UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Structural framework of c-Src activation by integrin β3

Blood, 2013-01, Vol.121 (4), p.700-706

2013

Volltextzugriff (PDF)

Fibrinogen interaction of CHO cells expressing chimeric αⅡb/αvβ3 integrin

Acta pharmacologica Sinica, 2008-02, Vol.29 (2), p.204-210

2008

Volltextzugriff (PDF)

Role and Mechanism of the Interaction of BCR-ABL with E3 Ligase c-CBL in Targeting Therapy of Chronic Myelogenous Leukemia

Zhongguo shi yan xue ye xue za zhi, 2017-02, Vol.25 (1), p.42

2017

Volltextzugriff (PDF)

A facile one-pot procedure for the transformation of acetonides into diacetates catalyzed with Bi(OTf)3·xH2O

Tetrahedron letters, 2008-04, Vol.49 (17), p.2714-2718

2008

Volltextzugriff (PDF)

Gene therapy for hemophilia B

Zhōnghuá xuèyèxué zázhì, 2013-09, Vol.34 (9), p.809-811

2013

Volltextzugriff (PDF)

Effect of the Integrin β3 Cytoplasmic NITY Motif on α II bβ3-Mediated Cell Functions in CHO Cell Model

Zhongguo shi yan xue ye xue za zhi, 2015-06, Vol.23 (3), p.768

2015

Volltextzugriff (PDF)

Myr-RKEFAK Peptide Selectively Regulates Outside-in Signaling Transduction-related Functions in Human Platelets

Zhongguo shi yan xue ye xue za zhi, 2015-06, Vol.23 (3), p.761

2015

Volltextzugriff (PDF)

Research progress on the effect of shear stress on thrombosis

Zhōnghuá xīnxuèguănbìng zázhì, 2013-10, Vol.41 (10), p.893

2013

Volltextzugriff (PDF)

The binding mechanisms of F VIII Trp1707Ser mutation-associated inhibitor

Zhōnghuá xuèyèxué zázhì, 2013-08, Vol.34 (8), p.691-695

2013

Volltextzugriff (PDF)

A single E726Q mutation in the membrane proximal α-helix of integrin β3 subunit induces membrane blebbing by disrupting the membrane-actin cortex interaction

Zhongguo shi yan xue ye xue za zhi, 2011-12, Vol.19 (6), p.1450

2011

Volltextzugriff (PDF)

Transgenic mouse models of the truncated platelet integrin β3 cytoplasmic tail established by stem cell transplantation

Zhongguo shi yan xue ye xue za zhi, 2013-06, Vol.21 (3), p.667

2013

Volltextzugriff (PDF)

Functional study of abnormal fibrinogen caused by Arg275His mutation in fibrinogen γ chain

Zhōnghuá xuèyèxué zázhì, 2013-03, Vol.34 (3), p.190-194

2013

Volltextzugriff (PDF)

Phenotype and genotype analysis of two Chinese pedigrees with type 3 von Willebrand diseases

Zhonghua yi xue yi chuan xue za zhi, 2012-10, Vol.29 (5), p.524

2012

Volltextzugriff (PDF)

The phenotypic and genotypic diagnosis of three Chinese patients with von Willebrand disease

Chung-hua nei kʿo tsa chih, 2012-10, Vol.51 (10), p.788

2012

Volltextzugriff (PDF)

Molecular analysis of a patient with hemophilia A caused by FVIII His99Arg mutation

Zhōnghuá xuèyèxué zázhì, 2011-09, Vol.32 (9), p.587-591

2011

Volltextzugriff (PDF)

Genotype and function analyses of four inherited dysfibrinogenemia pedigree caused by Arg16 amino acid substitution in fibrinogen Aα chain

Zhōnghuá xuèyèxué zázhì, 2012-06, Vol.33 (6), p.475-479

2012

Volltextzugriff (PDF)

Two novel mutations in one pedigree with hereditary Factor VII deficiency

Zhōnghuá xuèyèxué zázhì, 2011-03, Vol.32 (3), p.158-162

2011

Volltextzugriff (PDF)

Study of signal transduction mediated by integrin alphaIIbbeta3 using a dominant negative model

Zhongguo shi yan xue ye xue za zhi, 2009-08, Vol.17 (4), p.1026

2009

Volltextzugriff (PDF)

Molecular mechanisms of recurrent venous thrombosis in two pedigrees with type I antithrombin deficiency

Zhōnghuá xuèyèxué zázhì, 2011-12, Vol.32 (12), p.848-853

2011

Volltextzugriff (PDF)

Analysis of phenotype and genotype in three Chinese pedigrees with inherited dysfibrinogenemia

Zhōnghuá xuèyèxué zázhì, 2011-03, Vol.32 (3), p.153-157

2011

Volltextzugriff (PDF)

Analysis of phenotype and genotype in four Chinese pedigrees with inherited coagulation factor V deficiency.

