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Cognitive impairment can be broadly classified into two major subclasses based on the brain regions involved.
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The PPR proteins can be separated into two major subfamilies based on the nature of their PPR motifs and into several smaller subclasses based on their C-terminal domain structure (Lurin et al. 2004; O'Toole et al. 2008).
They can be divided into subclasses based on the tissue specificity and the function in mammals such as OBPs and major urinary proteins (MUPs) (Flower et al. 2000).
The paper further categorizes the literature into 11 subclasses based on the application area.
Synset and WordSense have subclasses based on the distinction of lexical groups.
PPR proteins are classified into different subclasses based on their domain architecture, which is often a reflection of their function.
T-ALL cases can be segregated into subclasses based on the expression of certain, subclass-defining oncogenes [1].
Eph receptors are divided into two subclasses based on their ligand specificities.
All FRT-like sequences were subdivided into classes and subclasses based on their sequence features.
The PI3K protein family is divided into three classes and several subclasses based on primary structure, regulation, and in vitro lipid substrate specificity.
The six mammalian Arfs can be categorized into three subclasses based on sequence similarities.
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