The embryonic myosin R672C mutation that underlies Freeman-Sheldon syndrome impairs cross-bridge detachment and cycling in adult skeletal muscle (Q35784455)

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scientific article published on 3 March 2015

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English	The embryonic myosin R672C mutation that underlies Freeman-Sheldon syndrome impairs cross-bridge detachment and cycling in adult skeletal muscle	scientific article published on 3 March 2015

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scholarly article

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2 March 2020

The embryonic myosin R672C mutation that underlies Freeman-Sheldon syndrome impairs cross-bridge detachment and cycling in adult skeletal muscle (English)

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2 March 2020

Freeman-Sheldon syndrome

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1

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2 March 2020

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Anita E Beck

2

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2 March 2020

Margaret J McMillin

3

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2 March 2020

F Steven Korte

4

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2 March 2020

Michael J Bamshad

5

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2 March 2020

Michael Regnier

6

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2 March 2020

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3 March 2015

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2 March 2020

Human Molecular Genetics

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2 March 2020

24

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2 March 2020

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2 March 2020

3348-3358

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2 March 2020

describes a project that uses

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11 June 2022

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1 reference

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inferred from PubMed ID database lookup

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1 reference

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inferred from PubMed ID database lookup

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1 reference

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inferred from PubMed ID database lookup

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1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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1 reference

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inferred from PubMed ID database lookup

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1 reference

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inferred from PubMed ID database lookup

Sarcomere popping requires stretch over a range where total tension decreases with length

1 reference

https://pubmed.ncbi.nlm.nih.gov/25740846

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based on heuristic

inferred from PubMed ID database lookup

Defective regulation of contractile function in muscle fibres carrying an E41K beta-tropomyosin mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/25740846

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Thin filament Ca2+ binding properties and regulatory unit interactions alter kinetics of tension development and relaxation in rabbit skeletal muscle

1 reference

https://pubmed.ncbi.nlm.nih.gov/25740846

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genotype-phenotype relationships in Freeman-Sheldon syndrome

1 reference

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inferred from PubMed ID database lookup

Identifiers

10.1093/HMG/DDV084

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25740846%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

PMC publication ID

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Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25740846%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25740846%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

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