Modelling pathogenesis and treatment of familial dysautonomia using patient-specific iPSCs. (Q37444336)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19693009%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

title

Modelling pathogenesis and treatment of familial dysautonomia using patient-specific iPSCs (English)

1 reference

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5 February 2020

0 references

1 reference

1 reference

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5 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19693009%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

Viviane Tabar

1 reference

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5 February 2020

Eirini P Papapetrou

1 reference

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5 February 2020

Hyesoo Kim

1 reference

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5 February 2020

Stuart M Chambers

1 reference

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5 February 2020

Mark J Tomishima

1 reference

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5 February 2020

Christopher A Fasano

1 reference

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5 February 2020

Yosif M Ganat

1 reference

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5 February 2020

Jayanthi Menon

1 reference

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5 February 2020

Fumiko Shimizu

1 reference

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5 February 2020

Agnes Viale

1 reference

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5 February 2020

Michel Sadelain

1 reference

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5 February 2020

language of work or name

English

0 references

publication date

19 August 2009

1 reference

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5 February 2020

1 reference

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5 February 2020

volume

461

1 reference

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5 February 2020

issue

7262

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5 February 2020

page(s)

402-406

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describes a project that uses

5 February 2020

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2784695/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

cites work

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23 August 2017

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23 August 2017

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Induced pluripotent stem cells generated from patients with ALS can be differentiated into motor neurons

23 August 2017

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Reprogramming of human somatic cells to pluripotency with defined factors

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Generation of functional hemangioblasts from human embryonic stem cells.

23 August 2017

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23 August 2017

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Familial dysautonomia: a review of the current pharmacological treatments

23 August 2017

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Derivation of midbrain dopamine neurons from human embryonic stem cells

23 August 2017

1 reference

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Familial dysautonomia is caused by mutations of the IKAP gene

23 August 2017

1 reference

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Tissue-specific expression of a splicing mutation in the IKBKAP gene causes familial dysautonomia

23 August 2017

1 reference

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The cellular function of MASH1 in autonomic neurogenesis

23 August 2017

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Forced expression of HoxB4 enhances hematopoietic differentiation by human embryonic stem cells.

14 September 2017

1 reference

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Development of the hemangioblast defines the onset of hematopoiesis in human ES cell differentiation cultures

14 September 2017

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Transcription impairment and cell migration defects in elongator-depleted cells: implication for familial dysautonomia

14 September 2017

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EGCG corrects aberrant splicing of IKAP mRNA in cells from patients with familial dysautonomia

14 September 2017

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Tocotrienols induce IKBKAP expression: a possible therapy for familial dysautonomia

14 September 2017

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Human ES cell-derived neural rosettes reveal a functionally distinct early neural stem cell stage

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Rescue of a human mRNA splicing defect by the plant cytokinin kinetin

2 September 2018

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Survival in familial dysautonomia: Impact of early intervention

2 September 2018

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IKAP localizes to membrane ruffles with filamin A and regulates actin cytoskeleton organization and cell migration

2 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19693009

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NATURE08320

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19693009%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

5 February 2020

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19693009%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

PubMed publication ID

19693009

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19693009%20AND%20SRC:MED&resulttype=core&format=json