Results 61 to 70 of about 20,082,992 (152)

Absence of Mutations at Codon 768 of the RET Proto-Oncogene in Sporadic and Hereditary Pheochromocytomas [PDF]

open access: yes, 1996
Sixteen sporadic pheochromocytomas, 3 pheochromocytomas in neurofibromatosis 1, and 4 pheochromocytomas in multiple endocrine neoplasia (MEN) 2A or 2B were screened for mutations at codon 768 of the RET proto-oncogene by AluI digestion of polymerase ...
(田中)小杉, 知里   +22 more
core  

Experimental implication of celiac ganglionotropic invasion of pancreatic‐cancer cells bearing c‐ret proto‐oncogene with reference to glial‐cell‐line‐derived neurotrophic factor (GDNF)

open access: yesInternational Journal of Cancer, 1999
Yuji Okada   +8 more
semanticscholar   +1 more source

Single nucleotide polymorphic alleles in the 5′ region of the RET proto-oncogene define a risk haplotype in Hirschsprung’s disease

open access: yesJournal of Medical Genetics, 2003
M. Sancandi   +10 more
semanticscholar   +1 more source

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

open access: yesEuropean Journal of Human Genetics, 2000
P. Griseri   +8 more
semanticscholar   +1 more source

Home - About - Disclaimer - Privacy