Results 111 to 120 of about 957,134 (321)

Molecular bases of the excretion of fetal bile acids and pigments through the fetal liver-placenta-maternal liver pathway

open access: yesAnnals of Hepatology, 2005
Since the excretion of potentially toxic cholephilic organic anions (COAs) produced by the fetus, such as bile acids and biliary pigments, cannot be performed by the fetal liver alone, the placenta and the maternal liver must play a key role ...
José J.G. Marín   +4 more
doaj   +1 more source

Effects of Maternal Low Protein Diet on Expression of Drug Transporters in the Blood-Brain Barrier of Adult Offspring [PDF]

open access: yes, 2012
Adverse uterine environment, manifested as low birth weight (LBW), has been shown to predispose individuals to hypertension, diabetes, and obesity by mechanisms that are just beginning to be understood.
Hastings, Bonnie L.
core   +1 more source

Fetal membrane imaging and the prediction of preterm birth: a systematic review, current issues, and future directions [PDF]

open access: gold, 2016
Vanessa Nunes   +5 more
openalex   +1 more source

Therapeutic strategies for MMAE‐resistant bladder cancer through DPP4 inhibition

open access: yesMolecular Oncology, EarlyView.
We established monomethyl auristatin E (MMAE)‐resistant bladder cancer (BC) cell lines by exposure to progressively increasing concentrations of MMAE in vitro. RNA sequencing showed DPP4 expression was increased in MMAE‐resistant BC cells. Both si‐DPP4 and the DPP4 inhibitor sitagliptin suppressed the viability of MMAE‐resistant BC cells.
Gang Li   +10 more
wiley   +1 more source

Reproductive organ on-a-chip technologies and assessments of the fetal-maternal interface

open access: yesFrontiers in Lab on a Chip Technologies
In this review, we discuss recent reproductive organ-on-a-chip (OoC) experiments that encompass multiple target areas of investigation, including model fabrication strategies, transport mechanisms, and immunology.
Hannah A. Richards   +4 more
doaj   +1 more source

Bacterial isolates from patients with preterm labor with and without preterm rupture of the fetal membranes [PDF]

open access: bronze, 1999
Hiroshige Mikamo   +5 more
openalex   +1 more source

Peroxidasin enables melanoma immune escape by inhibiting natural killer cell cytotoxicity

open access: yesMolecular Oncology, EarlyView.
Peroxidasin (PXDN) is secreted by melanoma cells and binds the NK cell receptor NKG2D, thereby suppressing NK cell activation and cytotoxicity. PXDN depletion restores NKG2D signaling and enables effective NK cell–mediated melanoma killing. These findings identify PXDN as a previously unrecognized immune evasion factor and a potential target to improve
Hsu‐Min Sung   +17 more
wiley   +1 more source

Optimum Mode of Delivery in Gestations Complicated by Preterm Premature Rupture of Membrane During 32-37 weeks of Gestation

open access: yesAdvanced Medical Journal
Background and objectives: Preterm premature rupture of membrane is amniotic fluid leakage due to fetal membrane rupture before 37 gestational weeks. The aim was to know the optimum mode of delivery in pregnant women with preterm premature rupture of ...
Shana Pishtiwan Mohammed Baqi   +1 more
doaj   +1 more source

Fetal collagenase gene-gene interactions: Is there evidence for amplification of preterm premature rupture of membrane (PPROM) risk? [PDF]

open access: bronze, 2005
Alison G. Cahill   +4 more
openalex   +1 more source

Dammarenediol II enhances etoposide‐induced apoptosis by targeting O‐GlcNAc transferase and Akt/GSK3β/mTOR signaling in liver cancer

open access: yesMolecular Oncology, EarlyView.
Etoposide induces DNA damage, activating p53‐dependent apoptosis via caspase‐3/7, which cleaves PARP1. Dammarenediol II enhances this apoptotic pathway by suppressing O‐GlcNAc transferase activity, further decreasing O‐GlcNAcylation. The reduction in O‐GlcNAc levels boosts p53‐driven apoptosis and influences the Akt/GSK3β/mTOR signaling pathway ...
Jaehoon Lee   +8 more
wiley   +1 more source

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