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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
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2015
2015
LIS1 is a microtubule (Mt) plus-end binding protein that interacts with the dynein/dynactin complex. In humans, LIS1 is required… Expand
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2009
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
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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
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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
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Highly Cited
1997
Highly Cited
1997
Forming the structure of the human brain involves extensive neuronal migration, a process dependent on cytoskeletal rearrangement… Expand
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1980
1980
Abstract The kinetics of malondialdehyde (MDA) re-appearance in human platelet density subpopulations after a single intake of… Expand
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