Associated Papers
A novel germline variant in RET gene resulting in an additional cysteine in a family with familial medullary thyroid carcinoma.
Oriola J et al.
Familial Cancer, 2021
Modification of multiple endocrine neoplasia 2A phenotype by cell membrane proximity of RET mutations in exon 10.
Machens A et al.
Endocrine-related Cancer, 2009
[Molecular biology, basic research and diagnosis of Hirschsprung's disease].
Martucciello G et al.
Der Pathologe, 2007
Self-association of the transmembrane domain of RET underlies oncogenic activation by MEN2A mutations.
Kjaer S et al.
Oncogene, 2006
Intrinsic susceptibility to misfolding of a hot-spot for Hirschsprung disease mutations in the ectodomain of RET.
Kjaer S et al.
Human Molecular Genetics, 2003
Association between c135G/A genotype and RET proto-oncogene germline mutations and phenotype of Hirschsprung's disease.
Fitze G et al.
Lancet (london, England), 2002
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