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Vincent Bours

Showing results (131-140 of 190) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|February 15, 2007
Mutations in the aryl hydrocarbon receptor interacting protein gene are not highly prevalent among subjects with sporadic pituitary adenomasAnne Barlier, Jean-François Vanbellinghen, Adrian F Daly, et al.
International Journal of Molecular Sciences|March 11, 2023
Diagnostic Performance of Immunohistochemistry Compared to Molecular Techniques for Microsatellite Instability and p53 Mutation Detection in Endometrial CancerSylvie Streel, Alixe Salmon, Adriane Dheur, et al.
Clinical Genetics|May 8, 2020
GREB1L variants in familial and sporadic hereditary urogenital adysplasia and Mayer-Rokitansky-Kuster-Hauser syndromeAdeline Jacquinet, Bouchra Boujemla, Corinne Fasquelle, et al.
Epidemics|June 28, 2023
Reconstruction of SARS-CoV-2 outbreaks in a primary school using epidemiological and genomic dataCécile Kremer, Andrea Torneri, Pieter J K Libin, et al.
Neuro-Oncology|October 1, 2015
Prognostic relevance of epilepsy at presentation in glioblastoma patientsSharon Berendsen, Meri Varkila, Jérôme Kroonen, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|August 26, 2004
In vitro and in vivo activity of the nuclear factor-kappaB inhibitor sulfasalazine in human glioblastomasPierre A Robe, Mohamed Bentires-Alj, Marianne Bonif, et al.
Molecular Cell|October 8, 2004
GSK3-mediated BCL-3 phosphorylation modulates its degradation and its oncogenicityPatrick Viatour, Emmanuel Dejardin, Michael Warnier, et al.
Neuro-Oncology|August 27, 2014
Connexin 30 expression inhibits growth of human malignant gliomas but protects them against radiation therapyMaria Artesi, Jerome Kroonen, Markus Bredel, et al.
Hematology (Amsterdam, Netherlands)|May 26, 2022
Does glucose-6-phosphate dehydrogenase deficiency worsen the clinical features of sickle cell disease? A multi-hospital-based cross-sectional studyPaul Kambale-Kombi, Roland Marini Djang'eing'a, Jean-Pierre Alworong'a Opara, et al.
Journal of Inherited Metabolic Disease|May 15, 2015
Mutation of the iron-sulfur cluster assembly gene IBA57 causes fatal infantile leukodystrophyFrançois-Guillaume Debray, Claudia Stümpfig, Arnaud V Vanlander, et al.
Pageof 19

Showing results (131-140 of 190) with videos related to

Sort By:
Pageof 19
The Journal of Clinical Endocrinology and Metabolism|February 15, 2007
Mutations in the aryl hydrocarbon receptor interacting protein gene are not highly prevalent among subjects with sporadic pituitary adenomasAnne Barlier, Jean-François Vanbellinghen, Adrian F Daly, et al.
International Journal of Molecular Sciences|March 11, 2023
Diagnostic Performance of Immunohistochemistry Compared to Molecular Techniques for Microsatellite Instability and p53 Mutation Detection in Endometrial CancerSylvie Streel, Alixe Salmon, Adriane Dheur, et al.
Clinical Genetics|May 8, 2020
GREB1L variants in familial and sporadic hereditary urogenital adysplasia and Mayer-Rokitansky-Kuster-Hauser syndromeAdeline Jacquinet, Bouchra Boujemla, Corinne Fasquelle, et al.
Epidemics|June 28, 2023
Reconstruction of SARS-CoV-2 outbreaks in a primary school using epidemiological and genomic dataCécile Kremer, Andrea Torneri, Pieter J K Libin, et al.
Neuro-Oncology|October 1, 2015
Prognostic relevance of epilepsy at presentation in glioblastoma patientsSharon Berendsen, Meri Varkila, Jérôme Kroonen, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|August 26, 2004
In vitro and in vivo activity of the nuclear factor-kappaB inhibitor sulfasalazine in human glioblastomasPierre A Robe, Mohamed Bentires-Alj, Marianne Bonif, et al.
Molecular Cell|October 8, 2004
GSK3-mediated BCL-3 phosphorylation modulates its degradation and its oncogenicityPatrick Viatour, Emmanuel Dejardin, Michael Warnier, et al.
Neuro-Oncology|August 27, 2014
Connexin 30 expression inhibits growth of human malignant gliomas but protects them against radiation therapyMaria Artesi, Jerome Kroonen, Markus Bredel, et al.
Hematology (Amsterdam, Netherlands)|May 26, 2022
Does glucose-6-phosphate dehydrogenase deficiency worsen the clinical features of sickle cell disease? A multi-hospital-based cross-sectional studyPaul Kambale-Kombi, Roland Marini Djang'eing'a, Jean-Pierre Alworong'a Opara, et al.
Journal of Inherited Metabolic Disease|May 15, 2015
Mutation of the iron-sulfur cluster assembly gene IBA57 causes fatal infantile leukodystrophyFrançois-Guillaume Debray, Claudia Stümpfig, Arnaud V Vanlander, et al.
Pageof 19