Results 41 to 50 of about 2,541,672 (233)

Increased expression of STAT3 and SOCS3 in placenta from hyperglycemic rats

open access: yesEuropean Journal of Histochemistry, 2019
Signal transducer and activator of transcription 3 (STAT3) is a transcription factor that is activated by interleukin (IL)-6 and IL-10 that generate nearly opposing responses.
Vanessa Dela Justina   +8 more
doaj   +1 more source

Recessive mutation in tetraspanin CD151 causes Kindler syndrome-like epidermolysis bullosa with multi-systemic manifestations including nephropathy [PDF]

open access: yes, 2018
Epidermolysis bullosa (EB) is caused by mutations in as many as 19 distinct genes. We have developed a next-generation sequencing (NGS) panel targeting genes known to be mutated in skin fragility disorders, including tetraspanin CD151 expressed in ...
Abiri, Maryam   +15 more
core   +1 more source

Potential of pre–gestational intake of Laportea interrupta L. (stinging nettle) leaf decoction as an aid for fetal–maternal health

open access: yesAsian Pacific Journal of Reproduction, 2015
Objective: To examine the potential of pre-gestational intake of Laportea interrupta L. (L. interrupta) leaf decoction as an aid for fetal-maternal health by determining its influence on embryonic implantation and growth, placental labyrinth vasculo ...
Jeriz Anne S. de Guzman   +3 more
doaj   +1 more source

Aggressive Surveillance Is Needed to Detect Endoleaks and Junctional Separation between Device Components after Zenith Fenestrated Aortic Reconstruction [PDF]

open access: yes, 2019
Background Junctional separation and resulting type IIIa endoleak is a well-known problem after EVAR (endovascular aneurysm repair). This complication results in sac pressurization, enlargement, and eventual rupture.
Dalsing, Michael C.   +7 more
core   +1 more source

Single-cell and spatial architecture of primary liver cancer

open access: yesCommunications Biology, 2023
Primary liver cancer (PLC) poses a leading threat to human health, and its treatment options are limited. Meanwhile, the investigation of homogeneity and heterogeneity among PLCs remains challenging.
Pei-Yun Zhou   +24 more
doaj   +1 more source

Modeling superimposed preeclampsia using Ang II (Angiotensin II) infusion in pregnant stroke-prone spontaneously hypertensive rats [PDF]

open access: yes, 2018
Hypertensive disorders of pregnancy are the second leading cause of maternal deaths worldwide. Superimposed preeclampsia is an increasingly common problem and often associated with impaired placental perfusion. Understanding the underlying mechanisms and
Beattie, Elisabeth   +7 more
core   +2 more sources

Maternal nano-titanium dioxide inhalation alters fetoplacental outcomes in a sexually dimorphic manner

open access: yesFrontiers in Toxicology, 2023
The placenta plays a critical role in nutrient-waste exchange between the maternal and fetal circulations, thus functioning as an interface that profoundly impacts fetal growth and development. The placenta has long been considered an asexual organ, but,
Julie A. Griffith   +19 more
doaj   +1 more source

Two‐ and three‐dimensional ultrasonographic features related to histopathology of the uterine endometrial‐myometrial junctional zone

open access: yesActa Obstetricia et Gynecologica Scandinavica, 2018
Our aim was to correlate junctional zone thickening and irregularity (junctional zone disease) and other ultrasonographic features of adenomyosis with the histopathology of the endometrial‐myometrial junctional zone.
C. Rasmussen, E. Hansen, M. Dueholm
semanticscholar   +1 more source

Neogenin Recruitment of the WAVE Regulatory Complex to Ependymal and Radial Progenitor Adherens Junctions Prevents Hydrocephalus

open access: yesCell Reports, 2017
Denudation of the ependyma due to loss of cell adhesion mediated by cadherin-based adherens junctions is a common feature of perinatal hydrocephalus. Junctional stability depends on the interaction between cadherins and the actin cytoskeleton.
Conor J. O’Leary   +7 more
doaj   +1 more source

Multigene Next-Generation Sequencing Panel Identifies Pathogenic Variants in Patients with Unknown Subtype of Epidermolysis Bullosa: Subclassification with Prognostic Implications [PDF]

open access: yes, 2017
Purpose: Epidermolysis bullosa (EB), the prototype of heritable blistering diseases, is caused by mutations in as many as 19 distinct genes. In this study, we evaluated the molecular basis of EB in 93 families, many of them of unknown subtype. Methods:
Abiri, Maryam   +15 more
core   +1 more source

Home - About - Disclaimer - Privacy