Advances in Down Syndrome Research:
"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...
Gespeichert in:
Weitere Verfasser: | |
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Format: | Elektronisch E-Book |
Sprache: | English |
Veröffentlicht: |
Vienna
Springer Vienna
2003
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Schriftenreihe: | Journal of Neural Transmission. Supplementa
67 |
Schlagworte: | |
Online-Zugang: | UBR01 URL des Erstveröffentlichers |
Zusammenfassung: | "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 |
Beschreibung: | 1 Online-Ressource (X, 242 p. 29 illus) |
ISBN: | 9783709167212 |
DOI: | 10.1007/978-3-7091-6721-2 |
Internformat
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520 | |a "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 | ||
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Datensatz im Suchindex
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any_adam_object | |
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dewey-hundreds | 600 - Technology (Applied sciences) |
dewey-ones | 616 - Diseases |
dewey-raw | 616 |
dewey-search | 616 |
dewey-sort | 3616 |
dewey-tens | 610 - Medicine and health |
discipline | Medizin |
doi_str_mv | 10.1007/978-3-7091-6721-2 |
format | Electronic eBook |
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indexdate | 2024-07-10T08:36:30Z |
institution | BVB |
isbn | 9783709167212 |
language | English |
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physical | 1 Online-Ressource (X, 242 p. 29 illus) |
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publishDate | 2003 |
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publisher | Springer Vienna |
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series2 | Journal of Neural Transmission. Supplementa |
spelling | Advances in Down Syndrome Research edited by G. Lubec Vienna Springer Vienna 2003 1 Online-Ressource (X, 242 p. 29 illus) txt rdacontent c rdamedia cr rdacarrier Journal of Neural Transmission. Supplementa 67 "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 Internal Medicine Neurosciences Human Genetics Molecular Medicine Pathology Pediatrics Internal medicine Human genetics Medicine Down-Syndrom (DE-588)4012849-0 gnd rswk-swf (DE-588)4143413-4 Aufsatzsammlung gnd-content Down-Syndrom (DE-588)4012849-0 s DE-604 Lubec, G. edt Erscheint auch als Druck-Ausgabe 9783211407769 Erscheint auch als Druck-Ausgabe 9783211407813 Erscheint auch als Druck-Ausgabe 9783709167229 https://doi.org/10.1007/978-3-7091-6721-2 Verlag URL des Erstveröffentlichers Volltext |
spellingShingle | Advances in Down Syndrome Research Internal Medicine Neurosciences Human Genetics Molecular Medicine Pathology Pediatrics Internal medicine Human genetics Medicine Down-Syndrom (DE-588)4012849-0 gnd |
subject_GND | (DE-588)4012849-0 (DE-588)4143413-4 |
title | Advances in Down Syndrome Research |
title_auth | Advances in Down Syndrome Research |
title_exact_search | Advances in Down Syndrome Research |
title_full | Advances in Down Syndrome Research edited by G. Lubec |
title_fullStr | Advances in Down Syndrome Research edited by G. Lubec |
title_full_unstemmed | Advances in Down Syndrome Research edited by G. Lubec |
title_short | Advances in Down Syndrome Research |
title_sort | advances in down syndrome research |
topic | Internal Medicine Neurosciences Human Genetics Molecular Medicine Pathology Pediatrics Internal medicine Human genetics Medicine Down-Syndrom (DE-588)4012849-0 gnd |
topic_facet | Internal Medicine Neurosciences Human Genetics Molecular Medicine Pathology Pediatrics Internal medicine Human genetics Medicine Down-Syndrom Aufsatzsammlung |
url | https://doi.org/10.1007/978-3-7091-6721-2 |
work_keys_str_mv | AT lubecg advancesindownsyndromeresearch |