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https://www.wildtypefoods.com/
Loaded with omega-3 and omega-6 fats, our salmon has all the nutritional benefits of wild fish, without any of the microplastics, mercury, parasites, or other common toxins. Sustainability. We cultivate our salmon indoors, in the middle of the city, in a closed system purpose-built to tread lighter on the planet.
https://www.bloomberg.com/profile/company/1587416D:US
Company profile page for Wild Type Inc including stock price, company news, press releases, executives, board members, and contact information
https://www.wildtypefoods.com/careers
Your work at Wildtype. Flexible schedule, up to 10 hours per month. Lead grocery shopping and preparation (including making seasoned sushi rice) for sushi, poke, smoked salmon, and cured salmon dishes (such as ceviche) for tastings with chefs, restaurateurs, investors and partners
https://www.bizapedia.com/ny/wildtype-inc.html
Wildtype, Inc. is a New York Domestic Business Corporation filed On October 2, 2014. The company's filing status is listed as Active and its File Number is 4645699. The Registered Agent on file for this company is C/O Cheng Lin and is located …
http://tbwaworldhealth.com/wildtype/
TBWA\WorldHealth Celebrates First Anniversary by Mobilizing Offices to "Do Good" on World Health Day. New York, NY - April 7, 2017. TBWA\WorldHealth, a global healthcare communications network, celebrated its first anniversary by kicking off an agency-wide collaborative effort to “Do Good” on behalf of others in honor of World Health Day ...
https://opencorpdata.com/us-ny/2333304
WILD-TYPE CREATIVE SOLUTIONS INC. is a business entity registered with New York State Department of State (NYSDOS). The DOS entity number is #2333304. The office address is located at 80 State Street, Albany, NEW YORK 12207-2543. The business is initally filed on January 11, 1999. The registered agent is Corporation Service Company. Entity Name.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4359312/
We co-cultured STKM2 cells with wild-type H. pylori strain 7.13 and its isogenic cagA − and cagE − mutants for 24 hours (MOI 100) and analyzed for expression of p53 and E-cadherin proteins. The latter mutant is functionally similar to 7.13 cagA − as it does not form the T4SS that is required for delivery of CagA into host cells.
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