Recent advances in animal and human pluripotent stem cell modeling of cardiac laminopathy (Q28077171)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27649756%20AND%20SRC:MED&resulttype=core&format=json

23 March 2020

review article

2 references

6 November 2020

Recent advances in animal and human pluripotent stem cell modeling of cardiac laminopathy (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27649756%20AND%20SRC:MED&resulttype=core&format=json

biomedical investigative technique

23 March 2020

main subject

dilated cardiomyopathy

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proteostasis deficiency

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23 March 2020

author name string

Yee-Ki Lee

1

2 references

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23 March 2020

Yu Jiang

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23 March 2020

Xin-Ru Ran

3

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23 March 2020

Yee-Man Lau

4

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23 March 2020

Kwong-Man Ng

5

2 references

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23 March 2020

Wing-Hon Kevin Lai

6

2 references

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23 March 2020

Chung-Wah Siu

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2 references

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23 March 2020

language of work or name

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20 September 2016

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23 March 2020

6 November 2020

Stem Cell Research & Therapy

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27649756%20AND%20SRC:MED&resulttype=core&format=json

23 March 2020

6 November 2020

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23 March 2020

page(s)

139

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23 March 2020

issue

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Creative Commons Attribution 4.0 International

23 March 2020

copyright license

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on focus list of Wikimedia project

6 November 2020

copyright status

copyrighted

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ScienceSource

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exact match

https://scigraph.springernature.com/pub.10.1186/s13287-016-0401-5

0 references

cites work

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Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease

20 March 2017

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Laminopathies and the long strange trip from basic cell biology to therapy

20 March 2017

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Human laminopathies: nuclei gone genetically awry

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The laminopathies: a clinical review

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Defects in nuclear structure and function promote dilated cardiomyopathy in lamin A/C-deficient mice

20 March 2017

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Modelling the long QT syndrome with induced pluripotent stem cells

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NF-κB activation impairs somatic cell reprogramming in ageing

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Truncated prelamin A expression in HGPS-like patients: a transcriptional study.

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Lamin A/C mutations in dilated cardiomyopathy

29 September 2017

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Induced pluripotent stem cells reveal functional differences between drugs currently investigated in patients with hutchinson-gilford progeria syndrome

29 September 2017

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Generation and characterization of a conditional deletion allele for Lmna in mice

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Depletion of extracellular signal-regulated kinase 1 in mice with cardiomyopathy caused by lamin A/C gene mutation partially prevents pathology before isoenzyme activation

29 September 2017

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Modeling of lamin A/C mutation premature cardiac aging using patient‐specific induced pluripotent stem cells

29 September 2017

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Pharmacological inhibition of c-Jun N-terminal kinase signaling prevents cardiomyopathy caused by mutation in LMNA gene

29 September 2017

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29 September 2017

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29 September 2017

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29 September 2017

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29 September 2017

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29 September 2017

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29 September 2017

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A human iPSC model of Hutchinson Gilford Progeria reveals vascular smooth muscle and mesenchymal stem cell defects

2 June 2018

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2 June 2018

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A progeroid syndrome in mice is caused by defects in A-type lamins

21 January 2018

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Expression of an LMNA-N195K variant of A-type lamins results in cardiac conduction defects and death in mice.

21 January 2018

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Nuclear envelope alterations in fibroblasts from LGMD1B patients carrying nonsense Y259X heterozygous or homozygous mutation in lamin A/C gene.

21 January 2018

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Heart transplantation in 7 patients from a single family with limb-girdle muscular dystrophy caused by lamin A/C mutation.

21 January 2018

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Implantable cardioverter-defibrillators in lamin A/C mutation carriers with cardiac conduction disorders.

21 January 2018

1 reference

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Nuclear accumulation of androgen receptor in gender difference of dilated cardiomyopathy due to lamin A/C mutations.

21 January 2018

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High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinics

21 January 2018

1 reference

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Long-Term Outcome and Risk Stratification in Dilated Cardiolaminopathies

21 January 2018

1 reference

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Unique Preservation of Neural Cells in Hutchinson- Gilford Progeria Syndrome Is Due to the Expression of the Neural-Specific miR-9 MicroRNA

21 January 2018

1 reference

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Mouse model carrying H222P- Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies

21 January 2018

1 reference

12 December 2020

Lamin A/C gene mutations in familial cardiomyopathy with advanced atrioventricular block and arrhythmia

1 reference

12 December 2020

Natural history of dilated cardiomyopathy due to lamin A/C gene mutations

1 reference

12 December 2020

Genetics of dilated cardiomyopathy

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12 December 2020

High Incidence of Sudden Death with Conduction System and Myocardial Disease Due to Lamins A and C Gene Mutation

1 reference

12 December 2020

A novel lamin A/C mutation in a family with dilated cardiomyopathy, prominent conduction system disease, and need for permanent pacemaker implantation

1 reference

12 December 2020

Metabolic and cardiac phenotype characterization in 37 atypical Dunnigan patients with nonfarnesylated mutated prelamin A

1 reference

12 December 2020

Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease

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12 December 2020

10.1186/S13287-016-0401-5

Identifiers

DOI

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27649756%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

23 March 2020

1 reference

9 September 2019

https://scigraph.springernature.com/pub.10.1186/s13287-016-0401-5

Fatcat ID

release_ojid335jpfdd3ksczjtvbs3fsu

1 reference

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24 November 2022

mapped directly with Wikidata item

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27649756%20AND%20SRC:MED&resulttype=core&format=json

23 March 2020

2 references