檢索結果 - Catherine Sullivan

  • Showing 1 - 15 results of 15
Refine Results
  1. 1
    TNFα and IL-1β influence the differentiation and migration of murine MSCs independently of the NF-κB pathway

    TNFα and IL-1β influence the differentiation and migration of murine MSCs independently of the NF-κB pathway 由 Catherine Sullivan, Ryan M. Porter, Chris H. Evans, Thomas Ritter, Georgina Shaw, Frank Barry, Mary Murphy

    出版 2014
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  2. 2
    High levels of vascular endothelial growth factor and its receptors (VEGFR-1, VEGFR-2, neuropilin-1) are associated with worse outcome in breast cancer

    High levels of vascular endothelial growth factor and its receptors (VEGFR-1, VEGFR-2, neuropilin-1) are associated with worse outcome in breast cancer 由 Sriparna Ghosh, Catherine Sullivan, Maciej P. Zerkowski, Annette M. Molinaro, David L. Rimm, Robert L. Camp, Gina G. Chung

    出版 2008
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  3. 3
    “Feeding the baby breast milk shouldn’t be a problem” breastfeeding confidence and intention in pregnant persons with type 2 diabetes mellitus from Thailand

    “Feeding the baby breast milk shouldn’t be a problem” breastfeeding confidence and intention in pregnant persons with type 2 diabetes mellitus from Thailand 由 Ratchanok Phonyiam, Chiao-Hsin Teng, Yamnia I. Cortés, Catherine Sullivan, Aunchalee E. L. Palmquist, Eric A. Hodges, Marianne Baernholdt

    出版 2025
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  4. 4
    PMCA2 regulates apoptosis during mammary gland involution and predicts outcome in breast cancer

    PMCA2 regulates apoptosis during mammary gland involution and predicts outcome in breast cancer 由 Joshua VanHouten, Catherine Sullivan, Caroline Bazinet, Tom Ryoo, Robert L. Camp, David L. Rimm, Gina G. Chung, John J. Wysolmerski

    出版 2010
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  5. 5
    Molecular Phenotypes in Triple Negative Breast Cancer from African American Patients Suggest Targets for Therapy

    Molecular Phenotypes in Triple Negative Breast Cancer from African American Patients Suggest Targets for Therapy 由 Robert Lindner, Catherine Sullivan, Onyinye Offor, Kimberly Lezon-Geyda, K. Halligan, Neal Fischbach, Mansi Shah, Veerle Bossuyt, Vincent Schulz, David Tuck, Lyndsay N. Harris

    出版 2013
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  6. 6
    Calcium-Sensing Receptor Promotes Breast Cancer by Stimulating Intracrine Actions of Parathyroid Hormone–Related Protein

    Calcium-Sensing Receptor Promotes Breast Cancer by Stimulating Intracrine Actions of Parathyroid Hormone–Related Protein 由 Wonnam Kim, Farzin M. Takyar, Karena Swan, Jaekwang Jeong, Joshua VanHouten, Catherine Sullivan, Pamela Dann, Herbert Yu, Nathalie Fiaschi‐Taesch, Wenhan Chang, John J. Wysolmerski

    出版 2016
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  7. 7
    PMCA2 regulates HER2 protein kinase localization and signaling and promotes HER2-mediated breast cancer

    PMCA2 regulates HER2 protein kinase localization and signaling and promotes HER2-mediated breast cancer 由 Jaekwang Jeong, Joshua VanHouten, Pamela Dann, Wonnam Kim, Catherine Sullivan, Herbert Yu, Lance A. Liotta, Virginia Espina, David F. Stern, Peter A. Friedman, John J. Wysolmerski

    出版 2016
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  8. 8
    Impact of Navigators on Completion of Steps in the Kidney Transplant Process

    Impact of Navigators on Completion of Steps in the Kidney Transplant Process 由 Catherine Sullivan, Janeen B. León, Srilekha S. Sayre, Marquisha Marbury, Michael Ivers, Julie Pencak, Kenneth A. Bodziak, Donald E. Hricik, Eric Morrison, Jeffrey M. Albert, Sankar D. Navaneethan, Christina M.Delos Reyes, Ashwini R. Sehgal

    出版 2012
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  9. 9
    De Novo Damaging DNA Coding Mutations Are Associated With Obsessive-Compulsive Disorder and Overlap With Tourette’s Disorder and Autism

    De Novo Damaging DNA Coding Mutations Are Associated With Obsessive-Compulsive Disorder and Overlap With Tourette’s Disorder and Autism 由 Carolina Cappi, Melody Oliphant, Zsanett Péter, Gwyneth Zai, Maria Conceição do Rosário, Catherine Sullivan, Abha R. Gupta, Ellen J. Hoffman, Manmeet Virdee, Emily Olfson, Sarah B. Abdallah, A. Jeremy Willsey, Roseli Gedanke Shavitt, Eurípedes C. Miguel, James L. Kennedy, Margaret A. Richter, Thomas Fernandez

