Concepedia

Author

EA Tuley

Howard Hughes Medical Institute

Also Known As

E A Tuley, E. Tuley, E.A. TULEY, E.A. Tuley, EA Tuley

13

Publications

1.2K

Citations

11

H-Index

10

Concepts

All Affiliations

Howard Hughes Medical InstituteJewish HospitalWashington University in St. Louis
ET

About

EA Tuley is an author at Howard Hughes Medical Institute specializing in food safety, hematology, and animal science.

Top Concepts

#ConceptH-IndexPublicationsCitations

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Medicine

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Immunology

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83

3

Pathology

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83

4

Clinical Genetics

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83

5

Food Safety

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85

EA Tuley

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10

Publications

1.1K

Citations

10

H-Index

YearCitations

Structure of the gene for human von Willebrand factor

D J Mancuso, EA Tuley, Lisa A. Westfield,

Journal of Biological Chemistry

1989

494

Dominant type 1 von Willebrand disease caused by mutated cysteine residues in the D3 domain of von Willebrand factor

Tadashi Matsushita, PH Reitsma, EA Tuley,

Blood

1996

137

von Willebrand disease type B: a missense mutation selectively abolishes ristocetin-induced von Willebrand factor binding to platelet glycoprotein Ib.

Ian Rabinowitz, EA Tuley, D J Mancuso,

Proceedings of the National Academy of Sciences

1992

98

The effect of temperature on the formation of mutagens in heated beef stock and cooked ground beef

Piero Dolara, B. Commoner, Antony J. Vithayathil,

Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis

1979

85

Expression of von Willebrand factor "Normandy": an autosomal mutation that mimics hemophilia A.

EA Tuley, Christine Gaucher, Sylvie Jorieux,

Proceedings of the National Academy of Sciences

1991

83

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

IR Peake, MB Liddell, Peter Moodie,

Blood

1990

71

Disulfide bonds required to assemble functional von Willebrand factor multimers.

Richard S. Thoma, Dan L. Crimmins, D W McCourt,

Journal of Biological Chemistry

1994

66

The mutation Arg (53)----Trp causes von Willebrand disease Normandy by abolishing binding to factor VIII. Studies with recombinant von Willebrand factor

Sylvie Jorieux, EA Tuley, Christine Gaucher,

Blood

1992

42

Recombinant von Willebrand factor Arg578–>Gln. A type IIB von Willebrand disease mutation affects binding to glycoprotein Ib but not to collagen or heparin.

Anna M. Randi, Sylvie Jorieux, EA Tuley,

Journal of Biological Chemistry

1992

33

Type IIB mutation His-505–>Asp implicates a new segment in the control of von Willebrand factor binding to platelet glycoprotein Ib.

Ian Rabinowitz, Anna M. Randi, Kenneth S. Shindler,

Journal of Biological Chemistry

1993

29

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