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Bruno Filipe Marques da Costa
AuthID:
R-000-2TS
Publications
Confirmed
To Validate
Document Source:
All
Document Type:
All Document Types
Article (49)
Review (9)
Abstract (3)
Article in Press (3)
Editorial Material (2)
Book Chapter (1)
Year Start - End:
2007
2008
2009
2010
2011
2012
2013
2014
2015
2016
2017
2018
2019
2020
2021
2022
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2025
2024
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2021
2020
2019
2018
2017
2016
2015
2014
2013
2012
2011
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2009
2008
2007
Order:
Year Dsc
Year Asc
Cit. WOS Dsc
IF WOS Dsc
Cit. Scopus Dsc
IF Scopus Dsc
Title Asc
Title Dsc
Results:
10
20
30
40
50
Confirmed Publications: 67
41
TITLE:
Understanding TERT Promoter Mutations: A Common Path to Immortality
AUTHORS:
Robert J A Bell
;
Tomas T Rube
; Ana Xavier Magalhaes;
Bruno M Costa
; Andrew Mancini; Jun S Song; Joseph F Costello;
PUBLISHED:
2016
,
SOURCE:
MOLECULAR CANCER RESEARCH,
VOLUME:
14,
ISSUE:
4
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
|
CIÊNCIAVITAE
42
TITLE:
A transcriptomic signature mediated by HOXA9 promotes human glioblastoma initiation, aggressiveness and resistance to temozolomide
AUTHORS:
Marta Pojo
; Celine S Goncalves; Ana Xavier Magalhaes;
Ana Isabel Oliveira
;
Tiago Goncalves
;
Sara Correia
;
Ana J Rodrigues
;
Sandra Costa
;
Luisa Pinto
; Afonso A Pinto;
Lopes, JM
;
Rui M Reis
;
Miguel Rocha
;
Nuno Sousa
;
Bruno M Costa
;
PUBLISHED:
2015
,
SOURCE:
ONCOTARGET,
VOLUME:
6,
ISSUE:
10
INDEXED IN:
Scopus
WOS
CrossRef
:
44
IN MY:
ORCID
|
CIÊNCIAVITAE
43
TITLE:
Expression of histone methyltransferases as novel biomarkers for renal cell tumor diagnosis and prognostication
AUTHORS:
Pires Luis, AS; Vieira Coimbra, M;
Vieira, FQ
; Costa Pinheiro, P; Silva Santos, R; Dias, PC; Antunes, L; Lobo, F; Oliveira, J; Goncalves, CS;
Costa, BM
;
Henrique, R
;
Carmen Jerónimo
;
PUBLISHED:
2015
,
SOURCE:
EPIGENETICS,
VOLUME:
10,
ISSUE:
11
INDEXED IN:
Scopus
WOS
CrossRef
Handle
IN MY:
ORCID
|
CIÊNCIAVITAE
44
TITLE:
Impact of TGF-β1 -509C/T and 869T/C polymorphisms on glioma risk and patient prognosis
AUTHORS:
Vieira de Castro, J; Goncalves, CS;
Costa, S
; Linhares, P; Vaz, R; Nabico, R; Amorim, J;
Viana Pereira, M
;
Reis, RM
;
Costa, BM
;
PUBLISHED:
2015
,
SOURCE:
Tumor Biology,
VOLUME:
36,
ISSUE:
8
INDEXED IN:
Scopus
CrossRef
IN MY:
ORCID
|
CIÊNCIAVITAE
45
TITLE:
Mesenchymal stem cells secretome as a modulator of the neurogenic niche: basic insights and therapeutic opportunities
Full Text
AUTHORS:
Antonio J Salgado
;
Joao C Sousa
;
Bruno M Costa
;
Ana O Pires
;
Antonio Mateus Pinheiro
;
Teixeira, FG
;
Luisa Pinto
;
Nuno Sousa
;
PUBLISHED:
2015
,
SOURCE:
FRONTIERS IN CELLULAR NEUROSCIENCE,
VOLUME:
9,
ISSUE:
JULY
INDEXED IN:
Scopus
WOS
CrossRef
:
73
IN MY:
ORCID
|
CIÊNCIAVITAE
46
TITLE:
MicroRNA-375 plays a dual role in prostate carcinogenesis
AUTHORS:
Costa Pinheiro, P; Ramalho Carvalho, J;
Vieira, FQ
; Torres Ferreira, J; Oliveira, J; Goncalves, CS;
Costa, BM
;
Henrique, R
;
Carmen Jerónimo
;
PUBLISHED:
2015
,
SOURCE:
CLINICAL EPIGENETICS,
VOLUME:
7,
ISSUE:
1
INDEXED IN:
Scopus
WOS
CrossRef
Handle
IN MY:
ORCID
|
CIÊNCIAVITAE
47
TITLE:
Transcriptional profiling of HOXA9-regulated genes in human glioblastoma cell models
AUTHORS:
Goncalves, CS; Xavier Magalhaes, A; Pojo, M; Oliveira, AI; Correia, S; Reis, RM;
Sousa, N
;
Rocha, M
;
Costa, BM
;
PUBLISHED:
2015
,
SOURCE:
GENOMICS DATA,
VOLUME:
5
INDEXED IN:
Scopus
WOS
IN MY:
ORCID
|
CIÊNCIAVITAE
48
TITLE:
Transcriptional profiling of HOXA9-regulated genes in human glioblastoma cell models
AUTHORS:
Céline S Gonçalves;
Ana Xavier-Magalhães
;
Marta Pojo
; Ana Isabel Oliveira; Sara Correia;
Rui M Reis
;
Nuno Sousa
;
Miguel Rocha
;
Bruno M Costa
;
PUBLISHED:
2015
,
SOURCE:
Genomics Data,
VOLUME:
5
INDEXED IN:
CrossRef
IN MY:
ORCID
|
CIÊNCIAVITAE
49
TITLE:
Variant Rett syndrome in a girl with a pericentric X-chromosome inversion leading to epigenetic changes and overexpression of the MECP2 gene
Full Text
AUTHORS:
Vieira, JP; Lopes, F;
Silva Fernandes, A
; Sousa, MV; Moura, S; Sousa, S;
Costa, BM
; Barbosa, M; Ylstra, B; Temudo, T; Lourenco, T;
Maciel, P
;
PUBLISHED:
2015
,
SOURCE:
INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE,
VOLUME:
46
INDEXED IN:
Scopus
WOS
IN MY:
ORCID
|
CIÊNCIAVITAE
50
TITLE:
Variant Rett syndrome in a girl with a pericentric X-chromosome inversion leading to epigenetic changes and overexpression of the MECP2 gene
Full Text
AUTHORS:
José Pedro Vieira; Fátima Lopes;
Anabela Silva-Fernandes
; Maria Vânia Sousa; Sofia Moura; Susana Sousa;
Bruno M Costa
; Mafalda Barbosa; Bauke Ylstra; Teresa Temudo; Teresa Lourenço;
Patrícia Maciel
;
PUBLISHED:
2015
,
SOURCE:
International Journal of Developmental Neuroscience,
VOLUME:
46
INDEXED IN:
CrossRef
IN MY:
ORCID
|
CIÊNCIAVITAE
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