Mouse angiotensin receptor genes Agtr1a and Agtr1b map to chromosomes 13 and 3

Augmentation of retinoic acid-induced granulocytic differentiation in HL-60 leukemia cells by serine/threonine protein phosphatase inhibitors.

FEBS letters·1992

Expression and regulation of the leukemia inhibitory factor/D factor gene in human T-cell leukemia virus type 1 infected T-cell lines.

Cancer research·1992

Effects of vagal stimulation on cesium-induced early afterdepolarizations and ventricular arrhythmias in rabbits.

Circulation·1992

[Clinical study on cefprozil fine granules].

The Japanese journal of antibiotics·1992

Immunohistochemical localization of hepatocyte growth factor protein in pancreas islet A-cells of man and rats.

Japanese journal of cancer research : Gann·1992

Columns for visual features of objects in monkey inferotemporal cortex.

Nature·1992

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

Mathematical Model to Assess Mutational Burden in Retinal Dystrophy Patients Negative to Mendelian Genetic Tests and Carriers of Multiple Recessive Variants.

Journal of ophthalmic & vision research·2026

A heritability-optimized method for functional prioritization of rare coding variants in complex traits.

Nature genetics·2026

WFS1 Deficiency Impairs PIAS4-Associated SUMOylation and Increases Ubiquitin-Mediated Spermatogenesis-Related Protein Degradation Leading to Testicular Male Infertility.

Advanced science (Weinheim, Baden-Wurttemberg, Germany)·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

Related Experiment Videos

Mouse angiotensin receptor genes Agtr1a and Agtr1b map to chromosomes 13 and 3

Related Concept Videos

Augmentation of retinoic acid-induced granulocytic differentiation in HL-60 leukemia cells by serine/threonine protein phosphatase inhibitors.

Expression and regulation of the leukemia inhibitory factor/D factor gene in human T-cell leukemia virus type 1 infected T-cell lines.

Effects of vagal stimulation on cesium-induced early afterdepolarizations and ventricular arrhythmias in rabbits.

[Clinical study on cefprozil fine granules].

Immunohistochemical localization of hepatocyte growth factor protein in pancreas islet A-cells of man and rats.

Columns for visual features of objects in monkey inferotemporal cortex.

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.

Mathematical Model to Assess Mutational Burden in Retinal Dystrophy Patients Negative to Mendelian Genetic Tests and Carriers of Multiple Recessive Variants.

A heritability-optimized method for functional prioritization of rare coding variants in complex traits.

WFS1 Deficiency Impairs PIAS4-Associated SUMOylation and Increases Ubiquitin-Mediated Spermatogenesis-Related Protein Degradation Leading to Testicular Male Infertility.

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.

Related Experiment Videos

Mouse angiotensin receptor genes Agtr1a and Agtr1b map to chromosomes 13 and 3

Related Concept Videos

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