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Annals of Hematology
|
June 5, 2003
A possible role of the P53 gene deletion as a prognostic factor in multiple myeloma
M 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 cancer
A 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 syndrome
C 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 patients
J 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 congenita
L 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 parasite
F 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 cancer
F 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 factor
W 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 retinopathy
P 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 carriers
C A Longui, S H V Lemos-Marini, B Figueiredo, et al.
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of 3
Search research articles
Search
Showing results (11-20 of 21) with videos related to
Sort By:
Page
of 3
Annals of Hematology
|
June 5, 2003
A possible role of the P53 gene deletion as a prognostic factor in multiple myeloma
M 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 cancer
A 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 syndrome
C 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 patients
J 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 congenita
L 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 parasite
F 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 cancer
F 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 factor
W 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 retinopathy
P 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 carriers
C A Longui, S H V Lemos-Marini, B Figueiredo, et al.
Page
of 3