Search Results - "Werner, Hendrikje"
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Disrupting the LINC complex by AAV mediated gene transduction prevents progression of Lamin induced cardiomyopathy
Published in Nature communications (05-08-2021)“…Mutations in the LaminA gene are a common cause of monogenic dilated cardiomyopathy. Here we show that mice with a cardiomyocyte-specific Lmna deletion develop…”
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Systematic in vivo candidate evaluation uncovers therapeutic targets for LMNA dilated cardiomyopathy and risk of Lamin A toxicity
Published in Journal of translational medicine (16-10-2023)“…Background Dilated cardiomyopathy (DCM) is a severe, non-ischemic heart disease which ultimately results in heart failure (HF). Decades of research on DCM have…”
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Regrowing the adult brain: NF-κB controls functional circuit formation and tissue homeostasis in the dentate gyrus
Published in PloS one (01-02-2012)“…Cognitive decline during aging is correlated with a continuous loss of cells within the brain and especially within the hippocampus, which could be regenerated…”
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The DtxR protein acting as dual transcriptional regulator directs a global regulatory network involved in iron metabolism of Corynebacterium glutamicum
Published in BMC genomics (09-02-2006)“…The knowledge about complete bacterial genome sequences opens the way to reconstruct the qualitative topology and global connectivity of transcriptional…”
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Rheb and mTOR Regulate Neuronal Polarity through Rap1B
Published in The Journal of biological chemistry (28-11-2008)“…The development of polarized hippocampal neurons with a single axon and multiple dendrites depends on the activity of phosphoinositide 3-kinase (PI3K) and the…”
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Nesprin-1 LINC complexes recruit microtubule cytoskeleton proteins and drive pathology in Lmna-mutant striated muscle
Published in Human molecular genetics (06-01-2023)“…Mutations in LMNA, the gene encoding A-type lamins, cause laminopathies-diseases of striated muscle and other tissues. The aetiology of laminopathies has been…”
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Abstract 13927: AAV Gene Therapy to Treat Underlying Cardiac Biomechanical Defects in Lmna Dilated Cardiomyopathy Improves Lifespan and Preserves Ejection Fraction in Lmna DCM Mouse Model
Published in Circulation (New York, N.Y.) (08-11-2022)“…Mutations in the LMNA gene are the second most common cause of genetic dilated cardiomyopathies (DCMs) with a prevalence of ~1/12500. Adeno-associated virus…”
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Abstract 12498: AAV-Mediated LINC Complex Uncoupling Ameliorates Pathology in a Mouse Model of LMNA Dilated Cardiomyopathy
Published in Circulation (New York, N.Y.) (07-11-2023)“…Abstract only Mutations in the LMNA gene, encoding lamin A/C, are one of the most frequent genetic causes of dilated cardiomyopathy. While gene therapy using…”
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Protein-Protein Interaction Mapping by 2C-BioID
Published in Current protocols in cell biology (01-09-2019)“…Protein-protein interactions (PPIs) add an essential layer of complexity to the information encoded by the genome. Modulation of such interactions is a key…”
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Dynamic composition of the nuclear envelope during mouse pre-implantation development
Published in Mechanisms of development (01-07-2017)Get full text
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Rheb and mTOR Regulate Neuronal Polarity through Rap1BS
Published in The Journal of biological chemistry (28-11-2008)“…The development of polarized hippocampal neurons with a single axon and multiple dendrites depends on the activity of phosphoinositide 3-kinase (PI3K) and the…”
Get full text
Journal Article -
12
Regrowing the Adult Brain: NF-[kappa]B Controls Functional Circuit Formation and Tissue Homeostasis in the Dentate Gyrus
Published in PloS one (01-02-2012)“…Cognitive decline during aging is correlated with a continuous loss of cells within the brain and especially within the hippocampus, which could be regenerated…”
Get full text
Journal Article