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Departments of Physiology and Biophysics, Morphology, Department of Biochemistry and Molecular Biology, Max‐Delbrück Center for Molecular Medicine (MDC), Biological Sciences Institute, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil
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, angiotensin. Figure 3 Phenotypic changes observed in mice with gene-targeted deletion of Mas. In this review, we will briefly highlight recent findings concerning the cardiovascular, renal, and metabolic roles of the ACE2/Ang-(1–7)/Mas axis. Furthermore, we
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London Regional Cancer Program, Biochemistry, 790 Commissioners Road, Room A4-921, London, Ontario, N6A 4L6 Canada Departments of
London Regional Cancer Program, Biochemistry, 790 Commissioners Road, Room A4-921, London, Ontario, N6A 4L6 Canada Departments of
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steroid receptor function by gene targeting in mice . Journal of Steroid Biochemistsry and Molecular Biology 93 107 – 112 . Xu Z Stokoe D Kane LP Weiss A 2002 The inducible expression of the tumor suppressor gene PTEN promotes apoptosis and
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-selective and conditional gene targeting approaches is necessary to better understand the role of these enzymes during the ovarian cycle and gestation. As previously mentioned, excess RA concentration is harmful to decidualization and implantation. Thus, actual
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ceramide-generating neutral sphingomyelinase 2 enzyme (nSMase2/SMPD3 – gene-targeted Smpd3 −/− and fro/fro mice) display gross skeletal abnormalities, including deformed long bones, short-limb dwarfism, hypomineralisation, delayed dentin mineralisation
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152 1347 – 1354 . ( doi:10.1210/en.2010-1068 ) Appelbaum L Vallone D Anzulovich A Ziv L Tom M Foulkes NS Gothilf Y 2006 Zebrafish arylalkylamine-N-acetyltranferase genes–targets for regulation of the circadian clock
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Department of Human Metabolism, Robert Hague Centre for Diabetes and Endocrinology, Medical School, The University of Sheffield, Sheffield S10 2RX, UK
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). This study additionally described the inhibition of nuclear factor κB (NFκB) activation, not only as a potential mechanism for decreased VCAM-1 expression, but also as a prospective modulator of several other inflammatory gene targets known to be
Centre for Neuroendocrinology and Department of Anatomy, Maurice Wilkins Centre for Molecular Biodiscovery, University of Otago, PO Box 913, Dunedin 9054, New Zealand
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function, including gene-targeting approaches that allow conditional regulation of prolactin responsive cells, will provide the impetus for a new wave of research to enhance our understanding of this fascinating system. Sixty years on from Geoffrey Harris
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. 2015 ). In 2015, use of the same MA-10 Leydig cells made deficient in TSPO by CRISPR/Cas9-mediated gene targeting indicated that PK11195 could stimulate steroidogenesis even in the absence of TSPO ( Tu et al . 2015 ). This work performed using three
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randomized controlled trial . European Journal of Obstetrics, Gynecology, and Reproductive Biology 200 . ( https://doi.org/10.1016/j.ejogrb.2016.02.009 ) 26963897 Kuhn R Torres RM 2002 Cre/loxP recombination system and gene targeting . Methods
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Endocrinology 52 11 – 28 . ( https://doi.org/10.1530/JME-13-0106 ) 24049066 Martinez-Sanchez A Nguyen-Tu MS Rutter GA 2015 DICER inactivation identifies pancreatic beta-cell “disallowed” genes targeted by microRNAs . Molecular Endocrinology
