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#Unit 5. Developmental Biology #Major histocompatibility complex #Part B Pointers
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#Unit 11. Evolution and Behavior

Dryopithecus -Australopithecus afarensis- Homo habilis - Homo erectus - Homo heidelbergensis-Neanderthal and Homo sapiens

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#Id: 8197

#Unit 2. Cellular Organization

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

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#Id: 7963

#Unit 2. Cellular Organization

A hereditary form of emphysema illustrates the detrimental effects that can result from misfolding of proteins in the ER.

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#Unit 3. Fundamental Processes

The lagging strand is synthesized discontinuously and the leading strand is synthesized continuously. This is called semidiscontinuous replication.

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#Unit 4. Cell Communication and Cell Signaling

PTEN can remove phosphate groups attached to serine,
threonine, and tyrosine residues in proteins, its ability to
remove the 3-phosphate from PI(3,4,5)P3 is its major function in cells.

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