검색어 : 통합검색[Human molecular genetics 3]
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921
- Curdlan and other bacterial (1→3)-β-d-glucans
- McIntosh, M.; Stone, B. A.; Stanisich, V. A.; ; (Applied microbiology and biotechnology, v.68, 2005, pp.163-173)
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922
- MicroRNA Expression Profiling Altered by Variant Dosage of Radiation Exposure
- Lee, Kuei-Fang; Chen, Yi-Cheng; Hsu, Paul Wei-Che; Liu, Ingrid Y.; Wu, Lawrence Shih-Hsin; Institute of Medical Sciences, Tzu Chi University, No. 701, Zhongyang Road, Section 3, Hualien 97004, Taiwan; Department of Computer Science & Information Engineering, Tamkang University, New Taipei City 25137, Taiwan; Bioinformatics Core Laboratory, Institute of Molecular Biology, Academia Sinica, Taipei 11529, Taiwan; Department of Molecular Biology and Human Genetics, Tzu Chi University, Hualien 97004, Taiwan; Institute of Medical Sciences, Tzu Chi University, No. 701, Zhongyang Road, Section 3, Hualien 97004, Taiwan; (BioMed research international, v.2014, 2014, pp.456323)
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923
- Genetic Evidence for a Link Between Favorable Adiposity and Lower Risk of Type 2 Diabetes, Hypertension, and Heart Disease
- Yaghootkar, Hanieh; Lotta, Luca A.; Tyrrell, Jessica; Smit, Roelof A.J.; Jones, Sam E.; Donnelly, Louise; Beaumont, Robin; Campbell, Archie; Tuke, Marcus A.; Hayward, Caroline; Ruth, Katherine S.; Padmanabhan, Sandosh; Jukema, J. Wouter; Palmer, Colin C.; Hattersley, Andrew; Freathy, Rachel M.; Langenberg, Claudia; Wareham, Nicholas J.; Wood, Andrew R.; Murray, Anna; Weedon, Michael N.; Sattar, Naveed; Pearson, Ewan; Scott, Robert A.; Frayling, Timothy M.; 1Genetics of Human Complex Traits, University of Exeter Medical School, University of Exeter, Exeter, U.K.; 2Medical Research Council Epidemiology Unit, Institute of Metabolic Science, University of Cambridge School of Clinical Medicine, Cambridge, U.K.; 1Genetics of Human Complex Traits, University of Exeter Medical School, University of Exeter, Exeter, U.K.; 3Department of Cardiology, Leiden University Medical Center, Leiden, the Netherlands; 1Genetics of Human Complex Traits, University of Exeter Medical School, University of Exeter, Exeter, U.K.; 5Division of Cardiovascular & Diabetes Medicine, Medical Research Institute, University of Dundee, Dundee, U.K.; 1Genetics of Human Complex Traits, University of Exeter Medical School, University of Exeter, Exeter, U.K.; 6Generation Scotland, Centre for Genomic and Experimental Medicine, Institute of Genetics and Molecular Medicine, University of; (Diabetes, v.65, 2016, pp.2448-2460)
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924
- Localization of a putative transcriptional regulator (ATRX) at pericentromeric heterochromatin and the short arms of acrocentric chromosomes
- McDowell, T. L.; Gibbons, R. J.; Sutherland, H.; O’Rourke, D. M.; Bickmore, W. A.; Pombo, A.; Turley, H.; Gatter, K.; Picketts, D. J.; Buckle, V. J.; Chapman, L.; Rhodes, D.; Higgs, D. R.; Medical Research Council Molecular Haematology Unit, Institute of Molecular Medicine, Oxford OX3 9DS, United Kingdom; Nuffield Department of Clinical Biochemistry and Cellular Science, University of Oxford, Oxford OX3 9DU, United Kingdom; Sir William Dunn School of Pathology, University of Oxford, Oxford OX1 3RE, United Kingdom; Medical Research Council Human Genetics Unit, Edinburgh EH4 2XU, United Kingdom; Ottawa General Hospital Research Institute, Ottawa, ON, Canada K1H 8L6; and Medical Research...; Medical Research Council Molecular Haematology Unit, Institute of Molecular Medicine, Oxford OX3 9DS, United Kingdom; Nuffield Department of Clinical Biochemistry and Cellular Science, University of Oxford, Oxford OX3 9DU, United Kingdom; Sir William Dunn School of Pathology, University of Oxford, Oxford OX1 3RE, United Kingdom; Medical Research Council Human Genetics Unit, Edinburgh EH4 2XU, United Kingdom; Ottawa General Hospital Research Institute, Ottawa, ON, Canada K1H 8L6; and Me; (Proceedings of the National Academy of Sciences of the United States of America, v.96, 1999, pp.13983-13988)
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925
- NRF2 and Hypoxia-Inducible Factors: Key Players in the Redox Control of Systemic Iron Homeostasis
- Duarte, Tiago L.; Talbot, Nick P.; Drakesmith, Hal; Instituto de Biologia Molecular e Celular, Instituto de Investigaç ã o e Inovaç ã o em Saú de (i3S), Universidade do Porto, Porto, Portugal.; Department of Physiology, Anatomy & Genetics, University of Oxford, Oxford, United Kingdom.; MRC Human Immunology Unit, MRC Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, University of Oxford, Oxford, United Kingdom.; (Antioxidants & redox signaling, v.35, 2021, pp.433-452)
