Results 111 to 120 of about 18,846 (258)

Placenta percreta: Histoplathological overview of a rare case

open access: yesJournal of Dr. NTR University of Health Sciences
Placenta percreta is a rare condition characterized by abnormal proliferation and penetration of the chorionic villi through the full thickness of myometrium and serosa. We present a case of 32-year-old female, G4P2L2A1 with low lying placenta.
Greeshma Sasmal   +4 more
doaj   +1 more source

CRISPR‐Cas9‐Generated TXNDC15 c.560delA Homozygous Mouse Model Exhibits Meckel–Gruber Syndrome Phenotype

open access: yesgenesis, Volume 64, Issue 1, February 2026.
ABSTRACT To determine whether TXNDC15 variation causes Meckel–Gruber syndrome (MKS), we assessed the pathogenicity of the frameshift variant c.560delA. A CRISPR–Cas9 generated mouse model carrying the equivalent Txndc15 c.512delA mutation was analyzed at embryonic day 15.5.
Yang Liu   +10 more
wiley   +1 more source

Multiple Regression Analysis of Ultrasound and Clinical Features for Quantitative Evaluation of Tubal Pregnancy Rupture

open access: yesJournal of Ultrasound in Medicine, Volume 45, Issue 2, Page 251-257, February 2026.
The aim is to search for quantitative indicators of ultrasound and clinical features that suggest tubal pregnancy rupture, and to identify independent risk factors for tubal pregnancy rupture through multiple regression analysis. Retrospective analysis of 166 cases of tubal pregnancy was confirmed by laparoscopy, including 97 cases of unruptured type ...
Shuang Gui   +4 more
wiley   +1 more source

Pregnancy and Delivery Outcomes in Vascular Ehlers–Danlos Syndrome: A Retrospective Multicentre Cohort Study

open access: yesBJOG: An International Journal of Obstetrics &Gynaecology, Volume 133, Issue 3, Page 463-470, February 2026.
ABSTRACT Objective We aim to increase knowledge on pregnancy and delivery risks in vascular Ehlers–Danlos Syndrome (vEDS). Our outcomes can contribute to establishing future guidelines for pregnancy and delivery management in women with vEDS. Design Retrospective multicentre cohort study.
Lisa M. van den Bersselaar   +13 more
wiley   +1 more source

A Novel Human Cellular System for Studying Normal Aging and for Anti‐Aging Discovery

open access: yesAging Cell, Volume 25, Issue 2, February 2026.
This study introduces a human cellular aging model using placental trophoblasts (hTSC‐STBs) that mimics key aging features like senescence and genomic instability. It aligns with human tissue aging and responds to anti‐aging treatments, offering a scalable platform to screen potential therapies and bridge lab findings to clinical applications ...
Zhen Feng   +14 more
wiley   +1 more source

Association between alkali and alkaline earth elements in chorionic villus and risk for spontaneous abortion

open access: yesEcotoxicology and Environmental Safety
Exposure to specific alkali and alkaline earth elements(AEs/AEEs) has been reported that are linked to an increased risk of spontaneous abortion. However, the direct evidence of exposure in the uterus are absent.
Meng Lin   +5 more
doaj   +1 more source

The Secretome of Human Trophoblast Stem Cells Attenuates Senescence‐Associated Traits

open access: yesAging Cell, Volume 25, Issue 2, February 2026.
Human trophoblast stem cell‐derived secretome/conditioned medium (hTSC‐CM) and the extracellular vesicles (EVs) therein suppress DNA damage and NF‐κB activation in senescent fibroblasts, in turn reducing the production of senescence‐associated secretory phenotype (SASP) factors. This study highlights hTSC‐CM and EVs as potential senotherapeutic agents.
Kotb Abdelmohsen   +18 more
wiley   +1 more source

Two Cases of Primary Ectopic Ovarian Pregnancy [PDF]

open access: yes, 2011
Primary ovarian pregnancy is one of the rarest varieties of ectopic pregnancies. Patients frequently present with abdominal pain and menstrual irregularities. Intrauterine devices have evolved as probable risk factors.
Ghosal, T   +3 more
core   +1 more source

Prenatal diagnosis and perinatal outcomes of fetuses with congenital duodenal obstruction: A nine‐year retrospective study from China

open access: yesActa Obstetricia et Gynecologica Scandinavica, Volume 105, Issue 2, Page 268-279, February 2026.
A retrospective study of 98 fetuses with congenital duodenal obstruction (CDO) revealed an overall genetic abnormality rate of 20.4%, with trisomy 21 being the predominant chromosomal anomaly. Comprehensive prenatal diagnostic testing is recommended for fetuses with suspected congenital duodenal obstruction, as the genetic findings exert substantial ...
Jianqin Lu   +16 more
wiley   +1 more source

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