Pages that link to "Q77481551"

The following pages link to Atypical MEN type 2B associated with two germline RET mutations on the same allele not involving codon 918 (Q77481551):

Displaying 30 items.

• RET Germline Mutations Identified by Exome Sequencing in a Chinese Multiple Endocrine Neoplasia Type 2A/Familial Medullary Thyroid Carcinoma Family (Q21135360) (← links)
• Molecular basis of medullary thyroid carcinoma: the role of RET polymorphisms (Q27010044) (← links)
• Paternal Age Effect Mutations and Selfish Spermatogonial Selection: Causes and Consequences for Human Disease (Q28259472) (← links)
• Mutations de RET et traitement préventif du cancer médullaire de la thyroïde (Q29011410) (← links)
• Multiple endocrine neoplasia 2B syndrome due to codon 918 mutation: clinical manifestation and course in early and late onset disease (Q30320428) (← links)
• Multiple endocrine neoplasia type 2 and familial medullary thyroid carcinoma: an update (Q33587821) (← links)
• Multiple endocrine neoplasia type 2. (Q34557491) (← links)
• A Drosophila model of multiple endocrine neoplasia type 2. (Q34589821) (← links)
• Tandem Germline RET Mutations in a Family Pathogenetic for Multiple Endocrine Neoplasia 2B, Confirmed by a Natural Experiment (Q35029690) (← links)
• Multiple endocrine neoplasias type 2B and RET proto-oncogene. (Q36012582) (← links)
• Molecular pathogenesis of MEN2-associated tumors (Q36121928) (← links)
• Pheochromocytoma-associated syndromes: genes, proteins and functions of RET, VHL and SDHx (Q36121945) (← links)
• Coexistence of Multiple Endocrine Neoplasia Type 2B and Chilaiditi Sign: A Case Report (Q36355221) (← links)
• The optimal range of RET mutations to be tested: European comments to the guidelines of the American Thyroid Association (Q36690582) (← links)
• Advanced medullary thyroid cancer: pathophysiology and management (Q36857218) (← links)
• A differential diagnosis of inherited endocrine tumors and their tumor counterparts (Q37023603) (← links)
• 2012 European thyroid association guidelines for genetic testing and its clinical consequences in medullary thyroid cancer (Q37290956) (← links)
• Molecular mechanisms of RET receptor-mediated oncogenesis in multiple endocrine neoplasia 2 (Q38010030) (← links)
• Novel tandem germline RET proto-oncogene mutations in a patient with multiple endocrine neoplasia type 2B: report of a case and a literature review of tandem RET mutations with in silico analysis (Q38087307) (← links)
• RET gene mutations (genotype and phenotype) of multiple endocrine neoplasia type 2 and familial medullary thyroid carcinoma (Q38202024) (← links)
• Hereditary Medullary Thyroid Cancer Genotype-Phenotype Correlation (Q38614498) (← links)
• A comprehensive overview of the role of the RET proto-oncogene in thyroid carcinoma (Q38730197) (← links)
• Disease associated mutations at valine 804 in the RET receptor tyrosine kinase confer resistance to selective kinase inhibitors (Q40547936) (← links)
• Multiple Endocrine Neoplasia Type 2B: Early Diagnosis by Multiple Mucosal Neuroma and Its DNA Analysis (Q41522198) (← links)
• Genetic and clinical features of multiple endocrine neoplasia types 1 and 2. (Q41667928) (← links)
• A Case of Multiple Endocrine Neoplasia Type 2B and Gangliomatosis of Gastrointestinal Tract. (Q42424055) (← links)
• Timing and extent of surgery in patients with familial medullary thyroid carcinoma/multiple endocrine neoplasia 2A-related RET mutations not affecting codon 634. (Q42469941) (← links)
• The development of rapid and accurate screening test for RET hotspot somatic and germline mutations in MEN2 syndromes. (Q53367275) (← links)
• Loss-of-function mutations of SCN10A encoding NaV1.8 α subunit of voltage-gated sodium channel in patients with human kidney stone disease. (Q55646299) (← links)
• The newly detected mutations in the RET proto-oncogene in exon 16 as a cause of sporadic medullary thyroid carcinoma (Q79294764) (← links)