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DataTítuloAutor(es)TipoAcesso
Mai-2009G2P[4] the most prevalent rotavirus genotype in 2007 winter season in an European non-vaccinated populationAntunes, Henedina; Afonso, Ariana; Iturriza, Miren, et al.ArtigoAcesso aberto
2016Gaps and barriers to tuberculosis screening among anti-tumor necrosis factor prescribersXerinda, Sandra; Oliveira, Olena; Lucas, Raquel, et al.ArtigoAcesso restrito UMinho
2019Gastrointestinal dysfunction in patients and mice expressing the autism-associated R451C mutation in neuroligin-3Hosie, Suzanne; Ellis, Melina; Swaminathan, Mathusi, et al.ArtigoAcesso aberto
2014Gellan gum-hyaluronic acid spongy-like hydrogels and cells from adipose tissue synergize promoting neoskin vascularizationCerqueira, Mariana Teixeira; Silva, Lucília Pereira; Santos, Tírcia Carlos, et al.ArtigoAcesso restrito UMinho
2014Gene disruption using zinc finger nuclease technologyGranja, Sara Costa; Marchiq, Ibtissam; Baltazar, Fátima, et al.Capítulo de livroAcesso restrito autor
2018Generation of a human induced pluripotent stem cell line (CSC-40) from a Parkinson's disease patient with a PINK1 p.Q456X mutationRuss, Kaspar; Marote, Ana Maria Franco Aveiro; Savchenko, Ekaterina, et al.ArtigoAcesso aberto
2018Generation of a human induced pluripotent stem cell line (CSC-42) from a patient with sporadic form of Parkinson's diseaseSavchenko, Ekaterina; Marote, Ana Maria Franco Aveiro; Russ, Kaspar, et al.ArtigoAcesso aberto
2018Generation of an induced pluripotent stem cell line (CSC-41) from a Parkinson's disease patient carrying a p.G2019S mutation in the LRRK2 geneMarote, Ana; Pomeshchik, Yuriy; Collin, Anna, et al.ArtigoAcesso aberto
Mar-2018Generation of an induced pluripotent stem cell line (CSC-44) from a Parkinson's disease patient carrying a compound heterozygous mutation (c.823C>T and EX6 del) in the PARK2 geneMarote, Ana Maria Franco Aveiro; Pomeshchik, Yuriy; Goldwurm, Stefano, et al.ArtigoAcesso aberto
Jan-2019Generation of an induced pluripotent stem cell line (CSC-46) from a patient with Parkinson's disease carrying a novel p.R301C mutation in the GBA geneGustavsson, Nadja; Marote, Ana; Pomeshchik, Yuriy, et al.ArtigoAcesso aberto
2018Generation of an integration-free induced pluripotent stem cell line (CSC-43) from a patient with sporadic Parkinson's diseaseMarote, Ana Maria Franco Aveiro; Pomeshchik, Yuriy; Goldwurm, Stefano, et al.ArtigoAcesso aberto
2019Genetic defects in fungal recognition and susceptibility to invasive pulmonary aspergillosisCunha, Cristina Amorim; Carvalho, AgostinhoArtigoAcesso aberto
2018Genetic deficiency of NOD2 confers resistance to invasive aspergillosisGresnigt, Mark S.; Cunha, Cristina; Jaeger, Martin, et al.ArtigoAcesso aberto
2016Genetic Determinants of Drug Resistance in Mycobacterium tuberculosis and Their Diagnostic ValueFarhat, Maha R.; Sultana, Razvan; Iartchouk, Oleg, et al.ArtigoAcesso restrito UMinho
Jul-2003Genetic interaction of CTLA-4 with HLA-DR15 in multiple sclerosis patientsAlizadeh, Mehdi; Babron, Marie-Claude; Birebent, Brigitte, et al.ArtigoAcesso restrito UMinho
2018Genetic profile and patient-reported outcomes in chronic obstructive pulmonary disease: A systematic reviewMelro, Hélder; Gomes, Jorge; Moura, Gabriela, et al.ArtigoAcesso aberto
Mar-2018Genetic variants of vascular endothelial growth factor predict risk and survival of gliomasLinhares, Paulo; Pereira, Marta Sofia Carvalho Ribeiro Viana; Ferreira, Mónica, et al.ArtigoAcesso aberto
2015Genome-wide association study identifies variants at 16p13 associated with survival in multiple myeloma patientsZiv, Elad; Dean, Eric; Hu, Donglei, et al.ArtigoAcesso aberto
Nov-2021Geological and hydrogeological review of a semi-arid region with conflicts to water availability (southeastern Brazil)Bhering, Apolo P.; Antunes, Isabel Margarida Horta Ribeiro; Marques, Eduardo A. G., et al.ArtigoAcesso aberto
2015Gestational age and fetal growth assessment among obstetriciansSousa-Santos, Ricardo F.; Mendes-Castro, Alfredo; Ferreira, Dânia, et al.ArtigoAcesso restrito autor
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