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검색어 : 통합검색[Human molecular genetics 3]

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801

mtDNA Chromatin-like Organization Is Gradually Established during Mammalian Embryogenesis

Marom, Shani; Blumberg, Amit; Kundaje, Anshul; Mishmar, Dan; Department of Life Sciences, Faculty of Natural Sciences, Ben-Gurion University of the Negev, Beer-Sheva 8410501, Israel; Department of Life Sciences, Faculty of Natural Sciences, Ben-Gurion University of the Negev, Beer-Sheva 8410501, Israel; Department of Genetics, Stanford University, Stanford, CA, USA; Department of Life Sciences, Faculty of Natural Sciences, Ben-Gurion University of the Negev, Beer-Sheva 8410501, Israel; (iscience, v.12, 2019, pp.141-151)
802

[Ancient DNA studies: from paleopathology to population genetics]

Verginelli, Fabio; Ottini, Laura; Esposito, Diana; Cama, Alessandro; Battista, Pasquale; Ciranni, Rosalba; Zavaglia, Katia; Mariani-Costantini, Renato; Fornaciari, Gino; ; (Medicina nei secoli, v.14, 2002, pp.587-607)
803

Reproductive Genetics. A de novo complex chromosomal rearrangement with a translocation 7;9 and 8q insertion in a male carrier with no infertility: Case report

Cai, Tao; Yu, Ping; Tagle, Danilo A.; Lu, David; Chen, Yiwang; Xia, Jiahui; National Laboratory of Medical Genetics, Hunan Medical University, Changsha, Peoples' Republic of China,; Genetics and Molecular Biology Branch, National Human Genome Research Institute, National Institute of Health, Building 49, Room 3A23, 49 Convent Drive MSC 4442, Bethesda, MD 20892-4442, and; Genetics and Molecular Biology Branch, National Human Genome Research Institute, National Institute of Health, Building 49, Room 3A23, 49 Convent Drive MSC 4442, Bethesda, MD 20892-4442, and; Veterans Affairs Medical Center and Georgetown University Medical Center, Washington, DC 20016, USA; Veterans Affairs Medical Center and Georgetown University Medical Center, Washington, DC 20016, USA; National Laboratory of Medical Genetics, Hunan Medical University, Changsha, Peoples' Republic of China,; (Human reproduction, v.16, 2001, pp.59-62)
804

Genetics of sex determination in man and mouse

Goodfellow, P. N.; Darling, S. M.; 1 Human Molecular Genetics Laboratory, Imperial Cancer Research Fund, Lincoln’s Inn Fields, London WC2A 3PX, UK; Mount Sinai Hospital Research Institute 2 , 600 University Avenue, Toronto, Ontario M5G 1X5, Canada; (Development, v.102, 1988, pp.251-258)
805

The wt1-heterozygous mouse; a model to study the development of glomerular sclerosis

Menke, Aswin L; IJpenberg, Annemieke; Fleming, Stewart; Ross, Allyson; Medine, Claire N; Patek, Charles E; Spraggon, Lee; Hughes, Jeremy; Clarke, Alan R; Hastie, Nicholas D; MRC Human Genetics Unit, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK; MRC Human Genetics Unit, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK; Department of Molecular and Cellular Pathology, Ninewells Hospital and Medical School, Dundee DD1 9SY, UK; MRC Human Genetics Unit, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK; MRC Human Genetics Unit, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK; Sir Alastair Currie Cancer Research UK Laboratories, Molecular Medicine Centre, Western General Hospital, Edinburgh EH4 2XU, UK; MRC Human Genetics Unit, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK; MRC Centre for Inflammation Research, University of Edinburgh, Teviot Place, Edinburgh EH8 9AG, UK; Cardiff School of Biosciences, Cardiff University, PO Box 911, Cardiff CF10 3US, UK; MRC Human Genetics Unit, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK; (The Journal of pathology : a journal of the Pathological Society of Great Britain and Ireland, v.200, 2003, pp.667-674)
806

Highlighting rare disease research with a GENETICS and G3 series on genetic models of rare diseases

Hieter, Philip; Andrews, Brenda; Fowler, Douglas; Bellen, Hugo; Michael Smith Laboratories, Department of Medical Genetics, University of British Columbia, Vancouver , BC , Canada; The Donnelly Centre and Department of Molecular Genetics, University of Toronto , Toronto, ON M5S 3E1 , Canada; Department of Genome Sciences and Department of Bioengineering, University of Washington , Seattle, WA , USA; Departments of Molecular and Human Genetics, and Neuroscience Neurological Research Institute, Texas Children's Hospital Baylor College of Medicine, Houston, TX, USA; (Genetics, v.224, 2023, pp.iyad121)
807