Zhōnghuá xuèyèxué zázhì, 2010-03, Vol.31 (3), p.149-153

2010

Volltextzugriff (PDF)

Phenotype and genotype analysis of three Chinese pedigrees with von Willebrand disease

Zhōnghuá xuèyèxué zázhì, 2011-02, Vol.32 (2), p.99-102

2011

Volltextzugriff (PDF)

Two new mutations of AT gene in type I inherited antithrombin deficiency.

Zhōnghuá xuèyèxué zázhì, 2010-03, Vol.31 (3), p.145-148

2010

Volltextzugriff (PDF)

Preparation and characterization of a monoclonal antibody against human c-Kit

Xi bao yu fen zi mian yi xue za zhi, 2009-07, Vol.25 (7), p.619

2009

Volltextzugriff (PDF)

Analysis of clinical features and genotype in three Chinese pedigrees with Glanzmann thrombasthenia

Zhōnghuá xuèyèxué zázhì, 2008-03, Vol.29 (3), p.149-153

2008

Volltextzugriff (PDF)

1 – 25 von 556

Suche als RSS-Feed

Aktive Filter

ThemaScience & Technology

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(289)
Mit Volltextzugriff
(423)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

Erscheinungsjahr

n.n

Thema

Humans
(88)
Male
(51)
Female
(47)
Animals
(30)
Adult
(27)
Middle Aged
(22)
Child
(18)
Aged
(16)
Infant
(16)
Treatment Outcome
(15)
China
(13)
Adolescent
(12)
Child, Preschool
(12)
Mutation
(12)
Pedigree
(12)
Mice
(10)
Phenotype
(10)
Rats
(9)
Follow-Up Studies
(8)
Genotype
(8)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

Menü

Weitere Dienste

Einstellungen

Structural framework of c-Src activation by integrin β3

Fibrinogen interaction of CHO cells expressing chimeric αⅡb/αvβ3 integrin

Role and Mechanism of the Interaction of BCR-ABL with E3 Ligase c-CBL in Targeting Therapy of Chronic Myelogenous Leukemia

A facile one-pot procedure for the transformation of acetonides into diacetates catalyzed with Bi(OTf)3·xH2O

Gene therapy for hemophilia B

Effect of the Integrin β3 Cytoplasmic NITY Motif on α II bβ3-Mediated Cell Functions in CHO Cell Model

Myr-RKEFAK Peptide Selectively Regulates Outside-in Signaling Transduction-related Functions in Human Platelets

Research progress on the effect of shear stress on thrombosis

The binding mechanisms of F VIII Trp1707Ser mutation-associated inhibitor

A single E726Q mutation in the membrane proximal α-helix of integrin β3 subunit induces membrane blebbing by disrupting the membrane-actin cortex interaction

Transgenic mouse models of the truncated platelet integrin β3 cytoplasmic tail established by stem cell transplantation

Functional study of abnormal fibrinogen caused by Arg275His mutation in fibrinogen γ chain

Phenotype and genotype analysis of two Chinese pedigrees with type 3 von Willebrand diseases

The phenotypic and genotypic diagnosis of three Chinese patients with von Willebrand disease

Molecular analysis of a patient with hemophilia A caused by FVIII His99Arg mutation

Genotype and function analyses of four inherited dysfibrinogenemia pedigree caused by Arg16 amino acid substitution in fibrinogen Aα chain

Two novel mutations in one pedigree with hereditary Factor VII deficiency

Study of signal transduction mediated by integrin alphaIIbbeta3 using a dominant negative model

Molecular mechanisms of recurrent venous thrombosis in two pedigrees with type I antithrombin deficiency

Analysis of phenotype and genotype in three Chinese pedigrees with inherited dysfibrinogenemia

Analysis of phenotype and genotype in four Chinese pedigrees with inherited coagulation factor V deficiency.

Phenotype and genotype analysis of three Chinese pedigrees with von Willebrand disease

Two new mutations of AT gene in type I inherited antithrombin deficiency.

Preparation and characterization of a monoclonal antibody against human c-Kit

Analysis of clinical features and genotype in three Chinese pedigrees with Glanzmann thrombasthenia

Aktive Filter

Suchergebnisse filtern