Isolation and mapping of a polymorphic DNA sequence pEKZ130 on chromosome 9 (D9S9)

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

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

Nucleic acids research·2026

RNA-Lexis: a probabilistic algorithm using a non-parametric segmentation logic to detect meaningful sequences in RNA.

Nucleic acids research·2026

Modulation of rob expression accelerates development of antibiotic resistance in Yersinia enterocolitica.

Nucleic acids research·2026

Lamin B1-dependent regulation of human separase in mitosis.

Nucleic acids research·2026

Neuronal activity-driven 3D chromatin dynamics in cortical pyramidal neurons depend on SATB2.

Nucleic acids research·2026

Chromatin accessibility classification of TAD boundaries discloses new architectural proteins.

Nucleic acids research·2026

Wilson disease associated with a novel variant in the ATP7B gene.

Frontiers in neurology·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

Related Experiment Videos

Isolation and mapping of a polymorphic DNA sequence pEKZ130 on chromosome 9 (D9S9)

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.

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

RNA-Lexis: a probabilistic algorithm using a non-parametric segmentation logic to detect meaningful sequences in RNA.

Modulation of rob expression accelerates development of antibiotic resistance in Yersinia enterocolitica.

Lamin B1-dependent regulation of human separase in mitosis.

Neuronal activity-driven 3D chromatin dynamics in cortical pyramidal neurons depend on SATB2.

Chromatin accessibility classification of TAD boundaries discloses new architectural proteins.

Wilson disease associated with a novel variant in the ATP7B gene.

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.

Related Experiment Videos

Isolation and mapping of a polymorphic DNA sequence pEKZ130 on chromosome 9 (D9S9)

Related Concept Videos

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