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Isabel Llano

Showing results (21-30 of 50) with videos related to

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The Journal of General Physiology|April 4, 2020
Differentially poised vesicles underlie fast and slow components of release at single synapsesKris Blanchard, Javier Zorrilla de San Martín, Alain Marty, et al.
Pediatric Dermatology|October 15, 2011
A novel mutation in the IRF6 gene associated with facial asymmetry in a family affected with Van der Woude syndromeLorena Miñones-Suárez, Alberto Mas-Vidal, Joaquin Fernandez-Toral, et al.
Genes|December 9, 2020
Novel Variant in <i>PLAG1</i> in a Familial Case with Silver-Russell Syndrome SuspicionYerai Vado, Arrate Pereda, Isabel Llano-Rivas, et al.
American Journal of Medical Genetics. Part A|April 13, 2011
In-frame deletion in FLNA causing familial periventricular heterotopia with skeletal dysplasia in malesElena Parrini, Isabel Llano Rivas, Joaquin Fernandez Toral, et al.
Frontiers in Cellular Neuroscience|August 4, 2015
An excitatory GABA loop operating in vivoGuadalupe Astorga, Jin Bao, Alain Marty, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 7, 2005
Developmental changes in parvalbumin regulate presynaptic Ca2+ signalingThibault Collin, Mireille Chat, Marie Gabrielle Lucas, et al.
Journal of Neurochemistry|June 4, 2020
Physiological involvement of presynaptic L-type voltage-dependent calcium channels in GABA release of cerebellar molecular layer interneuronsStéphanie Rey, Gilliane Maton, Shin'Ichiro Satake, et al.
Birth Defects Research|September 22, 2020
Prenatal and foetal autopsy findings in glutaric aciduria type IIAdriano Martinez-Aracil, Rebeca Ruiz-Onandi, Alvaro Perez-Rodriguez, et al.
Elife|May 14, 2020
Synergism of type 1 metabotropic and ionotropic glutamate receptors in cerebellar molecular layer interneurons in vivoJin Bao, Michael Graupner, Guadalupe Astorga, et al.
American Journal of Medical Genetics. Part A|April 23, 2015
Delineation of the clinically recognizable 17q22 contiguous gene deletion syndrome in a patient carrying the smallest microdeletion known to dateMaría Luisa Martínez-Fernández, Joaquin Fernández-Toral, Isabel Llano-Rivas, et al.
Pageof 5

Showing results (21-30 of 50) with videos related to

Sort By:
Pageof 5
The Journal of General Physiology|April 4, 2020
Differentially poised vesicles underlie fast and slow components of release at single synapsesKris Blanchard, Javier Zorrilla de San Martín, Alain Marty, et al.
Pediatric Dermatology|October 15, 2011
A novel mutation in the IRF6 gene associated with facial asymmetry in a family affected with Van der Woude syndromeLorena Miñones-Suárez, Alberto Mas-Vidal, Joaquin Fernandez-Toral, et al.
Genes|December 9, 2020
Novel Variant in <i>PLAG1</i> in a Familial Case with Silver-Russell Syndrome SuspicionYerai Vado, Arrate Pereda, Isabel Llano-Rivas, et al.
American Journal of Medical Genetics. Part A|April 13, 2011
In-frame deletion in FLNA causing familial periventricular heterotopia with skeletal dysplasia in malesElena Parrini, Isabel Llano Rivas, Joaquin Fernandez Toral, et al.
Frontiers in Cellular Neuroscience|August 4, 2015
An excitatory GABA loop operating in vivoGuadalupe Astorga, Jin Bao, Alain Marty, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 7, 2005
Developmental changes in parvalbumin regulate presynaptic Ca2+ signalingThibault Collin, Mireille Chat, Marie Gabrielle Lucas, et al.
Journal of Neurochemistry|June 4, 2020
Physiological involvement of presynaptic L-type voltage-dependent calcium channels in GABA release of cerebellar molecular layer interneuronsStéphanie Rey, Gilliane Maton, Shin'Ichiro Satake, et al.
Birth Defects Research|September 22, 2020
Prenatal and foetal autopsy findings in glutaric aciduria type IIAdriano Martinez-Aracil, Rebeca Ruiz-Onandi, Alvaro Perez-Rodriguez, et al.
Elife|May 14, 2020
Synergism of type 1 metabotropic and ionotropic glutamate receptors in cerebellar molecular layer interneurons in vivoJin Bao, Michael Graupner, Guadalupe Astorga, et al.
American Journal of Medical Genetics. Part A|April 23, 2015
Delineation of the clinically recognizable 17q22 contiguous gene deletion syndrome in a patient carrying the smallest microdeletion known to dateMaría Luisa Martínez-Fernández, Joaquin Fernández-Toral, Isabel Llano-Rivas, et al.
Pageof 5