검색어 : 통합검색[Human molecular genetics 3]
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851
- Robust CRISPR/Cas9 Genome Editing of the HUDEP-2 Erythroid Precursor Line Using Plasmids and Single-Stranded Oligonucleotide Donors
- Moir-Meyer, Gemma; Cheong, Pak Leng; Olijnik, Aude-Anais; Brown, Jill; Knight, Samantha; King, Andrew; Kurita, Ryo; Nakamura, Yukio; Gibbons, Richard J.; Higgs, Douglas R.; Buckle, Veronica J.; Babbs, Christian; MRC Molecular Haematology Unit, MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford OX3 9DS, UK; MRC Molecular Haematology Unit, MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford OX3 9DS, UK; MRC Molecular Haematology Unit, MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford OX3 9DS, UK; MRC Molecular Haematology Unit, MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford OX3 9DS, UK; Wellcome Trust Centre for Human Genetics, Oxford University, Oxford OX3 7BN, UK; MRC Molecular Haematology Unit, MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford OX3 9DS, UK; Department of Research and Development, Central Blood Institute, Japanese Red Cross Society, 1-1-3 Shibadaimon, Minato-ku, Tokyo 105-8521, Japan; RIKEN BioResource Research Center, Koyadai 3-1-1, Tsukuba 305-0074, Japan; MRC Molecular Haematology Unit, MRC Weatherall Institute of Molecular Medicine,; (Methods and protocols, v.1, 2018, pp.28)
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852
- SIAH1 targets the alternative splicing factor T-STAR for degradation by the proteasome
- Venables, Julian P.; Dalgliesh, Caroline; Paronetto, Maria Paolo; Skitt, Lindi; Thornton, Jared K.; Saunders, Philippa T.; Sette, Claudio; Jones, Keith T.; Elliott, David J.; ; (Human molecular genetics, v.13, 2004, pp.1525-1534)
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853
- Transcriptional repression by methylation of CpG
- MEEHAN, RICHARD; LEWIS, JOE; CROSS, SALLY; NAN, XINSHENG; JEPPESEN, PETER; BIRD, ADRIAN; Institute of Cell and Molecular Biology, University of Edinburgh, Kings Buildings, Edinburgh EH9 3JR, UK; Institute of Cell and Molecular Biology, University of Edinburgh, Kings Buildings, Edinburgh EH9 3JR, UK; Institute of Cell and Molecular Biology, University of Edinburgh, Kings Buildings, Edinburgh EH9 3JR, UK; Institute of Cell and Molecular Biology, University of Edinburgh, Kings Buildings, Edinburgh EH9 3JR, UK; MRC, Human Genetics Unit, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK; Institute of Cell and Molecular Biology, University of Edinburgh, Kings Buildings, Edinburgh EH9 3JR, UK; (Journal of cell science, v.1992, 1992, pp.9-14)
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854
- No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients
- Steinke, Verena; Rahner, Nils; Morak, Monika; Keller, Gisela; Schackert, Hans K; Gö rgens, Heike; Schmiegel, Wolff; Royer-Pokora, Brigitte; Dietmaier, Wolfgang; Kloor, Matthias; Engel, Christoph; Propping, Peter; Aretz, Stefan; 1Institute of Human Genetics, University of Bonn, Bonn, Germany; 1Institute of Human Genetics, University of Bonn, Bonn, Germany; [1] 2Institute of Human Genetics, Ludwig Maximilians University, Munich, Germany [2] 3Center of Medical Genetics, Munich, Germany; 4Department of Pathology, Munich University of Technology, Munich, Germany; 5Department of Surgical Research, Technische Universitä t Dresden, Dresden, Germany; 5Department of Surgical Research, Technische Universitä t Dresden, Dresden, Germany; 6Department of Medicine, Knappschaftskrankenhaus, Ruhr-University Bochum, Bochum, Germany; 7Institute of Human Genetics, Heinrich Heine University, Duesseldorf, Germany; 8Department of Pathology, University of Regensburg, Regensburg, Germany; 9Institute of Molecular Pathology, University of Heidelberg, Heidelberg, Germany; 10Institute for Medical Informatics, Statistics and Epidemiology, University of Leipzig, Leipzig, Germany; 1Institute of Human Genetics, University o; (European journal of human genetics : EJHG, v.16, 2008, pp.587-592)
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855
- Genetic determinants of plasma HDL-cholesterol levels in familial hypercholesterolemia
