Results 131 to 140 of about 2,739,321 (263)

Taqâlîd al-Zawâj fî al-I’tiqâd al-Jâwiy (al-Dirâsah al-Naqdiyyah).

open access: yesJournal of Comparative Study of Religions, 2020
This research focuses on solutions to the Javanese Muslim community in order to be able to carry out marriages with Javanese customs which are suitable with Islamic values and avoided from shirk. This research is a qualitative research with a cultural antrolopology approach.
Adib Fuadi Nuriz, Azzamul Azhar
openaire   +2 more sources

HDAC6 inhibition reverses axonal transport defects in motor neurons derived from FUS-ALS patients

open access: yesNature Communications, 2017
Amyotrophic lateral sclerosis (ALS) is a rapidly progressive neurodegenerative disorder due to selective loss of motor neurons (MNs). Mutations in the fused in sarcoma (FUS) gene can cause both juvenile and late onset ALS.
Wenting Guo   +25 more
semanticscholar   +1 more source

Plasma Neurofilament Heavy Chain Levels Correlate to Markers of Late Stage Disease Progression and Treatment Response in SOD1(G93A) Mice that Model ALS [PDF]

open access: yes, 2012
Background: Amyotrophic lateral sclerosis (ALS) is an incurable neurodegenerative disorder characterised by progressive degeneration of motor neurons leading to death, typically within 3–5 years of symptom onset. The diagnosis of ALS is largely reliant
Greensmith Linda   +24 more
core   +1 more source

Small molecule modulation of TDP-43 recruitment to stress granules prevents persistent TDP-43 accumulation in ALS/FTD

open access: yesNeuron, 2019
Stress granules (SGs) form during cellular stress and are implicated in neurodegenerative diseases such as amyotrophic lateral sclerosis and frontotemporal dementia (ALS/FTD). To yield insights into the role of SGs in pathophysiology, we performed a high-
Mark Y. Fang   +4 more
semanticscholar   +1 more source

Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

open access: yes, 2021
Importance: Juvenile amyotrophic lateral sclerosis (ALS) is a rare form of ALS characterized by age of symptom onset less than 25 years and a variable presentation. Objective: To identify the genetic variants associated with juvenile ALS. Design, Setting,
FALS Sequencing Consortium; American Genome Center; International ALS Genomics Consortium; and ITALSGEN Consortium
core  

Comparative Study of Structural and Functional Rearrangements in Skeletal Muscle Mitochondria of SOD1-G93A Transgenic Mice at Pre-, Early-, and Late-Symptomatic Stages of ALS Progression

open access: yesFrontiers in Bioscience-Landmark
Background: Amyotrophic lateral sclerosis (ALS) is a progressive multisystem disease characterized by limb and trunk muscle weakness that is attributed, in part, to abnormalities in mitochondrial ultrastructure and impaired ...
Natalia V. Belosludtseva   +4 more
doaj   +1 more source

Al-Alaqatu Al-Ilmiyati Baina Al-Ulamai Al-Jawina Wa Al-Faulati Al-Usminiyyina Fi Al-Qarni Al-Sadisa Asyara Al-Miladi Ila Qarni Al-Tamina Asyara Al-Miladi

open access: yesIslam Nusantara: Journal for the Study of Islamic History and Culture, 2022
Abstract For approximately five centuries, starting from 1571 and actually ending in 1924, the Ottoman Empire controlled the scientific centers in the Hejaz City. During that time, Ulama Jawi enjoyed the golden age of science. Thoriq Aziz, in his book entitled "Ulama-Ulama Nusantara yang Mempengaruhi Dunia" documented at least three Ulama from ...
openaire   +1 more source

ATXN2 and its neighbouring gene SH2B3 are associated with increased ALS risk in the Turkish population

open access: yes, 2012
Expansions of the polyglutamine (polyQ) domain (≥34) in Ataxin-2 (ATXN2) are the primary cause of spinocerebellar ataxia type 2 (SCA2). Recent studies reported that intermediate-length (27–33) expansions increase the risk of Amyotrophic Lateral Sclerosis
Hilmi Özçelik (5648923)   +35 more
core   +1 more source

A, The Al-DirᾹsah Al-TahlῙliyyah Li MuhtawᾹ Al-KitᾹb Al-MadrasῙy Li Ta’lῙm Al-Lugah Al-’Arabiyyah FῙ Al-Marhalah Al-ṠᾹnawiyyah ’AlᾹ AsᾹs Cefr (Al-Iṭar Al-Marja’Ῑ Al-Aurubbiy Al-Musytarak)

open access: yesRayah Al-Islam, 2022
Knowing the level of content of Arabic textbooks at the high school level is important because it is the starting point in preparing Arabic teaching materials at the university level. Without knowing the level, repetition can occur in determining the level and cause delays in increasing the linguistic level to a higher level.
openaire   +1 more source

ALS Genes in the Genomic Era and their Implications for FTD.

open access: yesTrends in Genetics, 2018
Amyotrophic lateral sclerosis (ALS) is a complex neurodegenerative disease, characterized genetically by a disproportionately large contribution of rare genetic variation.
H. Nguyen   +2 more
semanticscholar   +1 more source

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