Results 51 to 60 of about 17,532 (272)

Non-invasive prenatal screening: invasive implications and technological overreach

open access: yes, 2023
Cell-free foetal DNA (cffDNA) screening, herein referred to as non-invasive prenatal screening (NIPS), has seen widespread uptake as a preferred prenatal screening tool over the past decade. NIPS examines maternal serum for foetal genetic material and is
Kalle Amolins (16849723)
core   +3 more sources

Prenatal ultrasound screening for fetal anomalies and outcomes in high-risk pregnancies due to maternal HIV infection : a retrospective study [PDF]

open access: yes, 2013
Objective: To assess the prevalence of prenatal screening and of adverse outcome in high-risk pregnancies due to maternal HIV infection. Study design: The prevalence of prenatal screening in 330 pregnancies of HIV-positive women attending the ...
Louwen, Frank   +6 more
core   +1 more source

A two-year experience of non-invasive prenatal testing (NIPT) at an urban tertiary medical center in South Korea

open access: yesTaiwanese Journal of Obstetrics & Gynecology, 2019
Objective: To report our experience of implementing non-invasive prenatal testing (NIPT) in a tertiary urban academic medical center in South Korea.
Joseph J. Noh   +5 more
doaj   +1 more source

Correlation of neonatal blood serology with non-invasive prenatal screening test for RHD determination.

open access: yes, 2022
Correlation of neonatal blood serology with non-invasive prenatal screening test for RHD determination.
Bekele Chakiso (12257093)   +5 more
core   +1 more source

Progressive trends in prenatal genetic screening

open access: yesIberoamerican Journal of Medicine, 2022
According to the global report on birth defects in 2021, it is estimated that 8 million children are born with birth defects of genetic origin annually.
Kirolos Eskandar
doaj   +1 more source

Progressive trends in prenatal genetic screening

open access: yesJKS (Jurnal Kedokteran Syiah Kuala), 2023
According to the global report on birth defects in 2021, it is estimated that 8 million children are born with birth defects of genetic origin annually.
Kirolos S. Eskandar
doaj   +1 more source

Zinc Exposure Causes Disulfidptosis to Induce Miscarriage by Up‐Regulating GATA1/METTL1/SLC7A11 Axis

open access: yesAdvanced Science, EarlyView.
Zn exposure up‐regulates GATA1, promoting GATA1‐mediated METTL1 and SLC7A11 transcription. It also enhances METTL1‐mediated m7G modification on SLC7A11 mRNA, increasing SLC7A11 mRNA stability. Ultimately, Zn exposure up‐regulates SLC7A11 at both transcriptional and post‐transcriptional levels, causing disulfidptosis. Knockdown of murine Slc7a11, Gata1,
Wenxin Huang   +16 more
wiley   +1 more source

Non-invasive foetal sexing : medical test or a new tool for sex selection? [PDF]

open access: yes, 2011
Recent scientific developments in prenatal testing, based on foetal DNA in maternal blood, now allow non-invasive foetal sexing early in pregnancies at risk of a sex-linked disorder. In such cases, these novel non-invasive tests can improve prenatal care
Szczepura, Ala, Osipenko, Leeza
core  

Clinician views and experiences of non‐invasive prenatal genetic screening tests in Australia

open access: yesAustralian and New Zealand Journal of Obstetrics and Gynaecology, 2022
BackgroundNon‐invasive prenatal screening (NIPS) is being increasingly used by expectant parents. Much provision of this test in Australia is occurring in clinical settings where specialised genetic counselling is unavailable, such as general practice.
Shannon McKinn   +7 more
openaire   +5 more sources

G3BP1 Succinylation at K413 is Critical for Cardiac Function by Modulating PI3K‐AKT‐mTOR Signal Axis

open access: yesAdvanced Science, EarlyView.
Schematic illustrating the impact of G3BP1 succinylation at K413 on cardiac function. In the healthy human heart, G3BP1 succinylation maintains homeostatic mTOR signaling. In patients with dilated cardiomyopathy (DCM) and heart failure (HF), G3BP1 de‐succinylation induces RagA expression and disrupts the binding of the TSC1/2 complex, leading to the ...
Yuan Zhang   +9 more
wiley   +1 more source

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