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Ninja SS351 Foodi Power Pitcher System, Smoothie Bowl Maker, 4in
$105
Ninja SS351 Foodi Power Pitcher System, Smoothie Bowl Maker, 4in
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The blender system that crushes, food processes, makes smoothie bowls, and dough.
smartTORQUE is designed to power through heavy loads without stalling or the need to stir or shake.
Total speed control. Start slow and ramp up as needed for precision chopping and mixing.
Power Pitcher: Crush, chop, make smoothie bowls and dough conveniently in one pitcher.
Power Nutri Cup with better breakdown for smoother extractions, smoothies, and frozen drinks. (vs. BL480)
Power Nutri Bowl with Power Paddle powers through frozen foods with less liquid for perfectly thick smoothie bowls, nut butters, and blender ice cream.
6 preset Auto-iQ programs for one-touch smoothies, extractions, bowls, spreads, chopping, and dough.
Powerful 1400-peak-watt power-dense motor.
Versatility of 3 vessels for 1 baseâblend in the Power Pitcher, Power Nutri Cup, and Power Nutri Bowl and store just 1 base.
Includes 1400-peak-watt power-dense motor, 72-oz Power Pitcher (64 oz max liquid) with Total Crushing amp; Chopping Blade, Dough Blade, Cleaning Brush, (2) 24-oz Power Nutri Cups with spout lids, 14-oz Power Nutri Bowl with storage lid, Hybrid Edge Blades, and recipe inspiration guide.
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Product description
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Ninja SS351 Foodi Power Pitcher System, Smoothie Bowl Maker, 4in
Open access journal of the Ferrata-Storti Foundation, a no profit organization
Open access journal of the Ferrata-Storti Foundation, a no profit organization
This open-label, single-arm study investigated the long-term efficacy of tafasitamab plus lenalidomide in 81 patients with relapsed/refractory diffuse large B-cell lymphoma. The response rate was 57.5%, including complete responses in 40.0% of patients, and the median duration of response was 43.9 months. This treatment is a valuable option for patients not eligible for autologous stem-cell transplantation.
Grey zone lymphoma is a B-cell lymphoma, unclassifiable, with features intermediate between those of large B-cell lymphoma and classic Hodgkin lymphoma. The in-depth study of the two adolescent patients described in this case report expands the clinicopathological and genomic spectrum of this rare pediatric disease. Moreover, it provides information on their response to treatment.
The clinical picture of 56 patients with congenital amegakaryocytic thrombocytopenia due to MPL mutations was much more varied than previously thought. Twenty-five per cent of them had no signs of thrombocytopenia at birth, and 50% had non-hematologic defects. Pancytopenia developed in (nearly) all patients and hematopoietic stem-cell transplantation was effective in 87% of cases.
Sickle red blood cells exhibit abnormal adhesion to laminin mediated by Lu/BCAM protein at their surface. This study provides evidence of the involvement of oxidative stress in post-translational modifications of Lu/BCAM which impact the protein’s distribution and cis-interaction with glycophorin C at the cell surface activating its adhesive function in dense sickle red cells. The authors speculate that antioxidant drugs might attenuate this phenomenon.