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Polyglutamine Disorders

Overview of attention for book
Cover of 'Polyglutamine Disorders'

Table of Contents

  1. Altmetric Badge
    Book Overview
  2. Altmetric Badge
    Chapter 1 Clinical Features of Huntington’s Disease
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    Chapter 2 Genetic Rodent Models of Huntington Disease
  4. Altmetric Badge
    Chapter 3 Mitochondrial Dysfunction in Huntington’s Disease
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    Chapter 4 RNA Related Pathology in Huntington’s Disease
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    Chapter 5 X-Linked Spinal and Bulbar Muscular Atrophy: From Clinical Genetic Features and Molecular Pathology to Mechanisms Underlying Disease Toxicity
  7. Altmetric Badge
    Chapter 6 Spinocerebellar Ataxia Type 1: Molecular Mechanisms of Neurodegeneration and Preclinical Studies
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    Chapter 7 Spinocerebellum Ataxia Type 6: Molecular Mechanisms and Calcium Channel Genetics
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    Chapter 8 Spinocerebellar Ataxia Type 2
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    Chapter 9 Molecular Mechanisms and Therapeutic Strategies in Spinocerebellar Ataxia Type 7
  11. Altmetric Badge
    Chapter 10 Spinocerebellar Ataxia Type 17 (SCA17)
  12. Altmetric Badge
    Chapter 11 The Neuropathology of Spinocerebellar Ataxia Type 3/Machado-Joseph Disease
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    Chapter 12 Origins and Spread of Machado-Joseph Disease Ancestral Mutations Events
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    Chapter 13 Clinical Features of Machado-Joseph Disease
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    Chapter 14 Polyglutamine-Independent Features in Ataxin-3 Aggregation and Pathogenesis of Machado-Joseph Disease
  16. Altmetric Badge
    Chapter 15 Animal Models of Machado-Joseph Disease
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    Chapter 16 Towards the Identification of Molecular Biomarkers of Spinocerebellar Ataxia Type 3 (SCA3)/Machado-Joseph Disease (MJD)
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    Chapter 17 Planning Future Clinical Trials for Machado-Joseph Disease
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    Chapter 18 Molecular Mechanisms and Cellular Pathways Implicated in Machado-Joseph Disease Pathogenesis
  20. Altmetric Badge
    Chapter 19 Pharmacological Therapies for Machado-Joseph Disease
  21. Altmetric Badge
    Chapter 20 Gene Therapies for Polyglutamine Diseases
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    Chapter 21 Stem Cell-Based Therapies for Polyglutamine Diseases
Attention for Chapter 21: Stem Cell-Based Therapies for Polyglutamine Diseases
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Chapter title
Stem Cell-Based Therapies for Polyglutamine Diseases
Chapter number 21
Book title
Polyglutamine Disorders
Published in
Advances in experimental medicine and biology, January 2018
DOI 10.1007/978-3-319-71779-1_21
Pubmed ID
Book ISBNs
978-3-31-971778-4, 978-3-31-971779-1
Authors

Liliana S. Mendonça, Isabel Onofre, Catarina Oliveira Miranda, Rita Perfeito, Clévio Nóbrega, Luís Pereira de Almeida

Abstract

Polyglutamine (polyQ) diseases are a family of neurodegenerative disorders with very heterogeneous clinical presentations, although with common features such as progressive neuronal death. Thus, at the time of diagnosis patients might present an extensive and irreversible neuronal death demanding cell replacement or support provided by cell-based therapies. For this purpose stem cells, which include diverse populations ranging from embryonic stem cells (ESCs), to fetal stem cells, mesenchymal stromal cells (MSCs) or induced pluripotent stem cells (iPSCs) have remarkable potential to promote extensive brain regeneration and recovery in neurodegenerative disorders. This regenerative potential has been demonstrated in exciting pre and clinical assays. However, despite these promising results, several drawbacks are hampering their successful clinical implementation. Problems related to ethical issues, quality control of the cells used and the lack of reliable models for the efficacy assessment of human stem cells. In this chapter the main advantages and disadvantages of the available sources of stem cells as well as their efficacy and potential to improve disease outcomes are discussed.

X Demographics

X Demographics

The data shown below were collected from the profiles of 3 X users who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 30 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 30 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 7 23%
Student > Master 4 13%
Student > Ph. D. Student 4 13%
Other 1 3%
Student > Doctoral Student 1 3%
Other 2 7%
Unknown 11 37%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 6 20%
Medicine and Dentistry 3 10%
Neuroscience 3 10%
Pharmacology, Toxicology and Pharmaceutical Science 2 7%
Arts and Humanities 1 3%
Other 4 13%
Unknown 11 37%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 2. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 11 July 2018.
All research outputs
#13,580,944
of 23,023,224 outputs
Outputs from Advances in experimental medicine and biology
#1,901
of 4,964 outputs
Outputs of similar age
#220,048
of 442,364 outputs
Outputs of similar age from Advances in experimental medicine and biology
#61
of 237 outputs
Altmetric has tracked 23,023,224 research outputs across all sources so far. This one is in the 39th percentile – i.e., 39% of other outputs scored the same or lower than it.
So far Altmetric has tracked 4,964 research outputs from this source. They typically receive a little more attention than average, with a mean Attention Score of 6.1. This one has gotten more attention than average, scoring higher than 59% of its peers.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 442,364 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 48th percentile – i.e., 48% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 237 others from the same source and published within six weeks on either side of this one. This one has gotten more attention than average, scoring higher than 69% of its contemporaries.