Nuclear factor (NF)-κB and its associated pathways are major molecular regulators of blood-induced joint damage in a murine model of hemophilia-Reference-Cited by-同舟云学术

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Nuclear factor (NF)-κB and its associated pathways are major molecular regulators of blood-induced joint damage in a murine model of hemophilia

Published:2013-02 Issue:2 Volume:11 Page:293-306
ISSN:1538-7933
Container-title:Journal of Thrombosis and Haemostasis
language:en
Short-container-title:J Thromb Haemost

Author:

Sen D.¹,Chapla A.¹,Walter N.²,Daniel V.³,Srivastava A.¹⁴,Jayandharan G. R.¹⁴

Affiliation:

1. Department of Hematology; Christian Medical College; Vellore Tamil Nadu India

2. Department of General Pathology and Forensic Medicine; Christian Medical College; Vellore Tamil Nadu India

3. Department of Orthopedics; Christian Medical College; Vellore Tamil Nadu India

4. Centre for Stem Cell Research; Christian Medical College; Vellore Tamil Nadu India

Funder

G.R.J. from the Department of Science of Technology

Department of Biotechnology

Swarnajayanti Fellowship 2011

nnovative Young Biotechnologist award 2010

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/jth.12101/fullpdf

Reference84 articles.

1. Hemophilia and related bleeding disorders: a story of dismay and success;Mannucci;Hematology Am Soc Hematol Educ Program,2002

2. Rosendaal F, Aledort LM, Lusher JM, Rothschild C, Ingerslev J. Definitions in hemophilia. Recommendation of the scientific subcommittee on factor VIII and factor IX of the scientific and standardization committee of the International Society on Thrombosis and Haemostasis;White;Thromb Haemost,2001

3. A longitudinal study of orthopaedic outcomes for severe factor-VIII-deficient haemophiliacs. The Orthopaedic Outcome Study Group;Aledort;J Intern Med,1994

4. Meta-analytic evidence of increased breakthrough bleeding during prophylaxis with B-domain deleted factor VIII;Gruppo;Haemophilia,2004

5. Prophylaxis versus episodic treatment to prevent joint disease in boys with severe hemophilia;Manco-Johnson;N Engl J Med,2007

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2. Inflammatory diseases causing joint and bone destruction: rheumatoid arthritis and hemophilic arthropathy;Journal of Bone and Mineral Metabolism;2024-06-10

3. AAV mediated repression of Neat1 lncRNA combined with F8 gene augmentation mitigates pathological mediators of joint disease in haemophilia;Journal of Cellular and Molecular Medicine;2024-06

4. Stromal cell‐derived factor 1 alpha (SDF‐1alfa) and cartilage oligomeric matrix protein (COMP): Two potential signature biomarkers of radiological detectable hemophilic arthropathy;International Journal of Rheumatic Diseases;2024-02

5. Blood-Induced Arthropathy: A Major Disabling Complication of Haemophilia;Journal of Clinical Medicine;2023-12-30

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