Lista de obras - Daniel J Jagger - Dominio Público Uruguay

A deafness-associated mutant human connexin 26 improves the epithelial barrier in vitro

artículo científico publicado en 2007

A novel hearing-loss-related mutation occurring in the GJB2 basal promoter.

artículo científico publicado en 2007

A potassium current in guinea-pig outer hair cells activated by ion channel blocker DCDPC.

artículo científico publicado en 1998

A technique for slicing the rat cochlea around the onset of hearing

artículo científico publicado en 2000

A-type potassium currents dominate repolarisation of neonatal rat primary auditory neurones in situ ⬇️

artículo científico publicado el 1 de enero de 2002

ATP-gated currents in rat primary auditory neurones in situ arise from a heteromultimetric P2X receptor subunit assembly

artículo científico publicado en 2002

Allosteric modulation of native cochlear P2X receptors: insights from comparison with recombinant P2X2 receptors

artículo científico publicado en 2003

Alström Syndrome protein ALMS1 localizes to basal bodies of cochlear hair cells and regulates cilium-dependent planar cell polarity

artículo científico publicado en 2010

Assessing PCP in the cochlea of mammalian ciliopathy models

artículo científico publicado en 2012

Auditory hair cell precursors immortalized from the mammalian inner ear.

artículo científico publicado en 1998

Calcium signalling mediated by the 9 acetylcholine receptor in a cochlear cell line from the immortomouse

artículo científico publicado en 2000

Characterizing human vestibular sensory epithelia for experimental studies: new hair bundles on old tissue and implications for therapeutic interventions in ageing

artículo científico publicado en 2015

Compartmentalized and signal-selective gap junctional coupling in the hearing cochlea.

artículo científico publicado en 2006

Connexin30-mediated intercellular communication plays an essential role in epithelial repair in the cochlea

artículo científico publicado en 2013

Connexins and gap junctions in the inner ear--it's not just about K⁺ recycling

artículo científico publicado en 2014

Contractility in type III cochlear fibrocytes is dependent on non-muscle myosin II and intercellular gap junctional coupling

artículo científico publicado en 2012

Cx30 exhibits unique characteristics including a long half-life when assembled into gap junctions

artículo científico publicado en 2015

Defining the cellular environment in the organ of Corti following extensive hair cell loss: a basis for future sensory cell replacement in the Cochlea

artículo científico publicado en 2012

Development of gap junctional intercellular communication within the lateral wall of the rat cochlea

artículo científico publicado en 2011

Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates

scientific journal article

Disruption of SorCS2 reveals differences in the regulation of stereociliary bundle formation between hair cell types in the inner ear.

artículo científico publicado en 2017

Divergent membrane properties of mouse cochlear glial cells around hearing onset

artículo científico publicado en 2020

Functional P2X<sub>7</sub> Receptors in the Auditory Nerve of Hearing Rodents Localize Exclusively to Peripheral Glia

artículo científico publicado en 2021

Gap junctional coupling is essential for epithelial repair in the avian cochlea

artículo científico publicado en 2014

Identification of Persistent and Resurgent Sodium Currents in Spiral Ganglion Neurons Cultured from the Mouse Cochlea

artículo científico publicado en 2017

Ionic currents expressed in a cell line derived from the organ of Corti of the Immortomouse.

artículo científico publicado en 1999

Membrane properties of type II spiral ganglion neurones identified in a neonatal rat cochlear slice ⬇️

artículo científico publicado el 15 de octubre de 2003

Neuromodulation in the spiral ganglion: shaping signals from the organ of corti to the CNS.

artículo científico publicado en 2006

Olfactory ensheathing cells from the nasal mucosa and olfactory bulb have distinct membrane properties

scientific article published on 04 December 2019

P2X receptor signaling inhibits BDNF-mediated spiral ganglion neuron development in the neonatal rat cochlea

artículo científico publicado en 2007

Patterns of expression of Bardet-Biedl syndrome proteins in the mammalian cochlea suggest noncentrosomal functions

artículo científico publicado en 2009

Phosphoinositide Modulation of Heteromeric Kv1 Channels Adjusts Output of Spiral Ganglion Neurons from Hearing Mice

artículo científico publicado en 2015

Positional analysis of guinea pig inner hair cell membrane conductances: implications for regulation of the membrane filter.

artículo científico publicado en 2001

Potential role of purinergic signalling in cochlear pathology

artículo científico publicado en 2002

Purinergic regulation of sound transduction and auditory neurotransmission.

artículo científico publicado en 2002

Quantitative analysis of the expression of the glutamate-aspartate transporter and identification of functional glutamate uptake reveal a role for cochlear fibrocytes in glutamate homeostasis.

artículo científico publicado en 2009

Reducing Current Spread by Use of a Novel Pulse Shape for Electrical Stimulation of the Auditory Nerve.

artículo científico publicado en 2015

Regulation of ionic currents by protein kinase A and intracellular calcium in outer hair cells isolated from the guinea-pig cochlea

artículo científico publicado en 1999

Spinster homolog 2 (spns2) deficiency causes early onset progressive hearing loss

artículo científico publicado en 2014

TRPC-like conductance mediates restoration of intracellular Ca2+ in cochlear outer hair cells in the guinea pig and rat

The Alström syndrome protein, ALMS1, interacts with α-actinin and components of the endosome recycling pathway

artículo científico publicado en 2012

The Meckel-Gruber Syndrome protein TMEM67 (meckelin) regulates basal body planar polarization and non-canonical Wnt signalling via Wnt5a and ROR2.

