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European Journal of Medical Genetics|September 20, 2019
Attitudes towards Genetic Information Delivered by High-Throughput Sequencing among Molecular Geneticists, Genetic Counselors, Medical Advisors and Students in FranceVlad Titerlea, Doulaye Dembélé, Jean-Louis Mandel, et al.
Journal of Neurology|July 8, 2025
Vertigo and dizziness in genetic neurodevelopmental disorders: an international cross-sectional studyChristophe Lopez, Pauline Burger, Jean-Louis Mandel, et al.
Minerva Anestesiologica|January 18, 2018
Association between Bispectral Index System and airway obstruction: an observational prospective cohort analysis during third molar extractionsA Sassan Sabouri, Alireza Jafari, Paul Creighton, et al.
AJNR. American Journal of Neuroradiology|June 19, 2003
Chronic submasseteric abscess: anatomic, radiologic, and pathologic featuresKevin C Jones, John Silver, William S Millar, et al.
The Journal of Biological Chemistry|October 21, 2004
Hsp70 and Hsp40 chaperones do not modulate retinal phenotype in SCA7 miceDominique Helmlinger, Jacques Bonnet, Jean-Louis Mandel, et al.
Molecular Biology of the Cell|November 14, 2008
Cells lacking the fragile X mental retardation protein (FMRP) have normal RISC activity but exhibit altered stress granule assemblyMarie-Cécile Didiot, Murugan Subramanian, Eric Flatter, et al.
Biochemical and Biophysical Research Communications|February 16, 2002
Functional redundancy in the myotubularin familyJocelyn Laporte, Laurence Liaubet, François Blondeau, et al.
Neuron|June 24, 2003
CYFIP/Sra-1 controls neuronal connectivity in Drosophila and links the Rac1 GTPase pathway to the fragile X proteinAnnette Schenck, Barbara Bardoni, Caillin Langmann, et al.
Molecular Biology and Evolution|February 3, 2006
The evolutionary origin of peroxisomes: an ER-peroxisome connectionAgatha Schlüter, Stéphane Fourcade, Raymond Ripp, et al.
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