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International Journal of Cancer|July 9, 2004
Allelic loss but absence of mutations in the polyspecific transporter gene BWR1A on 11p15.5 in hepatoblastomaSteffen Albrecht, Wolfgang Hartmann, Farzad Houshdaran, et al.
Basic Research in Cardiology|July 14, 2012
Transcriptional regulation of Nox4 by histone deacetylases in human endothelial cellsDaniel Siuda, Ulrich Zechner, Nady El Hajj, et al.
Oncotarget|January 4, 2018
Integrin α5 triggers the metastatic potential in renal cell carcinomaInes Breuksch, Franz Prosinger, Fabian Baehr, et al.
Endocrine Connections|September 5, 2022
Comprehensive genetic testing approaches as the basis for personalized management of growth disturbances: current status and perspectivesDanielle Christine Maria van der Kaay, Anne Rochtus, Gerhard Binder, et al.
Journal of Immunology (Baltimore, Md. : 1950)|March 22, 2005
Linking C5 deficiency to an exonic splicing enhancer mutationNicole Pfarr, Dirk Prawitt, Michael Kirschfink, et al.
Pediatric Hematology and Oncology|June 11, 2016
Next-generation sequencing reveals germline mutations in an infant with synchronous occurrence of nephro- and neuroblastomaJohanna Theruvath, Alexandra Russo, Bettina Kron, et al.
Orphanet Journal of Rare Diseases|June 10, 2020
Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN)Thomas Eggermann, Miriam Elbracht, Ingo Kurth, et al.
European Journal of Human Genetics : EJHG|December 13, 2012
Frequency and characterization of DNA methylation defects in children born SGASusanne Bens, Andrea Haake, Julia Richter, et al.
Stem Cells (Dayton, Ohio)|December 8, 2004
In vitro cultured islet-derived progenitor cells of human origin express human albumin in severe combined immunodeficiency mouse liver in vivoMarc-Alexander von Mach, Jan Georg Hengstler, Marc Brulport, et al.
Clinical Epigenetics|May 7, 2016
Kaiso mediates human ICR1 methylation maintenance and H19 transcriptional fine regulationFlorian Bohne, David Langer, Ursula Martiné, et al.
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