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KINGFOM Ultra-Smooth PU Leather Writing Mat Lowest price challenge Shipping included Pad with Office Desk

KINGFOM Ultra-Smooth PU Leather Writing Pad Desk Mat with Office

$23

KINGFOM Ultra-Smooth PU Leather Writing Pad Desk Mat with Office

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Product description

Color:Brown-a006

KINGFOM Desk Mat amp; Mate enhances any desk and is perfect for use as a reading or writing surface, as well as housing your keyboard and mouse. Featuring an elegant textured surface and available in colors and different styles, the Desk Mat amp; Mate is a great addition to any workspace.

Wide Surface Area
Use the KINGFOM Desk Mat amp; Mate's wide surface area to accommodate a variety of the devices in your workspace. With enough room for your keyboard and mouse, and space enough for a sketchbook or journal, the Desk Mat amp; Mate is appropriate for a variety of uses. "br""br""b"Synthetic Leather Texture"br"A light synthetic leather texture on the Desk Mat amp; Mate feels great to the touch, and is combined with a non-glare surface to reduce eye strain. The surface is stain-resistant and is easy to clean."br""br""b"Use as Mousepad"br"The Desk Mat amp; Mate's texture allows it to be used as a mousepad; the Mat is suitable for any task - from basic computer use to design work. The Desk Mat also provides wrist support while typing, writing, or using the mouse, and will not move once placed on a desk due to its non-slip backing.

Technical Data:
★. Moddel NO.: A005/006
★. Brand Name: KINGFOM
★. Products Type: Office desk pad
★. Material: PU Leather
★. Color: brown/black
★. Size: 23.6'' x 17.7'' x 0.2'',clip width: 3 inches, thickness: 0.23 inches
★. Package: including 1 piece desk pad
★. Remarks: please do not rinse directly with water to clean it.
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KINGFOM Ultra-Smooth PU Leather Writing Pad Desk Mat with Office

CURRENT ISSUE
September, 2021

No. 106 (9)

2020 Impact Factor: 9.941 Submission > Acceptance: 52 days
ARTICLES IN THREE SENTENCES
Article

Long-term outcomes from the phase II L-MIND study of tafasitamab (MOR208) plus lenalidomide in patients with relapsed or refractory diffuse large B-cell lymphoma

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.

Johannes Duell et al.

Case Report

Clinical genomic profiling of novel grey zone lymphoma paired lesions with sequential central nervous system involvement in two adolescent patients

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.

Cagla Y. Benkli et al.

Article

CAMT-MPL: congenital amegakaryocytic thrombocytopenia caused by MPL mutations - heterogeneity of a monogenic disorder - a comprehensive analysis of 56 patients

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.

Manuela Germeshausen et al.

Article

Oxidative stress activates red cell adhesion to laminin in sickle cell disease

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.

Maria Alejandra Lizarralde-Iragorri et al.

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