C. Hackel

发表

Mutations in SRY and WT1 genes required for gonadal development are not responsible for XY partial gonadal dysgenesis.

A. Maciel-Guerra, G. Guerra Júnior, E. B. Tagliarini, 2005, Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas.

Identification of human chromosome 22 transcribed sequences with ORF expressed sequence tags.

F F Costa, A Habr-Gama, C Hackel, 2000, Proceedings of the National Academy of Sciences of the United States of America.

No association of the 5′ promoter region polymorphism of CYP17 gene with prostate cancer risk

M. Ribeiro, C. Hackel, A. Santos, 2002, Prostate Cancer and Prostatic Diseases.

The generation and utilization of a cancer-oriented representation of the human transcriptome by using expressed sequence tags

Marcio Luis Acencio, C. V. Jongeneel, John Quackenbush, 2003, Proceedings of the National Academy of Sciences of the United States of America.

Molecular mapping of an idic(Yp) chromosome in an Ullrich-Turner patient.

C. Hackel, A. Marques-de-Faria, M. Palandi de Mello, 2000, American journal of medical genetics.

A Novel Mutation (W718S) in the Steroid-Binding Domain of the Androgen Receptor Gene in a Boy with Ambiguous Genitalia and Hypergonadotrophic Hypogonadism

A. Maciel-Guerra, M. Ribeiro, C. Hackel, 1999 .

Detection of Borrelia burgdorferi in biological samples using the polymerase chain reaction assay.

A. Bollen, P. Gautier, A. Herzog, 1991, Research in microbiology.

New frameshift mutation in the 5α-reductase type 2 gene in a Brazilian patient with 5α-reductase deficiency

A. Maciel-Guerra, L. Ferraz, C. Hackel, 1999 .

Specific identification of Bordetella pertussis by the polymerase chain reaction.

S. Houard, A. Bollen, A. Herzog, 1989, Research in microbiology.

Specific identification of Mycobacterium leprae by the polymerase chain reaction.

F. Portaels, S. Houard, A. Bollen, 1990, Molecular and cellular probes.

Allelic 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.

J. Annichino-Bizzacchi, C. Hackel, J. Annichino‐Bizzacchi, 2000, Thrombosis research.

Diagnosis of 5α-Reductase Type 2 Deficiency: Contribution of Anti-Müllerian Hormone Evaluation

D. Damiani, G. Guerra‐Júnior, M. Toralles, 2005, Journal of pediatric endocrinology & metabolism : JPEM.

Evaluation of the Tubular and Interstitial Functions of the Testis in 46,XY Patients with Ambiguous Genitalia

M. de Castro, C. Lukas-Croisier, C. Hackel, 2000, Journal of pediatric endocrinology & metabolism : JPEM.

New frameshift mutation in the 5alpha-reductase type 2 gene in a Brazilian patient with 5alpha-reductase deficiency.

A. Maciel-Guerra, C. Hackel, G. G. Júnior, 1999, American journal of medical genetics.

Detection of Gly-196-Ser Mutation in 5α-Reductase Type II Gene in a Brazilian Patient with Female Assignment and Behavior

A. Maciel-Guerra, C. Hackel, M. Matias Baptista, 1998, Journal of pediatric endocrinology & metabolism : JPEM.

Cytogenetic analysis and detection of KAL-1 gene deletion with fluorescence in situ hybridization (FISH) in patients with Kallmann syndrome

A. Maciel-Guerra, C. Hackel, M. Baptista, 2001 .

A case of de novo i(12p) with 12q whole-arm translocation mosaicism.

C. Hackel, A. Marques-de-Faria, 1989, American journal of medical genetics.

I. Monlleó, M. B. Fontes, C. Hackel, 2004 .

[Genes involved in sex determination and differentiation].

C. Hackel, Maricilda Palandi Mello, Juliana de G Assumpção, 2005, Arquivos brasileiros de endocrinologia e metabologia.

Mutations of androgen receptor gene in Brazilian patients with male pseudohermaphroditism.

