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검색어 : 통합검색[Human molecular genetics 3]

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  • 71
    Duplication of the MYB oncogene in T cell acute lymphoblastic leukemia
    Lahortiga, Idoya; De Keersmaecker, Kim; Van Vlierberghe, Pieter; Graux, Carlos; Cauwelier, Barbara; Lambert, Frederic; Mentens, Nicole; Beverloo, H Berna; Pieters, Rob; Speleman, Frank; Odero, Maria D; Bauters, Marijke; Froyen, Guy; Marynen, Peter; Vandenberghe, Peter; Wlodarska, Iwona; Meijerink, Jules P P; Cools, Jan; [1] Human Genome Laboratory, Department of Molecular and Developmental Genetics, Vlaams Instituut voor Biotechnologie (VIB), Leuven, Belgium. [2] Human Genome Laboratory, Center for Human Genetics, Katholieke Universiteit (K.U.) Leuven, Leuven, Belgium. [3] Division of Oncology, Center for Applied Medical Research, University of Navarra, Pamplona, Spain.; [1] Human Genome Laboratory, Department of Molecular and Developmental Genetics, Vlaams Instituut voor Biotechnologie (VIB), Leuven, Belgium. [2] Human Genome Laboratory, Center for Human Genetics, Katholieke Universiteit (K.U.) Leuven, Leuven, Belgium.; Department of Pediatric Oncology/Hematology, Erasmus Medical Center/Sophia Children's Hospital, Rotterdam, The Netherlands.; [1] Human Genome Laboratory, Department of Molecular and Developmental Genetics, Vlaams Instituut voor Biotechnologie (VIB), Leuven, Belgium. [2] Human Genome Laboratory, Center for Human Genetics, Katholieke Universiteit (K.U.) Leuven, Leuven, Belgium. [3] D; (Nature genetics, v.39, 2007, pp.593-595)
  • 72
    AQP0 is a novel surface marker for deciphering abnormal erythropoiesis
    Wang, Tso-Fu; Lin, Guan-Ling; Chu, Sung-Chao; Chen, Chang-Chin; Liou, Yu-Shan; Chang, Hsin-Hou; Sun, Der-Shan; Departments of Hematology and Oncology, Hualien Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, Hualien, Taiwan, Republic of China; Department of Molecular Biology and Human Genetics, Tzu-Chi University, No. 701, Section 3, Zhong-Yang Road, Hualien, 97004 Taiwan, Republic of China; Departments of Hematology and Oncology, Hualien Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, Hualien, Taiwan, Republic of China; Department of Molecular Biology and Human Genetics, Tzu-Chi University, No. 701, Section 3, Zhong-Yang Road, Hualien, 97004 Taiwan, Republic of China; Department of Molecular Biology and Human Genetics, Tzu-Chi University, No. 701, Section 3, Zhong-Yang Road, Hualien, 97004 Taiwan, Republic of China; Department of Molecular Biology and Human Genetics, Tzu-Chi University, No. 701, Section 3, Zhong-Yang Road, Hualien, 97004 Taiwan, Republic of China; Department of Molecular Biology and Human Genetics, Tzu-Chi University, No. 701, Section 3, Zhong-Yang Road, Hua; (Stem cell research & therapy, v.12, 2021, pp.274)
  • 73
    <i>ST3GAL3</i> Mutations Impair the Development of Higher Cognitive Functions
    Hu, Hao; Eggers, Katinka; Chen, Wei; Garshasbi, Masoud; Motazacker, M.  Mahdi; Wrogemann, Klaus; Kahrizi, Kimia; Tzschach, Andreas; Hosseini, Masoumeh; Bahman, Ideh; Hucho, Tim; Mü hlenhoff, Martina; Gerardy-Schahn, Rita; Najmabadi, Hossein; Ropers, H.  Hilger; Kuss, Andreas  W.; Department for Human Molecular Genetics, Max-Planck Institute for Molecular Genetics, 14195 Berlin, Germany; Institute for Cellular Chemistry, Hannover Medical School, 30625 Hannover, Germany; Department for Human Molecular Genetics, Max-Planck Institute for Molecular Genetics, 14195 Berlin, Germany; Department for Human Molecular Genetics, Max-Planck Institute for Molecular Genetics, 14195 Berlin, Germany; Department for Human Molecular Genetics, Max-Planck Institute for Molecular Genetics, 14195 Berlin, Germany; Department of Biochemistry & Medical Genetics, University of Manitoba, Winnipeg R3E OJ9, Canada; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran 1985713834, Iran; Department for Human Molecular Genetics, Max-Planck Institute for Molecular Genetics, 14195 Berlin, Germany; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran 1985713834, Iran; Genetics Research Center, University of Social; (American journal of human genetics, v.89, 2011, pp.407-414)
  • 74
    Undiagnosed disease program in South Africa: Results from first 100 exomes
    Moosa, Shahida; Coetzer, Kimberly Christine; Lee, Eugene; Seo, Go Hun; Division of Molecular Biology and Human Genetics, Stellenbosch University, Cape Town, South Africa; Division of Molecular Biology and Human Genetics, Stellenbosch University, Cape Town, South Africa; 3billion Inc., Seoul, Republic of Korea; 3billion Inc., Seoul, Republic of Korea; (American Journal of Medical Genetics. Part A, v.188, 2022, pp.2684-2692)
  • 75
    Ulnar&#x2013;mammary syndrome with dysmorphic facies and mental retardation caused by a novel 1.28&#x2009;Mb deletion encompassing the TBX3 gene
