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Victoria Viart

Showing results (1-10 of 11) with videos related to

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European Journal of Human Genetics : EJHG|August 18, 2011
Functional analysis of a promoter variant identified in the CFTR gene in cis of a frameshift mutationVictoria Viart, Marie Des Georges, Mireille Claustres, et al.
Plos One|April 6, 2013
Phosphorylated C/EBPβ influences a complex network involving YY1 and USF2 in lung epithelial cellsVictoria Viart, Jessica Varilh, Estelle Lopez, et al.
Thrombosis and Haemostasis|May 26, 2012
Lethal factor VII deficiency due to novel mutations in the F7 promoter: functional analysis reveals disruption of HNF4 binding siteMuriel Giansily-Blaizot, Estelle Lopez, Victoria Viart, et al.
Prenatal Diagnosis|December 13, 2016
Germline mosaicism is a pitfall in PGD for X-linked disorders. Single sperm typing detects very low frequency paternal gonadal mosaicism in a case of recurrent chondrodysplasia punctata misattributed to a maternal originVictoria Viart, Marjolaine Willems, Aliya Ishmukhametova, et al.
The European Respiratory Journal|September 5, 2014
Transcription factors and miRNAs that regulate fetal to adult CFTR expression change are new targets for cystic fibrosisVictoria Viart, Anne Bergougnoux, Jennifer Bonini, et al.
Gene|April 10, 2012
Identification of a novel duplication CFTRdup2 and functional impact of large rearrangements identified in the CFTR geneMagali Taulan, Victoria Viart, Corinne Theze, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|March 24, 2015
Should diffuse bronchiectasis still be considered a CFTR-related disorder?Anne Bergougnoux, Victoria Viart, Julie Miro, et al.
Journal of Medical Genetics|October 26, 2010
Variants in CFTR untranslated regions are associated with congenital bilateral absence of the vas deferensEstelle Lopez, Victoria Viart, Caroline Guittard, et al.
Reproductive Biomedicine Online|December 6, 2017
Thirteen years' experience of 893 PGD cycles for monogenic disorders in a publicly funded, nationally regulated regional hospital serviceAnne Girardet, Aliya Ishmukhametova, Victoria Viart, et al.
European Journal of Human Genetics : EJHG|May 28, 2015
The improvement of the best practice guidelines for preimplantation genetic diagnosis of cystic fibrosis: toward an international consensusAnne Girardet, Victoria Viart, Stéphanie Plaza, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
European Journal of Human Genetics : EJHG|August 18, 2011
Functional analysis of a promoter variant identified in the CFTR gene in cis of a frameshift mutationVictoria Viart, Marie Des Georges, Mireille Claustres, et al.
Plos One|April 6, 2013
Phosphorylated C/EBPβ influences a complex network involving YY1 and USF2 in lung epithelial cellsVictoria Viart, Jessica Varilh, Estelle Lopez, et al.
Thrombosis and Haemostasis|May 26, 2012
Lethal factor VII deficiency due to novel mutations in the F7 promoter: functional analysis reveals disruption of HNF4 binding siteMuriel Giansily-Blaizot, Estelle Lopez, Victoria Viart, et al.
Prenatal Diagnosis|December 13, 2016
Germline mosaicism is a pitfall in PGD for X-linked disorders. Single sperm typing detects very low frequency paternal gonadal mosaicism in a case of recurrent chondrodysplasia punctata misattributed to a maternal originVictoria Viart, Marjolaine Willems, Aliya Ishmukhametova, et al.
The European Respiratory Journal|September 5, 2014
Transcription factors and miRNAs that regulate fetal to adult CFTR expression change are new targets for cystic fibrosisVictoria Viart, Anne Bergougnoux, Jennifer Bonini, et al.
Gene|April 10, 2012
Identification of a novel duplication CFTRdup2 and functional impact of large rearrangements identified in the CFTR geneMagali Taulan, Victoria Viart, Corinne Theze, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|March 24, 2015
Should diffuse bronchiectasis still be considered a CFTR-related disorder?Anne Bergougnoux, Victoria Viart, Julie Miro, et al.
Journal of Medical Genetics|October 26, 2010
Variants in CFTR untranslated regions are associated with congenital bilateral absence of the vas deferensEstelle Lopez, Victoria Viart, Caroline Guittard, et al.
Reproductive Biomedicine Online|December 6, 2017
Thirteen years' experience of 893 PGD cycles for monogenic disorders in a publicly funded, nationally regulated regional hospital serviceAnne Girardet, Aliya Ishmukhametova, Victoria Viart, et al.
European Journal of Human Genetics : EJHG|May 28, 2015
The improvement of the best practice guidelines for preimplantation genetic diagnosis of cystic fibrosis: toward an international consensusAnne Girardet, Victoria Viart, Stéphanie Plaza, et al.
Pageof 2