisk medicin and Enheten för biobanksforskning and Allmänmedicin and Umeå universitet and Medicin
Nature, ISSN 0028-0836, 2017, Volume 542, Issue 7640, pp. 186 - 190
Height is a highly heritable, classic polygenic trait with approximately 700 common associated variants identified through genome-wide association studies so... 
MISSING HERITABILITY | GENETIC ARCHITECTURE | INTERLEUKIN-11 | MUTATIONS | MULTIDISCIPLINARY SCIENCES | GENOME-WIDE ASSOCIATION | Stature | Genetic aspects | Observations | Genetic variation | Studies | Datasets | Disease | Genes | Deoxyribonucleic acid--DNA | Hälsovetenskaper | Folkhälsovetenskap, global hälsa, socialmedicin och epidemiologi | Medical and Health Sciences | Medicin och hälsovetenskap | Public Health, Global Health, Social Medicine and Epidemiology | Health Sciences
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15. Full Text Observation of the Doubly Charmed Baryon Xi(++)(cc)
by Dufour, L and Mulder, M and Onderwater, C. J. G and Pellegrino, Antonio and Tolk, S and van Veghel, M and LHCb Collaboration
Physical Review Letters, ISSN 0031-9007, 09/2017, Volume 119, Issue 11
A highly significant structure is observed in the Lambda K-+(c)-pi(+)pi(+) mass spectrum, where the Lambda(+)(c) baryon is reconstructed in the decay mode... 
MONTE-CARLO | GENERATOR | MASSES | B-C MESONS | DECAY | SPECTROSCOPY | HADRONIC PRODUCTION | VERSION | HEAVY BARYONS | GENXICC | PHYSICS, MULTIDISCIPLINARY | Physics - High Energy Physics - Experiment
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16. Full Text Abstracts of the HIV Research for Prevention Meeting, HIVR4P, 21-25 October, 2018, Madrid
AIDS Research and Human Retroviruses, ISSN 0889-2229, 10/2018, Volume 34, Issue S1, pp. 1 - 407
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17. Full Text Measurements of the branching fractions of $\Lambda_{c}^{+} \rightarrow p \pi^{-} \pi^{+}$, $\Lambda_{c}^{+} \rightarrow p K^{-} K^{+}$, and $\Lambda_{c}^{+} \rightarrow p \pi^{-} K^{+}
by LHCb collaboration and Aaij, R and Adeva, B and Adinolfi, M and Ajaltouni, Z and Akar, S and Albrecht, J and Alessio, F and Alexander, M and Albero, A. Alfonso and Ali, S and Alkhazov, G and Cartelle, P. Alvarez and AlvesJr, A. A and Amato, S and Amerio, S and Amhis, Y and An, L and Anderlini, L and Andreassi, G and Andreotti, M and Andrews, J. E and Appleby, R. B and Archilli, F and d'Argent, P and Romeu, J. Arnau and Artamonov, A and Artuso, M and Aslanides, E and Auriemma, G and Baalouch, M and Babuschkin, I and Bachmann, S and Back, J. J and Badalov, A and Baesso, C and Baker, S and Balagura, V and Baldini, W and Baranov, A and Barlow, R. J and Barschel, C and Barsuk, S and Barter, W and Baryshnikov, F and Batozskaya, V and Battista, V and Bay, A and Beaucourt, L and Beddow, J and Bedeschi, F and Bediaga, I and Beiter, A and Bel, L. J and Beliy, N and Bellee, V and Belloli, N and Belous, K and Belyaev, I and Ben-Haim, E and Bencivenni, G and Benson, S and Beranek, S and Berezhnoy, A and Bernet, R and Berninghoff, D and Bertholet, E and Bertolin, A and Betancourt, C and Betti, F and Bettler, M. -O and van Beuzekom, M and Bezshyiko, Ia and Bifani, S and Billoir, P and Birnkraut, A and Bitadze, A and Bizzeti, A and Bjørn, M and Blake, T and Blanc, F and Blouw, J and Blusk, S and Bocci, V and Boettcher, T and Bondar, A and Bondar, N and Bonivento, W and Bordyuzhin, I and Borgheresi, A and Borghi, S and Borisyak, M and Borsato, M and Bossu, F and Boubdir, M and Bowcock, T. J. V and Bowen, E and Bozzi, C and Braun, S and Britton, T and ...
11/2017
JHEP 03 (2018) 043 The ratios of the branching fractions of the decays $\Lambda_{c}^{+} \rightarrow p \pi^{-} \pi^{+}$, $\Lambda_{c}^{+} \rightarrow p K^{-}... 
Physics - High Energy Physics - Experiment
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18. Full Text Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals
by Dastani, Zari and Hivert, Marie-France and Timpson, Nicholas and Perry, John R. B and Yuan, Xin and Scott, Robert A and Henneman, Peter and Heid, Iris M and Kizer, Jorge R and Lyytikäinen, Leo-Pekka and Fuchsberger, Christian and Tanaka, Toshiko and Morris, Anew P and Small, Kerrin and Isaacs, Aaron and Beekman, Marian and Coassin, Stefan and Lohman, Kurt and Qi, Lu and Kanoni, Stavroula and Pankow, James S and Uh, Hae-Won and Wu, Ying and Bidulescu, Aurelian and Rasmussen-Torvik, Laura J and Greenwood, Celia M. T and Ladouceur, Martin and Grimsby, Jonna and Manning, Alisa K and Liu, Ching-Ti and Kooner, Jaspal and Mooser, Vincent E and Vollenweider, Peter and Kapur, Karen A and Chambers, John and Wareham, Nicholas J and Langenberg, Claudia and Frants, Rune and Willems-Vandijk, Ko and Oostra, Ben A and Willems, Sara M and Lamina, Claudia and Winkler, Thomas W and Psaty, Bruce M and Tracy, Russell P and Brody, Jennifer and Fouchier, Sigrid W and Hovingh, G. Kees and Boekholdt, S. Matthijs and Kastelein, John J. P and GLGC Investigators and DIAGRAM Consortium and MAGIC Consortium and MuTHER Consortium and Global B Pgen Consortium and MAGIC investigators and Procardis Consortium and DIAGRAM+ Consortium and GLGC Consortium and GIANT Consortium
PLoS genetics, ISSN 1553-7390, 2012, Volume 8, Issue 3, p. e1002607
Circulating levels of adiponectin, a hormone produced predominantly by adipocytes, are highly heritable and are inversely associated with type 2 diabetes... 
POPULATION | GENETIC-BASIS | VARIANTS | INSULIN-RESISTANCE | LIPID CONCENTRATIONS | GENETICS & HEREDITY | RISK | RECEPTOR | CORONARY-ARTERY-DISEASE | GENOME-WIDE ASSOCIATION | ADIPOSE-TISSUE | Gene Expression | Genetic Predisposition to Disease | Genome-Wide Association Study | Glucose Tolerance Test | Diabetes Mellitus, Type 2 - genetics | Humans | African Americans | European Continental Ancestry Group | Male | Cholesterol, HDL - genetics | Adiponectin - blood | Asian Continental Ancestry Group | Metabolic Networks and Pathways | Adiponectin - genetics | Insulin Resistance - genetics | Female | Polymorphism, Single Nucleotide | Waist-Hip Ratio | Type 2 diabetes | Physiological aspects | Development and progression | Genetic aspects | Research | Metabolism | Health aspects | Blood proteins | Meta-analysis | Medical research | Cardiovascular disease | Drug therapy | Insulin | Metabolic disorders | Medical and Health Sciences | Medicin och hälsovetenskap
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