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Academic Radiology, ISSN 1076-6332, 10/2019, Volume 26, Issue 10, pp. 1421 - 1431
Radiology education is suited to delivery via e-learning which may be used to fill gaps in knowledge and help prepare medical students for internship. There is... 
Medical students | Radiology | Medical education | E-learning | Diagnostic imaging | Adaptive tutorials | Internship programs | Methods
Journal Article
Journal of Urology, The, ISSN 0022-5347, 2017, Volume 197, Issue 4, pp. e1076 - e1076
Journal Article
Clinical Orthopaedics and Related Research, ISSN 0009-921X, 03/2013, Volume 471, Issue 3, pp. 871 - 877
Journal Article
by Tedja, Milly S and Wojciechowski, Robert and Hysi, Pirro G and Eriksson, Nicholas and Furlotte, Nicholas A and Verhoeven, Virginie J. M and Iglesias, Adriana I and Meester-Smoor, Magda A and Tompson, Stuart W and Fan, Qiao and Khawaja, Anthony P and Cheng, Ching-Yu and Höhn, René and Yamashiro, Kenji and Wenocur, Adam and Grazal, Clare and Haller, Toomas and Metspalu, Andres and Wedenoja, Juho and Jonas, Jost B and Wang, Ya Xing and Xie, Jing and Mitchell, Paul and Foster, Paul J and Klein, Barbara E. K and Klein, Ronald and Paterson, Andrew D and Hosseini, S. Mohsen and Shah, Rupal L and Williams, Cathy and Teo, Yik Ying and Tham, Yih Chung and Gupta, Preeti and Zhao, Wanting and Shi, Yuan and Saw, Woei-Yuh and Tai, E-Shyong and Sim, Xue Ling and Huffman, Jennifer E and Polašek, Ozren and Hayward, Caroline and Bencic, Goran and Rudan, Igor and Wilson, James F and Aung, Tin and Veluchamy, Amutha B and Burdon, Kathryn P and Campbell, Harry and Chen, Li Jia and Chen, Peng and Chen, Wei and Chew, Emily and Deangelis, Margaret M and Ding, Xiaohu and Döring, Angela and Evans, David M and Feng, Sheng and Fleck, Brian and Fogarty, Rhys D and Fondran, Jeremy R and Fossarello, Maurizio and Guo, Xiaobo and Haarman, Annet E. G and He, Mingguang and Howe, Laura D and Janmahasatian, Sarayut and Jhanji, Vishal and Kähönen, Mika and Kaprio, Jaakko and Kemp, John P and Khaw, Kay-Tee and Khor, Chiea-Chuen and Krapohl, Eva and Korobelnik, Jean-François and Lee, Kris and Li, Shi-Ming and Lu, Yi and Luben, Robert N and Mäkelä, Kari-Matti and McMahon, George and Meguro, Akira and Mihailov, Evelin and Miyake, Masahiro and Mizuki, Nobuhisa and Morrison, Margaux and Nangia, Vinay and Oexle, Konrad and Panda-Jonas, Songhomitra and Pang, Chi Pui and Pirastu, Mario and Plomin, Robert and Rantanen, Taina and Schache, Maria and Seppälä, Ilkka and Smith, George D and Pourcain, Beate St and Tam, Pancy O and Tideman, J. Willem L and Timpson, Nicholas J and Vaccargiu, Simona and ... and UK Biobank Eye Vis Consortium and CREAM and 23andMe Res Team and CREAM Consortium and 23andMe Research Team and UK Biobank Eye and Vision Consortium and The CREAM Consortium
Nature Genetics, ISSN 1061-4036, 06/2018, Volume 50, Issue 6, pp. 834 - 848
Journal Article
European Journal of Vascular & Endovascular Surgery, ISSN 1078-5884, 04/2019, Volume 57, Issue 4, pp. 554 - 560
Lower extremity amputation (LEA) is more common in people from lower socio-economic groups. This study examined this further by investigating the influence of... 
Scottish index of multiple deprivation | Lower extremity amputation | Quality of life | SURGERY | RATES | PERIPHERAL VASCULAR DISEASE | NEIGHBORHOOD | OUTCOMES | INDEX | Implants, Artificial | Prosthesis | Amputation | Index Medicus
Journal Article
Science, ISSN 0036-8075, 08/2014, Volume 345, Issue 6197, pp. 688 - 693
Spinal muscular atrophy (SMA) is a genetic disease caused by mutation or deletion of the survival of motor neuron 1 (SMN1) gene. A paralogous gene in humans,... 
SURVIVAL | EXON | PROTEIN | GENE | POLN | MULTIDISCIPLINARY SCIENCES | 3' ADENYLATION | INHIBITORS | Motor neurons | Genetic aspects | Longevity | Health aspects | Spinal muscular atrophy | RNA splicing | Signal transduction | Nervous system | Genetic disorders | Muscular system | Neurons | Proteins | Atrophy | Drugs | Muscles | Mice | Patients
Journal Article
PLoS ONE, ISSN 1932-6203, 10/2018, Volume 13, Issue 10, pp. e0206158 - e0206158
Nonsense mutations, resulting in a premature stop codon in the open reading frame of mRNAs are responsible for thousands of inherited diseases. Readthrough of... 
SYNTHETIC AMINOGLYCOSIDES | ZEBRAFISH | PTC124 | MULTIDISCIPLINARY SCIENCES | MOUSE MODEL | HUMAN GENETIC-DISEASES | DESIGNER AMINOGLYCOSIDES | CYSTIC-FIBROSIS | SUPPRESSION | ATALUREN | NONSENSE MUTATION | Gentamicins - chemistry | Antibiotics, Antineoplastic - pharmacology | Gentamicins - therapeutic use | Kidney Diseases - pathology | Humans | Cells, Cultured | Codon, Terminator - chemical synthesis | Rats | Male | Open Reading Frames - genetics | Zebrafish - embryology | Rats, Sprague-Dawley | Animals | Gentamicins - pharmacology | Embryo, Nonmammalian | Kidney Diseases - chemically induced | Codon, Nonsense - chemical synthesis | Protein Synthesis Inhibitors - pharmacology | Aminoglycosides - pharmacology | Open Reading Frames - drug effects | Genetic Diseases, Inborn - drug therapy | Protein Synthesis Inhibitors - therapeutic use | Aminoglycosides - therapeutic use | Aminoglycosides | Codon | Genetic translation | Health aspects | Physiological aspects | Genetic aspects | Research | Gene mutations | Gentamicin | Disease | Nonsense mutation | Toxicity | Genes | Clinical trials | Cytotoxicity | Proteins | Insurance pools | Rodents | Translation termination | Aminoglycoside antibiotics | Biocompatibility | Safety | Genetic disorders | Stop codon | Cystic fibrosis | Pharmacology | Chemical compounds | Hereditary diseases | Reinsurance | Antibiotics | Mutation | Codons | Index Medicus
Journal Article