Genetic mapping of the Na(+)-taurocholate cotransporting polypeptide to mouse chromosome 12

Microfluidic fabrication of 6-methoxyethylamino numonafide-eluting magnetic microspheres.

Acta biomaterialia·2013

A mutation in Tubb2b, a human polymicrogyria gene, leads to lethality and abnormal cortical development in the mouse.

Human molecular genetics·2013

Focusing forward genetics: a tripartite ENU screen for neurodevelopmental mutations in the mouse.

Genetics·2011

Histone H3K4 trimethylation by MLL3 as part of ASCOM complex is critical for NR activation of bile acid transporter genes and is downregulated in cholestasis.

American journal of physiology. Gastrointestinal and liver physiology·2011

Identification of a Van der Woude syndrome mutation in the cleft palate 1 mutant mouse.

Genesis (New York, N.Y. : 2000)·2010

Bevacizumab for recurrent ependymoma.

Neurology·2009

Assessment of auditory and vestibular function and gene therapy in the Snell's waltzer mouse model of human deafness and balance dysfunction.

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

Multi-omics integration and machine learning define an iron-sulfur cluster/zinc-binding protein prognostic signature in esophageal squamous cell carcinoma.

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

Genome-wide characterization of copy number variations in Nagami Mithun (Bos frontalis) using whole-genome resequencing.

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

ZDHHC5 may regulate the function of NKT cells and the immune response in Meniere's disease.

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

Genome-wide meta-analysis with 1,590,596 individuals identifies 12 novel risk loci for systemic lupus erythematosus.

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

Screening for candidate genes and cell populations associated with atherosclerotic calcification using single-cell RNA sequencing.

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

Causal Effects of Lipoproteins and Lipids on Atrial Fibrillation: A Mendelian Randomization Study.

Lipids·2026

Dissecting the shared genetic architecture and biological mechanisms linking sleep traits and suicide attempts: from variants to genes.

Molecular psychiatry·2026

Different properties of loss-of-function between variants in the LIPH gene responsible for autosomal recessive woolly hair and further characterization of C3orf52.

Journal of dermatological science·2026

Genetic Dissection of Wheat Heterosis Identifies Candidate Genes in Biparental and Diverse Hybrid Populations.

Plant biotechnology journal·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

Related Experiment Videos

Genetic mapping of the Na(+)-taurocholate cotransporting polypeptide to mouse chromosome 12

Related Concept Videos

Microfluidic fabrication of 6-methoxyethylamino numonafide-eluting magnetic microspheres.

A mutation in Tubb2b, a human polymicrogyria gene, leads to lethality and abnormal cortical development in the mouse.

Focusing forward genetics: a tripartite ENU screen for neurodevelopmental mutations in the mouse.

Histone H3K4 trimethylation by MLL3 as part of ASCOM complex is critical for NR activation of bile acid transporter genes and is downregulated in cholestasis.

Identification of a Van der Woude syndrome mutation in the cleft palate 1 mutant mouse.

Bevacizumab for recurrent ependymoma.

Assessment of auditory and vestibular function and gene therapy in the Snell's waltzer mouse model of human deafness and balance dysfunction.

Multi-omics integration and machine learning define an iron-sulfur cluster/zinc-binding protein prognostic signature in esophageal squamous cell carcinoma.

Genome-wide characterization of copy number variations in Nagami Mithun (Bos frontalis) using whole-genome resequencing.

ZDHHC5 may regulate the function of NKT cells and the immune response in Meniere's disease.

Genome-wide meta-analysis with 1,590,596 individuals identifies 12 novel risk loci for systemic lupus erythematosus.

Screening for candidate genes and cell populations associated with atherosclerotic calcification using single-cell RNA sequencing.

Causal Effects of Lipoproteins and Lipids on Atrial Fibrillation: A Mendelian Randomization Study.

Dissecting the shared genetic architecture and biological mechanisms linking sleep traits and suicide attempts: from variants to genes.

Different properties of loss-of-function between variants in the LIPH gene responsible for autosomal recessive woolly hair and further characterization of C3orf52.

Genetic Dissection of Wheat Heterosis Identifies Candidate Genes in Biparental and Diverse Hybrid Populations.

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.

Related Experiment Videos

Genetic mapping of the Na(+)-taurocholate cotransporting polypeptide to mouse chromosome 12

Related Concept Videos

Related Articles