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M B Melo

Showing results (11-20 of 21) with videos related to

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Annals of Hematology|June 5, 2003
A possible role of the P53 gene deletion as a prognostic factor in multiple myelomaM M Ortega, M B Melo, C A De Souza, et al.
Genetics and Molecular Research : GMR|June 23, 2010
GSTT1, GSTM1, and GSTP1 polymorphisms and chemotherapy response in locally advanced breast cancerA L Oliveira, F F O Rodrigues, R E Santos, et al.
Genetics and Molecular Research : GMR|February 6, 2007
The influence of parental origin of X chromosome genes on the stature of patients with 45 X Turner syndromeC Kochi, C A Longui, S H V Lemos-Marini, et al.
Journal of Medical Genetics|May 20, 2000
Novel mutation in the MYOC gene in primary open glaucoma patientsJ P Vasconcellos, M B Melo, V P Costa, et al.
Genetics and Molecular Research : GMR|June 19, 2007
A novel mutation in DAX1 gene causing different phenotypes in three siblings with adrenal hypoplasia congenitaL E P Calliari, C A Longui, M N Rocha, et al.
Parasitology International|September 24, 2002
How laminin-1 can be recognized by the protozoan parasite Tritrichomonas foetus: possible role played by the extracellular matrix glycoprotein in both cytoadhesion and cytotoxicity exerted by the parasiteF C Silva-Filho, S Kasai, M Nomizu, et al.
Genetics and Molecular Research : GMR|April 9, 2008
Correlation of polymorphism C3435T of the MDR-1 gene and the response of primary chemotherapy in women with locally advanced breast cancerF F O Rodrigues, R E Santos, M B Melo, et al.
Genes and Immunity|January 22, 2010
Early endosome localization and activity of RasGEF1b, a toll-like receptor-inducible Ras guanine-nucleotide exchange factorW A Andrade, A M Silva, V Souza Alves, et al.
Blood Cells, Molecules & Diseases|August 31, 2014
Increased circulating PEDF and low sICAM-1 are associated with sickle cell retinopathyP R S Cruz, R P C Lira, S A C Pereira Filho, et al.
Journal of Medical Genetics|May 4, 2004
Inhibin alpha-subunit (INHA) gene and locus changes in paediatric adrenocortical tumours from TP53 R337H mutation heterozygote carriersC A Longui, S H V Lemos-Marini, B Figueiredo, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Annals of Hematology|June 5, 2003
A possible role of the P53 gene deletion as a prognostic factor in multiple myelomaM M Ortega, M B Melo, C A De Souza, et al.
Genetics and Molecular Research : GMR|June 23, 2010
GSTT1, GSTM1, and GSTP1 polymorphisms and chemotherapy response in locally advanced breast cancerA L Oliveira, F F O Rodrigues, R E Santos, et al.
Genetics and Molecular Research : GMR|February 6, 2007
The influence of parental origin of X chromosome genes on the stature of patients with 45 X Turner syndromeC Kochi, C A Longui, S H V Lemos-Marini, et al.
Journal of Medical Genetics|May 20, 2000
Novel mutation in the MYOC gene in primary open glaucoma patientsJ P Vasconcellos, M B Melo, V P Costa, et al.
Genetics and Molecular Research : GMR|June 19, 2007
A novel mutation in DAX1 gene causing different phenotypes in three siblings with adrenal hypoplasia congenitaL E P Calliari, C A Longui, M N Rocha, et al.
Parasitology International|September 24, 2002
How laminin-1 can be recognized by the protozoan parasite Tritrichomonas foetus: possible role played by the extracellular matrix glycoprotein in both cytoadhesion and cytotoxicity exerted by the parasiteF C Silva-Filho, S Kasai, M Nomizu, et al.
Genetics and Molecular Research : GMR|April 9, 2008
Correlation of polymorphism C3435T of the MDR-1 gene and the response of primary chemotherapy in women with locally advanced breast cancerF F O Rodrigues, R E Santos, M B Melo, et al.
Genes and Immunity|January 22, 2010
Early endosome localization and activity of RasGEF1b, a toll-like receptor-inducible Ras guanine-nucleotide exchange factorW A Andrade, A M Silva, V Souza Alves, et al.
Blood Cells, Molecules & Diseases|August 31, 2014
Increased circulating PEDF and low sICAM-1 are associated with sickle cell retinopathyP R S Cruz, R P C Lira, S A C Pereira Filho, et al.
Journal of Medical Genetics|May 4, 2004
Inhibin alpha-subunit (INHA) gene and locus changes in paediatric adrenocortical tumours from TP53 R337H mutation heterozygote carriersC A Longui, S H V Lemos-Marini, B Figueiredo, et al.
Pageof 3