Associated Papers
Transcriptome analysis reveals effects of leukemogenic SHP2 mutations in biosynthesis of amino acids signaling.
Zhao Y et al.
Frontiers in Oncology, 2023
Modeling (not so) rare developmental disorders associated with mutations in the protein-tyrosine phosphatase SHP2.
Solman M et al.
Frontiers in Cell and Developmental Biology, 2022
Exploring the reason for increased activity of SHP2 caused by D61Y mutation through molecular dynamics.
Wang RR et al.
Computational Biology and Chemistry, 2019
Mutated Ptpn11 alters leukemic stem cell frequency and reduces the sensitivity of acute myeloid leukemia cells to Mcl1 inhibition.
Chen L et al.
Leukemia, 2015
The role of the protein tyrosine phosphatase SHP2 in cardiac development and disease.
Lauriol J et al.
Seminars in Cell & Developmental Biology, 2015
Structural and mechanistic insights into LEOPARD syndrome-associated SHP2 mutations.
Yu ZH et al.
The Journal of Biological Chemistry, 2013
Diverse biochemical properties of Shp2 mutants. Implications for disease phenotypes.
Keilhack H et al.
The Journal of Biological Chemistry, 2005
Select a paper to view details