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Lens Hi Low Auxiliary Lights Motorcycle Driving NEW before Max 43% OFF selling 70W 16000LM Spot

Lens Hi/Low Auxiliary Lights 16000LM Motorcycle 70W Spot Driving


Lens Hi/Low Auxiliary Lights 16000LM Motorcycle 70W Spot Driving


Connection method :Plug and play

product name

Apmatauto LED X6A external spotlight


1. Power: About 35W/PC,70W/2PCS 2.Current:about 2.8a/PCS,5.6a/2PCS 2. Voltage:12V-36V 3. Light Color: White 4. Luminous: 8000LM/PCS,16000LM/2PCS 5. Lifespan: 50000 hours 6. Waterproof: IP65 Waterproof 7.Dual Beam:High and Low Beam (The light was originally high beam and low beam)

7.light type: LED Lens With Perfect Cutting Line

8.Suitable for motorcycles, car,auto, vehicle,motos, ATVs, UTVs,cars, trucks,Scooter Lighting Easy to install,

Line group MODE

1.Low Beam 2.Hight Beam 3.two light flashing in the same time 4.two lights alternately flickering Volatge:DC 9V-36V Current:15A Electrical: On- Off TYPE:Electric On Off Switch(Fog Spotlight On Off Switch) Placement on Vehicle:Left, Right, Front Line length:about 2m

Package content

2PCS LED headlight bulb+A bracket+1Set Wire groups and Switches OR 2PCS LED headlight bulb+U bracket+1Set Wire groups and Switches OR 2PCS LED headlight bulb+G bracket+1Set Wire groups and Switches

Lens Hi/Low Auxiliary Lights 16000LM Motorcycle 70W Spot Driving

May, 2022

No. 107 (5)

2020 Impact Factor: 9.941 Submission > Acceptance: 80 days

Germline GATA2 variant disrupting endothelial eNOS function and angiogenesis can be restored by c-Jun/AP-1 upregulation

Germline GATA2 gene variants have been associated with several inherited and acquired hematologic disorders, and thrombosis has been reported in 25% of patients. Authors demonstrated that GATA2 deficiency is associated with defective expression of eNOS by platelets and endothelial cells with impaired NO production, suggesting that this may represent an important thrombogenic mechanism. They also identified a therapeutic option, through atorvastatin, able to restore eNOS expression and angiogenesis in GATA2 deficiency in vitro.

Giulio Purgatorio et al.


SF3B1-mutant myelodysplastic syndrome/myeloproliferative neoplasms: a unique molecular and prognostic entity

This study includes all consecutive WHO-defined MDS/MPN patients of Mayo Clinic from 1994 to 2020.Next-generation sequencing information at diagnosis was available for 444 (57%) patients. Authors combined all SF3B1-mutant MDS/MPN patients into one category (n=78) and compared them to their wild-type counterparts (n=446). Leukemia-free survival and overall survival in MDS/MPN patients with SF3B1 mutations were significantly better compared to SF31B wild-type MDS/MPN patients.

Abhishek A. Mangaonkar et al.


Toxicity and efficacy of chimeric antigen receptor T-cell therapy in patients with diffuse large B-cell lymphoma above the age of 70 years compared to younger patients – a matched control multicenter cohort study

Data regarding efficacy and toxicity of CAR-T cell therapy in the elderly, geriatric population are insufficient. This study explored the characteristics and outcome of 47 consecutive patients, 70 years or older, referred for CAR-T. The outcomes of CAR-T cell therapy are comparable between elderly, geriatric and younger patients, indicating that age as per se should not preclude CAR-T cell administration.

Ron Ram et al.


Prephase rituximab/prednisone therapy and aging-related, proinflammatory cytokine milieu in older, vulnerable patients with newly diagnosed diffuse large B-cell lymphoma

In this prospective pilot study, authors evaluated a rituximab/prednisone prephase treatment strategy in 33 older, vulnerable patients with newly diagnosed DLBCL. This prephase therapy was feasible with acceptable toxicity profiles and excellent long-term survival. Prephase therapy with rituximab/prednisone should be considered for all older, vulnerable DLBCL patients prior to curative intent, anthracycline-based chemoimmunotherapy.

Richard J. Lin et al.

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