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  • 1
    Publication Date: 1994-07-29
    Description: The zebrafish is rapidly becoming a popular model system for the study of vertebrate development because it is ideal for both embryological studies and genetic analysis. To determine if a retroviral vector pseudotyped with the envelope glycoprotein of the vesicular stomatitis virus could infect zebrafish embryos, and in particular, the cells destined to become the germ line, a pseudotyped virus was injected into blastula-stage zebrafish embryos. Fifty-one embryos were allowed to develop and eight transmitted proviral DNA to their progeny. Founders were mosaic, but as expected, transgenic F1's transmitted proviral DNA in a Mendelian fashion to the F2 progeny. Transgenic F1 fish inherited a single integrated provirus, and a single founder could transmit more than one viral integration to its progeny. These results demonstrate that this pantropic pseudotyped vector, originally developed for human gene therapy, will make the use of retroviral vectors in zebrafish possible.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lin, S -- Gaiano, N -- Culp, P -- Burns, J C -- Friedmann, T -- Yee, J K -- Hopkins, N -- CA14051/CA/NCI NIH HHS/ -- HD-20034/HD/NICHD NIH HHS/ -- HL-01855/HL/NHLBI NIH HHS/ -- etc. -- New York, N.Y. -- Science. 1994 Jul 29;265(5172):666-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Center for Cancer Research, Massachusetts Institute of Technology, Cambridge 02139.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/8036514" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Genetically Modified ; Base Sequence ; Cell Line ; DNA, Viral/analysis ; Genetic Vectors/*genetics ; Molecular Sequence Data ; Moloney murine leukemia virus/*genetics ; Proviruses/*genetics ; Vesicular stomatitis Indiana virus/*genetics ; Virus Integration/*genetics ; Zebrafish/embryology/*genetics
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 2
    Publication Date: 2011-11-26
    Description: B-type lamins, the major components of the nuclear lamina, are believed to be essential for cell proliferation and survival. We found that mouse embryonic stem cells (ESCs) do not need any lamins for self-renewal and pluripotency. Although genome-wide lamin-B binding profiles correlate with reduced gene expression, such binding is not directly required for gene silencing in ESCs or trophectoderm cells. However, B-type lamins are required for proper organogenesis. Defects in spindle orientation in neural progenitor cells and migration of neurons probably cause brain disorganizations found in lamin-B null mice. Thus, our studies not only disprove several prevailing views of lamin-Bs but also establish a foundation for redefining the function of the nuclear lamina in the context of tissue building and homeostasis.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3306219/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3306219/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kim, Youngjo -- Sharov, Alexei A -- McDole, Katie -- Cheng, Melody -- Hao, Haiping -- Fan, Chen-Ming -- Gaiano, Nicholas -- Ko, Minoru S H -- Zheng, Yixian -- R01 AR060042/AR/NIAMS NIH HHS/ -- R01 AR060042-02/AR/NIAMS NIH HHS/ -- R01 GM 56312/GM/NIGMS NIH HHS/ -- Howard Hughes Medical Institute/ -- Intramural NIH HHS/ -- New York, N.Y. -- Science. 2011 Dec 23;334(6063):1706-10. doi: 10.1126/science.1211222. Epub 2011 Nov 24.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Embryology, Carnegie Institution for Science, Baltimore, MD 21218, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22116031" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Body Size ; Brain/cytology/embryology ; Cell Cycle ; Cell Differentiation ; Cell Movement ; Cells, Cultured ; Chromatin/metabolism ; Embryonic Development ; Embryonic Stem Cells/cytology/*physiology ; Female ; Gene Expression Regulation, Developmental ; Gene Silencing ; Lamin Type B/genetics/metabolism/*physiology ; Male ; Mice ; Mice, Knockout ; Neural Stem Cells/cytology ; Neurons/cytology ; Nuclear Lamina/physiology ; Organ Size ; *Organogenesis ; Pluripotent Stem Cells/cytology/physiology ; Promoter Regions, Genetic ; Spindle Apparatus/physiology/ultrastructure ; Transcription, Genetic ; Trophoblasts/cytology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 3
    Publication Date: 1996-07-23
    Print ISSN: 0027-8424
    Electronic ISSN: 1091-6490
    Topics: Biology , Medicine , Natural Sciences in General
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