Linkage mapping of the mixed-lineage leukemia (Mll) gene to rat chromosome 8

Transgenic expression of CD36 in the spontaneously hypertensive rat is associated with amelioration of metabolic disturbances but has no effect on hypertension.

Physiological research·2003

Genetic isolation of quantitative trait loci for blood pressure development and renal mass on chromosome 5 in the spontaneously hypertensive rat.

Physiological research·2003

Genetic susceptibility to renal injury in hypertension.

Experimental nephrology·2001

Genetic isolation of a blood pressure quantitative trait locus on chromosome 2 in the spontaneously hypertensive rat.

Journal of hypertension·2001

Linkage mapping of the interleukin 1beta converting enzyme (Il1bc) and the glutamate receptor subunit KA1 (Grik4) genes to rat chromosome 8.

Folia biologica·2000

Genetic analysis of rat chromosome 1 and the Sa gene in spontaneous hypertension.

Hypertension (Dallas, Tex. : 1979)·2000

Development and validation of a high density SNP array for indigenous Indian pigs.

Mammalian genome : official journal of the International Mammalian Genome Society·2026

Integrative bioinformatics and machine learning reveal hub genes and immune signatures bridging type 2 diabetes mellitus, fracture susceptibility, and osteoblast differentiation dysfunction.

Mammalian genome : official journal of the International Mammalian Genome Society·2026

USP38 promotes breast cancer immune evasion and malignant progression by deubiquitinating and stabilizing PD-L1.

Mammalian genome : official journal of the International Mammalian Genome Society·2026

The role of impaired mitochondrial function in neurological manifestations of mitochondrial diseases.

Mammalian genome : official journal of the International Mammalian Genome Society·2026

Genomic analysis of breed composition and population structure in Montana composite cattle.

Mammalian genome : official journal of the International Mammalian Genome Society·2026

Metabolic convergence of diabetes and prostate cancer: from dysglycemia to tumor microenvironment reprogramming.

Mammalian genome : official journal of the International Mammalian Genome Society·2026

Founder mutations in movement disorders: global distribution, molecular mechanisms, and clinical consequences-a scoping review.

Neurogenetics·2026

Evaluation of genetic parameters affecting the reliability and effectiveness of kinship reconstruction in Forest and Tundra Nenets populations using X-STR markers.

Vavilovskii zhurnal genetiki i selektsii·2026

Case Report: A novel 1, 171 bp GCK promoter/exon 1 deletion in a Chinese pedigree: correcting a misdiagnosis of MODY10 based on an incidental INS variant.

Frontiers in endocrinology·2026

A novel variant c.1185_1196dup (p.(Gly396_Ser399dup)) in the SLC26A4 gene associated with recessive hearing loss.

Vavilovskii zhurnal genetiki i selektsii·2026

Optical genome mapping identifies clinically relevant somatic structural variation in epilepsy-affected brain tissue.

Genome research·2026

Genetic Susceptibility in Relative Maternal Protection From Type 1 Diabetes.

Diabetes care·2026

Related Experiment Videos

Linkage mapping of the mixed-lineage leukemia (Mll) gene to rat chromosome 8

Related Concept Videos

Transgenic expression of CD36 in the spontaneously hypertensive rat is associated with amelioration of metabolic disturbances but has no effect on hypertension.

Genetic isolation of quantitative trait loci for blood pressure development and renal mass on chromosome 5 in the spontaneously hypertensive rat.

Genetic susceptibility to renal injury in hypertension.

Genetic isolation of a blood pressure quantitative trait locus on chromosome 2 in the spontaneously hypertensive rat.

Linkage mapping of the interleukin 1beta converting enzyme (Il1bc) and the glutamate receptor subunit KA1 (Grik4) genes to rat chromosome 8.

Genetic analysis of rat chromosome 1 and the Sa gene in spontaneous hypertension.

Development and validation of a high density SNP array for indigenous Indian pigs.

Integrative bioinformatics and machine learning reveal hub genes and immune signatures bridging type 2 diabetes mellitus, fracture susceptibility, and osteoblast differentiation dysfunction.

USP38 promotes breast cancer immune evasion and malignant progression by deubiquitinating and stabilizing PD-L1.

The role of impaired mitochondrial function in neurological manifestations of mitochondrial diseases.

Genomic analysis of breed composition and population structure in Montana composite cattle.

Metabolic convergence of diabetes and prostate cancer: from dysglycemia to tumor microenvironment reprogramming.

Founder mutations in movement disorders: global distribution, molecular mechanisms, and clinical consequences-a scoping review.

Evaluation of genetic parameters affecting the reliability and effectiveness of kinship reconstruction in Forest and Tundra Nenets populations using X-STR markers.

Case Report: A novel 1, 171 bp GCK promoter/exon 1 deletion in a Chinese pedigree: correcting a misdiagnosis of MODY10 based on an incidental INS variant.

A novel variant c.1185_1196dup (p.(Gly396_Ser399dup)) in the SLC26A4 gene associated with recessive hearing loss.

Optical genome mapping identifies clinically relevant somatic structural variation in epilepsy-affected brain tissue.

Genetic Susceptibility in Relative Maternal Protection From Type 1 Diabetes.

Related Experiment Videos

Linkage mapping of the mixed-lineage leukemia (Mll) gene to rat chromosome 8

Related Concept Videos

Related Articles