Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome

The effects of HIV on cognitive and motor development in children born to HIV-seropositive women with no reported drug use: birth to 24 months.

Pediatrics·1995

The metanephric blastema differentiates into collecting system and nephron epithelia in vitro.

Development (Cambridge, England)·1995

The activation of a specific DNA binding protein by neutron irradiation.

International journal of radiation oncology, biology, physics·1995

Psychotropic drug use in relation to psychiatric symptoms in community-living persons with Alzheimer's disease.

Pharmacotherapy·1995

Intransal or intragastric immunization with proteosome-Shigella lipopolysaccharide vaccines protects against lethal pneumonia in a murine model of Shigella infection.

Infection and immunity·1995

Comprehensive tuberculosis control for patients at high risk for noncompliance.

American journal of respiratory and critical care medicine·1995

Exploring differences across pangenome-graph representations using Escherichia coli O157:H7 as a model.

Genomics·2026

Comprehensive analysis of differentially expressed mRNAs, lncRNAs, and miRNAs involved in ovarian differentiation and development in Qihe gibel carp (Carassius gibelio var. Qihe).

Genomics·2026

Genome-wide association and selective sweep analyses reveal genetic loci for teat number trait in pigs.

Genomics·2026

Effects of domestication on the body morphology and genetic diversity of the yellowfin seabream (Acanthopagrus latus).

Genomics·2026

A muskrat tissue atlas of small non-coding RNAs and their regulatory roles in muskrat musk secretion.

Genomics·2026

Dynamic transcriptomic landscape from bulk RNA-seq reveals critical mmu-miR-181a-5p/hif1a and mmu-miR-101a-3p/col1a1 modules for deep second-degree burn wound healing.

Genomics·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

Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome

Related Concept Videos

The effects of HIV on cognitive and motor development in children born to HIV-seropositive women with no reported drug use: birth to 24 months.

The metanephric blastema differentiates into collecting system and nephron epithelia in vitro.

The activation of a specific DNA binding protein by neutron irradiation.

Psychotropic drug use in relation to psychiatric symptoms in community-living persons with Alzheimer's disease.

Intransal or intragastric immunization with proteosome-Shigella lipopolysaccharide vaccines protects against lethal pneumonia in a murine model of Shigella infection.

Comprehensive tuberculosis control for patients at high risk for noncompliance.

Exploring differences across pangenome-graph representations using Escherichia coli O157:H7 as a model.

Comprehensive analysis of differentially expressed mRNAs, lncRNAs, and miRNAs involved in ovarian differentiation and development in Qihe gibel carp (Carassius gibelio var. Qihe).

Genome-wide association and selective sweep analyses reveal genetic loci for teat number trait in pigs.

Effects of domestication on the body morphology and genetic diversity of the yellowfin seabream (Acanthopagrus latus).

A muskrat tissue atlas of small non-coding RNAs and their regulatory roles in muskrat musk secretion.

Dynamic transcriptomic landscape from bulk RNA-seq reveals critical mmu-miR-181a-5p/hif1a and mmu-miR-101a-3p/col1a1 modules for deep second-degree burn wound healing.

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

Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome

Related Concept Videos

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