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Reduced von Willebrand factor secretion is associated with loss of Weibel-Palade body formation.

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Reduced von Willebrand factor secretion is associated with loss of Weibel-Palade body formation. / Castaman, G; Giacomelli, S H; Jacobi, P M; Obser, Tobias; Budde, U; Rodeghiero, F; Schneppenheim, Reinhard; Haberichter, S L.

in: J THROMB HAEMOST, Jahrgang 10, Nr. 5, 5, 2012, S. 951-958.

Publikationen: SCORING: Beitrag in Fachzeitschrift/Zeitung › SCORING: Zeitschriftenaufsatz › Forschung › Begutachtung

Harvard

Castaman, G, Giacomelli, SH, Jacobi, PM, Obser, T, Budde, U, Rodeghiero, F, Schneppenheim, R & Haberichter, SL 2012, 'Reduced von Willebrand factor secretion is associated with loss of Weibel-Palade body formation.', J THROMB HAEMOST, Jg. 10, Nr. 5, 5, S. 951-958. <http://www.ncbi.nlm.nih.gov/pubmed/22429825?dopt=Citation>

APA

Castaman, G., Giacomelli, S. H., Jacobi, P. M., Obser, T., Budde, U., Rodeghiero, F., Schneppenheim, R., & Haberichter, S. L. (2012). Reduced von Willebrand factor secretion is associated with loss of Weibel-Palade body formation. J THROMB HAEMOST, 10(5), 951-958. [5]. http://www.ncbi.nlm.nih.gov/pubmed/22429825?dopt=Citation

Vancouver

Castaman G, Giacomelli SH, Jacobi PM, Obser T, Budde U, Rodeghiero F et al. Reduced von Willebrand factor secretion is associated with loss of Weibel-Palade body formation. J THROMB HAEMOST. 2012;10(5):951-958. 5.

Bibtex

@article{e193b45732864bcb8d1de7dfee41f31f,
title = "Reduced von Willebrand factor secretion is associated with loss of Weibel-Palade body formation.",
abstract = "von Willebrand disease (VWD) is caused by mutations in von Willebrand factor (VWF) that have different pathophysiologic effect in causing low plasma VWF levels. Type 1 VWD includes quantitative plasma VWF deficiency with normal VWF structure and function.",
keywords = "Humans, Genetic Predisposition to Disease, Phenotype, Homozygote, Mutation, Missense, Heterozygote, Fluorescent Antibody Technique, Protein Multimerization, Transfection, Microscopy, Confocal, Protein Binding, HEK293 Cells, Down-Regulation, Collagen/metabolism, Platelet Glycoprotein GPIb-IX Complex/metabolism, Weibel-Palade Bodies/metabolism/*pathology/*secretion, von Willebrand Disease, Type 1/blood/genetics/*pathology, von Willebrand Factor/genetics/metabolism/*secretion, Humans, Genetic Predisposition to Disease, Phenotype, Homozygote, Mutation, Missense, Heterozygote, Fluorescent Antibody Technique, Protein Multimerization, Transfection, Microscopy, Confocal, Protein Binding, HEK293 Cells, Down-Regulation, Collagen/metabolism, Platelet Glycoprotein GPIb-IX Complex/metabolism, Weibel-Palade Bodies/metabolism/*pathology/*secretion, von Willebrand Disease, Type 1/blood/genetics/*pathology, von Willebrand Factor/genetics/metabolism/*secretion",
author = "G Castaman and Giacomelli, {S H} and Jacobi, {P M} and Tobias Obser and U Budde and F Rodeghiero and Reinhard Schneppenheim and Haberichter, {S L}",
year = "2012",
language = "English",
volume = "10",
pages = "951--958",
journal = "J THROMB HAEMOST",
issn = "1538-7933",
publisher = "Wiley-Blackwell",
number = "5",

}

RIS

TY - JOUR

T1 - Reduced von Willebrand factor secretion is associated with loss of Weibel-Palade body formation.

AU - Castaman, G

AU - Giacomelli, S H

AU - Jacobi, P M

AU - Obser, Tobias

AU - Budde, U

AU - Rodeghiero, F

AU - Schneppenheim, Reinhard

AU - Haberichter, S L

PY - 2012

Y1 - 2012

N2 - von Willebrand disease (VWD) is caused by mutations in von Willebrand factor (VWF) that have different pathophysiologic effect in causing low plasma VWF levels. Type 1 VWD includes quantitative plasma VWF deficiency with normal VWF structure and function.

AB - von Willebrand disease (VWD) is caused by mutations in von Willebrand factor (VWF) that have different pathophysiologic effect in causing low plasma VWF levels. Type 1 VWD includes quantitative plasma VWF deficiency with normal VWF structure and function.

KW - Humans

KW - Genetic Predisposition to Disease

KW - Phenotype

KW - Homozygote

KW - Mutation, Missense

KW - Heterozygote

KW - Fluorescent Antibody Technique

KW - Protein Multimerization

KW - Transfection

KW - Microscopy, Confocal

KW - Protein Binding

KW - HEK293 Cells

KW - Down-Regulation

KW - Collagen/metabolism

KW - Platelet Glycoprotein GPIb-IX Complex/metabolism

KW - Weibel-Palade Bodies/metabolism/pathology/secretion

KW - von Willebrand Disease, Type 1/blood/genetics/pathology

KW - von Willebrand Factor/genetics/metabolism/secretion

KW - Humans

KW - Genetic Predisposition to Disease

KW - Phenotype

KW - Homozygote

KW - Mutation, Missense

KW - Heterozygote

KW - Fluorescent Antibody Technique

KW - Protein Multimerization

KW - Transfection

KW - Microscopy, Confocal

KW - Protein Binding

KW - HEK293 Cells

KW - Down-Regulation

KW - Collagen/metabolism

KW - Platelet Glycoprotein GPIb-IX Complex/metabolism

KW - Weibel-Palade Bodies/metabolism/pathology/secretion

KW - von Willebrand Disease, Type 1/blood/genetics/pathology

KW - von Willebrand Factor/genetics/metabolism/secretion

M3 - SCORING: Journal article

VL - 10

SP - 951

EP - 958

JO - J THROMB HAEMOST

JF - J THROMB HAEMOST

SN - 1538-7933

IS - 5

M1 - 5

ER -