(Q54425556)

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The frequency of selected polymorphic variants of the RET gene in patients with medullary thyroid carcinoma and in the general population of central Poland.

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

29 May 2018

http://europepmc.org/abstract/MED/20521125

The frequency of selected polymorphic variants of the RET gene in patients with medullary thyroid carcinoma and in the general population of central Poland. (English)

1 reference

Europe PubMed Central

PubMed publication ID

29 May 2018

http://europepmc.org/abstract/MED/20521125

thyroid carcinoma

1 reference

based on heuristic

inferred from title

6

object named as

Jan Steffen

1 reference

Europe PubMed Central

PubMed publication ID

29 May 2018

http://europepmc.org/abstract/MED/20521125

author name string

Maria Sromek

1

1 reference

Europe PubMed Central

PubMed publication ID

29 May 2018

http://europepmc.org/abstract/MED/20521125

Malgorzata Czetwertyńska

2

1 reference

Europe PubMed Central

PubMed publication ID

29 May 2018

http://europepmc.org/abstract/MED/20521125

Elzbieta Skasko

3

1 reference

Europe PubMed Central

PubMed publication ID

29 May 2018

http://europepmc.org/abstract/MED/20521125

Joanna Zielińska

4

1 reference

Europe PubMed Central

PubMed publication ID

29 May 2018

http://europepmc.org/abstract/MED/20521125

Dorota Czapczak

5

1 reference

Europe PubMed Central

PubMed publication ID

29 May 2018

http://europepmc.org/abstract/MED/20521125

publication date

1 September 2010

1 reference

Europe PubMed Central

PubMed publication ID

29 May 2018

http://europepmc.org/abstract/MED/20521125

Endocrine Pathology

1 reference

Europe PubMed Central

PubMed publication ID

29 May 2018

http://europepmc.org/abstract/MED/20521125

21

1 reference

Europe PubMed Central

PubMed publication ID

29 May 2018

http://europepmc.org/abstract/MED/20521125

3

1 reference

Europe PubMed Central

PubMed publication ID

29 May 2018

http://europepmc.org/abstract/MED/20521125

178-185

1 reference

Europe PubMed Central

PubMed publication ID

29 May 2018

http://europepmc.org/abstract/MED/20521125

https://scigraph.springernature.com/pub.10.1007/s12022-010-9125-8

0 references

G691S, L769L and S836S ret proto-oncogene polymorphisms are not associated with higher risk to sporadic medullary thyroid carcinoma in Chilean patients

1 reference

https://api.crossref.org/works/10.1007%2FS12022-010-9125-8

21 January 2018

Specific polymorphisms in the RET proto-oncogene are over-represented in patients with Hirschsprung disease and may represent loci modifying phenotypic expression

1 reference

https://api.crossref.org/works/10.1007%2FS12022-010-9125-8

21 January 2018

Polymorphisms in exon 13 and intron 14 of the RET protooncogene: genetic modifiers of medullary thyroid carcinoma?

1 reference

https://pubmed.ncbi.nlm.nih.gov/20521125

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Activation of a novel human transforming gene, ret, by DNA rearrangement

1 reference

https://pubmed.ncbi.nlm.nih.gov/20521125

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

RET polymorphisms and sporadic medullary thyroid carcinoma in a Portuguese population

1 reference

https://pubmed.ncbi.nlm.nih.gov/20521125

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The phenotypes associated with ret mutations in the multiple endocrine neoplasia type 2 syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20521125

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evaluation of the role of RET polymorphisms/haplotypes as modifier loci for MEN 2, and analysis of the correlation with the type of RET mutation in a series of Spanish patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/20521125

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20521125

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The RET receptor: function in development and dysfunction in congenital malformation

1 reference

https://pubmed.ncbi.nlm.nih.gov/20521125

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

RET tyrosine kinase signaling in development and cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/20521125

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germline sequence variant S836S in the RET proto-oncogene is associated with low level predisposition to sporadic medullary thyroid carcinoma in the Spanish population

1 reference

https://pubmed.ncbi.nlm.nih.gov/20521125

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphisms G691S/S904S of RET as genetic modifiers of MEN 2A

1 reference

https://pubmed.ncbi.nlm.nih.gov/20521125

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A newly identified RET proto-oncogene polymorphism is found in a high number of endocrine tumor patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/20521125

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cloning and expression of the ret proto-oncogene encoding a tyrosine kinase with two potential transmembrane domains

1 reference

https://pubmed.ncbi.nlm.nih.gov/20521125

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The RET proto-oncogene: a molecular therapeutic target in thyroid cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/20521125

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The influence of gender, age, and RET polymorphisms on C-cell hyperplasia and medullary thyroid carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/20521125

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primary hyperparathyroidism as the leading symptom in a patient with a Y791F RET mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/20521125

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

How do synonymous mutations affect fitness?

1 reference

https://pubmed.ncbi.nlm.nih.gov/20521125

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple endocrine neoplasia type 2 and RET: from neoplasia to neurogenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/20521125

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Significance of the RET proto-oncogene polymorphisms in Turkish sporadic medullary thyroid carcinoma patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/20521125

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

RET polymorphisms in codons 769 and 836 are not associated with predisposition to medullary thyroid carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/20521125

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Over-representation of a germline RET sequence variant in patients with sporadic medullary thyroid carcinoma and somatic RET codon 918 mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/20521125

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A "silent" polymorphism in the MDR1 gene changes substrate specificity

1 reference

https://pubmed.ncbi.nlm.nih.gov/20521125

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The occurrence and the type of germline mutations in the RET gene in patients with medullary thyroid carcinoma and their unaffected kindred's from Central Poland

1 reference

https://pubmed.ncbi.nlm.nih.gov/20521125

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of the role of the Shine-Dalgarno sequence and mRNA secondary structure on the efficiency of translational initiation in the Euglena gracilis chloroplast atpH mRNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/20521125

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Folding dynamics and mechanism of beta-hairpin formation

1 reference

https://pubmed.ncbi.nlm.nih.gov/20521125

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

VARNA: Interactive drawing and editing of the RNA secondary structure

1 reference

https://pubmed.ncbi.nlm.nih.gov/20521125

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Codon usage tabulated from the international DNA sequence databases

1 reference

https://pubmed.ncbi.nlm.nih.gov/20521125

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Segregation of the V804L mutation and S836S polymorphism of exon 14 of the RET gene in an extended kindred with familial medullary thyroid cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/20521125

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germline-sequence variants S836S and L769L in the RE arranged during Transfection (RET) proto-oncogene are not associated with predisposition to sporadic medullary carcinoma in the French population

1 reference

https://pubmed.ncbi.nlm.nih.gov/20521125

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

RET as a diagnostic and therapeutic target in sporadic and hereditary endocrine tumors

1 reference

https://pubmed.ncbi.nlm.nih.gov/20521125

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

RET exon 11 (G691S) polymorphism is significantly more frequent in sporadic medullary thyroid carcinoma than in the general population

1 reference

https://pubmed.ncbi.nlm.nih.gov/20521125

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S12022-010-9125-8

1 reference

Europe PubMed Central

PubMed publication ID

29 May 2018

http://europepmc.org/abstract/MED/20521125

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 May 2018

http://europepmc.org/abstract/MED/20521125

ResearchGate publication ID

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