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Plant Direct|June 28, 2019
Weed presence altered biotic stress and light signaling in maize even when weeds were removed early in the critical weed-free periodDavid P Horvath, Stephanie Bruggeman, Janet Moriles-Miller, et al.BMC Genomics|May 20, 2015
Glyphosate's impact on vegetative growth in leafy spurge identifies molecular processes and hormone cross-talk associated with increased branchingMünevver Doğramacı, Michael E Foley, David P Horvath, et al.Functional & Integrative Genomics|May 15, 2012
Auxin and ABA act as central regulators of developmental networks associated with paradormancy in Canada thistle (Cirsium arvense)James V Anderson, Münevver Doğramacı, David P Horvath, et al.American Journal of Obstetrics and Gynecology|February 18, 2015
Impact of probiotics in women with gestational diabetes mellitus on metabolic health: a randomized controlled trialKaren L Lindsay, Lorraine Brennan, Maria A Kennelly, et al.American Journal of Medical Genetics. Part A|September 14, 2007
WT1 mutations in Meacham syndrome suggest a coelomic mesothelial origin of the cardiac and diaphragmatic malformationsMohnish Suri, Peter Kelehan, David O'neill, et al.American Journal of Human Genetics|March 29, 2005
Diversity and function of mutations in p450 oxidoreductase in patients with Antley-Bixler syndrome and disordered steroidogenesisNingwu Huang, Amit V Pandey, Vishal Agrawal, et al.Cell Reports|October 13, 2016
Astroglial-Mediated Remodeling of the Interhemispheric Midline Is Required for the Formation of the Corpus CallosumIlan Gobius, Laura Morcom, Rodrigo Suárez, et al.Genetics|September 29, 2011
Association between seed dormancy and pericarp color is controlled by a pleiotropic gene that regulates abscisic acid and flavonoid synthesis in weedy red riceXing-You Gu, Michael E Foley, David P Horvath, et al.Frontiers in Neurology|February 15, 2019
Extracranial and Intracranial Vasculopathy With "Moyamoya Phenomenon" in Association With Alagille SyndromeSiobhan Delaney, Ged O'Connor, William Reardon, et al.Human Mutation|June 17, 2005
Twenty-six novel EFNB1 mutations in familial and sporadic craniofrontonasal syndrome (CFNS)Ilse Wieland, William Reardon, Sibylle Jakubiczka, et al.Pageof 14