34 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
1 | 24501868 | [Blood transfusions suppress erythropoiesis in anemia of prematurity]. | 2013 | 1 |
2 | 22128160 | Identification of a key motif that determines the differential surface levels of RET and TrkB tyrosine kinase receptors and controls depolarization enhanced RET surface insertion. | 2012 Jan 13 | 2 |
3 | 16427628 | A PKC-mediated backup mechanism of the MXXCW motif-linked switch for initiating tyrosine kinase activities. | 2006 Feb 6 | 1 |
4 | 16829704 | De novo multiple endocrine neoplasia type 2B with noncardiogenic pulmonary edema as the presenting symptom. | 2006 Aug | 1 |
5 | 17102091 | Molecular implications of RET mutations for pheochromocytoma risk in multiple endocrine neoplasia 2. | 2006 Aug | 1 |
6 | 17108110 | Molecular mechanisms of RET receptor-mediated oncogenesis in multiple endocrine neoplasia 2B. | 2006 Nov 15 | 2 |
7 | 16254257 | p-p70S6K (Thr 389) Expression in nodular sclerosing hodgkin's disease as evidence for receptor tyrosine kinase signaling. | 2005 Autumn | 1 |
8 | 15379552 | Identification of major ERK-related phosphorylation sites in Gab1. | 2004 Sep 28 | 1 |
9 | 15485908 | Central role of the threonine residue within the p+1 loop of receptor tyrosine kinase in STAT3 constitutive phosphorylation in metastatic cancer cells. | 2004 Nov | 1 |
10 | 15531548 | Identification of a novel point mutation in the RET gene (Ala883Thr), which is associated with medullary thyroid carcinoma phenotype only in homozygous condition. | 2004 Nov | 1 |
11 | 12757658 | [A case report and pedigree study of a single point mutation in RET proto-oncogene and type 2B multiple endocrine neoplasia]. | 2003 Jan | 2 |
12 | 11839664 | RET oligonucleotide microarray for the detection of RET mutations in multiple endocrine neoplasia type 2 syndromes. | 2002 Feb | 1 |
13 | 11351254 | CGH alterations in medullary thyroid carcinomas in relation to the RET M918T mutation and clinical outcome. | 2001 Jun | 1 |
14 | 10871866 | Multiple endocrine neoplasia type 2B mutation in human RET oncogene induces medullary thyroid carcinoma in transgenic mice. | 2000 Jun 22 | 3 |
15 | 9621513 | Mutational analysis of the RET proto-oncogene in 71 Japanese patients with medullary thyroid carcinoma. | 1998 | 1 |
16 | 9706252 | [Early diagnosis of multiple endocrine neoplasia type 2 (MEN 2) by detection of mutated RET proto-oncogene carriers]. | 1998 | 1 |
17 | 9018112 | Distinct biological properties of two RET isoforms activated by MEN 2A and MEN 2B mutations. | 1997 Jan 23 | 2 |
18 | 9075701 | Only the substitution of methionine 918 with a threonine and not with other residues activates RET transforming potential. | 1997 Apr | 1 |
19 | 9393871 | The multiple endocrine neoplasia type 2B point mutation switches the specificity of the Ret tyrosine kinase towards cellular substrates that are susceptible to interact with Crk and Nck. | 1997 Nov 6 | 3 |
20 | 9398735 | A novel point mutation in the intracellular domain of the ret protooncogene in a family with medullary thyroid carcinoma. | 1997 Dec | 1 |
21 | 8557249 | Mutation analysis of the RET proto-oncogene in Dutch families with MEN 2A, MEN 2B and FMTC: two novel mutations and one de novo mutation for MEN 2A. | 1996 Jan | 1 |
22 | 8621456 | The multiple endocrine neoplasia type 2B point mutation alters long-term regulation and enhances the transforming capacity of the epidermal growth factor receptor. | 1996 Mar 8 | 3 |
23 | 8880581 | Multiple endocrine neoplasia type 2B (mucosal neuroma syndrome, Wagenmann-Froboese syndrome). | 1996 Sep | 1 |
24 | 8884827 | RET protooncogene mutational analysis in multiple endocrine neoplasia syndrome type 2B: case report and review of the literature. | 1996 Sep | 2 |
25 | 9074721 | [Neural crest and multiple endocrinopathies]. | 1996 | 1 |
26 | 7495285 | Absence of RET proto-oncogene point mutations in sporadic hyperplastic and neoplastic lesions of the parathyroid gland. | 1995 Dec | 1 |
27 | 7595167 | The RET proto-oncogene and cancer. | 1995 Oct | 1 |
28 | 7627271 | Tumor-specific mutations in the tyrosine kinase domain of the RET proto-oncogene in pheochromocytomas of sporadic type. | 1995 Apr | 2 |
29 | 7705835 | Detection of a germline mutation at codon 918 of the RET proto-oncogene in French MEN 2B families. | 1995 Apr | 2 |
30 | 8625130 | Analysis of RET protooncogene point mutations distinguishes heritable from nonheritable medullary thyroid carcinomas. | 1995 Aug 1 | 2 |
31 | 12114809 | Molecular Diagnosis of Multiple Endocrine Neoplasia (MEN) in Paraffin-Embedded Specimens. | 1995 Winter | 1 |
32 | 7906866 | A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma. | 1994 Jan 27 | 1 |
33 | 7911697 | Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumours. | 1994 Feb | 1 |
34 | 3001107 | Interaction of the insulin receptor kinase with serine/threonine kinases in vitro. | 1985 | 1 |