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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… Expand
National Institutes of Health

Papers overview

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2015
2015
PAFAH is specific for short acyl groups esterified at the sn-2 position of glycerol in phospholipids, and apart from PAF, it… Expand
Highly Cited
2009
Highly Cited
2009
Lissencephaly is a devastating neurological disorder caused by defective neuronal migration. LIS1 (official symbol PAFAH1B1, for… Expand
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2009
2009
Background:  Platelet activating factor (PAF), a pro‐inflammatory phospholipid, stimulates cytokine secretion from… Expand
2006
2006
Both neural development and prefrontal cortex function are known to be abnormal in schizophrenia and bipolar disorder. In order… Expand
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2006
2006
Spinal cord injury (SCI) causes male infertility, with low sperm motility the major long-term cause. It has been suggested in… Expand
2003
2003
Mutations in the human LIS1 gene cause the devastating brain disorder lissencephaly. LIS1 also regulates microtubule dynamics; it… Expand
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1999
1999
Lissencephaly patients are born with severe brain malformations and suffer from recurrent seizures. LIS1, the gene mutated in… Expand
1999
1999
Platelet‐activating factor is a phospholipid with several documented roles in the pre‐implantation embryo. Enzymes that belong to… Expand
Highly Cited
1997
Highly Cited
1997
Forming the structure of the human brain involves extensive neuronal migration, a process dependent on cytoskeletal rearrangement… Expand
1980
1980
Abstract The kinetics of malondialdehyde (MDA) re-appearance in human platelet density subpopulations after a single intake of… Expand