Results 161 to 170 of about 56,400 (202)

Association between severe childhood infections and subsequent risk of OCD is largely explained by shared familial factors. [PDF]

BMJ Ment Health
Pol-Fuster J, Kuja-Halkola R, Fernández de la Cruz L, Brikell I, Chang Z, D'Onofrio BM, Larsson H, Lichtenstein P, Beucke JC, De Schipper E, Mataix-Cols D.   +10 more
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Chemical Structures of Quinolinol Compounds Produced by Marine Pseudoalteromonas sp. A1-J11

Chemical Structures of Quinolinol Compounds Produced by Marine Pseudoalteromonas sp. A1-J11
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The 11th IJCAR automated theorem proving system competition – CASC-J11

AI Communications, 2023
The CADE ATP System Competition (CASC) is the annual evaluation of fully automatic, classical logic, Automated Theorem Proving (ATP) systems. CASC-J11 was the twenty-seventh competition in the CASC series. Twenty-four ATP systems competed in the various competition divisions.
Sutcliffe, G., Desharnais, M.
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Study on Wear Properties of J11 Wheel Steel with Nonuniform Microstructure

Journal of Materials Engineering and Performance, 2020
In 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.
Guan-Zhen Zhang, Chun-Peng Liu, Heng Zhang, Qian Li, Rui-Ming Ren   +4 more
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J11 Can Music Therapy Improve The Quality Of Life In Huntington's Disease?

Journal of Neurology, Neurosurgery & Psychiatry, 2014
Background 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.
M. van Bruggen-Rufi, R. Roos, W. Achterberg, A. Vink   +3 more
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J11 Contemporary dance improves motor function and body perception in huntington disease

Clinical therapeutics, 2018
Background 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 dance practice might be unsuitable and alternatives must be explored.
Iris Trinkler, Philippe Chéhère, Julie Salgues, Marie-Lorraine Monin, Sophie Tezenas du Montcel, Sonia Khani, Marcela Gargiulo, Alexandra Durr   +7 more
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Cloning and characterization of a thermostable and pH-stable cellobiohydrolase from Neocallimastix patriciarum J11

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 ...
Hui-Chang, Wang, Yo-Chia, Chen, Ching-Tsan, Huang, Ruey-Shyang, Hseu   +3 more
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Purification and characterization of a cellulolytic multienzyme complex produced by Neocallimastix patriciarum J11

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.
Hui-Chang, Wang, Yo-Chia, Chen, Ruey-Shyang, Hseu   +2 more
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Two new ketene derivatives from the endophytic fungus Daldinia eschscholtzii J11

Phytochemistry Letters, 2023
Song-Mei Lu, Cheng-Juan Liao, Yuan Xu, Teng-Yuan Gui, He-Lin Sui, Min Zhou   +5 more
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J11 Investigating phenocopies in a cohort of south african patients with a huntington’s disease-like phenotype

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, Amanda Krause
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