Speech identification and cortical potentials in individuals with auditory neuropathy

<p>Abstract</p> <p>Background</p> <p>Present study investigated the relationship between speech identification scores in quiet and parameters of cortical potentials (latency of P1, N1, and P2; and amplitude of N1/P2) in individuals with auditory neuropathy.</p> <p>Methods</p> <p>Ten individuals with auditory neuropathy (five males and five females) and ten individuals with normal hearing in the age range of 12 to 39 yr participated in the study. Speech identification ability was assessed for bi-syllabic words and cortical potentials were recorded for click stimuli.</p> <p>Results</p> <p>Results revealed that in individuals with auditory neuropathy, speech identification scores were significantly poorer than that of individuals with normal hearing. Individuals with auditory neuropathy were further classified into two groups, Good Performers and Poor Performers based on their speech identification scores. It was observed that the mean amplitude of N1/P2 of Poor Performers was significantly lower than that of Good Performers and those with normal hearing. There was no significant effect of group on the latency of the peaks. Speech identification scores showed a good correlation with the amplitude of cortical potentials (N1/P2 complex) but did not show a significant correlation with the latency of cortical potentials.</p> <p>Conclusion</p> <p>Results of the present study suggests that measuring the cortical potentials may offer a means for predicting perceptual skills in individuals with auditory neuropathy.</p

Synonymous Codon Usage Analysis of Thirty Two Mycobacteriophage Genomes

Synonymous codon usage of protein coding genes of thirty two completely sequenced mycobacteriophage genomes was studied using multivariate statistical analysis. One of the major factors influencing codon usage is identified to be compositional bias. Codons ending with either C or G are preferred in highly expressed genes among which C ending codons are highly preferred over G ending codons. A strong negative correlation between effective number of codons (Nc) and GC3s content was also observed, showing that the codon usage was effected by gene nucleotide composition. Translational selection is also identified to play a role in shaping the codon usage operative at the level of translational accuracy. High level of heterogeneity is seen among and between the genomes. Length of genes is also identified to influence the codon usage in 11 out of 32 phage genomes. Mycobacteriophage Cooper is identified to be the highly biased genome with better translation efficiency comparing well with the host specific tRNA genes

Mycobacteriophage Genome Database

Mycobacteriophage genome database (MGDB) is an exclusive repository of the 64 completely sequenced mycobacteriophages with annotated information. It is a comprehensive compilation of the various gene parameters captured from several databases pooled together to empower mycobacteriophage researchers. The MGDB (Version No.1.0) comprises of 6086 genes from 64 mycobacteriophages classified into 72 families based on ACLAME database. Manual curation was aided by information available from public databases which was enriched further by analysis. Its web interface allows browsing as well as querying the classification. The main objective is to collect and organize the complexity inherent to mycobacteriophage protein classification in a rational way. The other objective is to browse the existing and new genomes and describe their functional annotation

Cerebrospinal fluid adenosine deaminase and lysozyme levels in the diagnosis of tuberculous meningitis

Adenosine Deaminase Activity (ADA) and Lysozyme Activity (LYSA) were measured in the CSF of tuberculous meningitis (TBM) cases : 26 bacteriologically positive TBM (Group 1), 61 bacteriologically negative TBM (Group 2), 10 non-tuberculous meningitis (Group 3) and 17 control subjects (Group 4). The mean ADA levels in different groups in that order were found to be 11.6, 4.5, 4.4 and 0.8 U/l respectively. The mean LYSA levels in the same groups were 6.3, 2.1, 2.2 and 0.5 mcg/ml respectively. In bacteriologically positive TBM, the mean ADA and LYSA levels were significantly higher than the other three groups (p < 0.0001). An ADA level of 4U/l and LYSA tests were 96%, 82% and 85%, 95% respectively. When both the criteria were considered, the sensitivity and specificity were 91% and 93% respectively. Combination of both test definitions could give additional support to the diagnosis in 49% of 61 clinically suspected but bacteriologically negative TBM cases. Correlation of ADA and LYSA levels in CSF was found to be statistically significant (r = 0.59; p < 0.01)

Artificial Heart Neural Networks An Idea

Artificial Neural Networks Field (ANN Field) is an exciting field of research. ANN field took its inspiration from Human Brain. The heart and Brain are very important for the survival of Humans. Research Scientists published many articles by giving importance to Brain. But scientists have not yet explored much on the Heart which is another important part in addition to the Brain. The primary purpose of publishing this article is to show a path to ANN field Research Scientists by introducing the concept of Heart into Artificial Neural Networks. In this paper, we coined and defined Artificial Heart Neuron, which is the basic part of Artificial Heart Neural Networks Field (AHNN Field) in addition to Artificial Neuron. This work takes its inspiration from both Heart and Brain

Susceptibility of south Indian strains of Mycobacterium tuberculosis to tuberactinomycin

A total of 114 strains of Mycobacterium tuberculosis isolated from sputum samples of 114 patients of pulmonary tuberculosis in south India, were coded and tested for their in vitro susceptibility to tuberactinomycin (Tum) incorporated in Lowenstein-Jensen (LJ) medium. Of these strains, 95 (83.3%) and 15 (13.2%) were susceptible to Tum at 25 and 50 mg/l respectively. Only 4 (3.5%) strains were inhibited at 100 mg/l or more. Of the 37 drug sensitive strains, 2 (5.4%) were not susceptible to Tum at 25 mg/l compared to 17 (22.1%) of 77 strains-resistant to one or more of antituberculosis drugs (P <0.02). The drug susceptibility pattern of the strains revealed that there was no significant association of resistance between Tum and streptomycin or rifampicin or ethambutol or ethionamide or isoniazid. However, 15 (53.6%) of 28 kanamycin (K) resistant strains were not susceptible to Tum at 25 mg/l. This cross resistance between Tum and K was further studied in 24 and 15 K sensitive and resistant strains respectively, by correlating their proportion resistance at 16 mg/l and it was found to have a significant positive correlation (r = 0.55; X0.01)