Journal of General Microbiology · 2014 · 142 citations · 28 references
Life SciencesGeneticsMolecular GeneticsHuman GeneticsMedical GeneticsNeurogeneticsCochlear DisordersGenetic DisordersGenetic SyndromesHearing ImpairmentHearing LossInherited Disease TestingAncillary Molecular TestingGenetic TestingHearing Loss EtiologyMolecular Genetic DiagnosisMolecular Genetic TestingNon-syndromic Hearing LossSyndromic Hearing LossUsher Syndrome
Three strains of Streptococcus salivarius including a recent clinical isolate were found to possess Ca2(+)-dependent fructosyltransferase (FTF) activity. The extracellular FTF activity of cells grown on sucrose increased as much as 9-fold compared with cells grown on either glucose, fructose or galactose. This increase in activity was due not to induction of FTF by sucrose, but to the release of the cell-bound form of the enzyme. Studies with washed cells of S. salivarius ATCC 25975 showed that the extent of release of the cell-bound FTF activity was dependent upon the sucrose concentration up to 4 mM, at which concentration maximum release (95%) of cell-bound FTF occurred. Several lines of evidence suggested that either substrate binding or de novo synthesis of fructan is required for the release of the cell-bound FTF activity.
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Connexin-26 mutations in sporadic and inherited sensorineural deafness
Xavier Estivill, Paolo Fortina, Saul Surrey et al. · The Lancet · 1998 · 643 citations · Full text
GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study
Rikkert L. Snoeckx, P.L.M. Huygen, Delphine Feldmann et al. · The American Journal of Human Genetics · 2005 · 559 citations · Full text
Medicine, Genetics, Otolaryngology +12
Hereditary Hearing Loss and its Syndromes
Journal of Medical Genetics · 1995 · 512 citations · Full text
Medicine, Genetics, Otolaryngology +12