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P Fergelot

Showing results (11-20 of 29) with videos related to

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Blood Cells, Molecules & Diseases|September 23, 2000
The HFE gene undergoes alternate splicing processesA Thénié, M Orhant, I Gicquel, et al.
Clinical Chemistry|December 1, 1994
Rapid detection of 1078 delT mutation by PCR-mediated site-directed mutagenesis: detection of cystic fibrosis carriers in a celtic populationI Dorval, P Fergelot, C Dubourg, et al.
Clinical Genetics|March 18, 2017
Deletion of the transcription factor SOX4 is implicated in syndromic nephroblastomaA Trimouille, E Barouk-Simonet, S Charron, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|March 1, 1995
Tat-induced lesions in transgenic mice do not correlate with the HIV-1 LTR transactivationP Fergelot, T Molina, P Blanchet, et al.
Immunogenetics|January 1, 1995
A human homologue to the yeast omnipotent suppressor 45 maps 100 kb centromeric to HLA-AB Chauvel, I Dorval, P Fergelot, et al.
Nucleic Acids Research|January 11, 1993
Dispensable role of the NF-kappa B sites in the UV-induction of the HIV-1 LTR in transgenic miceA Zider, B Mashhour, P Fergelot, et al.
Human Mutation|January 1, 1995
French CF family genotype analysis shows that the R297Q mutation is a rare polymorphismI Dorval, P Jézéquel, B Chauvel, et al.
Human Molecular Genetics|September 5, 2001
Identification of an endogenous RNA transcribed from the antisense strand of the HFE geneA C Thénié, I M Gicquel, S Hardy, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|October 27, 2010
Bone status in a mouse model of genetic hemochromatosisP Guggenbuhl, P Fergelot, M Doyard, et al.
Clinical Chemistry|June 1, 1995
Structural analysis of CFTR gene in congenital bilateral absence of vas deferensP Jézéquel, I Dorval, P Fergelot, et al.
Pageof 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
Blood Cells, Molecules & Diseases|September 23, 2000
The HFE gene undergoes alternate splicing processesA Thénié, M Orhant, I Gicquel, et al.
Clinical Chemistry|December 1, 1994
Rapid detection of 1078 delT mutation by PCR-mediated site-directed mutagenesis: detection of cystic fibrosis carriers in a celtic populationI Dorval, P Fergelot, C Dubourg, et al.
Clinical Genetics|March 18, 2017
Deletion of the transcription factor SOX4 is implicated in syndromic nephroblastomaA Trimouille, E Barouk-Simonet, S Charron, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|March 1, 1995
Tat-induced lesions in transgenic mice do not correlate with the HIV-1 LTR transactivationP Fergelot, T Molina, P Blanchet, et al.
Immunogenetics|January 1, 1995
A human homologue to the yeast omnipotent suppressor 45 maps 100 kb centromeric to HLA-AB Chauvel, I Dorval, P Fergelot, et al.
Nucleic Acids Research|January 11, 1993
Dispensable role of the NF-kappa B sites in the UV-induction of the HIV-1 LTR in transgenic miceA Zider, B Mashhour, P Fergelot, et al.
Human Mutation|January 1, 1995
French CF family genotype analysis shows that the R297Q mutation is a rare polymorphismI Dorval, P Jézéquel, B Chauvel, et al.
Human Molecular Genetics|September 5, 2001
Identification of an endogenous RNA transcribed from the antisense strand of the HFE geneA C Thénié, I M Gicquel, S Hardy, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|October 27, 2010
Bone status in a mouse model of genetic hemochromatosisP Guggenbuhl, P Fergelot, M Doyard, et al.
Clinical Chemistry|June 1, 1995
Structural analysis of CFTR gene in congenital bilateral absence of vas deferensP Jézéquel, I Dorval, P Fergelot, et al.
Pageof 3