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P Fergelot

Showing results (21-30 of 29) with videos related to

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Blood Cells, Molecules & Diseases|August 14, 2001
Low penetrant hemochromatosis phenotype in eight families: no evidence of modifiers in the MHC regionS Sachot, R Moirand, A M Jouanolle, et al.
British Journal of Cancer|September 17, 2009
Absence of VHL gene alteration and high VEGF expression are associated with tumour aggressiveness and poor survival of renal-cell carcinomaJ-J Patard, N Rioux-Leclercq, D Masson, et al.
Annales De Genetique|January 9, 1999
Prevalence of the C282Y mutation in Brittany: penetrance of genetic hemochromatosis?A M Jouanolle, P Fergelot, M L Raoul, et al.
Clinical and Experimental Immunology|November 15, 2006
Interleukin-6 and vascular endothelial growth factor release by renal cell carcinoma cells impedes lymphocyte-dendritic cell cross-talkF Cabillic, F Bouet-Toussaint, O Toutirais, et al.
The British Journal of Dermatology|July 17, 2019
CFTR gene variants: a predisposition factor to aquagenic palmoplantar keratodermaC Raynal, E Girodon, M P Audrezet, et al.
American Journal of Medical Genetics. Part A|June 29, 2010
Rubinstein-Taybi syndrome and Hirschsprung disease in a patient harboring an intragenic deletion of the CREBBP geneB Isidor, G Podevin, C Camby, et al.
Nature Genetics|November 1, 1996
Haemochromatosis and HLA-HA M Jouanolle, G Gandon, P Jézéquel, et al.
Clinical Genetics|September 26, 2015
Fetal phenotypes in otopalatodigital spectrum disordersS Naudion, S Moutton, I Coupry, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|December 25, 2022
The multi-faceted nature of 15 CFTR exonic variations: Impact on their functional classification and perspectives for therapyA Bergougnoux, A Billet, C Ka, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Blood Cells, Molecules & Diseases|August 14, 2001
Low penetrant hemochromatosis phenotype in eight families: no evidence of modifiers in the MHC regionS Sachot, R Moirand, A M Jouanolle, et al.
British Journal of Cancer|September 17, 2009
Absence of VHL gene alteration and high VEGF expression are associated with tumour aggressiveness and poor survival of renal-cell carcinomaJ-J Patard, N Rioux-Leclercq, D Masson, et al.
Annales De Genetique|January 9, 1999
Prevalence of the C282Y mutation in Brittany: penetrance of genetic hemochromatosis?A M Jouanolle, P Fergelot, M L Raoul, et al.
Clinical and Experimental Immunology|November 15, 2006
Interleukin-6 and vascular endothelial growth factor release by renal cell carcinoma cells impedes lymphocyte-dendritic cell cross-talkF Cabillic, F Bouet-Toussaint, O Toutirais, et al.
The British Journal of Dermatology|July 17, 2019
CFTR gene variants: a predisposition factor to aquagenic palmoplantar keratodermaC Raynal, E Girodon, M P Audrezet, et al.
American Journal of Medical Genetics. Part A|June 29, 2010
Rubinstein-Taybi syndrome and Hirschsprung disease in a patient harboring an intragenic deletion of the CREBBP geneB Isidor, G Podevin, C Camby, et al.
Nature Genetics|November 1, 1996
Haemochromatosis and HLA-HA M Jouanolle, G Gandon, P Jézéquel, et al.
Clinical Genetics|September 26, 2015
Fetal phenotypes in otopalatodigital spectrum disordersS Naudion, S Moutton, I Coupry, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|December 25, 2022
The multi-faceted nature of 15 CFTR exonic variations: Impact on their functional classification and perspectives for therapyA Bergougnoux, A Billet, C Ka, et al.
Pageof 3