Defective dimerization of von Willebrand factor subunits due to a Cys --> Arg mutation in type IID von Willebrand disease

Gespeichert in:

Autor*in:	Schneppenheim, R. [verfasserIn] Brassard, J. Krey, S. Budde, U. Kunicki, T.J. Holmberg, L. Ware, J. Ruggeri, Z.M.

Format:	Artikel

Erschienen:	1996

Umfang:	6

Übergeordnetes Werk:	Enthalten in: Proceedings of the National Academy of Sciences of the United States of America - Washington, DC : NAS, 1877, 93(1996), 8, Seite 3581-3586
Übergeordnetes Werk:	volume:93 ; year:1996 ; number:8 ; pages:3581-3586 ; extent:6

Katalog-ID:	OLC1594994862

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245	1	0	\|a Defective dimerization of von Willebrand factor subunits due to a Cys --> Arg mutation in type IID von Willebrand disease
264		1	\|c 1996
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700	1		\|a Brassard, J. \|4 oth
700	1		\|a Krey, S. \|4 oth
700	1		\|a Budde, U. \|4 oth
700	1		\|a Kunicki, T.J. \|4 oth
700	1		\|a Holmberg, L. \|4 oth
700	1		\|a Ware, J. \|4 oth
700	1		\|a Ruggeri, Z.M. \|4 oth
773	0	8	\|i Enthalten in \|t Proceedings of the National Academy of Sciences of the United States of America \|d Washington, DC : NAS, 1877 \|g 93(1996), 8, Seite 3581-3586 \|w (DE-627)129505269 \|w (DE-600)209104-5 \|w (DE-576)014909189 \|x 0027-8424 \|7 nnns
773	1	8	\|g volume:93 \|g year:1996 \|g number:8 \|g pages:3581-3586 \|g extent:6
912			\|a GBV_USEFLAG_A
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912			\|a FID-LING
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912			\|a SSG-OLC-CHE
912			\|a SSG-OLC-MAT
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912			\|a SSG-OLC-PHA
912			\|a SSG-OLC-DE-84
912			\|a SSG-OPC-MAT
912			\|a SSG-OPC-FOR
912			\|a GBV_ILN_11
912			\|a GBV_ILN_20
912			\|a GBV_ILN_21
912			\|a GBV_ILN_22
912			\|a GBV_ILN_24
912			\|a GBV_ILN_40
912			\|a GBV_ILN_62
912			\|a GBV_ILN_65
912			\|a GBV_ILN_69
912			\|a GBV_ILN_70
912			\|a GBV_ILN_74
912			\|a GBV_ILN_105
912			\|a GBV_ILN_130
912			\|a GBV_ILN_154
912			\|a GBV_ILN_168
912			\|a GBV_ILN_171
912			\|a GBV_ILN_179
912			\|a GBV_ILN_211
912			\|a GBV_ILN_252
912			\|a GBV_ILN_290
912			\|a GBV_ILN_2001
912			\|a GBV_ILN_2002
912			\|a GBV_ILN_2003
912			\|a GBV_ILN_2004
912			\|a GBV_ILN_2005
912			\|a GBV_ILN_2006
912			\|a GBV_ILN_2007
912			\|a GBV_ILN_2010
912			\|a GBV_ILN_2011
912			\|a GBV_ILN_2015
912			\|a GBV_ILN_2021
912			\|a GBV_ILN_2141
912			\|a GBV_ILN_2190
912			\|a GBV_ILN_2192
912			\|a GBV_ILN_2219
912			\|a GBV_ILN_2221
912			\|a GBV_ILN_2237
912			\|a GBV_ILN_2409
912			\|a GBV_ILN_2410
912			\|a GBV_ILN_4012
912			\|a GBV_ILN_4029
912			\|a GBV_ILN_4035
912			\|a GBV_ILN_4037
912			\|a GBV_ILN_4046
912			\|a GBV_ILN_4082
912			\|a GBV_ILN_4103
912			\|a GBV_ILN_4112
912			\|a GBV_ILN_4125
912			\|a GBV_ILN_4219
912			\|a GBV_ILN_4266
912			\|a GBV_ILN_4305
912			\|a GBV_ILN_4306
912			\|a GBV_ILN_4307
912			\|a GBV_ILN_4309
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912			\|a GBV_ILN_4314
912			\|a GBV_ILN_4316
912			\|a GBV_ILN_4317
912			\|a GBV_ILN_4318
912			\|a GBV_ILN_4319
912			\|a GBV_ILN_4323
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952			\|d 93 \|j 1996 \|e 8 \|h 3581-3586 \|g 6

