Librería: Phatpocket Limited, Waltham Abbey, HERTS, Reino Unido
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Añadir al carritoCondición: Like New. Used - Like New. This is a brand new book! Your purchase helps support Sri Lankan Children's Charity 'The Rainbow Centre'. Our donations to The Rainbow Centre have helped provide an education and a safe haven to hundreds of children who live in appalling conditions.
Librería: Ria Christie Collections, Uxbridge, Reino Unido
EUR 225,98
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Añadir al carritoCondición: New. In.
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Añadir al carritoGebunden. Condición: New.
Librería: Mispah books, Redhill, SURRE, Reino Unido
EUR 292,88
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Añadir al carritoHardcover. Condición: Like New. Like New. book.
Librería: Revaluation Books, Exeter, Reino Unido
EUR 315,48
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Añadir al carritoHardcover. Condición: Brand New. 1st edition. 372 pages. 10.75x8.25x1.00 inches. In Stock.
Idioma: Inglés
Publicado por Springer, Wien, Springer Vienna, Springer, 2001
ISBN 10: 3211837329 ISBN 13: 9783211837320
Librería: AHA-BUCH GmbH, Einbeck, Alemania
EUR 282,80
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Añadir al carritoBuch. Condición: Neu. Neuware - When we worked on Down Syndrome brain in the past we have been focus ing on adult brain. This was a major step forwards as most work on Down Syndrome was carried out on fibroblasts or other tissues and, moreover, we introduced proteomics to identify and quantify brain protein expression. We considered evaluation of brain protein expression in Down Syndrome brain by and by more important than gene hunting at the nucleic acid level realiz ing the long unpredictable way from RNA to protein. The availability of fetal samples along with the proteomic appproach stimulated and reinforced studies on Down Syndrome brain. And indeed, it was found out that some observations on aberrant protein expression in adult Down Syndrome brain could not be verified in the fetal samples indi cating that neurodegeneration in adult Down Syndrome brain may have been responsible rather than trisomy 21. Using brains from the early second trimester of gestation led to the generation of a series of clues for the under standing of aberrant wiring of the brain in Down Syndrome and enabled the determination of altered key functions in early life; e. g. undetectably low drebrin was observed in Down Syndrome cortex, an integral constituent and marker for dendritic spines, main effectors of cross-talk between neurons. In addition, evaluation of the nature of the neuronal deficits in terms of neuro transmission markers could be established as well as neuronal density in fetal Down Syndrome cortex.