Search results
Results from the WOW.Com Content Network
To change this template's initial visibility, the |state= parameter may be used: {{Nucleus diseases | state = collapsed}} will show the template collapsed, i.e. hidden apart from its title bar. {{Nucleus diseases | state = expanded}} will show the template expanded, i.e. fully visible.
[[Category:Genetic disease and disorder templates by mechanism]] to the <includeonly> section at the bottom of that page. Otherwise, add <noinclude>[[Category:Genetic disease and disorder templates by mechanism]]</noinclude> to the end of the template code, making sure it starts on the same line as the code's last character.
Pages in category "Nucleus diseases" The following 6 pages are in this category, out of 6 total. This list may not reflect recent changes. C. Cornelia de Lange ...
These are transcribed in the nucleolus by RNA polymerase I. 45S is processed in the nucleus via 32S rRNA to 28S [6] and 5.8S, [7] and via 30S to 18S, [8] as shown in the diagram. 18S is a component of the ribosomal 40S subunit. 28S, 5.8S and 5S, [9] which is transcribed independently, are components
Nucleolus; Nucleus; Ribosome (dots as part of 5) Vesicle; ... An example of the template with all diagrams activated. Note: title bars are currently disabled in this ...
One hypothesized function of the dots is as a 'nuclear dump' or 'storage depot'. [21] The nuclear bodies may not all perform the same function. Sp140 associates with certain bodies and appears to be involved in transcriptional activation. [22] ND10 nuclear bodies have been shown to play a major role in chromatin regulation. [23]
DNA repair defects are seen in nearly all of the diseases described as accelerated aging disease, in which various tissues, organs or systems of the human body age prematurely. Because the accelerated aging diseases display different aspects of aging, but never every aspect, they are often called segmental progerias by biogerontologists .
In fact, DNA analysis of these two types of domains have shown that many sequences overlap, indicating that certain regions may switch between lamina-binding and nucleolus-binding. [35] NADs are associated with nucleolus function. The nucleolus is the largest sub-organelle within the nucleus and is the principal site for rRNA transcription.