검색어 : 통합검색[Human molecular genetics 3]
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191
- Down Regulation of FOXO1 Promotes Cell Proliferation in Cervical Cancer
- Prasad, Shyam Babu; Yadav, Suresh Singh; Das, Mitali; Govardhan, H. B.; Pandey, Lakshmi Kant; Singh, Sunita; Pradhan, Satyajit; Narayan, Gopeshwar; 1. Cancer Genetics Laboratory, Department of Molecular and Human Genetics, Banaras Hindu University, Varanasi-221 005, India; ; 1. Cancer Genetics Laboratory, Department of Molecular and Human Genetics, Banaras Hindu University, Varanasi-221 005, India; ; 1. Cancer Genetics Laboratory, Department of Molecular and Human Genetics, Banaras Hindu University, Varanasi-221 005, India; ; 2. Department of Radiotherapy and Radiation Medicine, Banaras Hindu University, Varanasi-221 005, India; ; 3. Department of Obstetrics and Gynaecology, Banaras Hindu University, Varanasi-221 005, India; ; 4. Department of Zoology, Mahila Mahavidyalaya; Banaras Hindu University, Varanasi-221 005, India.; 2. Department of Radiotherapy and Radiation Medicine, Banaras Hindu University, Varanasi-221 005, India; ; 1. Cancer Genetics Laboratory, Department of Molecular and Human Genetics, Banaras Hindu University, Varanasi-221 005, India; (Journal of Cancer, v.5, 2014, pp.655-662)
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192
- Next-Generation DNA Re-Sequencing Identifies Common Variants of TYR and HLA-A that Modulate the Risk of Generalized Vitiligo via Antigen Presentation
- Jin, Ying; Ferrara, Tracey; Gowan, Katherine; Holcomb, Cherie; Rastrou, Melinda; Erlich, Henry A; Fain, Pamela R; Spritz, Richard A; 1] Human Medical Genetics and Genomics Program, University of Colorado School of Medicine, Aurora, Colorado, USA [2] Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado, USA; Human Medical Genetics and Genomics Program, University of Colorado School of Medicine, Aurora, Colorado, USA; Human Medical Genetics and Genomics Program, University of Colorado School of Medicine, Aurora, Colorado, USA; Department of Human Genetics, Roche Molecular Systems, Pleasanton, California, USA; Department of Human Genetics, Roche Molecular Systems, Pleasanton, California, USA; Department of Human Genetics, Roche Molecular Systems, Pleasanton, California, USA; 1] Human Medical Genetics and Genomics Program, University of Colorado School of Medicine, Aurora, Colorado, USA [2] Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado, USA [3] Barbara Davis Center for Childhood Diabetes, University of Colorado School of Medicine, Aurora, Col; (Journal of investigative dermatology, v.132, 2012, pp.1730-1733)
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193
- VIP provides cellular protection through a specific splice variant of the PACAP receptor: A new neuroprotection target
- Pilzer, Inbar; Gozes, Illana; ; (Peptides, v.27, 2006, pp.2867-2876)
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194
- Genome-wide study of hair colour in UK Biobank explains most of the SNP heritability
- Morgan, Michael D.; Pairo-Castineira, Erola; Rawlik, Konrad; Canela-Xandri, Oriol; Rees, Jonathan; Sims, David; Tenesa, Albert; Jackson, Ian J.; MRC WIMM Centre for Computational Biology, MRC Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, Headington, Oxford, OX3 9DS UK; MRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Crewe Road, Edinburgh, EH4 2XU UK; Roslin Institute, University of Edinburgh, Easter Bush, Midlothian, EH25 9RG UK; MRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Crewe Road, Edinburgh, EH4 2XU UK; Dermatology, University of Edinburgh, Lauriston Building, Edinburgh, EH3 9HA UK; MRC WIMM Centre for Computational Biology, MRC Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, Headington, Oxford, OX3 9DS UK; MRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Crewe Road, Edinburgh, EH4 2XU UK; MRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Cr; (Nature communications, v.9, 2018, pp.5271)
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195
- Transgenic mice expressing mutated full-length HD cDNA: a paradigm for locomotor changes and selective neuronal loss in Huntington's disease
- Perutz, M. F.; Harper, P. S.; Ferguson-Smith, M. A.; Hemachandra Reddy, P.; Charles, Vinod; Williams, Maya; Miller, Georgina; Whetsell Jr., William O.; Tagle, Danilo A.; Genetics and Molecular Biology Branch, National Human Genome Research Institute, Building 49, Room 3A26, 49 Convent Drive MSC 4442, Bethesda, MD 20892,; Genetics and Molecular Biology Branch, National Human Genome Research Institute, Building 49, Room 3A26, 49 Convent Drive MSC 4442, Bethesda, MD 20892,; Genetics and Molecular Biology Branch, National Human Genome Research Institute, Building 49, Room 3A26, 49 Convent Drive MSC 4442, Bethesda, MD 20892,; Office of Research Services,Veterinary Resources Program, National Institutes of Health, Building 49, Room 3A26, 49 Convent Drive MSC 4442, Bethesda, MD 20892, USA; Department of Pathology,Vanderbilt University Medical Center, Nashville,TN 37232, USA; Genetics and Molecular Biology Branch, National Human Genome Research Institute, Building 49, Room 3A26, 49 Convent Drive MSC 4442, Bethesda, MD 20892,; (Philosophical transactions. Biological sciences, v.354, 1999, pp.1035-1045)
