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Current Molecular Medicine
|
October 13, 2010
MicroRNAs: macro challenges on understanding human biological functions and neurological diseases
C B Santos-Rebouças, M M G Pimentel
European Journal of Human Genetics : EJHG
|
October 19, 2006
Implication of abnormal epigenetic patterns for human diseases
C B Santos-Rebouças, M M G Pimentel
Disease Markers
|
September 5, 2009
Investigation of CBS, MTR, RFC-1 and TC polymorphisms as maternal risk factors for Down syndrome
N Fintelman-Rodrigues, J C Corrêa, J M Santos, et al.
Genetics and Molecular Research : GMR
|
February 15, 2008
LEPR p.Q223R, beta3-AR p.W64R and LEP c.-2548G>A gene variants in obese Brazilian subjects
S F P Duarte, E A Francischetti, V A Genelhu, et al.
International Journal of Molecular Medicine
|
July 18, 2002
Premature ovarian failure and FMR1 premutation co-segregation in a large Brazilian family
M C Machado-Ferreira, M A Costa-Lima, R T Boy, et al.
Genetics and Molecular Research : GMR
|
July 29, 2010
Beta3-adrenergic receptor polymorphism is related to cardiometabolic risk factors in obese Brazilian subjects
V A Genelhu, E A Francischetti, S F P Duarte, et al.
Genetics and Molecular Research : GMR
|
July 1, 2015
Screening for fragile X syndrome in males from specialized institutions in the northeast region of Brazil
M T M Viveiros, M D C Santos, J M Dos Santos, et al.
Disease Markers
|
December 20, 2008
The impact of folate pathway polymorphisms combined to nutritional deficiency as a maternal predisposition factor for Down syndrome
C B Santos-Rebouças, J C Corrêa, A Bonomo, et al.
Genetics and Molecular Research : GMR
|
January 20, 2016
Levels of mannose-binding lectin in individuals with visceral leishmaniasis in the northeast region of Brazil
E L da Silva, M Campos Júnior, S G Monteiro, et al.
European Journal of Neurology
|
May 7, 2010
Genetic analysis of LRRK2 functional domains in Brazilian patients with Parkinson's disease
C B Abdalla-Carvalho, C B Santos-Rebouças, B C Guimarães, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Current Molecular Medicine
|
October 13, 2010
MicroRNAs: macro challenges on understanding human biological functions and neurological diseases
C B Santos-Rebouças, M M G Pimentel
European Journal of Human Genetics : EJHG
|
October 19, 2006
Implication of abnormal epigenetic patterns for human diseases
C B Santos-Rebouças, M M G Pimentel
Disease Markers
|
September 5, 2009
Investigation of CBS, MTR, RFC-1 and TC polymorphisms as maternal risk factors for Down syndrome
N Fintelman-Rodrigues, J C Corrêa, J M Santos, et al.
Genetics and Molecular Research : GMR
|
February 15, 2008
LEPR p.Q223R, beta3-AR p.W64R and LEP c.-2548G>A gene variants in obese Brazilian subjects
S F P Duarte, E A Francischetti, V A Genelhu, et al.
International Journal of Molecular Medicine
|
July 18, 2002
Premature ovarian failure and FMR1 premutation co-segregation in a large Brazilian family
M C Machado-Ferreira, M A Costa-Lima, R T Boy, et al.
Genetics and Molecular Research : GMR
|
July 29, 2010
Beta3-adrenergic receptor polymorphism is related to cardiometabolic risk factors in obese Brazilian subjects
V A Genelhu, E A Francischetti, S F P Duarte, et al.
Genetics and Molecular Research : GMR
|
July 1, 2015
Screening for fragile X syndrome in males from specialized institutions in the northeast region of Brazil
M T M Viveiros, M D C Santos, J M Dos Santos, et al.
Disease Markers
|
December 20, 2008
The impact of folate pathway polymorphisms combined to nutritional deficiency as a maternal predisposition factor for Down syndrome
C B Santos-Rebouças, J C Corrêa, A Bonomo, et al.
Genetics and Molecular Research : GMR
|
January 20, 2016
Levels of mannose-binding lectin in individuals with visceral leishmaniasis in the northeast region of Brazil
E L da Silva, M Campos Júnior, S G Monteiro, et al.
European Journal of Neurology
|
May 7, 2010
Genetic analysis of LRRK2 functional domains in Brazilian patients with Parkinson's disease
C B Abdalla-Carvalho, C B Santos-Rebouças, B C Guimarães, et al.
Page
of 1