A. Maciel-Guerra, C. Hackel, D. Cabral, 1998, Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas.

[5alpha-reductase type 2 deficiency: experiences from Campinas (SP) and Salvador (BA)].

D. Damiani, G. Guerra‐Júnior, M. Toralles, 2005, Arquivos brasileiros de endocrinologia e metabologia.

Rarity of DNA sequence alterations in the promoter region of the human androgen receptor gene.

M. Ribeiro, C. Hackel, A. Santos, 2004, Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas.

A transcript finishing initiative for closing gaps in the human transcriptome.

Christine Hackel, Mari Cleide Sogayar, Silvana Giuliatti, 2004, Genome research.

The contribution of 700,000 ORF sequence tags to the definition of the human transcriptome

Emmanuel Dias-Neto, Sergio Verjovski-Almeida, Christine Hackel, 2001, Proceedings of the National Academy of Sciences of the United States of America.

Molecular analysis of KAL-1, GnRH-R, NELF and EBF2 genes in a series of Kallmann syndrome and normosmic hypogonadotropic hypogonadism patients.

C. Hackel, H. Garmes, M. Baptista, 2005, The Journal of endocrinology.

Identification and complete sequencing of novel human transcripts through the use of mouse orthologs and testis cDNA sequences.

Milton Faria, Flávio Henrique-Silva, Daniel Giannella-Neto, 2004, Genetics and molecular research : GMR.

Interphase Cytogenetics Using Fluorescence In Situ Hybridization: An Overview Of Its Application To Diffuse And Solid Tissue

Christine Hackel, Marileila Varella-Garcia, M. Varella‐Garcia, 1997 .

[Chromosome instability induced by agrochemicals among farm workers in Passo Fundo, Rio Grande do Sul, Brazil].

C. Hackel, A. Pacheco, 2002, Cadernos de saude publica.

Low expression of APAF-1XL in acute myeloid leukemia may be associated with the failure of remission induction therapy.

S. Saad, F. Costa, A. Fattori, 2008, Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas.

Polymorphisms in the DNA repair gene XRCC1 and susceptibility to alcoholic liver cirrhosis in older Southeastern Brazilians.

Christine Hackel, S. Z. Abdel‐Rahman, I. Cabral, 2002, Cancer letters.

Large-scale transcriptome analyses reveal new genetic marker candidates of head, neck, and thyroid cancer.

Emmanuel Dias-Neto, Sergio Verjovski-Almeida, Christine Hackel, 2005, Cancer research.

Correlation between histological criteria and human papillomavirus presence based on PCR assay in cervical biopsies

L. D. A. de Ângelo Andrade, E. B. Tagliarini, C. Hackel, 2003, International Journal of Gynecologic Cancer.

Allelic frequencies of six polymorphic markers for risk of prostate cancer.

M. Ribeiro, C. Hackel, A. Santos, 2002, Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas.

Two cases of Y; autosome translocations: A 45,X male and a clinically trisomy 18 patient.

D. Cavalcanti, N. Horelli-Kuitunen, M. de Mello, 1994, American journal of medical genetics.

New mutations, hotspots, and founder effects in Brazilian patients with steroid 5α-reductase deficiency type 2

L. E. Oliveira, Luiz E. Oliveira, G. Guerra‐Júnior, 2005, Journal of Molecular Medicine.

Duchenne muscular dystrophy in a girl with an (X;15) translocation.

M. I. Melaragno, D. Brunoni, C. Hackel, 1986, American journal of medical genetics.

Chromosomal aberrations in cultures of skin fibroblasts of leprosy patients.

C Hackel, B Beiguelman, B. Beiguelman, 1985, International journal of leprosy and other mycobacterial diseases : official organ of the International Leprosy Association.

Diagnosis of 5 alpha-reductase type 2 deficiency: Contribution of anti-Mullerian hormone evaluation

E. G. Stuchi-Perez, Christine Hackel, Lec Oliveira, 2005 .

Mutations of androgen receptor gene in Brazilian patients with male pseudohermaphroditism.

A. Maciel-Guerra, C. Hackel, D. Cabral, 1998, Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas.