Zobrazeno 1 - 9
of 9
pro vyhledávání: '"transgenní model"'
Autor:
Svobodová, Eva
Animal models of Alzheimer's disease display cognitive insufficiencies which mimic human symptoms and occur at a given age or post-treatment time. Animals are typically tested using canonical behavioral tests, lasting minutes and taking place mostly
Externí odkaz:
http://www.nusl.cz/ntk/nusl-445851
Autor:
Svobodová, Eva
Animal models of Alzheimer's disease display cognitive insufficiencies which mimic human symptoms and occur at a given age or post-treatment time. Animals are typically tested using canonical behavioral tests, lasting minutes and taking place mostly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2186::87253168abb2b9dd1f39cf11ac3c6009
http://www.nusl.cz/ntk/nusl-445851
http://www.nusl.cz/ntk/nusl-445851
Autor:
Gajdoš, Roman
Alzheimer's disease is a chronic, progressive, neurodegenerative disease. It belongs to the most common type of dementia and worldwide it is statistically the fifth cause of mortality. The most common morphological markers are insoluble β amyloid pl
Externí odkaz:
http://www.nusl.cz/ntk/nusl-410749
Autor:
Gajdoš, Roman
Alzheimer's disease is a chronic, progressive, neurodegenerative disease. It belongs to the most common type of dementia and worldwide it is statistically the fifth cause of mortality. The most common morphological markers are insoluble β amyloid pl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::b9bf634c14ec78b1ebf3030a4fe9d923
http://www.nusl.cz/ntk/nusl-463832
http://www.nusl.cz/ntk/nusl-463832
Analýza vybraných mitochondriálních proteinů ve svalové tkáni prasečího modelu Huntingtonovy choroby
Autor:
Dosoudilová, Žaneta
Huntington's disease (HD) is an autosomal dominant hereditary neurodegenerative disease characterized by motor, cognitive and behavioral disorders. HD is caused by expansion of CAG triplet (cytosine-adenosine-guanine) located in a gene on the short a
Externí odkaz:
http://www.nusl.cz/ntk/nusl-348332
Autor:
Dosoudilová, Žaneta
Huntington's disease (HD) is an autosomal dominant hereditary neurodegenerative disease characterized by motor, cognitive and behavioral disorders. HD is caused by expansion of CAG triplet (cytosine-adenosine-guanine) located in a gene on the short a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2186::75e1867d656454035fa7629b3da6a0b6
http://www.nusl.cz/ntk/nusl-348332
http://www.nusl.cz/ntk/nusl-348332
Autor:
Nepomucká, Kateřina
Diabetic nephropathy (DN) remains the most common cause of end stage renal failure. Nearly 10% of patients with diabetes develop nephropathy. Hyperglycaemia in the kidneys leads to the activation of alternative metabolic pathways of glucose (glycatio
Externí odkaz:
http://www.nusl.cz/ntk/nusl-340017
Autor:
Hampejsová, Zuzana
Loss of hearing affects more than 10 % of the population, and one newborn in a thousand is born with defects of the inner ear. Transcriptional factors involved in the development of inner ear are important in our understanding of the causes of inner
Externí odkaz:
http://www.nusl.cz/ntk/nusl-338188
Autor:
Nepomucká, Kateřina
Diabetic nephropathy (DN) remains the most common cause of end stage renal failure. Nearly 10% of patients with diabetes develop nephropathy. Hyperglycaemia in the kidneys leads to the activation of alternative metabolic pathways of glucose (glycatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::7b4e27176d7cd1356f9ac82fe588206e
http://www.nusl.cz/ntk/nusl-479544
http://www.nusl.cz/ntk/nusl-479544