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Elodee A. Tuley
Observed names:
E A Tuley,
E. Tuley,
E.A. TULEY,
E.A. Tuley,
EA Tuley,
ELODEE A. TULEY,
Elodee A Tuley,
Elodee Tuley
show all 8
Observed institutions:
Barnes-Jewish Hospital,
Howard Hughes Medical Institute,
Washington University in St. Louis,
Leiden University Medical Center,
University of Alabama at Birmingham,
Cardiff University,
University of Wales
show all 7
OpenAlex ID:
A5109977843
Structure of the gene for human von Willebrand factor
1989
·
D J Mancuso
, E A Tuley
, et al.
·
Journal of Biological Chemistry
·
488
Human von Willebrand factor gene and pseudogene: structural analysis and differentiation by polymerase chain reaction
1991
·
David J. Mancuso
, Elodee A. Tuley
, et al.
·
Biochemistry
·
230
Platelet-VWF complexes are preferred substrates of ADAMTS13 under fluid shear stress
2007
·
Kyuhwan Shim
, Patricia J. Anderson
, et al.
·
Blood
·
171
PDF
Incomplete embryonic lethality and fatal neonatal hemorrhage caused by prothrombin deficiency in mice
1998
·
Jiachun Xue
, Qingyu Wu
, et al.
·
Proceedings of the National Academy of Sciences
·
165
Dominant type 1 von Willebrand disease caused by mutated cysteine residues in the D3 domain of von Willebrand factor
1996
·
JC Eikenboom
, T Matsushita
, et al.
·
Blood
·
134
Cleavage of the ADAMTS13 Propeptide Is Not Required for Protease Activity
2003
·
Elaine M. Majerus
, Xinglong Zheng
, et al.
·
Journal of Biological Chemistry
·
129
Exosite interactions contribute to tension-induced cleavage of von Willebrand factor by the antithrombotic ADAMTS13 metalloprotease
2006
·
Weiqiang Gao
, Patricia J. Anderson
, et al.
·
Proceedings of the National Academy of Sciences
·
119
Localization of Disulfide Bonds in the Cystine Knot Domain of Human von Willebrand Factor
2000
·
Akira Katsumi
, Elodee A. Tuley
, et al.
·
Journal of Biological Chemistry
·
118
von Willebrand disease type B: a missense mutation selectively abolishes ristocetin-induced von Willebrand factor binding to platelet glycoprotein Ib.
1992
·
I Rabinowitz
, E A Tuley
, et al.
·
Proceedings of the National Academy of Sciences
·
94
The Kunitz-3 domain of TFPI-α is required for protein S–dependent enhancement of factor Xa inhibition
2010
·
Matthew Ndonwi
, Elodee A. Tuley
, et al.
·
Blood
·
92
Type 1 von Willebrand disease mutation Cys1149Arg causes intracellular retention and degradation of heterodimers: a possible general mechanism for dominant mutations of oligomeric proteins
2001
·
Imre Bodó
, Akira Katsumi
, et al.
·
Blood
·
83
The effect of temperature on the formation of mutagens in heated beef stock and cooked ground beef
1979
·
P. Dolara
, B. Commoner
, et al.
·
Mutation research. Fundamental and molecular mechanisms of mutagenesis
·
83
Expression of von Willebrand factor "Normandy": an autosomal mutation that mimics hemophilia A.
1991
·
E A Tuley
, C Gaucher
, et al.
·
Proceedings of the National Academy of Sciences
·
79
Molecular Mechanism and Classification of von Willebrand Disease
1995
·
J Evan Sadler
, Tadashi Matsushita
, et al.
·
Thrombosis and Haemostasis
·
78
Severe type III von Willebrand's disease caused by deletion of exon 42 of the von Willebrand factor gene: family studies that identify carriers of the condition and a compound heterozygous individual
1990
·
IR Peake
, MB Liddell
, et al.
·
Blood
·
71
Disulfide bonds required to assemble functional von Willebrand factor multimers.
1994
·
Z. Dong
, R.S. Thoma
, et al.
·
Journal of Biological Chemistry
·
66
TFPIβ is the GPI-anchored TFPI isoform on human endothelial cells and placental microsomes
2011
·
Thomas J. Girard
, Elodee Tuley
, et al.
·
Blood
·
59
PDF
Spontaneous mutation frequencies in Salmonella: Enhancement of G/C to A/T transitions and depression of deletion and frameshift mutation frequencies afforded by anoxic incubation
1984
·
Zlata Hartman
, Philip E. Hartman
, et al.
·
Environmental Mutagenesis
·
41
Rearranging Exosites in Noncatalytic Domains Can Redirect the Substrate Specificity of ADAMTS Proteases
2012
·
Weiqiang Gao
, Jian Zhu
, et al.
·
Journal of Biological Chemistry
·
39
PDF
The mutation Arg (53)----Trp causes von Willebrand disease Normandy by abolishing binding to factor VIII. Studies with recombinant von Willebrand factor
1992
·
S Jorieux
, EA Tuley
, et al.
·
Blood
·
38
PDF
Recombinant von Willebrand factor Arg578–>Gln. A type IIB von Willebrand disease mutation affects binding to glycoprotein Ib but not to collagen or heparin.
1992
·
A.M. Randi
, S Jorieux
, et al.
·
Journal of Biological Chemistry
·
33
DNA sequence changes of mutations in the histidine operon control region that decrease attenuation
1983
·
Wayne M. Barnes
, Elodee Tuley
·
Journal of Molecular Biology
·
32
Characterization of Partial Gene Deletions in Type III von Willebrand Disease with Alloantibody Inhibitors
1994
·
David J Mancuso
, Elodee A Tuley
, et al.
·
Thrombosis and Haemostasis
·
30
Type IIB mutation His-505–>Asp implicates a new segment in the control of von Willebrand factor binding to platelet glycoprotein Ib.
1993
·
I Rabinowitz
, A.M. Randi
, et al.
·
Journal of Biological Chemistry
·
29
Protein Z, protein Z‐dependent protease inhibitor (serpinA10), and the acute‐phase response
2012
·
T.J. GIRARD
, N.M. LASKY
, et al.
·
Journal of Thrombosis and Haemostasis
·
28
PDF
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Works count:
32
Citation count:
2,555
H-index:
25
I10-index:
26
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