BclI and MspI polymorphisms at the D6S90 locus

Same author

The clinical and genetic spectrum of spinocerebellar ataxia 14.

Neurology·2005

Same author

Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome.

Journal of medical genetics·2005

Same author

Spinocerebellar ataxia type 10 is rare in populations other than Mexicans.

Neurology·2002

Same author

Reduction of Purkinje cell pathology in SCA1 transgenic mice by p53 deletion.

Neurobiology of disease·2001

Same author

Mutations in the gene encoding methyl-CpG-binding protein 2 cause Rett syndrome.

Brain & development·2001

Same author

Requirement of Math1 for secretory cell lineage commitment in the mouse intestine.

Science (New York, N.Y.)·2001

Same journal

Correction to 'scSuperAnnotator: A platform for benchmarking comparison and visualizing automated cellular annotation methods for scRNA-seq data'.

Nucleic acids research·2026

Same journal

Correction to 'Differentiable partition function calculation for RNA'.

Nucleic acids research·2026

Same journal

Deployment of non-canonical splicing in tunicate genomes is mediated by divergent U2AF function and changing m6A modification in U1 and U6 snRNA.

Nucleic acids research·2026

Same journal

Bacillus subtilis DnaB forms multiple protein-protein interactions essential for DNA replication initiation.

Nucleic acids research·2026

Same journal

Multiple forms of protein-protein and DNA binding are exhibited by BrxC from the BREX phage restriction system.

Nucleic acids research·2026

Same journal

Biosynthesis of glycosylated 5-hydroxycytosine in the DNA of diverse viruses.

Nucleic acids research·2026

Related Experiment Videos

BclI and MspI polymorphisms at the D6S90 locus

Related Concept Videos

The clinical and genetic spectrum of spinocerebellar ataxia 14.

Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome.

Spinocerebellar ataxia type 10 is rare in populations other than Mexicans.

Reduction of Purkinje cell pathology in SCA1 transgenic mice by p53 deletion.

Mutations in the gene encoding methyl-CpG-binding protein 2 cause Rett syndrome.

Requirement of Math1 for secretory cell lineage commitment in the mouse intestine.

Correction to 'scSuperAnnotator: A platform for benchmarking comparison and visualizing automated cellular annotation methods for scRNA-seq data'.

Correction to 'Differentiable partition function calculation for RNA'.

Deployment of non-canonical splicing in tunicate genomes is mediated by divergent U2AF function and changing m6A modification in U1 and U6 snRNA.

Bacillus subtilis DnaB forms multiple protein-protein interactions essential for DNA replication initiation.

Multiple forms of protein-protein and DNA binding are exhibited by BrxC from the BREX phage restriction system.

Biosynthesis of glycosylated 5-hydroxycytosine in the DNA of diverse viruses.

Related Experiment Videos

BclI and MspI polymorphisms at the D6S90 locus

Related Concept Videos

Related Articles

The clinical and genetic spectrum of spinocerebellar ataxia 14.

Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome.

Spinocerebellar ataxia type 10 is rare in populations other than Mexicans.

Reduction of Purkinje cell pathology in SCA1 transgenic mice by p53 deletion.

Mutations in the gene encoding methyl-CpG-binding protein 2 cause Rett syndrome.

Requirement of Math1 for secretory cell lineage commitment in the mouse intestine.

Correction to 'scSuperAnnotator: A platform for benchmarking comparison and visualizing automated cellular annotation methods for scRNA-seq data'.

Correction to 'Differentiable partition function calculation for RNA'.

Deployment of non-canonical splicing in tunicate genomes is mediated by divergent U2AF function and changing m6A modification in U1 and U6 snRNA.

Bacillus subtilis DnaB forms multiple protein-protein interactions essential for DNA replication initiation.

Multiple forms of protein-protein and DNA binding are exhibited by BrxC from the BREX phage restriction system.

Biosynthesis of glycosylated 5-hydroxycytosine in the DNA of diverse viruses.