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Two Distinct Categories of Focal Deletions in Cancer Genomes | PLOS ONE
Zoom in of the 10q region containing focal homozygous deletion... | Download Scientific Diagram
Genome-wide somatic copy number alteration analysis and database construction for cervical cancer | SpringerLink
PDF) cIMPACT-NOW update 5: recommended grading criteria and terminologies for IDH-mutant astrocytomas. (2020) | Daniel J. Brat | 136 Citations
Focal chromosomal copy number aberrations in cancer—Needles in a genome haystack - ScienceDirect
Six-gene signature for predicting survival in patients with head and neck squamous cell carcinoma | Aging
Symmetry | Free Full-Text | Machine Learning Reveals Molecular Similarity and Fingerprints in Structural Aberrations of Somatic Cancer
Two Distinct Categories of Focal Deletions in Cancer Genomes - CSHL Scientific Digital Repository
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Frequent breakpoints of focal deletion and uniparental disomy in 22q11.1 or 11.2 segmental duplication region reveal distinct tumorigenesis in rhabdoid tumor of the kidney - Haruta - 2021 - Genes, Chromosomes and Cancer - Wiley Online Library
CNV Radar: an improved method for somatic copy number alteration characterization in oncology | BMC Bioinformatics | Full Text
Two Distinct Categories of Focal Deletions in Cancer Genomes | PLOS ONE
Estimation of copy number aberrations: Comparison of exome sequencing data with SNP microarrays identifies homozygous deletions of 19q13.2 and CIC in neuroblastoma
JCI Insight - Focal adhesion proteins Pinch1 and Pinch2 regulate bone homeostasis in mice
The PAX5 gene is frequently rearranged in BCR-ABL1-positive acute lymphoblastic leukemia but is not associated with outcome. A report on behalf of the GIMEMA Acute Leukemia Working Party | Haematologica
WWOX, the FRA16D gene: A target of and a contributor to genomic instability - Hussain - 2019 - Genes, Chromosomes and Cancer - Wiley Online Library
The Importance of Detecting Copy Number Variants (CNVs) in the Cancer Genome
Histopathologic subtype-specific genomic profiles of renal cell carcinomas identified by high-resolution whole-genome single nucleotide polymorphism array analysis
The focal deletion of chr6p21.32 encompassing HLA class II alleles. a... | Download Scientific Diagram
Clinical Cancer Research on Twitter: "Kline et al report on the results of PNOC003, a multi-center precision medicine trial for children and young adults with newly diagnosed diffuse intrinsic pontine glioma. https://t.co/MVhK6LA5fe #
Frontiers | Somatic Copy Number Alterations in Human Cancers: An Analysis of Publicly Available Data From The Cancer Genome Atlas
Recurrent Hemizygous Deletions in Cancers May Optimize Proliferative Potential | Science
Frontiers | Deletion of FUNDC2 and CMC4 on Chromosome Xq28 Is Sufficient to Cause Hypergonadotropic Hypogonadism in Men
Constitutional de novo deletion of the FBXW7 gene in a patient with focal segmental glomerulosclerosis and multiple primitive tumors | Scientific Reports