Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Megan W, Butler"'
Autor:
Peter Lee, Stephanie H. Abrams, Lynette A. Gillis, Reham Abdou, Nidhi Goyal, Nirav K. Desai, Kathryn E. Harlow, John F. Pohl, Carol Potter, Warren L. Shapiro, Henry C. Lin, Jennifer C. Arin, Karen F. Murray, Shikha S. Sundaram, Jennifer Panganiban, Marianne Kavan, Elizabeth L. Yu, Sarah A. Faasse, Ajay Jain, Kattayoun Kordy, Timothy A. Hadley, Stavra A. Xanthakos, James A. Proudfoot, Jeffrey B. Schwimmer, Sabina Ali, Kimberly P. Newton, Megan W. Butler, Bryan Rudolph, Naim Alkhouri, Shivali Joshi
Publikováno v:
Journal of pediatric gastroenterology and nutrition, vol 68, iss 2
J Pediatr Gastroenterol Nutr
J Pediatr Gastroenterol Nutr
OBJECTIVES: Nonalcoholic fatty liver disease (NAFLD) is common; however, no information is available on how pediatric gastroenterologists in the United States manage NAFLD. Therefore, study objectives were to: (1) understand how pediatric gastroenter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1fec6cc95783200c1526fb4682608d9
https://escholarship.org/uc/item/4sc2z8k0
https://escholarship.org/uc/item/4sc2z8k0
Autor:
Queenie K-G, Tan, Heidi, Cope, Rebecca C, Spillmann, Nicholas, Stong, Yong-Hui, Jiang, Marie T, McDonald, Jennifer A, Rothman, Megan W, Butler, Donald P, Frush, Ralph S, Lachman, Brendan, Lee, Carlos A, Bacino, Melanie J, Bonner, Chad M, McCall, Avani A, Pendse, Nicole, Walley, Vandana, Shashi, Joy D, Cogan
Publikováno v:
Cold Spring Harbor Molecular Case Studies
Recent evidence has implicated EFL1 in a phenotype overlapping Shwachman–Diamond syndrome (SDS), with the functional interplay between EFL1 and the previously known causative gene SBDS accounting for the similarity in clinical features. Relatively
Autor:
Colleen E. Wahl, Ingrid A. Holm, Jonathan A. Bernstein, Mitja I. Kurki, Annika M. Dries, Alexander Hoischen, Patrick Allard, Janet S. Sinsheimer, J. Scott Newberry, Maysantoine A. El-Dairi, David R. Adams, Anna C. Need, Mitchell Goheen, Camilo Toro, Outi Kuismin, Andrea L. Gropman, Fanny Kortüm, Lindsay C. Burrage, Braden E. Boone, Nicole M. Walley, Lori H. Handley, Daryl A. Scott, Donna Muzny, Jane S. Bellet, Lance H. Rodan, Catherine Groden, Paul Mazur, Christina G.S. Palmer, Megan W. Butler, Azamian S. Mashid, Brendan Lee, Peter G. Kranz, Alexa T. McCray, Yaping Yang, Hane Lee, David A. Sweetser, Lynne A. Wolfe, Richard Alan Lewis, Sylvia Klinkenberg, Trevor S. Frisby, Lea Latham, Elizabeth A. Worthey, Michele Nehrebecky, William J. Craigen, Donna M. Brown, Constance T. R. M. Stumpel, Laura A. Mamounas, Michael F. Wangler, Lauren C. Briere, Alanna E. Koehler, Sarah Sadozai, Shinya Yamamoto, Kate Frost, Michael Freemark, Carson R. Loomis, Slavé Petrovski, Christine M. Eng, Barbara K. Burton, Hugo J. Bellen, Angela L. Jones, Esteban C. Dell Angelica, A. Bacino, Camille L. Birch, David Goldstein, Tran A. Alyssa, Joan M. Stoler, Yong-hui Jiang, Scott E. Hickey, Paul R. Lee, Jennifer A. Sullivan, William A. Gahl, Christopher J. Adams, Rebecca C. Spillmann, Katherine H. Kim, Daryl Waggott, Seema R. Lalani, Denise J. Levy, René Santer, May V. Malicdan, Donna Novacic, John H. Postlethwait, Kimberly Splinter, Laurel A. Donnell-Fink, Jean M. Johnston, Richard