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Showing results (51-60 of 58) with videos related to

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Human Molecular Genetics|September 14, 2014
ILDR1 null mice, a model of human deafness DFNB42, show structural aberrations of tricellular tight junctions and degeneration of auditory hair cellsEva L Morozko, Ayako Nishio, Neil J Ingham, et al.
The Journal of Clinical Investigation|August 28, 2013
Tricellulin deficiency affects tight junction architecture and cochlear hair cellsGowri Nayak, Sue I Lee, Rizwan Yousaf, et al.
Nature Communications|April 8, 2017
Defective Gpsm2/Gα<sub>i3</sub> signalling disrupts stereocilia development and growth cone actin dynamics in Chudley-McCullough syndromeStephanie A Mauriac, Yeri E Hien, Jonathan E Bird, et al.
Human Molecular Genetics|August 13, 2003
Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degenerationTamar Ben-Yosef, Inna A Belyantseva, Thomas L Saunders, et al.
Nature Communications|May 26, 2018
Author Correction: Defective Gpsm2/Gα<sub>i3</sub> signalling disrupts stereocilia development and growth cone actin dynamics in Chudley-McCullough syndromeStephanie A Mauriac, Yeri E Hien, Jonathan E Bird, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|June 26, 2018
Gαi Proteins are Indispensable for HearingSandra Beer-Hammer, Sze Chim Lee, Stephanie A Mauriac, et al.
JCI Insight|February 8, 2022
The timing of auditory sensory deficits in Norrie disease has implications for therapeutic interventionDale Bryant, Valda Pauzuolyte, Neil J Ingham, et al.
Nature Genetics|September 20, 2005
Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebratesAlison J Ross, Helen May-Simera, Erica R Eichers, et al.
Pageof 6

Showing results (51-60 of 58) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 58 results.
Human Molecular Genetics|September 14, 2014
ILDR1 null mice, a model of human deafness DFNB42, show structural aberrations of tricellular tight junctions and degeneration of auditory hair cellsEva L Morozko, Ayako Nishio, Neil J Ingham, et al.
The Journal of Clinical Investigation|August 28, 2013
Tricellulin deficiency affects tight junction architecture and cochlear hair cellsGowri Nayak, Sue I Lee, Rizwan Yousaf, et al.
Nature Communications|April 8, 2017
Defective Gpsm2/Gα<sub>i3</sub> signalling disrupts stereocilia development and growth cone actin dynamics in Chudley-McCullough syndromeStephanie A Mauriac, Yeri E Hien, Jonathan E Bird, et al.
Human Molecular Genetics|August 13, 2003
Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degenerationTamar Ben-Yosef, Inna A Belyantseva, Thomas L Saunders, et al.
Nature Communications|May 26, 2018
Author Correction: Defective Gpsm2/Gα<sub>i3</sub> signalling disrupts stereocilia development and growth cone actin dynamics in Chudley-McCullough syndromeStephanie A Mauriac, Yeri E Hien, Jonathan E Bird, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|June 26, 2018
Gαi Proteins are Indispensable for HearingSandra Beer-Hammer, Sze Chim Lee, Stephanie A Mauriac, et al.
JCI Insight|February 8, 2022
The timing of auditory sensory deficits in Norrie disease has implications for therapeutic interventionDale Bryant, Valda Pauzuolyte, Neil J Ingham, et al.
Nature Genetics|September 20, 2005
Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebratesAlison J Ross, Helen May-Simera, Erica R Eichers, et al.
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