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Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2021 | 1 |
2022 | 2 |
2023 | 0 |
Search Results
3
results
Results by year
Page 1
CFTR corrector C17 is effective in muscular dystrophy, in vivo proof of concept in LGMDR3.
Hum Mol Genet. 2022 Feb 21;31(4):499-509. doi: 10.1093/hmg/ddab260.
Hum Mol Genet. 2022.
PMID: 34505136
Free PMC article.
KCNG1-Related Syndromic Form of Congenital Neuromuscular Channelopathy in a Crossbred Calf.
Jacinto JGP, Häfliger IM, Akyürek EE, Sacchetto R, Benazzi C, Gentile A, Drögemüller C.
Jacinto JGP, et al. Among authors: akyurek ee.
Genes (Basel). 2021 Nov 12;12(11):1792. doi: 10.3390/genes12111792.
Genes (Basel). 2021.
PMID: 34828398
Free PMC article.
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Differential Analysis of Gly211Val and Gly286Val Mutations Affecting Sarco(endo)plasmic Reticulum Ca2+-ATPase (SERCA1) in Congenital Pseudomyotonia Romagnola Cattle.
Akyürek EE, Busato F, Murgiano L, Bianchini E, Carotti M, Sandonà D, Drögemüller C, Gentile A, Sacchetto R.
Akyürek EE, et al.
Int J Mol Sci. 2022 Oct 15;23(20):12364. doi: 10.3390/ijms232012364.
Int J Mol Sci. 2022.
PMID: 36293223
Free PMC article.
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