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Coding region

XRCC2 coding region by high

XRCC2 coding region by high

... A sample size calculation (Kasiulevicious et al., 2006) indicated that the minimum sample size for this case-control study was ~45 for each group (controls and cases). In addition, the minimum odds ratio (OR) for signif- ...

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The fusion protein signal-peptide-coding region of canine distemper virus: a useful tool for phylogenetic reconstruction and lineage identification.

The fusion protein signal-peptide-coding region of canine distemper virus: a useful tool for phylogenetic reconstruction and lineage identification.

... (Fsp) coding region are extremely variable, suggesting that analysis of its sequence might be useful for strain characterization ...Fsp-coding region and H gene sequences of the same strains ...

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Biological basis of miRNA action when their targets are located in human protein coding region.

Biological basis of miRNA action when their targets are located in human protein coding region.

... We hypothesized that if site accessibility and/or local translation efficiency is important for miRNA action when miRNA target sites are located in human protein coding sequences, synonymous codons should be ...

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Is a non-synonymous SNP in the HvAACT1 coding region associated with

Is a non-synonymous SNP in the HvAACT1 coding region associated with

... HvAACT1 coding region, not only is the expression en- hanced but it also switches to the root apex, thereby altering the primary function of this gene, which is the release of ci- DOI: ...

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A pentanucleotide ATTTC repeat insertion in the non-coding region of DAB1, mapping to SCA37, causes spinocerebellar ataxia.

A pentanucleotide ATTTC repeat insertion in the non-coding region of DAB1, mapping to SCA37, causes spinocerebellar ataxia.

... chromosomal region 1p32. (D) Schematic physical map of the SCA candidate region; also depicted are the intronic repeat region with the XbaI restriction sites, the location of the Southern blot probe, ...

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Correction of the Caulobacter crescentus NA1000 genome annotation.

Correction of the Caulobacter crescentus NA1000 genome annotation.

... annotated coding regions and generate a file of regions where a one to one correspondence was ...annotated coding regions were detected opposite a high third position GC peak, the open reading frames (ORFs) ...

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Recent mitochondrial DNA mutations increase the risk of developing common late-onset human diseases.

Recent mitochondrial DNA mutations increase the risk of developing common late-onset human diseases.

... non-coding region of mtDNA (d-loop) showing allele frequencies in 7,729 control subjects and the position of alleles associated with eight common human diseases; where: AS = ankylosing spondylitis, IS = ...

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Sequence variation in the melanocortin-1 receptor(

Sequence variation in the melanocortin-1 receptor(

... the coding region of the melanocortin-1-receptor (MC1R) gene, and therefore its role underlying the dorsal color variation in two sympatric species of sand lizards (Liolaemus) that inhabit the southeastern ...

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Uncovering the rare variants of DLC1 isoform 1 and their functional effects in a Chinese sporadic congenital heart disease cohort.

Uncovering the rare variants of DLC1 isoform 1 and their functional effects in a Chinese sporadic congenital heart disease cohort.

... the coding region of DLC1 isoform 1 in 151 sporadic CHD patients and identified 13 non-synonymous rare variants (including 6 private variants) in the case ...N-terminal region of the DLC1 isoform 1 ...

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Bihao Caoa , Zhiyin Huanga , Guoju Chena and Jianjun Lei

Bihao Caoa , Zhiyin Huanga , Guoju Chena and Jianjun Lei

... This study was designed to control plant fertility by cell lethal gene Barnase expressing at specific developmental stage and in specific tissue of male organ under the control of Cre/loxP system, for heterosis breeding, ...

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Characterization of LEDGF/p75 genetic variants and association with HIV-1 disease progression.

Characterization of LEDGF/p75 genetic variants and association with HIV-1 disease progression.

... gene region, together with the CCR5 D32 variant can explain up to 13% of the observed variability in HIV-1 viremia [32] raising the need for further genetic studies to improve individualized prognosis in ...

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Arq. NeuroPsiquiatr.  vol.70 número12

Arq. NeuroPsiquiatr. vol.70 número12

... Taking this into account, we conducted a study with the aims of investigating a possible association between A/G COMT polymorphism in the non-coding region 3’ (rs165599) and schizophrenia, and also ...

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J. bras. pneumol.  vol.39 número2

J. bras. pneumol. vol.39 número2

... Objective: To evaluate the diagnostic contribution of molecular analysis of the cystic fibrosis transmembrane conductance regulator (CFTR) gene in patients suspected of having mild or atypical cystic fibrosis (CF). ...

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Dopa-responsive dystonia: functional analysis of single nucleotide substitutions within the 5' untranslated GCH1 region.

Dopa-responsive dystonia: functional analysis of single nucleotide substitutions within the 5' untranslated GCH1 region.

... upstream region [16–18] and intron-exon splice sites ...upstream region of the human GCH1 gene, three different single base pair (bp) substitutions have been identified at positions -22C>T [16,18], ...

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PDF EN Jornal Brasileiro de Pneumologia 2 9 english

PDF EN Jornal Brasileiro de Pneumologia 2 9 english

... Objective: To evaluate the diagnostic contribution of molecular analysis of the cystic fibrosis transmembrane conductance regulator (CFTR) gene in patients suspected of having mild or atypical cystic fibrosis (CF). ...

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Arq Bras Endocrinol Metab  vol.56 número3

Arq Bras Endocrinol Metab vol.56 número3

... Objective: To analyze the LEPR gene in obese children and to investigate the associations be- tween molecular indings and anthropometric and metabolic features. Subjects and methods: Thirty-two patients were evaluated ...

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Arq Bras Endocrinol Metab  vol.52 número8

Arq Bras Endocrinol Metab vol.52 número8

... Herein we report two sisters who presented the clinical and hormonal features typical of a combined form of 17 α-hydroxylase and 17,20-lyase defi ciency (1,2). The hor- monal profi le was based on elevated progesterone ...

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Novel point mutations in the ERG11 gene in clinical isolates of azole resistant Candida species

Novel point mutations in the ERG11 gene in clinical isolates of azole resistant Candida species

... The azoles are the class of medications most commonly used to fight infections caused by Candida sp. Typi- cally, resistance can be attributed to mutations in ERG11 gene (CYP51) which encodes the cytochrome P450 ...

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Polymorphism analysis of the hsp70 stress gene in Broiler chickens ( Gallus gallus ) of different breeds

Polymorphism analysis of the hsp70 stress gene in Broiler chickens ( Gallus gallus ) of different breeds

... Since birds are constantly challenged by heat stress in hot countries, many studies involving Hsp70 expression in broilers have been made. Gabriel (1996) showed that the expression of Hsp70 in the hepatocytes of broiler ...

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Genetic polymorphisms of paraoxonase 1 and susceptibility to atherogenesis

Genetic polymorphisms of paraoxonase 1 and susceptibility to atherogenesis

... A meta-analysis dealing with L55M, Q192R and C- 107T polymorphisms in relation to CHD demonstrated only a weak positive overall association between Q192R polymorphism and CHD, while the remaining L55M and C(-107)T ...

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