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Temporary Tattoos Kit Semi Permanent Tattoo, 3 Bottles 1.5 oz Ja

$9

Temporary Tattoos Kit Semi Permanent Tattoo, 3 Bottles 1.5 oz Ja

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Product description

TOOBITJagua Gel Temporary Tattoos Kit

Features
-Opaque semi-fluid tattoos gel/ink.
-100% real natural Jagua juice based, Ān-free/ No PPD.
-The color comes from the natural pigment addition that will naturally recedes in about 3-5 days.
-You can also use Alcohol to remove it. Prolonged exposure to water accelerates tattoo fading.
-Product expiration date, we recommended that should be used up within 3-4months after opening the bottle, no more than 6 months.

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Multiple Colors

Search: TOOBIT JAGUA
Black/Wine Red/Green/Brown
1. Black- should be the most popular colors for people
2. Dark Red - close to the wine red and suitable for women who wants some beautiful colors
3. Green- the color of green leaves, trees, expressing youth and vitality. If you paint a red flower on your skin, maybe also with a green leaf.
4. Brown - Insignificance: The color is a little light and not so vivid but natural very close to the skin color, elegant color.
Brown - //Advantage: brown contains the purest natural Jagua juice, with very little pigment added, will show a fascinating reddish brown on skin the next day after use
Please allow that the color may be slightly different from the picture, due to different computer screen display.

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Package Includes
-Tattoo paste bottles*3
-DIY stencils *Dozens pattern
-Disposable gloves*2
-Painting cotton swab*2
-Use Instruction*1

Tips:
We recommend taking a bit as a skin test before using large areas of skin.
I do hope that our tattoo gel will bring you a pleasant experience .

Temporary Tattoos Kit Semi Permanent Tattoo, 3 Bottles 1.5 oz Ja

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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