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He criticised the current system of incarceration as going completely against the purpose of youth justice, telling the hearing yesterday Don Dale in particular was run "like a human storage facility".
The head of Russian cryonics firm KrioRus, Danila Medvedev, looks inside a low-temperature human storage unit just outside Moscow.
Here we report that MLII knock-in mice, recapitulating the human storage disease, are runted with accompanying growth plate widening, low trabecular bone mass and cortical porosity.
Human skin and dermal vasculature contains high quantities of NO2- (8.4 µM) and nitrosothiols (2.9 µM), which can be recycled by environmental stimuli, such as UVA radiation, to form NO. –, The skin of a human weighs approximately 4 kg and can be considered the largest human storage organ for NO derivatives such nitrite and nitrosothiols.
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The cells of these mice exhibited a distinct cholesterol-storage disorder, and a subsequent in vitro survey of cell lines of human metabolic storage disorders revealed that NPC patient fibroblasts display a similar cholesterol-storage phenotype (Pentchev et al., 1986).
According to Hoffman & Senter (1978) the first real scientific study of imagery mnemonics was carried out at the University of Pennsylvania in the late 1950s, by Wallace, Turner, & Perkins, who were attempting to explore "the limits of human information storage".
As in human cases, storage is accompanied, by a high degree of neuronal ubiquitination.
Interestingly, mutations in MCOLN1 (the name of the TRPML1 gene) are solely responsible for the human lysosomal storage disorder (LSD) MLIV (mucolipidosis type IV) [ 21, 22].
On the other hand, the Bacteroides thetaiotaomicron branching enzyme is an attractive target for modeling human glycogen storage diseases in Bacteria.
Suitable control measures, such as removing rodents and preventing them from entering houses and human food storage buildings, should be taken to reduce incidence in this new disease-endemic region.
Finally (see Table 1), we investigated the amino-acid conservation in the positions mutated in the human glycogen storage diseases GSD3, GSD4, and APBD in orthologs of the human proteins (i.e. from sub-tree "A" for CBM_48 Alpha-amylase branCBM_48 Alpha-amylaseigure 4) from a wide variety of species, as well as in the paralogous Glgbranching from enzymes and Noseec punctiFigure
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