"Mutations in the tumor suppressor breast cancer susceptibility gene 1 BRCA1" trang 1 - tải miễn phí từ tailieuXANH
Parsing the synonymous mutations in the maize genome: Isoaccepting mutations are more advantageous in regions with codon co-occurrence bias

Parsing the synonymous mutations in the maize genome: Isoaccepting mutations are more advantageous in regions with codon co-occurrence bias
9    52    0
Gene characteristics predicting missense, nonsense and frameshift mutations in tumor samples

Gene characteristics predicting missense, nonsense and frameshift mutations in tumor samples
14    50    0
A spatial simulation approach to account for protein structure when identifying non-random somatic mutations

A spatial simulation approach to account for protein structure when identifying non-random somatic mutations
13    64    0
Comprehensive assessment of computational algorithms in predicting cancer driver mutations

Comprehensive assessment of computational algorithms in predicting cancer driver mutations
17    51    2
Comparison of germline versus somatic BAP1 mutations for risk of metastasis in uveal melanoma

Comparison of germline versus somatic BAP1 mutations for risk of metastasis in uveal melanoma
12    55    0
Utilizing protein structure to identify non-random somatic mutations

Utilizing protein structure to identify non-random somatic mutations
12    44    0
A patient with combined pituitary hormone deficiency and osteogenesis imperfecta associated with mutations in LHX4 and COL1A2

A patient with combined pituitary hormone deficiency and osteogenesis imperfecta associated with mutations in LHX4 and COL1A2
7    45    0
How many samples are needed to infer truly clonal mutations from heterogenous tumours?

How many samples are needed to infer truly clonal mutations from heterogenous tumours?
11    41    0
EGFR exon 20 insertion mutations and response to osimertinib in non-small-cell lung cancer

EGFR exon 20 insertion mutations and response to osimertinib in non-small-cell lung cancer
9    85    1
NOTCH1 mutations influence survival in chronic lymphocytic leukemia patients

NOTCH1 mutations influence survival in chronic lymphocytic leukemia patients
6    47    0
A probabilistic method for leveraging functional annotations to enhance estimation of the temporal order of pathway mutations during carcinogenesis

A probabilistic method for leveraging functional annotations to enhance estimation of the temporal order of pathway mutations during carcinogenesis
12    49    0
Using passenger mutations to estimate the timing of driver mutations and identify mutator alterations

Using passenger mutations to estimate the timing of driver mutations and identify mutator alterations
11    99    0
Recurrent mutations at estrogen receptor binding sites alter chromatin topology and distal gene expression in breast cancer

Recurrent mutations at estrogen receptor binding sites alter chromatin topology and distal gene expression in breast cancer
15    16    1
Similar response rates and survival with PARP inhibitors for patients with solid tumors harboring somatic versus Germline BRCA mutations: A Meta-analysis and systematic review

Similar response rates and survival with PARP inhibitors for patients with solid tumors harboring somatic versus Germline BRCA mutations: A Meta-analysis and systematic review
9    68    0
Báo cáo y học:

Báo cáo y học: " Transient antiretroviral therapy selecting for common HIV-1 mutations substantially accelerates the appearance of rare mutations"
13    48    0
Báo cáo hóa học:

Báo cáo hóa học: " Novel C16orf57 mutations in patients with Poikiloderma with Neutropenia: bioinformatic analysis of the protein and predicted effects of all reported mutations"
38    71    0
Báo cáo khoa học: BRCA1 16 years later: risk-associated BRCA1 mutations and their functional implications

Báo cáo khoa học: BRCA1 16 years later: risk-associated BRCA1 mutations and their functional implications
11    49    0
Diagnotic procedure development to detect common point mutations in fms-like tyrosine kinase 3 tyrosine kinase domain (FLT3-TKD)

Diagnotic procedure development to detect common point mutations in fms-like tyrosine kinase 3 tyrosine kinase domain (FLT3-TKD)
8    56    0
Identification and in silico analysis of GALNS mutations causing Morquio A syndrome in eight consanguineous families

Identification and in silico analysis of GALNS mutations causing Morquio A syndrome in eight consanguineous families
11    108    0
The analysis of partial dominance of intragenic mutations at the ADH locus in drosophila melanogaster at two different alcohol concentrations

The analysis of partial dominance of intragenic mutations at the ADH locus in drosophila melanogaster at two different alcohol concentrations
10    271    0
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