Inheritance, gene expression, and lignin characterization in a mutant pine deficient in cinnamyl alcohol dehydrogenase. -...
Homozygote, Lignin, Mutation, Phenotype, Substrate Specificity, Trees ...
AKT1 and TRH1 are required during root hair elongation in Arabidopsis. - Oxford Neuroscience
Arabidopsis, Arabidopsis Proteins, Cation Transport Proteins, Homozygote, Ion Transport, Mutation, Osmolar Concentration, ...
The effects of APOE on brain activity do not simply reflect the risk of Alzheimer's disease. - Oxford Neuroscience
... relative to ε3 homozygotes, during both tasks. The increased activation was due to decreased deactivation or paradoxical ... relative to ε3 homozygotes, during both tasks. The increased activation was due to decreased deactivation or paradoxical ...
Homozygous Mutations in TBC1D23 Lead to a Non-degenerative Form of Pontocerebellar Hypoplasia. - Oxford Neuroscience
Homozygote, Humans, Male, Microcephaly, Mutation, Pedigree, Phenotype, Zebrafish ...
Modulation of floral development by a gibberellin-regulated microRNA. - Oxford Neuroscience
Agrobacterium tumefaciens, Arabidopsis, Base Sequence, Conserved Sequence, Evolution, Molecular, Gibberellins, Homozygote, ...
Longitudinal MEMRI analysis of brain phenotypes in a mouse model of Niemann-Pick Type C disease. - Oxford Neuroscience
... and homozygote mutant NPC mice, as well as deformation-based morphometry (DBM) driven brain volume comparisons across genotypes ... and homozygote mutant NPC mice, as well as deformation-based morphometry (DBM) driven brain volume comparisons across genotypes ...
DAPK1 variants are associated with Alzheimer's disease and allele-specific expression. - Oxford Neuroscience
... whereas the risk for heterozygous subjects was not significantly different from that of major allele homozygotes. A second SNP ... Minor allele homozygotes had a consistently lower risk than major allele homozygotes in the discovery and initial two ... Minor allele homozygotes had a consistently lower risk than major allele homozygotes in the discovery and initial two ... whereas the risk for heterozygous subjects was not significantly different from that of major allele homozygotes. A second SNP ...
Congenital Myasthenic Syndrome Type 19 Is Caused by Mutations in COL13A1, Encoding the Atypical Non-fibrillar Collagen Type...
Homozygote, Humans, Male, Mice, Mutation, Myasthenic Syndromes, Congenital, Myoblasts, Neuromuscular Junction, Pedigree, ...