PAFAH1B1/Related Articles: Difference between revisions
< PAFAH1B1
Jump to navigation
Jump to search
imported>Daniel Mietchen m (Robot: Creating Related Articles subpage) |
imported>Daniel Mietchen m (manual clean-up) |
||
| Line 2: | Line 2: | ||
==Parent topics== | ==Parent topics== | ||
{{r|Gene}} | |||
{{r|Brain}} | |||
{{r|Brain development}} | |||
==Subtopics== | ==Subtopics== | ||
| Line 8: | Line 10: | ||
==Other related topics== | ==Other related topics== | ||
{{r|Lissencephaly}} | {{r|Lissencephaly}} | ||
{{r|Neuronal migration}} | |||
{{r|Gyrification}} | |||
Revision as of 14:40, 3 August 2009
- See also changes related to PAFAH1B1, or pages that link to PAFAH1B1 or to this page or whose text contains "PAFAH1B1".
Parent topics
- Gene [r]: The functional unit of heredity. [e]
- Brain [r]: The core unit of a central nervous system. [e]
- Brain development [r]: The build-up of the brain from ectodermal cells to a complex structure of neurons, glia and blood vessels. [e]
Subtopics
- Lissencephaly [r]: Condition in which the cortical surface is smooth, as opposed to gyrified. Normal in many mammals and transient in human fetal development but a disorder in humans born with it. [e]
- Neuronal migration [r]: The process by which nerve cells travel from the place of their last cell division to their final position in the brain. [e]
- Gyrification [r]: The folding process during brain development, or the extent of folding. [e]