排序调节表皮和神经元极性的基因.

MAGUKs, scaffolding proteins at cell junctions, are substrates of different proteases during apoptosis.

Cell death & disease·2011

From molecules to mammals: what's NOS got to do with it?

Acta physiologica Scandinavica·2003

Structure of the SH3-guanylate kinase module from PSD-95 suggests a mechanism for regulated assembly of MAGUK scaffolding proteins.

Molecular cell·2002

Polarized targeting of peripheral membrane proteins in neurons.

The Journal of biological chemistry·2001

PSD-93 knock-out mice reveal that neuronal MAGUKs are not required for development or function of parallel fiber synapses in cerebellum.

The Journal of neuroscience : the official journal of the Society for Neuroscience·2001

Electron microscopic immunocytochemical detection of PSD-95, PSD-93, SAP-102, and SAP-97 at postsynaptic, presynaptic, and nonsynaptic sites of adult and neonatal rat visual cortex.

Synapse (New York, N.Y.)·2001

A spliceosome-independent eukaryote generated by complete intron removal.

Cell·2026

Recent advances in Alzheimer's disease: From molecular mechanisms to therapeutic strategies.

Cell·2026

Bridging omics and physiology to build multimodal clocks of human aging.

Cell·2026

Rewriting Duchenne muscular dystrophy therapy.

Cell·2026

Photosynthetic medicine: Engineering a plant-derived nanofoundry to power mammalian cells.

Cell·2026

Map of spiking activity underlying change detection in the mouse visual system.

Cell·2026

MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

Scientific reports·2026

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

The Lancet. Microbe·2026

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

Frontiers in genetics·2026

A Novel <i>FN1</i> Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

Journal of clinical medicine·2026

The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

HLA·2026

Detailed Clinical Report of Four Individuals from a Nusayri Family with a Rare TNXB Variant: Classical-Like and Hypermobile Types of Ehlers-Danlos Syndrome.

Molecular syndromology·2026

相关实验视频

排序调节表皮和神经元极性的基因.

相关概念视频

MAGUKs, scaffolding proteins at cell junctions, are substrates of different proteases during apoptosis.

From molecules to mammals: what's NOS got to do with it?

Structure of the SH3-guanylate kinase module from PSD-95 suggests a mechanism for regulated assembly of MAGUK scaffolding proteins.

Polarized targeting of peripheral membrane proteins in neurons.

PSD-93 knock-out mice reveal that neuronal MAGUKs are not required for development or function of parallel fiber synapses in cerebellum.

Electron microscopic immunocytochemical detection of PSD-95, PSD-93, SAP-102, and SAP-97 at postsynaptic, presynaptic, and nonsynaptic sites of adult and neonatal rat visual cortex.

A spliceosome-independent eukaryote generated by complete intron removal.

Recent advances in Alzheimer's disease: From molecular mechanisms to therapeutic strategies.

Bridging omics and physiology to build multimodal clocks of human aging.

Rewriting Duchenne muscular dystrophy therapy.

Photosynthetic medicine: Engineering a plant-derived nanofoundry to power mammalian cells.

Map of spiking activity underlying change detection in the mouse visual system.

MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

A Novel <i>FN1</i> Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

Detailed Clinical Report of Four Individuals from a Nusayri Family with a Rare TNXB Variant: Classical-Like and Hypermobile Types of Ehlers-Danlos Syndrome.

相关实验视频

排序调节表皮和神经元极性的基因.

相关概念视频

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