Surface expression of platelet-type vonWillebrand disease (Gly→Val)233 mutation in CHO cells:: Effects on Mab and vWF binding

被引：0

作者：

Finch, CN ^{[1
]}

Bang, SM ^{[1
]}

Wise, KJ ^{[1
]}

Miller, JL ^{[1
]}

机构：

[1] SUNY Hlth Sci Ctr, Dept Pathol, Syracuse, NY 13210 USA

来源：

BLOOD | 1998年 / 92卷 / 10期

关键词：

D O I：

暂无

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

1416

引用

页码：344A / 345A

页数：2

共 19 条

[1] PATIENTS WITH PLATELET-TYPE VONWILLEBRAND DISEASE ARE HETEROZYGOUS FOR A GLY TO VAL SUBSTITUTION AT RESIDUE 233 OF PLATELET GPIB-ALPHA
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[2] PATIENTS WITH PLATELET-TYPE VONWILLEBRAND DISEASE ARE HETEROZYGOUS FOR A GLY TO VAL SUBSTITUTION AT RESIDUE-233 OF PLATELET GPLB-ALPHA
MILLER, JL
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[J]. ARTERIOSCLEROSIS, 1990, 10 (05): : A905 - A905
[3] Alterations in the intrinsic properties of the GPIbα-VWF tether bond define the kinetics of the platelet-type von Willebrand disease mutation, Gly233Val
Doggett, TA
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Lawshe, A
Miller, JL
Laurenzi, IJ
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Diacovo, TG
[J]. BLOOD, 2003, 102 (01) : 152 - 160
[4] CONFORMATIONAL ENERGY ANALYSIS OF THE SUBSTITUTION OF VAL FOR GLY-233 IN A FUNCTIONAL REGION OF PLATELET GPIB-ALPHA IN PLATELET-TYPE VONWILLEBRAND DISEASE
PINCUS, MR
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MILLER, JL
[J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1097 (02) : 133 - 139
[5] A second report of platelet-type von Willebrand disease with a Gly233Ser mutation in the GPIBA gene
Nurden, Paquita
Lanza, Francois
Bonnafous-Faurie, Cecile
Nurden, Alan
[J]. THROMBOSIS AND HAEMOSTASIS, 2007, 97 (02) : 319 - 321
[6] A RAPID VONWILLEBRAND FACTOR(VWF) BINDING TECHNIQUE THAT DISTINGUISHES TYPE-IIB FROM PLATELET-TYPE VONWILLEBRANDS DISEASE(VWD)
SCOTT, JP
MONTGOMERY, RR
ZUMWALT, KL
[J]. CLINICAL RESEARCH, 1988, 36 (03): : A418 - A418
[7] Identification of a novel point mutation in platelet glycoprotein Ibα Gly to Ser at residue 233, in a Japanese family with platelet-type von Willebrand disease
Matsubara, Y
Murata, M
Sugita, K
Ikeda, Y
[J]. JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2003, 1 (10) : 2198 - 2205
[8] Identification of a novel point mutation in platelet glycoprotein Ibα, Gly to Ser at residue 233, in a Japanese family with platelet-type von Willebrand disease.
Matsubara, Y
Murata, M
Sugita, K
Ikeda, Y
[J]. BLOOD, 2002, 100 (11) : 14A - 15A
[9] MUTATION IN THE GENE ENCODING THE ALPHA-CHAIN OF PLATELET GLYCOPROTEIN-IB IN PLATELET-TYPE VONWILLEBRAND DISEASE
MILLER, JL
CUNNINGHAM, D
LYLE, VA
FINCH, CN
[J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (11) : 4761 - 4765
[10] SUBSTITUTION OF VALINE FOR GLYCINE AT RESIDUE-233 OF PLATELET GPIB-ALPHA IN PLATELET-TYPE VONWILLEBRAND DISEASE CAUSES A DISCRETE CONFORMATIONAL CHANGE
PINCUS, MR
DYKES, DC
CARTY, RP
MILLER, JL
[J]. THROMBOSIS AND HAEMOSTASIS, 1991, 65 (06) : 770 - 770

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