Cargando…

Association of Complement Factor D and H Polymorphisms with Recurrent Pregnancy Loss

Recurrent pregnancy loss (RPL) is defined as two or more consecutive pregnancy losses prior to 20 weeks of gestation, and the incidence of RPL is estimated at 1% of all pregnancies. While the etiologies of RPL are diverse, immune function is considered to be an important cause of RPL. In particular,...

Descripción completa

Detalles Bibliográficos
Autores principales:	Cho, Hee Young, Park, Han Sung, Ko, Eun Ju, Ryu, Chang Soo, Kim, Jung Oh, Kim, Young Ran, Ahn, Eun Hee, Lee, Woo Sik, Kim, Nam Keun
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2019
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6981708/ https://www.ncbi.nlm.nih.gov/pubmed/31861421 http://dx.doi.org/10.3390/ijms21010017

Ejemplares similares

Association study of AGO1 and AGO2 genes polymorphisms with recurrent pregnancy loss
por: Kim, Young Ran, et al.
Publicado: (2019)

Association Study between Mucin 4 (MUC4) Polymorphisms and Idiopathic Recurrent Pregnancy Loss in a Korean Population
por: Kim, Ji-Hyang, et al.
Publicado: (2022)

Association of Polymorphisms in Plasminogen Activator Inhibitor-1 (PAI-1), Tissue Plasminogen Activator (tPA), and Renin (REN) with Recurrent Pregnancy Loss in Korean Women
por: Cho, Hee Young, et al.
Publicado: (2021)

3′-UTR Polymorphisms in the Vascular Endothelial Growth Factor Gene (VEGF) Contribute to Susceptibility to Recurrent Pregnancy Loss (RPL)
por: An, Hui Jeong, et al.
Publicado: (2019)

MTHFR 3′-untranslated region polymorphisms contribute to recurrent pregnancy loss risk and alterations in peripheral natural killer cell proportions
por: Kim, Eun Sun, et al.
Publicado: (2017)

Association of Polymorphisms in the Long Non-Coding RNA HOTAIR with Recurrent Pregnancy Loss in a Korean Population
por: Park, Hyeon Woo, et al.
Publicado: (2022)

Association of Polymorphisms in FSHR, INHA, ESR1, and BMP15 with Recurrent Implantation Failure
por: Ko, Eun-Ju, et al.
Publicado: (2023)

Genetic Polymorphisms in the 3′-Untranslated Regions of SMAD5, FN3KRP, and RUNX-1 Are Associated with Recurrent Pregnancy Loss
por: Kwon, Min-Jung, et al.
Publicado: (2022)

Association Study between the Polymorphisms of Matrix Metalloproteinase (MMP) Genes and Idiopathic Recurrent Pregnancy Loss
por: Park, Han Sung, et al.
Publicado: (2019)

Association between microRNA machinery gene polymorphisms and recurrent implantation failure
por: Lee, Yubin, et al.
Publicado: (2020)

Association between Platelet-Specific Collagen Receptor Glycoprotein 6 Gene Variants, Selected Biomarkers, and Recurrent Pregnancy Loss in Korean Women
por: An, Hui Jeong, et al.
Publicado: (2020)

Genetic Polymorphisms in miR-604A>G, miR-938G>A, miR-1302-3C>T and the Risk of Idiopathic Recurrent Pregnancy Loss
por: Cho, Sung-Hwan, et al.
Publicado: (2021)

Associations between microRNA (miR-25, miR-32, miR-125, and miR-222) polymorphisms and recurrent implantation failure in Korean women
por: Lee, Jeong Yong, et al.
Publicado: (2019)

The association of AGO1 (rs595961G>A, rs636832A>G) and AGO2 (rs11996715C>A, rs2292779C>G, rs4961280C>A) polymorphisms and risk of recurrent implantation failure
por: Ryu, Chang Soo, et al.
Publicado: (2019)

miR-27a and miR-449b polymorphisms associated with a risk of idiopathic recurrent pregnancy loss
por: Rah, HyungChul, et al.
Publicado: (2017)

Study of the Association between microRNA (miR-25T>C, miR-32C>A, miR-125C>T, and miR-222G>T) Polymorphisms and the Risk of Recurrent Pregnancy Loss in Korean Women
por: Lee, Jeong Yong, et al.
Publicado: (2020)

Genetic Variations miR-10aA>T, miR-30cA>G, miR-181aT>C, and miR-499bA>G and the Risk of Recurrent Pregnancy Loss in Korean Women
por: An, Hui-Jeong, et al.
Publicado: (2022)

Association of miR-938G>A Polymorphisms with Primary Ovarian Insufficiency (POI)-Related Gene Expression
por: Cho, Sung Hwan, et al.
Publicado: (2017)

