Elisabeth Ehler

WNT-3, expressed by motoneurons, regulates terminal arborization of neurotrophin-3-responsive spinal sensory neurons.

Neutral endopeptidase is activated in cardiomyocytes in human aortic valve stenosis and heart failure.

Measles virus spreads in rat hippocampal neurons by cell-to-cell contact and in a polarized fashion.

Extracellular signal-regulated protein kinase activation during reoxygenation is required to restore ischaemia-induced endothelial barrier failure.

The LIM-only protein DRAL/FHL2 interacts with and is a corepressor for the promyelocytic leukemia zinc finger protein.

Left but not right cardiac hypertrophy in atrial natriuretic peptide receptor-deficient mice is prevented by angiotensin type 1 receptor antagonist losartan.

Subcellular targeting of metabolic enzymes to titin in heart muscle may be mediated by DRAL/FHL-2.

Dilated cardiomyopathy: a disease of the intercalated disc?

PINCH2 is a new five LIM domain protein, homologous to PINCHand localized to focal adhesions.

Identification, characterization, and expression of a novel alpha-tropomyosin isoform in cardiac tissues in developing chicken.

Intermediate filament-co-localized molecules with myosin heavy chain epitopes define distinct cellular domains in hair follicles and epidermis.

M-band: a safeguard for sarcomere stability?

The sensitive giant: the role of titin-based stretch sensing complexes in the heart.

Design of artificial myocardial microtissues.

Myofibrillogenesis in the developing chicken heart: role of actin isoforms and of the pointed end actin capping protein tropomodulin during thin filament assembly.

Sequential myofibrillar breakdown accompanies mitotic division of mammalian cardiomyocytes.

The molecular composition of the sarcomeric M-band correlates with muscle fiber type.

Dimerisation of myomesin: implications for the structure of the sarcomeric M-band.

The kinase domain of titin controls muscle gene expression and protein turnover.

VEGF profiling and angiogenesis in human microtissues.

Involvement of palladin and alpha-actinin in targeting of the Abl/Arg kinase adaptor ArgBP2 to the actin cytoskeleton.

From A to Z and back? Multicompartment proteins in the sarcomere.

Establishment of cardiac cytoarchitecture in the developing mouse heart.

The sarcomeric M-band during development and in disease.

Unusual splicing events result in distinct Xin isoforms that associate differentially with filamin c and Mena/VASP.

Estrogen receptor alpha up-regulation and redistribution in human heart failure.

Probing the role of septins in cardiomyocytes.

Tissue-transplant fusion and vascularization of myocardial microtissues and macrotissues implanted into chicken embryos and rats.

Increased field resistance to Tilletia caries provided by a specific antifungal virus gene in genetically engineered wheat.

Re-expression of proteins involved in cytokinesis during cardiac hypertrophy.

Paxillin and ponsin interact in nascent costameres of muscle cells.

Palladin interacts with SH3 domains of SPIN90 and Src and is required for Src-induced cytoskeletal remodeling.

Myomesin 3, a novel structural component of the M-band in striated muscle.

Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy.

Targeted disruption of the mouse Csrp2 gene encoding the cysteine- and glycine-rich LIM domain protein CRP2 result in subtle alteration of cardiac ultrastructure.

Prox1 maintains muscle structure and growth in the developing heart.

Back to square one: what do we know about the functions of muscle LIM protein in the heart?

Muscle Research and Gene Ontology: New standards for improved data integration.

The sarcomere and sarcomerogenesis.

Overexpression of the transcription factor Hand1 causes predisposition towards arrhythmia in mice.

"MLP: A Stress Sensor Goes Nuclear" by Sylvia Gunkel, Jörg Heineke, Denise Hilfiker-Kleiner, Ralph Knöll, J Mol Cell Cardiol. 2009;47(4):423-5.

Identification of an emerin-beta-catenin complex in the heart important for intercalated disc architecture and beta-catenin localisation.

Proteomics analysis of the cardiac myofilament subproteome reveals dynamic alterations in phosphatase subunit distribution.

Ponsin interacts with Nck adapter proteins: implications for a role in cytoskeletal remodelling during differentiation of skeletal muscle cells.

CHAP is a newly identified Z-disc protein essential for heart and skeletal muscle function.

Stabilised beta-catenin in postnatal ventricular myocardium leads to dilated cardiomyopathy and premature death.

Thymosin beta4 facilitates epicardial neovascularization of the injured adult heart.

Normal passive viscoelasticity but abnormal myofibrillar force generation in human hypertrophic cardiomyopathy.

Interactions with M-band titin and calpain 3 link myospryn (CMYA5) to tibial and limb-girdle muscular dystrophies.

Novel missense mutations in exon 15 of desmoglein-2: role of the intracellular cadherin segment in arrhythmogenic right ventricular cardiomyopathy?

Mechanistic insights into arrhythmogenic right ventricular cardiomyopathy caused by desmocollin-2 mutations.

EH-myomesin splice isoform is a novel marker for dilated cardiomyopathy.

Cell biology. Gett'N-WASP stripes.

Novel role for p90 ribosomal S6 kinase in the regulation of cardiac myofilament phosphorylation.

Formin follows function: a muscle-specific isoform of FHOD3 is regulated by CK2 phosphorylation and promotes myofibril maintenance.

A novel desmocollin-2 mutation reveals insights into the molecular link between desmosomes and gap junctions.

Knockdown of embryonic myosin heavy chain reveals an essential role in the morphology and function of the developing heart.

Formin-g muscle cytoarchitecture.

Molecular changes in the heart of a severe case of arrhythmogenic right ventricular cardiomyopathy caused by a desmoglein-2 null allele.

RBM24: a 'regional business manager' in charge of the maintenance of sarcomeric protein expression 24 h a day?

Two distinct phosphorylation events govern the function of muscle FHOD3.

Myosin VI in skeletal muscle: its localization in the sarcoplasmic reticulum, neuromuscular junction and muscle nuclei.

Cardiomyocyte growth and sarcomerogenesis at the intercalated disc.