Dynamin 2 mutations associated with human diseases impair clathrin-mediated receptor endocytosis (Q84273176)

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3 February 2020

title

Dynamin 2 mutations associated with human diseases impair clathrin-mediated receptor endocytosis (English)

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3 February 2020

1

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3 February 2020

Jorge A Bevilacqua

4

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3 February 2020

Vehary Sakanyan

6

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3 February 2020

Pascale Guicheney

10

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3

Bernard Prudhon

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3 February 2020

2

Anne-Cécile Durieux

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3 February 2020

author name string

Adrien Herledan

5

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3 February 2020

Andoni Urtizberea

7

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3 February 2020

Luis Cartier

8

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3 February 2020

Norma B Romero

9

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publication date

1 October 2009

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3 February 2020

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3 February 2020

volume

30

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issue

10

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page(s)

1419-1427

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The role of phosphatidic acid in the regulation of the Ras/MEK/Erk signaling cascade

3 February 2020

cites work

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https://api.crossref.org/works/10.1002%2FHUMU.21086

7 January 2021

Mutations in dynamin 2 cause dominant centronuclear myopathy

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7 January 2021

Dynamin 2 mutations cause sporadic centronuclear myopathy with neonatal onset

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7 January 2021

A novel mutation in the dynamin 2 gene in a Charcot-Marie-Tooth type 2 patient: clinical and pathological findings

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7 January 2021

A new centronuclear myopathy phenotype due to a novel dynamin 2 mutation

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7 January 2021

The stalk region of dynamin drives the constriction of dynamin tubes

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7 January 2021

Identification of dynamin 2, an isoform ubiquitously expressed in rat tissues

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7 January 2021

Induction of mutant dynamin specifically blocks endocytic coated vesicle formation

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7 January 2021

Isolation of an ubiquitously expressed cDNA encoding human dynamin II, a member of the large GTP-binding protein family

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7 January 2021

Expression and purification of dynamin II domains and initial studies on structure and function

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7 January 2021

Subtle central and peripheral nervous system abnormalities in a family with centronuclear myopathy and a novel dynamin 2 gene mutation

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7 January 2021

Two novel mutations in dynamin-2 cause axonal Charcot-Marie-Tooth disease

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7 January 2021

Characterization of the muscle involvement in dynamin 2-related centronuclear myopathy.

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7 January 2021

Endocytosis proteins and cancer: a potential link?

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7 January 2021

Magnetic resonance imaging findings of leg musculature in Charcot-Marie-Tooth disease type 2 due to dynamin 2 mutation

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https://api.crossref.org/works/10.1002%2FHUMU.21086

7 January 2021

Dynamin-mediated internalization of caveolae.

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https://api.crossref.org/works/10.1002%2FHUMU.21086

7 January 2021

Clinical and histologic findings in autosomal centronuclear myopathy

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https://api.crossref.org/works/10.1002%2FHUMU.21086

7 January 2021

Role of dynamin in the formation of transport vesicles from the trans-Golgi network

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https://api.crossref.org/works/10.1002%2FHUMU.21086

7 January 2021

Regulation of Bin1 SH3 domain binding by phosphoinositides

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https://api.crossref.org/works/10.1002%2FHUMU.21086

7 January 2021

Dynamin is required for the activation of mitogen-activated protein (MAP) kinase by MAP kinase kinase

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https://api.crossref.org/works/10.1002%2FHUMU.21086

7 January 2021

Increased lysosome-related proteins in the skeletal muscles of distal myopathy with rimmed vacuoles

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https://api.crossref.org/works/10.1002%2FHUMU.21086

7 January 2021

Domain structure and function of dynamin probed by limited proteolysis.

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https://api.crossref.org/works/10.1002%2FHUMU.21086

7 January 2021

Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy

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https://api.crossref.org/works/10.1002%2FHUMU.21086

7 January 2021

Multiple distinct coiled-coils are involved in dynamin self-assembly

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https://api.crossref.org/works/10.1002%2FHUMU.21086

7 January 2021

Dynamin at the actin-membrane interface

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https://api.crossref.org/works/10.1002%2FHUMU.21086

7 January 2021

The dynamin superfamily: universal membrane tubulation and fission molecules?

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21086

7 January 2021

Alu-splice cloning of human Intersectin (ITSN), a putative multivalent binding protein expressed in proliferating and differentiating neurons and overexpressed in Down syndrome

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https://api.crossref.org/works/10.1002%2FHUMU.21086

7 January 2021

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https://api.crossref.org/works/10.1002%2FHUMU.21086

7 January 2021

Impairment of dynamin's GAP domain stimulates receptor-mediated endocytosis

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https://api.crossref.org/works/10.1002%2FHUMU.21086

7 January 2021

Identification of dynamin, a novel mechanochemical enzyme that mediates interactions between microtubules

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https://api.crossref.org/works/10.1002%2FHUMU.21086

7 January 2021

A model for dynamin self-assembly based on binding between three different protein domains

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7 January 2021

Dissecting DNA-protein and protein-protein interactions involved in bacterial transcriptional regulation by a sensitive protein array method combining a near-infrared fluorescence detection

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https://api.crossref.org/works/10.1002%2FHUMU.21086

7 January 2021

Dynamin 2 binds gamma-tubulin and participates in centrosome cohesion.

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https://api.crossref.org/works/10.1002%2FHUMU.21086

7 January 2021

Importance of the pleckstrin homology domain of dynamin in clathrin-mediated endocytosis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21086

7 January 2021

Ubiquitously expressed dynamin-II has a higher intrinsic GTPase activity and a greater propensity for self-assembly than neuronal dynamin-I

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21086

7 January 2021

The amphiphysin family of proteins and their role in endocytosis at the synapse

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21086

7 January 2021

Changes in synaptic expression of clathrin assembly protein AP180 in Alzheimer's disease analysed by immunohistochemistry

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21086

7 January 2021

Dynamin II interacts with syndecan-4, a regulator of focal adhesion and stress-fiber formation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21086

7 January 2021

Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21086

7 January 2021

Identifiers

DOI

10.1002/HUMU.21086

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19623537%20AND%20SRC:MED&resulttype=core&format=json

3 February 2020

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