نتایج جستجو برای: als gene

تعداد نتایج: 1166211  

Journal: :Sustainability 2021

Amaranthus palmeri S. Watson (Amaranthaceae Juss.) is a dioecious noxious weed, native to the Americas, which infests summer crops. It causes high crop losses, and rapidly evolves resistance herbicides. In Europe, A. was recorded mostly as casual alien, but in 2018 it reported infesting soybean field Italy, next year two more populations were found same area. Experiments conducted on these thre...

Journal: :Endocrinology 2000
A Suwanichkul Y R Boisclair R C Olney S K Durham D R Powell

During extrauterine life, insulin-like growth factors (IGFs) circulate in a ternary serum complex with one IGF-binding protein-3 (IGFBP-3) or IGFBP-5 protein and with a single acid-labile subunit (ALS). GH increases levels of this ternary complex; in mice, this effect is achieved in part by the ability of GH to stimulate mouse ALS (mALS) transcription through an interferon-gamma-activated seque...

2017
QianQian Wei QingQing Zhou YongPing Chen RuWei Ou Bei Cao YaQian Xu Jing Yang Hui-Fang Shang

Although the copper/zinc superoxide dismutase-1 (SOD1) gene has been identified in both familial ALS (FALS) and sporadic ALS (SALS), it has rarely been studied in Chinese patients with ALS, and there are few studies with large samples. This study sought to assess the prevalence of SOD1 mutations in Chinese ALS patients. We screened a cohort of 499 ALS patients (487 SALS and 12 FALS) from the De...

2008
John E. Landers Lijia Shi Ting-Jan Cho Jonathan D. Glass Christopher E. Shaw P. Nigel Leigh Frank Diekstra Meraida Polak Ildefonso Rodriguez-Leyva Stephan Niemann Bryan J. Traynor Diane Mckenna-Yasek Peter C. Sapp Ammar Al-Chalabi Anne-Marie A. Wills Robert H. Brown

Amyotrophic lateral sclerosis (ALS) is a progressive, neurodegenerative disorder of upper and lower motor neurons. Genetic variants in the paraoxonase gene cluster have been associated with susceptibility to sporadic ALS. Because these studies have yielded conflicting results, we have further investigated this association in a larger data set. Twenty SNPs spanning the paraoxonase gene cluster w...

Journal: :iranian journal of neurology 0
marzieh khani department of biology, school of science, university of tehran, tehran, iran afagh alavi department of biology, school of science, university of tehran, tehran, iran shahriar nafissi department of neurology, school of medicine, tehran university of medical sciences, tehran, iran elahe elahi department of biology and department of biotechnology, school of science, university of tehran, tehran, iran

background: amyotrophic lateral sclerosis (als) is the most common motor neuron disorder in european populations. als can be sporadic als (sals) or familial als (fals). among 20 known als genes, mutations in c9orf72 and superoxide dismutase 1 (sod1) are the most common genetic causes of the disease. whereas c9orf72 mutations are more common in western populations, the contribution of sod1 to al...

2017
Satoshi Iwakami Yoshiko Shimono Yohei Manabe Masaki Endo Hiroyuki Shibaike Akira Uchino Tohru Tominaga

Severe infestations of Alopecurus aequalis (shortawn foxtail), a noxious weed in wheat and barley cropping systems in Japan, can occur even after application of thifensulfuron-methyl, a sulfonylurea (SU) herbicide. In the present study, nine accessions of A. aequalis growing in a single wheat field were tested for sensitivity to thifensulfuron-methyl. Seven of the nine accessions survived appli...

Journal: :Human molecular genetics 2008
Simon Cronin Hylke M Blauw Jan H Veldink Michael A van Es Roel A Ophoff Daniel G Bradley Leonard H van den Berg Orla Hardiman

Amyotrophic lateral sclerosis (ALS) is an unrelenting neurodegenerative condition characterized by adult-onset loss of motor neurons. Genetic risk factors have been implicated in ALS susceptibility. Copy number variants (CNVs) account for more inter-individual genetic variation than SNPs and have the capacity to alter gene dose and phenotype. We sought to identify the contribution both of commo...

Journal: :Journal of molecular endocrinology 1997
P J Delhanty R C Baxter

The acid-labile subunit (ALS) of the ternary insulin-like growth factor-binding protein complex has a central role in controlling the bioavailability of circulating insulin-like growth factors. We have shown that gene expression of ALS is regulated by a number of factors, particularly growth hormone. Our aim was to characterize the ALS gene in order to define the mechanism of its regulation. So...

Journal: :European journal of neurology 2008
R M Liscic L T Grinberg J Zidar M A Gitcho N J Cairns

Major discoveries have been made in the recent past in the genetics, biochemistry and neuropathology of frontotemporal lobar degeneration (FTLD). TAR DNA-binding protein 43 (TDP-43), encoded by the TARDBP gene, has been identified as the major pathological protein of FTLD with ubiquitin-immunoreactive (ub-ir) inclusions (FTLD-U) with or without amyotrophic lateral sclerosis (ALS) and sporadic A...

2014
Takashi Ayaki Hidefumi Ito Hiroko Fukushima Takeshi Inoue Takayuki Kondo Akito Ikemoto Takeshi Asano Akemi Shodai Takuji Fujita Satoshi Fukui Hiroyuki Morino Satoshi Nakano Hirofumi Kusaka Hirofumi Yamashita Masafumi Ihara Riki Matsumoto Jun Kawamata Makoto Urushitani Hideshi Kawakami Ryosuke Takahashi

BACKGROUND Mutations in the valosin-containing protein (VCP) gene were first found to cause inclusion- body myopathy with early-onset Paget disease and frontotemporal dementia (IBMPFD). Mutations in the VCP gene were later reported to occur in familial amyotrophic lateral sclerosis (ALS). But the role of VCP in the neurodegenerative processes that occur in ALS remains unknown. The purpose of th...

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