Genesis of the Philadelphia chromosome: possible points of breakage in chromosome

Chromosomal location and some structural features of human clathrin light-chain genes (CLTA and CLTB).

Genomics·1994

Glial fibrillary acid protein, an astrocytic-specific marker, maps to human chromosome 17.

Genomics·1991

Chromosomal alterations in lymphocytes of patients with Balkan endemic nephropathy and of healthy individuals after incubation in vitro with ochratoxin A.

IARC scientific publications·1991

Induction of characteristic chromosomal aberrations, particularly X-trisomy, in cultured human lymphocytes treated by ochratoxin A, a mycotoxin implicated in Balkan endemic nephropathy.

Mutation research·1990

Mouse Hox-3.4: homeobox sequence and embryonic expression patterns compared with other members of the Hox gene network.

Development (Cambridge, England)·1990

The gene encoding peripheral myelin protein zero is located on mouse chromosome 1.

The Journal of neuroscience : the official journal of the Society for Neuroscience·1990

Diagnostic and mechanistic roles of miR-5584-5p in endometriosis via the FZD2-mediated Wnt/β-catenin EMT axis.

Hereditas·2026

Multi-omics mapping of TIMP1-associated stromal-myeloid remodeling in autoimmune gastritis and gastric cancer.

Hereditas·2026

Beyond the variant: hereditary cancer awareness in the multi-omics era.

Hereditas·2026

Hereditary breast cancer: emerging roles of non-coding RNAs.

Hereditas·2026

The prognostic value of miR-363-5p in colorectal cancer and its associated molecular mechanisms.

Hereditas·2026

MicroRNA-345-3p expression inhibits colorectal cancer liver metastasis by targeting KHDRBS1 and TGF-β signaling pathway.

Hereditas·2026

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

Genesis of the Philadelphia chromosome: possible points of breakage in chromosome

Related Concept Videos

Chromosomal location and some structural features of human clathrin light-chain genes (CLTA and CLTB).

Glial fibrillary acid protein, an astrocytic-specific marker, maps to human chromosome 17.

Chromosomal alterations in lymphocytes of patients with Balkan endemic nephropathy and of healthy individuals after incubation in vitro with ochratoxin A.

Induction of characteristic chromosomal aberrations, particularly X-trisomy, in cultured human lymphocytes treated by ochratoxin A, a mycotoxin implicated in Balkan endemic nephropathy.

Mouse Hox-3.4: homeobox sequence and embryonic expression patterns compared with other members of the Hox gene network.

The gene encoding peripheral myelin protein zero is located on mouse chromosome 1.

Diagnostic and mechanistic roles of miR-5584-5p in endometriosis via the FZD2-mediated Wnt/β-catenin EMT axis.

Multi-omics mapping of TIMP1-associated stromal-myeloid remodeling in autoimmune gastritis and gastric cancer.

Beyond the variant: hereditary cancer awareness in the multi-omics era.

Hereditary breast cancer: emerging roles of non-coding RNAs.

The prognostic value of miR-363-5p in colorectal cancer and its associated molecular mechanisms.

MicroRNA-345-3p expression inhibits colorectal cancer liver metastasis by targeting KHDRBS1 and TGF-β signaling pathway.

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

Genesis of the Philadelphia chromosome: possible points of breakage in chromosome

Related Concept Videos

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