Genetic mapping of the gene coding for the integrin beta 7 subunit to the distal part of mouse chromosome 15

Murine endogenous retroviruses.

Cellular and molecular life sciences : CMLS·2008

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

Impact of RAG transposon co-option on the evolution of the jawed vertebrate immune system.

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Intra-colony divergence and global allele sharing reflect purifying selection and recombination at the Botryllus histocompatibility factor locus.

Immunogenetics·2026

Naïve adaptive immune receptor repertoires in celiac disease assessed by machine learning; impact of the HLA-DQ2.5 allotype on the TCR repertoire.

Immunogenetics·2026

Genetic association of immunosenescence to immune decline.

Immunogenetics·2026

Causal relationship and pathogenic mechanism analysis of breast cancer and coronary heart disease based on mendelian randomization and transcriptome data analysis.

Immunogenetics·2026

Genotype-phenotype correlations in autoimmune and autoinflammatory diseases: An NGS-based immunogenetic cohort study.

Immunogenetics·2026

Biobank analysis of canine eye disease variants identifies new breed associations and a potential X-linked Retinoschisin 1 disease model.

G3 (Bethesda, Md.)·2026

Whole-Exome Sequencing Identifies a Rare CSRP3 Variant Associated With Familial Brugada Syndrome in a Lebanese Family.

Journal of cardiovascular electrophysiology·2026

Genetic Variants Associated with Ventricular Septal Defect in Malaysia: A Scoping Review of Current Evidence and Research Gaps.

Pediatric cardiology·2026

Genetic Insights into the Potential Causal Role of LIPA and LTA4H in Vitiligo: A Single-Cell Integrative Analysis.

Clinical, cosmetic and investigational dermatology·2026

Genome-wide selection signatures in Ramlıç sheep identified by complementary ROH and iHS analyses.

Frontiers in veterinary science·2026

Promoter variation in BraHDAC1 modulates stomatal regulation and thermotolerance in Brassica rapa.

The Plant cell·2026

Genetic mapping of the gene coding for the integrin beta 7 subunit to the distal part of mouse chromosome 15

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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.

Impact of RAG transposon co-option on the evolution of the jawed vertebrate immune system.

Intra-colony divergence and global allele sharing reflect purifying selection and recombination at the Botryllus histocompatibility factor locus.

Naïve adaptive immune receptor repertoires in celiac disease assessed by machine learning; impact of the HLA-DQ2.5 allotype on the TCR repertoire.

Genetic association of immunosenescence to immune decline.

Causal relationship and pathogenic mechanism analysis of breast cancer and coronary heart disease based on mendelian randomization and transcriptome data analysis.

Genotype-phenotype correlations in autoimmune and autoinflammatory diseases: An NGS-based immunogenetic cohort study.

Biobank analysis of canine eye disease variants identifies new breed associations and a potential X-linked Retinoschisin 1 disease model.

Whole-Exome Sequencing Identifies a Rare CSRP3 Variant Associated With Familial Brugada Syndrome in a Lebanese Family.

Genetic Variants Associated with Ventricular Septal Defect in Malaysia: A Scoping Review of Current Evidence and Research Gaps.

Genetic Insights into the Potential Causal Role of LIPA and LTA4H in Vitiligo: A Single-Cell Integrative Analysis.

Genome-wide selection signatures in Ramlıç sheep identified by complementary ROH and iHS analyses.

Promoter variation in BraHDAC1 modulates stomatal regulation and thermotolerance in Brassica rapa.

Genetic mapping of the gene coding for the integrin beta 7 subunit to the distal part of mouse chromosome 15

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