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American Journal of Human Genetics|December 1, 2009
Deletions and point mutations of LRRC50 cause primary ciliary dyskinesia due to dynein arm defectsNiki Tomas Loges, Heike Olbrich, Anita Becker-Heck, et al.
Brain : a Journal of Neurology|January 25, 2014
Sensory neuropathy with bone destruction due to a mutation in the membrane-shaping atlastin GTPase 3Uwe Kornak, Inès Mademan, Marte Schinke, et al.
Environmental Microbiology|November 17, 2006
Whole genome analysis of the marine Bacteroidetes'Gramella forsetii' reveals adaptations to degradation of polymeric organic matterMargarete Bauer, Michael Kube, Hanno Teeling, et al.
American Journal of Human Genetics|January 21, 2014
Mutations in PGAP3 impair GPI-anchor maturation, causing a subtype of hyperphosphatasia with mental retardationMalcolm F Howard, Yoshiko Murakami, Alistair T Pagnamenta, et al.
The Plant Journal : for Cell and Molecular Biology|April 28, 2023
A non-canonical function of Arabidopsis ERECTA proteins and a role of the SWI3B subunit of the SWI/SNF chromatin remodeling complex in gibberellin signalingElzbieta Sarnowska, Szymon Kubala, Pawel Cwiek, et al.
Nature|December 20, 2013
The genome of the recently domesticated crop plant sugar beet (Beta vulgaris)Juliane C Dohm, André E Minoche, Daniela Holtgräwe, et al.
Nature Genetics|January 15, 2002
Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetryHeike Olbrich, Karsten Häffner, Andreas Kispert, et al.
Science Translational Medicine|September 5, 2014
Effective diagnosis of genetic disease by computational phenotype analysis of the disease-associated genomeTomasz Zemojtel, Sebastian Köhler, Luisa Mackenroth, et al.
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|July 2, 2016
A high-density SNP genotyping array for Brassica napus and its ancestral diploid species based on optimised selection of single-locus markers in the allotetraploid genomeWayne E Clarke, Erin E Higgins, Joerg Plieske, et al.
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