Preliminary whole-exome sequencing reveals mutations that imply common tumorigenicity pathways in multiple endocrine neoplasia type 1 patients
about
Paraganglioma, pituitary adenoma, and osteosarcoma in a dog.MEN1 mutations and potentially MEN1-targeting miRNAs are responsible for menin deficiency in sporadic and MEN1 syndrome-associated primary hyperparathyroidism.Uncovering the heterogeneous genetic variations in two insulin-expressing tumors in a patient with MEN1.
P2860
Preliminary whole-exome sequencing reveals mutations that imply common tumorigenicity pathways in multiple endocrine neoplasia type 1 patients
description
2014 nî lūn-bûn
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2014年の論文
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2014年論文
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2014年論文
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2014年論文
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2014年論文
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2014年論文
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2014年论文
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2014年论文
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name
Preliminary whole-exome sequen ...... rine neoplasia type 1 patients
@ast
Preliminary whole-exome sequen ...... rine neoplasia type 1 patients
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type
label
Preliminary whole-exome sequen ...... rine neoplasia type 1 patients
@ast
Preliminary whole-exome sequen ...... rine neoplasia type 1 patients
@en
prefLabel
Preliminary whole-exome sequen ...... rine neoplasia type 1 patients
@ast
Preliminary whole-exome sequen ...... rine neoplasia type 1 patients
@en
P2093
P2860
P1433
P1476
Preliminary whole-exome sequen ...... rine neoplasia type 1 patients
@en
P2093
Elizabeth G Grubbs
F Anthony San Lucas
Jeffrey E Lee
Minerva Angélica Romero Arenas
Nancy D Perrier
Paul Scheet
Richard G Fowler
Thereasa A Rich
P2860
P304
1351-7; discussion 1357-8
P356
10.1016/J.SURG.2014.08.073
P407
P577
2014-11-11T00:00:00Z