검색어 : 통합검색[Human molecular genetics 3]
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171
- Smad3 Is a Key Nonredundant Mediator of Transforming Growth Factor β Signaling in Nme Mouse Mammary Epithelial Cells
- Dzwonek, Joanna; Preobrazhenska, Olena; Cazzola, Silvia; Conidi, Andrea; Schellens, Ann; van Dinther, Maarten; Stubbs, Andrew; Klippel, Anke; Huylebroeck, Danny; ten Dijke, Peter; Verschueren, Kristin; 1Laboratory of Molecular Biology, Center for Human Genetics, K.U.Leuven; 2Department of Molecular and Developmental Genetics (VIB11), VIB, Leuven, Belgium; 3Molecular Cell Biology, Leiden University Medical Center, Leiden, the Netherlands; 4Department of Bioinformatics, Erasmus University Medical Center, Rotterdam, the Netherlands; and 5Silence Therapeutics, Berlin, Germany; 1Laboratory of Molecular Biology, Center for Human Genetics, K.U.Leuven; 2Department of Molecular and Developmental Genetics (VIB11), VIB, Leuven, Belgium; 3Molecular Cell Biology, Leiden University Medical Center, Leiden, the Netherlands; 4Department of Bioinformatics, Erasmus University Medical Center, Rotterdam, the Netherlands; and 5Silence Therapeutics, Berlin, Germany; 1Laboratory of Molecular Biology, Center for Human Genetics, K.U.Leuven; 2Department of Molecular and Developmental Genetics (VIB11), VIB, Leuven, Belgium; 3Molecular Cell Biology, Leiden University Medical Center, Leiden, the Netherlands; 4D; (Molecular cancer research, v.7, 2009, pp.1342-1353)
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172
- The Principal Role of Ku in Telomere Length Maintenance Is Promotion of Est1 Association with Telomeres
- Williams, Jaime M.; Ouenzar, Faissal; Lemon, Laramie D.; Chartrand, Pascal; Bertuch, Alison A.; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030; Department of Biochemistry, Université de Montré al, Montré al, Qué bec, Canada H3C 3J7; Integrative Molecular and Biomedical Sciences Graduate Program, Baylor College of Medicine, Houston, Texas 77030; Department of Biochemistry, Université de Montré al, Montré al, Qué bec, Canada H3C 3J7; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030; (Genetics, v.197, 2014, pp.1123-1136)
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173
- IDO Induces Expression of a Novel Tryptophan Transporter in Mouse and Human Tumor Cells
- Silk, Jonathan D; Lakhal, Samira; Laynes, Robert; Vallius, Laura; Karydis, Ioannis; Marcea, Cornelius; Boyd, C A Richard; Cerundolo, Vincenzo; Medical Research Council Human Immunology Unit, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital , Headington OX3 9DS ,; Medical Research Council Human Immunology Unit, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital , Headington OX3 9DS ,; Department of Physiology, Anatomy and Genetics, University of Oxford , Oxford OX1 3QX ,; Medical Research Council Human Immunology Unit, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital , Headington OX3 9DS ,; Medical Research Council Human Immunology Unit, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital , Headington OX3 9DS ,; Medical Research Council Human Immunology Unit, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital , Headington OX3 9DS ,; Department of Physiology, Anatomy and Genetics, University of Oxford , Oxford OX1 3QX ,; Medical Research Council Human Immunology Unit, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital; (The journal of immunology : official journal of the American Association of Immunologists, v.187, 2011, pp.1617-1625)
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174
- Two Common Loss-of-Function Mutations within the Filaggrin Gene Predispose for Early Onset of Atopic Dermatitis
- Stemmler, Susanne; Parwez, Qumar; Petrasch-Parwez, Elisabeth; Epplen, Joerg T; Hoffjan, Sabine; 1Department of Human Genetics, Ruhr-University, Bochum, Germany; 2Private medical practice, Gladbeck, Germany; 3Department of Neuroanatomy and Molecular Brain Research, Ruhr-University, Bochum, Germany; 1Department of Human Genetics, Ruhr-University, Bochum, Germany; 1Department of Human Genetics, Ruhr-University, Bochum, Germany; (Journal of investigative dermatology, v.127, 2007, pp.722-724)
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175
- A mitotic recombination map proximal to the <i>APC </i> locus on chromosome 5q and assessment of influences on colorectal cancer risk
- Howarth, Kimberley; Ranta, Susanna; Winter, Eitan; Teixeira, Ana; Schaschl, Helmut; Harvey, John J; Rowan, Andrew; Jones, Angela; Spain, Sarah; Clark, Susan; Guenther, Thomas; Stewart, Aengus; Silver, Andrew; Tomlinson, Ian; Molecular and Population Genetics Laboratory, Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Oxford, OX3 7BN, UK; London Research Institute, Cancer Research UK, 44, Lincoln's Inn Fields, London, WC2A 3PX, UK; London Research Institute, Cancer Research UK, 44, Lincoln's Inn Fields, London, WC2A 3PX, UK; Molecular and Population Genetics Laboratory, Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Oxford, OX3 7BN, UK; London Research Institute, Cancer Research UK, 44, Lincoln's Inn Fields, London, WC2A 3PX, UK; London Research Institute, Cancer Research UK, 44, Lincoln's Inn Fields, London, WC2A 3PX, UK; London Research Institute, Cancer Research UK, 44, Lincoln's Inn Fields, London, WC2A 3PX, UK; Molecular and Population Genetics Laboratory, Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Oxford, OX3 7BN, UK; Molecular and Population Genetics Laboratory, Wellcome Trust Centre for H; (BMC medical genetics, v.10, 2009, pp.54-54)
