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Name
Melo, Joana Barbosa
 
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Results 1-27 of 27 (Search time: 0.241 seconds).

Issue DateTitleAuthor(s)TypeAccess
115-Jun-2009Analytical Approaches toward Successful Human Cell Metabolome Studies by NMR SpectroscopyDuarte, Iola F. ; Marques, Joana ; Ladeirinha, Ana F. ; Rocha, Cláudia ; Lamego, Inês ; Calheiros, Rita ; Silva, Tânia M. ; Marques, M. Paula M. ; Melo, Joana B. ; Carreira, Isabel M. ; Gil, Ana M. articleopenAccess
2May-2016BIRC3 alterations in chronic and B-cell acute lymphocytic leukemia patientsAlhourani, Eyad ; Othman, Moneeb A. K. ; Melo, Joana Barbosa ; Carreira, Isabel M. ; Grygalewicz, Beata; Vujić, Dragana; Zecević, Zeljko; Joksić, Gordana; Glaser, Anita ; Pohle, Beate; Schlie, Cordula; Hauke, Sven; Liehr, Thomas articleopenAccess
3Sep-2013Caraterização do perfil genómico do carcinoma pulmonarPortovedo, Sérgio Filipe de JesusmasterThesisopenAccess
42015Copy number variants prioritization after array-CGH analysis - a cohort of 1000 patientsCarreira, Isabel Marques ; Ferreira, Susana Isabel ; Matoso, Eunice ; Pires, Luís Miguel ; Ferrão, José ; Jardim, Ana ; Mascarenhas, Alexandra ; Pinto, Marta ; Lavoura, Nuno ; Pais, Claudia ; Paiva, Patrícia ; Simões, Lúcia ; Caramelo, Francisco ; Ramos, Lina ; Venâncio, Margarida ; Ramos, Fabiana; Beleza, Ana; Sá, Joaquim ; Saraiva, Jorge ; Melo, Joana Barbosa de articleopenAccess
52-May-2012Critical region in 2q31.2q32.3 deletion syndrome: Report of two phenotypically distinct patients, one with an additional deletion in Alagille syndrome regionFerreira, Susana Isabel ; Matoso, Eunice ; Venâncio, Margarida ; Saraiva, Jorge ; Melo, Joana B. ; Carreira, Isabel Marques articleopenAccess
62015Cutis Aplasia as a clinical hallmark for the syndrome associated with 19q13.11 deletion: the possible role for UBA2 geneMelo, Joana B. ; Estevinho, Alexandra ; Saraiva, Jorge; Ramos, Lina ; Carreira, Isabel M. articleopenAccess
723-Sep-2019Cytogenetics and Cytogenomics Evaluation in CancerRibeiro, Ilda Patrícia ; Melo, Joana Barbosa ; Carreira, Isabel Marques articleopenAccess
8May-2021DEPDC5 variant in focal cortical dysplasia: a case report and review of the literatureRibeiro, Joana de Jesus ; Pereira, Cristina Duarte ; Robalo, Conceição ; Pereira, Daniela J.; Duro, Diana ; Ramos, Fabiana ; Freire, António ; Melo, Joana B. articleopenAccess
92016Early detection and personalized treatment in oral cancer: the impact of omics approachesRibeiro, Ilda Patrícia ; Barroso, Leonor ; Marques, Francisco ; Melo, Joana Barbosa ; Carreira, Isabel Marques articleopenAccess
1022-Jun-2016Fibroblasts of Machado Joseph Disease patients reveal autophagy impairmentOnofre, Isabel ; Mendonça, Nuno ; Lopes, Sara ; Nobre, Rui J. ; Melo, Joana Barbosa ; Carreira, Isabel Marques ; Januário, Cristina ; Gonçalves, António Freire ; Almeida, Luís Pereira de articleopenAccess
11May-2018Generation and characterization of a human iPS cell line from a patient-related control to study disease mechanisms associated with DAND5 p.R152H alterationPars, Selin; Cristo, Fernando; Inácio, José M.; Rosas, Graça; Carreira, Isabel Marques ; Melo, Joana Barbosa ; Mendes, Patrícia; Martins, Duarte Saraiva; Almeida, Luís Pereira de ; Maio, José; Anjos, Rui ; Belo, José A.articleopenAccess
122017Genetic and epigenetic characterization of the tumors in a patient with a tongue primary tumor, a recurrence and a pharyngoesophageal second primary tumorRibeiro, Ilda Patrícia ; Marques, Francisco ; Barroso, Leonor ; Miguéis, Jorge ; Caramelo, Francisco ; Santos, André ; Julião, Maria J.; Melo, Joana B. ; Carreira, Isabel M. articleopenAccess
132018Genomic and epigenetic signatures associated with survival rate in oral squamous cell carcinoma patientsRibeiro, Ilda Patrícia ; Caramelo, Francisco ; Esteves, Luísa ; Oliveira, Camila ; Marques, Francisco ; Barroso, Leonor ; Melo, Joana Barbosa ; Carreira, Isabel Marques articleopenAccess
1424-Oct-2017Genomic predictive model for recurrence and metastasis development in head and neck squamous cell carcinoma patientsRibeiro, Ilda Patrícia ; Caramelo, Francisco ; Esteves, Luísa ; Menoita, Joana ; Marques, Francisco ; Barroso, Leonor ; Miguéis, Jorge ; Melo, Joana Barbosa ; Carreira, Isabel Marques articleopenAccess
