Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Greg L, Finney"'
Autor:
Maia M Chan, Jason M Wooden, Mark Tsang, Diana M Gilligan, Dinesh K Hirenallur-S, Greg L Finney, Eric Rynes, Michael Maccoss, Julita A Ramirez, Heon Park, Brian M Iritani
Publikováno v:
PLoS ONE, Vol 8, Iss 2, p e54902 (2013)
Hematopoietic protein-1 (Hem-1) is a hematopoietic cell specific member of the WAVE (Wiskott-Aldrich syndrome verprolin-homologous protein) complex, which regulates filamentous actin (F-actin) polymerization in many cell types including immune cells.
Externí odkaz:
https://doaj.org/article/3a3f8926de9342c888d922f1f26fd247
Autor:
Eric Rynes, Michael J. MacCoss, Raymond F. Robledo, Jason M. Wooden, Diana M. Gilligan, Luanne L. Peters, Amy J. Lambert, Greg L. Finney
Publikováno v:
Blood Cells, Molecules, and Diseases. 47:85-94
Hemolytic anemia is one of the most common inherited disorders. To identify candidate proteins involved in hemolytic anemia pathophysiology, we utilized a label-free comparative proteomic approach to detect differences in RBCs from normal and beta-ad
Autor:
Amy J. Lambert, Jason M. Wooden, Greg L. Finney, Raymond F. Robledo, Michael J. MacCoss, Luanne L. Peters, Diana M. Gilligan, Eric Rynes
Publikováno v:
British Journal of Haematology. 154:492-501
Spherocytosis is one of the most common inherited disorders, yet presents with a wide range of clinical severity. While several genes have been found mutated in patients with spherocytosis, the molecular basis for the variability in severity of haemo
Autor:
Brian M. Iritani, Greg L. Finney, Eric Rynes, Maia M. Chan, Julita A. Ramirez, Michael J. MacCoss, Heon Park, Diana M. Gilligan, Jason M. Wooden, Mark Tsang, Dinesh K. Hirenallur-S
Publikováno v:
PLoS ONE, Vol 8, Iss 2, p e54902 (2013)
PLoS ONE
PLoS ONE
Hematopoietic protein-1 (Hem-1) is a hematopoietic cell specific member of the WAVE (Wiskott-Aldrich syndrome verprolin-homologous protein) complex, which regulates filamentous actin (F-actin) polymerization in many cell types including immune cells.
Autor:
Jason M, Wooden, Greg L, Finney, Eric, Rynes, Michael J, Maccoss, Amy J, Lambert, Raymond F, Robledo, Luanne L, Peters, Diana M, Gilligan
Publikováno v:
British journal of haematology. 154(4)
Spherocytosis is one of the most common inherited disorders, yet presents with a wide range of clinical severity. While several genes have been found mutated in patients with spherocytosis, the molecular basis for the variability in severity of haemo
Publikováno v:
Briefings in functional genomicsproteomics. 8(2)
The ultimate goal of most shotgun proteomic pipelines is the discovery of novel biomarkers to direct the development of quantitative diagnostics for the detection and treatment of disease. Differential comparisons of biological samples identify candi
Autor:
Raymond F. Robledo, Eric Rynes, Michael J. MacCoss, Greg L. Finney, Diana M. Gilligan, Luanne L. Peters, Amy J. Lambert, Jason M. Wooden
Publikováno v:
Blood Cells, Molecules, and Diseases. 48:145
This article has been retracted; please see Elsevier Policy on Article Withdrawal (http://www.elsevier.com/locate/withdrawalpolicy). This article has been retracted at the request of the editor as the data in the paper are largely duplicated in a pap
Publikováno v:
Blood. 110:1728-1728
Inherited hemolytic anemia (spherocytosis or elliptocytosis) is one of the most common inherited diseases with an incidence of 1:2500 to 1:5000 in populations of Northern European descent. While it is known that mild to severe inherited hemolytic ane
Publikováno v:
Blood. 108:1569-1569
Inherited hemolytic anemia (spherocytosis or elliptocytosis) is one of the most common inherited diseases with an incidence of 1:2500 to 1:5000 in populations of Northern European descent. Mild to severe inherited hemolytic anemias can arise from def
Autor:
Chan, Maia M.1, Wooden, Jason M.2, Tsang, Mark1, Gilligan, Diana M.2, Hirenallur-S, Dinesh K.1, Finney, Greg L.3, Rynes, Eric3, MacCoss, Michael3, Ramirez, Julita A.1, Park, Heon1, Iritani, Brian M.1 biritani@uw.edu
Publikováno v:
PLoS ONE. Feb2013, Vol. 8 Issue 2, p1-16. 16p.