| 1 |
33084974 | A novel germline variant in RET gene resulting in an additional cysteine in a family with familial medullary thyroid carcinoma. | 2021 Jul |
9 |
| 2 |
33754314 | Kidney malformations and Hirschsprung's disease in carriers of cysteine mutations in exon 10 of the RET proto-oncogene. | 2021 Jul |
2 |
| 3 |
31711124 | REToma: a cancer subtype with a shared driver oncogene. | 2020 Apr 22 |
1 |
| 4 |
32064171 | Peptides containing the MXXCW motif inhibit oncogenic RET kinase activity with a novel mechanism of action. | 2020 |
4 |
| 5 |
32948239 | Total colonic aganglionosis and cleft palate in a newborn with Janus-cysteine 618 mutation of RET proto-oncogene: a case report. | 2020 Sep 18 |
1 |
| 6 |
31392261 | Cryo-EM structure of the activated RET signaling complex reveals the importance of its cysteine-rich domain. | 2019 Jul |
6 |
| 7 |
27704398 | The RET E616Q Variant is a Gain of Function Mutation Present in a Family with Features of Multiple Endocrine Neoplasia 2A. | 2017 Mar |
3 |
| 8 |
28181547 | Differences in the transcriptome of medullary thyroid cancer regarding the status and type of RET gene mutations. | 2017 Feb 9 |
1 |
| 9 |
28506408 | Genetics of medullary thyroid cancer: An overview. | 2017 May |
2 |
| 10 |
26572832 | Variability in penetrance of multiple endocrine neoplasia 2A with amino acid substitutions in RET codon 634. | 2016 Feb |
5 |
| 11 |
26780347 | Commentary to Gorelenkova Miller and Mieyal (2015): sulfhydryl-mediated redox signaling in inflammation: role in neurodegenerative diseases. | 2016 Apr |
2 |
| 12 |
25638620 | Clinical and genetic correlations of familial Hirschsprung's disease. | 2015 Feb |
2 |
| 13 |
25831049 | Anti-tumour effects of antibodies targeting the extracellular cysteine-rich region of the receptor tyrosine kinase EphB4. | 2015 Apr 10 |
1 |
| 14 |
26033033 | C-Cell Neoplasia in Asymptomatic Carriers of RET Mutation in Extracellular Cysteine-Rich and Intracellular Tyrosine Kinase Domain. | 2015 Aug |
1 |
| 15 |
24449676 | A patient with an apparently sporadic pheochromocytoma with a rearranged during transfection codon 635 variant: a mild form of multiple endocrine neoplasia type 2? | 2014 Apr |
3 |
| 16 |
24643705 | Genetic disorders of pediatric MEN2A patients in the south of Spain. | 2014 Nov |
3 |
| 17 |
25242331 | RET recognition of GDNF-GFRα1 ligand by a composite binding site promotes membrane-proximal self-association. | 2014 Sep 25 |
1 |
| 18 |
23554805 | Integrated DNA-based/biochemical screening for early diagnosis of multiple endocrine neoplasia type 2A (MEN2A). | 2013 Mar |
2 |
| 19 |
23113396 | [Hirschsprung's disease and medullary carcinoma of the thyroids: two diseases in a monogenetic disorder]. | 2012 Apr |
1 |
| 20 |
20497437 | RET codon 804 mutations in multiple endocrine neoplasia 2: genotype-phenotype correlations and implications in clinical management. | 2011 Jan |
3 |
| 21 |
21110809 | Development of RET kinase inhibitors for targeted cancer therapy. | 2011 |
1 |
| 22 |
20119574 | A Korean family of familial medullary thyroid cancer with Cys618Ser RET germline mutation. | 2010 Feb |
6 |
| 23 |
20152359 | Familial associations in medullary thyroid carcinoma with Hirschsprung disease: the role of the RET-C620 "Janus" genetic variation. | 2010 Feb |
1 |
| 24 |
20235151 | A redox-linked novel pathway for arsenic-mediated RET tyrosine kinase activation. | 2010 May 15 |
9 |
| 25 |
20473317 | Mammal-restricted elements predispose human RET to folding impairment by HSCR mutations. | 2010 Jun |
1 |
| 26 |
