retoncogene

由FCastinetti著作·2023—In1993,mutationsintheRET(rearrangedduringtransfection)proto-oncogenewereidentifiedbyMulliganandcolleaguesasresponsibleforMEN- ...,由TCChang著作·2013—TheRealWorldofApplicationofRETOncogeneDeterminationintheManagementofMultipleEndocrineNeoplasiaType2inTaiwan·摘要·關鍵字·延伸閱讀·國際替代 ...,TheRETproto-oncogeneonchromosome10q11playsakeyroleinthegenesisofmedullarycarcinoma...

Thirty Years of Progress Thanks to the RET Oncogene

由 F Castinetti 著作 · 2023 — In 1993, mutations in the RET (rearranged during transfection) proto-oncogene were identified by Mulligan and colleagues as responsible for MEN- ...

The Real World of Application of RET Oncogene ...

由 TC Chang 著作 · 2013 — The Real World of Application of RET Oncogene Determination in the Management of Multiple Endocrine Neoplasia Type 2 in Taiwan · 摘要 · 關鍵字 · 延伸閱讀 · 國際替代 ...

RET Proto-Oncogene

The RET proto-oncogene on chromosome 10q11 plays a key role in the genesis of medullary carcinoma. The RET gene, which has 21 exons, encodes a receptor tyrosine ...

A comprehensive overview of the role of the RET proto

由 C Romei 著作 · 2016 · 被引用 329 次 — The RET proto-oncogene is located on the long arm of chromosome 10 (10q11.2). The protein that RET encodes is a cellular tyrosine kinase ...

RET proto

The RET proto-oncogene encodes a receptor tyrosine kinase for members of the glial cell line-derived neurotrophic factor (GDNF) family of extracellular ...

The RET proto

由 SM Jhiang 著作 · 2000 · 被引用 375 次 — The RET proto-oncogene was identified as the susceptibility gene for multiple endocrine neoplasia type 2 (MEN 2), an inherited cancer syndrome ...

RET proto

由 C Eng 著作 · 1999 · 被引用 441 次 — The RET proto-oncogene, located on chromosome subband 10q11.2, encodes a receptor tyrosine kinase expressed in tissues and tumors derived from neural crest.

5979 - Gene ResultRET ret proto

5 天前 — This gene encodes a transmembrane receptor and member of the tyrosine protein kinase family of proteins. Binding of ligands such as GDNF ...

RET oncogene

由 YF Mak 著作 · 1996 · 被引用 41 次 — RET mutations have been identified as the underlying cause of two congenital diseases that predominately affect tissues of neural crest origin: the MEN 2 ...