Alpha-actinin-3 (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Alpha-actinin-3" in English language version.

refsWebsite

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11nih.gov

4^th place

6doi.org

2^nd place

2ensembl.org

1,626^th place

1,007^th place

1uniprot.org

5,673^rd place

6,418^th place

1semanticscholar.org

11^th place

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1harvard.edu

18^th place

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doi.org

Beggs AH, Byers TJ, Knoll JH, Boyce FM, Bruns GA, Kunkel LM (May 1992). "Cloning and characterization of two human skeletal muscle alpha-actinin genes located on chromosomes 1 and 11". The Journal of Biological Chemistry. 267 (13): 9281–9288. doi:10.1016/S0021-9258(19)50420-3. PMID 1339456.
North KN, Yang N, Wattanasirichaigoon D, Mills M, Easteal S, Beggs AH (April 1999). "A common nonsense mutation results in alpha-actinin-3 deficiency in the general population". Nature Genetics. 21 (4): 353–354. doi:10.1038/7675. PMID 10192379. S2CID 19882092.
Pickering C, Kiely J (2017). "ACTN3: More than Just a Gene for Speed". Frontiers in Physiology. 8: 1080. doi:10.3389/fphys.2017.01080. PMC 5741991. PMID 29326606.
Hogarth MW, Houweling PJ, Thomas KC, Gordish-Dressman H, Bello L, Pegoraro E, et al. (January 2017). "Evidence for ACTN3 as a genetic modifier of Duchenne muscular dystrophy". Nature Communications. 8 (1): 14143. Bibcode:2017NatCo...814143H. doi:10.1038/ncomms14143. PMC 5290331. PMID 28139640.
Seto JT, Lek M, Quinlan KG, Houweling PJ, Zheng XF, Garton F, MacArthur DG, Raftery JM, Garvey SM, Hauser MA, Yang N, Head SI, North KN (2011). "Deficiency of α-actinin-3 is associated with increased susceptibility to contraction-induced damage and skeletal muscle remodeling". Human Molecular Genetics. 20 (15): 2914–2927. doi:10.1093/hmg/ddr196. PMID 21536590. Retrieved 15 February 2022.
Chan Y, Tong HQ, Beggs AH, Kunkel LM (July 1998). "Human skeletal muscle-specific alpha-actinin-2 and -3 isoforms form homodimers and heterodimers in vitro and in vivo". Biochemical and Biophysical Research Communications. 248 (1): 134–139. doi:10.1006/bbrc.1998.8920. PMID 9675099.

ensembl.org

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000248746 – Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000006457 – Ensembl, May 2017

harvard.edu

ui.adsabs.harvard.edu

Hogarth MW, Houweling PJ, Thomas KC, Gordish-Dressman H, Bello L, Pegoraro E, et al. (January 2017). "Evidence for ACTN3 as a genetic modifier of Duchenne muscular dystrophy". Nature Communications. 8 (1): 14143. Bibcode:2017NatCo...814143H. doi:10.1038/ncomms14143. PMC 5290331. PMID 28139640.

nih.gov

pubmed.ncbi.nlm.nih.gov

Beggs AH, Byers TJ, Knoll JH, Boyce FM, Bruns GA, Kunkel LM (May 1992). "Cloning and characterization of two human skeletal muscle alpha-actinin genes located on chromosomes 1 and 11". The Journal of Biological Chemistry. 267 (13): 9281–9288. doi:10.1016/S0021-9258(19)50420-3. PMID 1339456.
North KN, Yang N, Wattanasirichaigoon D, Mills M, Easteal S, Beggs AH (April 1999). "A common nonsense mutation results in alpha-actinin-3 deficiency in the general population". Nature Genetics. 21 (4): 353–354. doi:10.1038/7675. PMID 10192379. S2CID 19882092.
Pickering C, Kiely J (2017). "ACTN3: More than Just a Gene for Speed". Frontiers in Physiology. 8: 1080. doi:10.3389/fphys.2017.01080. PMC 5741991. PMID 29326606.
Hogarth MW, Houweling PJ, Thomas KC, Gordish-Dressman H, Bello L, Pegoraro E, et al. (January 2017). "Evidence for ACTN3 as a genetic modifier of Duchenne muscular dystrophy". Nature Communications. 8 (1): 14143. Bibcode:2017NatCo...814143H. doi:10.1038/ncomms14143. PMC 5290331. PMID 28139640.
Seto JT, Lek M, Quinlan KG, Houweling PJ, Zheng XF, Garton F, MacArthur DG, Raftery JM, Garvey SM, Hauser MA, Yang N, Head SI, North KN (2011). "Deficiency of α-actinin-3 is associated with increased susceptibility to contraction-induced damage and skeletal muscle remodeling". Human Molecular Genetics. 20 (15): 2914–2927. doi:10.1093/hmg/ddr196. PMID 21536590. Retrieved 15 February 2022.
Chan Y, Tong HQ, Beggs AH, Kunkel LM (July 1998). "Human skeletal muscle-specific alpha-actinin-2 and -3 isoforms form homodimers and heterodimers in vitro and in vivo". Biochemical and Biophysical Research Communications. 248 (1): 134–139. doi:10.1006/bbrc.1998.8920. PMID 9675099.

ncbi.nlm.nih.gov

"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Entrez Gene: ACTN3 actinin, alpha 3".
Pickering C, Kiely J (2017). "ACTN3: More than Just a Gene for Speed". Frontiers in Physiology. 8: 1080. doi:10.3389/fphys.2017.01080. PMC 5741991. PMID 29326606.
Hogarth MW, Houweling PJ, Thomas KC, Gordish-Dressman H, Bello L, Pegoraro E, et al. (January 2017). "Evidence for ACTN3 as a genetic modifier of Duchenne muscular dystrophy". Nature Communications. 8 (1): 14143. Bibcode:2017NatCo...814143H. doi:10.1038/ncomms14143. PMC 5290331. PMID 28139640.

semanticscholar.org

api.semanticscholar.org

North KN, Yang N, Wattanasirichaigoon D, Mills M, Easteal S, Beggs AH (April 1999). "A common nonsense mutation results in alpha-actinin-3 deficiency in the general population". Nature Genetics. 21 (4): 353–354. doi:10.1038/7675. PMID 10192379. S2CID 19882092.

uniprot.org

"ACTN3 - Alpha-actinin-3 - Homo sapiens (Human) - ACTN3 gene & protein". www.uniprot.org. Retrieved 22 April 2022.