Manipulating the mouse genome: implications for neurobiology

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Immunoregulation of host-versus-graft responses in the uterus.

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The missense mutation W290R in Fgfr2 causes developmental defects from aberrant IIIb and IIIc signaling.

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Forward genetic screen of mouse reveals dominant missense mutation in the P/Q-type voltage-dependent calcium channel, CACNA1A.

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Genetic regulation of stem cell origins in the mouse embryo.

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Ethological learning during the critical period resets synaptic setpoints in mouse binocular visual cortex.

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Amygdala astrocytes encode anxiety states.

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Lactylation drives oligodendrocyte differentiation and (re)myelination.

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Autonomic C1 neurons promote anxiety via activation of vlPAG.

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

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Manipulating the mouse genome: implications for neurobiology

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Genome Wide Conditional Mouse Knockout Resources.

Developmental differences in the expression of FGF receptors between human and mouse embryos.

Immunoregulation of host-versus-graft responses in the uterus.

The missense mutation W290R in Fgfr2 causes developmental defects from aberrant IIIb and IIIc signaling.

Forward genetic screen of mouse reveals dominant missense mutation in the P/Q-type voltage-dependent calcium channel, CACNA1A.

Genetic regulation of stem cell origins in the mouse embryo.

Ethological learning during the critical period resets synaptic setpoints in mouse binocular visual cortex.

Decide when to cooperate.

Amygdala astrocytes encode anxiety states.

Lactylation drives oligodendrocyte differentiation and (re)myelination.

Beyond neurotoxicity: A new face of 6-hydroxydopamine in cancer immunity.

Autonomic C1 neurons promote anxiety via activation of vlPAG.

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.

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Manipulating the mouse genome: implications for neurobiology

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