Cloning of a DSS1 pseudogene (DSS1P1) and mapping to human chromosome band 5q14

Genetic and epigenetic heterogeneity in cancer: the ultimate challenge for drug therapy.

Current drug targets·2010

Nuclear matrix association: switching to the invasive cytotrophoblast.

Placenta·2010

Spectrum of mutations in the CFTR gene of patients with classical and atypical forms of cystic fibrosis from southwestern Sweden: identification of 12 novel mutations.

Genetic testing·2002

Identification of the human cortactin-binding protein-2 gene from the autism candidate region at 7q31.

Genomics·2001

A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome.

Nature genetics·2001

Sperm nuclear matrix association of the PRM1-->PRM2-->TNP2 domain is independent of Alu methylation.

Molecular human reproduction·2001

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

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

Deciphering pervasive domestication and active "dark matter" of proviruses in prokaryotes via precision border mapping.

Science advances·2026

Related Experiment Videos

Cloning of a DSS1 pseudogene (DSS1P1) and mapping to human chromosome band 5q14

Related Concept Videos

Genetic and epigenetic heterogeneity in cancer: the ultimate challenge for drug therapy.

Nuclear matrix association: switching to the invasive cytotrophoblast.

Spectrum of mutations in the CFTR gene of patients with classical and atypical forms of cystic fibrosis from southwestern Sweden: identification of 12 novel mutations.

Identification of the human cortactin-binding protein-2 gene from the autism candidate region at 7q31.

A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome.

Sperm nuclear matrix association of the PRM1-->PRM2-->TNP2 domain is independent of Alu methylation.

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.

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.

Deciphering pervasive domestication and active "dark matter" of proviruses in prokaryotes via precision border mapping.

Related Experiment Videos

Cloning of a DSS1 pseudogene (DSS1P1) and mapping to human chromosome band 5q14

Related Concept Videos

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