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28篇 您的检索式:作者名="Presneau"
    题名 作者 年代 出处 被引量
1Brachyury, a crucial regulator of notochordal development, is a novel biomarker for ehordomas 显示文摘Vujovic S Henderson S Presneau N 2006J Pathot2006,209,2:1
2Potential therapeutic tar- gets for ehordoma : P13 K/AKT/TSCI/TSC2/mTOR pathway 显示文摘Presneau N Shalaby A Idowu B 2009Br J Cancer2009,100,9:1
3Comparative analysis of loss of heterozygosity of specific chromosome 3, 13, 17,and X loci and TP53 mutations in human epithelial ovarian cancer显示文摘Manderson EN Presneau N Provencher D 2002Mol Carcinog2002,34,2:1
4Comparative analysis of loss of heterozygosity of specific chromosome 3, 13, 17, and X loci and TP53 mutations in human epithelial ovarian cancer显示文摘Manderson EN Presneau N Provencher D 0,,:1
5The role of epidermal growth factor receptor in chordoma pathogenesis:a potential therapeutic target显示文摘Shalaby A Presneau N Ye H 0,,03:1
6Rapid detection of BRCA-1 germline mutations by the protein truncation test in Tunisian families显示文摘Monastiri K Ben Ahmed S Presneau N 0,,09:1
7Com- parative analysis of loss of heterozygosity of specific chromosome 3,13,17,and X loci and TP53 mutations in human epithelial ovarian cancer显示文摘Manderson EN Presneau N Provencher D 2002Mol Carcinog2002,34,2:1
8Role of the transcription factor T(brachyury)in the pathogenesis of sporadic chordoma:A genetic and function-based study显示文摘Presneau N Shalaby A Ye H 2011J Pathol2011,223,3:1
9GNAS1 mutations occur more commonly than previously thought in intramuscular myxoma显示文摘Delaney D Diss T C Presneau N 0,,05:1
10The quest for a tumor suppressor gene phenotype 显示文摘Presneau N Manderson EN Tonin PN 2003Curr Mol Med2003,3,7:1
11Distinct H3F3A and H3F3B driver mutations define chondroblastoma and giant cell tumor of bone显示文摘Behjati S Tarpey PS Presneau N 2013Nat Genet2013,45,12:1
12The role of epidermal growth factor receptor in chordoma pathogenesis: A potential therapeutic target 显示文摘Shalaby A Presneau N Ye H 2011J Pathol2011,223,3:1
13Brachyury, a crucial regulator of notochordal development, is a novel bi- omarker for chordomas 显示文摘Vujovic S Henderson S Presneau N 2006J Pathol2006,209,2:1
14Familial tumoral calcinosis and hyperostosis-hyperphosphataemia syndrome are different manifestations of the same disease:novel missense mutations in GALNT3显示文摘Joseph L Hing SN Presneau N 0,,:1
15Role of the tran- scription factor T (brachyury) in the pathogenesis of spo- radic chordoma: a genetic and functional-based study显示文摘Presneau N Shalaby A Ye H 2010J Patho12010,223,3:1
16Brachyury, a crucial regulator of notochordal development, is a novel biomarker for chordomas显示文摘Vujovic S Henderson S Presneau N 2006J Pathol2006,209,2:1
17A molecular map of mesenchymal tumors 显示文摘Henderson SR Guiliano D Presneau N 2005Genome Biol2005,6,9:1
18GNAS1 mutations previously thought in intramuscular myxoma 显示文摘Delaney D Diss TC Presneau N occur more commonly than 2009Mod Pathol2009,22,5:1
19GNAS I mutations occur more commonly than previously thought in intramuscular myxoma显示文摘Delaney D Diss TC Presneau N 2009Mod Pathol2009,22,5:1
20GNAS 1 mutations occur more commonly than previously thought in intramuscular myxoma显示文摘Delaney D Diss TC Presneau N 2009Mod Pathol2009,22,5:1
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