Isochromosome 17q- in acute promyelocytic leukemia. Molecular characterization by fluorescence in situ hybridization

Translocation (14;19)(q32;q13.1) in a Young Patient who Developed a Large Cell Lymphoma after an Initial Diagnosis of CLL.

Leukemia & lymphoma·2016

Two Translocations: a Follicular Variant 2; 18 and a Burkitt 8;14 in a Small Non Cleaved Non Hodgkin's Lymphoma.

Leukemia & lymphoma·2016

Bone marrow WT1 levels at diagnosis, post-induction and post-intensification in adult de novo AML.

Leukemia·2013

Adverse impact of IDH1 and IDH2 mutations in primary AML: experience of the Spanish CETLAM group.

Leukemia research·2012

CALM/AF10-positive leukemias show upregulation of genes involved in chromatin assembly and DNA repair processes and of genes adjacent to the breakpoint at 10p12.

Leukemia·2011

Breakpoints of 11q25 in three similar cases of B non Hodgkin's lymphoma.

Leukemia & lymphoma·2011

A pericentric inv(9)(p22q34) of the der(9)t(9;22)(q34;q11.2) is a recurrent secondary anomaly in Ph-positive leukemia.

Cancer genetics and cytogenetics·2010

Translocation (3;8)(q27;q24) in two cases of triple hit lymphoma.

Cancer genetics and cytogenetics·2010

Screening for DNA copy number aberrations in mucinous adenocarcinoma arising from the minor salivary gland: two case reports.

Cancer genetics and cytogenetics·2010

Screening for common copy-number variants in cancer genes.

Cancer genetics and cytogenetics·2010

Trisomy 17 in congenital plexiform (multinodular) cellular schwannoma.

Cancer genetics and cytogenetics·2010

Chromosomal alterations in Malaysian patients with nasopharyngeal carcinoma analyzed by comparative genomic hybridization.

Cancer genetics and cytogenetics·2010

Identification and validation of feature genes using a ferroptosis-informed analytical framework in medulloblastoma.

Frontiers in pediatrics·2026

Genome-wide CRISPR screens identify shared and context-specific regulators of podocyte resistance to oxidative injury.

Renal failure·2026

Genotype and arrhythmic risk in dilated cardiomyopathy.

European heart journal·2026

Gene-Guided Therapy in Type 2 Diabetes Mellitus: An Integrative Review of the Pharmacogenetics of Metformin and Sodium-Glucose Cotransporter-2 Inhibitors.

Endocrinology, diabetes & metabolism·2026

Evaluating the effects of metronidazole, metformin, and onion extract on GAPDH activity and nitric oxide production in Blastocystis sp. cultures: a biochemical and therapeutic approach.

BMC complementary medicine and therapies·2026

Excess endopolyploidy associated with cellular defects in neo-autotetraploid Arabidopsis arenosa is in part corrected by a naturally evolved allele of CYCD3;2.

The New phytologist·2026

Related Experiment Videos

Isochromosome 17q- in acute promyelocytic leukemia. Molecular characterization by fluorescence in situ hybridization

Related Concept Videos

Translocation (14;19)(q32;q13.1) in a Young Patient who Developed a Large Cell Lymphoma after an Initial Diagnosis of CLL.

Two Translocations: a Follicular Variant 2; 18 and a Burkitt 8;14 in a Small Non Cleaved Non Hodgkin's Lymphoma.

Bone marrow WT1 levels at diagnosis, post-induction and post-intensification in adult de novo AML.

Adverse impact of IDH1 and IDH2 mutations in primary AML: experience of the Spanish CETLAM group.

CALM/AF10-positive leukemias show upregulation of genes involved in chromatin assembly and DNA repair processes and of genes adjacent to the breakpoint at 10p12.

Breakpoints of 11q25 in three similar cases of B non Hodgkin's lymphoma.

A pericentric inv(9)(p22q34) of the der(9)t(9;22)(q34;q11.2) is a recurrent secondary anomaly in Ph-positive leukemia.

Translocation (3;8)(q27;q24) in two cases of triple hit lymphoma.

Screening for DNA copy number aberrations in mucinous adenocarcinoma arising from the minor salivary gland: two case reports.

Screening for common copy-number variants in cancer genes.

Trisomy 17 in congenital plexiform (multinodular) cellular schwannoma.

Chromosomal alterations in Malaysian patients with nasopharyngeal carcinoma analyzed by comparative genomic hybridization.

Identification and validation of feature genes using a ferroptosis-informed analytical framework in medulloblastoma.

Genome-wide CRISPR screens identify shared and context-specific regulators of podocyte resistance to oxidative injury.

Genotype and arrhythmic risk in dilated cardiomyopathy.

Gene-Guided Therapy in Type 2 Diabetes Mellitus: An Integrative Review of the Pharmacogenetics of Metformin and Sodium-Glucose Cotransporter-2 Inhibitors.

Evaluating the effects of metronidazole, metformin, and onion extract on GAPDH activity and nitric oxide production in Blastocystis sp. cultures: a biochemical and therapeutic approach.

Excess endopolyploidy associated with cellular defects in neo-autotetraploid Arabidopsis arenosa is in part corrected by a naturally evolved allele of CYCD3;2.

Related Experiment Videos

Isochromosome 17q- in acute promyelocytic leukemia. Molecular characterization by fluorescence in situ hybridization

Related Concept Videos

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