Karpas 422 (DSMZ) | Bioz | Ratings For Life-Science Research
Focal chromosomal copy number aberrations in cancer—Needles in a genome haystack - ScienceDirect
Focal chromosomal copy number aberrations in cancer—Needles in a genome haystack - ScienceDirect
Recurrent Hemizygous Deletions in Cancers May Optimize Proliferative Potential | Science
Cancers | Free Full-Text | The Effect of Atm Loss on Radiosensitivity of a Primary Mouse Model of Pten-Deleted Brainstem Glioma
Overview of all mutations, focal deletions, 6q deletions, and TCR... | Download Scientific Diagram
Six-gene signature for predicting survival in patients with head and neck squamous cell carcinoma | Aging
Genome-wide somatic copy number alteration analysis and database construction for cervical cancer | SpringerLink
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 #
Recurrent deletions of IKZF1 in pediatric acute myeloid leukemia | Haematologica
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
JCI Insight - Focal adhesion proteins Pinch1 and Pinch2 regulate bone homeostasis in mice
Frontiers | Somatic Copy Number Alterations in Human Cancers: An Analysis of Publicly Available Data From The Cancer Genome Atlas
Two Distinct Categories of Focal Deletions in Cancer Genomes | PLOS ONE
Histopathologic subtype-specific genomic profiles of renal cell carcinomas identified by high-resolution whole-genome single nucleotide polymorphism array analysis
Figures and data in The novel lncRNA lnc-NR2F1 is pro-neurogenic and mutated in human neurodevelopmental disorders | eLife
Pan-cancer analysis of homozygous deletions in primary tumours uncovers rare tumour suppressors | Nature Communications
Cumulative haploinsufficiency and triplosensitivity drive aneuploidy patterns and shape the cancer genome. - Abstract - Europe PMC