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Dominique Vidaud

Showing results (21-30 of 90) with videos related to

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British Journal of Haematology|February 21, 2006
Prothrombin Saint-Denis: a natural variant with a point mutation resulting in Asp to Glu substitution at position 552 in prothrombinStanislas Rouy, Dominique Vidaud, Jean-Luc Alessandri, et al.
Human Mutation|August 26, 2003
CFTR mutations in patients from Colombia: implications for local and regional molecular diagnosis programsGenoveva Keyeux, Clemencia Rodas, Thierry Bienvenu, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|July 19, 2006
Global proteomic analysis of microdissected cirrhotic nodules reveals significant biomarkers associated with clonal expansionNathalie Guedj, Delphine Dargere, Françoise Degos, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|June 3, 2004
Molecular profiles of neurofibromatosis type 1-associated plexiform neurofibromas: identification of a gene expression signature of poor prognosisPascale Lévy, Ivan Bièche, Karen Leroy, et al.
European Journal of Human Genetics : EJHG|February 2, 2023
Comment on Intragenic inversions in NF1 gene as pathogenic mechanism in neurofibromatosis type 1Laurence Pacot, Albain Chansavang, Sébastien Jacques, et al.
European Journal of Human Genetics : EJHG|July 24, 2008
Characterization of a 7.6-Mb germline deletion encompassing the NF1 locus and about a hundred genes in an NF1 contiguous gene syndrome patientEric Pasmant, Aurélie de Saint-Trivier, Ingrid Laurendeau, et al.
Brain Research. Molecular Brain Research|June 5, 2003
Quantitative RT-PCR reveals a ubiquitous but preferentially neural expression of the KIS gene in rat and humanIvan Bièche, Valérie Manceau, Patrick A Curmi, et al.
Rheumatology (Oxford, England)|January 26, 2010
Increase in type II collagen turnover after iron depletion in patients with hereditary haemochromatosisPascal Richette, Claire Eymard, Michelle Deberg, et al.
Gut|September 29, 2006
Liver fibrosis in women with chronic hepatitis C: evidence for the negative role of the menopause and steatosis and the potential benefit of hormone replacement therapyLiana Codes, Tarik Asselah, Dominique Cazals-Hatem, et al.
Hepatology (Baltimore, Md.)|June 29, 2007
Telangiectatic adenoma: an entity associated with increased body mass index and inflammationValérie Paradis, Axelle Champault, Maxime Ronot, et al.
Pageof 9

Showing results (21-30 of 90) with videos related to

Sort By:
Pageof 9
British Journal of Haematology|February 21, 2006
Prothrombin Saint-Denis: a natural variant with a point mutation resulting in Asp to Glu substitution at position 552 in prothrombinStanislas Rouy, Dominique Vidaud, Jean-Luc Alessandri, et al.
Human Mutation|August 26, 2003
CFTR mutations in patients from Colombia: implications for local and regional molecular diagnosis programsGenoveva Keyeux, Clemencia Rodas, Thierry Bienvenu, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|July 19, 2006
Global proteomic analysis of microdissected cirrhotic nodules reveals significant biomarkers associated with clonal expansionNathalie Guedj, Delphine Dargere, Françoise Degos, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|June 3, 2004
Molecular profiles of neurofibromatosis type 1-associated plexiform neurofibromas: identification of a gene expression signature of poor prognosisPascale Lévy, Ivan Bièche, Karen Leroy, et al.
European Journal of Human Genetics : EJHG|February 2, 2023
Comment on Intragenic inversions in NF1 gene as pathogenic mechanism in neurofibromatosis type 1Laurence Pacot, Albain Chansavang, Sébastien Jacques, et al.
European Journal of Human Genetics : EJHG|July 24, 2008
Characterization of a 7.6-Mb germline deletion encompassing the NF1 locus and about a hundred genes in an NF1 contiguous gene syndrome patientEric Pasmant, Aurélie de Saint-Trivier, Ingrid Laurendeau, et al.
Brain Research. Molecular Brain Research|June 5, 2003
Quantitative RT-PCR reveals a ubiquitous but preferentially neural expression of the KIS gene in rat and humanIvan Bièche, Valérie Manceau, Patrick A Curmi, et al.
Rheumatology (Oxford, England)|January 26, 2010
Increase in type II collagen turnover after iron depletion in patients with hereditary haemochromatosisPascal Richette, Claire Eymard, Michelle Deberg, et al.
Gut|September 29, 2006
Liver fibrosis in women with chronic hepatitis C: evidence for the negative role of the menopause and steatosis and the potential benefit of hormone replacement therapyLiana Codes, Tarik Asselah, Dominique Cazals-Hatem, et al.
Hepatology (Baltimore, Md.)|June 29, 2007
Telangiectatic adenoma: an entity associated with increased body mass index and inflammationValérie Paradis, Axelle Champault, Maxime Ronot, et al.
Pageof 9