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Virginie S Vervoort

Showing results (1-10 of 7) with videos related to

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Gene|February 3, 2007
Splice variants and expression patterns of SHEP1, BCAR3 and NSP1, a gene family involved in integrin and receptor tyrosine kinase signalingVirginie S Vervoort, Séverine Roselli, Robert G Oshima, et al.
American Journal of Medical Genetics. Part A|February 8, 2006
AGTR2 in brain development and functionVirginie S Vervoort, Greagory Guzauskas, John Archie, et al.
Transgenic Research|November 21, 2007
A novel Flk1-TVA transgenic mouse model for gene delivery to angiogenic vasculatureVirginie S Vervoort, Mark Lu, Fatima Valencia, et al.
Annals of Neurology|July 6, 2004
POMGnT1 gene alterations in a family with neurological abnormalitiesVirginie S Vervoort, Kenton R Holden, Kennedy C Ukadike, et al.
European Journal of Human Genetics : EJHG|October 31, 2002
Genomic rearrangements of EYA1 account for a large fraction of families with BOR syndromeVirginie S Vervoort, Richard J H Smith, Jane O'Brien, et al.
Human Mutation|May 18, 2004
Branchio-oto-renal syndrome: the mutation spectrum in EYA1 and its phenotypic consequencesEugene H Chang, Maithilee Menezes, Nicole C Meyer, et al.
Science (New York, N.Y.)|June 29, 2002
AGTR2 mutations in X-linked mental retardationVirginie S Vervoort, Michael A Beachem, Penny S Edwards, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Gene|February 3, 2007
Splice variants and expression patterns of SHEP1, BCAR3 and NSP1, a gene family involved in integrin and receptor tyrosine kinase signalingVirginie S Vervoort, Séverine Roselli, Robert G Oshima, et al.
American Journal of Medical Genetics. Part A|February 8, 2006
AGTR2 in brain development and functionVirginie S Vervoort, Greagory Guzauskas, John Archie, et al.
Transgenic Research|November 21, 2007
A novel Flk1-TVA transgenic mouse model for gene delivery to angiogenic vasculatureVirginie S Vervoort, Mark Lu, Fatima Valencia, et al.
Annals of Neurology|July 6, 2004
POMGnT1 gene alterations in a family with neurological abnormalitiesVirginie S Vervoort, Kenton R Holden, Kennedy C Ukadike, et al.
European Journal of Human Genetics : EJHG|October 31, 2002
Genomic rearrangements of EYA1 account for a large fraction of families with BOR syndromeVirginie S Vervoort, Richard J H Smith, Jane O'Brien, et al.
Human Mutation|May 18, 2004
Branchio-oto-renal syndrome: the mutation spectrum in EYA1 and its phenotypic consequencesEugene H Chang, Maithilee Menezes, Nicole C Meyer, et al.
Science (New York, N.Y.)|June 29, 2002
AGTR2 mutations in X-linked mental retardationVirginie S Vervoort, Michael A Beachem, Penny S Edwards, et al.
Pageof 1