Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Mikayla S. Borthwick"'
Autor:
Christopher P. Vellano, Michael G. White, Miles C. Andrews, Manoj Chelvanambi, Russell G. Witt, Joseph R. Daniele, Mark Titus, Jennifer L. McQuade, Fabio Conforti, Elizabeth M. Burton, Matthew J. Lastrapes, Gabriel Ologun, Alexandria P. Cogdill, Golnaz Morad, Peter Prieto, Alexander J. Lazar, Yanshuo Chu, Guangchun Han, M. A. Wadud Khan, Beth Helmink, Michael A. Davies, Rodabe N. Amaria, Jeffrey J. Kovacs, Scott E. Woodman, Sapna Patel, Patrick Hwu, Michael Peoples, Jeffrey E. Lee, Zachary A. Cooper, Haifeng Zhu, Guang Gao, Hiya Banerjee, Mike Lau, Jeffrey E. Gershenwald, Anthony Lucci, Emily Z. Keung, Merrick I. Ross, Laura Pala, Eleonora Pagan, Rossana Lazcano Segura, Qian Liu, Mikayla S. Borthwick, Eric Lau, Melinda S. Yates, Shannon N. Westin, Khalida Wani, Michael T. Tetzlaff, Lauren E. Haydu, Mikhila Mahendra, XiaoYan Ma, Christopher Logothetis, Zachary Kulstad, Sarah Johnson, Courtney W. Hudgens, Ningping Feng, Lorenzo Federico, Georgina V. Long, P. Andrew Futreal, Swathi Arur, Hussein A. Tawbi, Amy E. Moran, Linghua Wang, Timothy P. Heffernan, Joseph R. Marszalek, Jennifer A. Wargo
Publikováno v:
Nature. 613:E3-E3
Autor:
Diana L. Moreno, Mikayla S. Borthwick, Leah Peralta, Wai Kin Chan, Brenda Melendez, Qian Zhang, Nisha Gokul, Melinda S. Yates
Publikováno v:
Cancer Prevention Research. 16:P015-P015
Background: Lynch syndrome (LS) is a hereditary cancer syndrome carrying roughly 60% lifetime risk of endometrial cancer (EC) development. LS-EC is caused by mutations in mismatch repair genes (most commonly MSH2), which lead to DNA repair deficiency
Autor:
Bryan Fellman, Qian Zhang, Rosemarie Schmandt, Joseph A. Dottino, Kayleah Cumpian, Antonios G. Mikos, Yunyun Jiang, Karen H. Lu, Mikayla S. Borthwick, Hannah A. Pearce, Brenda Melendez, Emma Watson, Joseph Celestino, Ying Yuan, Melinda S. Yates, Sarita R. Shah
Publikováno v:
J Control Release
Non-surgical treatment options for low-grade endometrial cancer and precancerous lesions are a critical unmet need for women who wish to preserve fertility or are unable to undergo hysterectomy. The PI3K/AKT/mTOR pathway is frequently activated in en
Autor:
Pamela T. Soliman, Russell Broaddus, Mikayla S. Borthwick, Brenda Melendez, Melinda S. Yates, Laurie J. McKenzie, Richard K. Yang, Karen H. Lu, Bryan Fellman, Ying Yuan, Qian Zhang, David S. Loose, Joseph A. Dottino
Publikováno v:
Am J Obstet Gynecol
Background Obesity is a well-known risk factor for endometrial cancer, but the mechanisms of obesity-related carcinogenesis are not well defined, particularly for premenopausal women. With the continuing obesity epidemic, increases in the incidence o
Autor:
Kwartler CS; Division of Medical Genetics, Department of Internal Medicine, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX 77030., Pedroza AJ; Department of Cardiothoracic Surgery, Stanford University, Stanford, CA 94305., Kaw A; Division of Medical Genetics, Department of Internal Medicine, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX 77030., Guan P; Division of Medical Genetics, Department of Internal Medicine, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX 77030., Ma S; Division of Medical Genetics, Department of Internal Medicine, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX 77030.; Current address: Department Medicine, Michigan State University, East Lansing, MI 48824., Duan XY; Division of Medical Genetics, Department of Internal Medicine, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX 77030., Kernell C; Division of Medical Genetics, Department of Internal Medicine, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX 77030., Wang C; Division of Medical Genetics, Department of Internal Medicine, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX 77030., Pinelo JEE; Division of Medical Genetics, Department of Internal Medicine, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX 77030., Bowen MSB; Division of Medical Genetics, Department of Internal Medicine, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX 77030., Chen J; Division of Medical Genetics, Department of Internal Medicine, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX 77030., Zhong Y; Department of Epigenetics and Molecular Carcinogenesis, The University of Texas MD Anderson Cancer Center, Smithville, TX 78957., Sinha S; Wellcome-MRC Cambridge Stem Cell Institute, University of Cambridge, Cambridge, United Kingdom., Shen X; Institute of Cancer Research, Shenzhen Bay Laboratory, Shenzhen, China., Fischbein MP; Department of Cardiothoracic Surgery, Stanford University, Stanford, CA 94305., Milewicz DM; Division of Medical Genetics, Department of Internal Medicine, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX 77030.
Publikováno v:
Nature cardiovascular research [Nat Cardiovasc Res] 2023 Oct; Vol. 2 (10), pp. 937-955. Date of Electronic Publication: 2023 Sep 28.