about
Development and application of a DNA microarray-based yeast two-hybrid systemRBM20, a gene for hereditary cardiomyopathy, regulates titin splicingNibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndromeHereditary isolated renal magnesium loss maps to chromosome 11q23.Inflammation-induced acute phase response in skeletal muscle and critical illness myopathyFamilial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 geneGenome search for susceptibility loci of common idiopathic generalised epilepsies[Molecular-cytogenetic analysis of ancient DNA (aDNA) from preparations from the Meckel collection in Halle (Saale)].Fine mapping and single nucleotide polymorphism association results of candidate genes for asthma and related phenotypes.The genome sequence of the spontaneously hypertensive rat: Analysis and functional significanceShort-term weightlessness produced by parabolic flight maneuvers altered gene expression patterns in human endothelial cells.Splitting schizophrenia: periodic catatonia-susceptibility locus on chromosome 15q15A genetic basis for mechanosensory traits in humansGene localization for an autosomal dominant familial periodic fever to 12p13Genomic approach to identify factors that drive the formation of three-dimensional structures by EA.hy926 endothelial cells.Genome-wide analysis indicates more Asian than Melanesian ancestry of Polynesians.Progress and prospects in rat genetics: a community view.SNP and haplotype mapping for genetic analysis in the rat.PTHR1 loss-of-function mutations in familial, nonsyndromic primary failure of tooth eruptionDifferential gene expression profile and altered cytokine secretion of thyroid cancer cells in space.Characterization of the genomic structure and function of regions influencing renin and angiogenesis in the SS rat.Identification of Stim1 as a candidate gene for exaggerated sympathetic response to stress in the stroke-prone spontaneously hypertensive rat.The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21Localisation of a gene for an autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia, and distinctive facies to chromosome 15q26.1A.05: COMPARISON OF THE WHOLE GENOME SEQUENCE REVEALED GENETICALLY DISTINCT LOCI BETWEEN SHR/IZM AND SHRSP/IZM.The Slavic NBN Founder Mutation: A Role for Reproductive Fitness?Borna disease virus-induced neuronal degeneration dependent on host genetic background and prevented by soluble factors.A trans-acting locus regulates an anti-viral expression network and type 1 diabetes riskGenome sequencing reveals loci under artificial selection that underlie disease phenotypes in the laboratory ratCombined sequence-based and genetic mapping analysis of complex traits in outbred rats.Differential gene expression of human chondrocytes cultured under short-term altered gravity conditions during parabolic flight maneuvers.Retention of lysosomal protein CLN5 in the endoplasmic reticulum causes neuronal ceroid lipofuscinosis in Asian sibship.Genome-wide linkage scan for bladder exstrophy-epispadias complex.Systems Genetics Analysis of a Recombinant Inbred Mouse Cell Culture Panel Reveals Wnt Pathway Member Lrp6 as a Regulator of Adult Hippocampal Precursor Cell Proliferation.Impaired p53-mediated DNA damage response, cell-cycle disturbance and chromosome aberrations in Nijmegen breakage syndrome lymphoblastoid cell lines.Linkage studies exclude the AT-V gene(s) from the translocation breakpoints in an AT-V patient.Diaphragmatic spinal muscular atrophy with respiratory distress is heterogeneous, and one form Is linked to chromosome 11q13-q21.[Primary failure of eruption (PFE). Clinical and molecular genetics analysis].Two genomic regions of chromosomes 1 and 18 explain most of the stroke susceptibility under salt loading in stroke-prone spontaneously hypertensive rat/Izm.IL-11 is a crucial determinant of cardiovascular fibrosis.
P50
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P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Kathrin Saar
@en
Kathrin Saar
@es
Kathrin Saar
@nl
Kathrin Saar
@sl
type
label
Kathrin Saar
@en
Kathrin Saar
@es
Kathrin Saar
@nl
Kathrin Saar
@sl
prefLabel
Kathrin Saar
@en
Kathrin Saar
@es
Kathrin Saar
@nl
Kathrin Saar
@sl
P106
P21
P31
P496
0000-0002-4483-1557