    Klopocki, Eva; Neumann, Luitgard M; Tö nnies, Holger; Ropers, Hans-Hilger; Mundlos, Stefan; Ullmann, Reinhard; 1Institute of Medical Genetics, Charité Universitä tsmedizin Berlin, Berlin, Germany; 2Institute of Human Genetics, Charité Universitä tsmedizin Berlin, Berlin, Germany; 2Institute of Human Genetics, Charité Universitä tsmedizin Berlin, Berlin, Germany; 3Max-Planck Institute for Molecular Genetics, Berlin, Germany; 1Institute of Medical Genetics, Charité Universitä tsmedizin Berlin, Berlin, Germany; 3Max-Planck Institute for Molecular Genetics, Berlin, Germany; (European journal of human genetics : EJHG, v.14, 2006, pp.1274-1279)
  • 76
    Physical and Genetic Linkage of Glutaminase (<i>Gls</i>), Signal Transducer and Activator of Transcription 1 (<i>Stat1</i>), and Xeroderma Pigmentosum Complementation Group G (<i>Xpg</i>) on Mouse Proximal Chromosome 1
    Lé vy, Nicolas; Boettger-Tong, Holly; Dohmae, Kayoko; Agoulnik, Alexander I.; Ty, Theresa I.; Nishimune, Yoshitake; Bishop, Colin E.; Department of Obstetrics and Gynecology, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, 77030; Department of Obstetrics and Gynecology, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, 77030; Research Institute for Microbial Diseases, Osaka University, Yamadaoka 3-1, Suita, Osaka, 565, Japan; Department of Obstetrics and Gynecology, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, 77030; Department of Obstetrics and Gynecology, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, 77030; Research Institute for Microbial Diseases, Osaka University, Yamadaoka 3-1, Suita, Osaka, 565, Japan; Department of Obstetrics and Gynecology, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, 77030; (Genomics, v.54, 1998, pp.355-356)
  • 77
    <i>Fgfr1</i> and <i>Fgfr2</i> have distinct differentiation- and proliferation-related roles in the developing mouse skull vault
    Iseki, S.; Wilkie, A. O. M.; Morriss-Kay, G. M.; 1 Department of Human Anatomy and Genetics, South Parks Road, Oxford OX1 3QX, UK; 3 Institute of Molecular Medicine, John Radcliffe Hospital, Headington, Oxford OX3 9DS, UK; 1 Department of Human Anatomy and Genetics, South Parks Road, Oxford OX1 3QX, UK; (Development, v.126, 1999, pp.5611-5620)
  • 78
    Mechanisms of change in gene copy number
    Hastings, P. J.; Lupski, James R.; Rosenberg, Susan M.; Ira, Grzegorz; Department of Molecular and Human Genetics, Houston, Texas 77030, USA.; [1] Department of Molecular and Human Genetics, Houston, Texas 77030, USA. [2] Department of Pediatrics, Baylor College of Medicine, One Baylor Plaza, Houston, Texas 77030, USA. [3] Texas Children's Hospital, 1102 Bates, Houston, Texas 77030, USA.; [1] Department of Molecular and Human Genetics, Houston, Texas 77030, USA. [2] Department of Biochemistry and Molecular Biology, Houston, Texas 77030, USA. [3] Department of Molecular Virology and Microbiology, Houston, Texas 77030, USA. [4] The Dan L. Duncan Cancer Center, Baylor College of Medicine, One Baylor Plaza, Houston, Texas 77030, USA.; Department of Molecular and Human Genetics, Houston, Texas 77030, USA.; (Nature reviews. Genetics, v.10, 2009, pp.551-564)
  • 79
    Delayed male germ cell sex-specification permits transition into embryonal carcinoma cells with features of primed pluripotency
    Dawson, Emily P.; Lanza, Denise G.; Webster, Nicholas J.; Benton, Susan M.; Suetake, Isao; Heaney, Jason D.; Department of Molecular and Human Genetics, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA; Department of Molecular and Human Genetics, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA; Department of Molecular and Human Genetics, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA; Department of Molecular and Human Genetics, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA; Institute for Protein Research, Osaka University, 3-2 Yamadaoka, Suita, Osaka 565-0871, Japan; Department of Molecular and Human Genetics, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA; (Development, v.145, 2018, pp.dev156612-dev156612)
  • 80
    Islet1 is a direct transcriptional target of the homeodomain transcription factor Shox2 and rescues the Shox2-mediated bradycardia
    Hoffmann, Sandra; Berger, Ina M.; Glaser, Anne; Bacon, Claire; Li, Li; Gretz, Norbert; Steinbeisser, Herbert; Rottbauer, Wolfgang; Just, Steffen; Rappold, Gudrun; Department of Human Molecular Genetics, Institute of Human Genetics, University Heidelberg, INF 366, 69120 Heidelberg, Germany; Department of Internal Medicine II, University of Ulm, Albert-Einstein-Allee 23, 89081 Ulm, Germany; Department of Human Molecular Genetics, Institute of Human Genetics, University Heidelberg, INF 366, 69120 Heidelberg, Germany; Department of Human Molecular Genetics, Institute of Human Genetics, University Heidelberg, INF 366, 69120 Heidelberg, Germany; Medical Research Center, University Heidelberg, Theodor-Kutzer-Ufer 1-3, 68167 Mannheim, Germany; Medical Research Center, University Heidelberg, Theodor-Kutzer-Ufer 1-3, 68167 Mannheim, Germany; Division of Developmental Genetics, Institute of Human Genetics, University Heidelberg, INF 366, 69120 Heidelberg, Germany; Department of Internal Medicine II, University of Ulm, Albert-Einstein-Allee 23, 89081 Ulm, Germany; Department of Internal Medicine II, University of Ulm, Albert-Einstein-Allee 23, 89081; (Basic research in cardiology, v.108, 2013, pp.339)

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