Browsing by Author Hackel, C

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

or enter first few letters:  
Showing results 1 to 20 of 30  next >
PreviewIssue DateTitleAuthor(s)AdvisorType
1999New frameshift mutation in the 5 alpha-reductase type 2 gene in a Brazilian patient with 5 alpha-reductase deficiencyFerraz, LFC; Baptista, MTM; Maciel-Guerra, AT; Junior, GG; Hackel, C-Artigo de periódico
2002Polymorphisms in the DNA repair gene XRCC1 and susceptibility to alcoholic liver cirrhosis in older Southeastern BraziliansRossit, ARB; Cabral, IR; Hackel, C; da Silva, RDMA; Froes, NDTC; Abdel-Rahman, SZ-Artigo de periódico
2000Evaluation of the tubular and interstitial functions of the testis in 46,XY patients with ambiguous genitaliaStuchi-Perez, EG; Lukas-Croisier, C; De Castro, M; Baptista, MTM; Scolfaro, MR; Marques-De-Faria, AP; Hackel, C; Maciel-Guerra, AT; Guerra, G-Artigo de periódico
2005New mutations, hotspots, and founder effects in Brazilian patients with steroid 5 alpha-reductase deficiency type 2Hackel, C; Oliveira, LEC; Ferraz, LFC; Tonini, MMO; Silva, DN; Toralles, MB; Stuchi-Perez, EG; Guerra, G-Artigo de periódico
2001The contribution of 700,000 ORF sequence tags to the definition of the human transcriptomeCamargo, AA; Samaia, HPB; Dias-Neto, E; Simao, DF; Migotto, IA; Briones, MRS; Costa, FF; Nagai, MA; Verjovski-Almeida, S; Zago, MA; Andrade, LEC; Carrer, H; El-Dorry, HFA; Espreafico, EM; Habr-Gama, A; Giannella-Neto, D; Goldman, GH; Gruber, A; Hackel, C; Kimura, ET; Maciel, RMB; Marie, SKN; Martins, EAL; Nobrega, MP; Paco-Larson, ML; Pardini, MIMC; Pereira, GG; Pesquero, JB; Rodrigues, V; Rogatto, SR; da Silva, IDCG; Sogayar, MC; Sonati, MDF; Tajara, EH; Valentini, SR; Alberto, FL; Amaral, MEJ; Aneas, I; Arnaldi, LAT; de Assis, AM; Bengtson, MH; Bergamo, NA; Bombonato, V; de Camargo, MER; Canevari, RA; Carraro, DM; Cerutti, JM; Correa, MLC; Correa, RFR; Costa, MCR; Curcio, C; Hokama, POM; Ferreira, AJS; Furuzawa, GK; Gushiken, T; Ho, PL; Kimura, E; Krieger, JE; Leite, LCC; Majumder, P; Marins, M; Marques, ER; Melo, ASA; Melo, M; Mestriner, CA; Miracca, EC; Miranda, DC; Nascimento, ALTO; Nobrega, FG; Ojopi, EPB; Pandolfi, JRC; Pessoa, LG; Prevedel, AC; Rahal, P; Rainho, CA; Reis, EMR; Ribeiro, ML; da Ros, N; de Sa, RG; Sales, MM; Sant'anna, SC; dos Santos, ML; da Silva, AM; da Silva, NP; Silva, WA; da Silveira, RA; Sousa, JF; Stecconi, D; Tsukumo, F; Valente, V; Soares, F; Moreira, ES; Nunes, DN; Correa, RG; Zalcberg, H; Carvalho, AF; Reis, LFL; Brentani, RR; Simpson, AJG; de Souza, SJ-Artigo de periódico
2000Identification of human chromosome 22 transcribed sequences with ORF expressed sequence tagsde Souza, SJ; Camargo, AA; Briones, MRS; Costa, FF; Nagai, MA; Verjovski-Almeida, S; Zago, MA; Andrade, LEC; Carrer, H; El-Dorry, HFA; Espreafico, EM; Habr-Gama, A; Giannella-Neto, D; Goldman, GH; Gruber, A; Hackel, C; Kimura, ET; Maciel, RMB; Marie, SKN; Martins, EAL; Nobrega, MP; Paco-Larson, ML; Pardini, MIMC; Pereira, GG; Pesquero, JB; Rodrigues, V; Rogatto, SR; da Silva, IDCG; Sogayar, MC; Sonati, MD; Tajara, EH; Valentini, SR; Acencio, M; Alberto, FL; Amaral, MEJ; Aneas, I; Bengtson, MH; Carraro, DM; Carvalho, AF; Carvalho, LH; Cerutti, JM; Correa, MLC; Costa, MCR; Curcio, C; Gushiken, T; Ho, PL; Kimura, E; Leite, LCC; Maia, G; Majumder, P; Marins, M; Matsukuma, A; Melo, ASA; Mestriner, CA; Miracca, EC; Miranda, DC; Nascimento, ALTO; Nobrega, FG; Ojopi, EPB; Pandolfi, JRC; Pessoa, LG; Rahal, P; Rainho, CA; da Ro's, N; de Sa, RG; Sales, MM; da Silva, NP; Silva, TC; da Silva, W; Simao, DF; Sousa, JF; Stecconi, D; Tsukumo, F; Valente, V; Zalcberg, H; Bretani, RR; Reis, LFL; Dias-Neto, E; Simpson, AJG-Artigo de periódico
