Genetic mapping of the mouse prosaposin gene (Psap) to mouse chromosome 10

Murine endogenous retroviruses.

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Murine leukemia virus in organs of senescence-prone and -resistant mouse strains.

Mechanisms of ageing and development·2002

Identification and genetic mapping of the mouse Fkbp9 gene encoding a new member of FK506-binding protein family.

Molecules and cells·2001

The mouse gap junction gene connexin29 is highly expressed in sciatic nerve and regulated during brain development.

Biological chemistry·2001

Mouse histamine N-methyltransferase: cDNA cloning, expression, gene cloning and chromosomal localization.

Inflammation research : official journal of the European Histamine Research Society ... [et al.]·2001

Intracellular domains of mouse connexin26 and -30 affect diffusional and electrical properties of gap junction channels.

The Journal of membrane biology·2001

Integrative profiling of multi-modal plasma cfRNA signatures enables detection and prognostic risk stratification in breast cancer.

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Metabolomics and network pharmacology identify three key bioactive organic acid metabolites in Amomum tsao-ko.

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New genomic and transposable element annotation of the microsporidian parasite Anncaliia algerae.

Genomics·2026

Comprehensive evaluation of new sequencer T20 and well-established T7 with 507 human samples.

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A chromosome-level genome assembly and developmental transcriptome profiling reveal stage-specific remodeling of the molecular chaperone system in Helicoverpa armigera.

Genomics·2026

Enhancer-promoter interaction maps in pig implantation tissue identify candidate cis-regulatory elements and regulatory variants.

Genomics·2026

T2T-CHM13 reference genome reduces mapping bias and enhances alignment accuracy at disease-associated variants.

iScience·2026

Genome-wide exploration of coat color-associated loci in Hokkaido Native Horses, with a novel locus implicated in the roan phenotype.

Journal of equine science·2026

Diagnostic limitations of routine low-coverage CNV-seq in detecting mosaic paternal uniparental disomy in Beckwith-Wiedemann syndrome: a case report.

Frontiers in medicine·2026

Cataract GWAS meta-analysis and multi-omics Mendelian randomisation inform disease mechanisms and candidate target prioritisation.

EBioMedicine·2026

Cross-Ethnic Replication of Intersectin-1 as a Parkinson's Disease Susceptibility Gene in a Large Chinese Cohort.

Movement disorders : official journal of the Movement Disorder Society·2026

Chromosomal abnormalities in isolated persistent left superior vena cava: A systematic review and meta-analysis.

Turkish journal of obstetrics and gynecology·2026

Related Experiment Videos

Genetic mapping of the mouse prosaposin gene (Psap) to mouse chromosome 10

Related Concept Videos

Murine endogenous retroviruses.

Murine leukemia virus in organs of senescence-prone and -resistant mouse strains.

Identification and genetic mapping of the mouse Fkbp9 gene encoding a new member of FK506-binding protein family.

The mouse gap junction gene connexin29 is highly expressed in sciatic nerve and regulated during brain development.

Mouse histamine N-methyltransferase: cDNA cloning, expression, gene cloning and chromosomal localization.

Intracellular domains of mouse connexin26 and -30 affect diffusional and electrical properties of gap junction channels.

Integrative profiling of multi-modal plasma cfRNA signatures enables detection and prognostic risk stratification in breast cancer.

Metabolomics and network pharmacology identify three key bioactive organic acid metabolites in Amomum tsao-ko.

New genomic and transposable element annotation of the microsporidian parasite Anncaliia algerae.

Comprehensive evaluation of new sequencer T20 and well-established T7 with 507 human samples.

A chromosome-level genome assembly and developmental transcriptome profiling reveal stage-specific remodeling of the molecular chaperone system in Helicoverpa armigera.

Enhancer-promoter interaction maps in pig implantation tissue identify candidate cis-regulatory elements and regulatory variants.

T2T-CHM13 reference genome reduces mapping bias and enhances alignment accuracy at disease-associated variants.

Genome-wide exploration of coat color-associated loci in Hokkaido Native Horses, with a novel locus implicated in the roan phenotype.

Diagnostic limitations of routine low-coverage CNV-seq in detecting mosaic paternal uniparental disomy in Beckwith-Wiedemann syndrome: a case report.

Cataract GWAS meta-analysis and multi-omics Mendelian randomisation inform disease mechanisms and candidate target prioritisation.

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Genetic mapping of the mouse prosaposin gene (Psap) to mouse chromosome 10

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