排序方式: 共有15条查询结果,搜索用时 15 毫秒
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Histones and cancer test 总被引:1,自引:0,他引:1
E W Johns J A Pritchard J L Moore W H Sutherland C A Joslin J A Forrester A J Davies A M Neville R G Fish 《Nature》1973,245(5420):98-99
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Improved auditory spatial tuning in blind humans. 总被引:17,自引:0,他引:17
Despite reports of improved auditory discrimination capabilities in blind humans and visually deprived animals, there is no general agreement as to the nature or pervasiveness of such compensatory sensory enhancements. Neuroimaging studies have pointed out differences in cerebral organization between blind and sighted humans, but the relationship between these altered cortical activation patterns and auditory sensory acuity remains unclear. Here we compare behavioural and electrophysiological indices of spatial tuning within central and peripheral auditory space in congenitally blind and normally sighted but blindfolded adults to test the hypothesis (raised by earlier studies of the effects of auditory deprivation on visual processing) that the effects of visual deprivation might be more pronounced for processing peripheral sounds. We find that blind participants displayed localization abilities that were superior to those of sighted controls, but only when attending to sounds in peripheral auditory space. Electrophysiological recordings obtained at the same time revealed sharper tuning of early spatial attention mechanisms in the blind subjects. Differences in the scalp distribution of brain electrical activity between the two groups suggest a compensatory reorganization of brain areas in the blind that may contribute to the improved spatial resolution for peripheral sound sources. 相似文献
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Infantile-onset symptomatic epilepsy syndrome caused by a homozygous loss-of-function mutation of GM3 synthase 总被引:8,自引:0,他引:8
Simpson MA Cross H Proukakis C Priestman DA Neville DC Reinkensmeier G Wang H Wiznitzer M Gurtz K Verganelaki A Pryde A Patton MA Dwek RA Butters TD Platt FM Crosby AH 《Nature genetics》2004,36(11):1225-1229
We identified an autosomal recessive infantile-onset symptomatic epilepsy syndrome associated with developmental stagnation and blindness. Assuming a founder effect in a large Old Order Amish pedigree, we carried out a genome-wide screen for linkage and identified a single region of homozygosity on chromosome 2p12-p11.2 spanning 5.1 cM (maximum lod score of 6.84). We sequenced genes in the region and identified a nonsense mutation in SIAT9, which is predicted to result in the premature termination of the GM3 synthase enzyme (also called lactosylceramide alpha-2,3 sialyltransferase). GM3 synthase is a member of the sialyltransferase family and catalyzes the initial step in the biosynthesis of most complex gangliosides from lactosylceramide. Biochemical analysis of plasma glycosphingolipids confirmed that affected individuals lack GM3 synthase activity, as marked by a complete lack of GM3 ganglioside and its biosynthetic derivatives and an increase in lactosylceramide and its alternative derivatives. Although the relationship between defects in ganglioside catabolism and a range of lysosomal storage diseases is well documented, this is the first report, to our knowledge, of a disruption of ganglioside biosynthesis associated with human disease. 相似文献
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The gene ST7 has recently been implicated as the broad-range tumor suppressor on human chromosome 7q31.1. We did not detect somatic mutations in ST7 in any of 149 primary ovarian, breast or colon carcinomas. These data suggest that epigenetic downregulation or haploinsufficiency, rather than somatic genetic alterations, may be the primary mechanism of abrogation of ST7 function in these tumor types. 相似文献
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Casey G Neville PJ Plummer SJ Xiang Y Krumroy LM Klein EA Catalona WJ Nupponen N Carpten JD Trent JM Silverman RH Witte JS 《Nature genetics》2002,32(4):581-583
RNASEL (encoding ribonuclease L) has recently been proposed as a candidate for the hereditary prostate cancer (HPC1) gene. We determined that the RNASEL variant Arg462Gln has three times less enzymatic activity than the wildtype and is significantly associated with prostate cancer risk (P = 0.007). At least one copy of the mutated allele that causes this substitution is carried by nearly 60% of the men in our study. Men that are heterozygous with respect to the mutated allele have 50% greater risk of prostate cancer than non-carriers, and homozygotes have more than double the risk. 相似文献
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A F Arnsten D S Segal H J Neville S A Hillyard D S Janowsky L L Judd F E Bloom 《Nature》1983,304(5928):725-727
Previous research on the behavioural functions of endogenous opioid systems in rodents suggested a possible opioid role in the regulation of attention. This proposal was consistent with reports that opiate administration in man impairs the ability to concentrate while opiate antagonists augment behavioural and electrophysiological indices of arousal and attention. We examined the effects of the opiate antagonist naloxone on electrophysiological measures of attention in normal human subjects, using a paradigm which dissociates selective information processing from concurrent processes of general arousal or alertness that may be present. We now report electrophysiological evidence that naloxone improves the selectivity of auditory attention in the presence of competing sources of stimuli. These findings indicate a role for the endogenous opioid systems in the regulation of selective attention in man. 相似文献