نتایج جستجو برای: پدیدهی knock

تعداد نتایج: 15981  

Journal: :International Journal of Engine Research 2022

Knock research is an essential study because knock limits spark-ignition (SI) engine power output, durability, noise, fuel consumption, and emission performance. The thermal efficiency of can be improved by increasing the compression ratio, but at same time it leads to possibility end gas autoignition inside chamber. objective this work was show effect three different ratios (CRs) 8.5, 9.5, 10....

2003
James Allen Fill David B. Wilson

We analyze the two-player game of Knock ’em Down, asymptotically as the number of tokens to be knocked down becomes large. Optimal play requires mixed strategies with deviations of order √ n from the naive law-of-large numbers allocation.

Journal: :Cell Reports 2021

(Cell Reports 33, 108456-1–108456-8.e1–e5; December 1, 2020) In the originally published version of this article, Eran Elhaik was incorrectly spelled in author list. The corrected list appears here and with article online. authors regret error. Rare Variant Burden Analysis within Enhancers Identifies CAV1 as an ALS Risk GeneCooper-Knock et al.Cell ReportsDecember 01, 2020In BriefCooper-Knock al...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2001
M Asahi X Wang T Mori T Sumii J C Jung M A Moskowitz M E Fini E H Lo

Deleterious processes of extracellular proteolysis may contribute to the progression of tissue damage after acute brain injury. We recently showed that matrix metalloproteinase-9 (MMP-9) knock-out mice were protected against ischemic and traumatic brain injury. In this study, we examined the mechanisms involved by focusing on relevant MMP-9 substrates in blood-brain barrier, matrix, and white m...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2008
Cuie Qiu Thomas Zeyda Brian Johnson Ute Hochgeschwender Luis de Lecea Melanie K Tallent

The K(+) M-current (I(M), Kv7) is an important regulator of cortical excitability, and mutations in these channels cause a seizure disorder in humans. The neuropeptide somatostatin (SST), which has antiepileptic properties, augments I(M) in hippocampal CA1 pyramidal neurons. We used SST receptor knock-out mice and subtype-selective ligands to investigate the receptor subtype that couples to I(M...

Journal: :Cancer research 2005
Ee Hong Tan Shing Chuan Hooi Mirtha Laban Esther Wong Sathivel Ponniah Aileen Wee Nai-dy Wang

The CCAAT/enhancer binding protein alpha (C/EBPalpha) is vital for establishing normal hepatic energy homeostasis and moderating hepatocellular growth. CEBPA loss-of-function mutations identified in acute myeloid leukemia patients support a tumor suppressor role for C/EBPalpha. Recent work showed reductions of C/EBPalpha levels in human hepatocellular carcinoma with the reductions correlating t...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2014
Eva Mracsko Arthur Liesz Ana Stojanovic Wilson Pak-Kin Lou Matthias Osswald Wei Zhou Simone Karcher Frank Winkler Ana Martin-Villalba Adelheid Cerwenka Roland Veltkamp

Neuroinflammation plays a key role in secondary brain damage after stroke. Although deleterious effects of proinflammatory cytokines are well characterized, direct cytotoxic effects of invading immune cells on the ischemic brain and the importance of their antigen-dependent activation are essentially unknown. Here we examined the effects of adaptive and innate immune cells-cytotoxic T lymphocyt...

2017
Nikita Zabinyakov Garrett Bullivant Feng Cao Matilde Fernandez Ojeda Zheng Ping Jia Xiao-Yan Wen James J Dowling Gajja S Salomons Saadet Mercimek-Andrews

Pyridoxine dependent epilepsy (PDE) is caused by likely pathogenic variants in ALDH7A1 (PDE-ALDH7A1) and inherited autosomal recessively. Neurotoxic alpha-amino adipic semialdehyde (alpha-AASA), piperideine 6-carboxylate and pipecolic acid accumulate in body fluids. Neonatal or infantile onset seizures refractory to anti-epileptic medications are clinical features. Treatment with pyridoxine, ar...

2007
Chen Lai Xian Lin Jayanth Chandran Hoon Shim Wan-Jou Yang Huaibin Cai

The G59S missense mutation at the conserved microtubule-binding domain of p150 , a major component of dynein/dynactin complex, has been linked to an autosomal dominant form of motor neuron disease (MND). To study how this mutation affects the function of the dynein/dynactin complex and contributes to motor neuron degeneration, we generated p150 glued G59S knock-in mice. We found that the G59S m...

Journal: :Thrombosis and haemostasis 2008
Paul E Monahan

The study of coagulation factors has been rapidly advanced by studies performed in genetically engineered mouse strains. Investigation of factor IX (FIX) has benefited from excellent gene-deleted mouse models that recapitulate many of the features of human haemophilia B. Moreover, advanced positional cloning techniques and availability of technology to allow not only knock-out mice, but also kn...

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