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Human Mutation, ISSN 1059-7794, 08/2011, Volume 32, Issue 8, pp. 894 - 899
Journal Article
Methods in Molecular Biology, ISSN 1064-3745, 2017, Volume 1498, pp. 191 - 197
In silico prediction methods have increasingly been valuable and popular in molecular biology, especially in human genetics, for deleteriousness prediction to... 
dbscSNV | dbNSFP | Functional prediction | Splice site | Database | In silico | Nonsynonymous | Protocol | Single nucleotide variant | Computational Biology - methods | Gene Expression - genetics | Computer Simulation | Humans | Databases, Genetic | Polymorphism, Single Nucleotide - genetics | Genome, Human - genetics | Index Medicus
Journal Article
Nucleic Acids Research, ISSN 0305-1048, 12/2014, Volume 42, Issue 22, pp. 13534 - 13544
In silico tools have been developed to predict variants that may have an impact on pre-mRNA splicing. The major limitation of the application of these tools to... 
DEFECTS | GENE | DATABASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | DISEASE | SITES | MUTATIONS | IDENTIFICATION | ABERRANT | CANCER | DBNSFP | Genetic Variation | RNA Splice Sites | Alternative Splicing | Position-Specific Scoring Matrices | Artificial Intelligence | Computer Simulation | Genes, Neoplasm | Humans | Genome, Human | Genomics - methods | Index Medicus | Data Resources and Analyses
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 04/2015, Volume 24, Issue 8, pp. 2125 - 2137
Journal Article
by Sims, Rebecca and Van Der Lee, Sven J and Naj, Adam C and Bellenguez, Céline and Badarinarayan, Nandini and Jakobsdottir, Johanna and Kunkle, Brian W and Boland, Anne and Raybould, Rachel and Bis, Joshua C and Martin, Eden R and Grenier-Boley, Benjamin and Heilmann-Heimbach, Stefanie and Chouraki, Vincent and Kuzma, Amanda B and Sleegers, Kristel and Vronskaya, Maria and Ruiz, Agustin and Graham, Robert R and Olaso, Robert and Hoffmann, Per and Grove, Megan L and Vardarajan, Badri N and Hiltunen, Mikko and Nöthen, Markus M and White, Charles C and Hamilton-Nelson, Kara L and Epelbaum, Jacques and Maier, Wolfgang and Choi, Seung-Hoan and Beecham, Gary W and Dulary, Cécile and Herms, Stefan and Smith, Albert V and Funk, Cory C and Derbois, Céline and Forstner, Andreas J and Ahmad, Shahzad and Li, Hongdong and Bacq, Delphine and Harold, Denise and Satizabal, Claudia L and Valladares, Otto and Squassina, Alessio and Thomas, Rhodri and Brody, Jennifer A and Qu, Liming and Sánchez-Juan, Pascual and Morgan, Taniesha and Wolters, Frank J and Zhao, Yi and Garcia, Florentino Sanchez and Denning, Nicola and Fornage, Myriam and Malamon, John and Naranjo, Maria Candida Deniz and Majounie, Elisa and Mosley, Thomas H and Dombroski, Beth and Wallon, David and Lupton, Michelle K and Dupuis, Josée and Whitehead, Patrice and Fratiglioni, Laura and Medway, Christopher and Jian, Xueqiu and Mukherjee, Shubhabrata and Keller, Lina and Brown, Kristelle and Lin, Honghuang and Cantwell, Laura B and Panza, Francesco and McGuinness, Bernadette and Moreno-Grau, Sonia and Burgess, Jeremy D and Solfrizzi, Vincenzo and Proitsi, Petra and Adams, Hieab H and Allen, Mariet and Seripa, Davide and Pastor, Pau and Cupples, L Adrienne and Price, Nathan D and Hannequin, Didier and Frank-García, Ana and Levy, Daniel and Chakrabarty, Paramita and Caffarra, Paolo and Giegling, Ina and Beiser, Alexa S and Giedraitis, Vilmantas and Hampel, Harald and Garcia, Melissa E and Wang, Xue and Lannfelt, Lars and Mecocci, Patrizia and Eiriksdottir, Gudny and Crane, Paul K and Pasquier, Florence and Boccardi, Virginia and ... and EADI and GERAD PERADES and ARUKConsortium and CHARGE and ADGC and GERAD/PERADES, CHARGE, ADGC, EADI and ARUK Consortium and Stockholms universitet and Centrum för forskning om äldre och åldrande (ARC), (tills m KI) and Samhällsvetenskapliga fakulteten
Nature Genetics, ISSN 1061-4036, 09/2017, Volume 49, Issue 9, pp. 1373 - 1384
Journal Article
by Malik, Rainer and Chauhan, Ganesh and Traylor, Matthew and Sargurupremraj, Muralidharan and Okada, Yukinori and Mishra, Aniket and Rutten-Jacobs, Loes and Giese, Anne-Katrin and Van Der Laan, Sander W and Gretarsdottir, Solveig and Anderson, Christopher D and Chong, Michael and Adams, Hieab H. H and Ago, Tetsuro and Almgren, Peter and Amouyel, Philippe and Ay, Hakan and Bartz, Traci M and Benavente, Oscar R and Bevan, Steve and Boncoraglio, Giorgio B and Brown, Robert D and Butterworth, Adam S and Carrera, Caty and Carty, Cara L and Chasman, Daniel I and Chen, Wei-Min and Cole, John W and Correa, Adolfo and Cotlarciuc, Ioana and Cruchaga, Carlos and Danesh, John and De Bakker, Paul I. W and Destefano, Anita L and Den Hoed, Marcel and Duan, Qing and Engelter, Stefan T and