about
Morphology of nuclear transcriptionLoss of the Suv39h histone methyltransferases impairs mammalian heterochromatin and genome stabilityNucleoli, nucleolar chromosomes and ribosomal genes in the human spermatocyte.Expression patterns of protein C inhibitor in mouse development.Distinct chromatin signature of histone H3 variant H3.3 in human cells.c-erbB-3: a nuclear protein in mammary epithelial cells.Hepatocyte specific expression of an oncogenic variant of β-catenin results in cholestatic liver diseaseIdentification of a rare COCH mutation by whole-exome sequencing : Implications for personalized therapeutic rehabilitation in an Austrian family with non-syndromic autosomal dominant late-onset hearing loss.A single allele of Hdac2 but not Hdac1 is sufficient for normal mouse brain development in the absence of its paralog.hVps37A Status affects prognosis and cetuximab sensitivity in ovarian cancer.Characterization of NKIP: a novel, Na+/K+-ATPase interacting protein mediates neural differentiation and apoptosis.Loss of novel mda-7 splice variant (mda-7s) expression is associated with metastatic melanoma.Whole-exome sequencing to identify the cause of congenital sensorineural hearing loss in carriers of a heterozygous GJB2 mutation.A FGF3 mutation associated with differential inner ear malformation, microtia, and microdontia.Immunohistochemical expression analysis of Cx43, Cx26, c-KIT and PlAP in contralateral testis biopsies of patients with non-seminomatous testicular germ cell tumor.LEM4/ANKLE-2 deficiency impairs post-mitotic re-localization of BAF, LAP2α and LaminA to the nucleus, causes nuclear envelope instability in telophase and leads to hyperploidy in HeLa cells.A novel missense NDP mutation [p.(Cys93Arg)] with a manifesting carrier in an austrian family with Norrie disease.A Novel Mutation in SLC26A4 Causes Nonsyndromic Autosomal Recessive Hearing Impairment.The role of alternative GJB2 transcription in screening for neonatal sensorineural deafness in Austria.The promoter mutation c.-259C>T (-3438C>T) is not a common cause of non-syndromic hearing impairment in Austria.Identification of a SNP in a regulatory region of GJB2 associated with idiopathic nonsyndromic autosomal recessive hearing loss in a multicenter study.Despite a lack of otoacoustic emission, word recognition is not seriously influenced in a TECTA DFNA8/12 family.Connexin 26 mutations in cases of sensorineural deafness in eastern Austria.In focus in Vienna: the cell nucleus.Hepatocyte specific expression of an oncogenic variant of β-catenin results in lethal metabolic dysfunction in mice.Lamina-associated Polypeptide 2-α Forms Homo-trimers via Its C Terminus, and Oligomerization Is Unaffected by a Disease-causing MutationA Novel Connexin 26 Mutation Associated with Autosomal Recessive Sensorineural DeafnessHistone deacetylase 1 expression is inversely correlated with age in the short-lived fish Nothobranchius furzeriHuman ribosomal RNA gene repeats are localized in the dense fibrillar component of nucleoli: light and electron microscopic in situ hybridization in human Sertoli cellsTranscribed and nontranscribed parts of the human ribosomal gene repeat show a similar pattern of distribution in nucleoliThe transcription unit of ribosomal genes is attached to the nuclear skeletonSignal amplification at the ultrastructural level using biotinylated tyramides and immunogold detectionRibosomal gene transcription is organized in foci within nucleolar componentsArrangement of individual human ribosomal DNA fragments on stretched DNA fibersRecruitment of bone-marrow-derived cells by skeletal and cardiac muscle in adult dystrophic mdx miceMale fertility and protein C inhibitor/plasminogen activator inhibitor-3 (PCI): localization of PCI in mouse testis and failure of single plasminogen activator knockout to restore spermatogenesis in PCI-deficient miceMapping of cellular compartments based on ultrastructural immunogold labelingLamina-associated polypeptide 2alpha forms complexes with heat shock proteins Hsp70 and Hsc70 in vivoNucleolus and chromatinSomatic cell reprogramming by transfection with liposomal agents
P50
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P50
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researcher
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wetenschapper
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հետազոտող
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C Schöfer
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C Schöfer
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C Schöfer
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C Schöfer
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C Schöfer
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C Schöfer
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C Schöfer
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C Schöfer
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C Schöfer
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C Schöfer
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C Schöfer
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C Schöfer
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C Schöfer
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C Schöfer
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C Schöfer
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P106
P1153
24327364700
P31
P496
0000-0001-9570-5692