"Structural mutation" trang 1 - tải miễn phí từ tailieuXANH
Highly efficient correction of structural mutations of 450 kb KIT locus in kidney cells of Yorkshire pig by CRISPR/Cas9

Highly efficient correction of structural mutations of 450 kb KIT locus in kidney cells of Yorkshire pig by CRISPR/Cas9
8    35    1
Báo cáo khoa học: Enhanced thermostability of methyl parathion hydrolase from Ochrobactrum sp. M231 by rational engineering of a glycine to proline mutation

Báo cáo khoa học: Enhanced thermostability of methyl parathion hydrolase from Ochrobactrum sp. M231 by rational engineering of a glycine to proline mutation
8    40    0
3D deep convolutional neural networks for amino acid environment similarity analysis

3D deep convolutional neural networks for amino acid environment similarity analysis
23    135    0
Predicting the most deleterious missense nsSNPs of the protein isoforms of the human HLA-G gene and in silico evaluation of their structural and functional consequences

Predicting the most deleterious missense nsSNPs of the protein isoforms of the human HLA-G gene and in silico evaluation of their structural and functional consequences
27    9    1
Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genome

Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genome
21    166    2
Báo cáo khoa học: Structural effects of a dimer interface mutation on catalytic activity of triosephosphate isomerase The role of conserved residues and complementary mutations

Báo cáo khoa học: Structural effects of a dimer interface mutation on catalytic activity of triosephosphate isomerase The role of conserved residues and complementary mutations
15    44    0
Báo cáo khóa học: Disruption of the interaction between the Rieske iron–sulfur protein and cytochrome b in the yeast bc1 complex owing to a human disease-associated mutation within cytochrome b

Báo cáo khóa học: Disruption of the interaction between the Rieske iron–sulfur protein and cytochrome b in the yeast bc1 complex owing to a human disease-associated mutation within cytochrome b
7    28    0
Prediction of sensitivity to gefitinib/ erlotinib for EGFR mutations in NSCLC based on structural interaction fingerprints and multilinear principal component analysis

Prediction of sensitivity to gefitinib/ erlotinib for EGFR mutations in NSCLC based on structural interaction fingerprints and multilinear principal component analysis
13    56    0
EGFR Mutant Structural Database: Computationally predicted 3D structures and the corresponding binding free energies with gefitinib and erlotinib

EGFR Mutant Structural Database: Computationally predicted 3D structures and the corresponding binding free energies with gefitinib and erlotinib
10    68    0
Quantum coupled mutation finder: Predicting functionally or structurally important sites in proteins using quantum Jensen-Shannon divergence and CUDA programming

Quantum coupled mutation finder: Predicting functionally or structurally important sites in proteins using quantum Jensen-Shannon divergence and CUDA programming
17    44    0
Metabolome and transcriptome analyses of the molecular mechanisms of flower color mutation in tobacco

Metabolome and transcriptome analyses of the molecular mechanisms of flower color mutation in tobacco
10    65    1
Genome analysis and pleiotropy assessment using causal networks with loss of function mutation and metabolomics

Genome analysis and pleiotropy assessment using causal networks with loss of function mutation and metabolomics
16    59    1
Long-read individual-molecule sequencing reveals CRISPR-induced genetic heterogeneity in human ESCs

Long-read individual-molecule sequencing reveals CRISPR-induced genetic heterogeneity in human ESCs
14    197    1
Evaluation of the structural impact of the missense mutation JAK2 V617F in janus kinase 2 by docking study

Evaluation of the structural impact of the missense mutation JAK2 V617F in janus kinase 2 by docking study
6    9    1
VARS1 mutations associated with neurodevelopmental disorder are located on a short amino acid stretch of the anticodon-binding domain

VARS1 mutations associated with neurodevelopmental disorder are located on a short amino acid stretch of the anticodon-binding domain
12    9    2
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