Varaico: Literature-Extracted Genetic Variants

Gene:RET
Variant:p.D1017N
Back to variants list

RET

NM_020975.6:p.D1017N

Associated Papers

Looking for RET alterations in thyroid cancer: clinical relevance, methodology and timing.

Elisei R et al.

Endocrine, 2023

Rare RET Variant p.D707E in a Chinese Pedigree with Hereditary Medullary Thyroid Carcinoma.

Zhang L et al.

Pathobiology : Journal of Immunopathology, Molecular and Cellular Biology, 2017

Chasing the ubiquitous RET proto-oncogene in South African MEN2 families--implications for the surgeon.

Moore SW et al.

South African Journal of Surgery. Suid-afrikaanse Tydskrif Vir Chirurgie, 2010

Familial medullary carcinoma prevention, risk evaluation, and RET in children of families with MEN2.

Moore SW et al.

Journal of Pediatric Surgery, 2007

Molecular mechanisms of RET-induced Hirschsprung pathogenesis.

Lantieri F et al.

Annals of Medicine, 2006

The RET proto-oncogene induces apoptosis: a novel mechanism for Hirschsprung disease.

Bordeaux MC et al.

The Embo Journal, 2000

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."