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Showing results (731-740 of 885) with videos related to

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Scientific Reports|May 28, 2021
Multimodal evaluation of hypoxia in brain metastases of lung cancer and interest of hypoxia image-guided radiotherapyAurélien Corroyer-Dulmont, Samuel Valable, Jade Fantin, et al.
Frontiers in Microbiology|November 13, 2023
Pharmacokinetic-pharmacodynamic cutoff values for benzylpenicillin in horses to support the establishment of clinical breakpoints for benzylpenicillin antimicrobial susceptibility testing in horsesElodie A Lallemand, Alain Bousquet-Mélou, Laura Chapuis, et al.
European Journal of Human Genetics : EJHG|August 13, 2002
Refinement of the NHS locus on chromosome Xp22.13 and analysis of five candidate genesAnnick Toutain, Benoît Dessay, Nathalie Ronce, et al.
Science (New York, N.Y.)|April 9, 2011
Association of TALS developmental disorder with defect in minor splicing component U4atac snRNAPatrick Edery, Charles Marcaillou, Mourad Sahbatou, et al.
Neurology|March 17, 2000
Homogeneous phenotype of the gypsy limb-girdle MD with the gamma-sarcoglycan C283Y mutationL Merlini, J C Kaplan, C Navarro, et al.
Nature Communications|August 14, 2021
CRISPR-Cas9 globin editing can induce megabase-scale copy-neutral losses of heterozygosity in hematopoietic cellsJ Boutin, J Rosier, D Cappellen, et al.
Cell Death & Disease|September 15, 2024
SMAC mimetic drives microglia phenotype and glioblastoma immune microenvironmentEmmanuel Snacel-Fazy, Aurélie Soubéran, Magali Grange, et al.
Human Mutation|April 15, 2021
Novel missense mutations in PTCHD1 alter its plasma membrane subcellular localization and cause intellectual disability and autism spectrum disorderJudith Halewa, Sylviane Marouillat, Manon Dixneuf, et al.
Journal of Medical Genetics|August 21, 2007
Cardio-facio-cutaneous and Noonan syndromes due to mutations in the RAS/MAPK signalling pathway: genotype-phenotype relationships and overlap with Costello syndromeCaroline Nava, Nadine Hanna, Caroline Michot, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|December 25, 2012
Selective involvement of serum response factor in pressure-induced myogenic tone in resistance arteriesKevin Retailleau, Bertrand Toutain, Guillaume Galmiche, et al.
Pageof 89

Showing results (731-740 of 885) with videos related to

Sort By:
Pageof 89
Scientific Reports|May 28, 2021
Multimodal evaluation of hypoxia in brain metastases of lung cancer and interest of hypoxia image-guided radiotherapyAurélien Corroyer-Dulmont, Samuel Valable, Jade Fantin, et al.
Frontiers in Microbiology|November 13, 2023
Pharmacokinetic-pharmacodynamic cutoff values for benzylpenicillin in horses to support the establishment of clinical breakpoints for benzylpenicillin antimicrobial susceptibility testing in horsesElodie A Lallemand, Alain Bousquet-Mélou, Laura Chapuis, et al.
European Journal of Human Genetics : EJHG|August 13, 2002
Refinement of the NHS locus on chromosome Xp22.13 and analysis of five candidate genesAnnick Toutain, Benoît Dessay, Nathalie Ronce, et al.
Science (New York, N.Y.)|April 9, 2011
Association of TALS developmental disorder with defect in minor splicing component U4atac snRNAPatrick Edery, Charles Marcaillou, Mourad Sahbatou, et al.
Neurology|March 17, 2000
Homogeneous phenotype of the gypsy limb-girdle MD with the gamma-sarcoglycan C283Y mutationL Merlini, J C Kaplan, C Navarro, et al.
Nature Communications|August 14, 2021
CRISPR-Cas9 globin editing can induce megabase-scale copy-neutral losses of heterozygosity in hematopoietic cellsJ Boutin, J Rosier, D Cappellen, et al.
Cell Death & Disease|September 15, 2024
SMAC mimetic drives microglia phenotype and glioblastoma immune microenvironmentEmmanuel Snacel-Fazy, Aurélie Soubéran, Magali Grange, et al.
Human Mutation|April 15, 2021
Novel missense mutations in PTCHD1 alter its plasma membrane subcellular localization and cause intellectual disability and autism spectrum disorderJudith Halewa, Sylviane Marouillat, Manon Dixneuf, et al.
Journal of Medical Genetics|August 21, 2007
Cardio-facio-cutaneous and Noonan syndromes due to mutations in the RAS/MAPK signalling pathway: genotype-phenotype relationships and overlap with Costello syndromeCaroline Nava, Nadine Hanna, Caroline Michot, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|December 25, 2012
Selective involvement of serum response factor in pressure-induced myogenic tone in resistance arteriesKevin Retailleau, Bertrand Toutain, Guillaume Galmiche, et al.
Pageof 89