artículo científico publicado en 2015

The Meckel-Gruber syndrome protein TMEM67 controls basal body positioning and epithelial branching morphogenesis in mice via the non-canonical Wnt pathway ⬇️

artículo científico publicado en 2015

The Membrane Properties of Cochlear Root Cells are Consistent with Roles in Potassium Recirculation and Spatial Buffering

artículo científico publicado en 2010

The enigmatic root cell - emerging roles contributing to fluid homeostasis within the cochlear outer sulcus

artículo científico publicado en 2012

The fast activating potassium current, I(K,f), in guinea-pig inner hair cells is regulated by protein kinase A.

artículo científico publicado en 1999

The inner ear contains heteromeric channels composed of cx26 and cx30 and deafness-related mutations in cx26 have a dominant negative effect on cx30.

artículo científico publicado en 2003

The timing of auditory sensory deficits in Norrie disease has implications for therapeutic intervention

artículo científico publicado en 2022

Lista de obras de Daniel J Jagger

A deafness-associated mutant human connexin 26 improves the epithelial barrier in vitro

A novel hearing-loss-related mutation occurring in the GJB2 basal promoter.

A potassium current in guinea-pig outer hair cells activated by ion channel blocker DCDPC.

A technique for slicing the rat cochlea around the onset of hearing

A-type potassium currents dominate repolarisation of neonatal rat primary auditory neurones in situ ⬇️

ATP-gated currents in rat primary auditory neurones in situ arise from a heteromultimetric P2X receptor subunit assembly

Allosteric modulation of native cochlear P2X receptors: insights from comparison with recombinant P2X2 receptors

Alström Syndrome protein ALMS1 localizes to basal bodies of cochlear hair cells and regulates cilium-dependent planar cell polarity

Assessing PCP in the cochlea of mammalian ciliopathy models

Auditory hair cell precursors immortalized from the mammalian inner ear.

Calcium signalling mediated by the 9 acetylcholine receptor in a cochlear cell line from the immortomouse

Characterizing human vestibular sensory epithelia for experimental studies: new hair bundles on old tissue and implications for therapeutic interventions in ageing

Compartmentalized and signal-selective gap junctional coupling in the hearing cochlea.

Connexin30-mediated intercellular communication plays an essential role in epithelial repair in the cochlea

Connexins and gap junctions in the inner ear--it's not just about K⁺ recycling

Contractility in type III cochlear fibrocytes is dependent on non-muscle myosin II and intercellular gap junctional coupling

Cx30 exhibits unique characteristics including a long half-life when assembled into gap junctions

Defining the cellular environment in the organ of Corti following extensive hair cell loss: a basis for future sensory cell replacement in the Cochlea

Development of gap junctional intercellular communication within the lateral wall of the rat cochlea

Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates

Disruption of SorCS2 reveals differences in the regulation of stereociliary bundle formation between hair cell types in the inner ear.

Divergent membrane properties of mouse cochlear glial cells around hearing onset

Functional P2X<sub>7</sub> Receptors in the Auditory Nerve of Hearing Rodents Localize Exclusively to Peripheral Glia

Gap junctional coupling is essential for epithelial repair in the avian cochlea

Identification of Persistent and Resurgent Sodium Currents in Spiral Ganglion Neurons Cultured from the Mouse Cochlea

Ionic currents expressed in a cell line derived from the organ of Corti of the Immortomouse.

Membrane properties of type II spiral ganglion neurones identified in a neonatal rat cochlear slice ⬇️

Neuromodulation in the spiral ganglion: shaping signals from the organ of corti to the CNS.

Olfactory ensheathing cells from the nasal mucosa and olfactory bulb have distinct membrane properties

P2X receptor signaling inhibits BDNF-mediated spiral ganglion neuron development in the neonatal rat cochlea

Patterns of expression of Bardet-Biedl syndrome proteins in the mammalian cochlea suggest noncentrosomal functions

Phosphoinositide Modulation of Heteromeric Kv1 Channels Adjusts Output of Spiral Ganglion Neurons from Hearing Mice

Positional analysis of guinea pig inner hair cell membrane conductances: implications for regulation of the membrane filter.

Potential role of purinergic signalling in cochlear pathology

Purinergic regulation of sound transduction and auditory neurotransmission.

Quantitative analysis of the expression of the glutamate-aspartate transporter and identification of functional glutamate uptake reveal a role for cochlear fibrocytes in glutamate homeostasis.

Reducing Current Spread by Use of a Novel Pulse Shape for Electrical Stimulation of the Auditory Nerve.

Regulation of ionic currents by protein kinase A and intracellular calcium in outer hair cells isolated from the guinea-pig cochlea

Spinster homolog 2 (spns2) deficiency causes early onset progressive hearing loss

TRPC-like conductance mediates restoration of intracellular Ca2+ in cochlear outer hair cells in the guinea pig and rat

The Alström syndrome protein, ALMS1, interacts with α-actinin and components of the endosome recycling pathway

The Meckel-Gruber Syndrome protein TMEM67 (meckelin) regulates basal body planar polarization and non-canonical Wnt signalling via Wnt5a and ROR2.

The Meckel-Gruber syndrome protein TMEM67 controls basal body positioning and epithelial branching morphogenesis in mice via the non-canonical Wnt pathway ⬇️

The Membrane Properties of Cochlear Root Cells are Consistent with Roles in Potassium Recirculation and Spatial Buffering

The enigmatic root cell - emerging roles contributing to fluid homeostasis within the cochlear outer sulcus

The fast activating potassium current, I(K,f), in guinea-pig inner hair cells is regulated by protein kinase A.

The inner ear contains heteromeric channels composed of cx26 and cx30 and deafness-related mutations in cx26 have a dominant negative effect on cx30.

The timing of auditory sensory deficits in Norrie disease has implications for therapeutic intervention