UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 59

Sortiert nach

Clinical Consequences and Molecular Bases of Low Fibrinogen Levels

International journal of molecular sciences, 2018-01, Vol.19 (1), p.192

2018

Volltextzugriff (PDF)

Whole Blood Thromboelastometry by ROTEM and Thrombin Generation by Genesia According to the Genotype and Clinical Phenotype in Congenital Fibrinogen Disorders

International journal of molecular sciences, 2021-02, Vol.22 (5), p.2286

2021

Volltextzugriff (PDF)

Venous Thrombosis and Thrombocyte Activity in Zebrafish Models of Quantitative and Qualitative Fibrinogen Disorders

International journal of molecular sciences, 2021-01, Vol.22 (2), p.655

2021

Volltextzugriff (PDF)

Targeted mutation of zebrafish fga models human congenital afibrinogenemia

Blood, 2014-04, Vol.123 (14), p.2278-2281

2014

Volltextzugriff (PDF)

Fibrinogen Łódź: a new cause of dysfibrinogenemia associated with recurrent thromboembolic arterial events

Polskie archiwum medycyny wewne̦trznej, 2019-12, Vol.129 (12), p.934-935

2019

Volltextzugriff (PDF)

A Novel Nonsense Mutation in FGB (c.1421G>A; p.Trp474Ter) in the Beta Chain of Fibrinogen Causing Hypofibrinogenemia with Bleeding Phenotype

Biomedicines, 2020-12, Vol.8 (12), p.605

2020

Volltextzugriff (PDF)

Loss of Dicer in Sertoli Cells Has a Major Impact on the Testicular Proteome of Mice

Molecular & cellular proteomics, 2011-04, Vol.10 (4), p.M900587MCP200, Article M900587-MCP200

2011

Volltextzugriff (PDF)

C2orf62 and TTC17 are involved in actin organization and ciliogenesis in zebrafish and human

PloS one, 2014-01, Vol.9 (1), p.e86476-e86476

2014

Volltextzugriff (PDF)

DNA methylation profiling of the fibrinogen gene landscape in human cells and during mouse and zebrafish development

PloS one, 2013-08, Vol.8 (8), p.e73089

2013

Volltextzugriff (PDF)

A liver enhancer in the fibrinogen gene cluster

Blood, 2011-01, Vol.117 (1), p.276-282

2011

Volltextzugriff (PDF)

Case Report: Unmasked Inherited Dysfibrinogenemia After Everolimus Therapy

Frontiers in medicine, 2020-11, Vol.7, p.591546

2020

Volltextzugriff (PDF)

Illustrated State-of-the-Art Capsules of the ISTH 2020 Congress

Research and practice in thrombosis and haemostasis, 2021-07, Vol.5 (5), p.e12532

2021

Volltextzugriff (PDF)

Illustrated State‐of‐the‐Art Capsules of the ISTH 2021 Congress

Research and practice in thrombosis and haemostasis, 2021-07, Vol.5 (5), p.e12532-n/a, Article e12532

2021

Volltextzugriff (PDF)

When fibrin(ogen) is too loud, silence it

Blood, 2022-03, Vol.139 (9), p.1261-1262

Neerman-Arbez, Marguerite

2022

Volltextzugriff (PDF)

Outcome of donor splice site mutations accounting for congenital afibrinogenemia reflects order of intron removal in the fibrinogen alpha gene (FGA)

Blood, 2003-03, Vol.101 (5), p.1851-1856

2003

Volltextzugriff (PDF)

Deletion of 3 residues from the C-terminus of MCFD2 affects binding to ERGIC-53 and causes combined factor V and factor VIII deficiency

Blood, 2008-02, Vol.111 (3), p.1299-1301

2008

Volltextzugriff (PDF)

Deletion of the fibrogen alpha-chain gene (FGA) causes congenital afibrogenemia

The Journal of clinical investigation, 1999-01, Vol.103 (2), p.215-218

1999

Volltextzugriff (PDF)

Manipulating the quality control pathway in transfected cells: low temperature allows rescue of secretion-defective fibrinogen mutants

Haematologica (Roma), 2008-02, Vol.93 (2), p.224-231

2008

Volltextzugriff (PDF)

Integrated analysis of mRNA and miRNA expression in response to interleukin-6 in hepatocytes

Data in brief, 2015-09, Vol.4 (C), p.226-228

2015

Volltextzugriff (PDF)

Molecular mechanisms accounting for fibrinogen deficiency: from large deletions to intracellular retention of misfolded proteins

Journal of thrombosis and haemostasis, 2007-07, Vol.5 (s1), p.125-131

2007

Volltextzugriff (PDF)

