نتایج جستجو برای: htra1

تعداد نتایج: 528  

Journal: :Molecular Vision 2008
Peter J Francis Hong Zhang Andrew DeWan Josephine Hoh Michael L Klein

PURPOSE To estimate the joint effects of single nucleotide polymorphisms (SNPs) in the genes complement factor H (CFH), HtrA serine peptidase 1 (HTRA1), and age-related maculopathy susceptibility 2 (LOC387715/ARMS2) in a Caucasian age related macular degeneration (AMD) case-control cohort. METHODS We genotyped three SNPs, rs1061170 (exon 9, CFH), rs11200638 (HTRA1 promoter, -512 bp), and rs10...

2017
Olga Rotan Katharina N Severin Simon Pöpsel Alexander Peetsch Melisa Merdanovic Michael Ehrmann Matthias Epple

The efficient intracellular delivery of (bio)molecules into living cells remains a challenge in biomedicine. Many biomolecules and synthetic drugs are not able to cross the cell membrane, which is a problem if an intracellular mode of action is desired, for example, with a nuclear receptor. Calcium phosphate nanoparticles can serve as carriers for small and large biomolecules as well as for syn...

Journal: :Vision Research 2008
Daniel Gibbs Zhenglin Yang Ryan Constantine Xiang Ma Nicola J. Camp Xian Yang Hayou Chen Adam Jorgenson Vincent Hau Andrew DeWan Jiexi Zeng Jennifer Harmon Jeanette Buehler John M. Brand Josephine Hoh D. Joshua Cameron Manjusha Dixit Zongzhong Tong Kang Zhang

Age-related macular degeneration (AMD) is a complex disorder with genetic and environmental influences. The genetic influences affecting AMD are not well understood and few genes have been consistently implicated and replicated for this disease. A polymorphism (rs11200638) in a transcription factor binding site of the HTRA1 gene has been described, in previous reports, as being most significant...

Alireza Irani, Amin Reza Nikpoor, Fazel Gorjipour, Hajar Aryan, Hossein Nazari, Kazem Mousavizadeh, Khalil Ghasemi Falavarjani, Mohammad Askari, Mohammad Hosein Sanati, Mohsen Mazidi,

Background: Half of the cases of vision loss in people under 60 years of age have been attributed to age-related macular degeneration (AMD). This is a multifactorial disease with late onset. It has been demonstrated that many different genetic loci are implicated in the risk of developing AMD in different populations. In the current study, we investigated the association of high-temperature &lr...

Journal: :Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2004
Toshio Fukutake

Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL) is a single-gene disorder directly affecting the cerebral small blood vessels, that is caused by mutations in the HTRA1 gene encoding HtrA serine peptidase/protease 1 (HTRA1). CARASIL is the second known genetic form of ischemic, nonhypertensive, cerebral small-vessel disease with an identified...

Journal: :reports of biochemistry and molecular biology 0
mohammad askari department of biotechnology, pasteur institute of iran, tehran, iran amin reza nikpoor department of immunology, school of medicine, mashhad university of medical sciences, mashhad, iran fazel gorjipour physiology research center, faculty of medicine, iran university of medical sciences, tehran, iran mohsen mazidi biochemistry and nutrition research center, mashhad university of medical sciences, mashhad, mohammad hosein sanati national institute for genetic engineering and biotechnology, tehran, iran hajar aryan fazeli-sanati genetic laboratory, tehran, iran

background: half of the cases of vision loss in people under 60 years of age have been attributed to age-related macular degeneration (amd). this is a multifactorial disease with late onset. it has been demonstrated that many different genetic loci are implicated in the risk of developing amd in different populations. in the current study, we investigated the association of high-temperature ‎re...

Journal: :PLoS Medicine 2007
Anne E Hughes Nick Orr Chris Patterson Hossein Esfandiary Ruth Hogg Vivienne McConnell Giuliana Silvestri Usha Chakravarthy

BACKGROUND Age-related macular degeneration (AMD) is the major cause of blindness in the elderly. Those with the neovascular end-stage of disease have irreversible loss of central vision. AMD is a complex disorder in which genetic and environmental factors play a role. Polymorphisms in the complement factor H (CFH) gene, LOC387715, and the HTRA1 promoter are strongly associated with AMD. Smokin...

Journal: :Journal of Analytical Science and Technology 2022

Abstract Extracellular matrix (ECM) proteins play a pivotal role in cell growth and differentiation. To characterize aged ECM proteins, we compared the proteomes by shotgun method of young (passage #15) late senescent #40) human dermal fibroblasts (HDFs) using SDS-PAGE coupled with LC–MS/MS. The relative abundance identified was determined mol% individual as semi-quantitative index. Fifteen inc...

2012
Gergely Losonczy Attila Vajas Lili Takács Erika Dzsudzsák Ágnes Fekete Éva Márhoffer László Kardos Éva Ajzner Begoña Hurtado Pablo Garcia de Frutos András Berta István Balogh

Age-related macular degeneration (AMD) is the leading cause of blindness in the elderly in the developed world. Numerous genetic factors contribute to the development of the multifactorial disease. We performed a case-control study to assess the risk conferred by known and candidate genetic polymorphisms on the development of AMD. We searched for genetic interactions and for differences in dry ...

2014
Michael W. Risør Ebbe Toftgaard Poulsen Line R. Thomsen Thomas F. Dyrlund Tania A. Nielsen Niels Chr. Nielsen Kristian W. Sanggaard Jan J. Enghild

Human HtrA1 (high-temperature requirement protein A1) belongs to a conserved family of serine proteases involved in protein quality control and cell fate. The homotrimeric ubiquitously expressed protease has chymotrypsin-like specificity and primarily targets hydrophobic stretches in selected or misfolded substrate proteins. In addition, the enzyme is capable of exerting autolytic activity by r...

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