Frequent epigenetic inactivation of the SLIT2 gene in gliomas

Dallol, Ashraf; Krex, Dietmar; Hesson, Luke; Eng, Charis; Maher, Eamonn R; Latif, Farida; 1Section of Medical and Molecular Genetics, Division of Reproductive and Child Health, University of Birmingham, Birmingham B15 2TT, UK; 2Department of Neurosurgery, Universitä tsklinikum Carl Gustav Carus Technische Universitä t Dresden, Fetscherstraße 74, 01307 Dresden, Germany; 1Section of Medical and Molecular Genetics, Division of Reproductive and Child Health, University of Birmingham, Birmingham B15 2TT, UK; 3Clinical Cancer Genetics and Human Cancer Genetics Programs, Comprehensive Cancer Center, and the Division of Human Genetics, Department of Internal Medicine, The Ohio State University, Columbus, OH, USA; [1] 1Section of Medical and Molecular Genetics, Division of Reproductive and Child Health, University of Birmingham, Birmingham B15 2TT, UK [2] 4Cancer Research UK, Renal Molecular Oncology Research Group, University of Birmingham, Birmingham B15 2TG, UK; [1] 1Section of Medical and Molecular Genetics, Division of Reproductive and Child Health, University of; (Oncogene, v.22, 2003, pp.4611-4616)
808

CRISPR-Cas12a-integrated transgenes in genomic safe harbors retain high expression in human hematopoietic iPSC-derived lineages and primary cells

Vlassis, Arsenios; Jensen, Tanja L.; Mohr, Marina; Jedrzejczyk, Dominika J.; Meng, Xiangyou; Kovacs, Gergo; Morera-Gó mez, Martí ; Barghetti, Andrea; Muyo Abad, Sergi; Baumgartner, Roland F.; Natarajan, Kedar N.; Nielsen, Lars K.; Warnecke, Tanya; Gill, Ryan T.; Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, Kemitorvet 220, 2800 Kongens Lyngby, Denmark; Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, Kemitorvet 220, 2800 Kongens Lyngby, Denmark; Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, Kemitorvet 220, 2800 Kongens Lyngby, Denmark; Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, Kemitorvet 220, 2800 Kongens Lyngby, Denmark; Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, Kemitorvet 220, 2800 Kongens Lyngby, Denmark; DTU Bioengineering, Technical University of Denmark, Søltofts Plads 224, 2800 Kongens Lyngby, Denmark; Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, Kemitorvet 220, 2800 Kongens Lyngby, Denmark; Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, Kem; (iscience, v.26, 2023, pp.108287)
809

Interrogating cell type-specific cooperation of transcriptional regulators in 3D chromatin

Yi, Xianfu; Zheng, Zhanye; Xu, Hang; Zhou, Yao; Huang, Dandan; Wang, Jianhua; Feng, Xiangling; Zhao, Ke; Fan, Xutong; Zhang, Shijie; Dong, Xiaobao; Wang, Zhao; Shen, Yujun; Cheng, Hui; Shi, Lei; Li, Mulin Jun; School of Biomedical Engineering and Technology, Tianjin Medical University, Tianjin 300070, China; Department of Pharmacology, Tianjin Key Laboratory of Inflammation Biology, School of Basic Medical Sciences, Tianjin Medical University, Tianjin 300070, China; Department of Bioinformatics, The Province and Ministry Co-sponsored Collaborative Innovation Center for Medical Epigenetics, Tianjin Medical University, Tianjin 300070, China; Department of Bioinformatics, The Province and Ministry Co-sponsored Collaborative Innovation Center for Medical Epigenetics, Tianjin Medical University, Tianjin 300070, China; Department of Bioinformatics, The Province and Ministry Co-sponsored Collaborative Innovation Center for Medical Epigenetics, Tianjin Medical University, Tianjin 300070, China; Department of Bioinformatics, The Province and Ministry Co-sponsored Collaborative Innovation Center for Medical Epigenetics, Tianjin Medical University, Tianjin 300070, China; Department of Bioinformat; (iscience, v.24, 2021, pp.103468)
810

SDHAF2 (PGL2-SDH5) and Hereditary Head and Neck Paraganglioma

Kunst, Henricus P.M.; Rutten, Martijn H.; de Mö nnink, Jan-Pieter; Hoefsloot, Lies H.; Timmers, Henri J.L.M.; Marres, Henri A.M.; Jansen, Jeroen C.; Kremer, Hannie; Bayley, Jean-Pierre; Cremers, Cor W.R.J.; Authors' Affiliations: Departments of 1Otorhinolaryngology, Head and Neck Surgery, 2Human Genetics, and 3Endocrinology, Radboud University Nijmegen Medical Center, and 4Donders Institute for Brain, Cognition and Behavior and 5Nijmegen Centre for Molecular Life Sciences, Radboud University Nijmegen, Nijmegen, the Netherlands; 6Department of Otorhinolaryngology, Maxima Medical Centre, Eindhoven, the Netherlands; and Departments of 7Otorhinolaryngology and 8Human Genetics, Leiden University Medical Center, Leiden, the Netherlands; Authors' Affiliations: Departments of 1Otorhinolaryngology, Head and Neck Surgery, 2Human Genetics, and 3Endocrinology, Radboud University Nijmegen Medical Center, and 4Donders Institute for Brain, Cognition and Behavior and 5Nijmegen Centre for Molecular Life Sciences, Radboud University Nijmegen, Nijmegen, the Netherlands; 6Department of Otorhinolaryngology, Maxima Medical Centre, Eindhoven, the Netherlands; and Departments of 7Otorhinolaryngology and 8Human; (Clinical Cancer research : an official journal of the American Association for Cancer Research, v.17, 2011, pp.247-254)

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