Zobrazeno 1 - 10
of 209
pro vyhledávání: '"Otterud BE"'
Publikováno v:
The Journal of Infectious Diseases, 2008 Feb 01. 197(3), 340-346.
Externí odkaz:
https://www.jstor.org/stable/30087697
Autor:
Bleakley, Marie *, Otterud, Brith E., Richardt, Julia L., Mollerup, Audrey D., Hudecek, Michael, Nishida, Tetsuya, Chaney, Colette N., Warren, Edus H., Leppert, Mark F., Riddell, Stanley R.
Publikováno v:
In Blood 10 June 2010 115(23):4923-4933
Autor:
Butterfield, Russell J., Ramachandran, Deepa, Hasstedt, Sandra J., Otterud, Brith E., Leppert, Mark F., Swoboda, Kathryn J., Flanigan, Kevin M.
Publikováno v:
In Neuromuscular Disorders 2009 19(4):279-287
Autor:
Nori Matsunami, Dexter Hadley, Charles H Hensel, G Bryce Christensen, Cecilia Kim, Edward Frackelton, Kelly Thomas, Renata Pellegrino da Silva, Jeff Stevens, Lisa Baird, Brith Otterud, Karen Ho, Tena Varvil, Tami Leppert, Christophe G Lambert, Mark Leppert, Hakon Hakonarson
Publikováno v:
PLoS ONE, Vol 8, Iss 1, p e52239 (2013)
Structural variation is thought to play a major etiological role in the development of autism spectrum disorders (ASDs), and numerous studies documenting the relevance of copy number variants (CNVs) in ASD have been published since 2006. To determine
Externí odkaz:
https://doaj.org/article/8f019b4696504a81b6489786168f61ab
Autor:
Neklason Deborah W, Tuohy Therese M, Stevens Jeffery, Otterud Brith, Baird Lisa, Kerber Richard A, Samowitz Wade S, Kuwada Scott K, Leppert Mark F, Burt Randall W
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 8, Iss Suppl 1, p O4 (2010)
Externí odkaz:
https://doaj.org/article/e8dc8c9df6f24281a8b5f873342969d5
Autor:
Brith Otterud, Timothy C. Beals, Mark Leppert, Michael J. Redd, David Grunwald, Jeff Stevens, Michael J. Jurynec, Allen D. Sawitzke
Osteoarthritis (OA) is a common debilitating disease characterized by abnormal remodeling of the cartilage and bone of the articular joint. Ameliorating therapeutics are lacking due to limited understanding of the molecular pathways affecting disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db1f4760e4156740a4380650f92e2e2e
https://europepmc.org/articles/PMC6620756/
https://europepmc.org/articles/PMC6620756/
Akademický článek
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Autor:
Warren, E.H1,2, Otterud, B.E3, Linterman, R.W1, Brickner, A.G4, Engelhard, V.H4, Leppert, M.F3, Martin, P.J1,2, Riddell, S.R1,2
Publikováno v:
Tissue Antigens. Apr2002, Vol. 59 Issue 4, p293-303. 11p.
Autor:
Gabriel D. Bonnell, Steven B. Bleyl, Shawn Levy, Neil E. Bowles, Norisada Matsunami, Douglas C. Nielsen, Jeff Stevens, Mark Leppert, Cammon B. Arrington, Brith Otterud
Publikováno v:
Circulation: Cardiovascular Genetics. 5:175-182
Background— A number of single gene defects have been identified in patients with isolated or nonsyndromic congenital heart defects (CHDs). However, due to significant genetic heterogeneity, candidate gene approaches have had limited success in fin
Autor:
Stanley R. Riddell, Marie Bleakley, Michael Hudecek, Julia L. Richardt, Audrey D. Mollerup, Mark Leppert, Edus H. Warren, Colette Chaney, Brith Otterud, Tetsuya Nishida
Publikováno v:
Blood. 115:4923-4933
T-cell immunotherapy that targets minor histocompatibility (H) antigens presented selectively by recipient hematopoietic cells, including leukemia, could prevent and treat leukemic relapse after hematopoietic cell transplantation without causing graf