Inequities in the Time to Colon Cancer Diagnosis Among Individuals With Severe Psychiatric Illness by Jonah H. Gorodensky, Laura Davis, Rebecca Griffiths, Oyedeji Ayonrinde, Colleen Webber, Timothy P. Hanna, Natalie Coburn, Alyson L. Mahar

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Assessments of prostate cancer cell functions highlight differences between a pan‐PI3K/mTOR inhibitor, gedatolisib, and single‐node inhibitors of the PI3K/AKT/mTOR pathway by Adrish Sen, Salmaan Khan, Stefano Rossetti, Aaron Broege, Ian MacNeil, Ann DeLaForest, Jhomary Molden, Laura Davis, Charles Iversrud, Megan Seibel, Ross Kopher, Stephen Schulz, Lance Laing

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Lessons learned from 5 years of pegvaliase in US clinics: A case series by Erin Cooney, Zineb Ammous, Tricia Bender, Gillian E. Clague, Marilyn Clifford, Angela Crutcher, Laura Davis-Keppen, Kirsten Havens, Melissa Lah, Stephanie Sacharow, Amarilis Sanchez-Valle, Erika Vucko, Bridget Wardley, Leah Wessenberg, Hans C. Andersson

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Relationship between experiencing a challenge or delay accessing contraception and contraceptive self-efficacy: Data from a 2022 nationally representative online survey by Alex Schulte, Ariana H. Bennett, Jennet Arcara, Jamie Bardwell, Aisha Chaudhri, Laura Davis, Brittni Frederiksen, Elizabeth Jones, Catherine Labiran, Raegan McDonald-Mosley, Whitney Rice, Tara Stein, Ena Suseth Valladares, Kari White, Cassondra Marshall, Anu Manchikanti Gomez

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P777: Genome sequencing detects transposable element (TE) insertions in two diagnostic challenging cases by Revathi Rajkumar, Anjana Chandrasekhar, Zinayida Schlachetzki, Samin Sajan, Brittany Thomas, Becky Milewski, Joshua Lowry, Richard Wang, Jon Albay, Danny Miller, Kaitlyn Burns, Laura Davis-Keppen, Nora Urraca, Kerri Bosfield, Katherine Cung, Erin Venti, Ryan Taft, Denise Perry, Akanchha Kesari

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An mRNA vaccine encoding five conserved Group A Streptococcus antigens by Nichaela Harbison-Price, Ismail Sebina, Rhiannon A. Bolton, Meredith Finn, Amanda J. Cork, Isabel G. Courtney, Steven Hancock, Ruby Pelingon, Johanna Richter, Olivia Ericsson, Shannon Green, Celeste Cuellar, Laura Davis, Brody Pullinger, Jack Na, Gayathiri Elangovan, David M. P. De Oliveira, Bodie F. Curren, Nia Bickham, Miguel Aguirre, Christina Dold, Stephan Brouwer, Obadiah Plante, Gabrielle T. Belz, Mark J. Walker

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Multiple molecular diagnoses identified through genome sequencing in individuals with suspected rare disease by Alka Malhotra, Erin Thorpe, Alison J. Coffey, Revathi Rajkumar, Josephine Adjeman, Naomi Dianne Naa Adjeley Adjetey, Sharron Aglobitse, Felix Allotey, Todor Arsov, Joyce Ashong, Ebenezer Vincent Badoe, Donald Basel, Yvonne Brew, Chester Brown, Kerri Bosfield, Kari Casas, Mario Cornejo-Olivas, Laura Davis-Keppen, Abbey Freed, Kate Gibson, Parul Jayakar, Marilyn C. Jones, Martina Kawome, Aimé Lumaka, Ursula Maier, Prince Makay, Gioconda Manassero, Marilyn Marbell-Wilson, Charles Marcuccilli, Diane Masser-Frye, Julie McCarrier, Hannah-Sharon Mills, Jeny Balazar Montoya, Gerrye Mubungu, Mamy Ngole, Jorge Perez, Eniko Pivnick, Milagros M. Duenas-Roque, Hildegard Pena Salguero, Arturo Serize, Marwan Shinawi, Fabio Sirchia, Claudia Soler-Alfonso, Alan Taylor, Lauren Thompson, Gail Vance, Adeline Vanderver, Keith Vaux, Danita Velasco, Samuel Wiafe, Ryan J. Taft, Denise L. Perry, Akanchha Kesari

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