A comparative study of cDNA microarray analysis of familial and sporadic...
Many genes and signalling pathways controlling cell proliferation, death and differentiation, as well as genomic integrity, are involved in cancer development. Techniques, such as cDNA microarrays,...
View ArticleEvaluation of methylenetetrahydrofolate reductase C677T gene polymorphism...
The etiology of human recurrent fetal loss is associated with methylenetetrahydrofolate reductase (MTHFR) C677T gene polymorphism. Several conflicting reports on MTHFR gene polymorphism increases the...
View ArticleTeeth are bones: Signature genes and molecules that underwrite odontogenesis
Understanding the molecular genetics of odontogenesis (tooth development) can unlock innovative avenues to genetically engineer teeth for therapy. In this review, emerging insights into the genetic...
View ArticlePreparation and partial characterization of monoclonal antibody against human...
Phosphodiesterase 5 (PDE5) is a catalytic enzyme for degradation of cyclic guanosine monophosphate (cGMP) in human smooth muscle cells. Inhibition of this enzyme by certain chemicals including...
View ArticleAssociation of insertion/deletion polymorphism of Alu angiotensin converting...
The objective of the study is to know the frequencies of insertion/deletion (I/D) allele and association of angiotensin converting enzyme (ACE), I/D polymorphism in Jammu and Kashmir (JK) populations...
View ArticleA study of correlation between CYP2C9 gene polymorphism and Warfarin...
In this study, we investigated the correlation between CYP2C9 gene polymorphism and maintenance dose of Warfarin in 300 patients who were the Han population derived from the Affiliated Yan An Hospital...
View ArticleMutation N308T of protein tyrosine phosphatase SHP-2 in two Senegalese...
Noonan syndrome is a genetic autosomal dominant disorder characterized by facial dysmorphy, short stature, delayed puberty and congenital heart defects. The first gene implicated in this syndrome is...
View ArticleThe codon 17 polymorphism of the CTLA4 gene in type 1 diabetes mellitus in...
The aim of this work was to study the polymorphism in CTLA4 gene in insulin-dependent diabetes mellitus (IDDM) type I patients in Baghdad population. To achieve this goal, blood samples were collected...
View ArticleMeta-analysis of methylenetetrahydrofolate reductase (MTHFR) A1298C...
Polymorphisms in key genes involving the folate pathway have been reported to be associated with the risk of orofacial cleft (OFC) and several studies were published with conflicting results. A...
View ArticleEvaluation of BNC2 as a new candidate gene for hypospadias
In order to evaluate the use of the BNC2 gene in clinical practice regarding hypospadias, the presence of the impact of mutations in BNC2 gene in males who had been treated surgically for hypospadias...
View ArticleThe impact of genome information on mate selection: From the African perspective
Mate selection in humans is an important social activity which is central to every individuals life. The debate on the ethics of generating and using genetic information has been of concern to several...
View ArticleEvaluation of methylenetetrahydrofolate reductase C677T gene polymorphism...
The etiology of human recurrent fetal loss is associated with methylenetetrahydrofolate reductase (MTHFR) C677T gene polymorphism. Several conflicting reports on MTHFR gene polymorphism increases the...
View ArticleTeeth are bones: Signature genes and molecules that underwrite odontogenesis
Understanding the molecular genetics of odontogenesis (tooth development) can unlock innovative avenues to genetically engineer teeth for therapy. In this review, emerging insights into the genetic...
View ArticlePreparation and partial characterization of monoclonal antibody against human...
Phosphodiesterase 5 (PDE5) is a catalytic enzyme for degradation of cyclic guanosine monophosphate (cGMP) in human smooth muscle cells. Inhibition of this enzyme by certain chemicals including...
View ArticleAssociation of insertion/deletion polymorphism of Alu angiotensin converting...
The objective of the study is to know the frequencies of insertion/deletion (I/D) allele and association of angiotensin converting enzyme (ACE), I/D polymorphism in Jammu and Kashmir (JK) populations...
View ArticleA study of correlation between CYP2C9 gene polymorphism and Warfarin...
In this study, we investigated the correlation between CYP2C9 gene polymorphism and maintenance dose of Warfarin in 300 patients who were the Han population derived from the Affiliated Yan An Hospital...
View ArticleMutation N308T of protein tyrosine phosphatase SHP-2 in two Senegalese...
Noonan syndrome is a genetic autosomal dominant disorder characterized by facial dysmorphy, short stature, delayed puberty and congenital heart defects. The first gene implicated in this syndrome is...
View ArticleThe codon 17 polymorphism of the CTLA4 gene in type 1 diabetes mellitus in...
The aim of this work was to study the polymorphism in CTLA4 gene in insulin-dependent diabetes mellitus (IDDM) type I patients in Baghdad population. To achieve this goal, blood samples were collected...
View ArticleMeta-analysis of methylenetetrahydrofolate reductase (MTHFR) A1298C...
Polymorphisms in key genes involving the folate pathway have been reported to be associated with the risk of orofacial cleft (OFC) and several studies were published with conflicting results. A...
View ArticleEvaluation of BNC2 as a new candidate gene for hypospadias
In order to evaluate the use of the BNC2 gene in clinical practice regarding hypospadias, the presence of the impact of mutations in BNC2 gene in males who had been treated surgically for hypospadias...
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