Congenital afibrinogenemia: identification and expression of a missense mutation in FGB impairing fibrinogen secretion

Blood, 2003-12, Vol.102 (13), p.4413-4415

2003

Volltextzugriff (PDF)

Fibrinogen Gene Mutations Accounting for Congenital Afibrinogenemia

Annals of the New York Academy of Sciences, 2001-01, Vol.936 (1), p.496-508

NEERMAN-ARBEZ, MARGUERITE

2001

Volltextzugriff (PDF)

αIIbβ3 variants defined by next-generation sequencing: Predicting variants likely to cause Glanzmann thrombasthenia

Proceedings of the National Academy of Sciences - PNAS, 2015-04, Vol.112 (15), p.E1898-E1907

2015

Volltextzugriff (PDF)

Natural history of patients with congenital dysfibrinogenemia

Blood, 2015-01, Vol.125 (3), p.553-561

2015

Volltextzugriff (PDF)

To aggregate or not to aggregate

Journal of thrombosis and haemostasis, 2007-10, Vol.5 (10), p.1997-1998

NEERMAN‐ARBEZ, M.

2007

Volltextzugriff (PDF)

1 – 25 von 59

Suche als RSS-Feed

Aktive Filter

KollektionElektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(56)
Mit Volltextzugriff
(58)

Publikationsform

Artikel
(57)
Berichte
(2)

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(42)
Life Sciences & Biomedicine
(39)
Humans
(28)
Animals
(22)
Hematology
(22)
Fibrinogen - Genetics
(20)
Afibrinogenemia - Genetics
(14)
Biological And Medical Sciences
(13)
Biochemistry & Molecular Biology
(11)
Fibrinogen
(11)
Hematologic And Hematopoietic Diseases
(11)
Male
(11)
Medical Sciences
(11)
Female
(10)
Mutation
(10)
Platelet Diseases And Coagulopathies
(9)
Fibrinogen - Metabolism
(8)
Molecular Sequence Data
(7)
Fibrin
(6)
Fibrinogen - Chemistry
(6)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Clinical Consequences and Molecular Bases of Low Fibrinogen Levels

Whole Blood Thromboelastometry by ROTEM and Thrombin Generation by Genesia According to the Genotype and Clinical Phenotype in Congenital Fibrinogen Disorders

Venous Thrombosis and Thrombocyte Activity in Zebrafish Models of Quantitative and Qualitative Fibrinogen Disorders

Targeted mutation of zebrafish fga models human congenital afibrinogenemia

Fibrinogen Łódź: a new cause of dysfibrinogenemia associated with recurrent thromboembolic arterial events

A Novel Nonsense Mutation in FGB (c.1421G>A; p.Trp474Ter) in the Beta Chain of Fibrinogen Causing Hypofibrinogenemia with Bleeding Phenotype

Loss of Dicer in Sertoli Cells Has a Major Impact on the Testicular Proteome of Mice

C2orf62 and TTC17 are involved in actin organization and ciliogenesis in zebrafish and human

DNA methylation profiling of the fibrinogen gene landscape in human cells and during mouse and zebrafish development

A liver enhancer in the fibrinogen gene cluster

Case Report: Unmasked Inherited Dysfibrinogenemia After Everolimus Therapy

Illustrated State-of-the-Art Capsules of the ISTH 2020 Congress

Illustrated State‐of‐the‐Art Capsules of the ISTH 2021 Congress

When fibrin(ogen) is too loud, silence it

Outcome of donor splice site mutations accounting for congenital afibrinogenemia reflects order of intron removal in the fibrinogen alpha gene (FGA)

Deletion of 3 residues from the C-terminus of MCFD2 affects binding to ERGIC-53 and causes combined factor V and factor VIII deficiency

Deletion of the fibrogen alpha-chain gene (FGA) causes congenital afibrogenemia

Manipulating the quality control pathway in transfected cells: low temperature allows rescue of secretion-defective fibrinogen mutants

Integrated analysis of mRNA and miRNA expression in response to interleukin-6 in hepatocytes

Molecular mechanisms accounting for fibrinogen deficiency: from large deletions to intracellular retention of misfolded proteins

Congenital afibrinogenemia: identification and expression of a missense mutation in FGB impairing fibrinogen secretion

Fibrinogen Gene Mutations Accounting for Congenital Afibrinogenemia

αIIbβ3 variants defined by next-generation sequencing: Predicting variants likely to cause Glanzmann thrombasthenia

Natural history of patients with congenital dysfibrinogenemia

To aggregate or not to aggregate

Aktive Filter

Suchergebnisse filtern