검색어 : 통합검색[Human molecular genetics 3]
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701
- Testis-determining factor and Y-linked sex reversal
- Hawkins, J. Ross; Koopman, Peter; Berta, Philippe; Human Molecular Genetics Laboratory, Imperial Cancer Research Fund, Lincoln's Inn Fields, London WC2A 3PX, UK; Laboratory of Eukaryotic Molecular Genetics, MRC National Institute for Medical Research, The Ridgeway, Mill Hill, London NW7 1AA, UK; Centre de Recherches de Biochimie Macromoleculaire, CNRS/INSERM BP 5O51, Route de Mende, 34033 Montpellier Cedex, France; (Current opinion in genetics & development, v.1, 1991, pp.30-33)
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702
- MAPK phosphatase DUSP16/MKP-7, a candidate tumor suppressor for chromosome region 12p12–13, reduces BCR-ABL-induced transformation
- Hoornaert, Inge; Marynen, Peter; Goris, Jozef; Sciot, Raf; Baens, Mathijs; 1Human Genome Laboratory, Department of Human Genetics, Flanders Interuniversity Institute for Biotechnology (VIB), Katholieke Universiteit Leuven, Herestraat 49, B-3000 Leuven, Belgium; 1Human Genome Laboratory, Department of Human Genetics, Flanders Interuniversity Institute for Biotechnology (VIB), Katholieke Universiteit Leuven, Herestraat 49, B-3000 Leuven, Belgium; 2Department of Molecular Cell Biology, Division of Biochemistry, Katholieke Universiteit Leuven, Herestraat 49, B-3000 Leuven, Belgium; 3Department of Pathology, Katholieke Universiteit Leuven, Herestraat 49, B-3000 Leuven, Belgium; 1Human Genome Laboratory, Department of Human Genetics, Flanders Interuniversity Institute for Biotechnology (VIB), Katholieke Universiteit Leuven, Herestraat 49, B-3000 Leuven, Belgium; (Oncogene, v.22, 2003, pp.7728-7736)
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703
- The role of <i>IL-16</i> gene polymorphisms in endometriosis
- Matalliotakis, Michail; Zervou, Maria I.; Eliopoulos, Elias; Matalliotaki, Charoula; Rahmioglu, Nilufer; Kalogiannidis, Ioannis; Zondervan, Krina; Spandidos, Demetrios A.; Matalliotakis, Ioannis; Goulielmos, George N.; Department of Obstetrics and Gynecology, Venizeleio General Hospital, 71409 Heraklion, Crete; Section of Molecular Pathology and Human Genetics, Department of Internal Medicine, School of Medicine, University of Crete, 71003 Heraklion, Crete; Laboratory of Genetics, Department of Biotechnology, Agricultural University of Athens, 11855 Athens, Greece; Department of Obstetrics and Gynecology, Venizeleio General Hospital, 71409 Heraklion, Crete; Wellcome Trust Centre for Human Genetics; 3rd Department of Obstetrics and Gynaecology, Aristotle University of Thessaloniki, 54124 Thessaloniki; Wellcome Trust Centre for Human Genetics; Laboratory of Clinical Virology, Medical School, University of Crete, 71003 Heraklion, Crete, Greece; Department of Obstetrics and Gynecology, Venizeleio General Hospital, 71409 Heraklion, Crete; Section of Molecular Pathology and Human Genetics, Department of Internal Medicine, School of Medicine, University of Crete, 71003 Heraklion, Crete; (International journal of molecular medicine, v.41, 2018, pp.1469-1476)
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704
- Mutation screening and association analysis of six candidate genes for autism on chromosome 7q
- Bonora, Elena; Lamb, Janine A; Barnby, Gabrielle; Sykes, Nuala; Moberly, Thomas; Beyer, Kim S; Klauck, Sabine M; Poustka, Firtz; Bacchelli, Elena; Blasi, Francesca; Maestrini, Elena; Battaglia, Agatino; Haracopos, Demetrios; Pedersen, Lennart; Isager, Torben; Eriksen, Gunna; Viskum, Birgitte; Sorensen, Ester-Ulsted; Brondum-Nielsen, Karen; Cotterill, Rodney; Engeland, Herman von; Jonge, Maretha de; Kemner, Chantal; Steggehuis, Karlijn; Scherpenisse, Margret; Rutter, Michael; Bolton, Patrick F; Parr, Jeremy R; Poustka, Annemarie; Bailey, Anthony J; Monaco, Anthony P; 1The Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK; 1The Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK; 1The Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK; 1The Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK; 1The Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK; 2Department of Molecular Genome Analysis, Deutsches Krebsforschungszentrum, Heidelberg, Germany; 2Department of Molecular Genome Analysis, Deutsches Krebsforschungszentrum, Heidelberg, Germany; 3Department of Child and Adolescent Psychiatry, University of Frankfurt, Frankfurt, Germany; 4University of Bologna, Dipartimento di Biologia Evoluzionistica Sperimentale and Lab Genetica Medica, Policlinico S. Orsola-Malpighi, Bologna, Italy; 4University of Bologna, Dipartimento di Biologia Evoluzionistica Sperimentale and Lab Genetica Medica, Policlinico S. Orsola-Malpighi, Bologna, Ital; (European journal of human genetics : EJHG, v.13, 2005, pp.198-207)
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705
- Assignment of the gene (EPLG2) encoding a high-affinity binding protein for the receptor tyrosine kinase Elk to a 200-kilobasepair region in human chromosome Xq12
- Fletcher, Frederick A.; Huebner, Kay; Shaffer, Lisa G.; Fairweather, Nicholas D.; Monaco, Anthony P.; Mü ller, Ulrich; Druck, Teresa; Simoneaux, Denise K.; Chelly, Jamel; Belmont, John W.; Beckmann, M.Patricia; Lyman, Stewart D.; Immunex Research and Development Corporation, Seattle, Washington 98101, USA; Jefferson Cancer Institute, Thomas Jefferson Medical College, Philadelphia, Pennsylvania 19107, USA; Institute for Molecular Genetics, Baylor College of Medicine, Houston, Texas 77030, USA; Imperial Cancer Research Fund Laboratories, Institute of Molecular Medicine, John Radcliffe Hospital, Oxford, England, OX3 9DU; Imperial Cancer Research Fund Laboratories, Institute of Molecular Medicine, John Radcliffe Hospital, Oxford, England, OX3 9DU; Justus-Liebig University, Institute of Human Genetics, Giessen, Germany, D-35392; Jefferson Cancer Institute, Thomas Jefferson Medical College, Philadelphia, Pennsylvania 19107, USA; Institute for Molecular Genetics, Baylor College of Medicine, Houston, Texas 77030, USA; Imperial Cancer Research Fund Laboratories, Institute of Molecular Medicine, John Radcliffe Hospital, Oxford, England, OX3 9DU; Institute for Molecular Genetics, Baylor College of Medicine, Houst; (Genomics, v.25, 1995, pp.334-335)
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706
- The length of lipids bound to human CD1d molecules modulates the affinity of NKT cell TCR and the threshold of NKT cell activation
- McCarthy, Corinna; Shepherd, Dawn; Fleire, Sebastian; Stronge, Victoria S.; Koch, Michael; Illarionov, Petr A.; Bossi, Giovanna; Salio, Mariolina; Denkberg, Galit; Reddington, Faye; Tarlton, Andrea; Reddy, B. Gopal; Schmidt, Richard R.; Reiter, Yoram; Griffiths, Gillian M.; van der Merwe, P. Anton; Besra, Gurdyal S.; Jones, E. Yvonne; Batista, Facundo D.; Cerundolo, Vincenzo; Tumour Immunology Unit, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, Cancer Research UK Receptor Structure Research Group, Division of Structural Biology, Wellcome Trust Centre for Human Genetics, and Sir William Dunn School of Pathology, University of Oxford, Oxford OX3 9DS, UK; Tumour Immunology Unit, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, Cancer Research UK Receptor Structure Research Group, Division of Structural Biology, Wellcome Trust Centre for Human Genetics, and Sir William Dunn School of Pathology, University of Oxford, Oxford OX3 9DS, UK; Lymphocyte Interaction Laboratory, London Research Institute, Cancer Research UK, London WC2A 3PX, UK; Tumour Immunology Unit, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, Cancer Research UK Receptor Structure Research Group, Division of Structural Biology, Wellcome Trust Centre for Human Genetics, and Sir William Dunn School of Pathology, University of Oxford,; (The Journal of experimental medicine, v.204, 2007, pp.1131-1144)
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707
- Smoking-Related Gene Expression in Laser Capture-Microdissected Human Lung
- Tan, Xiang-Lin; Wang, Tao; Xiong, Shengli; Kumar, Shalini V.; Han, Weiguo; Spivack, Simon D.; Authors' Affiliations: 1Division of Pulmonary Medicine, Department of Medicine, 2Department of Epidemiology and Population Health, and 3Department of Genetics, Albert Einstein College of Medicine, Bronx, New York; and 4Laboratory of Human Toxicology and Molecular Epidemiology, Wadsworth Center, New York State Department of Health, Albany, New York; Authors' Affiliations: 1Division of Pulmonary Medicine, Department of Medicine, 2Department of Epidemiology and Population Health, and 3Department of Genetics, Albert Einstein College of Medicine, Bronx, New York; and 4Laboratory of Human Toxicology and Molecular Epidemiology, Wadsworth Center, New York State Department of Health, Albany, New York; Authors' Affiliations: 1Division of Pulmonary Medicine, Department of Medicine, 2Department of Epidemiology and Population Health, and 3Department of Genetics, Albert Einstein College of Medicine, Bronx, New York; and 4Laboratory of Human Toxicology and Molecular Epidemiology, Wadsworth Center,; (Clinical Cancer research : an official journal of the American Association for Cancer Research, v.15, 2009, pp.7562-7570)
