INT9243
From wiki-pain
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Sentences Mentioned In
Key: | Protein | Mutation | Event | Anatomy | Negation | Speculation | Pain term | Disease term |
Expression of the telencephalic transcription factor FOXG128 was detected in the NE cells by RT-PCR at day 17 of differentiation (Figure 3B) and by immunostaining at day 25 of differentiation (Figure 3D). | |||||||||||||||
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Increased HbF production was associated with demethylation of two restriction enzyme sites 5' to the two gamma-globin genes. | |||||||||||||||
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The generation of the region-specific neural cells positive for FOXG1, OTX2 or HOXB4 was comparable between TZ1 and YZ1 hiPSC, and H9 hESC. | |||||||||||||||
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Mature neural progenitors weakly express telencephalic markers, but strong expression of BF1, EN2 and OTX2 but not EN1 reveals their forebrain character. | |||||||||||||||
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Based on these results, we suggest that noxious mechanical stimulation of the skin produces changes of HBF, either as a reflex response via activation of the hepatic sympathetic nerves or as a passive response to systemic circulatory changes, depending on the sites stimulated. | |||||||||||||||
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Interestingly, at D42 the cells expressed the ventral diencephalon marker RX, telencephalic marker BF1 [20], [21], as well as the hindbrain marker GBX2 (Figure 4E). | |||||||||||||||
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In this study, higher HbF and fewer vascular complications were found in the low LDH groups. | |||||||||||||||
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This group also had lower hemoglobin concentrations, serum arginine, arginine to ornithine ratios, and fetal hemoglobin (HbF) levels. | |||||||||||||||
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Nevertheless, the degree of hemolysis varies among patients and its intensity is modulated by HbF expression and co-incident ? | |||||||||||||||
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Levels of HBF, HO2D, and MEGX were measured at BASELINE, after lung injury (INJURY time point), and after addition of PEEP (PEEP time point). | |||||||||||||||
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thalassemia and/or a gene for raised HbF production (XmnI polymorphism). | |||||||||||||||
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These factors are the presence of silent or mild beta-thalassemia alleles associated with a high residual output of beta globin, the co-inheritance of alpha thalassemia and/or of genetic determinants able to sustain a continuous production of gamma globin chains (HbF) in adult life [18]. | |||||||||||||||
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Other mutations increasing HbF production are those associated with deletional and non-deletional HPFH linked to the beta globin gene cluster. | |||||||||||||||
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The hemoglobin (Hb) profile and HbF levels were investigated by high performance liquid chromatography (HPLC/VARIANT I; BIO-RAD, CA, USA).
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General Comments
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