Results 81 to 90 of about 9,082,756 (299)
, 2012 Based on simulation of one-dimensional coal and gas outburst and energy conservation principle, a mechanism on spalling lamination and a formula of the lamination characteristic length were promoted.
Yanjina, Song, Guoqiangb, Cheng
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The 9th International RASopathies Symposium
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT The RASopathies are a group of congenital disorders with overlapping clinical manifestations that are caused by pathogenic germline or early somatic variants that result in the hyperactivation of the RAS/mitogen‐activated protein kinase (MAPK) signaling pathway.
Pau Castel +41 more
wiley +1 more source
Lymphatic Abnormalities in Noonan Syndrome Extend Beyond Clinically Apparent Disease
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Lymphatic disease represents a well‐described manifestation of Noonan syndrome (NS), yet the full phenotypic spectrum remains incompletely characterized, especially in asymptomatic individuals. We conducted a cross‐sectional study including 10 individuals with NS (four with peripheral lymphedema and six without) and 10 age‐ and sex‐matched ...
Inger Norlyk Sheyanth +7 more
wiley +1 more source
Advances in Civil Engineering, 2020 For the quantitative recognition and characterization of the flow characteristics of polymorphism coalbed gas in tectonic coal, experiments on pore morphology, pore diameter distribution, and methane adsorption law in outburst tectonic coal were carried ...
Jiazhuo Li +7 more
doaj +1 more source
Numerical analysis on energy-reducing and outburst-eliminating mechanism in coal mass with reaming and cavitation [PDF]
Hydraulic flushing technology had been widely used in the process of gas enhanced extraction in soft coal mass. However, few studies had revealed the energy-reducing and outburst-eliminating mechanism in hydraulic flushing coal mass from the perspective ...
Jiamei CHANG +8 more
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American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Autosomal recessive loss‐of‐function variants in PPP1R13L cause an ultra‐rare cardiocutaneous syndrome characterized by rapidly progressive arrhythmogenic cardiomyopathy (ACM). PPP1R13L encodes iASPP, which has two potentially overlapping mechanisms driving ACM as both a regulator of NFκB‐mediated inflammation and a binding partner within the ...
Aaron Renberg +9 more
wiley +1 more source
An April 1991 outburst from 4U0115+63 observed by BATSE
, 1993 4U0115+63 is a recurrent transient X-ray pulsar in a moderately eccentric orbit with a Be star companion, V635 Cas. Many outbursts from this system have been reported over the past twenty years; yet despite the apparent relation between optical outbursts
Cominsky, L. +5 more
core +2 more sources
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Multiple Acyl‐CoA Dehydrogenase Deficiency (MADD) is an autosomal recessive inborn error of metabolism caused by biallelic pathogenic variants in one of three known genes: ETFA, ETFB, and ETFDH. It can cause multisystem dysfunction, including cardiomyopathy in severe cases.
Yutaka Furuta +17 more
wiley +1 more source
Shock and Vibration, 2019 With mining depths increasing, coal and gas outburst disasters are becoming more and more serious and complicated, which directly restricts the production efficiency of coal mines.
Linchao Dai +6 more
doaj +1 more source