Results 141 to 150 of about 97,443 (231)

In vitro differentiation and ultrastructure of human extravillous trophoblast (EVT) cells

open access: hybrid, 1993
Olga Genbačev   +3 more
openalex   +1 more source

Highly Tunable and Cell‐Remodelable Thiol‐ene Alginate‐Peptide Crosslinked Hydrogels to Recreate Cellular and Organoid Microenvironments for Biofabrication

open access: yesAdvanced Healthcare Materials, Volume 15, Issue 9, 6 March 2026.
Norbornene‐functionalized alginate is crosslinked with a di‐thiolated peptide sequence cleavable by cell‐secreted matrix metalloproteinases and decorated with cell‐adhesion peptides upon exposure to UV. Thyroid follicles, endometrial and intestinal organoids are encapsulated in a gentle manner with high cell viability and correct phenotype ...
Julia Fernández‐Pérez   +8 more
wiley   +1 more source

Endogenous retroviral elements LTR8B and MER65 rewire PSG9 regulation to control trophoblast syncytialization and pre-eclampsia risk. [PDF]

open access: yesGenome Biol
Singh M   +20 more
europepmc   +1 more source

Enrichment of circulating trophoblasts from maternal blood using filtration-based Metacell® technology

open access: gold, 2022
Jana Weymaere   +6 more
openalex   +1 more source

Endometrial Assembloid Model Reveals Endometrial Gland Development Regulation by Estradiol‐Driven WNT7B Suppression

open access: yesAdvanced Science, Volume 13, Issue 13, 3 March 2026.
This study developed a 3D endometrial assembloid model to study how uterine glands form and develop. They discovered key interactions between different cell types and identified WNT7B as a regulator controlled by estradiol‐mediated TGFβ1‐VDR interaction.
Xintong Li   +12 more
wiley   +1 more source

Imaging Of A Three Dimensional Model System For Invasive Growth Of Trophoblasts

open access: green, 2020
Gerit Moser   +5 more
openalex   +1 more source

Paternal MHC expression on mouse trophoblast affects uterine vascularization and fetal growth [PDF]

open access: bronze, 2011
Zofia E. Madeja   +8 more
openalex   +1 more source

A Novel Homozygous CUL7 Variant in an Iranian Patient Expands the Genetic Spectrum of 3 M Syndrome

open access: yesClinical Case Reports, Volume 14, Issue 3, March 2026.
ABSTRACT 3 M syndrome (3MS) is a rare autosomal recessive disorder characterized by severe prenatal and postnatal growth retardation, distinctive facial features, and skeletal abnormalities, while cognitive development remains unaffected. This study reports a novel homozygous pathogenic variant in the CUL7 gene identified in an Iranian girl with ...
Maryam Arefzadeh   +8 more
wiley   +1 more source

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