5'RNA-Seq identifies Fhl1 as a genetic modifier in cardiomyopathy. (Q37602194)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24509080%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

title

5'RNA-Seq identifies Fhl1 as a genetic modifier in cardiomyopathy (English)

1 reference

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7 March 2020

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1 reference

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7 March 2020

Polakit Teekakirikul

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7 March 2020

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Barbara McDonough

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7 March 2020

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J G Seidman

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7 March 2020

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Philip L De Jager

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7 March 2020

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Christine E Seidman

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7 March 2020

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Joshua M Gorham

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7 March 2020

Danos C Christodoulou

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object named as

Danos C Christodoulou

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7 March 2020

2

Hiroko Wakimoto

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7 March 2020

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Steve R DePalma

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7 March 2020

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Daniel S Herman

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7 March 2020

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David A Conner

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Jochen Daniel Muehlschlegel

7 March 2020

19

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Jochen D Muehlschlegel

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7 March 2020

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Martha L Bulyk

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7 March 2020

author name string

Kenji Onoue

3

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7 March 2020

David M McKean

10

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7 March 2020

Andrea A Domenighetti

11

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7 March 2020

Anton Aboukhalil

12

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7 March 2020

Stephen Chang

13

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7 March 2020

Gyan Srivastava

14

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7 March 2020

Ju Chen

17

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7 March 2020

language of work or name

English

0 references

publication date

10 February 2014

1 reference

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Journal of Clinical Investigation

7 March 2020

published in

1 reference

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7 March 2020

volume

124

1 reference

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7 March 2020

issue

3

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7 March 2020

page(s)

1364-1370

1 reference

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The UCSC genome browser and associated tools

7 March 2020

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23 August 2017

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23 August 2017

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23 August 2017

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23 August 2017

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An FHL1-containing complex within the cardiomyocyte sarcomere mediates hypertrophic biomechanical stress responses in mice

23 August 2017

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A global view of gene activity and alternative splicing by deep sequencing of the human transcriptome

23 August 2017

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23 August 2017

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23 August 2017

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Expression profiling of cardiac genes in human hypertrophic cardiomyopathy: insight into the pathogenesis of phenotypes

23 August 2017

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The Genetic Basis for Cardiomyopathy

23 August 2017

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An abnormal Ca(2+) response in mutant sarcomere protein-mediated familial hypertrophic cardiomyopathy

23 August 2017

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A calcineurin-dependent transcriptional pathway for cardiac hypertrophy

23 August 2017

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The significance of digital gene expression profiles

23 August 2017

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A mouse model of familial hypertrophic cardiomyopathy

23 August 2017

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A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation

23 August 2017

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Structural organization of the human reduced folate carrier gene: evidence for 5' heterogeneity in lymphoblast mRNA.

23 August 2017

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Serum cardiac troponin I is related to increased left ventricular wall thickness, left ventricular dysfunction, and male gender in hypertrophic cardiomyopathy.

28 September 2017

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Evidence for FHL1 as a novel disease gene for isolated hypertrophic cardiomyopathy

25 June 2018

1 reference

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Cardiac myosin binding protein-C mutations in families with hypertrophic cardiomyopathy: disease expression in relation to age, gender, and long term outcome.

1 September 2018

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Regulation of ompA mRNA stability: the role of a small regulatory RNA in growth phase-dependent control.

1 September 2018

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Experimental cardiac fibrosis: differential time course of responses to mineralocorticoid-salt administration

1 September 2018

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1 September 2018

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The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms

1 September 2018

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1 September 2018

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Sex hormone receptor gene variation associated with phenotype in male hypertrophic cardiomyopathy patients

1 September 2018

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3 December 2018

Identifiers

DOI

10.1172/JCI70108

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24509080%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24509080%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

1 reference