Language mechanisms and reading disorder: a modular approach.
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Nodular lymphoid hyperplasia (NLH) has been firmly associated with syndromes of hypogammaglobulinemia but not with selective absence of IgA. We report the case of a 5-yr-old girl with the triad of selective IgA deficiency, NLH of the small bowel, and giardiasis. Results of an extensive immunologic investigation, including immunohistochemical examinations of small bowel biopsies, support the hypothesis that the basic defect responsible for IgA deficiency in this patient was the failure of precursor IgM-bearing lymphocytes to differentiate into IgA-producing plasma cells. Furthermore, the abundance of IgM-bearing cells in biopsy specimens demonstrates the existence of a compensatory mechanism in the intestine to substitute IgM for the absent IgA.
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Silencer elements, by analogy to enhancer elements, function independently of their position and orientation. We show that the chicken lysozyme silencer S-2.4 kb has many other characteristics in common with enhancer elements. The silencer is comprised of modules that independently repress gene activity--repression being increased synergistically when different or identical modules are combined. Repression is effective both on a complete and on a minimal promoter consisting of a TATA box only. One silencer module is bound in vitro by a 75-93 kd protein, termed NeP1; the other can be bound either by the product of the oncogene v-erbA or by the thyroid hormone receptor. This erbA binding site is unusual in that the palindromic sequence is inverted.
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We describe an instrumentation package built for the measurement of stabilizing forces in thoraco-lumbar-sacral-hip-knee-ankle orthoses. The system uses inexpensive and robust transducers mounted on the orthoses. Instrumentation is contained in a back-pack; the associated software package may be used for a wide variety of transducer applications.
The new expression vector system CYTEXP is designed to facilitate the optimization of both transcription and translation in Escherichia coli, while at the same time allowing the exchange of its major components using unique restriction sites. In vitro mutagenesis can be performed in situ using single-stranded DNA generated from the bacteriophage f1 ORI sequence. The basic vector pCYTEXP1 bears a synthetic copy of the intercistronic sequence that enhances the translation of the E. coli atpE gene. Reading frames can be inserted directly downstream of this sequence. The bacteriophage lambda promoters, the atpE sequence, the bacteriophage fd transcriptional terminator, the f1 ORI, and the amp antibiotic resistance gene are all borne on exchangeable "modules." Thus, both the efficiency and the conditions of expression of cloned genes can be readily optimized.
The new release of MOL3D, a molecular modeling program written in FORTRAN, contains not only enhanced graphic capabilities, but also an improved module for intermolecular calculations that allows rigid and flexible docking. Various interfaces have been added to some well-known and widely diffused programs, such as MM2, AMBER and MOPAC, and to the Cambridge Crystallographic Database. Finally a graph manager and a samples database have been added, which allow efficient searches with various requirements concerning structural templates, pharmacophoric three-dimensional (3D) constraints, and the field of biological activity, if any.
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Multiunit mapping techniques were used to investigate whether or not units with ON- and OFF-center receptive fields occur in an orderly arrangement in the cat lateral geniculate nucleus. In the A layers, ON- and OFF-center sites were partially segregated in the dimension parallel to the laminae, with ON-center sites predominant at the dorsal surface of each layer and OFF-center sites relatively more numerous at the ventral surface of the layer. Microelectrode tracks were placed to traverse the visual field map in the nucleus parallel to projection lines, parallel to isoelevation lines and parallel to isoazimuth lines. The tracks placed parallel to projection lines contained long sequences of units of the same center sign, providing evidence that ON and OFF zones are organized in vertical modules which span much or all of the thickness of a layer. The tracks placed parallel to isoelevation and isoazimuth lines contained alternating clusters of ON- and OFF-center sites. These clusters were larger in the dimension representing isoelevation than in the dimension representing isoazimuth. Taken together, these results indicate that the cat lateral geniculate nucleus contains ON and OFF modules oriented perpendicular to the layers.
The mature forms of the extracellular muramidase-2 of Enterococcus hirae and Streptococcus faecalis autolysin have very similar primary structures. Each consists of an active-site-containing N-terminal domain fused to a multiple-repeat C-terminal domain. Polypeptide segments occurring at equivalent places in these two bacterial wall lytic enzymes have homologues in two phage lysozymes and in three functionally unrelated proteins, illustrating the principle that protein molecules frequently are constructed from modules that are linked in a single polypeptide chain.
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