Isolation and mapping of a polymorphic DNA sequence (pHHH163) on chromosome 18 [D18S21]

Genomic analysis of Fas and FasL genes and absence of correlation with disease progression in AIDS.

Immunogenetics·2004

Genomic analysis of Th1-Th2 cytokine genes in an AIDS cohort: identification of IL4 and IL10 haplotypes associated with the disease progression.

Genes and immunity·2003

A genomewide scan for loci predisposing to type 2 diabetes in a U.K. population (the Diabetes UK Warren 2 Repository): analysis of 573 pedigrees provides independent replication of a susceptibility locus on chromosome 1q.

American journal of human genetics·2001

Trans-ethnic fine mapping of a quantitative trait locus for circulating angiotensin I-converting enzyme (ACE).

Human molecular genetics·2001

Associations of distinct variants of the intestinal mucin gene MUC3A with ulcerative colitis and Crohn's disease.

Journal of human genetics·2001

A first high-density map of 981 biallelic markers on human chromosome 14.

Genomics·2000

Synergistic interaction between the macrophage polarizing signals IL-4 and IFNγ is controlled by the STAT6/STAT1/IRF1 axis.

Nucleic acids research·2026

PCRD-seq: proximity crosslinking-induced RNA depletion sequencing for low-input chromatin-associated transcriptome profiling.

Nucleic acids research·2026

Modeling conformational transitions in DNA, RNA, and protein-nucleic acid complexes.

Nucleic acids research·2026

Genetic studies with a uracil DNA glycosylase biosensor support a role for mitochondrial UNG1 in nuclear uracil repair.

Nucleic acids research·2026

Dual-mode application of transcriptional regulation and DNA editing using the ultra-compact TnpB system.

Nucleic acids research·2026

Imaging and mechanism of DNA-DNA recognition mediated by divalent ions.

Nucleic acids research·2026

β-cell 14-3-3-ζ and sex are key regulators of α-cell form and function.

Endocrinology·2026

Haplotype-resolved genome assembly of female Vernicia montana elucidates its W-specific sex-determination region.

Horticulture research·2026

Tailless (TLX) terminates the neural stem cell temporal cascade in both the optic lobe and central brain.

Development (Cambridge, England)·2026

Tactile deprivation induces Sex-Dependent cytoarchitectural remodeling in limbic circuits and alters Anxiety-Like behavior in mice.

Brain research·2026

Atypical auditory cortical lateralization and hearing loss-associated temporal volume reductions in youth with chromosome 22q11.2 deletion syndrome: Preliminary implications for psychosis risk.

Psychiatry research. Neuroimaging·2026

Glucose Transporter Deficiency Syndrome Type 1 (Glut1-DS): New Insights From a Brazilian Cohort of Patients.

JIMD reports·2026

Related Experiment Videos

Isolation and mapping of a polymorphic DNA sequence (pHHH163) on chromosome 18 [D18S21]

Related Concept Videos

Genomic analysis of Fas and FasL genes and absence of correlation with disease progression in AIDS.

Genomic analysis of Th1-Th2 cytokine genes in an AIDS cohort: identification of IL4 and IL10 haplotypes associated with the disease progression.

A genomewide scan for loci predisposing to type 2 diabetes in a U.K. population (the Diabetes UK Warren 2 Repository): analysis of 573 pedigrees provides independent replication of a susceptibility locus on chromosome 1q.

Trans-ethnic fine mapping of a quantitative trait locus for circulating angiotensin I-converting enzyme (ACE).

Associations of distinct variants of the intestinal mucin gene MUC3A with ulcerative colitis and Crohn's disease.

A first high-density map of 981 biallelic markers on human chromosome 14.

Synergistic interaction between the macrophage polarizing signals IL-4 and IFNγ is controlled by the STAT6/STAT1/IRF1 axis.

PCRD-seq: proximity crosslinking-induced RNA depletion sequencing for low-input chromatin-associated transcriptome profiling.

Modeling conformational transitions in DNA, RNA, and protein-nucleic acid complexes.

Genetic studies with a uracil DNA glycosylase biosensor support a role for mitochondrial UNG1 in nuclear uracil repair.

Dual-mode application of transcriptional regulation and DNA editing using the ultra-compact TnpB system.

Imaging and mechanism of DNA-DNA recognition mediated by divalent ions.

β-cell 14-3-3-ζ and sex are key regulators of α-cell form and function.

Haplotype-resolved genome assembly of female Vernicia montana elucidates its W-specific sex-determination region.

Tailless (TLX) terminates the neural stem cell temporal cascade in both the optic lobe and central brain.

Tactile deprivation induces Sex-Dependent cytoarchitectural remodeling in limbic circuits and alters Anxiety-Like behavior in mice.

Atypical auditory cortical lateralization and hearing loss-associated temporal volume reductions in youth with chromosome 22q11.2 deletion syndrome: Preliminary implications for psychosis risk.

Glucose Transporter Deficiency Syndrome Type 1 (Glut1-DS): New Insights From a Brazilian Cohort of Patients.

Related Experiment Videos

Isolation and mapping of a polymorphic DNA sequence (pHHH163) on chromosome 18 [D18S21]

Related Concept Videos

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