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D Borgel

Explore the profile of D Borgel including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 28
Citations 180
Followers 0
Related Specialties
Hematology
Cardiology & Vascular Diseases
General Medicine
Top 10 Co-Authors
S Gandrille
M Aiach
M Alhenc-Gelas
P Gaussem
T Kaabache
C Matheron
J Duchemin
F Bernardi
P H Reitsma
C Abdo
Published In
Thromb Haemost
J Thromb Haemost
Blood Coagul Fibrinolysis
Hum Genet
Nat Med
Affiliations
Soon will be listed here.
Recent Articles
1.
Author Correction: Long-term safety and efficacy of lentiviral hematopoietic stem/progenitor cell gene therapy for Wiskott-Aldrich syndrome
Magnani A, Semeraro M, Adam F, Booth C, Dupre L, Morris E, et al.
Nat Med . 2022 Aug; 28(10):2217. PMID: 35945284
No abstract available.
2.
Long-term safety and efficacy of lentiviral hematopoietic stem/progenitor cell gene therapy for Wiskott-Aldrich syndrome
Magnani A, Semeraro M, Adam F, Booth C, Dupre L, Morris E, et al.
Nat Med . 2022 Jan; 28(1):71-80. PMID: 35075289
Patients with Wiskott-Aldrich syndrome (WAS) lacking a human leukocyte antigen-matched donor may benefit from gene therapy through the provision of gene-corrected, autologous hematopoietic stem/progenitor cells. Here, we present comprehensive, long-term...
3.
A chemically-modified inactive antithrombin as a potent antagonist of fondaparinux and heparin anticoagulant activity
Fazavana J, Bianchini E, Saller F, Smadja C, Picard V, Taverna M, et al.
J Thromb Haemost . 2013 Apr; 11(6):1128-36. PMID: 23581397
Background: Heparin and its analogs, mediating their anticoagulant activity through antithrombin (AT) activation, remain largely used for the preventive and curative treatment of thrombosis. The major adverse reaction of these...
4.
Vascular endothelial growth factor, as compared with placental growth factor, is increased in severe sepsis but not in organ failure
Smadja D, Borgel D, Diehl J, Gaussem P
J Thromb Haemost . 2012 Mar; 10(5):974-6. PMID: 22385934
No abstract available.
5.
Novel human pathological mutations. Gene symbol: PROS1. Disease: Protein S deficiency
Pintao M, Garcia A, Borgel D, Alhenc-Gelas M, Spek C, de Visser M, et al.
Hum Genet . 2010 Jan; 127(1):121. PMID: 20108435
No abstract available.
6.
Gross deletions/duplications in PROS1 are relatively common in point mutation-negative hereditary protein S deficiency
Pintao M, Garcia A, Borgel D, Alhenc-Gelas M, Spek C, de Visser M, et al.
Hum Genet . 2009 May; 126(3):449-56. PMID: 19466456
Hereditary protein S (PS) deficiency is an autosomal disorder caused by mutations in the PS gene (PROS1). Conventional PCR-based mutation detection identifies PROS1 point mutations in approximately 50% of the...
7.
Plasma levels of the growth arrest-specific gene 6 product (Gas6) and antiplatelet drug responsiveness in healthy subjects
Burnier L, Borgel D, Angelillo-Scherrer A, Fontana P
J Thromb Haemost . 2006 Sep; 4(10):2283-4. PMID: 16999853
No abstract available.
8.
The protein S thrombin-sensitive region modulates phospholipid binding and the gamma-carboxyglutamic acid-rich (Gla) domain conformation in a non-specific manner
Saller F, Kaabache T, Aiach M, Gandrille S, Borgel D
J Thromb Haemost . 2006 Feb; 4(3):704-6. PMID: 16460467
No abstract available.
9.
Molecular bases of type II protein S deficiency: the I203-D204 deletion in the EGF4 domain alters GLA domain function
Baroni M, Mazzola G, Kaabache T, Borgel D, Gandrille S, Vigano DAngelo S, et al.
J Thromb Haemost . 2006 Jan; 4(1):186-91. PMID: 16409468
Objective: To characterize the first type II protein S (PS) deficiency affecting the epidermal growth factor (EGF)4 domain, a calcium-binding module with a poorly defined functional role. Patients: The proband...
10.
Sepsis and coagulation
Diehl J, Borgel D
Curr Opin Crit Care . 2005 Sep; 11(5):454-60. PMID: 16175032
Purpose Of Review: There is considerable evidence that dysregulation of the coagulation and fibrinolytic systems plays a major role in the pathophysiology of severe sepsis, with a special focus on...