Isolation and mapping of a polymorphic DNA sequence (pTB10.171) on chromosome 10 [D10S19]

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

Nuclear receptor Nur77 resolves the inflammatory response of macrophages primarily by regulating expression of AP-1 transcription factors and their target genes.

Nucleic acids research·2026

When circular RNAs meet the genome: CiR-loops as chromatin regulators and disease drivers.

Nucleic acids research·2026

SpliceImpactR maps alternative RNA processing events driving protein functional diversity.

Nucleic acids research·2026

The leading region of many plasmids is adapted for translational efficiency.

Nucleic acids research·2026

Binary-SPA: a reference-free method for cell annotation in high-resolution spatial transcriptomics.

Nucleic acids research·2026

DeepPNI: a language- and graph-based model for mutation-driven protein-nucleic acid binding energetics.

Nucleic acids research·2026

Newborn screening and biobanking for preventable genetic disorders in Mongolia: A developing country perspective.

Regenerative therapy·2026

Whole-genome resequencing with multidimensional annotation revealed pathogenic networks in sirenomelia.

Italian journal of pediatrics·2026

Human Loss-of-Function ZNRF3 Mutation Impairs Adipose Thermogenesis and Drives Subcutaneous Fat Expansion.

Diabetes·2026

Integrated genetic identification and molecular dynamics simulations in a novel LOXL3 genetic mutation associated with Stickler syndrome.

Frontiers in genetics·2026

The ZBTB16/CUL3/ROC1 ubiquitin ligase drives the degradation of pathogenic pendrin (SLC26A4) protein variants.

Journal of biomedical science·2026

Identification and functional characterization of a SUZ12 frameshift variant in a Chinese family with Imagawa-Matsumoto syndrome.

BMC medical genomics·2026

Related Experiment Videos

Isolation and mapping of a polymorphic DNA sequence (pTB10.171) on chromosome 10 [D10S19]

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.

Nuclear receptor Nur77 resolves the inflammatory response of macrophages primarily by regulating expression of AP-1 transcription factors and their target genes.

When circular RNAs meet the genome: CiR-loops as chromatin regulators and disease drivers.

SpliceImpactR maps alternative RNA processing events driving protein functional diversity.

The leading region of many plasmids is adapted for translational efficiency.

Binary-SPA: a reference-free method for cell annotation in high-resolution spatial transcriptomics.

DeepPNI: a language- and graph-based model for mutation-driven protein-nucleic acid binding energetics.

Newborn screening and biobanking for preventable genetic disorders in Mongolia: A developing country perspective.

Whole-genome resequencing with multidimensional annotation revealed pathogenic networks in sirenomelia.

Human Loss-of-Function ZNRF3 Mutation Impairs Adipose Thermogenesis and Drives Subcutaneous Fat Expansion.

Integrated genetic identification and molecular dynamics simulations in a novel LOXL3 genetic mutation associated with Stickler syndrome.

The ZBTB16/CUL3/ROC1 ubiquitin ligase drives the degradation of pathogenic pendrin (SLC26A4) protein variants.

Identification and functional characterization of a SUZ12 frameshift variant in a Chinese family with Imagawa-Matsumoto syndrome.

Related Experiment Videos

Isolation and mapping of a polymorphic DNA sequence (pTB10.171) on chromosome 10 [D10S19]

Related Concept Videos

Related Articles