User profiles for Daniel J. Jagger
Daniel JaggerUniversity College London Verified email at ucl.ac.uk Cited by 2873 |
Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates
…, H May-Simera, ER Eichers, M Kai, J Hill, DJ Jagger… - Nature …, 2005 - nature.com
The evolutionarily conserved planar cell polarity (PCP) pathway (or noncanonical Wnt
pathway) drives several important cellular processes, including epithelial cell polarization, cell …
pathway) drives several important cellular processes, including epithelial cell polarization, cell …
[HTML][HTML] Connexins and gap junctions in the inner ear – it's not just about K+ recycling
DJ Jagger, A Forge - Cell and tissue research, 2015 - Springer
Normal development, function and repair of the sensory epithelia in the inner ear are all
dependent on gap junctional intercellular communication. Mutations in the connexin genes …
dependent on gap junctional intercellular communication. Mutations in the connexin genes …
[HTML][HTML] The Alström syndrome protein, ALMS1, interacts with α-actinin and components of the endosome recycling pathway
Alström syndrome (ALMS) is a progressive multi-systemic disorder characterized by cone-rod
dystrophy, sensorineural hearing loss, childhood obesity, insulin resistance and cardiac, …
dystrophy, sensorineural hearing loss, childhood obesity, insulin resistance and cardiac, …
Compartmentalized and signal-selective gap junctional coupling in the hearing cochlea
DJ Jagger, A Forge - Journal of Neuroscience, 2006 - Soc Neuroscience
Gap junctional intercellular communication (GJIC) plays a major role in cochlear function.
Recent evidence suggests that connexin 26 (Cx26) and Cx30 are the major constituent …
Recent evidence suggests that connexin 26 (Cx26) and Cx30 are the major constituent …
Auditory hair cell precursors immortalized from the mammalian inner ear
…, P Lawlor, JF Ashmore, DJ Jagger… - … of the Royal …, 1998 - royalsocietypublishing.org
Mammalian auditory hair cells are few in number, experimentally inaccessible, and do not
proliferate postnatally or in vitro. Immortal cell lines with the potential to differentiate into …
proliferate postnatally or in vitro. Immortal cell lines with the potential to differentiate into …
[HTML][HTML] Defining the cellular environment in the organ of Corti following extensive hair cell loss: a basis for future sensory cell replacement in the Cochlea
RR Taylor, DJ Jagger, A Forge - PloS one, 2012 - journals.plos.org
Background Following the loss of hair cells from the mammalian cochlea, the sensory epithelium
repairs to close the lesions but no new hair cells arise and hearing impairment ensues. …
repairs to close the lesions but no new hair cells arise and hearing impairment ensues. …
Membrane properties of type II spiral ganglion neurones identified in a neonatal rat cochlear slice
DJ Jagger, GD Housley - The Journal of physiology, 2003 - Wiley Online Library
Neuro‐anatomical studies in the mammalian cochlea have previously identified a subpopulation
of approximately 5% of primary auditory neurones, designated type II spiral ganglion …
of approximately 5% of primary auditory neurones, designated type II spiral ganglion …
[HTML][HTML] Characterizing human vestibular sensory epithelia for experimental studies: new hair bundles on old tissue and implications for therapeutic interventions in …
RR Taylor, DJ Jagger, SR Saeed, P Axon… - Neurobiology of …, 2015 - Elsevier
Balance disequilibrium is a significant contributor to falls in the elderly. The most common
cause of balance dysfunction is loss of sensory cells from the vestibular sensory epithelia of …
cause of balance dysfunction is loss of sensory cells from the vestibular sensory epithelia of …
Inhibition of YAP/TAZ-driven TEAD activity prevents growth of NF2-null schwannoma and meningioma
Schwannoma tumours typically arise on the eighth cranial nerve and are mostly caused by
loss of the tumour suppressor Merlin (NF2). There are no approved chemotherapies for these …
loss of the tumour suppressor Merlin (NF2). There are no approved chemotherapies for these …
The Meckel-Gruber syndrome protein TMEM67 controls basal body positioning and epithelial branching morphogenesis in mice via the non-canonical Wnt pathway
…, C Toomes, CA Johnson, DJ Jagger - Disease models & …, 2015 - journals.biologists.com
Ciliopathies are a group of developmental disorders that manifest with multi-organ anomalies.
Mutations in TMEM67 (MKS3) cause a range of human ciliopathies, including Meckel-…
Mutations in TMEM67 (MKS3) cause a range of human ciliopathies, including Meckel-…