21542403 | Chasing the ubiquitous RET proto-oncogene in South African MEN2 families--implications for the surgeon. | 2010 Nov |
1 |
| 27 |
18248647 | The Y606C RET mutation causes a receptor gain of function. | 2008 Aug |
1 |
| 28 |
18365214 | Multiple endocrine neoplasia syndromes, children, Hirschsprung's disease and RET. | 2008 May |
1 |
| 29 |
17270543 | Familial medullary carcinoma prevention, risk evaluation, and RET in children of families with MEN2. | 2007 Feb |
1 |
| 30 |
17279407 | [Molecular biology, basic research and diagnosis of Hirschsprung's disease]. | 2007 Mar |
1 |
| 31 |
17453286 | Genotype-phenotype based surgical concept of hereditary medullary thyroid carcinoma. | 2007 May |
1 |
| 32 |
17895320 | RET genetic screening in patients with medullary thyroid cancer and their relatives: experience with 807 individuals at one center. | 2007 Dec |
1 |
| 33 |
16469774 | A novel activating mutation in the RET tyrosine kinase domain mediates neoplastic transformation. | 2006 Jul |
1 |
| 34 |
16732321 | Self-association of the transmembrane domain of RET underlies oncogenic activation by MEN2A mutations. | 2006 Nov 9 |
12 |
| 35 |
16954442 | An in-frame complex germline mutation in the juxtamembrane intracellular domain causing RET activation in familial medullary thyroid carcinoma. | 2006 Sep |
1 |
| 36 |
17065770 | Study of the RET gene and his implication in thyroid cancer: Morocco case family. | 2006 Jul-Sep |
3 |
| 37 |
17102091 | Molecular implications of RET mutations for pheochromocytoma risk in multiple endocrine neoplasia 2. | 2006 Aug |
1 |
| 38 |
17260470 | [RET gene cys 634 trp mutation in a multiple endocrine neoplasia type 2A kindred]. | 2006 Dec |
5 |
| 39 |
16029119 | RET proto-oncogene: a review and update of genotype-phenotype correlations in hereditary medullary thyroid cancer and associated endocrine tumors. | 2005 Jun |
1 |
| 40 |
16277170 | Multiple endocrine neoplasia type 2A/localized cutaneous lichen amyloidosis associated with malignant pheochromocytoma and ganglioneuroma. | 2005 Sep |
1 |
| 41 |
16343103 | Multiple endocrine neoplasia 2A due to a unique C609S RET mutation presents with pheochromocytoma and reduced penetrance of medullary thyroid carcinoma. | 2005 Dec |
3 |
| 42 |
15240641 | A novel point mutation of the RET protooncogene involving the second intracellular tyrosine kinase domain in a family with medullary thyroid carcinoma. | 2004 Jul |
1 |
| 43 |
15271413 | RET oncogene mutations in 75 cases of familial medullary thyroid carcinoma in Japan. | 2004 Jul-Aug |
2 |
| 44 |
12606135 | Multiple endocrine neoplasia type 2A: an unusual clinical presentation and association with renal dysplasia. | 2003 Mar |
1 |
| 45 |
12630912 | The soluble ectodomain of RetC634Y inhibits both the wild-type and the constitutively active Ret. | 2003 Jun 15 |
3 |
| 46 |
12734540 | Cys611Ser mutation in RET proto-oncogene in a kindred with medullary thyroid carcinoma and Hirschsprung's disease. | 2003 May |
8 |
| 47 |
14602786 | A novel germ-line point mutation in RET exon 8 (Gly(533)Cys) in a large kindred with familial medullary thyroid carcinoma. | 2003 Nov |
3 |
| 48 |
11935126 | RET mutation profile and variable clinical manifestations in a family with multiple endocrine neoplasia type 2A and Hirschsprung's disease. | 2002 Apr |
2 |
| 49 |
11944888 | Evidence of both extra- and intracellular cysteine targets of protein modification for activation of RET kinase. | 2002 Apr 12 |
4 |
| 50 |
12033991 | A PCR-mutagenesis strategy for rapid detection of mutations in codon 634 of the ret proto-oncogene related to MEN 2A. | 2002 May 21 |
2 |