Results 21 to 30 of about 7,212 (260)

c‐Rel–dependent Chk2 signaling regulates the DNA damage response limiting hepatocarcinogenesis

open access: yesHepatology, EarlyView., 2022
In response to genotoxic injury, c‐Rel upregulates ATM‐Chk2‐p53 pathway DNA damage proteins to limiting hepatocarcinogenesis. Abstract Background and Aims Hepatocellular carcinoma (HCC) is a leading cause of cancer‐related death. The NF‐κB transcription factor family subunit c‐Rel is typically protumorigenic; however, it has recently been reported as a
Jack Leslie   +17 more
wiley   +1 more source

Treatment of rosacea patients with broadband pulse light emission using smooth pulse and photon recirculation technologies

open access: yesVestnik Dermatologii i Venerologii, 2017
Goal of the study. To assess the efficacy and safety of using broadband pulse light emission with smooth pulse and photon recirculation technologies in the treatment of patients suffering from erythematous and papulous subtypes of rosacea.
A. A. Kubanova, Y. B. Makhakova
doaj   +1 more source

Hereditary haemorrhagic telangiectasia: A case report

open access: yesSAGE Open Medical Case Reports, 2021
Background: Hereditary haemorrhagic telangiectasia is an autosomal dominant genetic disorder characterized by abnormalities in blood vessel formation. The clinical manifestations of patients affected with hereditary haemorrhagic telangiectasia include ...
Asfandyar Mufti   +3 more
doaj   +1 more source

Life-threatening anaemia in patient with hereditary haemorrhagic telangiectasia (Rendu-Osler-Weber syndrome)

open access: yesOpen Medicine, 2020
Hereditary haemorrhagic telangiectasia (HHT), also known as Rendu-Osler-Weber syndrome, is a rare autosomal dominant vascular disorder. Patients with HHT may present with a wide spectrum of clinical manifestations from epistaxis to clinically significant
Mikołajczyk-Solińska Melania   +4 more
doaj   +1 more source

Brainstem capillary telangiectasias in a pacient with central vestibular syndrome [PDF]

open access: yesRomanian Journal of Neurology, 2010
Capillary telangiectasias repesent one of the four types of brainstem vascular malformations, characterized by multiple thin-walled vascular channels, interposed between normal brain parenchyma of unknown etiology. They are most of the time an incidental
Athena Mergeani, Florina Antochi
doaj   +1 more source

Hyperosmotic stress induces PARP1‐mediated HPF1‐dependent mono(ADP‐ribosyl)ation

open access: yesFEBS Letters, EarlyView.
Sorbitol‐induced hyperosmotic stress rapidly induces reversible mono(ADP‐ribosyl)ation (MARylation) on PARP1 without the signs of genotoxic signaling. We show that PARP1 autoMARylation is HPF1 dependent and forms hydroxylamine‐resistant O‐glycosidic linkages.
Anna Georgina Kopasz   +11 more
wiley   +1 more source

Sclerotherapy. Step by step. Telangiectasia

open access: yesАмбулаторная хирургия, 2019
The article  presents classification, diagnostic  principles  and  modern  technique of phlebosclerosing treatment  of lower limbs telangiectasias.
V. Yu. Bogachev
doaj   +1 more source

Rendu-Osler-Weber syndrome: dermatological approach [PDF]

open access: yesAnais Brasileiros de Dermatologia, 2015
The Rendu-Osler-Weber syndrome is a rare systemic fibrovascular dysplasia, recognized by mucocutaneous telangiectasias, arteriovenous malformations, epistaxis and family history.
Aline Blanco Barbosa   +5 more
doaj   +1 more source

KDM7A and KDM1A inhibition suppresses tumour promoting pathways in prostate cancer

open access: yesMolecular Oncology, EarlyView.
Treatment resistance is a major challenge for patients with advanced prostate cancer. This study examined an alternative approach to target the major prostate cancer‐promoting pathway by targeting epigenetic factors, whose levels are higher in tumours.
Jennie N Jeyapalan   +16 more
wiley   +1 more source

Loss of IGF‐1R impairs DNA‐PKcs recruitment to chromatin leading to defective end‐joining

open access: yesMolecular Oncology, EarlyView.
IGF‐1R promotes radioresistance by facilitating DNA‐PKcs recruitment to chromatin, enabling non‐homologous end‐joining (NHEJ) repair of double‐strand breaks. Inhibition or loss of IGF‐1R disrupts this recruitment to damage sites, driving compensatory reliance on microhomology‐mediated end‐joining (MMEJ) repair.
Matthew O. Ellis   +3 more
wiley   +1 more source

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