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The US ambassador to Mexico has announced that she is stepping down in May.Roberta Jacobson made the announcement in a tweet in Spanish on Thursday, "I will be departing at the beginning of May, in search of other opportunities."The resignation comes at a time when US relations with Mexico have been strained over issues related to trade and migration and, Jacobson ended her tweet stating, "We are Stronger Together!""I do it knowing the US-Mexico relationship is strong and vital and that this amazing Mission Mexico team will continue to ensure it remains so," she adds. "At this time, I have no news to share on my successor."Jacobson is an experienced US diplomat who was nominated to the position in 2015 by then-President Barack Obama and confirmed the following spring.She was closely involved with the Obama administrations' efforts to reopen diplomatic relations with Cuba in her previous role at the helm of the agency's western hemisphere bureau.John Kerry, who served as secretary of state under Obama, paid tribute to Jacobson on Twitter: 'Whether it was Mexico, Colombia, Cuba and more - Roberta demonstrated the difference diplomacy can make to advance American interests and build peace.'Last weekend, Mexican President Enrique Pe?a Nieto called off an official trip to Washington to meet with President Donald Trump after a tense phone call.CNN previously reported Pe?a Nieto was tentatively planning the trip for March, a White House official said, but the official confirmed that the trip was put on hold following the phone call, which took place on February 20.The-CNN-Wire? & ? 2018 Cable News Network, Inc., a Time Warner Company. All rights reserved. 1688

The Synthetic Turf Field Recycled Tire Crumb Rubber Research Under the Federal Research Action Plan (FRAP) Final Report: Part 1 - Tire Crumb Characterization has been released. It summarizes the first part of the research study that was conducted under the FRAP. The second part, Exposure Characterization, which will include information from a biomonitoring study that CDC/ATSDR is conducting, will be released later. For more information about the study and timeline, see our website on the Federal Research on Recycled Tire Crumb Used on Playing Fields at 567

The U.S. decline in cigarette smoking could be stalling while the adult vaping rate appears to be rising, according to a government report released Thursday.About 14% of U.S adults were cigarette smokers last year, the third year in a row the annual survey found that rate. But health officials said a change in the methodology make it hard to compare that to the same 14% reported for 2017 and 2018.The adult smoking rate last saw a substantial drop in 2017, when it fell from 16% the year before.The new figures from the Centers for Disease Control and Prevention mean there are more than 34 million adult smokers in the U.S.Meanwhile, about 4.5% of adults were counted as current e-cigarette users last year — about 11 million people.That rate appears to be up from 3.2% in 2018 and 2.8% in 2017. But again, officials said that comparing 2019 with earlier years is difficult because of the survey change.The CDC figures are based on responses from about 32,000 people.Health officials have long called tobacco use the nation’s leading cause of preventable disease and death.___The Associated Press Health & Science Department receives support from the Howard Hughes Medical Institute’s Department of Science Education. The AP is solely responsible for all content. 1279

The US Food and Drug Administration approved two cancer treatments, Vitrakvi and Xospata, this week after expedited reviews.Vitrakvi, approved Monday, is "a treatment for adult and pediatric patients whose cancers have a specific genetic feature (biomarker)."The FDA said in a statement that it is the second approved cancer treatment that is based on a tumor biomarker instead of the place in the body where the tumor originated.Vitrakvi will be used for the treatment of solid tumors that have an NTRK (neurotrophic receptor tyrosine kinase) gene fusion that do not have a known resistance mutation, that are not metastatic or where surgical removal is likely to lead to severe morbidity, and that have no alternative treatments or have progressed after treatments.NTRK genes are rare but occur in many types of cancer, the FDA said, such as mammary analogue secretory carcinoma and infantile fibrosarcoma.Xospata tablets, approved Wednesday, are for the "treatment of adult patients who have relapsed or refractory acute myeloid leukemia (AML) with a FLT3 mutation," according to the FDA.Alongside the tablets, the agency also approved a diagnostic to detect the mutation."Approximately 25 to 30 percent of patients with AML have a mutation in the FLT3 gene. These mutations are associated with a particularly aggressive form of the disease and a higher risk of relapse," Dr. Richard Pazdur, director of the FDA's Oncology Center of Excellence, said in the statement.AML is a rapidly progressing cancer that affects the numbers of normal blood cells and calls for continuous transfusions, the FDA said.Both treatments were granted Priority Review designation.Priority Review, established in 1992, means the FDA aims to review the drug or treatment within six months, opposed to 10 months for a standard review."A Priority Review designation will direct overall attention and resources to the evaluation of applications for drugs that, if approved, would be significant improvements in the safety or effectiveness of the treatment, diagnosis, or prevention of serious conditions when compared to standard applications," the FDA says.Both treatments also received?orphan drug?designation, a status granted to drugs for rare diseases or conditions. 2261

The stars have aligned. New Season of #BB22 August 5th: https://t.co/9aJHMKZMCl. pic.twitter.com/uZ0ex6rwTP— Big Brother (@CBSBigBrother) July 23, 2020 159