Falcone, Guido J and Gottesman, Rebecca F and Grewal, Raji P and Gudnason, Vilmundur and Gustafsson, Stefan and Haessler, Jeffrey and Harris, Tamara B and Hassan, Ahamad and Havulinna, Aki S and Heckbert, Susan R and Holliday, Elizabeth G and Howard, George and Hsu, Fang-Chi and Hyacinth, Hyacinth I and Ikram, M. Arfan and Ingelsson, Erik and Irvin, Marguerite R and Jian, Xueqiu and Jiménez-Conde, Jordi and Johnson, Julie A and Jukema, J. Wouter and Kanai, Masahiro and Keene, Keith L and Kissela, Brett M and Kleindorfer, Dawn O and Kooperberg, Charles and Kubo, Michiaki and Lange, Leslie A and Langefeld, Carl D and Langenberg, Claudia and Launer, Lenore J and Lee, Jin-Moo and Lemmens, Robin and Leys, Didier and Lewis, Cathryn M and Lin, Wei-Yu and Lindgren, Arne G and Lorentzen, Erik and Magnusson, Patrik K and Maguire, Jane and Manichaikul, Ani and McArdle, Patrick F and Meschia, James F and Mitchell, Braxton D and Mosley, Thomas H and Nalls, Michael A and Ninomiya, Toshiharu and O'Donnell, Martin J and Psaty, Bruce M and Pulit, Sara L and Rannikmäe, Kristiina and Reiner, Alexander P and Rexrode, Kathryn M and Rice, Kenneth and Rich, Stephen S and Ridker, Paul M and Rost, Natalia S and Rothwell, Peter M and Rotter, Jerome I and Rundek, Tatjana and Sacco, Ralph L and Sakaue, Saori and Sale, Michele M and ... and AFGen Consortium and UK Young Lacunar DNA Study and EPIC-CVD Consortium and Int Stroke Genetics Consortium ISG and INVENT Consortium and Int Genomics Blood Pressure iGEN and MEGASTROKE Consortium and COMPASS Consortium and METASTROKE Consortium and EPIC-InterAct Consortium and Cohorts Heart Aging Res Genomic and BioBank Japan Cooperative Hosp Grp and NINDS Stroke Genetics Network Si and STARNET and Neurology Working Grp Charge Con and Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium and International Stroke Genetics Consortium (ISGC) and NINDS Stroke Genetics Network (SiGN) and International Genomics of Blood Pressure (iGEN-BP) Consortium and BioBank Japan Cooperative Hospital Group and Neurology Working Group of the CHARGE Consortium and Science for Life Laboratory, SciLifeLab and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för immunologi, genetik och patologi and Medicinsk genetik och genomik and Geriatrik and Kardiovaskulär epidemiologi and Uppsala universitet and Institutionen för medicinska vetenskaper and Molekylär epidemiologi and Institutionen för folkhälso- och vårdvetenskap
Nature Genetics, ISSN 1061-4036, 04/2018, Volume 50, Issue 4, pp. 524 - 537
Journal Article
地质学报:英文版, ISSN 1000-9515, 2017, Volume 91, Issue S1, pp. 229 - 230
<正>1 Introduction Geochemical mapping at national and continental scales continues to present challenges worldwide due to variations in geologic and... 
GEOSCIENCES, MULTIDISCIPLINARY | Temporal distribution | Spatial discrimination | Spatial analysis | Comparative studies | Geochemistry | Rocks | Data | Regolith
Journal Article
The FEBS Journal, ISSN 1742-464X, 06/2017, Volume 284, Issue 11, pp. 1738 - 1747
Osteomyelitis is an inflammation of the bone and bone marrow that occurs as a consequence of infections mainly attributed to Staphylococcus aureus . In a... 
osteomyelitis | 3L1 | osteogenesis | CHI | Notch signaling | CHI3L1 | PROTEIN | BIOCHEMISTRY & MOLECULAR BIOLOGY | RUNX2 | OSTEOCLASTOGENESIS | NOTCH SIGNALING PATHWAY | MICE | BONE | MUTATIONS | EXPRESSION | RNA, Small Interfering - genetics | Up-Regulation | Femur - pathology | Chitinase-3-Like Protein 1 - antagonists & inhibitors | Gene Expression Profiling | Jagged-1 Protein - biosynthesis | Femur - microbiology | Osteomyelitis - metabolism | RNA Interference | Chitinase-3-Like Protein 1 - physiology | Osteomyelitis - pathology | Cytokines - genetics | Staphylococcal Infections - metabolism | Bone Resorption | Signal Transduction | Mice, Inbred C57BL | Chitinase-3-Like Protein 1 - genetics | Bacterial Load | Osteoclasts - metabolism | Jagged-1 Protein - genetics | Receptor, Notch1 - biosynthesis | Animals | Osteomyelitis - microbiology | Mice | Receptor, Notch1 - genetics | Cytokines - biosynthesis | Inflammation - physiopathology | Osteomyelitis | Inflammation | Analysis | Staphylococcus aureus | Staphylococcus aureus infections | Chitinase | Animal models | Destruction | Genes | Osteoblasts | Blood | Signal transduction | Alterations | Control | Mouse devices | Computed tomography | Mineralization | Rodents | Penicillin | Bone marrow | Biocompatibility | Inhibition | Jagged1 protein | Bone (cortical) | Cytokines | RNA-mediated interference | Interference | Bone turnover | Ribonucleic acid--RNA | Gene expression | Patients | Osteoclastogenesis | Osteoblastogenesis | Osteoclasts | Notch protein | Differentiation | Osteogenesis | Index Medicus
Journal Article