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21篇 您的检索式：作者名="MENIN C"

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	题名	作者	年代	出处	被引量
1	Association between MDM2-SNP309 and age at colorectal cancer diagnosis according to p53 mutation status显示文摘	MENIN C SCAINI M C DE SALVO G L	2006	J Natl Cancer lnst2006，98，4：	1
2	MDM2 SNP309 accelerates colorectal tumour formation in women显示文摘	Bond GL Menin C Bertorelle R	2006	J Med Genet2006，43，12：	1
3	Survivin expression impacts prognostically on NSCLC but not SCLC显示文摘	Rosato A Menin C Boldrin D	2013	Lung Cancer2013，79，2：	1
4	Survivin expression impacts prognostically on NSCLC but not SCLC显示文摘	ROSATO A MENIN C BOLDRIN D	2013	Lung Cancer2013，79，2：	1
5	Anomalous tran- scripts and allelic deletions of the FHIT gene in human esopha- geal eancer显示文摘	Menin C Santacatterina M Zambon A	2000	Cancer Genet Cytogenet2000，119，：	1
6	Anomalous tran- scripts and allelic deletious of the FHIT gene in human esopha- geal cancer显示文摘	Menin C Santacatterina M Zambon A	2000	Cancer Genet Cytogenet2000，119，：	1
7	Hepatosplenic gammadeha T-cell lymphoma presenting with immune-mediated thrombocytopenia and hemolytic anemia (Evans' syndrome)显示文摘	Motta G Vianello F Menin C	2002	Am J Hematol2002，69，4：	1
8	Smeared Crack Models for Reinforced Concrete Beams by Finite Element Method 显示文摘	Menin R C G Trautwein L M Bittencourt T N	2009	Ibracon Structures and Materials Journal2009，2，2：	1
9	Lack of association between androgen receptor CAG polymorphism and familial breast/ovarian cancer显示文摘	Banna G	2001	Cancer Lett2001，168，1：	1
10	Hepatosplenic gammadelta T-cell lymphoma presenting with immune-mediated thrombocytopenia and hemolytic anemia (Evans' syndrome)显示文摘	VIANELLO F MENIN C	2002	Am J Hematol2002，69，4：	1
11	Anomalous transcripts and allelic deletions of the FHIT gene in human esophageal cancer 显示文摘	Menin C Sanacatterina M Zambon A	2000	Cancer Genet Cytogenet2000，119，1：	1
12	Anomalous transcripts and alleic deletions of the FHIT gene in huamn esophageal cancer显示文摘	Santacatterina M Iambom A	2000	Cancer Genet Cytogenet2000，119，1：	1
13	Anomalous transcripts and allelic deletions of the FHIT gene in human esophageal cancer 显示文摘	Menin C Santacatterina M Zambon A	2000	Cancer Genet Cytogenet2000，119，：	1
14	Genomic rearrangements account for more than one-third of the BRCA1 mutations in northern Italian breast/ovarian cancer families显示文摘	Montagna MP Menin C Agata S		0，，：	1
15	TP53 gene mutations in gastric carcinoma detected by polymerase chain reaction/singlestrand conformation polymorphism analysis of archival material 显示文摘	Andrea E Baffa R Menin C	1995	Cancer Res Clin Oncol1995，121，：	1
16	STAT3 pathway is activat- ed in ALK-positive large B-cell lymphoma carrying SQSTM1- ALK rearrangement and provides a possible therapeutic target 显示文摘	d'Amore ES Visco C Menin A	2013	Am J Surg Pathol2013，37，5：	1
17	Macrocomp-artmentation of total creatine in cardiomyocytes revisited显示文摘	Menin L Panchichkina M Keriel C	2001	Mol Cell Biochem2001，220，12：	1
18	Survivin expression impacts prognostically on NSCLC but not SCLC 显示文摘	Rosato A Menin C Boldrin D	2013	Lung Cancer2013，79，2：	1
19	Anomalous transcripts and alleic deletion of the FHIT gene in human esophageal cancer 显示文摘	Menin C Santacatterina M Iambom A	2000	Cancer Cenet Cytogenet2000，119，1：	1
20	Anomalous transcripts and allelic deletions of the FHIT gene in human esophageal cancer显示文摘	Menin C Santacatterina M Zambon A	2000	Cancer Genet Cytogenet2000，119，1：	1

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