Analysis of C3 Gene Variants in Patients With Idiopathic Recurrent Spontaneous Pregnancy Loss
Published 2018 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Analysis of C3 Gene Variants in Patients With Idiopathic Recurrent Spontaneous Pregnancy Loss
Authors
Keywords
-
Journal
Frontiers in Immunology
Volume 9, Issue -, Pages -
Publisher
Frontiers Media SA
Online
2018-08-07
DOI
10.3389/fimmu.2018.01813
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- The role of complement inhibitors beyond controlling inflammation
- (2017) A. M. Blom JOURNAL OF INTERNAL MEDICINE
- Regulator-dependent mechanisms of C3b processing by factor I allow differentiation of immune responses
- (2017) Xiaoguang Xue et al. NATURE STRUCTURAL & MOLECULAR BIOLOGY
- Regulator-dependent mechanisms of C3b processing by factor I allow differentiation of immune responses
- (2017) Xiaoguang Xue et al. NATURE STRUCTURAL & MOLECULAR BIOLOGY
- Analysis of Complement C3 Gene Reveals Susceptibility to Severe Preeclampsia
- (2017) A. Inkeri Lokki et al. Frontiers in Immunology
- Complement component C3 - The “Swiss Army Knife” of innate immunity and host defense
- (2016) Daniel Ricklin et al. IMMUNOLOGICAL REVIEWS
- Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans
- (2016) Paul Laissue et al. Open Biology
- Dynamics of complement activation in aHUS and how to monitor eculizumab therapy
- (2014) M. Noris et al. BLOOD
- Analysis of Rare Variants in the C3 Gene in Patients with Age-Related Macular Degeneration
- (2014) Maheswara R. Duvvari et al. PLoS One
- Complement Activation and Regulation in Preeclamptic Placenta
- (2014) Anna Inkeri Lokki et al. Frontiers in Immunology
- Analysis of genes coding for CD46, CD55, and C4b-binding protein in patients with idiopathic, recurrent, spontaneous pregnancy loss
- (2013) Frida C. Mohlin et al. EUROPEAN JOURNAL OF IMMUNOLOGY
- Rare variants in CFI, C3 and C9 are associated with high risk of advanced age-related macular degeneration
- (2013) Johanna M Seddon et al. NATURE GENETICS
- Identification of a rare coding variant in complement 3 associated with age-related macular degeneration
- (2013) Xiaowei Zhan et al. NATURE GENETICS
- Evaluation and treatment of recurrent pregnancy loss: a committee opinion
- (2012) FERTILITY AND STERILITY
- Preeclampsia Is Characterized by Placental Complement Dysregulation
- (2012) Aletta Buurma et al. HYPERTENSION
- Allelic Variants of Complement Genes Associated with Dense Deposit Disease
- (2011) M. A. Abrera-Abeleda et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
- Common polymorphisms in C3, factor B, and factor H collaborate to determine systemic complement activity and disease risk
- (2011) M. Heurich et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Complement component C3 functions as an embryotrophic factor in early postimplantation rat embryos
- (2010) Makoto Usami et al. INTERNATIONAL JOURNAL OF DEVELOPMENTAL BIOLOGY
- An Alternative Role of C1q in Cell Migration and Tissue Remodeling: Contribution to Trophoblast Invasion and Placental Development
- (2010) C. Agostinis et al. JOURNAL OF IMMUNOLOGY
- Easy genotyping of complement C3 ‘slow’ and ‘fast’ allotypes by tetra-primer amplification refractory mutation system PCR
- (2010) Benedetta Peruzzi et al. MOLECULAR AND CELLULAR PROBES
- Complement 3 deficiency impairs early pregnancy in mice
- (2009) Wang-Ngai Chow et al. MOLECULAR REPRODUCTION AND DEVELOPMENT
- Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome
- (2008) V. Fremeaux-Bacchi et al. BLOOD
Find the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
SearchCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now