PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 23730215-6 2013 We have also found that a single mutation of the Tyr(644) or Tyr(664) residue of the C terminus of NPM-ALK to phenylalanine decreases significantly, but does not completely abolish, the association between NPM-ALK and IGF-IR. Tyrosine 49-52 ALK receptor tyrosine kinase Homo sapiens 103-106 23730215-6 2013 We have also found that a single mutation of the Tyr(644) or Tyr(664) residue of the C terminus of NPM-ALK to phenylalanine decreases significantly, but does not completely abolish, the association between NPM-ALK and IGF-IR. Tyrosine 49-52 ALK receptor tyrosine kinase Homo sapiens 210-213 23730215-6 2013 We have also found that a single mutation of the Tyr(644) or Tyr(664) residue of the C terminus of NPM-ALK to phenylalanine decreases significantly, but does not completely abolish, the association between NPM-ALK and IGF-IR. Tyrosine 61-64 ALK receptor tyrosine kinase Homo sapiens 103-106 23730215-6 2013 We have also found that a single mutation of the Tyr(644) or Tyr(664) residue of the C terminus of NPM-ALK to phenylalanine decreases significantly, but does not completely abolish, the association between NPM-ALK and IGF-IR. Tyrosine 61-64 ALK receptor tyrosine kinase Homo sapiens 210-213 23730215-7 2013 The purpose of this study was to determine whether the dual mutation of Tyr(644) and Tyr(664) abrogates the association and interactions between NPM-ALK and IGF-IR. Tyrosine 72-75 ALK receptor tyrosine kinase Homo sapiens 149-152 23730215-7 2013 The purpose of this study was to determine whether the dual mutation of Tyr(644) and Tyr(664) abrogates the association and interactions between NPM-ALK and IGF-IR. Tyrosine 85-88 ALK receptor tyrosine kinase Homo sapiens 149-152 23730215-10 2013 Importantly, we found that the dual mutation of Tyr(644) and Tyr(664) diminishes the oncogenic effects of NPM-ALK, including its ability to induce anchorage-independent colony formation and to sustain cellular transformation, proliferation, and migration. Tyrosine 48-51 ALK receptor tyrosine kinase Homo sapiens 110-113 23730215-10 2013 Importantly, we found that the dual mutation of Tyr(644) and Tyr(664) diminishes the oncogenic effects of NPM-ALK, including its ability to induce anchorage-independent colony formation and to sustain cellular transformation, proliferation, and migration. Tyrosine 61-64 ALK receptor tyrosine kinase Homo sapiens 110-113 23730215-11 2013 Furthermore, the association between NPM-ALK and IGF-IR through Tyr(644) and Tyr(664) appears to contribute to maintaining the stability of NPM-ALK protein. Tyrosine 64-67 ALK receptor tyrosine kinase Homo sapiens 41-44 23730215-11 2013 Furthermore, the association between NPM-ALK and IGF-IR through Tyr(644) and Tyr(664) appears to contribute to maintaining the stability of NPM-ALK protein. Tyrosine 64-67 ALK receptor tyrosine kinase Homo sapiens 144-147 23730215-11 2013 Furthermore, the association between NPM-ALK and IGF-IR through Tyr(644) and Tyr(664) appears to contribute to maintaining the stability of NPM-ALK protein. Tyrosine 77-80 ALK receptor tyrosine kinase Homo sapiens 144-147