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PAFAH1B1 wt Allele

Known as: LIS2, Platelet-Activating Factor Acetylhydrolase, Isoform Ib, Alpha Subunit 45kDa wt Allele, Platelet-Activating Factor Acetylhydrolase, Isoform Ib, Alpha Subunit (45kD) Gene 
Human PAFAH1B1 wild-type allele is located in the vicinity of 17p13.3 and is approximately 92 kb in length. This allele, which encodes platelet… 
National Institutes of Health

Papers overview

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Highly Cited
2009
Highly Cited
2009
Lissencephaly is a devastating neurological disorder caused by defective neuronal migration. LIS1 (official symbol PAFAH1B1, for… 
2009
2009
Background:  Platelet activating factor (PAF), a pro‐inflammatory phospholipid, stimulates cytokine secretion from… 
2006
2006
Spinal cord injury (SCI) causes male infertility, with low sperm motility the major long-term cause. It has been suggested in… 
2003
2003
Mutations in the human LIS1 gene cause the devastating brain disorder lissencephaly. LIS1 also regulates microtubule dynamics; it… 
Review
2000
Review
2000
1999
1999
Lissencephaly patients are born with severe brain malformations and suffer from recurrent seizures. LIS1, the gene mutated in… 
Review
1999
Review
1999
Classical lissencephaly is a severe human neuronal migration disorder characterized by a smooth cerebral surface and a paucity of… 
Highly Cited
1997
Highly Cited
1997
Forming the structure of the human brain involves extensive neuronal migration, a process dependent on cytoskeletal rearrangement…