Assignment of the gene for NADH diaphorase Dia-1 to Mouse chromosome 15

Genomic structure of the human unconventional myosin VI gene.

Gene·2001

A variable myopathy associated with heterozygosity for the R503C mutation in the carnitine palmitoyltransferase II gene.

Molecular genetics and metabolism·2000

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2.

Nature genetics·1999

Cysteine substitutions in epidermal growth factor-like domains of fibrillin-1: distinct effects on biochemical and clinical phenotypes.

American journal of human genetics·1999

Williams-Beuren syndrome: genes and mechanisms.

Human molecular genetics·1999

Novel mutations in the Wiskott-Aldrich syndrome protein gene and their effects on transcriptional, translational, and clinical phenotypes.

Human mutation·1999

Two-dimensional electrophoresis of peptides from human-CHO cell hybrids containing human chromosome 21.

Somatic cell genetics·1983

Secondary mutation resistant to 7-ketocholesterol rescues a sterol metabolic defect in amphotericin B-resistant Chinese hamster cell line.

Somatic cell genetics·1983

Expression of recessive Aprt- mutations in mouse CAK cells resulting from chromosome loss and duplication.

Somatic cell genetics·1983

Chromosome assignment of genes encoding the alpha and beta subunits of glycoprotein hormones in man and mouse.

Somatic cell genetics·1983

LPS-nonresponsive variants of mouse B cell lymphoma, 70Z/3: isolation and characterization.

Somatic cell genetics·1983

Assignment of gene(s) coding for antigen defined by monoclonal antibody 2B2.

Somatic cell genetics·1983

Genetic covariance between plant biparental populations: concept and estimation.

Heredity·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

Related Experiment Videos

Assignment of the gene for NADH diaphorase Dia-1 to Mouse chromosome 15

Related Concept Videos

Genomic structure of the human unconventional myosin VI gene.

A variable myopathy associated with heterozygosity for the R503C mutation in the carnitine palmitoyltransferase II gene.

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2.

Cysteine substitutions in epidermal growth factor-like domains of fibrillin-1: distinct effects on biochemical and clinical phenotypes.

Williams-Beuren syndrome: genes and mechanisms.

Novel mutations in the Wiskott-Aldrich syndrome protein gene and their effects on transcriptional, translational, and clinical phenotypes.

Two-dimensional electrophoresis of peptides from human-CHO cell hybrids containing human chromosome 21.

Secondary mutation resistant to 7-ketocholesterol rescues a sterol metabolic defect in amphotericin B-resistant Chinese hamster cell line.

Expression of recessive Aprt- mutations in mouse CAK cells resulting from chromosome loss and duplication.

Chromosome assignment of genes encoding the alpha and beta subunits of glycoprotein hormones in man and mouse.

LPS-nonresponsive variants of mouse B cell lymphoma, 70Z/3: isolation and characterization.

Assignment of gene(s) coding for antigen defined by monoclonal antibody 2B2.

Genetic covariance between plant biparental populations: concept and estimation.

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.

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

Related Experiment Videos

Assignment of the gene for NADH diaphorase Dia-1 to Mouse chromosome 15

Related Concept Videos

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