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2021 HP OMEN 15.6Ã¢ÂÂ FHD 144Hz Laptop Computer, 3rd Gen AMD R
2021 HP OMEN 15.6Ã¢ÂÂ FHD 144Hz Laptop Computer, 3rd Gen AMD R
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ãUpgradedãSeal is opened for upgrade only, 1-Year warranty on Upgraded RAM/SSD from Snow Bell, and original 1-Year Manufacture warranty on remaining components. ã15.6" FHD 144Hz IPS Displayã1920 x 1080 resolution boasts impressive color and clarity, Anti-Glare Energy-efficient WLED screen.
ãAMD 3rd Generation Ryzen 7-4800H ProcessorãUltra-low-voltage platform. Octal-core, 16-way processing provides maximum high-efficiency power to go.
ã32GB DDR4 RAMãPlenty of high-bandwidth RAM to smoothly run your games as well as multiple programs. ã2TB PCIe SSDãSave files fast and store more data. With massive amounts of storage and advanced communication power, great for major gaming, multiple servers, backups, and more.
ã4 Zone RGB Backlit KeyboardãTouchpad with scroll and multitouch capability, Allows you to enjoy comfortable and accurate typing, even in dim lighting.ãNVIDIA GeForce GTX 1660 Ti GraphicsãBacked by 6GB GDDR6 dedicated video memory provide solid image quality for Internet use, movies, basic photo editing and casual gaming. Audio by Bang amp; Olufsen with dual speakers amp; Built-in HD webcam with dual array microphone.
ãWindows 10 Home includedã6-cell Lithium-ion polymer battery. 14.1" x 9.8" x 0.9â, 5.42 lbs. 3x USB 3.0 Type A, 1x USB 3.1 Type C, 1x Headphone/Microphone Combo, 1x HDMI, 1x Media card reader. Xbox Game Pass for PC. Wireless-AC + Bluetooth, Mica Silver, Bonus 32GB SnowBell USB Card.
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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.