"Multiple mutations" trang 1 - tải miễn phí từ tailieunhanh
Overview and clinical significance of multiple mutations in individual genes in hepatocellular carcinoma

Overview and clinical significance of multiple mutations in individual genes in hepatocellular carcinoma
12    1    1
Breast cancer and synchronous multiple primary lung adenocarcinomas with heterogeneous mutations: A case report

Breast cancer and synchronous multiple primary lung adenocarcinomas with heterogeneous mutations: A case report
6    47    1
SigsPack, a package for cancer mutational signatures

SigsPack, a package for cancer mutational signatures
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Isma: An R package for the integrative analysis of mutations detected by multiple pipelines

Isma: An R package for the integrative analysis of mutations detected by multiple pipelines
9    84    1
A CRISPR/Cas9 toolkit for multiplex genome editing in plants

A CRISPR/Cas9 toolkit for multiplex genome editing in plants
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Combined targeting of MEK and the glucocorticoid receptor for the treatment of RAS-mutant multiple myeloma

Combined targeting of MEK and the glucocorticoid receptor for the treatment of RAS-mutant multiple myeloma
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Germline and somatic mutations in patients with multiple primary melanomas: A next generation sequencing study

Germline and somatic mutations in patients with multiple primary melanomas: A next generation sequencing study
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Comparison of orthopaedic manifestations of multiple epiphyseal dysplasia caused by MATN3 versus COMP mutations: A case control study

Comparison of orthopaedic manifestations of multiple epiphyseal dysplasia caused by MATN3 versus COMP mutations: A case control study
8    51    1
Truncating CHRNG mutations associated with interfamilial variability of the severity of the Escobar variant of multiple pterygium syndrome

Truncating CHRNG mutations associated with interfamilial variability of the severity of the Escobar variant of multiple pterygium syndrome
8    15    1
Large-scale mutational analysis in the EXT1 and EXT2 genes for Japanese patients with multiple osteochondromas

Large-scale mutational analysis in the EXT1 and EXT2 genes for Japanese patients with multiple osteochondromas
7    12    1
Báo cáo y học:

Báo cáo y học: " Mutations that permit residual CFTR function delay acquisition of multiple respiratory pathogens in CF patients"
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Báo cáo y học:

Báo cáo y học: "The evolution of HIV-1 reverse transcriptase in route to acquisition of Q151M multi-drug resistance is complex and involves mutations in multiple domains"
11    57    0
Báo cáo y học:

Báo cáo y học: "APOBEC3G induces a hypermutation gradient: purifying selection at multiple steps during HIV-1 replication results in levels of G-to-A mutations that are high in DNA, intermediate in cellular viral RNA, and low in virion RNA"
15    33    0
Analysis of hereditary cancer syndromes by using a panel of genes: Novel and multiple pathogenic mutations

Analysis of hereditary cancer syndromes by using a panel of genes: Novel and multiple pathogenic mutations
19    102    0
Use of the QIAGEN GeneReader NGS system for detection of KRAS mutations, validated by the QIAGEN Therascreen PCR kit and alternative NGS platform

Use of the QIAGEN GeneReader NGS system for detection of KRAS mutations, validated by the QIAGEN Therascreen PCR kit and alternative NGS platform
8    69    1
Targeted deep sequencing of mucinous ovarian tumors reveals multiple overlapping RAS-pathway activating mutations in borderline and cancerous neoplasms

Targeted deep sequencing of mucinous ovarian tumors reveals multiple overlapping RAS-pathway activating mutations in borderline and cancerous neoplasms
10    43    1
Machine learning classifier for identification of damaging missense mutations exclusive to human mitochondrial DNA-encoded polypeptides

Machine learning classifier for identification of damaging missense mutations exclusive to human mitochondrial DNA-encoded polypeptides
11    57    1
LowMACA: Exploiting protein family analysis for the identification of rare driver mutations in cancer

LowMACA: Exploiting protein family analysis for the identification of rare driver mutations in cancer
12    55    1
Coupled mutation finder: A new entropybased method quantifying phylogenetic noise for the detection of compensatory mutations

Coupled mutation finder: A new entropybased method quantifying phylogenetic noise for the detection of compensatory mutations
12    25    1
Causal mutations from adaptive laboratory evolution are outlined by multiple scales of genome annotations and conditionspecificity

Causal mutations from adaptive laboratory evolution are outlined by multiple scales of genome annotations and conditionspecificity
16    46    1