152015High rates of submicroscopic aberrations in karyotypically normal acute lymphoblastic leukemiaOthman, Moneeb A. K. ; Melo, Joana B. ; Carreira, Isabel M. ; Rincic, Martina ; Glaser, Anita ; Grygalewicz, Beata; Gruhn, Bernd; Wilhelm, Kathleen; Rittscher, Katharina; Meyer, Britta; Silva, Maria Luiza Macedo; de Jesus Marques Salles, Terezinha; Liehr, Thomas articleopenAccess
1614-Aug-2023Interaction between genetics and the adherence to the Mediterranean diet: the risk for age-related macular degeneration. Coimbra Eye Study Report 8Barreto, Patrícia ; Farinha, Cláudia ; Coimbra, Rita ; Cachulo, Maria da Luz ; Melo, Joana Barbosa ; Lechanteur, Yara; Hoyng, Carel B.; Cunha-Vaz, José ; Silva, Rufino articleopenAccess
172015Isochromosome 17q in Chronic Lymphocytic LeukemiaAlhourani, Eyad ; Rincic, Martina ; Melo, Joana B. ; Carreira, Isabel M. ; Glaser, Anita ; Pohle, Beate; Schlie, Cordula; Liehr, Thomas articleopenAccess
187-May-2021Mitochondrial Alterations in Fibroblasts of Early Stage Bipolar Disorder PatientsMarques, Ana P. ; Resende, Rosa ; Silva, Diana F. ; Batista, Mariana ; Pereira, Daniela ; Wildenberg, Brigite ; Morais, Sofia ; Macedo, António ; Pais, Claudia ; Melo, Joana B. ; Madeira, Nuno ; Pereira, Cláudia F. articleopenAccess
192017MLPA analysis in a cohort of patients with autismPeixoto, Sara ; Melo, Joana B. ; Ferrão, José ; Pires, Luís M. ; Lavoura, Nuno ; Pinto, Marta ; Oliveira, Guiomar ; Carreira, Isabel M. articleopenAccess
202009Molecular cytogenetic characterisation of a mosaic add(12)(p13.3) with an inv dup(3)(q26.31 → qter) detected in an autistic boyCarreira, Isabel M. ; Melo, Joana B. ; Rodrigues, Carlos F. D. ; Backx, Liesbeth; Vermeesch, Joris; Weise, Anja; Kosyakova, Nadezda; Oliveira, Guiomar ; Matoso, Eunice articleopenAccess
21Feb-2020Molecular cytogenetic pilot study on pleomorphic adenomas of salivary glandsThielker, Jovanna; Weise, Anja; Othman, Moneeb A. K. ; Carreira, Isabel M. ; Melo, Joana B. ; Von Eggeling, Ferdinand; Guntinas-Lichius, Orlando; Ziegler, Monika; Liehr, Thomas articleopenAccess
222014A Novel Cryptic Three-Way Translocation t(2;9;18)(p23.2;p21.3;q21.33) with Deletion of Tumor Suppressor Genes in 9p21.3 and 13q14 in a T-Cell Acute Lymphoblastic LeukemiaOthman, Moneeb A. K. ; Rincic, Martina ; Melo, Joana B. ; Carreira, Isabel M. ; Alhourani, Eyad ; Hunstig, Friederike ; Glaser, Anita ; Liehr, Thomas articleopenAccess
2329-Apr-2022Nucleolin Overexpression Predicts Patient Prognosis While Providing a Framework for Targeted Therapeutic Intervention in Lung CancerFernandes, Ângela Valério ; Fonseca, Nuno A. ; Gonçalves, Nélio ; Cruz, Ana F. ; Pereira, Marta I. ; Gregório, Ana C. ; Moura, Vera ; Ladeirinha, Ana F. ; Alarcão, Ana ; Gonçalves, Joana ; Abrunhosa, Antero ; Melo, Joana B. ; Carvalho, Lina ; Simões, Sérgio ; Moreira, João N. articleopenAccess
243-Apr-2023Resective Epilepsy Surgery and Respective Histopathological Diagnoses: A Retrospective Cohort StudyJesus-Ribeiro, Joana ; Rebelo, Olinda ; Bento, Conceição; Pereira, Cristina Maria Gonçalves ; Robalo, Conceição ; Rito, Manuel; Pereira, Ricardo; Costa, José Augusto; Melo, Joana Barbosa ; Freire, António ; Santana, Isabel ; Sales, Francisco articleopenAccess
2518-Jun-2021The Enhanced Efficacy of Intracellular Delivery of Doxorubicin/C6-Ceramide Combination Mediated by the F3 Peptide/Nucleolin System Is Supported by the Downregulation of the PI3K/Akt PathwayCruz, Ana F. ; Caleiras, Mariana B. ; Fonseca, Nuno A. ; Gonçalves, Nélio ; Mendes, Vera M. ; Sampaio, Susana F. ; Moura, Vera ; Melo, Joana B. ; Almeida, Ramiro D. ; Manadas, Bruno ; Simões, Sérgio Paulo ; Moreira, João N. articleopenAccess
26May-2020Upper aerodigestive tract carcinoma: Development of a (epi)genomic predictive model for recurrence and metastasisRibeiro, Ilda Patrícia ; Caramelo, Francisco ; Ribeiro, Margarida ; Machado, Ana; Miguéis, Jorge ; Marques, Francisco; Carreira, Isabel Marques ; Melo, Joana Barbosa articleopenAccess
2720-Jul-2010X-chromosome terminal deletion in a female with premature ovarian failure: Haploinsufficiency of X-linked genes as a possible explanationFerreira, Susana I. ; Matoso, Eunice ; Pinto, Marta ; Almeida, Joana ; Liehr, Thomas ; Melo, Joana B. ; Carreira, Isabel M. articleopenAccess