Targeting mammalian genes--rats join in and mice move ahead

Human stem cell-based embryo models: innovation, ethics, and policy.

Human reproduction (Oxford, England)·2026

Stem cell-based embryo models: The 2021 ISSCR stem cell guidelines revisited.

Stem cell reports·2025

A comprehensive human embryo reference tool using single-cell RNA-sequencing data.

Nature methods·2024

A fibronectin gradient remodels mixed-phase mesoderm.

Science advances·2024

When boundaries benefit science and society.

Cell·2024

An Irak1-Mecp2 tandem duplication mouse model for the study of MECP2 duplication syndrome.

Disease models & mechanisms·2024

Precise genomic integration of large DNA fragments by donor-directed annealing using prime editing.

Nature biotechnology·2026

Donor-complementary prime editing enables precise kilobase and library-compatible DNA insertions.

Nature biotechnology·2026

Megascale microbiome analysis with DartUniFrac.

Nature biotechnology·2026

Engineered bacterial siderophore production accelerates rock weathering for carbon removal.

Nature biotechnology·2026

Transferable genetic toolsets for nonmodel gut Clostridia enable in vivo reversible control of metabolite production.

Nature biotechnology·2026

Adaptive model-guided protein evolution with sparse data optimizes compact eukaryotic genome editors.

Nature biotechnology·2026

Spatial Genetic Mapping of Normal Human Prostate Tissue Identifies Epithelial Compartments Enriched for Prostate Cancer Association.

Molecular carcinogenesis·2026

AGG repeat expansion and aggregation of BIN1 in multiple system atrophy.

Brain : a journal of neurology·2026

[Optical genome mapping analysis of a Chinese pedigree with a complex balanced translocation involving four chromosomes].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics·2026

[Pathogenicity analysis and prenatal genetic counseling for five Chinese pedigrees harboring a hemizygous c.-32C>G variant of FGF13 gene].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics·2026

Interim analysis of an international multi-site prospective natural history study evaluating the clinical presentation and progression of Leigh syndrome spectrum disorders.

Therapeutic advances in rare disease·2026

Systematic genotype-phenotype mapping and transcriptomic analyses highlight SEMA6A as a candidate for neuronal migration defects in 5q22-q23 deletions.

Journal of human genetics·2026

Related Experiment Videos

Targeting mammalian genes--rats join in and mice move ahead

Related Concept Videos

Human stem cell-based embryo models: innovation, ethics, and policy.

Stem cell-based embryo models: The 2021 ISSCR stem cell guidelines revisited.

A comprehensive human embryo reference tool using single-cell RNA-sequencing data.

A fibronectin gradient remodels mixed-phase mesoderm.

When boundaries benefit science and society.

An Irak1-Mecp2 tandem duplication mouse model for the study of MECP2 duplication syndrome.

Precise genomic integration of large DNA fragments by donor-directed annealing using prime editing.

Donor-complementary prime editing enables precise kilobase and library-compatible DNA insertions.

Megascale microbiome analysis with DartUniFrac.

Engineered bacterial siderophore production accelerates rock weathering for carbon removal.

Transferable genetic toolsets for nonmodel gut Clostridia enable in vivo reversible control of metabolite production.

Adaptive model-guided protein evolution with sparse data optimizes compact eukaryotic genome editors.

Spatial Genetic Mapping of Normal Human Prostate Tissue Identifies Epithelial Compartments Enriched for Prostate Cancer Association.

AGG repeat expansion and aggregation of BIN1 in multiple system atrophy.

[Optical genome mapping analysis of a Chinese pedigree with a complex balanced translocation involving four chromosomes].

[Pathogenicity analysis and prenatal genetic counseling for five Chinese pedigrees harboring a hemizygous c.-32C>G variant of FGF13 gene].

Interim analysis of an international multi-site prospective natural history study evaluating the clinical presentation and progression of Leigh syndrome spectrum disorders.

Systematic genotype-phenotype mapping and transcriptomic analyses highlight SEMA6A as a candidate for neuronal migration defects in 5q22-q23 deletions.

Related Experiment Videos

Targeting mammalian genes--rats join in and mice move ahead

Related Concept Videos

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