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196
- Structural Basis for LMO2-Driven Recruitment of the SCL:E47 <sub>bHLH</sub> Heterodimer to Hematopoietic-Specific Transcriptional Targets
- El Omari, Kamel; Hoosdally, Sarah J.; Tuladhar, Kapil; Karia, Dimple; Hall-Ponselé , Elisa; Platonova, Olga; Vyas, Paresh; Patient, Roger; Porcher, Catherine; Mancini, Erika J.; Division of Structural Biology, The Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, UK; MRC Molecular Hematology Unit, Weatherall Institute of Molecular Medicine, University of Oxford, Oxford OX3 9DS, UK; MRC Molecular Hematology Unit, Weatherall Institute of Molecular Medicine, University of Oxford, Oxford OX3 9DS, UK; Division of Structural Biology, The Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, UK; MRC Molecular Hematology Unit, Weatherall Institute of Molecular Medicine, University of Oxford, Oxford OX3 9DS, UK; Division of Structural Biology, The Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, UK; MRC Molecular Hematology Unit, Weatherall Institute of Molecular Medicine, University of Oxford, Oxford OX3 9DS, UK; MRC Molecular Hematology Unit, Weatherall Institute of Molecular Medicine, University of Oxford, Oxford OX3 9DS, UK; MRC Molecular Hematology Unit, Weatherall Insti; (Cell reports, v.4, 2013, pp.135-147)
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197
- Activation of the lectin DC-SIGN induces an immature dendritic cell phenotype triggering Rho-GTPase activity required for HIV-1 replication
- Hodges, Ashleigh; Sharrocks, Katherine; Edelmann, Mariola; Baban, Dilair; Moris, Arnaud; Schwartz, Olivier; Drakesmith, Hal; Davies, Kay; Kessler, Benedikt; McMichael, Andrew; Simmons, Alison; Medical Research Council Human Immunology Unit, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, Headington, Oxford OX3 9DS, UK.; Medical Research Council Human Immunology Unit, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, Headington, Oxford OX3 9DS, UK.; The Henry Wellcome Building for Molecular Physiology, University of Oxford, Oxford OX3 7BN, UK.; Medical Research Council Functional Genetics Unit, Department of Human Anatomy and Genetics, University of Oxford, Oxford OX1 3QX, UK.; Groupe Virus et Immunité , Institut Pasteur, 75724 Paris, Cedex 15, France.; Groupe Virus et Immunité , Institut Pasteur, 75724 Paris, Cedex 15, France.; Molecular Immunology Group, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, Headington, Oxford OX3 9DS, UK.; Medical Research Council Functional Genetics Unit, Department of Human Anatomy and Genetics, University of Oxford, Oxford OX1 3QX, UK.; The Henry Wellcome Building; (Nature immunology, v.8, 2007, pp.569-577)
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198
- Genetic and electrophysiological studies of drosophila syntaxin-1A demonstrate its role in nonneuronal secretion and neurotransmission
- Schulze, Karen L; Broadie, Kendal; Perin, Mark S; Bellen, Hugo J; Howard Hughes Medical Institute Department of Molecular and Human Genetics USA; Department of Zoology University of Cambridge Cambridge CB2 3EJ England; Division of Neuroscience Baylor College of Medicine Houston, Texas 77030 USA; Howard Hughes Medical Institute Department of Molecular and Human Genetics USA; (Cell, v.80, 1995, pp.311-320)
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199
- Dimerization of presenilin-1 in vivo: suggestion of novel regulatory mechanisms leading to higher order complexes
- Hé bert, Sé bastien S; Godin, Chantal; Tomiyama, Takami; Mori, Hiroshi; Lé vesque, Georges; ; (Biochemical and biophysical research communications, v.301, 2003, pp.119-126)
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200
- Mutations in <i>SPATA7</i> Cause Leber Congenital Amaurosis and Juvenile Retinitis Pigmentosa
- Wang, Hui; den Hollander, Anneke I.; Moayedi, Yalda; Abulimiti, Abuduaini; Li, Yumei; Collin, Rob W.J.; Hoyng, Carel B.; Lopez, Irma; Abboud, Emad B.; Al-Rajhi, Ali A.; Bray, Molly; Lewis, Richard Alan; Lupski, James R.; Mardon, Graeme; Koenekoop, Robert K.; Chen, Rui; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA; Department of Human Genetics, Nijmegen Centre for Molecular Life Sciences, Radboud University Nijmegen Medical Centre, 6500 HB, Nijmegen, The Netherlands; Department of Neuroscience, Baylor College of Medicine, Houston, TX 77030, USA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA; Department of Human Genetics, Nijmegen Centre for Molecular Life Sciences, Radboud University Nijmegen Medical Centre, 6500 HB, Nijmegen, The Netherlands; Department of Ophthalmology, Nijmegen Centre for Molecular Life Sciences, Radboud University Nijmegen Medical Centre, 6500 HB, Nijmegen, The Netherlands; McGill Ocular Genetics Center, McGill University Health Center, Montreal, Quebec H3H 1P3, Canada; King Khaled Eye Specialist Hospital, P.O. Box 7191, Riyad; (American journal of human genetics, v.86, 2010, pp.293-293)
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