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[PDF] Top 20 Neurotensin receptor 1 gene (NTSR1) polymorphism is associated with working memory.

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Neurotensin receptor 1 gene (NTSR1) polymorphism is associated with working memory.

Neurotensin receptor 1 gene (NTSR1) polymorphism is associated with working memory.

... NTSR1 gene, which may or may not have functional consequence on the ...in gene expression [44], mRNA secondary structure formation [45], and transcriptional suppression of the genes ...It is possible ... See full document

7

BsmI polymorphism in the vitamin D receptor gene is associated with 25-hydroxy vitamin D levels in individuals with cognitive decline

BsmI polymorphism in the vitamin D receptor gene is associated with 25-hydroxy vitamin D levels in individuals with cognitive decline

... mean ± standard deviation, and nonparametric variables such as medians (interquartile range). Categorical variables were presented as percentages. Parametric variables were evalu- ated by the Student’s T-test to compare ... See full document

7

Rev. Bras. Psiquiatr.  vol.39 número3

Rev. Bras. Psiquiatr. vol.39 número3

... (BDNF) is an important nerve growth factor linked with development and neural ...Val66Met polymorphism in the BDNF gene has been associated with a significant impact on episodic ... See full document

2

The Pro12Ala polymorphism in the peroxisome proliferator-activated receptor gamma-2 gene (PPARγ2) is associated with increased risk of coronary artery disease: a meta-analysis.

The Pro12Ala polymorphism in the peroxisome proliferator-activated receptor gamma-2 gene (PPARγ2) is associated with increased risk of coronary artery disease: a meta-analysis.

... Pro12Ala polymorphism with CAD risk is not precisely clarified ...Pro12Ala polymorphism with CAD, the results remained ...this is one of the largest systematic reviews of the ... See full document

14

A Common Polymorphism of the Human Cardiac Sodium Channel Alpha Subunit (SCN5A) Gene Is Associated with Sudden Cardiac Death in Chronic Ischemic Heart Disease.

A Common Polymorphism of the Human Cardiac Sodium Channel Alpha Subunit (SCN5A) Gene Is Associated with Sudden Cardiac Death in Chronic Ischemic Heart Disease.

... associations with specific forms of cardiac death only (sudden, arrhythmogenic, ischemic ...adrenergic receptor, nitric oxide synthase 1 adaptor protein, ryanodine receptor 2, sodium channel ... See full document

10

The polymorphism of the serotonin-2A receptor T102C is associated with age

The polymorphism of the serotonin-2A receptor T102C is associated with age

... it is important to understand the biological role of serotonin ...5-HT is an ancestral molecule that has recently acted as a neurotransmitter, regulating several brain functions, as well as being involved ... See full document

6

Fractures of the proximal femur: correlation with vitamin D receptor gene polymorphism

Fractures of the proximal femur: correlation with vitamin D receptor gene polymorphism

... are associated with a larger number of deaths, with dis- ability and greater medical costs than all other osteoporotic fractures taken together (2,3) and therefore represent a consider- able ... See full document

7

A polymorphism in the HLA-DPB1 gene is associated with susceptibility to multiple sclerosis.

A polymorphism in the HLA-DPB1 gene is associated with susceptibility to multiple sclerosis.

... on gene expression ...this gene [1]. VDREs are bound by the vitamin D receptor (VDR) which acts as a ligand activated transcription factor, and the VDRE upstream of HLA-DRB1 is highly ... See full document

7

Arq. NeuroPsiquiatr.  vol.71 número7

Arq. NeuroPsiquiatr. vol.71 número7

... Ninety-nine patients with probable AD and 111 healthy control subjects were enrolled for analysis. he demograph- ic data of groups are shown in Table 1. Diferent subsamples were analyzed: early-onset AD ... See full document

5

Association of T174M polymorphism of angiotensinogen gene with essential hypertension: A meta-analysis

Association of T174M polymorphism of angiotensinogen gene with essential hypertension: A meta-analysis

... T174M polymorphism demonstrated a significant increase in the risk of essential hypertension in Asians (10 studies were in- cluded and four of them were Chinese) and in mixed/other populations (including African, ... See full document

7

The Drosophila melanogaster methuselah gene: a novel gene with ancient functions.

The Drosophila melanogaster methuselah gene: a novel gene with ancient functions.

... (Fig. 1) show that the choice of the alignment algorithm influences the conclusion on which one is the oldest mth-like ...taken with care. However, some inferences can be made in combination ... See full document

12

Polimorfismos dos genes apolipoproteínas E e A5 e relação com parâmetros bioquímicos e hemostáticos em dislipidêmicos

Polimorfismos dos genes apolipoproteínas E e A5 e relação com parâmetros bioquímicos e hemostáticos em dislipidêmicos

... Atherosclerosis is a complex process due to multiple genetic and environmental interactions that modify not only lipid metabolism but also the coagulation system and inflammatory ...Dyslipidemia is the most ... See full document

176

Inattentional Blindness and Individual Differences in Cognitive Abilities.

Inattentional Blindness and Individual Differences in Cognitive Abilities.

... Each participant completed ten easy practice trials (smaller arm 4.5°) before the threshold- ing began. Once the threshold had been determined for an individual, the critical trial occurred immediately and without ... See full document

27

Survey of mutations in prolificacy genes in Santa Ines and Morada Nova sheep

Survey of mutations in prolificacy genes in Santa Ines and Morada Nova sheep

... Other prolific ovine lineages have been studied and mutations in the gene of bone morphogenetic protein 15 (BMP-15) were implicated (Galloway et al., 2000, Liao et al., 2004). The BMP-15 consists of a growth ... See full document

7

XmnI polymorphism is associated with fetal hemoglobin levels in hypoplastic syndromes

XmnI polymorphism is associated with fetal hemoglobin levels in hypoplastic syndromes

... There are many factors that could change the level of HbF in adults, such as age, sex, polymorphisms, β-globin locus control region (LCR) and HbF persistence. Among the poly- morphic genetic markers of the β-globin ... See full document

2

Acute leukemia in early childhood

Acute leukemia in early childhood

... MLL gene fusion but may also increase the risk of the occurrence of further ...interact with environmental, dietary, mater- nal, and other factors to modulate the devel- opment of acute ...MLL gene ... See full document

12

Arq. Bras. Cardiol.  vol.89 número6

Arq. Bras. Cardiol. vol.89 número6

... Assim como é importante conhecer a epidemiologia dos fatores de risco clássicos para HAS e avaliar o impacto que cada um deles tem sobre a morbidade e a mortalidade relacionadas à HAS, o conhecimento de fatores de risco ... See full document

7

Clinics  vol.66 número11

Clinics vol.66 número11

... G1 with the ADA*1/*1 and ADA*1/*2 genotypes were ...not associated with the presence or absence of ...are associated with miscarriages, but their influence may be ... See full document

5

Thyrotoxic Periodic Paralysis and Polymorphisms of the , , and  Genes in Men with Graves Disease

Thyrotoxic Periodic Paralysis and Polymorphisms of the , , and Genes in Men with Graves Disease

... Each reaction was performed with 100 ng of genomic DNA, 0.5 units of Taq polymerase (Takara Shuzo, Otsu, Japan), 2 pmol of each primer, and 4 nmol of each deoxynucleotide in a total reac- tion volume of 20 μL ... See full document

5

Arq. Bras. Cardiol.  vol.97 número6

Arq. Bras. Cardiol. vol.97 número6

... The approval for the study was granted by the Hospital Socor and Ethical Research Committee of the Universidade Federal de Minas Gerais. Informed consent was obtained from all participants, and the relevant clinical ... See full document

6

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