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Ana Isabel Fernandes Grangeia
AuthID:
R-000-K8X
Publications
Confirmed
To Validate
Document Source:
All
Document Type:
All Document Types
Article (29)
Abstract (3)
Editorial Material (2)
Article in Press (2)
Review (1)
Correction (1)
Letter (1)
Year Start - End:
2004
2005
2006
2007
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2005
2004
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: 39
31
TITLE:
Association of cystic fibrosis genetic modifiers with congenital bilateral absence of the vas deferens
AUTHORS:
Viktoria Havasi;
Steven M Rowe
;
Peter N Kolettis
;
Didem Dayangac
; Ahmet Sahin;
Ana Grangeia
;
Filipa Carvalho
;
Alberto Barros
;
Mario Sousa
;
Lluis Bassas
; Teresa Casals; Eric J Sorscher;
PUBLISHED:
2010
,
SOURCE:
FERTILITY AND STERILITY,
VOLUME:
94,
ISSUE:
6
INDEXED IN:
Scopus
WOS
CrossRef
:
17
IN MY:
ORCID
|
CIÊNCIAVITAE
32
TITLE:
Molecular and functional characterization of CBAVD-causing mutations located in CFTR nucleotide-binding domains
AUTHORS:
Ana Grangeia
; Rene Barro Soria;
Filipa Carvalho
;
Ana M Damas
;
Ana Colette Mauricio
;
Karl Kunzelmann
;
Alberto Barros
;
Mario Sousa
;
PUBLISHED:
2008
,
SOURCE:
CELLULAR PHYSIOLOGY AND BIOCHEMISTRY,
VOLUME:
22,
ISSUE:
1-4
INDEXED IN:
Scopus
WOS
CrossRef
:
7
IN MY:
ORCID
|
CIÊNCIAVITAE
33
TITLE:
Molecular characterisation of the cystic fibrosis transmembrane conductance regulator gene in congenital absence of the vas deferens
AUTHORS:
Grangeia, A
;
Sa, R
;
Carvalho, F
; Martin, J; Girodon, E; Ferraz, L;
Barros, A
; Sousa, M;
PUBLISHED:
2007
,
SOURCE:
23rd Annual Meeting of the European-Society-of-Human-Reproduction-and-Embryology
in
HUMAN REPRODUCTION,
VOLUME:
22
INDEXED IN:
WOS
IN MY:
ORCID
34
TITLE:
Molecular characterization of the cystic fibrosis transmembrane conductance regulator gene in congenital absence of the vas deferens
AUTHORS:
Ana Grangeia
;
Rosalia Sa
;
Filipa Carvalho
; Josiane Martin; Emmanuelle Girodon; Joaquina Silva; Luis Ferraz;
Alberto Barros
;
Mario Sousa
;
PUBLISHED:
2007
,
SOURCE:
GENETICS IN MEDICINE,
VOLUME:
9,
ISSUE:
3
INDEXED IN:
Scopus
WOS
CrossRef
:
26
IN MY:
ORCID
|
CIÊNCIAVITAE
35
TITLE:
CFTR rearrangements in CAVD patients
AUTHORS:
Grangeia, A
;
Carvalho, F
; Girodon, E; Silva, J; Sousa, M;
Barros, A
;
PUBLISHED:
2006
,
SOURCE:
22nd Annual Meeting of the European-Society-of-Human-Reproduction-and-Embryology
in
HUMAN REPRODUCTION,
VOLUME:
21
INDEXED IN:
WOS
IN MY:
ORCID
36
TITLE:
A novel missense mutation P1290S at exon-20 of the CFTR gene in a Portuguese patient with congenital bilateral absence of the vas deferens
AUTHORS:
Grangeia, A
;
Carvalho, F
;
Fernandes, S
; Silva, J;
Sousa, M
;
Barros, A
;
PUBLISHED:
2005
,
SOURCE:
FERTILITY AND STERILITY,
VOLUME:
83,
ISSUE:
2
INDEXED IN:
Scopus
WOS
CrossRef
:
8
IN MY:
ORCID
|
CIÊNCIAVITAE
37
TITLE:
A RhoGAP protein as a main immune suppressive factor in the Leptopilina boulardi (Hymenoptera, Figitidae)–Drosophila melanogaster interaction
Full Text
AUTHORS:
Labrosse, C; Stasiak, K; Lesobre, J;
Grangeia, A
; Huguet, E; J.M Drezen; Poirie, M;
PUBLISHED:
2005
,
SOURCE:
Insect Biochemistry and Molecular Biology,
VOLUME:
35,
ISSUE:
2
INDEXED IN:
CrossRef
:
110
IN MY:
ORCID
|
CIÊNCIAVITAE
38
TITLE:
CFTR gene mutations in congenital absence of vas deferens [Estudo das mutações do gene CFTR na ausência congénita dos canais deferentes]
AUTHORS:
Grangeia, A
;
Carvalho, F
;
Sousa, M
;
Barros, A
;
PUBLISHED:
2004
,
SOURCE:
Arquivos de Medicina,
VOLUME:
18,
ISSUE:
1-2
INDEXED IN:
Scopus
IN MY:
ORCID
|
CIÊNCIAVITAE
39
TITLE:
Characterization of cystic fibrosis conductance transmembrane regulator gene mutations and IVS8 poly(T) variants in Portuguese patients with congenital absence of the vas deferens
AUTHORS:
Grangeia, A
; Niel, F;
Carvalho, F
;
Fernandes, S
; Ardalan, A; Girodon, E; Silva, J;
Ferras, L
;
Sousa, M
;
Barros, A
;
PUBLISHED:
2004
,
SOURCE:
HUMAN REPRODUCTION,
VOLUME:
19,
ISSUE:
11
INDEXED IN:
Scopus
WOS
CrossRef
:
35
IN MY:
ORCID
|
CIÊNCIAVITAE
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