Human TaqI RFLP recognized by neurofilament gene probes

Channeling Vision: CaV1.4-A Critical Link in Retinal Signal Transmission.

BioMed research international·2018

Cone dystrophy and ectopic synaptogenesis in a Cacna1f loss of function model of congenital stationary night blindness (CSNB2A).

Channels (Austin, Tex.)·2017

Congenital stationary night blindness in mice - a tale of two Cacna1f mutants.

Advances in experimental medicine and biology·2010

X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F gene.

Journal of medical genetics·2006

A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants.

Human genetics·2001

Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.

Nature genetics·2000

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

PCRD-seq: proximity crosslinking-induced RNA depletion sequencing for low-input chromatin-associated transcriptome profiling.

Nucleic acids research·2026

Modeling conformational transitions in DNA, RNA, and protein-nucleic acid complexes.

Nucleic acids research·2026

From operating room to circuit mechanisms: Clinical basic science partnerships as a strategic model for human neuroscience.

Epilepsia·2026

Regulatory architecture controlling terminal differentiation of an interoceptive paraneuron in Caenorhabditis elegans.

Development (Cambridge, England)·2026

Distinct differentiation trajectories leave lasting impacts on gene regulation and function of V2a neurons.

Nature communications·2026

Single-cell profiling of natural killer/T-cell lymphoma reveals stratified immune features and potential therapeutic implications.

Nature communications·2026

Activity and Functional Connectivity of Lumbar Spinal Interneurons at Rest: Irregular, Sparse Yet Structured.

The Journal of neuroscience : the official journal of the Society for Neuroscience·2026

Mechanistic characterization and inhibition of PAD4-dependent NETosis following experimental neonatal hypoxic-ischemic brain injury.

Experimental neurology·2026

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Human TaqI RFLP recognized by neurofilament gene probes

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Channeling Vision: CaV1.4-A Critical Link in Retinal Signal Transmission.

Cone dystrophy and ectopic synaptogenesis in a Cacna1f loss of function model of congenital stationary night blindness (CSNB2A).

Congenital stationary night blindness in mice - a tale of two Cacna1f mutants.

X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F gene.

A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants.

Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.

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.

PCRD-seq: proximity crosslinking-induced RNA depletion sequencing for low-input chromatin-associated transcriptome profiling.

Modeling conformational transitions in DNA, RNA, and protein-nucleic acid complexes.

From operating room to circuit mechanisms: Clinical basic science partnerships as a strategic model for human neuroscience.

Regulatory architecture controlling terminal differentiation of an interoceptive paraneuron in Caenorhabditis elegans.

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Human TaqI RFLP recognized by neurofilament gene probes

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