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708
- Consanguinity in Centre d’Étude du Polymorphisme Humain (CEPH) pedigrees
- Stevens, Eric L; Heckenberg, Greg; Baugher, Joseph D; Roberson, Elisha DO; Downey, Thomas J; Pevsner, Jonathan; Program in Human Genetics, Johns Hopkins School of Medicine, Baltimore, MD, USA; Partek Inc., St Louis, MO, USA; Program in Biochemistry, Cellular, and Molecular Biology, Johns Hopkins School of Medicine, Baltimore, MD, USA; Program in Human Genetics, Johns Hopkins School of Medicine, Baltimore, MD, USA; Partek Inc., St Louis, MO, USA; 1] Program in Human Genetics, Johns Hopkins School of Medicine, Baltimore, MD, USA [2] Department of Neurology, Hugo Moser Institute at the Kennedy Krieger Institute, Baltimore, MD, USA [3] Department of Psychiatry and Behavioral Sciences, Johns Hopkins School of Medicine, Baltimore, MD, USA; (European journal of human genetics : EJHG, v.20, 2012, pp.657-667)
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709
- Human genetic and metabolite variation reveals that methylthioadenosine is a prognostic biomarker and an inflammatory regulator in sepsis
- Wang, Liuyang; Ko, Emily R.; Gilchrist, James J.; Pittman, Kelly J.; Rautanen, Anna; Pirinen, Matti; Thompson, J. Will; Dubois, Laura G.; Langley, Raymond J.; Jaslow, Sarah L.; Salinas, Raul E.; Rouse, D. Clayburn; Moseley, M. Arthur; Mwarumba, Salim; Njuguna, Patricia; Mturi, Neema; Williams, Thomas N.; Scott, J. Anthony G.; Hill, Adrian V. S.; Woods, Christopher W.; Ginsburg, Geoffrey S.; Tsalik, Ephraim L.; Ko, Dennis C.; Department of Molecular Genetics and Microbiology, School of Medicine, Duke University, Durham, NC 27710, USA.; Duke Regional Hospital, Department of Medicine, School of Medicine, Duke University, Durham, NC 27710, USA.; Wellcome Trust Centre for Human Genetics, Roosevelt Drive, University of Oxford, Oxford OX3 7BN, U.K.; Department of Molecular Genetics and Microbiology, School of Medicine, Duke University, Durham, NC 27710, USA.; Wellcome Trust Centre for Human Genetics, Roosevelt Drive, University of Oxford, Oxford OX3 7BN, U.K.; Wellcome Trust Centre for Human Genetics, Roosevelt Drive, University of Oxford, Oxford OX3 7BN, U.K.; Proteomics and Metabolomics Core Facility, Duke University Medical Center, Durham, NC 27710, USA.; Proteomics and Metabolomics Core Facility, Duke University Medical Center, Durham, NC 27710, USA.; Department of Pharmacology and Center for Lung Biology, University of South Alabama College of Medicine, Mobile, AL 36688, USA.; Department of Molecula; (Science advances, v.3, 2017, pp.e1602096)
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710
- Characterization of ATP7A missense mutants suggests a correlation between intracellular trafficking and severity of Menkes disease
- Skjørringe, Tina; Amstrup Pedersen, Per; Salling Thorborg, Sidsel; Nissen, Poul; Gourdon, Pontus; Birk Møller, Lisbeth; Applied Human Genetics, Kennedy Center, Department of Clinical Genetics, Copenhagen University, Rigshospitalet, Glostrup Denmark; Department of Biology, August Krogh Building, University of Copenhagen, Universitetsparken 13, DK-2100 Copenhagen OE, Denmark; Applied Human Genetics, Kennedy Center, Department of Clinical Genetics, Copenhagen University, Rigshospitalet, Glostrup Denmark; Centre for Membrane Pumps in Cells and Disease-PUMKIN, Aarhus University, Department of Molecular Biology, Gustav Wieds Vej 10C, DK-8000 Aarhus C, Denmark; Department of Biomedical Sciences, University of Copenhagen, Blegdamsvej 3B, DK-2200 Copenhagen, Denmark; Applied Human Genetics, Kennedy Center, Department of Clinical Genetics, Copenhagen University, Rigshospitalet, Glostrup Denmark; (Scientific reports, v.7, 2017, pp.757)
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