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allfields	(DE-627)OLC1594994862 (DE-599)GBVOLC1594994862 DE-627 ger DE-627 rakwb 570 000 500 500 AVZ LING fid BIODIV fid Schneppenheim, R. verfasserin aut Defective dimerization of von Willebrand factor subunits due to a Cys --> Arg mutation in type IID von Willebrand disease 1996 6 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier Brassard, J. oth Krey, S. oth Budde, U. oth Kunicki, T.J. oth Holmberg, L. oth Ware, J. oth Ruggeri, Z.M. oth Enthalten in Proceedings of the National Academy of Sciences of the United States of America Washington, DC : NAS, 1877 93(1996), 8, Seite 3581-3586 (DE-627)129505269 (DE-600)209104-5 (DE-576)014909189 0027-8424 nnns volume:93 year:1996 number:8 pages:3581-3586 extent:6 GBV_USEFLAG_A SYSFLAG_A GBV_OLC FID-LING FID-BIODIV SSG-OLC-PHY SSG-OLC-CHE SSG-OLC-MAT SSG-OLC-FOR SSG-OLC-PHA SSG-OLC-DE-84 SSG-OPC-MAT SSG-OPC-FOR GBV_ILN_11 GBV_ILN_20 GBV_ILN_21 GBV_ILN_22 GBV_ILN_24 GBV_ILN_40 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_74 GBV_ILN_105 GBV_ILN_130 GBV_ILN_154 GBV_ILN_168 GBV_ILN_171 GBV_ILN_179 GBV_ILN_211 GBV_ILN_252 GBV_ILN_290 GBV_ILN_2001 GBV_ILN_2002 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2015 GBV_ILN_2021 GBV_ILN_2141 GBV_ILN_2190 GBV_ILN_2192 GBV_ILN_2219 GBV_ILN_2221 GBV_ILN_2237 GBV_ILN_2409 GBV_ILN_2410 GBV_ILN_4012 GBV_ILN_4029 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4082 GBV_ILN_4103 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4219 GBV_ILN_4266 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4309 GBV_ILN_4310 GBV_ILN_4314 GBV_ILN_4316 GBV_ILN_4317 GBV_ILN_4318 GBV_ILN_4319 GBV_ILN_4323 AR 93 1996 8 3581-3586 6
spelling	(DE-627)OLC1594994862 (DE-599)GBVOLC1594994862 DE-627 ger DE-627 rakwb 570 000 500 500 AVZ LING fid BIODIV fid Schneppenheim, R. verfasserin aut Defective dimerization of von Willebrand factor subunits due to a Cys --> Arg mutation in type IID von Willebrand disease 1996 6 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier Brassard, J. oth Krey, S. oth Budde, U. oth Kunicki, T.J. oth Holmberg, L. oth Ware, J. oth Ruggeri, Z.M. oth Enthalten in Proceedings of the National Academy of Sciences of the United States of America Washington, DC : NAS, 1877 93(1996), 8, Seite 3581-3586 (DE-627)129505269 (DE-600)209104-5 (DE-576)014909189 0027-8424 nnns volume:93 year:1996 number:8 pages:3581-3586 extent:6 GBV_USEFLAG_A SYSFLAG_A GBV_OLC FID-LING FID-BIODIV SSG-OLC-PHY SSG-OLC-CHE SSG-OLC-MAT SSG-OLC-FOR SSG-OLC-PHA SSG-OLC-DE-84 SSG-OPC-MAT SSG-OPC-FOR GBV_ILN_11 GBV_ILN_20 GBV_ILN_21 GBV_ILN_22 GBV_ILN_24 GBV_ILN_40 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_74 GBV_ILN_105 GBV_ILN_130 GBV_ILN_154 GBV_ILN_168 GBV_ILN_171 GBV_ILN_179 GBV_ILN_211 GBV_ILN_252 GBV_ILN_290 GBV_ILN_2001 GBV_ILN_2002 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2015 GBV_ILN_2021 GBV_ILN_2141 GBV_ILN_2190 GBV_ILN_2192 GBV_ILN_2219 GBV_ILN_2221 GBV_ILN_2237 GBV_ILN_2409 GBV_ILN_2410 GBV_ILN_4012 GBV_ILN_4029 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4082 GBV_ILN_4103 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4219 GBV_ILN_4266 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4309 GBV_ILN_4310 GBV_ILN_4314 GBV_ILN_4316 GBV_ILN_4317 GBV_ILN_4318 GBV_ILN_4319 GBV_ILN_4323 AR 93 1996 8 3581-3586 6
