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Mice, Inbred C57BL
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Saturday, November 21, 2009

Genetic complexity of absence seizures in substrains of C3H mice.

15 Dec 2009 Absence epilepsy is a common form of idiopathic generalized epilepsy whose etiology is poorly understood because of genetic and phenotypic heterogeneity. The inbred mouse strain C3H/He exhibits spontaneous absence seizures characterized by spike and ... Read more...


Osteoblast differentiation is functionally associated with decreased AMP kinase activity.

29 Nov 2009 Osteoblasts, originating from mesenchymal stem cells, play a pivotal role in bone formation and mineralization. Several transcription factors including runt-related transcription factor 2 (Runx2) have been reported to be essential for osteoblast ... Read more...


Rab22B is expressed in the CNS astroglia lineage and plays a role in epidermal growth factor receptor trafficking in A431 cells.

29 Nov 2009 The expression profile and functions of the brain-enriched Rab22B/Rab31 small GTPase had remained uncharacterized. Using specific antibodies against Rab22B, we found the protein to be exceptionally enriched in nestin and RC2-positive radial glia of ... Read more...

 

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Technical information about 'Mice, Inbred C57BL'

Descriptor UI: D008810

Alternative terms: Mice, Inbred C57BL; C57BL Mice, Inbred; Inbred C57BL Mice; Mouse, Inbred C57BL; C57BL Mouse, Inbred; Inbred C57BL Mouse; Mice, C57BL; C57BL Mice; Mouse, C57BL; C57BL Mouse;

Related Mesh Headings: Carcinoma, Lewis Lung;

Allowable Qualifiers: abnormalities; anatomy & histology; blood; cerebrospinal fluid; classification; embryology; genetics; growth & development; immunology; injuries; metabolism; microbiology; parasitology; physiology; psychology; surgery; urine; virology;

Tree Number: B01.050.157.520.420; B01.050.199.520.520.420; B01.150.900.649.865.635.505.500.400.420;

History Note: 74(72)

Technical Notes: NIM when exper animal: no qualif; when IM, qualif permitted; do not forget also to check tag MICE

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