Provisional assignment of MPI, PKM2, PGM3, and ME1 to Chinese hamster chromosome 4

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Increased frequencies of the killer immunoglobulin-like receptor genes KIR2DL2 and KIR2DS2 are associated with neuroblastoma.

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Cell death & disease·2014

Identification of circulating microRNAs in HNF1A-MODY carriers.

Diabetologia·2013

MicroRNA-204 increases sensitivity of neuroblastoma cells to cisplatin and is associated with a favourable clinical outcome.

British journal of cancer·2012

Modulation of neuroblastoma disease pathogenesis by an extensive network of epigenetically regulated microRNAs.

Oncogene·2012

Role of nuclear background and in vivo environment in variable segregation behavior of the aging-dependent T414G mutation at critical control site for human fibroblast mtDNA replication.

Somatic cell and molecular genetics·2004

Polycation-mediated transfection: how to overcome undesirable side effects of sticky DNA complexes.

Somatic cell and molecular genetics·2004

Chemically induced premature chromosome condensation in human fibroblast cell lines: fundamental study for applications to the biodosimetry of local exposure.

Somatic cell and molecular genetics·2004

Removal of UV photoproducts from an adenovirus-encoded reporter gene following infection of unirradiated and UV-irradiated human fibroblasts.

Somatic cell and molecular genetics·2004

Damage-repair kinetics and early adaptive response induced by gamma rays in murine leukocytes in vivo.

Somatic cell and molecular genetics·2004

Defective NF-kappaB signaling in dedifferentiated hepatoma cells.

Somatic cell and molecular genetics·2004

Rare missense variants identified by whole-genome sequencing in men with oligoasthenoteratozoospermia: An experimental study.

International journal of reproductive biomedicine·2026

Whole-Exome Sequencing Reveals the Genetic Landscape and Genotype-Phenotype Spectrum of Dystonia in a Chinese Cohort.

CNS neuroscience & therapeutics·2026

Genome-wide analysis of 439 mass spectrometry-based proteomic profiles in a population of 15,035 Scottish individuals.

Nature communications·2026

Generation of a human induced pluripotent stem cell line (PNUYHi004-A) from a patient with hereditary spastic paraplegia type 46 (SPG46) carrying compound heterozygous GBA2 variants.

Stem cell research·2026

Polygenic Risk Scores for Islet Autoantibody Positive Early-Stage Type 1 Diabetes Pre-Screening.

Diabetes, obesity & metabolism·2026

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Clinical genetics·2026

Related Experiment Videos

Provisional assignment of MPI, PKM2, PGM3, and ME1 to Chinese hamster chromosome 4

Related Concept Videos

A physiologically relevant 3D collagen-based scaffold-neuroblastoma cell system exhibits chemosensitivity similar to orthotopic xenograft models.

Increased frequencies of the killer immunoglobulin-like receptor genes KIR2DL2 and KIR2DS2 are associated with neuroblastoma.

MYCN repression of Lifeguard/FAIM2 enhances neuroblastoma aggressiveness.

Identification of circulating microRNAs in HNF1A-MODY carriers.

MicroRNA-204 increases sensitivity of neuroblastoma cells to cisplatin and is associated with a favourable clinical outcome.

Modulation of neuroblastoma disease pathogenesis by an extensive network of epigenetically regulated microRNAs.

Role of nuclear background and in vivo environment in variable segregation behavior of the aging-dependent T414G mutation at critical control site for human fibroblast mtDNA replication.

Polycation-mediated transfection: how to overcome undesirable side effects of sticky DNA complexes.

Chemically induced premature chromosome condensation in human fibroblast cell lines: fundamental study for applications to the biodosimetry of local exposure.

Removal of UV photoproducts from an adenovirus-encoded reporter gene following infection of unirradiated and UV-irradiated human fibroblasts.

Damage-repair kinetics and early adaptive response induced by gamma rays in murine leukocytes in vivo.

Defective NF-kappaB signaling in dedifferentiated hepatoma cells.

Rare missense variants identified by whole-genome sequencing in men with oligoasthenoteratozoospermia: An experimental study.

Whole-Exome Sequencing Reveals the Genetic Landscape and Genotype-Phenotype Spectrum of Dystonia in a Chinese Cohort.

Genome-wide analysis of 439 mass spectrometry-based proteomic profiles in a population of 15,035 Scottish individuals.

Generation of a human induced pluripotent stem cell line (PNUYHi004-A) from a patient with hereditary spastic paraplegia type 46 (SPG46) carrying compound heterozygous GBA2 variants.

Polygenic Risk Scores for Islet Autoantibody Positive Early-Stage Type 1 Diabetes Pre-Screening.

Analysis of Genomic Testing of Congenital Heart Disease in a Cohort From a Consanguineous Population.

Related Experiment Videos

Provisional assignment of MPI, PKM2, PGM3, and ME1 to Chinese hamster chromosome 4

Abstract:

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