Luna Simona Pane
Overview
Explore the profile of Luna Simona Pane including associated specialties, affiliations and a list of published articles.
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10
Citations
323
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0
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Recent Articles
1.
Li S, Akrap N, Cerboni S, Porritt M, Wimberger S, Lundin A, et al.
Nat Commun
. 2021 May;
12(1):2832.
PMID: 33972550
No abstract available.
2.
Li S, Akrap N, Cerboni S, Porritt M, Wimberger S, Lundin A, et al.
Nat Commun
. 2021 Jan;
12(1):497.
PMID: 33479216
Prokaryotic restriction enzymes, recombinases and Cas proteins are powerful DNA engineering and genome editing tools. However, in many primary cell types, the efficiency of genome editing remains low, impeding the ...
3.
Carreras A, Pane L, Nitsch R, Madeyski-Bengtson K, Porritt M, Akcakaya P, et al.
BMC Biol
. 2019 Jan;
17(1):4.
PMID: 30646909
Background: Plasma concentration of low-density lipoprotein (LDL) cholesterol is a well-established risk factor for cardiovascular disease. Inhibition of proprotein convertase subtilisin/kexin type 9 (PCSK9), which regulates cholesterol homeostasis, has recently...
4.
Coelho M, Li S, Pane L, Firth M, Ciotta G, Wrigley J, et al.
BMC Biol
. 2018 Dec;
16(1):150.
PMID: 30593278
Background: Base Editing is a precise genome editing method that uses a deaminase-Cas9 fusion protein to mutate cytidine to thymidine in target DNA in situ without the generation of a...
5.
Schick R, Mekies L, Shemer Y, Eisen B, Hallas T, Ben Jehuda R, et al.
PLoS One
. 2018 Oct;
13(10):e0205719.
PMID: 30332462
Aims: Dilated cardiomyopathy (DCM), a myocardial disorder that can result in progressive heart failure and arrhythmias, is defined by ventricular chamber enlargement and dilatation, and systolic dysfunction. Despite extensive research,...
6.
Pane L, Fulcoli F, Cirino A, Altomonte A, Ferrentino R, Bilio M, et al.
Dis Model Mech
. 2018 Sep;
11(9).
PMID: 30166330
The gene is haploinsufficient in 22q11.2 deletion syndrome (22q11.2DS), and genetic evidence from human patients and mouse models points to a major role of this gene in the pathogenesis of...
7.
Chen Z, Xian W, Bellin M, Dorn T, Tian Q, Goedel A, et al.
Eur Heart J
. 2017 Feb;
38(4):292-301.
PMID: 28182242
No abstract available.
8.
Rocchetti M, Sala L, Dreizehnter L, Crotti L, Sinnecker D, Mura M, et al.
Cardiovasc Res
. 2017 Feb;
113(5):531-541.
PMID: 28158429
Aims: Calmodulin (CaM) is a small protein, encoded by three genes (CALM1-3), exerting multiple Ca2+-dependent modulatory roles. A mutation (F142L) affecting only one of the six CALM alleles is associated...
9.
Gramlich M, Pane L, Zhou Q, Chen Z, Murgia M, Schotterl S, et al.
EMBO Mol Med
. 2015 Mar;
7(5):562-76.
PMID: 25759365
Frameshift mutations in the TTN gene encoding titin are a major cause for inherited forms of dilated cardiomyopathy (DCM), a heart disease characterized by ventricular dilatation, systolic dysfunction, and progressive...
10.
Pane L, Zhang Z, Ferrentino R, Huynh T, Cutillo L, Baldini A
Hum Mol Genet
. 2012 Feb;
21(11):2485-96.
PMID: 22367967
The developmental role of the T-box transcription factor Tbx1 is exquisitely dosage-sensitive. In this study, we performed a microarray-based transcriptome analysis of E9.5 embryo tissues across a previously generated Tbx1...