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TLS Online TPP Program

#Id: 8197


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

#Unit 2. Cellular Organization #Peroxisome & Lysosome #Part B Pointers
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TLS Online TPP Program

#Id: 653

#Unit 3. Fundamental Processes

A more potent mutagen translates into a greater number of revertant colonies.

TLS Online TPP Program

#Id: 9861

#Unit 6. System Physiology – Plant

LOV2 domain is essential for blue light–induced kinase activation and autophosphorylation of the phototropin photoreceptor.

TLS Online TPP Program

#Id: 3870

#Unit 5. Developmental Biology

Secreted GABA then acts on prestalk cells to induce the cell-surface exposure of the serine protease domain of the ABC transporter TagC.

TLS Online TPP Program

#Id: 9276

#Unit 6. System Physiology – Plant

NodA is an N-acyltransferase that catalyzes the addition of a fatty acyl chain.
NodB is a chitin-oligosaccharide deacetylase that removes the acetyl group from the terminal nonreducing sugar.
NodC is a chitin-oligosaccharide synthase that links N-acetyl-D-glucosamine monomers.

TLS Online TPP Program

#Id: 1052

#Unit 5. Developmental Biology

Hox9 and Hox10 paralogues specify the stylopod

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