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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.

#Section 3: Genetics, Cellular and Molecular Biology #Peroxisome & Lysosome #Part B Pointers
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TLS Online TPP Program

#Id: 8963

#Section 3: Genetics, Cellular and Molecular Biology

If the duplicate is redundant and does not provide a fitness benefit, it will be lost by deletion or the accumulation of loss of-function mutations.
A second fate is that a duplicate can simply retain its original function.
TLS Online TPP Program

#Id: 8532

#Section 3: Genetics, Cellular and Molecular Biology

Catastrophe 
The change from growth to shrinkage
TLS Online TPP Program

#Id: 8206

#Section 3: Genetics, Cellular and Molecular Biology

Plant vacuole act as
a storage organelle for nutrients and waste products
a degradative compartment
an economical way of increasing cell size
a controller of turgor pressure
TLS Online TPP Program

#Id: 9296

#Section 2: General Biology
TLS Online TPP Program

#Id: 8323

#Section 3: Genetics, Cellular and Molecular Biology