Isolation and mapping of a polymorphic DNA sequence (cTBQ20) on chromosome 10 [D10S31]

The D2 receptor occupancy profile of loxapine determined using PET.

Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology·1996

Loss of retinoic acid receptors in mouse skin and skin tumors is associated with activation of the ras(Ha) oncogene and high risk for premalignant progression.

Cancer research·1996

Two distinct apolipoprotein B alleles in mice generated by a single 'in-out' targeting.

Gene·1996

Insulin resistance in patients with essential hypertension can occur in the absence of microalbuminuria.

American journal of hypertension·1996

Familial amyotrophic lateral sclerosis with a mutation in exon 4 of the Cu/Zn superoxide dismutase gene: pathological and immunocytochemical changes.

Acta neuropathologica·1996

Mouse monoclonal antipeptide antibodies specific for cholesteryl ester transfer protein (CETP).

Hybridoma·1996

AID self-assembly and multistranded DNA binding drive synapsis in class switch recombination.

Nucleic acids research·2026

Coronavirus NSP14 drives internal m7G modification to rewire host splicing and promote viral replication.

Nucleic acids research·2026

Insights into the recruitment of the H3K4me3 reader Spp1 by the meiotic double-strand break protein Mer2.

Nucleic acids research·2026

Newly synthesized histones: passive or active players in the regulation of epigenetic inheritance?

Nucleic acids research·2026

ETfinder: harnessing conserved C-terminal tails of single-stranded DNA-binding proteins for mining and engineering RecET systems in non-model microbial chassis.

Nucleic acids research·2026

MOSAIC enables selective transfer and fairness-aware generalization in cross-species DNA methylation prediction.

Nucleic acids research·2026

Molecular characterization of FAM222B as a novel disease gene for dominant cardiovascular laterality defects.

Scientific reports·2026

Genetic architecture and inheritance patterns of Leber hereditary optic neuropathy among 419 Chinese pedigrees carrying the ND4 11778G>A mutation.

Journal of genetics and genomics = Yi chuan xue bao·2026

Integrating LNA-qPCR and full-length SMN1 sequencing for precision SMA carrier screening: large-scale validation in 30,849 individuals.

Clinica chimica acta; international journal of clinical chemistry·2026

Novel splice site variants in GBA1 are associated with Gaucher disease and genotype-phenotype correlations.

Brain & development·2026

High-Resolution Physical Mapping and Chromosomal Transmission in Sugarcane Progeny.

The Journal of heredity·2026

Loci Associated With Susceptibility to Biliary Atresia-A Genome-Wide Association Study in Taiwan.

Pediatrics international : official journal of the Japan Pediatric Society·2026

Related Experiment Videos

Isolation and mapping of a polymorphic DNA sequence (cTBQ20) on chromosome 10 [D10S31]

Related Concept Videos

The D2 receptor occupancy profile of loxapine determined using PET.

Loss of retinoic acid receptors in mouse skin and skin tumors is associated with activation of the ras(Ha) oncogene and high risk for premalignant progression.

Two distinct apolipoprotein B alleles in mice generated by a single 'in-out' targeting.

Insulin resistance in patients with essential hypertension can occur in the absence of microalbuminuria.

Familial amyotrophic lateral sclerosis with a mutation in exon 4 of the Cu/Zn superoxide dismutase gene: pathological and immunocytochemical changes.

Mouse monoclonal antipeptide antibodies specific for cholesteryl ester transfer protein (CETP).

AID self-assembly and multistranded DNA binding drive synapsis in class switch recombination.

Coronavirus NSP14 drives internal m7G modification to rewire host splicing and promote viral replication.

Insights into the recruitment of the H3K4me3 reader Spp1 by the meiotic double-strand break protein Mer2.

Newly synthesized histones: passive or active players in the regulation of epigenetic inheritance?

ETfinder: harnessing conserved C-terminal tails of single-stranded DNA-binding proteins for mining and engineering RecET systems in non-model microbial chassis.

MOSAIC enables selective transfer and fairness-aware generalization in cross-species DNA methylation prediction.

Molecular characterization of FAM222B as a novel disease gene for dominant cardiovascular laterality defects.

Genetic architecture and inheritance patterns of Leber hereditary optic neuropathy among 419 Chinese pedigrees carrying the ND4 11778G>A mutation.

Integrating LNA-qPCR and full-length SMN1 sequencing for precision SMA carrier screening: large-scale validation in 30,849 individuals.

Novel splice site variants in GBA1 are associated with Gaucher disease and genotype-phenotype correlations.

High-Resolution Physical Mapping and Chromosomal Transmission in Sugarcane Progeny.

Loci Associated With Susceptibility to Biliary Atresia-A Genome-Wide Association Study in Taiwan.

Related Experiment Videos

Isolation and mapping of a polymorphic DNA sequence (cTBQ20) on chromosome 10 [D10S31]

Related Concept Videos

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