glycerophosphoinositol 4,5-bisphosphate and Deafness

glycerophosphoinositol 4,5-bisphosphate has been researched along with Deafness in 3 studies

Research

Studies (3)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (33.33)	29.6817
2010's	1 (33.33)	24.3611
2020's	1 (33.33)	2.80

Authors

Authors	Studies
An, J; Cho, HS; Choi, BY; Choi, HB; Choi, IS; Gee, HY; Han, JH; Kang, TM; Kim, A; Kim, BJ; Kim, E; Kim, MY; Kim, N; Kim, NKD; Koh, YI; Lee, C; Lee, SM; Lee, SY; Oh, DY; Park, M; Park, WY; Yi, N	1
Anselmi, F; Arslan, E; Bortolozzi, M; Calì, B; Ciubotaru, CD; Crispino, G; De Camilli, P; Majumder, P; Mammano, F; Pozzan, T; Ramirez, FG; Rodriguez, L; Scimemi, P; Simeonato, E	1
Bartles, JR; Loomis, PA; Mugnaini, E; Sekerková, G; Zheng, L	1

Reviews

1 review(s) available for glycerophosphoinositol 4,5-bisphosphate and Deafness

Article	Year
Espins and the actin cytoskeleton of hair cell stereocilia and sensory cell microvilli. Cellular and molecular life sciences : CMLS, 2006, Volume: 63, Issue:19-20 Topics: Actin Cytoskeleton; Animals; Calcium; Cilia; Deafness; Hair Cells, Auditory; Humans; Mice; Microfilament Proteins; Microvilli; Neurons, Afferent; Phosphatidylinositol 4,5-Diphosphate; Proline; Protein Isoforms	2006

Other Studies

2 other study(ies) available for glycerophosphoinositol 4,5-bisphosphate and Deafness

Article	Year
Novel KCNQ4 variants in different functional domains confer genotype- and mechanism-based therapeutics in patients with nonsyndromic hearing loss. Experimental & molecular medicine, 2021, Volume: 53, Issue:7 Topics: Deafness; Female; Genotype; HEK293 Cells; Humans; KCNQ Potassium Channels; Male; Mutation, Missense; Patch-Clamp Techniques; Pedigree; Phenotype; Phosphatidylinositol 4,5-Diphosphate; Potassium; Protein Domains	2021
Reduced phosphatidylinositol 4,5-bisphosphate synthesis impairs inner ear Ca2+ signaling and high-frequency hearing acquisition. Proceedings of the National Academy of Sciences of the United States of America, 2012, Aug-28, Volume: 109, Issue:35 Topics: Age Factors; Animals; Animals, Newborn; Calcium Signaling; Connexins; Deafness; Evoked Potentials, Auditory, Brain Stem; Gap Junctions; Hair Cells, Auditory; Hearing; Mechanotransduction, Cellular; Mice; Mice, Inbred C57BL; Mice, Knockout; NF-kappa B; Organ of Corti; Phenotype; Phosphatidylinositol 4,5-Diphosphate; Phosphotransferases (Alcohol Group Acceptor); Pitch Perception	2012

Article

Year

Novel KCNQ4 variants in different functional domains confer genotype- and mechanism-based therapeutics in patients with nonsyndromic hearing loss.

Experimental & molecular medicine, 2021, Volume: 53, Issue:7

Topics: Deafness; Female; Genotype; HEK293 Cells; Humans; KCNQ Potassium Channels; Male; Mutation, Missense; Patch-Clamp Techniques; Pedigree; Phenotype; Phosphatidylinositol 4,5-Diphosphate; Potassium; Protein Domains

2021

Reduced phosphatidylinositol 4,5-bisphosphate synthesis impairs inner ear Ca2+ signaling and high-frequency hearing acquisition.

Proceedings of the National Academy of Sciences of the United States of America, 2012, Aug-28, Volume: 109, Issue:35

Topics: Age Factors; Animals; Animals, Newborn; Calcium Signaling; Connexins; Deafness; Evoked Potentials, Auditory, Brain Stem; Gap Junctions; Hair Cells, Auditory; Hearing; Mechanotransduction, Cellular; Mice; Mice, Inbred C57BL; Mice, Knockout; NF-kappa B; Organ of Corti; Phenotype; Phosphatidylinositol 4,5-Diphosphate; Phosphotransferases (Alcohol Group Acceptor); Pitch Perception

2012