Results 181 to 190 of about 5,300 (235)
Some of the next articles are maybe not open access.
Study on Wear Properties of J11 Wheel Steel with Nonuniform Microstructure
Journal of Materials Engineering and Performance, 2020In actual wheel–rail systems, a nonuniform microstructure of the wheel and rail materials is a serious problem. A double-disk rolling wear test device was used to study the influence of the nonuniform microstructure on the wear properties of wheel materials in the present study.
Guanqun Zhang +4 more
semanticscholar +2 more sources
Biochemical and Biophysical Research Communications, 2014
Understanding the roles of the components of the multienzyme complex of the anaerobial cellulase system, acting on complex substrates, is crucial to the development of efficient cellulase systems for industrial applications such as converting lignocellulose to sugars for bioethanol production.
Huichang Wang, Yo-Chia Chen, R. Hseu
semanticscholar +3 more sources
Understanding the roles of the components of the multienzyme complex of the anaerobial cellulase system, acting on complex substrates, is crucial to the development of efficient cellulase systems for industrial applications such as converting lignocellulose to sugars for bioethanol production.
Huichang Wang, Yo-Chia Chen, R. Hseu
semanticscholar +3 more sources
Protein Expression and Purification, 2013
An 1888-bp cDNA designated celA, isolated from a cDNA library of Neocallimastix patriciarum J11 was cloned. The celA had an open reading frame of 1530 bp encoding J11 CelA of 510 amino acids. The primary structure analysis of J11 CelA revealed a complete cellulose-binding domain at the N-terminal, followed by an Asn, Ala, Gly, Gln and Pro-rich linker ...
Huichang Wang +3 more
semanticscholar +3 more sources
An 1888-bp cDNA designated celA, isolated from a cDNA library of Neocallimastix patriciarum J11 was cloned. The celA had an open reading frame of 1530 bp encoding J11 CelA of 510 amino acids. The primary structure analysis of J11 CelA revealed a complete cellulose-binding domain at the N-terminal, followed by an Asn, Ala, Gly, Gln and Pro-rich linker ...
Huichang Wang +3 more
semanticscholar +3 more sources
J11 Can Music Therapy Improve The Quality Of Life In Huntington’s Disease?
Journal of Neurology, Neurosurgery & Psychiatry, 2014Background Since there is no cure for Huntington’s disease (HD) yet the intention of all forms of treatment is to improve quality of life. All treatment must be individually tailored, as the symptoms and signs are different for each person and change over time. Music therapy (MT) recognises individual needs and can be adapted to meet them.
Karen Jones +4 more
semanticscholar +2 more sources
J11 Contemporary dance improves motor function and body perception in huntington disease
Clinical therapeutics, 2018Background Physical exercise improves neurological conditions, but adherence is hard to establish. Dance might be a promising alternative. However, for patients with Huntington Disease (HD), who suffer from rhythmic movement execution deficits, metric ...
I. Trinkler +7 more
semanticscholar +2 more sources
Putting a minicomputer onto a chip-PDP-11 to J11
Microprocessors and Microsystems, 1984Abstract The architecture and instruction set of the PDP-11 are outlined. The construction of the J11 is given followed by software facilities that distinguish the processor. Hardware implementation is examined and the results of performance benchmarks given.
openaire +4 more sources
Journal of Neurology, Neurosurgery & Psychiatry, 2016
Background Huntington’s disease (HD) is caused by an unstable expanded trinucleotide (CAG) repeat in the huntingtin (HTT) gene. Presentation involves a clinical triad of symptoms: behavioural problems, movement disorder and cognitive decline. Elsewhere, between 1 and 7% of individuals diagnosed do not carry the mutation and are said to have an HD ...
Fiona K. Baine, A. Krause
semanticscholar +2 more sources
Background Huntington’s disease (HD) is caused by an unstable expanded trinucleotide (CAG) repeat in the huntingtin (HTT) gene. Presentation involves a clinical triad of symptoms: behavioural problems, movement disorder and cognitive decline. Elsewhere, between 1 and 7% of individuals diagnosed do not carry the mutation and are said to have an HD ...
Fiona K. Baine, A. Krause
semanticscholar +2 more sources
Journal of Neurology, Neurosurgery & Psychiatry, 2012
Background and Aims The characteristic symptoms of chorea in Huntington9s disease, have been related to a dysfunction of dopamine transmission. Furthermore, psychological symptoms like anhedonia and altered motivation and drive as functions of the dopaminergic reward system are common and often manifest already early in the course of the disease ...
K. Malejko +4 more
semanticscholar +2 more sources
Background and Aims The characteristic symptoms of chorea in Huntington9s disease, have been related to a dysfunction of dopamine transmission. Furthermore, psychological symptoms like anhedonia and altered motivation and drive as functions of the dopaminergic reward system are common and often manifest already early in the course of the disease ...
K. Malejko +4 more
semanticscholar +2 more sources
Two new ketene derivatives from the endophytic fungus Daldinia eschscholtzii J11
Phytochemistry Letters, 2023Song Lu +5 more
semanticscholar +2 more sources

