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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2009 | 1 |
2010 | 2 |
2011 | 1 |
2020 | 1 |
2021 | 1 |
2024 | 0 |
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Page 1
Studying the "Rigid-Flexible" Properties of Polymeric Micelle Core-Forming Segments with a Hydrophobic Phthalocyanine Probe Using NMR and UV Spectroscopy.
Langmuir. 2021 Apr 13;37(14):4316-4330. doi: 10.1021/acs.langmuir.1c00328. Epub 2021 Apr 1.
Langmuir. 2021.
PMID: 33794644
Free PMC article.
Hydrophobically Functionalized Poly(Acrylic Acid) Comprising the Ester-Type Labile Spacer: Synthesis and Self-Organization in Water.
Lamch Ł, Ronka S, Moszyńska I, Warszyński P, Wilk KA.
Lamch Ł, et al. Among authors: moszynska i.
Polymers (Basel). 2020 May 22;12(5):1185. doi: 10.3390/polym12051185.
Polymers (Basel). 2020.
PMID: 32455970
Free PMC article.
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Dysmyelinating and demyelinating Charcot-Marie-Tooth disease associated with two myelin protein zero gene mutations.
Drac H, Kabzińska D, Moszyńska I, Strugalska-Cynowska H, Hausmanowa-Petrusewicz I, Kochański A.
Drac H, et al. Among authors: moszynska i.
J Appl Genet. 2011 May;52(2):177-83. doi: 10.1007/s13353-010-0003-3. Epub 2010 Nov 3.
J Appl Genet. 2011.
PMID: 21107784
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The 5' regulatory sequence of the PMP22 in the patients with Charcot-Marie-Tooth disease.
Sinkiewicz-Darol E, Kabzińska D, Moszyńska I, Kochański A.
Sinkiewicz-Darol E, et al. Among authors: moszynska i.
Acta Biochim Pol. 2010;57(3):373-7. Epub 2010 Sep 15.
Acta Biochim Pol. 2010.
PMID: 20842290
Free article.
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A newly identified Thr99fsX110 mutation in the PMP22 gene associated with an atypical phenotype of the hereditary neuropathy with liability to pressure palsies.
Moszyńska I, Kabzińska D, Sinkiewicz-Darol E, Kochański A.
Moszyńska I, et al.
Acta Biochim Pol. 2009;56(4):627-30. Epub 2009 Oct 15.
Acta Biochim Pol. 2009.
PMID: 19830275
Free article.
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