[acetyl-CoA carboxylase] kinase activity

Known as: acetyl-CoA carboxylase kinase activity, AMPK, ACK2 
Catalysis of the reaction: ATP + [acetyl-CoA carboxylase] = ADP + [acetyl-CoA carboxylase] phosphate. [EC:2.7.11.27, MetaCyc:[ACETYL-COA-CARBOXYLASE… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1988-2017
024619882017

Papers overview

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Highly Cited
2007
Highly Cited
2007
Upon intravenous transplantation, hematopoietic stem cells (HSCs) can home to specialized niches, yet most HSCs fail to engraft… (More)
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Highly Cited
1999
Highly Cited
1999
BACKGROUND & AIMS Interstitial cells of Cajal (ICC) serve as pacemaker cells and mediators of neurotransmission from the enteric… (More)
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Highly Cited
1996
Highly Cited
1996
The injection of an antagonistic anti-murine c-kit monoclonal antibody ACK2 during mouse embryonic development produced three… (More)
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Highly Cited
1995
Highly Cited
1995
In vivo injection of a neutralizing, monoclonal antibody (ACK2) to the receptor tyrosine kinase (c-kit) disrupts the normal… (More)
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Highly Cited
1994
Highly Cited
1994
The proto-oncogene c-kit, encoding a receptor-type tyrosine kinase, is allelic with the W locus of the mouse. The stromal cell… (More)
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1993
1993
The protooncogene c-kit encodes a receptor type tyrosine kinase and is allelic with the W locus of mice. SLF, the c-Kit ligand… (More)
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Highly Cited
1991
Highly Cited
1991
Recent studies have shown that the dominant white spotting (W) locus encodes the proto-oncogene c-kit, a member of the tyrosine… (More)
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Highly Cited
1991
Highly Cited
1991
The expression and function of a receptor tyrosine kinase, c-kit, in the adult bone marrow of the mouse were investigated by… (More)
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Highly Cited
1991
Highly Cited
1991
Previous studies on mice bearing various mutations within the c-kit gene, dominant white spotting (W), indicate the functional… (More)
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Highly Cited
1988
Highly Cited
1988
We have examined the sites phosphorylated on acetyl-CoA carboxylase by three protein kinases which have been shown to inactivate… (More)
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