Correction: Advanced Immunolabeling Method for Optical Volumetric Imaging Reveals Dystrophic Neurites of Dopaminergic Neurons in Alzheimer’s Disease Mouse Brain

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: 1 Online-Ressource.

Language: Englisch

Bibliographic citation: Correction: Advanced Immunolabeling Method for Optical Volumetric Imaging Reveals Dystrophic Neurites of Dopaminergic Neurons in Alzheimer’s Disease Mouse Brain ; day:19 ; month:12 ; year:2023 ; pages:1
Molecular neurobiology ; (19.12.2023), 1

Creator: Baek, Soonbong
Jang, Jaemyung
Jung, Hyun Jin
Lee, Hyeyoung
Choe, Youngshik

Contributor: SpringerLink (Online service)

DOI: 10.1007/s12035-023-03878-8

URN: urn:nbn:de:101:1-2024030321010670277067

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:54 AM CEST

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Baek, Soonbong
Jang, Jaemyung
Jung, Hyun Jin
Lee, Hyeyoung
Choe, Youngshik
SpringerLink (Online service)

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Advanced Immunolabeling Method for Optical Volumetric Imaging Reveals Dystrophic Neurites of Dopaminergic Neurons in Alzheimer’s Disease Mouse Brain

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Sequential formation of different layers of dystrophic neurites in Alzheimer’s brains

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Applying Joint Graph Embedding to Study Alzheimer’s Neurodegeneration Patterns in Volumetric Data

In vivo human molecular neuroimaging of dopaminergic vulnerability along the Alzheimer’s disease phases

Early neurone loss in Alzheimer’s disease : cortical or subcortical?

Abnormal accumulation of extracellular vesicles in hippocampal dystrophic axons and regulation by the primary cilia in Alzheimer’s disease

The Alzheimer’s β-secretase BACE1 localizes to normal presynaptic terminals and to dystrophic presynaptic terminals surrounding amyloid plaques

Neuron-level explainable AI for Alzheimer’s Disease assessment from fundus images

Dystrophic (senescent) rather than activated microglial cells are associated with tau pathology and likely precede neurodegeneration in Alzheimer’s disease

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Advanced Immunolabeling Method for Optical Volumetric Imaging Reveals Dystrophic Neurites of Dopaminergic Neurons in Alzheimer’s Disease Mouse Brain

Dystrophic neurites express C9orf72 in Alzheimer's disease brains

Sequential formation of different layers of dystrophic neurites in Alzheimer’s brains

Accumulation of saposin in dystrophic neurites is linked to impaired lysosomal functions in Alzheimer’s disease brains

Applying Joint Graph Embedding to Study Alzheimer’s Neurodegeneration Patterns in Volumetric Data

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Neuron-level explainable AI for Alzheimer’s Disease assessment from fundus images

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Correction: Advanced Immunolabeling Method for Optical Volumetric Imaging Reveals Dystrophic Neurites of Dopaminergic Neurons in Alzheimer’s Disease Mouse Brain

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Other Objects (12)

Advanced Immunolabeling Method for Optical Volumetric Imaging Reveals Dystrophic Neurites of Dopaminergic Neurons in Alzheimer’s Disease Mouse Brain

Dystrophic neurites express C9orf72 in Alzheimer's disease brains

Sequential formation of different layers of dystrophic neurites in Alzheimer’s brains

Accumulation of saposin in dystrophic neurites is linked to impaired lysosomal functions in Alzheimer’s disease brains

Applying Joint Graph Embedding to Study Alzheimer’s Neurodegeneration Patterns in Volumetric Data

In vivo human molecular neuroimaging of dopaminergic vulnerability along the Alzheimer’s disease phases

Early neurone loss in Alzheimer’s disease : cortical or subcortical?

Abnormal accumulation of extracellular vesicles in hippocampal dystrophic axons and regulation by the primary cilia in Alzheimer’s disease

The Alzheimer’s β-secretase BACE1 localizes to normal presynaptic terminals and to dystrophic presynaptic terminals surrounding amyloid plaques

Neuron-level explainable AI for Alzheimer’s Disease assessment from fundus images

Dystrophic (senescent) rather than activated microglial cells are associated with tau pathology and likely precede neurodegeneration in Alzheimer’s disease

Distinct volumetric features of cerebrospinal fluid distribution in idiopathic normal-pressure hydrocephalus and Alzheimer’s disease

Advanced Immunolabeling Method for Optical Volumetric Imaging Reveals Dystrophic Neurites of Dopaminergic Neurons in Alzheimer’s Disease Mouse Brain

Dystrophic neurites express C9orf72 in Alzheimer's disease brains

Sequential formation of different layers of dystrophic neurites in Alzheimer’s brains

Accumulation of saposin in dystrophic neurites is linked to impaired lysosomal functions in Alzheimer’s disease brains

Applying Joint Graph Embedding to Study Alzheimer’s Neurodegeneration Patterns in Volumetric Data

In vivo human molecular neuroimaging of dopaminergic vulnerability along the Alzheimer’s disease phases

Early neurone loss in Alzheimer’s disease : cortical or subcortical?

Abnormal accumulation of extracellular vesicles in hippocampal dystrophic axons and regulation by the primary cilia in Alzheimer’s disease

The Alzheimer’s β-secretase BACE1 localizes to normal presynaptic terminals and to dystrophic presynaptic terminals surrounding amyloid plaques

Neuron-level explainable AI for Alzheimer’s Disease assessment from fundus images

Dystrophic (senescent) rather than activated microglial cells are associated with tau pathology and likely precede neurodegeneration in Alzheimer’s disease

Distinct volumetric features of cerebrospinal fluid distribution in idiopathic normal-pressure hydrocephalus and Alzheimer’s disease

Advanced Immunolabeling Method for Optical Volumetric Imaging Reveals Dystrophic Neurites of Dopaminergic Neurons in Alzheimer’s Disease Mouse Brain

Dystrophic neurites express C9orf72 in Alzheimer's disease brains

Sequential formation of different layers of dystrophic neurites in Alzheimer’s brains

Accumulation of saposin in dystrophic neurites is linked to impaired lysosomal functions in Alzheimer’s disease brains

Applying Joint Graph Embedding to Study Alzheimer’s Neurodegeneration Patterns in Volumetric Data

In vivo human molecular neuroimaging of dopaminergic vulnerability along the Alzheimer’s disease phases

Early neurone loss in Alzheimer’s disease : cortical or subcortical?

Abnormal accumulation of extracellular vesicles in hippocampal dystrophic axons and regulation by the primary cilia in Alzheimer’s disease

The Alzheimer’s β-secretase BACE1 localizes to normal presynaptic terminals and to dystrophic presynaptic terminals surrounding amyloid plaques

Neuron-level explainable AI for Alzheimer’s Disease assessment from fundus images

Dystrophic (senescent) rather than activated microglial cells are associated with tau pathology and likely precede neurodegeneration in Alzheimer’s disease

Distinct volumetric features of cerebrospinal fluid distribution in idiopathic normal-pressure hydrocephalus and Alzheimer’s disease

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