Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Kathy Leppig"'
Autor:
Patrick Van Bogaert, Kevin Farrell, David Webb, Kathy Leppig, Adela Della Marina, Richard Tomlinson, Peter E. Clayton, Baziel G.M. van Engelen, Todd Arthur, Vincent Laugel, Tom G.J. Hofste, C. Rauscher, Nadia Bahi-Buisson, Hans Holthausen, Stephanie Gross, F. Ebinger, Brigitte Chabrol, Rob Forsyth, Axel Panzer, Nils O. Nilsson, Michael Champion, Loreto Martorell, Ron A. Wevers, Marcel M. Verbeek, Inger Sandvig, Wilhelmina G. Leen, Christophe M. R. Rouselle, Maike Leferink, Katherine Lachlan, Bwee Tien Poll-The, Helen Mundy, Parol Sykora, Hans Scheffer, Bernhard Weschke, Ines Carrilho, Michèl A.A.P. Willemsen, Ming K. Lim, Athanasios Evangeliou, Joe McMenamin, Stephanie Grunewald, Jolita Bekhof, Marije E. C. Meuwissen, Christian de Goede, Thomas Scheffner, Elizabeth J. Donner, Joerg Klepper, John Trounce, Grazia M.S. Mancini, Eamonn Sheridan, Diana Ballhausen, Sandeep Jayawant, Neil Simpson, James Coldwell
Publikováno v:
Brain, vol. 133, no. 3, pp. 655-670
Brain, 133, 655-70
Brain, 133, 655-670. Oxford University Press
Brain
Brain, 133(Part 3), 655-670. Oxford University Press
Brain, 133, Pt 3, pp. 655-70
Brain, 133, 655-70
Brain, 133, 655-670. Oxford University Press
Brain
Brain, 133(Part 3), 655-670. Oxford University Press
Brain, 133, Pt 3, pp. 655-70
Contains fulltext : 88466.pdf (Publisher’s version ) (Closed access) Glucose transporter-1 deficiency syndrome is caused by mutations in the SLC2A1 gene in the majority of patients and results in impaired glucose transport into the brain. From 2004
Autor:
Gail P. Jarvik, Laura M. Amendola, Jonathan S. Berg, Kyle Brothers, Ellen W. Clayton, Wendy Chung, Barbara J. Evans, James P. Evans, Stephanie M. Fullerton, Carlos J. Gallego, Nanibaa’ A. Garrison, Stacy W. Gray, Ingrid A. Holm, Iftikhar J. Kullo, Lisa Soleymani Lehmann, Cathy McCarty, Cynthia A. Prows, Heidi L. Rehm, Richard R. Sharp, Joseph Salama, Saskia Sanderson, Sara L. Van Driest, Marc S. Williams, Susan M. Wolf, Wendy A. Wolf, Wylie Burke, John Harley, Melanie Myers, Bahram Namjou, Sander Vinks, John Connolly, Brendan Keating, Glenn Gerhard, Agnes Sundaresan, Gerard Tromp, David Crosslin, Kathy Leppig, Cathy Wicklund, Christopher Chute, John Lynch, Mariza De Andrade, John Heit, Jen McCormick, Murray Brilliant, Terrie Kitchner, Marylyn Ritchie, Erwin Böttinger, Inga Peter, Stephen Persell, Laura Rasmussen-Torvik, Tracy McGregor, Dan Roden, Armand Antommaria, Rosetta Chiavacci, Andy Faucett, David Ledbetter, Janet Williams, Andrea Hartzler, Carolyn R. Rohrer Vitek, Norm Frost, Kadija Ferryman, Carol Horowitz, Rosamond Rhodes, Randi Zinberg, Sharon Aufox, Vivian Pan, Rochelle Long, Erin Ramos, Jackie Odgis, Anastasia Wise, Sara Hull, Jonathan Gitlin, Robert Green, Danielle Metterville, Amy McGuire, Sek Won Kong, Sue Trinidad, David Veenstra, Myra Roche, Debra Skinner, Kelly Raspberry, Julianne O’Daniel, Will Parsons, Christine Eng, Susan Hilsenbeck, Dean Karavite, Laura Conlin, Nancy Spinner, Ian Krantz, Marni Falk, Avni Santani, Elizabeth Dechene, Matthew Dulik, Barbara Bernhardt, Scott Schuetze, Jessica Everett, Michele Caroline Gornick, Ben Wilfond, Holly Tabor, Amy A. Lemke, Sue Richards, Katrina Goddard, Greg Cooper, Kelly East, Greg Barsh, Barbara Koenig, Eliezer Van Allen, Judy Garber, Jeremy Garrett, Ma’n Zawati, Michelle Lewis, Sarah Savage, Maureen Smith, Sameek Roychowdhury, Alice Bailey, Benjamin Berkman, Charlisse Caga Anan, Lucia Hindorff, Carolyn Hutter, Rosalind King, Rongling Li, Nicole Lockhart, Jean McEwen, Derek Scholes, Sheri Schully, Kathie Sun
Publikováno v:
American journal of human genetics. 94(6)
As more research studies incorporate next-generation sequencing (including whole-genome or whole-exome sequencing), investigators and institutional review boards face difficult questions regarding which genomic results to return to research participa
Autor:
Marijane Krohn, Qinyuan Low, Molly Hogan, Warren Kearney, Julie Mason, Beth Virnig, Takeshi Kondoh, F. Arthur Mcmorris, Jeanne Forbes, Michael McCormack, Kelly Feil, Tom Gasser, Alberto Hayek, Janice L. B. Byrne, Catherine Palmer, Beth Mueller, Sonny K. Chong, Raj Kapur, Bruce Blazer, Delbert H. Dayton, Sandy Maynard, Mark Hirschel, Peter D'ascoli, Soe Soe Thwin, Kathy Weese, Lillie Mae Padilla, Lee Ducat, Jeff Miller, John Q. Trojanowski, John P. Conrad, Anne Peterson, Kenneth Ward, Virginia Lee, Sharon Bledsoe, Ted Rigley, Judy Christianson, Bryan E. Hainline, Alan Fantel, Kathy Leppig, Catherine Verfaillie, D. Ware Branch, Susan Shen Schwarz, Jeff Blount, Ted Eastlund, Takashi Okagaki, Feng C. Zhou, Beverly Norris, Walter C. Low, Ying Jie, Helen Newman Gage, Stephen A. Heifetz, Preston Williams, Sharon Hillier, Yung Hsiao Chiang, Debra Kahlenbeck, Thomas Norwood, Daniel Peavy, Tara Vick, Ranjita Sengupta, Thomas J. Gill, Laura Coultrip, Lisa Pundt, Gayl Chrysler
Publikováno v:
JAMA: The Journal of the American Medical Association. 273:66
Objective. —To assess the potential availability and utility of fetal tissues obtained from spontaneous abortions and from ectopic pregnancies for human transplantation therapy. Design. —Tissue collection and analysis by personnel skilled in tiss