Results 171 to 180 of about 75,155 (200)
Some of the next articles are maybe not open access.
Nature New Biology, 1972
INVESTIGATION of a tumour system requires a ready supply of tissue and ability to manipulate the growing environment. In vivo methods of maintenance are preferred, because the tissue is morphologically similar to the original, the therapeutic: toxicity ratio of possible treatments can be assessed and agents affecting tumour growth indirectly by ...
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INVESTIGATION of a tumour system requires a ready supply of tissue and ability to manipulate the growing environment. In vivo methods of maintenance are preferred, because the tissue is morphologically similar to the original, the therapeutic: toxicity ratio of possible treatments can be assessed and agents affecting tumour growth indirectly by ...
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MeCP2 Dysfunction in Humans and Mice
Journal of Child Neurology, 2005Rett syndrome is a leading cause of postnatal neurodevelopmental regression. Rett syndrome is caused by mutations in MECP2, the gene encoding methyl-CpG binding protein 2. In up to 96% of all classic cases, Rett syndrome cases are caused by mutations or deletions in MECP2.
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In Vivo Imaging in Humanized Mice
2008The radiological modalities that are currently utilized as critical components in clinical medicine have also been adapted to small-animal imaging, among which are ultrasound imaging, X-ray computerized tomography (CT), magnetic resonance imaging (MRI), positron emission tomography (PET), and single-photon emission computed tomography (SPECT).
H, Masuda +5 more
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Modifier genes in mice and humans
Nature Reviews Genetics, 2001An emerging theme of studies with spontaneous, engineered and induced mutant mice is that phenotypes often depend on genetic background, implying that genetic modifiers have a role in guiding the functional consequences of genetic variation. Understanding the molecular and cellular basis by which modifier genes exert their influence will provide ...
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Modeling Human Epilepsies in Mice
Epilepsia, 2001Summary: Two categories of mouse models of human epilepsy are now contributing to the experimental analysis of inherited seizure disorders. The first type includes homologous genetic models arrived at in the classic way; the genes from human inherited epilepsy syndromes are cloned, and mice are recreated with functionally identical mutations.
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Of Mice and Men: The Human Sciences and the Humanities
The Hastings Center Report, 1980openaire +2 more sources
Proceedings of the National Academy of Sciences of the United States of America, 2023
Prasanta K Dash +2 more
exaly
Prasanta K Dash +2 more
exaly
New generation humanized mice for virus research: Comparative aspects and future prospects
Virology, 2013Ramesh Akkina
exaly
Humanized Mice for the Study of Immuno-Oncology
Trends in Immunology, 2018Philippe De La Rochere +2 more
exaly