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926
- A knockin mouse model for human <i>ATP4a<sup>R703C</sup></i> mutation identified in familial gastric neuroendocrine tumors recapitulates the premalignant condition of the human disease and suggests new therapeutic strategies
- Calvete, Oriol; Varro, Andrea; Pritchard, D. Mark; Barroso, Alicia; Oteo, Marta; Morcillo, Miguel Á ngel; Vargiu, Pierfrancesco; Dodd, Steven; Garcia, Miriam; Reyes, José ; Ortega, Sagrario; Benitez, Javier; Human Genetics Group , Spanish National Cancer Research Center (CNIO) , Madrid 28029 , Spain; Department of Cellular and Molecular Physiology , Institute of Translational Medicine, University of Liverpool , Liverpool L69 3BX , UK; Department of Cellular and Molecular Physiology , Institute of Translational Medicine, University of Liverpool , Liverpool L69 3BX , UK; Human Genetics Group , Spanish National Cancer Research Center (CNIO) , Madrid 28029 , Spain; Centro de Investigaciones Energé ticas, Medioambientales y Tecnoló gicas (CIEMAT) , Madrid 28040 , Spain; Centro de Investigaciones Energé ticas, Medioambientales y Tecnoló gicas (CIEMAT) , Madrid 28040 , Spain; Transgenic Mice Core Unit , Spanish National Cancer Research Center (CNIO) , Madrid 28029 , Spain; Department of Cellul; (Disease models & mechanisms : DMM, v.9, 2016, pp.975-984)
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927
- Mouse genetics provides insight into folliculogenesis, fertilization and early embryonic development
- Amleh, Asma; Dean, Jurrien; ; (Human reproduction update, v.8, 2002, pp.395-403)
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928
- Bi-allelic <i>ACBD6</i> variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders
- Kaiyrzhanov, Rauan; Rad, Aboulfazl; Lin, Sheng-Jia; Bertoli-Avella, Aida; Kallemeijn, Wouter W; Godwin, Annie; Zaki, Maha S; Huang, Kevin; Lau, Tracy; Petree, Cassidy; Efthymiou, Stephanie; Karimiani, Ehsan Ghayoor; Hempel, Maja; Normand, Elizabeth A; Rudnik-Schö neborn, Sabine; Schatz, Ulrich A; Baggelaar, Marc P; Ilyas, Muhammad; Sultan, Tipu; Alvi, Javeria Raza; Ganieva, Manizha; Fowler, Ben; Aanicai, Ruxandra; Tayfun, Gulsen Akay; Al Saman, Abdulaziz; Alswaid, Abdulrahman; Amiri, Nafise; Asilova, Nilufar; Shotelersuk, Vorasuk; Yeetong, Patra; Azam, Matloob; Babaei, Meisam; Monajemi, Gholamreza Bahrami; Mohammadi, Pouria; Samie, Saeed; Banu, Selina Husna; Pinto Basto, Jorge; Kortü m, Fanny; Bauer, Mislen; Bauer, Peter; Beetz, Christian; Garshasbi, Masoud; Issa, Awatif Hameed; Eyaid, Wafaa; Ahmed, Hind; Hashemi, Narges; Hassanpour, Kazem; Herman, Isabella; Ibrohimov, Sherozjon; Abdul-Majeed, Ban A; Imdad, Maria; Isrofilov, Ma; Department of Neuromuscular Diseases, UCL Institute of Neurology , London WC1N 3BG , UK; Cellular and Molecular Research Center, Sabzevar University of Medical Sciences , Sabzevar 009851 , Iran; Genes & Human Disease Research Program, Oklahoma Medical Research Foundation , Oklahoma City, OK 73104 , USA; Department of Medical Genetics, CENTOGENE GmbH , 18055 Rostock , Germany; Department of Chemistry, Imperial College London, Molecular Sciences Research Hub , London W12 0BZ , UK; European Xenopus Resource Centre-XenMD, School of Biological Sciences, University of Portsmouth , Portsmouth PO1 2DT , UK; Clinical Genetics Department, Human Genetics and Genome Research Institute, National Research Centre , 12622 Cairo , Egypt; Genes & Human Disease Research Program, Oklahoma Medical Research Foundation , Oklahoma City, OK 73104 , USA; Department of Neuromuscular Diseases, UCL Institute of Neurology , London WC1N 3BG , UK; Genes & Human Disease Research Program, Oklahoma Medical Rese; (Brain : a journal of neurology, v.147, 2024, pp.1436-1456)
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929
- Liver sphingomyelin synthase 1 deficiency causes steatosis, steatohepatitis, fibrosis, and tumorigenesis: An effect of glucosylceramide accumulation
- Li, Zhiqiang; Chiang, Yeun-po; He, Mulin; Worgall, Tilla S.; Zhou, Hongwen; Jiang, Xian-Cheng; Department of Cell Biology, SUNY Downstate Health Sciences University, Brooklyn, NY, USA; Department of Cell Biology, SUNY Downstate Health Sciences University, Brooklyn, NY, USA; Department of Cell Biology, SUNY Downstate Health Sciences University, Brooklyn, NY, USA; Department of Medicine, Columbia University, New York, USA; Nanjing Medical University, Nanjing, China; Department of Cell Biology, SUNY Downstate Health Sciences University, Brooklyn, NY, USA; (iscience, v.24, 2021, pp.103449)
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930
- [Ethical guidelines on genetic testing and gene therapy].
- Fukushima, Yoshimitsu; ; (日本臨牀 = Japanese journal of clinical medicine, v.63, 2005, pp.389-393)
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