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Croquette

Showing results (171-180 of 197) with videos related to

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Angewandte Chemie (International Ed. in English)|January 22, 2015
Photoswitching kinetics and phase-sensitive detection add discriminative dimensions for selective fluorescence imagingJérôme Querard, Tal-Zvi Markus, Marie-Aude Plamont, et al.
Psychiatry Research|October 1, 1998
Genotype-phenotype relationship in female carriers of the premutation and full mutation of FMR-1P Franke, M Leboyer, M Gänsicke, et al.
European Journal of Clinical Pharmacology|July 30, 2009
Cannabis and benzodiazepines as determinants of methadone trough plasma concentration variability in maintenance treatment: a transnational studyRichard Hallinan, Séverine Crettol, Kingsley Agho, et al.
Light, Science & Applications|December 5, 2018
Macroscale fluorescence imaging against autofluorescence under ambient lightRuikang Zhang, Raja Chouket, Marie-Aude Plamont, et al.
Drug and Alcohol Dependence|December 3, 2014
A randomized, controlled trial of combined cognitive-behavioral therapy plus prize-based contingency management for cocaine dependenceSylvie A Petitjean, Kenneth M Dürsteler-MacFarland, Marina Croquette Krokar, et al.
European Journal of Human Genetics : EJHG|February 1, 2007
Recurrent rearrangements in the proximal 15q11-q14 region: a new breakpoint cluster specific to unbalanced translocationsCécile Mignon-Ravix, Danielle Depetris, Judith J Luciani, et al.
Respiratory Medicine and Research|July 6, 2026
Effectiveness and tolerance of respiratory rehabilitation in suspected pulmonary hypertension associated with chronic obstructive pulmonary diseaseChristian Giffa, Salomé Courat-Beuvon, Magali Croquette, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 1, 1997
[Fragile X syndrome is still unrecognized: efficacy of molecular diagnosis in mentally retarded probands]M Cossée, C Moutou, V Biancalana, et al.
Journal of Medical Genetics|September 10, 2003
Telomeric 22q13 deletions resulting from rings, simple deletions, and translocations: cytogenetic, molecular, and clinical analyses of 32 new observationsJ J Luciani, P de Mas, D Depetris, et al.
Communications Biology|January 30, 2021
Detection of genetic variation and base modifications at base-pair resolution on both DNA and RNAZhen Wang, Jérôme Maluenda, Laurène Giraut, et al.
Pageof 20

Showing results (171-180 of 197) with videos related to

Sort By:
Pageof 20
Angewandte Chemie (International Ed. in English)|January 22, 2015
Photoswitching kinetics and phase-sensitive detection add discriminative dimensions for selective fluorescence imagingJérôme Querard, Tal-Zvi Markus, Marie-Aude Plamont, et al.
Psychiatry Research|October 1, 1998
Genotype-phenotype relationship in female carriers of the premutation and full mutation of FMR-1P Franke, M Leboyer, M Gänsicke, et al.
European Journal of Clinical Pharmacology|July 30, 2009
Cannabis and benzodiazepines as determinants of methadone trough plasma concentration variability in maintenance treatment: a transnational studyRichard Hallinan, Séverine Crettol, Kingsley Agho, et al.
Light, Science & Applications|December 5, 2018
Macroscale fluorescence imaging against autofluorescence under ambient lightRuikang Zhang, Raja Chouket, Marie-Aude Plamont, et al.
Drug and Alcohol Dependence|December 3, 2014
A randomized, controlled trial of combined cognitive-behavioral therapy plus prize-based contingency management for cocaine dependenceSylvie A Petitjean, Kenneth M Dürsteler-MacFarland, Marina Croquette Krokar, et al.
European Journal of Human Genetics : EJHG|February 1, 2007
Recurrent rearrangements in the proximal 15q11-q14 region: a new breakpoint cluster specific to unbalanced translocationsCécile Mignon-Ravix, Danielle Depetris, Judith J Luciani, et al.
Respiratory Medicine and Research|July 6, 2026
Effectiveness and tolerance of respiratory rehabilitation in suspected pulmonary hypertension associated with chronic obstructive pulmonary diseaseChristian Giffa, Salomé Courat-Beuvon, Magali Croquette, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 1, 1997
[Fragile X syndrome is still unrecognized: efficacy of molecular diagnosis in mentally retarded probands]M Cossée, C Moutou, V Biancalana, et al.
Journal of Medical Genetics|September 10, 2003
Telomeric 22q13 deletions resulting from rings, simple deletions, and translocations: cytogenetic, molecular, and clinical analyses of 32 new observationsJ J Luciani, P de Mas, D Depetris, et al.
Communications Biology|January 30, 2021
Detection of genetic variation and base modifications at base-pair resolution on both DNA and RNAZhen Wang, Jérôme Maluenda, Laurène Giraut, et al.
Pageof 20