2000Allelic frequencies of three VNTRs in intron 40 of the human von Willebrand factor gene in types 1, 2, and 3 von Willebrand disease patients and controls of a Brazilian populationMazzini, J; Hackel, C; Annichino-Bizzacchi, JM-Artigo de periódico
1999Determination of the allele frequencies of three polymorphisms in the promoter region of the human protein C gene in three Brazilian ethnic groupsMendes, CPO; Hackel, C; Arruda, VR; Annichino-Bizzacchi, JM-Artigo de periódico
1998Detection of Gly-196-Ser mutation in 5 alpha-reductase type II gene in a Brazilian patient with female assignment and behaviorFerraz, LFC; Guerra, G; Baptista, MTM; Maciel-Guerra, AT; Hackel, C-Artigo de periódico
2005Diagnosis of 5 alpha-reductase type 2 deficiency: Contribution of anti-Mullerian hormone evaluationStuchi-Perez, EG; Hackel, C; Oliveira, LEC; Ferraz, LFC; Oliveira, LC; Nunes-Silva, D; Toralles, MB; Steinmetz, L; Damiani, D; Maciel-Guerra, AT; Guerra, G-Artigo de periódico
2005Large-scale transcriptome analyses reveal new genetic marker candidates of head, neck, and thyroid cancerReis, EM; Ojopi, EPB; Alberto, FL; Rahal, P; Tsukumo, F; Mancini, UM; Guimaraes, GS; Thompson, GMA; Camacho, C; Miracca, E; Carvalho, AL; Machado, AA; Paquola, ACM; Cerutti, JM; da Silva, AM; Pereira, GG; Valentini, SR; Nagai, MA; Kowalski, LP; Verjovski-Almeida, S; Tajara, EH; Dias-Neto, E; Bengtson, MH; Canevari, RA; Carazzolle, MF; Colin, C; Costa, FF; Costa, MC; Estecio, MR; Esteves, LI; Federico, MH; Guimaraes, PE; Hackel, C; Kimura, ET; Leoni, SG; Maciel, RM; Maistro, S; Mangone, FR; Massirer, KB; Matsuo, SE; Nobrega, FG; Nobrega, MP; Nunes, DN; Nunes, F; Pandolfi, JR; Pardini, MI; Pasini, FS; Peres, T; Rainho, CA; Dos Reis, PP; Rodrigus-Lisoni, FC; Rogatto, SR; dos Santos, A; dos Santos, PC; Sogayar, MC; Zanelli, CF-Artigo de periódico
2004Correlation between histological criteria and human papillomavirus presence based on PCR assay in cervical biopsiesSalvia, PND; Bergo, SM; Bonesso-Sabadini, PIP; Tagliarini, EB; Hackel, C; Andrade, LALD-Artigo de periódico
2002No association of the 5 ' promoter region polymorphism of CVP17 gene with prostate cancer riskdos Santos, A; Ribeiro, ML; Mesquita, JC; Carvalho-Salles, AB; Hackel, C-Artigo de periódico
2000Molecular mapping of an idic(Yp) chromosome in an Ullrich-Turner patientAssumpcao, JG; Hackel, C; Marques-de-Faria, AP; de Mello, MP-Artigo de periódico
2005Molecular analysis of KAL-1, GnRH-R, NELF and EBF2 genes in a series of Kallmann syndrome and normosmic hypogonadotropic hypogonadism patientsTrarbach, EB; Baptista, MTM; Garmes, HM; Hackel, C-Artigo de periódico
1998A novel mutation in a Brazilian patient with glycogen storage disease type 1aSartorato, EL; Reis, FC; Norato, DYJ; Hackel, C-Artigo de periódico
2005Mutations In Sry And Wt1 Genes Required For Gonadal Development Are Not Responsible For Xy Partial Gonadal Dysgenesis.Tagliarini, E B; Assumpção, J G; Scolfaro, M R; Mello, M P de; Maciel-Guerra, A T; Guerra Júnior, G; Hackel, C-Artigo de periódico
2008Low Expression Of Apaf-1xl In Acute Myeloid Leukemia May Be Associated With The Failure Of Remission Induction Therapy.Benites, B D; Fattori, A; Hackel, C; Lorand-Metze, I; De Souza, C A; Schulz, E; Costa, F F; Saad, S T O-Artigo de periódico
1998Mutations Of Androgen Receptor Gene In Brazilian Patients With Male Pseudohermaphroditism.Cabral, D F; Maciel-Guerra, A T; Hackel, C-Artigo de periódico
2000Allelic Frequencies Of Three Vntrs In Intron 40 Of The Human Von Willebrand Factor Gene In Types 1, 2, And 3 Von Willebrand Disease Patients And Controls Of A Brazilian Population.Mazzini, J; Hackel, C; Annichino-Bizzacchi, J M-Artigo de periódico