Results 121 to 130 of about 353,849 (343)

ATF3 Deficiency Exacerbates Ageing‐Induced Atherosclerosis and Clinical Intervention Strategy

open access: yesAdvanced Science, EarlyView.
Targeting ATF3 with terazosin to against VSMC Senescence and atherosclerosis. TZ reduces the binding affinity of YTHDF2 to Atf3 mRNA, while enhancing mRNA stability. ATF3 promotes Atg7 transcription, enhancing autophagy. ATG7 binds to ATF3 in the cytoplasm, facilitating ATF3 translocation to the nucleus and establishing positive feedback. By modulating
Hao Nie   +11 more
wiley   +1 more source

Genital Vulvar Lichen Sclerosus in Monozygotic Twin Women: A Case Report and Review of the Literature

open access: yesCase Reports in Dermatology, 2013
Lichen sclerosus et atrophicus is a skin disease of multifactorial etiology which appears in patients with genetic or hormonal predisposition and autoimmune disease.
Georgeta Doulaveri   +4 more
doaj   +1 more source

Phosphorus Vacancy‐Induced Built‐In Electric Field for Electromagnetic Properties Modulation

open access: yesAdvanced Science, EarlyView.
The advantages of defect‐induced polarization resulting from group VA anion vacancies, particularly phosphorus vacancies (VP) are analyzed in comparison to the anion vacancies of other elements. P atoms possess both plentiful high‐energy unpaired valence electrons in 3p orbitals and moderate nonmetallicity, thus the selection of VP for regulating EM ...
Yu Zhang   +8 more
wiley   +1 more source

The awareness of the citizens of Swietokrzyskie Voivodeship on the genetic predisposition on cancer

open access: yesJournal of Education, Health and Sport, 2017
Introduction: Cancers are the major concern of the modern world, they are in fact the fourth most common cause of death in the world and second in developed countries. The root cause of tumour development lies in genetics.
Izabela Kamila Wojarska
doaj   +1 more source

Attitudes Toward Updated Genetic Testing Among Patients with Unexplained Mismatch Repair Deficiency [PDF]

open access: yes, 2018
Individuals who have colorectal cancer (CRC) or endometrial cancer (EC) displaying loss of immunohistochemical (IHC) staining of one or more mismatch repair (MMR) proteins without a causative germline mutation are said to have unexplained mismatch repair
Omark, Jessica
core   +1 more source

Macrophage‐Mediated Transport of Insoluble Indirubin Induces Hepatic Injury During Intestinal Inflammation

open access: yesAdvanced Science, EarlyView.
Plant‐derived bioactive molecules with low solubility and permeability induce hepatocyte injury, though the mechanisms driving their hepatic effects remain poorly understood. This study identifies a novel transport pathway in which poorly soluble indirubin accumulates in the liver via macrophage‐mediated uptake in Peyer's patches, exacerbating hepatic ...
Yiqi Xu   +9 more
wiley   +1 more source

Genetics and Economic Mobility [PDF]

open access: yes, 2008
Presents a literature review on the link between genetic traits, such as cognitive skills, health, mental health, personality, and appearance, and academic and economic success.
Jessica Kronstadt
core  

SUMOylation is a Translatable Target in Hypoxic MNPs Regulating Retinal Vasculopathy

open access: yesAdvanced Science, EarlyView.
During ischemic retinopathy/retinal vasculopathy, UBC9‐mediated SUMOylation in retinal macrophages enhances their pro‐angiogenic capacity via hypoxia‐induced SUMOylation of FUS at K327/K502. This modification suppresses FUS binding to the Vegfa mRNA 3’UTR, stabilizing transcripts and facilitating VEGFA production. Targeting UBC9 inhibition can serve as
Zheng Zhong   +9 more
wiley   +1 more source

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