ASPM protein, human

Known as: Abnormal Spindle-Like Microcephaly-Associated Protein, Abnormal Spindle Protein Homolog, Asp Homolog 
Abnormal spindle-like microcephaly-associated protein (3477 aa, ~410 kDa) is encoded by the human ASPM gene. This protein plays a role in the… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

2011-2017
01220112017

Papers overview

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Review
2018
Review
2018
  • 2018
Microcephaly is a genetically heterogeneous disorder and is one of the frequently notable conditions in paediatric neuropathology… (More)
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2018
2018
A new study suggests an evolutionary mechanism — involving abnormal spindle-like microcephaly-associated protein — that, in part… (More)
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Review
2017
Review
2017
  • 2017
Microcephaly is a genetically heterogeneous disorder and is one of the frequently notable conditions in paediatric neuropathology… (More)
  • figure 1
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2017
2017
Microcephaly is a genetically heterogeneous disorder and is one of the frequently notable conditions in paediatric neuropathology… (More)
  • figure 1
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2013
2013
BACKGROUND Quantification of viral RNA levels and CD4 cell count determinations are the most widely used laboratory assays… (More)
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2011
2011
Background:The clinico-pathological and molecular heterogeneity of epithelial ovarian cancer (EOC) complicates its early… (More)
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