Browsing by Author Hackel, C

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PreviewIssue DateTitleAuthor(s)AdvisorType
2004A transcript finishing initiative for closing gaps in the human transcriptomeSogayar, MC; Camargo, AA; Bettoni, F; Carraro, DM; Pires, LC; Parmigiani, MB; Ferreira, EN; Moreira, ES; Latorre, MRDO; Simpson, AJG; Cruz, LO; Degaki, TL; Festa, F; Massirer, KB; Camargo, F; Camargo, LP; Cunha, MAV; De Souza, SJ; Faria, M; Giuliatti, S; Kopp; Oliviera, PSL; Paiva, PB; Pereira, AA; Pinheiro, DG; Puga, RD; Souza, JES; Albuquerque, DM; Andrade, LEC; Baia, GS; Briones, MRS; Cavaleiro-Luna, AMS; Cerutti, JM; Costa, FF; Constanzi-Strauss, E; Espreafico, EM; Ferrasi, AC; Ferro, ES; Fortes, MAHZ; Furchi, JRF; Gianella-Neto, D; Goldman, GH; Goldman, MHS; Gruber, A; Guimaraes, GS; Hackel, C; Henrique-Silva, F; Kimura, ET; Leoni, SG; Macedo, C; Malnic, B; Manzini, CV; Marie, SKN; Martinez-Rossi, NM; Menossi, M; Miracca, EC; Nagai, MA; Nobrega, FG; Nobrega, MP; Oba-Shinjo, SM; Oliviera, MK; Orabona, GM; Otsuke, AY; Paco-Larson, ML; Paixao, BMC; Pandolfi, JRC; Pardini, MIMC; Passos-Bueno, MR; Passos, GAS; Pesquero, JB; Pessoa, JG; Rahal, P; Rainho, CA; Reis, CP; Ricca, TI; Rodriguez, V; Rogatto, SR; Romano, CM; Romeiro, JG; Rossi, A; Sa, RG; Sales, MM; SantAnna, SC; Santarosa, PL; Segato, F; Silva, WA; Silva, IDCG; Silva, NP; Soares-Costa, A; Sonati, MF; Strauss, BE; Tajara, EH; Valentini, SR; Villanova, FE; Ward, LS; Zanette, DL-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
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
1998Mutations Of Androgen Receptor Gene In Brazilian Patients With Male Pseudohermaphroditism.Cabral, D F; Maciel-Guerra, A T; Hackel, C-Artigo de periódico
1999New Frameshift Mutation In The 5alpha-reductase Type 2 Gene In A Brazilian Patient With 5alpha-reductase Deficiency.Ferraz, L F; Mathias Baptista, M T; Maciel-Guerra, A T; Júnior, G G; 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
1998Detection Of Gly-196-ser Mutation In 5alpha-reductase Type Ii Gene In A Brazilian Patient With Female Assignment And Behavior.Caldas Ferraz, L F; Guerra, G; Matias Baptista, M T; Maciel-Guerra, A T; 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
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
1989A Case Of De Novo I(12p) With 12q Whole-arm Translocation Mosaicism.Marques-de-Faria, A P; Hackel, C-Artigo de periódico
2004Rarity Of Dna Sequence Alterations In The Promoter Region Of The Human Androgen Receptor Gene.Cabral, D F; Santos, A; Ribeiro, M L; Mesquita, J C; Carvalho-Salles, A B; Hackel, C-Artigo de periódico
2000Molecular Mapping Of An Idic(yp) Chromosome In An Ullrich-turner Patient.Godoy Assumpção, J; Hackel, C; Marques-De-Faria, A P; Palandi de Mello, M-Artigo de periódico
2002Allelic Frequencies Of Six Polymorphic Markers For Risk Of Prostate Cancer.Ribeiro, M L; Santos, A; Carvalho-Salles, A B; Hackel, C-Artigo de periódico
1994Two Cases Of Y; Autosome Translocations: A 45,x Male And A Clinically Trisomy 18 Patient.Farah, S B; Ramos, C F; de Mello, M P; Sartorato, E L; Horelli-Kuitunen, N; Lopes, V L; Cavalcanti, D P; Hackel, C-Artigo de periódico
-1-Uns- -1Correlation Between Histological Criteria And Human Papillomavirus Presence Based On Pcr Assay In Cervical Biopsies.Salvia, P N D; Bergo, S M; Bonesso-Sabadini, P I P; Tagliarini, E B; Hackel, C; De Angelo Andrade, L A L-Artigo de periódico
2002No Association Of The 5' Promoter Region Polymorphism Of Cyp17 Gene With Prostate Cancer Risk.dos Santos, A; Ribeiro, M L; Mesquita, J C; Carvalho-Salles, A B; Hackel, C-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
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
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