allfields_unstemmed	(DE-627)OLC1594994862 (DE-599)GBVOLC1594994862 DE-627 ger DE-627 rakwb 570 000 500 500 AVZ LING fid BIODIV fid Schneppenheim, R. verfasserin aut Defective dimerization of von Willebrand factor subunits due to a Cys --> Arg mutation in type IID von Willebrand disease 1996 6 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier Brassard, J. oth Krey, S. oth Budde, U. oth Kunicki, T.J. oth Holmberg, L. oth Ware, J. oth Ruggeri, Z.M. oth Enthalten in Proceedings of the National Academy of Sciences of the United States of America Washington, DC : NAS, 1877 93(1996), 8, Seite 3581-3586 (DE-627)129505269 (DE-600)209104-5 (DE-576)014909189 0027-8424 nnns volume:93 year:1996 number:8 pages:3581-3586 extent:6 GBV_USEFLAG_A SYSFLAG_A GBV_OLC FID-LING FID-BIODIV SSG-OLC-PHY SSG-OLC-CHE SSG-OLC-MAT SSG-OLC-FOR SSG-OLC-PHA SSG-OLC-DE-84 SSG-OPC-MAT SSG-OPC-FOR GBV_ILN_11 GBV_ILN_20 GBV_ILN_21 GBV_ILN_22 GBV_ILN_24 GBV_ILN_40 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_74 GBV_ILN_105 GBV_ILN_130 GBV_ILN_154 GBV_ILN_168 GBV_ILN_171 GBV_ILN_179 GBV_ILN_211 GBV_ILN_252 GBV_ILN_290 GBV_ILN_2001 GBV_ILN_2002 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2015 GBV_ILN_2021 GBV_ILN_2141 GBV_ILN_2190 GBV_ILN_2192 GBV_ILN_2219 GBV_ILN_2221 GBV_ILN_2237 GBV_ILN_2409 GBV_ILN_2410 GBV_ILN_4012 GBV_ILN_4029 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4082 GBV_ILN_4103 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4219 GBV_ILN_4266 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4309 GBV_ILN_4310 GBV_ILN_4314 GBV_ILN_4316 GBV_ILN_4317 GBV_ILN_4318 GBV_ILN_4319 GBV_ILN_4323 AR 93 1996 8 3581-3586 6
allfieldsGer	(DE-627)OLC1594994862 (DE-599)GBVOLC1594994862 DE-627 ger DE-627 rakwb 570 000 500 500 AVZ LING fid BIODIV fid Schneppenheim, R. verfasserin aut Defective dimerization of von Willebrand factor subunits due to a Cys --> Arg mutation in type IID von Willebrand disease 1996 6 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier Brassard, J. oth Krey, S. oth Budde, U. oth Kunicki, T.J. oth Holmberg, L. oth Ware, J. oth Ruggeri, Z.M. oth Enthalten in Proceedings of the National Academy of Sciences of the United States of America Washington, DC : NAS, 1877 93(1996), 8, Seite 3581-3586 (DE-627)129505269 (DE-600)209104-5 (DE-576)014909189 0027-8424 nnns volume:93 year:1996 number:8 pages:3581-3586 extent:6 GBV_USEFLAG_A SYSFLAG_A GBV_OLC FID-LING FID-BIODIV SSG-OLC-PHY SSG-OLC-CHE SSG-OLC-MAT SSG-OLC-FOR SSG-OLC-PHA SSG-OLC-DE-84 SSG-OPC-MAT SSG-OPC-FOR GBV_ILN_11 GBV_ILN_20 GBV_ILN_21 GBV_ILN_22 GBV_ILN_24 GBV_ILN_40 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_74 GBV_ILN_105 GBV_ILN_130 GBV_ILN_154 GBV_ILN_168 GBV_ILN_171 GBV_ILN_179 GBV_ILN_211 GBV_ILN_252 GBV_ILN_290 GBV_ILN_2001 GBV_ILN_2002 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2015 GBV_ILN_2021 GBV_ILN_2141 GBV_ILN_2190 GBV_ILN_2192 GBV_ILN_2219 GBV_ILN_2221 GBV_ILN_2237 GBV_ILN_2409 GBV_ILN_2410 GBV_ILN_4012 GBV_ILN_4029 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4082 GBV_ILN_4103 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4219 GBV_ILN_4266 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4309 GBV_ILN_4310 GBV_ILN_4314 GBV_ILN_4316 GBV_ILN_4317 GBV_ILN_4318 GBV_ILN_4319 GBV_ILN_4323 AR 93 1996 8 3581-3586 6
