Zellweger syndrome

Autosomal recessive Mutations in any of a dozen different peroxins, the most common being Pex1, cause an impairment in peroxisomal protein import.

TLS Online TPP Program

#Id: 10377

#XL - Q Biochemistry

TLS Online TPP Program

#Id: 9187

#XL - T Zoology

Positive Selection: The Spread of Beneficial Mutations

TLS Online TPP Program

#Id: 9266

#XL - R Botany

N2 constitutes about 80% of the earth’s atmosphere, but the stability of its triple bond renders it inert and metabolically inaccessible to most organisms.

TLS Online TPP Program

#Id: 8601

#XL - R Botany

TLS Online TPP Program

#Id: 10020

#XL - T Zoology

The C-terminal segment of Smo binds Cos2, and Smo is stabilized from degradation