High-resolution genetic mapping of the hypodactyly (Hd) locus on mouse chromosome 6

Triangular nanoperforation and band engineering of InGaAs quantum wells: a lithographic route toward Dirac cones in III-V semiconductors.

Nanotechnology·2019

Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome.

Journal of medical genetics·2009

A comparative molecular analysis of developing mouse forelimbs and hindlimbs using serial analysis of gene expression (SAGE).

Genome research·2001

A novel frameshift mutation in exon 23 of ATP7A (MNK) results in occipital horn syndrome and not in Menkes disease.

American journal of human genetics·2001

Identification and prevention of a GC content bias in SAGE libraries.

Nucleic acids research·2001

Sodium channel beta subunits mediate homophilic cell adhesion and recruit ankyrin to points of cell-cell contact.

The Journal of biological chemistry·2001

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

Generation of miR-141/200c conditional knockout mice from knockout-first, reporter-tagged parent and functional validation of the floxed allele.

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

Machine learning identifies ac4C-related prognostic signature and TUBA1C as therapeutic target in COAD.

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

Long non-coding RNAs link DNA methylation to immune regulatory networks in bovine subclinical mastitis.

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

Identification of a metastasis-associated prognostic gene signature in osteosarcoma through integrated bioinformatics and functional analysis.

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

Obesity and reduced renal corticomedullary differentiation on T1 mapping: a population-based UK Biobank study.

International urology and nephrology·2026

Evaluating the pathogenic significance of unique chromosomal variants in craniosynostosis using patient-derived induced pluripotent stem cells and mouse modelling.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

[Genetic and functional characterization of a novel KIT splicing variant in a Chinese three-generation pedigree with piebaldism].

Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences·2026

Genome-wide association study of sarcopenia index reveals sex-stratified genetic architecture.

Biology of sex differences·2026

Whole-Exome Sequencing in a Consanguinity-Enriched South Indian Retinitis Pigmentosa Cohort: Diagnostic Yield and Molecular Spectrum.

Ophthalmology science·2026

Genetic analysis, reproductive decision-making, and pregnancy outcomes in 51 Chinese osteogenesis imperfecta families.

Journal of assisted reproduction and genetics·2026

Related Experiment Videos

High-resolution genetic mapping of the hypodactyly (Hd) locus on mouse chromosome 6

Related Concept Videos

Triangular nanoperforation and band engineering of InGaAs quantum wells: a lithographic route toward Dirac cones in III-V semiconductors.

Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome.

A comparative molecular analysis of developing mouse forelimbs and hindlimbs using serial analysis of gene expression (SAGE).

A novel frameshift mutation in exon 23 of ATP7A (MNK) results in occipital horn syndrome and not in Menkes disease.

Identification and prevention of a GC content bias in SAGE libraries.

Sodium channel beta subunits mediate homophilic cell adhesion and recruit ankyrin to points of cell-cell contact.

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.

Generation of miR-141/200c conditional knockout mice from knockout-first, reporter-tagged parent and functional validation of the floxed allele.

Machine learning identifies ac4C-related prognostic signature and TUBA1C as therapeutic target in COAD.

Long non-coding RNAs link DNA methylation to immune regulatory networks in bovine subclinical mastitis.

Identification of a metastasis-associated prognostic gene signature in osteosarcoma through integrated bioinformatics and functional analysis.

Obesity and reduced renal corticomedullary differentiation on T1 mapping: a population-based UK Biobank study.

Evaluating the pathogenic significance of unique chromosomal variants in craniosynostosis using patient-derived induced pluripotent stem cells and mouse modelling.

[Genetic and functional characterization of a novel KIT splicing variant in a Chinese three-generation pedigree with piebaldism].

Genome-wide association study of sarcopenia index reveals sex-stratified genetic architecture.

Whole-Exome Sequencing in a Consanguinity-Enriched South Indian Retinitis Pigmentosa Cohort: Diagnostic Yield and Molecular Spectrum.

Genetic analysis, reproductive decision-making, and pregnancy outcomes in 51 Chinese osteogenesis imperfecta families.

Related Experiment Videos

High-resolution genetic mapping of the hypodactyly (Hd) locus on mouse chromosome 6

Related Concept Videos

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