    出版 2019
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  10. 10
    No Evidence for Association of Autism with Rare Heterozygous Point Mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contactins

    No Evidence for Association of Autism with Rare Heterozygous Point Mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contacti... 由 John D. Murdoch, Abha R. Gupta, Stephan Sanders, Michael F. Walker, John F. Keaney, Thomas Fernandez, Michael T. Murtha, Samuel Anyanwu, G Ober, Melanie J. Raubeson, Nicholas M. DiLullo, Natalie M. Villa, Zainabdul Waqar, Catherine Sullivan, Luis A. González, A. Jeremy Willsey, So-Yeon Choe, Benjamin M. Neale, Mark J. Daly, Matthew W. State

    出版 2015
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  11. 11
    Structural Determinants of Signal Speed: A Multimodal Investigation of Face Processing in Autism Spectrum Disorder

    Structural Determinants of Signal Speed: A Multimodal Investigation of Face Processing in Autism Spectrum Disorder 由 Campbell R Coleman, Madelyn G. Nance, Zachary Jacokes, T. Jason Druzgal, Vardan Arutiunian, Anna Kresse, Catherine Sullivan, Megha Santhosh, Emily Neuhaus, Heather Borland, Raphael Bernier, Susan Y. Bookheimer, Mirella Dapretto, Allison Jack, Shafali Jeste, James C. McPartland, Adam Naples, Daniel H. Geschwind, Abha R. Gupta, Sara Jane Webb, Kevin A. Pelphrey, John D. Van Horn, Benjamin T. Newman, Meghan H. Puglia

    出版 2025
    獲取全文
    Pré-impressão
    加到收藏夾
    Saved in:
  12. 12
    De Novo Insertions and Deletions of Predominantly Paternal Origin Are Associated with Autism Spectrum Disorder

    De Novo Insertions and Deletions of Predominantly Paternal Origin Are Associated with Autism Spectrum Disorder 由 Shan Dong, Michael F. Walker, Nicholas Carriero, Michael DiCola, A. Jeremy Willsey, Adam Yongxin Ye, Zainulabedin Waqar, Luis Eduardo González, John D. Overton, Stephanie Frahm, John F. Keaney, Nicole A. Teran, Jeanselle Dea, Jeffrey D. Mandell, Vanessa H. Bal, Catherine Sullivan, Nicholas M. DiLullo, Rehab O. Khalil, Jake Gockley, Zafer Yüksel, Sinem M Sertel, A. Gulhan Ercan‐Sencicek, Abha R. Gupta, Shrikant Mane, Michael Sheldon, Andrew I. Brooks, Kathryn Roeder, Bernie Devlin, Matthew W. State, Liping Wei, Stephan Sanders

    出版 2014
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  13. 13
    The contribution of de novo coding mutations to autism spectrum disorder

    The contribution of de novo coding mutations to autism spectrum disorder 由 Ivan Iossifov, Brian J. O’Roak, Stephan Sanders, Michael Ronemus, Niklas Krumm, Dan Levy, Holly A.F. Stessman, Kali Witherspoon, Laura Vives, Karynne Patterson, Joshua D. Smith, Bryan Paeper, Deborah A. Nickerson, Jeanselle Dea, Shan Dong, Luis Eduardo González, Jeffrey D. Mandell, Shrikant Mane, Michael T. Murtha, Catherine Sullivan, Michael F. Walker, Zainulabedin Waqar, Liping Wei, A. Jeremy Willsey, Boris Yamrom, Yoonha Lee, Ewa Grabowska, Ertuğrul Dalkıç, Zihua Wang, Steven C. Marks, Peter Andrews, Anthony Leotta, Jude Kendall, Inessa Hakker, Julie Rosenbaum, Beicong Ma, Linda Rodgers, Jennifer Troge, Giuseppe Narzisi, Seungtai Yoon, Michael C. Schatz, Kenny Ye, W. Richard McCombie, Jay Shendure, Evan E. Eichler, Matthew W. State, Michael Wigler

    出版 2014
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  14. 14
    Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes

    Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes 由 Xueya Zhou, Pamela Feliciano, Chang Shu, Tianyun Wang, Irina Astrovskaya, Jacob B. Hall, Joseph Obiajulu, Jessica Wright, Shwetha C. Murali, Simon Xu, Leo Brueggeman, Taylor R. Thomas, Olena Marchenko, Christopher Fleisch, Sarah D. Barns, LeeAnne Green Snyder, Bing Han, Timothy S. Chang, Tychele N. Turner, William T. Harvey, Andrew Nishida, Brian J. O’Roak, Daniel H. Geschwind, Adrienne Adams, Alpha Amatya, Alicia Andrus, Asif Bashar, Anna F. Berman, Alison Brown, Alexies Camba, Amanda C. Gulsrud, Anthony D. Krentz, Amanda D. Shocklee, Amy Esler, Alex E. Lash, Anne Fanta, Ali Fatemi, Angela Fish, Alexandra Goler, Antonio González, Anibal Gutierrez, Antonio Y. Hardan, Amy Hess, Anna Hirshman, Alison Holbrook, J. Andrea, Anthony J. Griswold, Angela Gruber, A Jarratt, Anna Jelinek, Alissa Jorgenson, Aline Juárez, Annes Kim, Alex Kitaygorodsky, Addie Luo, Angela L. Rachubinski, Allison Wainer, Amy M. Daniels, Anup Mankar, Andrew L. Mason, Alexandra Miceli, Anna Milliken, Amy Morales-Lara, Alexandra N. Stephens, Ai Nhu Nguyen, Amy Nicholson, Anna Marie Paolicelli, Alexander P. McKenzie, Abha R. Gupta, A Raven, Anna Rhea, Andrea Simon, Aubrie Soucy, Amy Swanson, Anthony Sziklay, Amber Tallbull, Angela Tesng, Audrey W. M. Ward, Allyson Zick, Brittani A. Hilscher, Brandi Bell, Barbara Enright, B. E. Robertson, Brenda Hauf, Bill Jensen, Brandon Lobisi, Brianna M. Vernoia, Brady Schwind, Bonnie VanMetre, Craig A. Erickson, Catherine Sullivan, Charles F. Albright, Claudine Anglo, Cate Buescher, Catherine C. Bradley, Claudia Campo-Soria, Cheryl Cohen, Costanza Colombi, Chris Diggins, Catherine Edmonson

    出版 2022
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  15. 15
    The children's brain tumor network (CBTN) - Accelerating research in pediatric central nervous system tumors through collaboration and open science

    The children's brain tumor network (CBTN) - Accelerating research in pediatric central nervous system tumors through collaboration and open science 由 Jena Lilly, Jo Lynne Rokita, Jennifer Mason, Tatiana Patton, Stephanie Stefankiewiz, David Higgins, Gerri Trooskin, Carina A. Larouci, Kamnaa Arya, Elizabeth Appert, Allison P. Heath, Yuankun Zhu, Miguel Brown, Bo Zhang, Bailey Farrow, Shannon Robins, Allison M. Morgan, Thinh Q. Nguyen, Elizabeth Frenkel, Kaitlin Lehmann, Emily Drake, Catherine Sullivan, Alexa Plisiewicz, Noel Coleman, Luke Patterson, Mateusz Koptyra, Zeinab Helili, Nicholas Van Kuren, Nathan Young, Meen Chul Kim, Christopher Friedman, Alex Lubneuski, Christopher Blackden, Marti Williams, Valérie Baubet, Lamiya Tauhid, Jamie Galanaugh, Katie Boucher, Heba Ijaz, Kristina A. Cole, Namrata Choudhari, Mariarita Santi, Robert W. Moulder, Jonathan Waller, Whitney Rife, Sharon J. Diskin, Marion K. Mateos, D. Williams Parsons, Ian F. Pollack, Stewart Goldman, Sarah Leary, Chiara Caporalini, Anna Maria Buccoliero, Mirko Scagnet, David Haussler, Derek Hanson, Ron Firestein, Jason E. Cain, Joanna J. Phillips, Nalin Gupta, Sabine Mueller, Gerald A. Grant, Michelle Monje, Sonia Partap, Jeffrey P. Greenfield, Rintaro Hashizume, Amy Smith, Shida Zhu, James M. Johnston, Jason Fangusaro, Matthew A. Miller, Matthew D. Wood, Sharon Gardner, Claire L. Carter, Laura M. Prolo, Jared Pisapia, Katherine Pehlivan, Andrea Franson, Toba N. Niazi, Josh Rubin, Mohamed S Abdelbaki, David S. Ziegler, Holly Lindsay, Ana Guerreiro Stücklin, Nicolas U. Gerber, Olena M. Vaske, Carolyn Quinsey, Brian R. Rood, Javad Nazarian, Eric H. Raabe, Eric M. Jackson, Stacie Stapleton, Robert M. Lober, David E. Kram, Carl Koschmann, Phillip B. Storm, Rishi Lulla, Michael Prados, Adam Resnick, Angela J. Waanders

    出版 2022
    獲取全文
    Artigo
    加到收藏夾
    Saved in:

檢索工具: