Uniparental disomies, homozygous deletions, amplifications, and target genes in mantle cell lymphoma revealed by integrative high-resolution whole-genome profiling. - Wikidata - wikimedia - TriplyDB

Uniparental disomies, homozygous deletions, amplifications, and target genes in mantle cell lymphoma revealed by integrative high-resolution whole-genome profiling.

Uniparental disomies, homozygous deletions, amplifications, and target genes in mantle cell lymphoma revealed by integrative high-resolution whole-genome profiling.

http://www.wikidata.org/entity/Q37143660

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Risk factors for etiology and prognosis of mantle cell lymphoma The EMT activator ZEB1 promotes tumor growth and determines differential response to chemotherapy in mantle cell lymphoma.Low ATM protein expression and depletion of p53 correlates with olaparib sensitivity in gastric cancer cell lines.Mantle cell lymphoma in the era of precision medicine-diagnosis, biomarkers and therapeutic agents The copper chelator ATN-224 induces caspase-independent cell death in diffuse large B cell lymphoma Integrative and comparative genomics analysis of early hepatocellular carcinoma differentiated from liver regeneration in young and old Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium Fas-associated factor 1 inhibits tumor growth by suppressing Helicobacter pylori-induced activation of NF-κB signaling in human gastric carcinoma Mantle cell lymphoma: report of the 2010 Mantle Cell Lymphoma Consortium Workshop.Recent advances in mantle cell lymphoma: report of the 2012 Mantle Cell Lymphoma Consortium Workshop.An integrated Bayesian analysis of LOH and copy number data.Copy neutral loss of heterozygosity: a novel chromosomal lesion in myeloid malignancies Epigenetic activation of SOX11 in lymphoid neoplasms by histone modifications.The expression of FAS-associated factor 1 and heat shock protein 70 in ovarian cancer.Pathway discovery in mantle cell lymphoma by integrated analysis of high-resolution gene expression and copy number profiling.Cell-cycle reprogramming for PI3K inhibition overrides a relapse-specific C481S BTK mutation revealed by longitudinal functional genomics in mantle cell lymphoma Non-nodal type of mantle cell lymphoma is a specific biological and clinical subgroup of the disease.p97-containing complexes in proliferation control and cancer: emerging culprits or guilt by association?Mantle cell lymphoma: biology, pathogenesis, and the molecular basis of treatment in the genomic era Numerical and structural genomic aberrations are reliably detectable in tissue microarrays of formalin-fixed paraffin-embedded tumor samples by fluorescence in-situ hybridization.Fas-associated factor (Faf1) is a novel CD40 interactor that regulates CD40-induced NF-κB activation via a negative feedback loop.Common genetic variants related to genomic integrity and risk of papillary thyroid cancer Acquired genomic copy number aberrations and survival in chronic lymphocytic leukemia.Genome wide copy number analysis of paediatric Burkitt lymphoma using formalin-fixed tissues reveals a subset with gain of chromosome 13q and corresponding miRNA over expression Investigation of Rho-Kinase Expressions and Polymorphisms in Mantle Cell Lymphoma Patients.Relax with CouchDB--into the non-relational DBMS era of bioinformatics Patterns of somatic uniparental disomy identify novel tumor suppressor genes in colorectal cancer.Fas-associated factor 1 is a scaffold protein that promotes β-transducin repeat-containing protein (β-TrCP)-mediated β-catenin ubiquitination and degradation Molecular pathogenesis of mantle cell lymphoma.Arsenic trioxide rewires mantle cell lymphoma response to bortezomib Integrative genomics reveals mechanisms of copy number alterations responsible for transcriptional deregulation in colorectal cancer.Reduced FAF1 Expression and Helicobacter Infection: Correlations with Clinicopathological Features in Gastric Cancer.Chromatin-associated degradation is defined by UBXN-3/FAF1 to safeguard DNA replication fork progression.CCND2 rearrangements are the most frequent genetic events in cyclin D1(-) mantle cell lymphoma.Role of p97/VCP (Cdc48) in genome stability.ATM deficiency sensitizes mantle cell lymphoma cells to poly(ADP-ribose) polymerase-1 inhibitors.Molecular subsets of mantle cell lymphoma defined by the IGHV mutational status and SOX11 expression have distinct biologic and clinical features New developments in the pathology of malignant lymphoma: a review of the literature published from August to December 2008.Landscape of somatic mutations and clonal evolution in mantle cell lymphoma.FAS-associated factor 1 (FAF1): diverse functions and implications for oncogenesis.

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Uniparental disomies, homozygous deletions, amplifications, and target genes in mantle cell lymphoma revealed by integrative high-resolution whole-genome profiling.

http://www.wikidata.org/entity/Q37143660

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2008 nî lūn-bûn

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Uniparental disomies, homozygo ...... lution whole-genome profiling.

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Uniparental disomies, homozygo ...... lution whole-genome profiling.

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Uniparental disomies, homozygo ...... lution whole-genome profiling.

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Uniparental disomies, homozygo ...... lution whole-genome profiling.

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Elena M Hartmann

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P2860

Molecular allelokaryotyping of pediatric acute lymphoblastic leukemias by high-resolution single nucleotide polymorphism oligonucleotide genomic microarray

Global variation in copy number in the human genome

Highly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide-polymorphism genotyping microarrays

Genetic and molecular pathogenesis of mantle cell lymphoma: perspectives for new targeted therapeutics.

c-Myc-regulated microRNAs modulate E2F1 expression

Detection of large-scale variation in the human genome

Segmental duplications and copy-number variation in the human genome.

Identification and characterization of a novel gene, C13orf25, as a target for 13q31-q32 amplification in malignant lymphoma

Large-scale copy number polymorphism in the human genome

Structure, dynamics and functions of promyelocytic leukaemia nuclear bodies

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