N-terminal extensions of the human AMPD2 polypeptide influence ATP regulation of isoform L
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
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1. Clinical and genetic spectrum of AMPD2-related pontocerebellar hypoplasia type 9;European Journal of Human Genetics;2018-02-20
2. A novel AMPD2 mutation outside the AMP deaminase domain causes pontocerebellar hypoplasia type 9;American Journal of Medical Genetics Part A;2017-02-07
3. AMPD3-deficient mice exhibit increased erythrocyte ATP levels but anemia not improved due to PK deficiency;Genes to Cells;2012-10-18
4. Overexpression of AMP‐metabolizing enzymes controls adenine nucleotide levels and AMPK activation in HEK293T cells;The FASEB Journal;2012-03-13
5. Proteinuria in AMPD2-deficient mice;Genes to Cells;2011-12-29
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