Association between HOX Transcript Antisense RNA Single-Nucleotide Variants and Recurrent Implantation Failure
por: Lee, Jeong Yong, et al.
Publicado: (2021)

Genetic Variants in MicroRNA Machinery Genes Are Associate with Idiopathic Recurrent Pregnancy Loss Risk
por: Jung, Yong Wook, et al.
Publicado: (2014)

Correction: Kim, N.K., et al. Study of the Association between microRNA (miR-25T>C, miR-32C>A, miR-125C>T, and miR-222G>T) Polymorphisms and the Risk of Recurrent Pregnancy Loss in Korean Women. Genes 2020, 11, 354
por: Lee, Jeong Yong, et al.
Publicado: (2020)

Single nucleotide polymorphisms at miR-146a/196a2 and their primary ovarian insufficiency-related target gene regulation in granulosa cells
por: Cho, Sung Hwan, et al.
Publicado: (2017)

Identification of Single Nucleotide Polymorphisms as Biomarkers for Recurrent Pregnancy Loss in Korean Women
por: Kim, Hye In, et al.
Publicado: (2022)

Genetic Association between Inflammatory-Related Polymorphism in STAT3, IL-1β, IL-6, TNF-α and Idiopathic Recurrent Implantation Failure
por: Kwon, Min Jung, et al.
Publicado: (2023)

Analysis of the Association Between MicroRNA Biogenesis Gene Polymorphisms and Venous Thromboembolism in Koreans
por: Ko, Eun Ju, et al.
Publicado: (2019)

Methylenetetrahydrofolate Reductase Polymorphisms and Risk of Recurrent Pregnancy Loss: a Case-Control Study
por: Hwang, Kyu Ri, et al.
Publicado: (2017)

Pregnancy outcomes of elective induction in low-risk term pregnancies: A propensity-score analysis
por: Na, Eun Duc, et al.
Publicado: (2019)

Distribution of Intracranial Major Artery Stenosis/Occlusion According to RNF213 Polymorphisms
por: Kim, Jinkwon, et al.
Publicado: (2020)

Association of Plasminogen Activator Inhibitor-1 (PAI-1) Gene Polymorphisms with Osteoporotic Vertebral Compression Fractures (OVCFs) in Postmenopausal Women
por: Kim, Jung Oh, et al.
Publicado: (2016)

A study of associations between CUBN, HNF1A, and LIPC gene polymorphisms and coronary artery disease
por: Park, Han Sung, et al.
Publicado: (2020)

Outcomes of Empirical Treatment With Intravenous Immunoglobulin G Combined With Low-Dose Aspirin in Women With Unexplained Recurrent Pregnancy Loss
por: Kim, Ju Hee, et al.
Publicado: (2022)

Association of Thymidylate Synthase (TS) Gene Polymorphisms with Incidence and Prognosis of Coronary Artery Disease
por: Kim, Jung Oh, et al.
Publicado: (2023)

The Synergistic Effect of Plasminogen Activator Inhibitor-1 (PAI-1) Polymorphisms and Metabolic Syndrome on Coronary Artery Disease in the Korean Population
por: Park, Han Sung, et al.
Publicado: (2020)

Pathogenetic factors involved in recurrent pregnancy loss from multiple aspects
por: Pei, Chang-Zhu, et al.
Publicado: (2019)

MiR-10a, 27a, 34b/c, and 300 Polymorphisms are Associated with Ischemic Stroke Susceptibility and Post-Stroke Mortality
por: Ryu, Chang Soo, et al.
Publicado: (2020)

Genetic associations between the miRNA polymorphisms miR-130b (rs373001), miR-200b (rs7549819), and miR-495 (rs2281611) and colorectal cancer susceptibility
por: Kim, Eun-Gyo, et al.
Publicado: (2019)

Liquid biopsy prediction of axillary lymph node metastasis, cancer recurrence, and patient survival in breast cancer: A meta-analysis
por: Lee, Ju-Han, et al.
Publicado: (2018)

Circulating Extracellular-Vesicle-Incorporated MicroRNAs as Potential Biomarkers for Ischemic Stroke in Patients With Cancer
por: Bang, Oh Young, et al.
Publicado: (2023)

Pregnancy-Associated Breast Disease: Radiologic Features and Diagnostic Dilemmas
por: Son, Eun Ju, et al.
Publicado: (2006)

The 3′-UTR Polymorphisms in the Thymidylate Synthase (TS) Gene Associated with the Risk of Ischemic Stroke and Silent Brain Infarction
por: Kim, Jung Oh, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_i4dc71th3p6j79nmpe9pjcc4e0