Showing results (1-10 of 37) with videos related to
Sort By:
Pageof 4
Journal of Chemical Ecology|May 3, 2007
The effects of a naturally produced benzoquinone on microbes common to flourAnn Yezerski, Carla Ciccone, Jill Rozitski, et al.Glycoconjugate Journal|December 26, 2012
Murine isoforms of UDP-GlcNAc 2-epimerase/ManNAc kinase: Secondary structures, expression profiles, and response to ManNAc therapyTal Yardeni, Katherine Jacobs, Terren K Niethamer, et al.Biochemistry|September 14, 2011
Identification, tissue distribution, and molecular modeling of novel human isoforms of the key enzyme in sialic acid synthesis, UDP-GlcNAc 2-epimerase/ManNAc kinaseTal Yardeni, Tsering Choekyi, Katherine Jacobs, et al.Metabolomics : Official Journal of the Metabolomic Society|March 5, 2019
A metabolomics-based approach for non-invasive screening of fetal central nervous system anomaliesJacopo Troisi, Annamaria Landolfi, Laura Sarno, et al.Molecular Genetics and Metabolism Reports|April 22, 2014
Two novel compound heterozygous mutations in OPA3 in two siblings with OPA3-related 3-methylglutaconic aciduriaChristina Lam, Linda K Gallo, Richard Dineen, et al.American Journal of Medical Genetics. Part A|June 18, 2016
Delayed diagnosis in a house of correction: Smith-Magenis syndrome due to a de novo nonsense RAI1 variantPatra Yeetong, Thierry Vilboux, Carla Ciccone, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 26, 2008
Allele-specific silencing of the dominant disease allele in sialuria by RNA interferenceRiko D Klootwijk, Paul J M Savelkoul, Carla Ciccone, et al.Molecular Genetics and Metabolism|August 23, 2005
Single nucleotide polymorphisms in the dystroglycan gene do not correlate with disease severity in hereditary inclusion body myopathyEmily Gottlieb, Carla Ciccone, Daniel Darvish, et al.Plos One|August 23, 2011
Molecular analysis of the Retinoic Acid Induced 1 gene (RAI1) in patients with suspected Smith-Magenis syndrome without the 17p11.2 deletionThierry Vilboux, Carla Ciccone, Jan K Blancato, et al.Journal of the Neurological Sciences|September 25, 2010
Brain alteration in a Nude/SCID fetus carrying FOXN1 homozygous mutationStefania Amorosi, Ilaria Vigliano, Ennio Del Giudice, et al.Pageof 4