"gene variants" trang 4 - tải miễn phí từ tailieuXANH
Cepip: Context-dependent epigenomic weighting for prioritization of regulatory variants and disease-associated genes

Cepip: Context-dependent epigenomic weighting for prioritization of regulatory variants and disease-associated genes
15    277    2
Stable enhancers are active in development, and fragile enhancers are associated with evolutionary adaptation

Stable enhancers are active in development, and fragile enhancers are associated with evolutionary adaptation
17    19    1
Exome sequencing identifies gene variants and networks associated with extreme respiratory outcomes following preterm birth

Exome sequencing identifies gene variants and networks associated with extreme respiratory outcomes following preterm birth
10    6    1
Methylation of the first exon in the erythropoietin receptor gene does not correlate with its mRNA and protein level in cancer cells

Methylation of the first exon in the erythropoietin receptor gene does not correlate with its mRNA and protein level in cancer cells
9    5    1
Uncovering a multitude of human glucocorticoid receptor variants: An expansive survey of a single gene

Uncovering a multitude of human glucocorticoid receptor variants: An expansive survey of a single gene
15    5    1
Population size influences the type of nucleotide variations in humans

Population size influences the type of nucleotide variations in humans
12    7    1
Detecting TF-miRNA-gene network based modules for 5hmC and 5mC brain samples: A intra- and inter-species case-study between human and rhesus

Detecting TF-miRNA-gene network based modules for 5hmC and 5mC brain samples: A intra- and inter-species case-study between human and rhesus
22    2    1
Association between sequence variants in panicle development genes and the number of spikelets per panicle in rice

Association between sequence variants in panicle development genes and the number of spikelets per panicle in rice
11    2    1
Rare intronic variants of TCF7L2 arising by selective sweeps in an indigenous population from Mexico

Rare intronic variants of TCF7L2 arising by selective sweeps in an indigenous population from Mexico
15    2    1
Monoamine oxidase B gene variants associated with attention deficit hyperactivity disorder in the Indo-Caucasoid population from West Bengal

Monoamine oxidase B gene variants associated with attention deficit hyperactivity disorder in the Indo-Caucasoid population from West Bengal
15    2    1
The genetic variants in 3’ untranslated region of voltage-gated sodium channel alpha 1 subunit gene affect the mRNA-microRNA interactions and associate with epilepsy

The genetic variants in 3’ untranslated region of voltage-gated sodium channel alpha 1 subunit gene affect the mRNA-microRNA interactions and associate with epilepsy
12    2    1
C14orf132 gene is possibly related to extremely low birth weight

C14orf132 gene is possibly related to extremely low birth weight
5    2    1
New population-based exome data question the pathogenicity of some genetic variants previously associated with Marfan syndrome

New population-based exome data question the pathogenicity of some genetic variants previously associated with Marfan syndrome
8    2    1
Associations of the uric acid related genetic variants in SLC2A9 and ABCG2 loci with coronary heart disease risk

Associations of the uric acid related genetic variants in SLC2A9 and ABCG2 loci with coronary heart disease risk
7    2    1
The prognostic impact of GSTM1/GSTP1 genetic variants in bladder Cancer

The prognostic impact of GSTM1/GSTP1 genetic variants in bladder Cancer
11    46    0
Advantages of a next generation sequencing targeted approach for the molecular diagnosis of retinoblastoma

Advantages of a next generation sequencing targeted approach for the molecular diagnosis of retinoblastoma
9    61    0
Variants at the 9p21 locus and melanoma risk

Variants at the 9p21 locus and melanoma risk
15    70    0
MAP-RSeq: Mayo Analysis Pipeline for RNA sequencing

MAP-RSeq: Mayo Analysis Pipeline for RNA sequencing
11    91    0
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