"Comparative Genomic Hybridization" trang 1 - tải miễn phí từ tailieunhanh
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
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báo cáo khoa học:

báo cáo khoa học: "Genomic profiling of plasmablastic lymphoma using array comparative genomic hybridization (aCGH): revealing significant overlapping genomic lesions with diffuse large B-cell lymphoma"
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The EMSY gene collaborates with CCND1 in non-small cell lung carcinogenesis

The EMSY gene collaborates with CCND1 in non-small cell lung carcinogenesis
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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
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Báo cáo hóa học:

Báo cáo hóa học: " Chromosomal 16p microdeletion in Rubinstein-Taybi syndrome detected by oligonucleotide-based array comparative genomic hybridization: a case report"
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Báo cáo y học:

Báo cáo y học: " Ring chromosome 13 syndrome characterized by high resolution array based comparative genomic hybridization in patient with 47, XYY syndrome: a case report."
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Amplification and overexpression of CTTN and CCND1 at chromosome 11q13 in Esophagus squamous cell carcinoma (ESCC) of North Eastern Chinese population

Amplification and overexpression of CTTN and CCND1 at chromosome 11q13 in Esophagus squamous cell carcinoma (ESCC) of North Eastern Chinese population
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CAISMOV24, a new human low-grade serous ovarian carcinoma cell line

CAISMOV24, a new human low-grade serous ovarian carcinoma cell line
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Identification of BRCA1-like triple-negative breast cancers by quantitative multiplexligation-dependent probe amplification (MLPA) analysis of BRCA1-associated chromosomal regions: A validation study

Identification of BRCA1-like triple-negative breast cancers by quantitative multiplexligation-dependent probe amplification (MLPA) analysis of BRCA1-associated chromosomal regions: A validation study
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Combined comparative genomic hybridization and transcriptomic analyses of ovarian granulosa cell tumors point to novel candidate driver genes

Combined comparative genomic hybridization and transcriptomic analyses of ovarian granulosa cell tumors point to novel candidate driver genes
11    47    1
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    39    1
The genetic basis for inactivation of Wnt pathway in human osteosarcoma

The genetic basis for inactivation of Wnt pathway in human osteosarcoma
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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
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Pyloric gland adenoma of the cystic duct with malignant transformation: Report of a case with a review of the literature

Pyloric gland adenoma of the cystic duct with malignant transformation: Report of a case with a review of the literature
10    59    1
Phân lớp dữ liệu CGH dự đoán bệnh ung thư ở người

Phân lớp dữ liệu CGH dự đoán bệnh ung thư ở người
11    58    1
Prenatal diagnosis of distal 13q deletion syndrome in a fetus with esophageal atresia: A case report and review of the literature

Prenatal diagnosis of distal 13q deletion syndrome in a fetus with esophageal atresia: A case report and review of the literature
6    1    1
SubPatCNV: Approximate subspace pattern mining for mapping copy-number variations

SubPatCNV: Approximate subspace pattern mining for mapping copy-number variations
12    46    1
Screening populations for copy number variation using genotyping-by-sequencing: a proof of concept using soybean fast neutron mutants

Screening populations for copy number variation using genotyping-by-sequencing: a proof of concept using soybean fast neutron mutants
16    52    1