(Q24302244)

vesicle transport along microtubule

GOA release 2020-03-11

1 reference

neuronal ceroid lipofuscinosis

GOA release 2020-03-11

1 reference

8

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author name string

Kristiina Uusi-Rauva

1

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Aija Kyttälä

2

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Rik van der Kant

3

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Jouni Vesa

4

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Kimmo Tanhuanpää

5

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Jacques Neefjes

6

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Vesa M Olkkonen

Cellular and Molecular Life Sciences

7

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language of work or name

English

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publication date

June 2012

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published in

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volume

69

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issue

12

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page(s)

2075-89

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cites work

CLN3, the protein associated with batten disease: structure, function and localization

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Defective intracellular transport of CLN3 is the molecular basis of Batten disease (JNCL)

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Membrane trafficking and mitochondrial abnormalities precede subunit c deposition in a cerebellar cell model of juvenile neuronal ceroid lipofuscinosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Two motifs target Batten disease protein CLN3 to lysosomes in transfected nonneuronal and neuronal cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

CLN3 protein is targeted to neuronal synapses but excluded from synaptic vesicles: new clues to Batten disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Isolation of a novel gene underlying batten disease, CLN3

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

The neuronal ceroid-lipofuscinoses: from past to present

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Autophagy is disrupted in a knock-in mouse model of juvenile neuronal ceroid lipofuscinosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

A novel role of the Batten disease gene CLN3: association with BMP synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

CLN3P, the Batten's disease protein, is a novel palmitoyl-protein Delta-9 desaturase.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

btn1, the Schizosaccharomyces pombe homologue of the human Batten disease gene CLN3, regulates vacuole homeostasis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

CLN3 protein regulates lysosomal pH and alters intracellular processing of Alzheimer's amyloid-beta protein precursor and cathepsin D in human cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Elevated lysosomal pH in neuronal ceroid lipofuscinoses (NCLs)

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Action of BTN1, the yeast orthologue of the gene mutated in Batten disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

A role in vacuolar arginine transport for yeast Btn1p and for human CLN3, the protein defective in Batten disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Defective lysosomal arginine transport in juvenile Batten disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

A function retained by the common mutant CLN3 protein is responsible for the late onset of juvenile neuronal ceroid lipofuscinosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Interactions between the juvenile Batten disease gene, CLN3, and the Notch and JNK signalling pathways.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

The Batten disease gene CLN3 is required for the response to oxidative stress.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Neuronal vulnerability of CLN3 deletion to calcium-induced cytotoxicity is mediated by calsenilin

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Interaction between Sdo1p and Btn1p in the Saccharomyces cerevisiae model for Batten disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

A novel interaction of CLN3 with nonmuscle myosin-IIB and defects in cell motility of Cln3(-/-) cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

S. pombe btn1, the orthologue of the Batten disease gene CLN3, is required for vacuole protein sorting of Cpy1p and Golgi exit of Vps10p

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Loss of the Batten disease gene CLN3 prevents exit from the TGN of the mannose 6-phosphate receptor.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Novel interactions of CLN3 protein link Batten disease to dysregulation of fodrin-Na+, K+ ATPase complex.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Interconnections of CLN3, Hook1 and Rab proteins link Batten disease to defects in the endocytic pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Visual deficits in a mouse model of Batten disease are the result of optic nerve degeneration and loss of dorsal lateral geniculate thalamic neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Batten disease (JNCL) is linked to disturbances in mitochondrial, cytoskeletal, and synaptic compartments.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Regulation of caveolin-1 membrane trafficking by the Na/K-ATPase.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Biosynthesis and intracellular targeting of the CLN3 protein defective in Batten disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Assays for interaction between Rab7 and oxysterol binding protein related protein 1L (ORP1L).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Dynein-mediated vesicle transport controls intracellular Salmonella replication

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Activation of endosomal dynein motors by stepwise assembly of Rab7-RILP-p150Glued, ORP1L, and the receptor betalll spectrin

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

The Rab7 effector protein RILP controls lysosomal transport by inducing the recruitment of dynein-dynactin motors

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Changes in lysosome shape and distribution correlated with changes in cytoplasmic pH

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Kinesin-2 is a motor for late endosomes and lysosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

A 30-year follow-up of a neuronal ceroid lipofuscinosis patient with mutations in CLN3 and protracted disease course.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Molecular characterization of the 50-kD subunit of dynactin reveals function for the complex in chromosome alignment and spindle organization during mitosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Point mutation of adenosine triphosphate-binding motif generated rigor kinesin that selectively blocks anterograde lysosome membrane transport

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Targeted disruption of mouse conventional kinesin heavy chain, kif5B, results in abnormal perinuclear clustering of mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Rab-interacting lysosomal protein (RILP): the Rab7 effector required for transport to lysosomes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Structural basis for recruitment of RILP by small GTPase Rab7

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Cholesterol sensor ORP1L contacts the ER protein VAP to control Rab7-RILP-p150 Glued and late endosome positioning

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Identification of a transactivation motif in the CLN3 protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

AP-1 and AP-3 facilitate lysosomal targeting of Batten disease protein CLN3 via its dileucine motif.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Interaction among Btn1p, Btn2p, and Ist2p reveals potential interplay among the vacuole, amino acid levels, and ion homeostasis in the yeast Saccharomyces cerevisiae

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Btn2, a Hook1 ortholog and potential Batten disease-related protein, mediates late endosome-Golgi protein sorting in yeast

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Rab7: a key to lysosome biogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Rab 7: an important regulator of late endocytic membrane traffic

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Rab7 regulates late endocytic trafficking downstream of multivesicular body biogenesis and cargo sequestration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Role of the small GTPase Rab7 in the late endocytic pathway.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Rabring7, a novel Rab7 target protein with a RING finger motif

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

The oxysterol-binding protein homologue ORP1L interacts with Rab7 and alters functional properties of late endocytic compartments

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

FYCO1 is a Rab7 effector that binds to LC3 and PI3P to mediate microtubule plus end-directed vesicle transport

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Rubicon controls endosome maturation as a Rab7 effector

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Rab proteins and endocytic trafficking: potential targets for therapeutic intervention

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Rab5 and Rab7 control endocytic sorting along the axonal retrograde transport pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

The small GTPase Rab7 controls the endosomal trafficking and neuritogenic signaling of the nerve growth factor receptor TrkA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Mutations in the small GTP-ase late endosomal protein RAB7 cause Charcot-Marie-Tooth type 2B neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Lysosomal activity associated with developmental axon pruning

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Rab7 is required for the normal progression of the autophagic pathway in mammalian cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Role for Rab7 in maturation of late autophagic vacuoles

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Mutant Rab7 causes the accumulation of cathepsin D and cation-independent mannose 6-phosphate receptor in an early endocytic compartment

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00018-011-0913-1

Isolation of a novel gene underlying Batten disease, CLN3. The International Batten Disease Consortium

21 January 2018

1 reference

12 December 2020

Opposing motor activities of dynein and kinesin determine retention and transport of MHC class II-containing compartments

1 reference

12 December 2020

Apoptosis as the mechanism of neurodegeneration in Batten's disease.

1 reference

12 December 2020

The rab7 GTPase resides on a vesicular compartment connected to lysosomes

1 reference

12 December 2020

On the effects of weak bases and monensin on sorting and processing of lysosomal enzymes in human cells

1 reference

12 December 2020