Critical level statistics and anomalously localized states at the Anderson transition [PDF]
We study the level-spacing distribution function $P(s)$ at the Anderson transition by paying attention to anomalously localized states (ALS) which contribute to statistical properties at the critical point.
A. G. Aronov +22 more
core +1 more source
Single copy/knock-in models of ALS SOD1 in C. elegans suggest loss and gain of function have different contributions to cholinergic and glutamatergic neurodegeneration [PDF]
Mutations in Cu/Zn superoxide dismutase 1 (SOD1) lead to Amyotrophic Lateral Sclerosis (ALS), a neurodegenerative disease that disproportionately affects glutamatergic and cholinergic motor neurons.
Baskoylu, Saba N +10 more
core +3 more sources
Screening of the transcriptional regulatory regions of vascular endothelial growth factor receptor 2 (VEGFR2) in amyotrophic lateral sclerosis [PDF]
Background Vascular endothelial growth factor (VEGF) has neurotrophic activity which is mediated by its main agonist receptor, VEGFR2. Dysregulation of VEGF causes motor neurone degeneration in a mouse model of amyotrophic lateral sclerosis (ALS), and
Brockington, A. +4 more
core +3 more sources
Al-Tasybīh al-Tamṡīlī, al-Tasybīh Gair al-Tamṡīlī, al-Tasybīh al-Ḍimnī, dan al-Tasybīh al-Maqlūb
Tulisan ini membahas kajian balāgah yaitu ilmu tentang retorika dan stilistika bahasa. Balāgah merupakan salah satu dari sekian banyak disiplin ilmu yang dipergunakan untuk menafsirkan ayat-ayat al-Qur’ān. Ilmu Balāgah mencakup bayān, ma‘ānī, dan badī’ yang satu sama lain saling melengkapi sehingga ketiganya penting untuk dipelajari.
openaire +2 more sources
Noninvasive ¹³C-octanoic acid breath test shows delayed gastric emptying in patients with amyotrophic lateral sclerosis [PDF]
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder characterized by progressive loss of motor neurons. However, ALS has been recognized to also involve non-motor systems.
Folwaczny, Christian +6 more
core +1 more source
Broad clinical phenotypes associated with TAR-DNA binding protein (TARDBP) mutations in amyotrophic lateral sclerosis [PDF]
The finding of TDP-43 as a major component of ubiquitinated protein inclusions in amyotrophic lateral sclerosis (ALS) has led to the identification of 30 mutations in the transactive response-DNA binding protein (TARDBP) gene, encoding TDP-43.
A Yokoseki +46 more
core +1 more source
Digital terrain models (DTM) based on airborne laser scanning (ALS) are an important source for identifying and monitoring archaeological sites and landscapes. However, a DTM is only one of many representations of a given surface.
Michael Doneus +2 more
doaj +1 more source
Structural Diversity of Sense and Antisense RNA Hexanucleotide Repeats Associated with ALS and FTLD
The hexanucleotide expansion GGGGCC located in C9orf72 gene represents the most common genetic cause of amyotrophic lateral sclerosis (ALS) and frontotemporal lobar dementia (FTLD).
Tim Božič +4 more
doaj +1 more source
Al-Ma‘had al-Turāthī wa al-Ta’hīl al- Mihanī:Tajribah Nūr al-Jadīd al-Tawaqu‘i al-Mustaqbal
This paper will discuss the characteristics of pesantren education in relation to vocational education, background and objectives by taking the case of boarding Nurul Jadid, Karanganyar, Paiton, Probolinggo, East Java.Unlike what Abdurrahman Wahid once argues, since the 1970's, the pesantren, traditional Islamic boarding schools, have not been ...
Murodi Murodi, Hamid. W Wahid
openaire +1 more source
Objectives: Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease with an unclear etiology. This study aimed to assess chronic heavy metal exposure in ALS patients in South Korea by comparing hair concentrations of common (Hg, Pb,
Jae-Kook Yoo +8 more
doaj +1 more source

