(Q35132215)

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Beta-actin deficiency with oxidative posttranslational modifications in Rett syndrome erythrocytes: insights into an altered cytoskeletal organization

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scholarly article

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Europe PubMed Central

PubMed publication ID

6 August 2017

Beta-actin deficiency with oxidative posttranslational modifications in Rett syndrome erythrocytes: insights into an altered cytoskeletal organization (English)

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Europe PubMed Central

PubMed publication ID

6 August 2017

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Alessio Cortelazzo

1

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24671107%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

Silvia Leoncini

6

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Europe PubMed Central

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11 June 2020

12

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24671107%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

14

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24671107%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

Giuseppe Valacchi

11

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Giuseppe Valacchi

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11 June 2020

Alessandra Pecorelli

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Alessandra Pecorelli

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11 June 2020

Cinzia Signorini

5

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Cinzia Signorini

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11 June 2020

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Claudio De Felice

2

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11 June 2020

Giuseppe Belmonte

4

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Europe PubMed Central

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11 June 2020

Gloria Zollo

7

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11 June 2020

Antonietta Capone

8

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11 June 2020

Cinzia Della Giovampaola

9

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Europe PubMed Central

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11 June 2020

Claudia Sticozzi

10

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Europe PubMed Central

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11 June 2020

Roberto Guerranti

13

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Europe PubMed Central

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11 June 2020

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publication date

26 March 2014

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Europe PubMed Central

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6 August 2017

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Europe PubMed Central

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11 June 2020

9

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24671107%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

3

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Europe PubMed Central

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11 June 2020

e93181

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24671107%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

copyright license

Creative Commons Attribution 4.0 International

26 March 2014

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April 2022 Public Data File from Crossref

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Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3966888/fullTextXML

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Antiproliferative effect of two novel COX-2 inhibitors on human keratinocytes

1 reference

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The role of oxidative stress in Rett syndrome: an overview.

1 reference

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Native ultrastructure of the red cell cytoskeleton by cryo-electron tomography

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13 July 2018

MeCP2 and Rett syndrome: reversibility and potential avenues for therapy.

1 reference

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13 July 2018

Diverse protective roles of the actin cytoskeleton during oxidative stress

1 reference

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13 July 2018

Actin structure and function.

1 reference

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13 July 2018

Rett syndrome: revised diagnostic criteria and nomenclature

1 reference

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13 July 2018

Reversibility of functional deficits in experimental models of Rett syndrome.

1 reference

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13 July 2018

MeCP2 functions largely cell-autonomously, but also non-cell-autonomously, in neuronal maturation and dendritic arborization of cortical pyramidal neurons

1 reference

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MeCP2 involvement in the regulation of neuronal alpha-tubulin production

1 reference

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13 July 2018

Mecp2 deficiency leads to delayed maturation and altered gene expression in hippocampal neurons

1 reference

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Partial rescue of MeCP2 deficiency by postnatal activation of MeCP2.

1 reference

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Mechanisms of disease: neurogenetics of MeCP2 deficiency

1 reference

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Molecular genetics of Rett syndrome: when DNA methylation goes unrecognized

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4-Hydroxy-2-nonenal: a product and mediator of oxidative stress

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Dendritic anomalies in disorders associated with mental retardation

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The current state of two-dimensional electrophoresis with immobilized pH gradients

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13 July 2018

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

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The structure of an open state of beta-actin at 2.65 A resolution

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Pathobiochemical aspects of cytoskeleton components.

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Selective dendritic alterations in the cortex of Rett syndrome

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Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

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Dendritic cytoskeletal protein expression in mental retardation: an immunohistochemical study of the neocortex in Rett syndrome.

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Delayed maturation of neuronal architecture and synaptogenesis in cerebral cortex of Mecp2-deficient mice.

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Widespread changes in dendritic and axonal morphology in Mecp2-mutant mouse models of Rett syndrome: evidence for disruption of neuronal networks

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MeCP2 deficiency is associated with impaired microtubule stability

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Morphological changes and oxidative damage in Rett Syndrome erythrocytes.

1 reference

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Systemic oxidative stress in classic Rett syndrome.

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Identifiers

10.1371/JOURNAL.PONE.0093181

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Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24671107%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

2014PLoSO...993181C

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PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24671107%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24671107%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

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