Results 101 to 110 of about 3,770 (221)

Haplophyllum tuberculatum: An overview [PDF]

open access: yes, 2016
Introduction: Haplophyllum tuberculatum, belonging to the Rutaceae family, is distributed in south-eastern regions of Iran, particularly in Baloochestan.
Arbabi, Mina.   +3 more
core  

Fluorescence studies of natural photosensitizers in oncology and antimicrobial therapy

open access: yesНаучно-технический вестник информационных технологий, механики и оптики
The article provides an overview of current paper on the use of natural photosensitizers for photodynamic therapy and photodynamic inactivation of microorganisms.
D. O. Evtifeev   +3 more
doaj   +1 more source

Solar-Light-Activated Photochemical Skin Injury Induced by Highly Oxygenated Compounds of Sosnovsky’s Hogweed

open access: yesPhotochem
Sosnovsky’s hogweed (Heracleum sosnowskyi Manden.) is an invasive plant species widely distributed across Eastern Europe and Russia that poses a serious threat to human health due to its pronounced phototoxic properties.
Valery M. Dembitsky   +1 more
doaj   +1 more source

British Association of Dermatologists and British Photodermatology Group guidelines for the safe and effective use of psoralen-ultraviolet A therapy 2015 [PDF]

open access: yes, 2016
Abel EA   +65 more
core   +2 more sources

Bioactive phytochemicals modulating skin depigmentation, inflammation and cardiovascular pathways

open access: yesPharmacological Research - Modern Chinese Medicine
Introduction: Vitiligo (leukoderma) is a chronic autoimmune disorder characterized by selective melanocyte loss, resulting in depigmented skin patches.
Trilochan Satapathy, Anjali Minj
doaj   +1 more source

Photoallergic Contact Dermatitis to Brosimum Wood [PDF]

open access: yes, 2008
Brandão, FM   +4 more
core   +1 more source

In vivo mapping of nucleosomes using psoralen-DNA crosslinking and primer extension [PDF]

open access: yes, 2017
By the use of psoralen crosslinking and primer extension, a method was developed which allows the analysis of chromatin structure in vivo.
Sogo, José M., Wellinger, Ralf Erik
core  

Investigation of FANCA mutations in greek patients [PDF]

open access: yes, 2013
Background: Fanconi anemia (FA) is a rare genetic disease characterized by considerable heterogeneity. Fifteen subtypes are currently recognised and deletions of the Fanconi anemia complementation group A (FANCA) gene account for more than 65% of FA ...
Fryssira, Elena   +8 more
core  

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