| Preview | Issue Date | Title | Author(s) | Advisor | Type |
| - | Combination Of Angiotensin-converting Enzyme And Methylenetetrahydrofolate Reductase Gene Polymorphisms As Determinant Risk Factors For Chronic Allograft Dysfunction. | de Alvarenga, M P S; Pavarino-Bertelli, E C; Abbud-Filho, M; Ferreira-Baptista, M A S; Haddad, R; Eberlin, M N; Goloni-Bertollo, E M | - | Artigo de periódico |
| 2010 | Novel Deletion Alleles Carrying Cyp21a1p/a2 Chimeric Genes In Brazilian Patients With 21-hydroxylase Deficiency. | Coeli, Fernanda B; Soardi, Fernanda C; Bernardi, Renan D; de Araújo, Marcela; Paulino, Luciana C; Lau, Ivy F; Petroli, Reginaldo J; de Lemos-Marini, Sofia H V; Baptista, Maria T M; Guerra-Júnior, Gil; de-Mello, Maricilda P | - | Artigo de periódico |
| 2006 | Yeast Oxidative Stress Response. Influences Of Cytosolic Thioredoxin Peroxidase I And Of The Mitochondrial Functional State. | Demasi, Ana P D; Pereira, Gonçalo A G; Netto, Luis E S | - | Artigo de periódico |
| 2007 | Molecular Genetics Study Of Deafness In Brazil: 8-year Experience. | de Oliveira, Camila Andréa; Alexandrino, Fabiana; Christiani, Thalita Vitachi; Steiner, Carlos Eduardo; Cunha, José Luiz Rosemberis; Guerra, Andréa Trevas Maciel; Sartorato, Edi Lúcia | - | Artigo de periódico |
| 2013 | Optimization Of Simultaneous Screening Of The Main Mutations Involved In Non-syndromic Deafness Using The Taqman® Openarray™ Genotyping Platform. | Martins, Fábio Tadeu Arrojo; Ramos, Priscila Zonzini; Svidnicki, Maria Carolina Costa Melo; Castilho, Arthur Menino; Sartorato, Edi Lúcia | - | Artigo de periódico |
| 1996 | Molecular Analysis Of Cyp21 And C4 Genes In Brazilian Families With The Classical Form Of Steroid 21-hydroxylase Deficiency. | de-Araujo, M; Sanches, M R; Suzuki, L A; Guerra, G; Farah, S B; de-Mello, M P | - | Artigo de periódico |
| 2013 | Study Of Candidate Genes For Dyslexia In Brazilian Individuals. | Svidnicki, M C C M; Salgado, C A; Lima, R F; Ciasca, S M; Secolin, R; Pomilio, M C A; Junqueira, P A; Pinto, M S; Pereira, M M; Sartorato, E L | - | Artigo de periódico |
| 2012 | Thrombomodulin Is Required For The Antithrombotic Activity Of Thrombin Mutant W215a/e217a In A Mouse Model Of Arterial Thrombosis. | Vicente, Cristina P; Weiler, Hartmut; Di Cera, Enrico; Tollefsen, Douglas M | - | Artigo de periódico |
| 1999 | Mutation Distribution And Cyp21/c4 Locus Variability In Brazilian Families With The Classical Form Of The 21-hydroxylase Deficiency. | Paulino, L C; Araujo, M; Guerra, G; Marini, S H; De Mello, M P | - | Artigo de periódico |
| 2003 | Simple Fluorescent Pcr Method For Detection Of Large Deletions In The Beta-globin Gene Cluster. | De Andrade, Tiago Gomes; Saad, Sara Teresinha Olalla; Sonati, Maria de Fatima; Costa, Fernando Ferreira | - | Artigo de periódico |
| - | Abo Blood Group In Amerindians From Brazilian Amazon. | Barjas-Castro, M L; Soares, M C P; Menezes, R C; Carvalho, M H M; Costa, F F; Saad, S T O | - | Artigo de periódico |
| - | Cystic Fibrosis Transmembrane Conductance Regulator Gene Mutations And Glutathione S-transferase Null Genotypes In Cystic Fibrosis Patients In Brazil. | Lima, Carmen Silvia Passos; Ortega, Manoela Marques; Marson, Fernando Augusto Lima; Zulli, Roberto; Ribeiro, Antônio Fernando; Bertuzzo, Carmen Silvia | - | Artigo de periódico |
| 2001 | High Prevalence Of Alpha-thalassemia Among Individuals With Microcytosis And Hypochromia Without Anemia. | Borges, E; Wenning, M R; Kimura, E M; Gervásio, S A; Costa, F F; Sonati, M F | - | Artigo de periódico |
| 2002 | Hemoglobin H Disease Resulting From The Association Of The - Alpha 3.7 Rightward Deletion And The (alpha Alpha)mm Deletion In A Brazilian Patient. | Wenning, M R S C; Harteveld, C L; Giordano, P C; Kimura, E M; Saad, S T O; Costa, F F; Sonati, M F | - | Artigo de periódico |
| 2002 | Alpha-thalassemia Does Not Significantly Contribute To The Low Mcv Level Of Hb C Trait. | Silva, Nadia M; Soledade, Cinira S; Costa, Fernando F; Sonati, Maria F | - | Artigo de periódico |
| 2011 | Genomic Imbalances Detected Through Array Cgh In Fetuses With Holoprosencephaly. | Machado, Isabela Nelly; Heinrich, Juliana Karina; Barini, Ricardo | - | Artigo de periódico |
| 2003 | The Hansenula Polymorpha Mox Gene Presents Two Alternative Transcription Start Points Differentially Utilized And Sensitive To Respiratory Activity. | Genu, Victor; Gödecke, Stefanie; Hollenberg, Cornelis P; Pereira, Gonçalo G | - | Artigo de periódico |
| 2005 | Rhnull Syndrome: Identification Of A Novel Mutation In Rhce. | Rosa, K A; Reid, M E; Lomas-Francis, C; Powell, V I; Costa, F F; Stinghen, S T; Watanabe, A M; Carboni, E K; Baldon, J P; Jucksch, M M F; Castilho, L | - | Artigo de periódico |
| 2005 | Molecular Analysis Of Kal-1, Gnrh-r, Nelf And Ebf2 Genes In A Series Of Kallmann Syndrome And Normosmic Hypogonadotropic Hypogonadism Patients. | Trarbach, Ericka B; Baptista, Maria T M; Garmes, Heraldo M; Hackel, Christine | - | Artigo de periódico |
| - | A Naturally Occurring Deletion In The Sry Promoter Region Affecting The Sp1 Binding Site Is Associated With Sex Reversal. | Assumpção, J G; Ferraz, L F Caldas; Benedetti, C E; Maciel-Guerra, A T; Guerra, G; Marques-de-Faria, A P; Baptista, M T Matias; de Mello, M P | - | Artigo de periódico |
Repositório da Produção Científica e Intelectual da Unicamp