Identification and chromosomal mapping of a duplicated X-specific human sequence

'The current mental health status of children and young people with JIA, and their wider family': a charity partner collaboration survey.

Pediatric rheumatology online journal·2023

Measures of lamb production efficiency in a temperate grass-based system differing in ewe prolificacy potential and stocking rate.

Journal of animal science·2017

Effect of ewe prolificacy potential and stocking rate on ewe and lamb performance in a grass-based lamb production system.

Journal of animal science·2017

Susceptibility of metallothionein-null mice to paraquat.

Environmental toxicology and pharmacology·2011

Methylation of novel markers of fragile X alleles is inversely correlated with FMRP expression and FMR1 activation ratio.

Human molecular genetics·2010

ZNF397, a new class of interphase to early prophase-specific, SCAN-zinc-finger, mammalian centromere protein.

Chromosoma·2008

Comprehensive post-transcriptional modification profiles in individual Staphylococcus aureus tRNA species.

Nucleic acids research·2026

CTDP1 governs a Pol II phosphorylation intermediate and coordinates Mediator recruitment, transcription efficiency, and splicing.

Nucleic acids research·2026

DEPACE-seq enables high-fidelity, single-nucleotide-resolution mapping of abasic sites and characterization of dynamic and long-lived AP landscapes in mammalian genomes.

Nucleic acids research·2026

Functional analysis of natural variation in the RNA-binding protein CsrA across the bacterial domain predicts regulatory activity.

Nucleic acids research·2026

miRNA-mediated cell-to-cell communications boost DNA repair during the radioadaptive response.

Nucleic acids research·2026

Synonymous mutations in essential genes infrequently produce fitness effects in human cell lines.

Nucleic acids research·2026

Multi-omics identification of ZFPM2 and CD44 as key candidates for testicular size in sheep.

Theriogenology·2026

Complex epilepsy phenotype associated with chromosome 2q24.2-q24.3 deletion involving sodium channel gene cluster.

Annals of the Child Neurology Society·2026

Purine Metabolism-Related Pathogenic Genes in Trigeminal Neuralgia: A Multiomics Mendelian Randomization Study.

Pain research & management·2026

Carrier frequency of autosomal recessive monogenic disorders in the peruvian population.

Frontiers in genetics·2026

Detecting pathogenic structural variation in families with undiagnosed rare disease in a national genome project.

European journal of human genetics : EJHG·2026

Genome shuffling enables quantitative trait locus mapping in Bacillus subtilis.

Nature communications·2026

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Identification and chromosomal mapping of a duplicated X-specific human sequence

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'The current mental health status of children and young people with JIA, and their wider family': a charity partner collaboration survey.

Measures of lamb production efficiency in a temperate grass-based system differing in ewe prolificacy potential and stocking rate.

Effect of ewe prolificacy potential and stocking rate on ewe and lamb performance in a grass-based lamb production system.

Susceptibility of metallothionein-null mice to paraquat.

Methylation of novel markers of fragile X alleles is inversely correlated with FMRP expression and FMR1 activation ratio.

ZNF397, a new class of interphase to early prophase-specific, SCAN-zinc-finger, mammalian centromere protein.

Comprehensive post-transcriptional modification profiles in individual Staphylococcus aureus tRNA species.

CTDP1 governs a Pol II phosphorylation intermediate and coordinates Mediator recruitment, transcription efficiency, and splicing.

DEPACE-seq enables high-fidelity, single-nucleotide-resolution mapping of abasic sites and characterization of dynamic and long-lived AP landscapes in mammalian genomes.

Functional analysis of natural variation in the RNA-binding protein CsrA across the bacterial domain predicts regulatory activity.

miRNA-mediated cell-to-cell communications boost DNA repair during the radioadaptive response.

Synonymous mutations in essential genes infrequently produce fitness effects in human cell lines.

Multi-omics identification of ZFPM2 and CD44 as key candidates for testicular size in sheep.

Complex epilepsy phenotype associated with chromosome 2q24.2-q24.3 deletion involving sodium channel gene cluster.

Purine Metabolism-Related Pathogenic Genes in Trigeminal Neuralgia: A Multiomics Mendelian Randomization Study.

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Identification and chromosomal mapping of a duplicated X-specific human sequence

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