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Results of search for 'au:"Macgillivray, R T A"'
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Authors
Bauer, N
Brown, L A
Carter, C J
Carter, I S R
Chou, E M H
Clarke, B J
Di Cera, E
Dower, N A
Hewitt, J
Hudson, D M
Jackson, S C
Krisinger, M J
MacGillivray, R T A
Macgillivray, R T A
Page, M J
Panak, P J
Pryzdial, E L G
Pu, C H
Smith, V C
Wu, J K
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Topics
Adolescent
Aged
Allosteric Regulation
Amino Acid Sequence
Animals
Arginine
Base Sequence
Binding Sites
Blood Coagulation
Blood Proteins
Carbonates
Catalytic Domain
Chromosomes, Human, X
Humans
Male
Mutation
Pedigree
Sequence Deletion
chemistry
genetics
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English
Your search returned 6 results.
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1.
Determinants of specificity in coagulation proteases.
[electronic resource]
by
Page, M J
Macgillivray, R T A
Di Cera, E
Producer:
20060427
In:
Journal of thrombosis and haemostasis : JTH
vol. 3
Online resources:
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2.
Complexation of Cm(III) with the recombinant N-lobe of human serum transferrin studied by time-resolved laser fluorescence spectroscopy (TRLFS).
[electronic resource]
by
Bauer, N
Smith, V C
MacGillivray, R T A
Panak, P J
Producer:
20150831
In:
Dalton transactions (Cambridge, England : 2003)
vol. 44
Online resources:
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3.
Severe protein S deficiency resulting from two novel mutations in PROS1 presenting with a relatively mild clinical phenotype.
[electronic resource]
by
Carter, I S R
Hewitt, J
Pu, C H
Wu, J K
Carter, C J
Macgillivray, R T A
Producer:
20080813
In:
Journal of thrombosis and haemostasis : JTH
vol. 6
Online resources:
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4.
Severe prothrombin deficiency caused by prothrombin-Edmonton (R-4Q) combined with a previously undetected deletion.
[electronic resource]
by
Wong, A Y K
Hewitt, J
Clarke, B J
Hudson, D M
Krisinger, M J
Dower, N A
MacGillivray, R T A
Producer:
20070108
In:
Journal of thrombosis and haemostasis : JTH
vol. 4
Online resources:
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5.
Molecular characterization of a 4,409,480 bp deletion of the human X chromosome in a patient with haemophilia B.
[electronic resource]
by
Hewitt, J
Chou, E M H
Brown, L A
Smith, V C
Yong, S L
Wadsworth, L D
Wu, J K
Macgillivray, R T A
Producer:
20150220
In:
Haemophilia : the official journal of the World Federation of Hemophilia
vol. 20
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6.
Coagulation factor X Arg386 specifically affects activation by the intrinsic pathway: a novel patient mutation.
[electronic resource]
by
Vanden Hoek, A L
Talbot, K
Carter, I S R
Vickars, L
Carter, C J
Jackson, S C
MacGillivray, R T A
Pryzdial, E L G
Producer:
20130605
In:
Journal of thrombosis and haemostasis : JTH
vol. 10
Online resources:
Available from publisher's website
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