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The Journal of Clinical Investigation|September 16, 1999
Characterization of a novel cellular defect in patients with phenotypic homozygous familial hypercholesterolemiaD Norman, X M Sun, M Bourbon, et al.Oncotarget|July 10, 2015
Requirement of novel amino acid fragments of orphan nuclear receptor TR3/Nur77 for its functions in angiogenesisYan Li, Pierre M Bourbon, Marianne A Grant, et al.Journal of Medical Genetics|May 5, 2009
Genetic diagnosis of familial hypercholesterolaemia: the importance of functional analysis of potential splice-site mutationsM Bourbon, M A Duarte, A C Alves, et al.Molecular and Cellular Biology|February 7, 2001
Distinctive features of Drosophila alternative splicing factor RS domain: implication for specific phosphorylation, shuttling, and splicing activationE Allemand, R Gattoni, H M Bourbon, et al.Clinical Genetics|May 22, 2008
Variable phenotypic expression of homozygous familial hypobetalipoproteinaemia due to novel APOB gene mutationsE Di Leo, L Magnolo, M Bertolotti, et al.Genetical Research|December 6, 2001
Dominant modifiers of the polyhomeotic extra-sex-combs phenotype induced by marked P element insertional mutagenesis in DrosophilaM O Fauvarque, P Laurenti, A Boivin, et al.Microvascular Research|June 19, 2021
A novel transcriptional complex on the VE-cadherin promoter regulated the downregulation of VE-cadherin in the Down Syndrome Candidate Region 1 isoform 1L-mediated angiogenesisShiqiang Hou, Gengming Niu, Xin Liu, et al.Microvascular Research|October 27, 2019
Orphan nuclear receptor TR3/Nur77 biologics inhibit tumor growth by targeting angiogenesis and tumor cellsChen Chen, Yan Li, Shiqiang Hou, et al.Scientific Reports|December 9, 2015
Structural analysis of APOB variants, p.(Arg3527Gln), p.(Arg1164Thr) and p.(Gln4494del), causing Familial Hypercholesterolaemia provides novel insights into variant pathogenicityJ A Fernández-Higuero, A Etxebarria, A Benito-Vicente, et al.Gene|October 18, 2002
Characterization of the nm23-M2, nm23-M3 and nm23-M4 mouse genes: comparison with their human orthologsK Massé, S Dabernat, P-M Bourbon, et al.Pageof 5