allfieldsSound	(DE-627)OLC1594994862 (DE-599)GBVOLC1594994862 DE-627 ger DE-627 rakwb 570 000 500 500 AVZ LING fid BIODIV fid Schneppenheim, R. verfasserin aut Defective dimerization of von Willebrand factor subunits due to a Cys --> Arg mutation in type IID von Willebrand disease 1996 6 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier Brassard, J. oth Krey, S. oth Budde, U. oth Kunicki, T.J. oth Holmberg, L. oth Ware, J. oth Ruggeri, Z.M. oth Enthalten in Proceedings of the National Academy of Sciences of the United States of America Washington, DC : NAS, 1877 93(1996), 8, Seite 3581-3586 (DE-627)129505269 (DE-600)209104-5 (DE-576)014909189 0027-8424 nnns volume:93 year:1996 number:8 pages:3581-3586 extent:6 GBV_USEFLAG_A SYSFLAG_A GBV_OLC FID-LING FID-BIODIV SSG-OLC-PHY SSG-OLC-CHE SSG-OLC-MAT SSG-OLC-FOR SSG-OLC-PHA SSG-OLC-DE-84 SSG-OPC-MAT SSG-OPC-FOR GBV_ILN_11 GBV_ILN_20 GBV_ILN_21 GBV_ILN_22 GBV_ILN_24 GBV_ILN_40 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_74 GBV_ILN_105 GBV_ILN_130 GBV_ILN_154 GBV_ILN_168 GBV_ILN_171 GBV_ILN_179 GBV_ILN_211 GBV_ILN_252 GBV_ILN_290 GBV_ILN_2001 GBV_ILN_2002 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2015 GBV_ILN_2021 GBV_ILN_2141 GBV_ILN_2190 GBV_ILN_2192 GBV_ILN_2219 GBV_ILN_2221 GBV_ILN_2237 GBV_ILN_2409 GBV_ILN_2410 GBV_ILN_4012 GBV_ILN_4029 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4082 GBV_ILN_4103 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4219 GBV_ILN_4266 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4309 GBV_ILN_4310 GBV_ILN_4314 GBV_ILN_4316 GBV_ILN_4317 GBV_ILN_4318 GBV_ILN_4319 GBV_ILN_4323 AR 93 1996 8 3581-3586 6
source	Enthalten in Proceedings of the National Academy of Sciences of the United States of America 93(1996), 8, Seite 3581-3586 volume:93 year:1996 number:8 pages:3581-3586 extent:6
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authorswithroles_txt_mv	Schneppenheim, R. @@aut@@ Brassard, J. @@oth@@ Krey, S. @@oth@@ Budde, U. @@oth@@ Kunicki, T.J. @@oth@@ Holmberg, L. @@oth@@ Ware, J. @@oth@@ Ruggeri, Z.M. @@oth@@
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title	Defective dimerization of von Willebrand factor subunits due to a Cys --> Arg mutation in type IID von Willebrand disease
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title_full	Defective dimerization of von Willebrand factor subunits due to a Cys --> Arg mutation in type IID von Willebrand disease
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title_sort	defective dimerization of von willebrand factor subunits due to a cys --> arg mutation in type iid von willebrand disease
title_auth	Defective dimerization of von Willebrand factor subunits due to a Cys --> Arg mutation in type IID von Willebrand disease
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title_short	Defective dimerization of von Willebrand factor subunits due to a Cys --> Arg mutation in type IID von Willebrand disease
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author2	Brassard, J. Krey, S. Budde, U. Kunicki, T.J. Holmberg, L. Ware, J. Ruggeri, Z.M.
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Defective dimerization of von Willebrand factor subunits due to a Cys --> Arg mutation in type IID von Willebrand disease

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