- van Aalst-Cohen, Emily S; Jansen, Angelique C M; Boekholdt, S Matthijs; Tanck, Michael W T; Fontecha, Marcel R; Cheng, Suzanne; Li, Jia; Defesche, Joep C; Kuivenhoven, Jan Albert; Kastelein, John J P; 1Department of Vascular Medicine, Academic Medical Center, Amsterdam, The Netherlands; 1Department of Vascular Medicine, Academic Medical Center, Amsterdam, The Netherlands; 2Department of Cardiology, Academic Medical Center, Amsterdam, The Netherlands; 3Department of Clinical Epidemiology and Biostatistics, Academic Medical Center, Amsterdam, The Netherlands; 4Department of Human Genetics, Roche Molecular Systems, Inc., Alameda, CA, USA; 4Department of Human Genetics, Roche Molecular Systems, Inc., Alameda, CA, USA; 4Department of Human Genetics, Roche Molecular Systems, Inc., Alameda, CA, USA; 1Department of Vascular Medicine, Academic Medical Center, Amsterdam, The Netherlands; 1Department of Vascular Medicine, Academic Medical Center, Amsterdam, The Netherlands; 1Department of Vascular Medicine, Academic Medical Center, Amsterdam, The Netherlands; (European journal of human genetics : EJHG, v.13, 2005, pp.1137-1142)
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856
- DNA methyltransferase 1o functions during preimplantation development to preclude a profound level of epigenetic variation
- Cirio, M. Cecilia; Martel, Josee; Mann, Mellissa; Toppings, Marc; Bartolomei, Marisa; Trasler, Jacquetta; Chaillet, J. Richard; Department of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USA; Montreal Children's Hospital of the McGill University Health Centre, Department of Pediatrics, Department of Human Genetics, Department of Pharmacology and Therapeutics, McGill University, Montreal, Qué bec H3H 1P3, Canada; Department of Cell and Developmental Biology, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA; Montreal Children's Hospital of the McGill University Health Centre, Department of Pediatrics, Department of Human Genetics, Department of Pharmacology and Therapeutics, McGill University, Montreal, Qué bec H3H 1P3, Canada; Department of Cell and Developmental Biology, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA; Montreal Children's Hospital of the McGill University Health Centre, Department of Pediatrics, Department of Human Genetics, Department of Pharmacology and Therapeutics; (Developmental biology, v.324, 2008, pp.139-150)
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857
- [Trends of genomic researches for drug discoveries]
- Nemoto, Y; ; (日本臨牀 = Japanese journal of clinical medicine, v.56, 1998, pp.224-232)
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858
- Biochemistry and genetics of monoamine oxidase
- Weyler, W.; Hsu, Y.-P.P.; Breakafield, X.O.; ; (Pharmacology & therapeutics, v.47, 1990, pp.391-417)
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859
- SPOCS: software for predicting and visualizing orthology/paralogy relationships among genomes
- Curtis, Darren S.; Phillips, Aaron R.; Callister, Stephen J.; Conlan, Sean; McCue, Lee Ann; 1Computational & Statistical Analytics Division, Pacific Northwest National Laboratory, 2Biological Sciences Division, Pacific Northwest National Laboratory, Richland, WA 99352, USA, 3Genetics and Molecular Biology Branch, National Human Genome Research Institute, NIH, Bethesda, MD 20892, USA and 4Computational Sciences & Mathematics Division, Pacific Northwest National Laboratory, Richland, WA 99352, USA; 1Computational & Statistical Analytics Division, Pacific Northwest National Laboratory, 2Biological Sciences Division, Pacific Northwest National Laboratory, Richland, WA 99352, USA, 3Genetics and Molecular Biology Branch, National Human Genome Research Institute, NIH, Bethesda, MD 20892, USA and 4Computational Sciences & Mathematics Division, Pacific Northwest National Laboratory, Richland, WA 99352, USA; 1Computational & Statistical Analytics Division, Pacific Northwest National Lab; (Bioinformatics, v.29, 2013, pp.2641-2642)
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860
- Where the genome meets the connectome: understanding how genes shape human brain connectivity
- Arnatkeviciute Aurina; Fulcher Ben; Bellgrove Mark; Fornito Alex; ; (, v., 2021, )
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