A BclI RFLP for DXS296 (VK21) near the fragile X

Gastric adenocarcinoma and proximal polyposis of the stomach (GAPPS): a new autosomal dominant syndrome.

Gut·2011

De novo SCN1A mutations in migrating partial seizures of infancy.

Neurology·2011

Recurrence risk of epilepsy and mental retardation in females due to parental mosaicism of PCDH19 mutations.

Neurology·2011

The role of neuronal GABA(A) receptor subunit mutations in idiopathic generalized epilepsies.

Neuroscience letters·2009

Deletions or duplications in KCNQ2 can cause benign familial neonatal seizures.

Journal of medical genetics·2007

Generalized epilepsy with febrile seizures plus-associated sodium channel beta1 subunit mutations severely reduce beta subunit-mediated modulation of sodium channel function.

Neuroscience·2007

LUCas: Light-Uncaged Cas13a using photocleavable interfering guide RNAs.

Nucleic acids research·2026

Fluorescent reporter assay reveals ribonucleotides promote mismatch correction in vivo.

Nucleic acids research·2026

Large-scale mutational analysis uncovers molecular mechanisms governing dual RNA functions in transposons.

Nucleic acids research·2026

Temporal dynamics of intragenic enhancer RNAs regulate Lin28a expression in response to external stimuli in embryonic stem cells.

Nucleic acids research·2026

PCNA-RECQL5-RPRD1B recruit repair components to stressed replication forks to promote survival of BRCA1-deficient cancer cells.

Nucleic acids research·2026

Synergistic interaction between the macrophage polarizing signals IL-4 and IFNγ is controlled by the STAT6/STAT1/IRF1 axis.

Nucleic acids research·2026

Benchmarking Denoising Strategies and Nucleic Acid Templates for ITS2 Amplicon Sequencing of Gut Mycobiome.

FASEB journal : official publication of the Federation of American Societies for Experimental Biology·2026

Draft genome sequence of Barnettozyma sp. NCYC 4493 from a UK industrial source.

Microbiology resource announcements·2026

Multi-kingdom gut microbiota analyses identify biomarkers of different types of pediatric short bowel syndrome.

mSystems·2026

Related Experiment Videos

A BclI RFLP for DXS296 (VK21) near the fragile X

Related Concept Videos

Gastric adenocarcinoma and proximal polyposis of the stomach (GAPPS): a new autosomal dominant syndrome.

De novo SCN1A mutations in migrating partial seizures of infancy.

Recurrence risk of epilepsy and mental retardation in females due to parental mosaicism of PCDH19 mutations.

The role of neuronal GABA(A) receptor subunit mutations in idiopathic generalized epilepsies.

Deletions or duplications in KCNQ2 can cause benign familial neonatal seizures.

Generalized epilepsy with febrile seizures plus-associated sodium channel beta1 subunit mutations severely reduce beta subunit-mediated modulation of sodium channel function.

LUCas: Light-Uncaged Cas13a using photocleavable interfering guide RNAs.

Fluorescent reporter assay reveals ribonucleotides promote mismatch correction in vivo.

Large-scale mutational analysis uncovers molecular mechanisms governing dual RNA functions in transposons.

Temporal dynamics of intragenic enhancer RNAs regulate Lin28a expression in response to external stimuli in embryonic stem cells.

PCNA-RECQL5-RPRD1B recruit repair components to stressed replication forks to promote survival of BRCA1-deficient cancer cells.

Synergistic interaction between the macrophage polarizing signals IL-4 and IFNγ is controlled by the STAT6/STAT1/IRF1 axis.

Benchmarking Denoising Strategies and Nucleic Acid Templates for ITS2 Amplicon Sequencing of Gut Mycobiome.

Draft genome sequence of Barnettozyma sp. NCYC 4493 from a UK industrial source.

Multi-kingdom gut microbiota analyses identify biomarkers of different types of pediatric short bowel syndrome.

Related Experiment Videos

A BclI RFLP for DXS296 (VK21) near the fragile X

Related Concept Videos

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