32
TITLE: Dynein and Mast/Orbit/CLASP have antagonistic roles in regulating kinetochore-microtubule plus-end dynamics
AUTHORS: Rita Reis; Talia Feijao; Susana Gouveia; Antonio J Pereira ; Irina Matos; Sampaio, P ; Helder Maiato ; Claudio E Sunkel ;
PUBLISHED: 2009, SOURCE: JOURNAL OF CELL SCIENCE, VOLUME: 122, ISSUE: 14
INDEXED IN: Scopus WOS CrossRef: 21
34
TITLE: Bruton Tyrosine Kinase (BTK) mutations in X-linked agammaglobulinaemia (XLA)  Full Text
AUTHORS: Fernandes, S; Sousa, S; Faria, E; Marques, L; Victor, B; Martins, M; Vassal, H; Gusmao, R; Barros, A ;
PUBLISHED: 2008, SOURCE: 13th European-Soc-for-Immunodeficiencies/10th Int-Patient-Org-for-Primary-Immunodeficiencies/8th Int-Nursing-Group-for-Immunodeficiencies Meeting in CLINICAL AND EXPERIMENTAL IMMUNOLOGY, VOLUME: 154
INDEXED IN: WOS
35
TITLE: Identification of new breakpoints in AZFb and AZFc
AUTHORS: Paula Costa; Rita Goncalves; Cristina Ferras ; Susana Fernandes; Ana Teresa Fernandes; Marrio Sousa ; Alberto Barros ;
PUBLISHED: 2008, SOURCE: MOLECULAR HUMAN REPRODUCTION, VOLUME: 14, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef: 33
36
TITLE: Abnormal methylation of imprinted genes in human sperm is associated with oligozoospermia
AUTHORS: Marques, CJ ; Costa, P; Vaz, B; Carvalho, F ; Fernandes, S; Barros, A ; Sousa, M ;
PUBLISHED: 2008, SOURCE: MOLECULAR HUMAN REPRODUCTION, VOLUME: 14, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef: 291
37
TITLE: Prevalence of structural autosomal abnormalities in 10248 infertile portuguese patients
AUTHORS: Lima, ; Doria, S ; Fernandes, S; Madureira, C; Almeida, C; Lemos, F; Reis, F; Pereira, S; Sousa, M; Barros, A ;
PUBLISHED: 2007, SOURCE: 6th European Cytogenetics Conference in CHROMOSOME RESEARCH, VOLUME: 15
INDEXED IN: WOS
38
TITLE: DAZ gene copies: evidence of Y chromosome evolution
AUTHORS: Ana Teresa Fernandes; Susana Fernandes; Rita Goncalves; Rosalia S ; Paula Costa; Alexandra Rosa; Cristina Ferras ; Mario Sousa ; Antonio Brehm; Alberto Barros ;
PUBLISHED: 2006, SOURCE: MOLECULAR HUMAN REPRODUCTION, VOLUME: 12, ISSUE: 8
INDEXED IN: Scopus WOS CrossRef: 16
40
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
Page 4 of 5. Total results: 45.