Primary hyperparathyroidism, C-cell hyperplasia and papillary thyroid carcinoma in a patient with RET germline polymorphism S836S

No abstract is available for this paper.

• Publication year

  2002

• Venue

  Langenbeck's archives of surgery (Print)

• Publication date

  2002-09-27

• Fields of study

  Medicine

• Identifiers
  DOI 10.1007/s00423-002-0321-yPMID 12410354
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Papillary Thyroid Carcinoma in Patients with RET Proto-Oncogene Germline Mutation

  2002cited by this paper
• Expression and alternative splicing of c-ret RNA in papillary thyroid carcinomas

  2001cited by this paper
• Germline sequence variant S836S in the RET proto‐oncogene is associated with low level predisposition to sporadic medullary thyroid carcinoma in the Spanish population

  2001influential reference
• Genotype-phenotype correlations in hereditary medullary thyroid carcinoma: oncological features and biochemical properties.

  2001cited by this paper
• Expression of the RET proto‐oncogene in papillary thyroid carcinoma and its correlation with clinical outcome

  2001influential reference
• A single-nucleotide polymorphic variant of the RET proto-oncogene is underrepresented in sporadic Hirschsprung disease

  2000cited by this paper
• Variable expressivity of familial medullary thyroid carcinoma (FMTC) due to a RET V804M (GTG-->ATG) mutation.

  2000cited by this paper
• RET rearrangements in papillary thyroid carcinomas and adenomas detected by interphase FISH

  2000influential reference
• RET proto-oncogene in the development of human cancer.

  1999influential reference
• Expression of wild-type ret, ret/PTC and ret/PTC variants in papillary thyroid carcinoma in Germany

  1999cited by this paper
• Over-representation of a germline RET sequence variant in patients with sporadic medullary thyroid carcinoma and somatic RET codon 918 mutation

  1999cited by this paper
• Genotype-phenotype correlation of patients with multiple endocrine neoplasia type 2 in Japan.

  1998cited by this paper
• Molecular biology of the MEN2 gene

  1998influential reference
• Genetic alterations of the RET proto-oncogene in familial and sporadic pheochromocytomas.

  1997cited by this paper
• A novel splice site associated polymorphism in the tuberous sclerosis 2 (TSC2) gene may predispose to the development of sporadic gangliogliomas.

  1997cited by this paper
• Two alleles of the human paraoxonase gene produce different amounts of mRNA. An explanation for differences in serum concentrations of paraoxonase associated with the (Leu-Met54) polymorphism.

  1997cited by this paper
• Alternative splicing of exon 3 of the human growth hormone receptor is the result of an unusual genetic polymorphism.

  1996cited by this paper
• DNA polymorphisms and conditions for SSCP analysis of the 20 exons of the ret proto-oncogene.

  1995cited by this paper
• DNA polymorphisms and conditions for SSCP analysis of the 20 exons of the ret proto-oncogene.

  1994cited by this paper
• Expression of papillary thyroid carcinoma in multiple endocrine neoplasia type 2A.

  1993cited by this paper

• The RET polymorphic allele S836S is associated with early metastatic disease in patients with hereditary or sporadic medullary thyroid carcinoma.

  2010cites this paper
• Germline polymorphisms of RET and GFRA1 genes in patients with medullary thyroid carcinoma

  2006cites this paper