Isolation and mapping of a polymorphic DNA sequence (pB3.811) on chromosome 12 [D12S33]

Mining the plasma proteome: Evaluation of enrichment methods for depth and reproducibility.

Journal of proteomics·2025

Dunnigan lipodystrophy syndrome: French National Diagnosis and Care Protocol (PNDS; Protocole National de Diagnostic et de Soins).

Orphanet journal of rare diseases·2022

[Fighting against unexplained sudden death].

Annales de cardiologie et d'angeiologie·2021

Clinical correlations and long-term follow-up in 100 patients with sarcoglycanopathies.

European journal of neurology·2020

Guidance for the care of neuromuscular patients during the COVID-19 pandemic outbreak from the French Rare Health Care for Neuromuscular Diseases Network.

Revue neurologique·2020

Selected mitochondrial DNA landscapes activate the SIRT3 axis of the UPRmt to promote metastasis.

Oncogene·2017

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 (pB3.811) on chromosome 12 [D12S33]

Related Concept Videos

Mining the plasma proteome: Evaluation of enrichment methods for depth and reproducibility.

Dunnigan lipodystrophy syndrome: French National Diagnosis and Care Protocol (PNDS; Protocole National de Diagnostic et de Soins).

[Fighting against unexplained sudden death].

Clinical correlations and long-term follow-up in 100 patients with sarcoglycanopathies.

Guidance for the care of neuromuscular patients during the COVID-19 pandemic outbreak from the French Rare Health Care for Neuromuscular Diseases Network.

Selected mitochondrial DNA landscapes activate the SIRT3 axis of the UPRmt to promote metastasis.

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 (pB3.811) on chromosome 12 [D12S33]

Related Concept Videos

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