Detalles de la búsqueda
1.
Recurrent ETNK1 mutations in atypical chronic myeloid leukemia.
Blood
; 125(3): 499-503, 2015 Jan 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-25343957
2.
FusionAnalyser: a new graphical, event-driven tool for fusion rearrangements discovery.
Nucleic Acids Res
; 40(16): e123, 2012 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-22570408
3.
Gene expression signature of non-involved lung tissue associated with survival in lung adenocarcinoma patients.
Carcinogenesis
; 34(12): 2767-73, 2013 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-23978379
4.
A computational procedure to identify significant overlap of differentially expressed and genomic imbalanced regions in cancer datasets.
Nucleic Acids Res
; 37(15): 5057-70, 2009 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-19542187
5.
Candidate Genes and MiRNAs Linked to the Inverse Relationship Between Cancer and Alzheimer's Disease: Insights From Data Mining and Enrichment Analysis.
Front Genet
; 10: 846, 2019.
Artículo
en Inglés
| MEDLINE | ID: mdl-31608105
6.
Genome-wide screening of copy number alterations and LOH events in renal cell carcinomas and integration with gene expression profile.
Mol Cancer
; 7: 6, 2008 Jan 14.
Artículo
en Inglés
| MEDLINE | ID: mdl-18194544
7.
[Combined vaccine against measles, mumps, rubella and varicella and recommendations for varicella immunization in Italy?]. / Il vaccino quadruplo contro morbillo, parotite, rosolia e varicella modificherà le indicazioni per la profilassi dell'infezione da virus varicella zoster in italia?
Ig Sanita Pubbl
; 63(6): 715-22, 2007.
Artículo
en Italiano
| MEDLINE | ID: mdl-18216886
8.
Erratum: OncoScore: a novel, Internet-based tool to assess the oncogenic potential of genes.
Sci Rep
; 7: 46823, 2017 05 22.
Artículo
en Inglés
| MEDLINE | ID: mdl-28530230
9.
OncoScore: a novel, Internet-based tool to assess the oncogenic potential of genes.
Sci Rep
; 7: 46290, 2017 04 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-28387367
10.
Read-through transcripts in normal human lung parenchyma are down-regulated in lung adenocarcinoma.
Oncotarget
; 7(19): 27889-98, 2016 May 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-27058892
11.
CEQer: a graphical tool for copy number and allelic imbalance detection from whole-exome sequencing data.
PLoS One
; 8(10): e74825, 2013.
Artículo
en Inglés
| MEDLINE | ID: mdl-24124457
12.
Identification of novel point mutations in splicing sites integrating whole-exome and RNA-seq data in myeloproliferative diseases.
Mol Genet Genomic Med
; 1(4): 246-59, 2013 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-24498620
13.
Whole genome SNP genotyping and exome sequencing reveal novel genetic variants and putative causative genes in congenital hyperinsulinism.
PLoS One
; 8(7): e68740, 2013.
Artículo
en Inglés
| MEDLINE | ID: mdl-23869231
14.
Recurrent SETBP1 mutations in atypical chronic myeloid leukemia.
Nat Genet
; 45(1): 18-24, 2013 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-23222956
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