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176
- In vivo characterization of regulatory polymorphisms by allele-specific quantification of RNA polymerase loading
- Knight, Julian C.; Keating, Brendan J.; Rockett, Kirk A.; Kwiatkowski, Dominic P.; [1] Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, UK. [2] Department of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts 02138, USA.; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, UK.; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, UK.; [1] Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, UK. [2] University Department of Pediatrics, John Radcliffe Hospital, Oxford OX3 9DU, UK.; (Nature genetics, v.33, 2003, pp.469-475)
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177
- Cell Cycle Regulation by NF-YC in <i>Drosophila</i> Eye Imaginal Disc: Implications for Synchronization in the Non-Proliferative Region
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Avellino, Anthony;
Peng, Chen-Huan;
Lin, Ming-Der;
Department of Molecular Biology and Human Genetics, Tzu Chi University, 701 Zhongyang Rd., Sec. 3, Hualien 97004, Taiwan;
anthonyavellino39@gmail.com ; Department of Orthopedics, Hualien Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, 707 Zhongyang Rd., Sec. 3, Hualien 97002, Taiwan;peng0913@gmail.com ; Department of Molecular Biology and Human Genetics, Tzu Chi University, 701 Zhongyang Rd., Sec. 3, Hualien 97004, Taiwan;anthonyavellino39@gmail.com ; (International journal of molecular sciences, v.24, 2023, pp.12203)
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178
- Localizing the RPGR protein along the cilium: a new method to determine efficacies to treat RPGR mutations
- Da Costa, R; Glaus, E; Tiwari, A; Kloeckener-Gruissem, B; Berger, W; Neidhardt, J; 1] Department of Human Genetics, Faculty of Medicine and Health Sciences, University of Oldenburg, Oldenburg, Germany [2] Institute of Medical Molecular Genetics, University of Zurich, Schlieren, Switzerland; Institute of Medical Molecular Genetics, University of Zurich, Schlieren, Switzerland; Institute of Medical Molecular Genetics, University of Zurich, Schlieren, Switzerland; 1] Institute of Medical Molecular Genetics, University of Zurich, Schlieren, Switzerland [2] Department of Biology, ETH Zurich, Zurich, Switzerland; 1] Institute of Medical Molecular Genetics, University of Zurich, Schlieren, Switzerland [2] Neuroscience Center Zurich, University of Zurich and ETH Zurich, Zurich, Switzerland [3] Zurich Center for Integrative Human Physiology (ZIHP), University of Zurich, Zurich, Switzerland; 1] Department of Human Genetics, Faculty of Medicine and Health Sciences, University of Oldenburg, Oldenburg, Germany [2] Institute of Medical Molecular Genetics, University of Zurich; (Gene therapy, v.22, 2015, pp.413-420)
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179
- Genetic risk factors of ME/CFS: a critical review
- Dibble, Joshua J; McGrath, Simon J; Ponting, Chris P; MRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh , Crewe Road South, Edinburgh EH4 2XU, UK; Wrekin , Prospect Road, Monmouth NP25 3SZ, UK; MRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh , Crewe Road South, Edinburgh EH4 2XU, UK; (Human molecular genetics, v.29, 2020, pp.R117-R124)
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180
- Delineation of mechanisms and regions of dosage imbalance in complex rearrangements of 1p36 leads to a putative gene for regulation of cranial suture closure
- Gajecka, Marzena; Yu, Wei; Ballif, Blake C; Glotzbach, Caron D; Bailey, Kristen A; Shaw, Chad A; Kashork, Catherine D; Heilstedt, Heidi A; Ansel, David A; Theisen, Aaron; Rice, Ritva; Rice, David P C; Shaffer, Lisa G; 1Health Research and Education Center, Washington State University, Spokane, WA, USA; 3Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA; [1] 1Health Research and Education Center, Washington State University, Spokane, WA, USA [2] 3Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA; [1] 1Health Research and Education Center, Washington State University, Spokane, WA, USA [2] 2Sacred Heart Medical Center, Spokane, WA, USA; [1] 1Health Research and Education Center, Washington State University, Spokane, WA, USA [2] 2Sacred Heart Medical Center, Spokane, WA, USA; 3Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA; 3Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA; 3Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA; 4Department of Medicine, Children's Hospital, Boston, MA, USA; 1Health Rese; (European journal of human genetics : EJHG, v.13, 2005, pp.139-149)
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