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Phospho-N-acetylmuramoyl-pentapeptide-transferase

Known as: phospho-N-acetylmuramoyl pentapeptide transferase, phospho-N-acetylmuramyl-pentapeptide translocase, phospho N-acetylmuramoyl-pentapeptide transferase 
National Institutes of Health

Papers overview

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Highly Cited
2012
Highly Cited
2012
(G2019S) mutation of leucine-rich repeat kinase 2 (LRRK2) is the most common genetic cause of both familial and sporadic… Expand
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Highly Cited
2011
Highly Cited
2011
A multiplexed electrochemical immunoassay integrating enzyme amplification and electric field-driven strategy was developed for… Expand
Highly Cited
2011
Highly Cited
2011
Activation of Group I metabotropic glutamate receptors (mGluRs) in rat hippocampus induces a form of long-term depression (LTD… Expand
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Highly Cited
2007
Highly Cited
2007
PURPOSE Endoplasmic reticulum (ER) stress has been implicated in a wide variety of neurodegenerative disorders of the central… Expand
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Highly Cited
2006
Highly Cited
2006
Receptor-operated Ca2+ entry (ROCE) and store-operated Ca2+ entry (SOCE) are known to be inhibited by tyrosine kinase inhibitors… Expand
Highly Cited
2003
Highly Cited
2003
Kainic acid induces excitotoxicity and nerve cell degeneration in vulnerable regions of rat brain, most markedly in hippocampus… Expand
Highly Cited
2000
Highly Cited
2000
SecA insertion and deinsertion through SecYEG drive preprotein translocation at the Escherichia coli inner membrane. We present… Expand
Highly Cited
2000
Highly Cited
2000
Abstract: The activity of tyrosine hydroxylase, the rate‐limiting enzyme in the biosynthesis of dopamine, is stimulated by… Expand
Highly Cited
1990
Highly Cited
1990
Synthetic peptides based on the threonine phosphorylation site and proposed inhibitory site of DARPP-32 (dopamine- and cAMP… Expand
Highly Cited
1982
Highly Cited
1982
The μ and δ opiate receptors, postulated on the basis of pharmacological observations, have been well characterized in ligand… Expand