Results 141 to 150 of about 2,373 (254)

Serum estradiol (E2), progesterone (P), and human chorionic gonadotropin (HCG), D-dimer (D-D) fibrinogen (FIB) levels after low molecular weight heparin sodium on preventing miscarriage in patients with adverse pregnancy and delivery. [PDF]

J Med Biochem
Pei L, Wang T, Yang Q.
europepmc   +1 more source

USP9X as a Candidate Mediator of Prenatal Aspirin‐Induced Ovarian Reserve Reduction in Offspring Mice

Advanced Science, Volume 13, Issue 16, 18 March 2026.
This study suggests that prenatal aspirin exposure is associated with reduced ovarian reserve in offspring, associated with HDAC1‐linked epigenetic downregulation of Usp9x as a candidate mechanism. These preclinical findings provide new insights into fetal‐origin ovarian disorders and contribute to the evidence base concerning aspirin's gestational ...
Yating Li, Caiyun Ge, Wai Yen Yim, Hui Feng, Tiancheng Wu, Lu Chen, Qiaohua Xiong, Shumin Pan, Mei Wang, Huijun Chen, Yuanzhen Zhang, Hui Wang   +11 more
wiley   +1 more source

Prevention of ovarian hyperstimulation syndrome: optimizing habitual stimulation strategies. [PDF]

F S Rep
Quaas AM.
europepmc   +1 more source

Metabolic Reprogramming Driven by Trophoblasts and Decidual XCR1+PMN‐MDSC Crosstalk Controls Adverse Outcomes Associated With Advanced Maternal Age

Advanced Science, Volume 13, Issue 16, 18 March 2026.
The interaction between trophoblasts and decidual polymorphonuclear myeloid‐derived suppressor cells (dPMN‐MDSCs) via the XCL1–XCR1 axis is crucial for fetal development during the third trimester. Disruption of this axis impairs FOXO1 activity and causes metabolic imbalance in dPMN‐MDSCs, contributing to adverse outcomes associated with advanced ...
Meiqi Chen, Yuxiong Guo, Qing Zhao, Jingping Liu, Shuyi Kuang, Zhengcong Huang, Chenlin Lv, Shuxiu Xu, Zekai Zhuang, Anyan Yang, Jing Li, Kai Wu, Yumei He   +12 more
wiley   +1 more source

Recurrent pregnancy loss, psychological distress and wellbeing support for women: a mixed-methods analysis. [PDF]

BMC Womens Health
Aventin Á, Robinson M, White J, Galeotti M.   +3 more
europepmc   +1 more source

Time‐Efficient and Informatic‐Skill‐Light Gap‐Filling for Telomere‐to‐Telomere Genome Assembly

Advanced Science, Volume 13, Issue 14, 9 March 2026.
The paper introduces a novel auxiliary software toolbox GapSuite, consisting of two tools Gap‐Aid and Gap‐Graph, which guides users to fill gaps in chromosome‐level genome assembly using sequence‐extension‐based and assembly‐graph‐based strategies. The two tools enable users with limited informatics expertise to efficiently complete gap‐filling on ...
Dong Xu, Xianjia Zhao, Lianguang Shang, Shaolong Tian, Yanchun Li, Huaming Wen, Qiang Xu, Dongxi Li, Weihua Pan   +8 more
wiley   +1 more source

Identification of potential NAD-related biomarkers of recurrent miscarriage risk. [PDF]

Hum Reprod
Cuny H, Shand AW, Goth J, Sheng DZ, Tossey T, Martin EMMA, Sipka A, Aleshin O, Schneuer FJ, Nassar N, Dunwoodie SL.   +10 more
europepmc   +1 more source

Soybean growth habit influence on development, yield, and seed quality in North Carolina full‐season soybean production

Agronomy Journal, Volume 118, Issue 2, March/April 2026.
Abstract North Carolina soybean [Glycine max (L.) Merr.] production has historically relied on later maturing determinate varieties, but recent availability of later maturing indeterminate varieties has raised questions about growth habit effects on soybean production in the region. This study evaluated the impact of soybean growth habit (indeterminate
Lilly R. Bunch, Rachel A. Vann, Dominic D. Reisig, Guy D. Collins, Kelly O'Reilly, Donald R. Stokes   +5 more
wiley   +1 more source

Protecting Embryo with Chinese Herbal Medicine for Treating Habitual Miscarriages----- 4 Cases Study Enclosed [PDF]

Perceptions in Reproductive Medicine, 2018
openaire   +1 more source

GATA3 Deletion Associated With Juvenile Idiopathic Arthritis: Expanding the Phenotypic Spectrum of Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia (HDR) Syndrome

American Journal of Medical Genetics Part A, Volume 200, Issue 3, Page 733-737, March 2026.
ABSTRACT Hypoparathyroidism, sensorineural deafness, and renal dysplasia (HDR) syndrome is caused by pathogenic variants in the GATA3 gene located on chromosome 10p14. Here we present a 10‐year‐old girl with HDR syndrome who also has oligoarticular juvenile idiopathic arthritis (JIA).
Lauren N. Meiss, Amanda V. Karam, Julia Shalen, David E. Tunkel, Belina Y. Yi, Kelsey S. Guthrie, Emily M. Kudalkar, Anna E. Patrick, Sonja A. Rasmussen   +8 more
wiley   +1 more source