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Association of toll-interacting protein gene polymorphisms with atopic dermatitisEvaluation of the toll-like receptor 6 Ser249Pro polymorphism in patients with asthma, atopic dermatitis and chronic obstructive pulmonary disease.Pannexin1 stabilizes synaptic plasticity and is needed for learning.Characterization of connexin31.1-deficient mice reveals impaired placental developmentCcdc66 null mutation causes retinal degeneration and dysfunctionCellular and subcellular localization of paralemmin-1, a protein involved in cell shape control, in the rat brain, adrenal gland and kidneyMolecular characterization and immunohistochemical localization of palmdelphin, a cytosolic isoform of the paralemmin protein family implicated in membrane dynamicsNeuroanatomical correlates of suicide in psychosis: the possible role of von Economo neuronsLoss of connexin36 increases retinal cell vulnerability to secondary cell loss.Efficacy of fumaric acid esters in the R6/2 and YAC128 models of Huntington's disease.Expression pattern of lacZ reporter gene representing connexin36 in transgenic mice.SOX9 duplication linked to intersex in deer.Association of variation in the LAMA3 gene, encoding the alpha-chain of laminin 5, with atopic dermatitis in a German case-control cohort.Haplotype-defined linkage region for gPRA in Schapendoes dogs.Unintended spread of a biosafety level 2 recombinant retrovirus.Olfactory neuron-specific expression of A30P α-synuclein exacerbates dopamine deficiency and hyperactivity in a novel conditional model of early Parkinson's disease stages.Cellular and subcellular localization of Huntingtin [corrected] aggregates in the brain of a rat transgenic for Huntington disease.Inactivation of ceramide synthase 6 in mice results in an altered sphingolipid metabolism and behavioral abnormalities.Generalized progressive retinal atrophy in the Irish Glen of Imaal Terrier is associated with a deletion in the ADAM9 gene.First appraisal of brain pathology owing to A30P mutant alpha-synuclein.Progressive retinal atrophy in Schapendoes dogs: mutation of the newly identified CCDC66 gene.Immunohistochemical detection of the neuronal connexin36 in the mouse central nervous system in comparison to connexin36-deficient tissues.Fine-structural analysis and connexin expression in the retina of a transgenic model of Huntington's disease.Is the retina affected in Huntington disease?Behavioral abnormalities precede neuropathological markers in rats transgenic for Huntington's disease.Postsynaptic NO/cGMP increases NMDA receptor currents via hyperpolarization-activated cyclic nucleotide-gated channels in the hippocampus.Von Economo neuron density in the anterior cingulate cortex is reduced in early onset schizophrenia.Exome Sequencing Reveals AGBL5 as Novel Candidate Gene and Additional Variants for Retinitis Pigmentosa in Five Turkish Families.Neurodegeneration and motor dysfunction in a conditional model of Parkinson's disease.Signal transducer and activator of transcription 3-mediated regulation of miR-199a-5p links cardiomyocyte and endothelial cell function in the heart: a key role for ubiquitin-conjugating enzymes.Neurodegeneration in the olfactory bulb and olfactory deficits in the -/- mouse model for retinal degenerationNo evidence of an association between polymorphisms in the IRAK-M gene and atopic dermatitis in a German cohortPolymorphisms in NACHT-LRR (NLR) genes in atopic dermatitisTwo Common Loss-of-Function Mutations within the Filaggrin Gene Predispose for Early Onset of Atopic DermatitisCorrection: Pannexin1 Stabilizes Synaptic Plasticity and Is Needed for LearningVariation in the BDNF and NGFB genes in German atopic dermatitis patientsTheta-burst transcranial magnetic stimulation alters cortical inhibition
P50
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P50
name
Elisabeth Petrasch-Parwez
@en
type
label
Elisabeth Petrasch-Parwez
@en
prefLabel
Elisabeth Petrasch-Parwez
@en