proline and Vestibular Diseases

proline has been researched along with Vestibular Diseases in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (50.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Bartles, JR; Changyaleket, B; Loomis, PA; Mugnaini, E; Sekerková, G; Whitlon, DS; Zheng, L	1
Bom, SJ; Brunner, HG; Brunt, TM; Cremers, CW; Cremers, FP; de Kok, YJ; Huygen, PL; Kemperman, MH; Morton, CC; Robertson, NG; van Beusekom, E; van der Velde-Visser, SD; Verhagen, WI	1

Other Studies

2 other study(ies) available for proline and Vestibular Diseases

Article	Year
Espins are multifunctional actin cytoskeletal regulatory proteins in the microvilli of chemosensory and mechanosensory cells. The Journal of neuroscience : the official journal of the Society for Neuroscience, 2004, Jun-09, Volume: 24, Issue:23 Topics: Actins; Animals; Animals, Newborn; Blotting, Western; Calcium; Chemoreceptor Cells; Cytoskeletal Proteins; Deafness; Female; Fluorescent Antibody Technique; Hair Cells, Auditory; Immunoenzyme Techniques; Immunohistochemistry; Male; Mechanoreceptors; Mice; Mice, Inbred Strains; Microfilament Proteins; Microvilli; Polymers; Proline; Protein Isoforms; Rats; Rats, Sprague-Dawley; Signal Transduction; Transfection; Type C Phospholipases; Vestibular Diseases	2004
A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects. Human molecular genetics, 1999, Volume: 8, Issue:2 Topics: Age of Onset; Amino Acid Substitution; Base Sequence; Chromosome Mapping; Chromosomes, Human, Pair 14; Deafness; DNA; DNA Mutational Analysis; Extracellular Matrix Proteins; Female; Genes, Dominant; Genetic Linkage; Hearing Loss, Sensorineural; Humans; Male; Microsatellite Repeats; Pedigree; Point Mutation; Proline; Proteins; Serine; Vestibular Diseases	1999

Article

Year

Espins are multifunctional actin cytoskeletal regulatory proteins in the microvilli of chemosensory and mechanosensory cells.

The Journal of neuroscience : the official journal of the Society for Neuroscience, 2004, Jun-09, Volume: 24, Issue:23

Topics: Actins; Animals; Animals, Newborn; Blotting, Western; Calcium; Chemoreceptor Cells; Cytoskeletal Proteins; Deafness; Female; Fluorescent Antibody Technique; Hair Cells, Auditory; Immunoenzyme Techniques; Immunohistochemistry; Male; Mechanoreceptors; Mice; Mice, Inbred Strains; Microfilament Proteins; Microvilli; Polymers; Proline; Protein Isoforms; Rats; Rats, Sprague-Dawley; Signal Transduction; Transfection; Type C Phospholipases; Vestibular Diseases

2004

A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects.

Human molecular genetics, 1999, Volume: 8, Issue:2

Topics: Age of Onset; Amino Acid Substitution; Base Sequence; Chromosome Mapping; Chromosomes, Human, Pair 14; Deafness; DNA; DNA Mutational Analysis; Extracellular Matrix Proteins; Female; Genes, Dominant; Genetic Linkage; Hearing Loss, Sensorineural; Humans; Male; Microsatellite Repeats; Pedigree; Point Mutation; Proline; Proteins; Serine; Vestibular Diseases

1999