Alvaro Rendon

Cellular localization of the vesicular inhibitory amino acid transporter in the mouse and human retina.

Dystrophin isoform Dp7l is present in lamellipodia and focal complexes in human astrocytoma cells U-373 MG.

Targeted inactivation of dystrophin gene product Dp71: phenotypic impact in mouse retina.

Voltage-gated channels and calcium homeostasis in mammalian rod photoreceptors.

Absence of Dp71 in mdx3cv mouse spermatozoa alters flagellar morphology and the distribution of ion channels and nNOS.

Molecular cloning and protein expression of Duchenne muscular dystrophy gene products in porcine retina.

The sarcoglycan-sarcospan complex localization in mouse retina is independent from dystrophins.

Rural telemedicine infrastructure and services in the Department of Cauca, Colombia.

Improving epidemiologic surveillance and health promoter training in rural Latin America through information and communication technologies.

A novel isoform of delta-sarcoglycan is localized at the sarcoplasmic reticulum of mouse skeletal muscle.

Platelet adhesion: structural and functional diversity of short dystrophin and utrophins in the formation of dystrophin-associated-protein complexes related to actin dynamics.

Distribution of vesicular glutamate transporters in rat and human retina.

Role of dystrophins and utrophins in platelet adhesion process.

The glutamate transporter EAAT5 works as a presynaptic receptor in mouse rod bipolar cells.

The toxicity of the PrP106-126 prion peptide on cultured photoreceptors correlates with the prion protein distribution in the mammalian and human retina.

Utrophins compensate for Dp71 absence in mdx3cv in adhered platelets.

Kir4.1 and AQP4 associate with Dp71- and utrophin-DAPs complexes in specific and defined microdomains of Müller retinal glial cell membrane.

A deficit of brain dystrophin 71 impairs hypothalamic osmostat.

Functional implication of Dp71 in osmoregulation and vascular permeability of the retina.

Mammalian retinal horizontal cells are unconventional GABAergic neurons.

Expression of dystrophins and the dystrophin-associated-protein complex by pituicytes in culture.

Characterization of Dp71Δ(78-79), a novel dystrophin mutant that stimulates PC12 cell differentiation.

Reevaluation of dystrophin localization in the mouse retina.

Dystrophin Dp71: the smallest but multifunctional product of the Duchenne muscular dystrophy gene.

Dp71 gene disruption alters the composition of the dystrophin-associated protein complex and neuronal nitric oxide synthase expression in the hypothalamic supraoptic and paraventricular nuclei.

AAV-mediated gene delivery in Dp71-null mouse model with compromised barriers.

Slight alteration of the electroretinogram in mice lacking dystrophin dp71.

A vital signs telemonitoring system - interoperability supported by a personal health record systema and a cloud service.

Lack of dystrophin protein Dp71 results in progressive cataract formation due to loss of fiber cell organization.