Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Matthew Dulik"'
Autor:
Emma Bedoukian, Sara Reichert, Elizabeth DeChene, Alexandra Heck, Jennifer Hershey, Morgan McManus, Michelle Marchese, Surabhi Mulchandani, Francis Jeshira Reynoso Santos, K. Taylor Wild, Kathleen Wood, Laura Conlin, Matthew Dulik, Ramakrishnan Rajagopalan, Nancy Spinner, Ian Krantz
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101431- (2024)
Externí odkaz:
https://doaj.org/article/5bba578230e346c995d309d6d4d32d65
Autor:
Tanaya Jadhav, Avery Zucco, Matt Aruta, Matthew Dulik, Laura Conlin, Ramakrishnan Rajagopalan, Jing Wang
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101741- (2024)
Externí odkaz:
https://doaj.org/article/ae6f3c60b9424f3a88559ba09dea1484
Autor:
Jing Wang, Ada Chan, James Peterson, Kathleen Wood, Maria Alejandra Diaz-Miranda, Archana Tara, Amy Goldstein, Zarazuela Zolkipli-Cunningham, Elizabeth M. McCormick, Colleen Muraresku, Matthew Dulik, Douglas Wallace, Marni Falk
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100628- (2023)
Externí odkaz:
https://doaj.org/article/1e45c3f3454a4a3aaa32154fd2238203
Autor:
Margaret A Gustafson, Elizabeth M McCormick, Lalith Perera, Matthew J Longley, Renkui Bai, Jianping Kong, Matthew Dulik, Lishuang Shen, Amy C Goldstein, Shana E McCormack, Benjamin L Laskin, Bart P Leroy, Xilma R Ortiz-Gonzalez, Meredith G Ellington, William C Copeland, Marni J Falk
Publikováno v:
PLoS ONE, Vol 14, Iss 9, p e0221829 (2019)
Mitochondrial DNA (mtDNA) genome integrity is essential for proper mitochondrial respiratory chain function to generate cellular energy. Nuclear genes encode several proteins that function at the mtDNA replication fork, including mitochondrial single
Externí odkaz:
https://doaj.org/article/63b1a4fb63464668996acd615bcb408a
Autor:
Erfan Aref-Eshghi, Kajia Cao, Weixuan Fu, Kathleen Wood, Nancy Spinner, Matthew Dulik, Laura Conlin, Jing Wang, Minjie Luo
Publikováno v:
Genetics in Medicine. 24:S197-S198
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