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AMPD2 gene

Known as: ADENOSINE MONOPHOSPHATE DEAMINASE 2, AMPD isoform L, SPG63 
 
National Institutes of Health

Papers overview

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2019
2019
Soft‐tissue sarcomas are rare, heterogeneous, and often aggressive mesenchymal cancers. Many of them are associated with poor… Expand
Review
2019
Review
2019
Pontocerebellar hypoplasia type 9 (PCH9) is a rare autosomal recessive neurodegenerative disorder with prenatal onset caused by… Expand
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2019
2019
Background Systemic lupus erythematosus (SLE) is a multisystemic autoimmune disease with various clinical manifestations… Expand
2018
2018
BackgroundSystemic lupus erythematosus (SLE) is a multisystemic autoimmune disease with various clinical manifestations… Expand
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2018
2018
The protein-coding gene adenosine monophosphate deaminase (AMPD) 2 plays a critical role in energy metabolism by converting… Expand
2015
2015
Objective: To determine the molecular basis of a severe neurologic disorder in a large consanguineous family with complete… Expand
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2015
2015
Hibernating animals develop fatty liver when active in summertime and undergo a switch to a fat oxidation state in the winter. We… Expand
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2012
2012
We investigated whether overexpression of AMP‐metabolizing enzymes in intact cells would modulate oligomycin‐induced AMPK… Expand
2012
2012
The AMPD2 gene, a member of the AMPD gene family encoding AMP deaminase, is widely expressed in nonmuscle tissues including… Expand
Highly Cited
2012
Highly Cited
2012
Fatty liver (hepatic steatosis) is associated with nucleotide turnover, loss of ATP and generation of adenosine monophosphate… Expand
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