"Genomic alterations" trang 1 - tải miễn phí từ tailieuXANH
Array comparative genomic hybridization analysis discloses chromosome copy number alterations as indicators of patient outcome in lymph node-negative breast cancer

Array comparative genomic hybridization analysis discloses chromosome copy number alterations as indicators of patient outcome in lymph node-negative breast cancer
12    57    0
Cribriform and intraductal prostate cancer are associated with increased genomic instability and distinct genomic alterations

Cribriform and intraductal prostate cancer are associated with increased genomic instability and distinct genomic alterations
11    75    0
PTEN genomic deletion predicts prostate cancer recurrence and is associated with low AR expression and transcriptional activity

PTEN genomic deletion predicts prostate cancer recurrence and is associated with low AR expression and transcriptional activity
9    64    0
Clinically significant genomic alterations in the Chinese and Western patients with intrahepatic cholangiocarcinoma

Clinically significant genomic alterations in the Chinese and Western patients with intrahepatic cholangiocarcinoma
10    46    1
Genomic changes and biochemical alterations of seed protein and oil content in a subset of fast neutron induced soybean mutants

Genomic changes and biochemical alterations of seed protein and oil content in a subset of fast neutron induced soybean mutants
12    65    0
Genomic profiling of Chinese patients with urothelial carcinoma

Genomic profiling of Chinese patients with urothelial carcinoma
11    62    1
Báo cáo khoa học:

Báo cáo khoa học: "Genomic alterations of primary tumor and blood in invasive ductal carcinoma of breast"
11    45    0
Báo cáo y học:

Báo cáo y học: " Microenvironmental genomic alterations reveal signaling networks for head and neck squamous cell carcinoma"
15    45    0
báo cáo khoa học:

báo cáo khoa học: " The role of complex genomic alterations in neuroblastoma risk estimation"
4    28    0
In vitro activity of a G-quadruplexstabilizing small molecule that synergizes with Navitoclax to induce cytotoxicity in acute myeloid leukemia cells

In vitro activity of a G-quadruplexstabilizing small molecule that synergizes with Navitoclax to induce cytotoxicity in acute myeloid leukemia cells
11    40    0
Multi-region and single-cell sequencing reveal variable genomic heterogeneity in rectal cancer

Multi-region and single-cell sequencing reveal variable genomic heterogeneity in rectal cancer
11    106    0
Germline EMSY sequence alterations in hereditary breast cancer and ovarian cancer families

Germline EMSY sequence alterations in hereditary breast cancer and ovarian cancer families
8    138    0
CCNE1 amplification is associated with poor prognosis in patients with triple negative breast cancer

CCNE1 amplification is associated with poor prognosis in patients with triple negative breast cancer
11    50    0
The genomic and transcriptomic landscape of anaplastic thyroid cancer: Implications for therapy

The genomic and transcriptomic landscape of anaplastic thyroid cancer: Implications for therapy
11    52    0
Chromosomal imbalances in human bladder urothelial carcinoma: Similarities and differences between biopsy samples and cancer stem-like cells

Chromosomal imbalances in human bladder urothelial carcinoma: Similarities and differences between biopsy samples and cancer stem-like cells
10    59    0
Copy number alterations in small intestinal neuroendocrine tumors determined by array comparative genomic hybridization

Copy number alterations in small intestinal neuroendocrine tumors determined by array comparative genomic hybridization
13    52    0
Cancer prognosis prediction using somatic point mutation and copy number variation data: A comparison of gene‑level and pathway‑based models

Cancer prognosis prediction using somatic point mutation and copy number variation data: A comparison of gene‑level and pathway‑based models
19    56    0
The diagnostic application of RNA sequencing in patients with thyroid cancer: An analysis of 851 variants and 133 fusions in 524 genes

The diagnostic application of RNA sequencing in patients with thyroid cancer: An analysis of 851 variants and 133 fusions in 524 genes
10    59    0
Chromatin spatial organization of wild type and mutant peanuts reveals high-resolution genomic architecture and interaction alterations

Chromatin spatial organization of wild type and mutant peanuts reveals high-resolution genomic architecture and interaction alterations
21    161    1
Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome

Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome
21    41    2
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