L. Maas, Alexandra J. McCarty, Gretchen Golas, Sarah K. Nicholas, Donna M. Krasnewich, David D. Draper, Cynthia J. Tifft, Cecilia Esteves, David M. Koeller, John A. Phillips, Chris A. Walsh, Palotie Aarno, Gary D. Clark, Howard J. Jacob, Katherine E. Schaffer, Magdalena Walkiewicz, Satu Korpi-Heikkila, Karin Oberndorff, David P. Bick, Isabel Hardee, Valerie Maduro, John J. Mulvihill, Elizabeth A. Burke, Thomas C. Markello, Yvonne L. Latour, Adam P. Liebendorder, Ashok Balasubramanyam, David J. Eckstein, Elizabeth L. Krieg, M. T. Cho, Teri A. Manolio, Katherine R. Chao, Alan H. Beggs, Patricia A. Zornio, Valerie Gartner, Chyau Yueh C Lau, Monte Westerfield, Issac S. Kohane, Jyoti G. Dayal, Rena A. Godfrey, Thomas O. Metz, John H. Newman, Brett H. Graham, Alec A. Weech, Joe Lazar, Mike Warburton, Anastasia L. Wise, Nicholas Stong, Shweta U. Dhar, Matthew R. Herzog, Joel B. Krier, Jennefer N. Kohler, Guoyun Yu, Neil A. Hanchard, Edwin K. Silverman, Christine M. Shuss, Kim A. Strong, Olli Pietilainen, Casey Martin, Mariska Davids, Prashant Sharma, Joseph Loscalzo, Lorraine Potocki, Nathanial J. Tolman, Joy D. Cogan, Matthew Might, Barbara N. Pusey, Naghmeh Dorrani, Sharyn A. Lincoln, Euan A. Ashley, Mahim Jain, Jennifer L. Murphy, Stan F. Nelson, Patricia A. Ward, Shawn Levy, Kelly Schoch, Katrina M. Dipple, Paul G. Fisher, Cynthia M. Cooper, Vandana Shashi, Juan C. Pallais, Martha Ann Keels, Jennifer E. Posey, Heather M. McLaughlin, Calum A. MacRae, Eric Vilain, Molly C. Schroeder, Mary E. Hackbarth, Sara P. Thomas, Lisa Emrick, Ariane Soldatos, Allyn McConkie-Rosell, Ellen Macnamara, Melanie J. Bonner, Hayk Barseghyan, Tyra Estwick, Alejandro E. Mercedes, Malik Alawi, Maja Hempel, Matthew T. Wheeler, Jordan S. Orange, Paolo M. Moretti, Brenda Iglesias, Rachel Ramoni, Loren D M Pena, Zaheer M. Valivullah, Mary 'Gracie' G. Gordon, Rizwan Hamid, Jeanette C. Papp, Dan C. Dorset, Jill A. Rosenfeld
Publikováno v:
American Journal of Human Genetics, 99, 991-999
American Journal of Human Genetics, 99, 4, pp. 991-999
American Journal of Human Genetics, 100, 1, pp. 179
American Journal of Human Genetics, 100, 179
American Journal of Human Genetics, 99(4), 991-999. Cell Press
American Journal of Human Genetics, 99, 4, pp. 991-999
American Journal of Human Genetics, 100, 1, pp. 179
American Journal of Human Genetics, 100, 179
American Journal of Human Genetics, 99(4), 991-999. Cell Press
Item does not contain fulltext The ASXL genes (ASXL1, ASXL2, and ASXL3) participate in body patterning during embryogenesis and encode proteins involved in epigenetic regulation and assembly of transcription factors to specific genomic loci. Germline
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b44e4831dd3e02760631dd22e1bbb1d6
http://hdl.handle.net/2066/167201
http://hdl.handle.net/2066/167201
Autor:
Amber Burt, Liyong Wang, Stephan Züchner, William K. Scott, Todd L. Edwards, Jeffery M. Vance, Eden R. Martin, Megan W. Butler
Publikováno v:
Annals of Human Genetics. 75:201-210
Vitamin D and vitamin D receptor (VDR) have been postulated as environmental and genetic factors in neurodegeneration disorders including multiple sclerosis (MS), Alzheimer disease (AD), and recently Parkinson disease (PD). Given the sparse data on P