نتایج جستجو برای: aloxe3

تعداد نتایج: 25  

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2003
Zheyong Yu Claus Schneider William E Boeglin Lawrence J Marnett Alan R Brash

Lipoxygenase (LOX) enzymes form fatty acid hydroperoxides used in membrane remodeling and cell signaling. Mammalian epidermal LOX type 3 (eLOX3) is distinctive in totally lacking this typical oxygenase activity. Surprisingly, genetic evidence has linked mutations in eLOX3 or a colocalizing enzyme, 12R-LOX, to disruption of the normal permeability barrier of the skin [Jobard, F., Lefèvre, C., Ka...

2012
Gabriella Andreotti Stella Koutros Sonja I. Berndt Kathryn Hughes Barry Lifang Hou Jane A. Hoppin Dale P. Sandler Jay H. Lubin Laurie A. Burdette Jeffrey Yuenger Meredith Yeager Laura E. Beane Freeman Michael C. R. Alavanja

Background. Lipid metabolism processes have been implicated in prostate carcinogenesis. Since several pesticides are lipophilic or are metabolized via lipid-related mechanisms, they may interact with variants of genes in the lipid metabolism pathway. Methods. In a nested case-control study of 776 cases and 1444 controls from the Agricultural Health Study (AHS), a prospective cohort study of pes...

Journal: :Acta dermato-venereologica 2014
Kana Tanahashi Kazumitsu Sugiura Kenji Asagoe Yumi Aoyama Keiji Iwatsuki Masashi Akiyama

Collodion babies are newborns encased in a glistening membrane that cracks in a characteristic manner within 48 h and desquamates in large lamellae after a few days. Most collodion babies later develop one of the several types of autosomal recessive congenital ichthyoses (ARCI), such as lamellar ichthyosis (LI) or congenital ichthyosiform erythroderma; however, about 10% heal spontaneously (1)....

2015
Tao Wang Chenchen Xu Xiping Zhou Chunjia Li Hongbing Zhang Bill Q. Lian Jonathan J. Lee Jun Shen Yuehua Liu Christine Guo Lian Andrzej Slominski

Non-bullous congenital ichthyosiform erythroderma (NBCIE) is a hereditary disorder of keratinization caused by pathogenic variants in genes encoding enzymes important to lipid processing and terminal keratinocyte differentiation. Impaired function of these enzymes can cause pathologic epidermal scaling, significantly reduced skin barrier function. In this study, we have performed a focused, gen...

Journal: :Journal of Investigative Dermatology 2023

Dupilumab, a monoclonal antibody that targets IL-4Ra, has shown significant clinical benefits in modulation of type 2(T2) inflammation atopic dermatitis(AD). To date, there are no detailed proteomic studies longitudinal changes AD skin proteins patients treated with dupilumab. Assessments lesional and non-lesional 20 during 16 weeks dupilumab treatment were done by tape stripping(STS) compared ...

Journal: :Journal of dermatological science 2006
Masashi Akiyama

Autosomal recessive congenital ichthyoses (ARCI) include several severe subtypes including harlequin ichthyosis (HI), lamellar ichthyosis and non-bullous congenital ichthyosiform erythroderma. Patients with these severe types of ichthyoses frequently show severe hyperkeratosis and scales over a large part of the body surface form birth and their quality of life is often severely affected. Recen...

Journal: :Acta dermato-venereologica 2016
Maritta Hellström Pigg Anette Bygum Agneta Gånemo Marie Virtanen Flemming Brandrup Andreas D Zimmer Alrun Hotz Anders Vahlquist Judith Fischer

Autosomal recessive congenital ichthyosis (ARCI) represents a heterogeneous group of rare disorders of cornification with 3 major subtypes: harlequin ichthyosis (HI), lamellar ichthyosis (LI) and congenital ichthyosiform erythroderma (CIE). A 4th subtype has also been proposed: pleomorphic ichthyosis (PI), characterized by marked skin changes at birth and subsequently mild symptoms. In nationwi...

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