Project Start
1999-12-01
Project End
2000-11-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
8
Fiscal Year
2000
Total Cost
$348,958
Indirect Cost
Name
University of Washington
Department
Type
DUNS #
135646524
City
Seattle
State
WA
Country
United States
Zip Code
98195
Parisi, Melissa A; Lipman, Neil S; Clarke, Christine M et al. (2005) Evaluation of Hox11L1 in the fmc/fmc rat model of chronic intestinal pseudo-obstruction. J Pediatr Surg 40:1760-5
Cooper, Laurence J N; Topp, Max S; Pinzon, Cris et al. (2004) Enhanced transgene expression in quiescent and activated human CD8+ T cells. Hum Gene Ther 15:648-58
Leppig, Kathleen A; Sybert, Virginia P; Ross, Judith L et al. (2004) Phenotype and X inactivation in 45,X/46,X,r(X) cases. Am J Med Genet A 128A:276-84
Parisi, Melissa A; Baldessari, Audrey E; Iida, Malissa H K et al. (2003) Genetic background modifies intestinal pseudo-obstruction and the expression of a reporter gene in Hox11L1-/- mice. Gastroenterology 125:1428-40
Weldin, Josh; Jack, Rhona; Dugaw, Kathryn et al. (2003) Quercetin, an over-the-counter supplement, causes neuroblastoma-like elevation of plasma homovanillic acid. Pediatr Dev Pathol 6:547-51
Dinulos, James G H; Mentele, Laurel; Fredericks, L Page et al. (2003) Keratinocyte expression of human beta defensin 2 following bacterial infection: role in cutaneous host defense. Clin Diagn Lab Immunol 10:161-6
Johnston, Donna L; Meshinchi, Soheil; Opheim, Kent E et al. (2003) Progenitor cell involvement is predictive of response to induction chemotherapy in paediatric acute myeloid leukaemia. Br J Haematol 123:431-5
Parisi, Melissa A; Kapur, Raj P; Neilson, Ian et al. (2002) Hydrocephalus and intestinal aganglionosis: is L1CAM a modifier gene in Hirschsprung disease? Am J Med Genet 108:51-6
Bender, M A; Roach, J N; Halow, J et al. (2001) Targeted deletion of 5'HS1 and 5'HS4 of the beta-globin locus control region reveals additive activity of the DNaseI hypersensitive sites. Blood 98:2022-7
Leppig, K A; Disteche, C M (2001) Ring X and other structural X chromosome abnormalities: X inactivation and phenotype. Semin Reprod Med 19:147-57

Showing the most recent 10 out of 32 publications