Advances in Down Syndrome Research / Journal of Neural Transmission. Supplementa Bd.67 (PDF)
(Sprache: Englisch)
"Advances in Down Syndrome Research" represents updated research in several areas of Down Syndrome (DS).
A new promising animal model of DS is reported and this opens new opportunities to study pathomechanisms and pharmacological approaches as it is more...
A new promising animal model of DS is reported and this opens new opportunities to study pathomechanisms and pharmacological approaches as it is more...
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"Advances in Down Syndrome Research" represents updated research in several areas of Down Syndrome (DS).
A new promising animal model of DS is reported and this opens new opportunities to study pathomechanisms and pharmacological approaches as it is more than difficult to carry out studies in humans and the clinical features are highly variable. In terms of biology, cell cycle and stem cell studies and in terms of biochemistry, relevance of studies on a specific protein kinase, channels, transporters, superoxide dismutase, antioxidant system, chromosome assembly factor and other important biological structures are provided. And again, the gene dosage hypothesis is addressed and although the vast majority of chromosome 21 gene products is unchanged in fetal DS brain, a few specific chromosome 21 encoded structures including transcription factors are indeed overexpressed although findings in fetal DS are different from those in adult DS brain when Alzheimer-like neuropathology supervenes.
A new promising animal model of DS is reported and this opens new opportunities to study pathomechanisms and pharmacological approaches as it is more than difficult to carry out studies in humans and the clinical features are highly variable. In terms of biology, cell cycle and stem cell studies and in terms of biochemistry, relevance of studies on a specific protein kinase, channels, transporters, superoxide dismutase, antioxidant system, chromosome assembly factor and other important biological structures are provided. And again, the gene dosage hypothesis is addressed and although the vast majority of chromosome 21 gene products is unchanged in fetal DS brain, a few specific chromosome 21 encoded structures including transcription factors are indeed overexpressed although findings in fetal DS are different from those in adult DS brain when Alzheimer-like neuropathology supervenes.
Bibliographische Angaben
- 2013, 2003, 242 Seiten, Englisch
- Herausgegeben: Gert Lubec
- Verlag: Springer Vienna
- ISBN-10: 3709167213
- ISBN-13: 9783709167212
- Erscheinungsdatum: 13.03.2013
Abhängig von Bildschirmgröße und eingestellter Schriftgröße kann die Seitenzahl auf Ihrem Lesegerät variieren.
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- Größe: 31 MB
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Sprache:
Englisch
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