Results 91 to 100 of about 12,622 (181)
EFFICIENCY ANALYSIS OF HASHING METHODS FOR FILE SYSTEMS IN USER MODE [PDF]
Научно-технический вестник информационных технологий, механики и оптики, 2013 The article deals with characteristics and performance of interaction protocols between virtual file system and file system, their influence on processing power of microkernel operating systems. User mode implementation of ext2 file system for MINIX 3 OS
E. Y. Ivanov, M. S. Kosyakov
doaj
Assessment of Noise Reduction Concepts for Leading-Edge Slat Noise [PDF]
The leading-edge slat of a high-lift airfoil can be a significant noise contributor during aircraft landing. This paper summarizes the effects of several passive noise reduction devices on the 30P30N high-lift airfoil.
Cattafesta, Louis N., III +7 more
core +1 more source
Mutation Screening of the EXT1 and EXT2 Genes in Patients with Hereditary Multiple Exostoses
The American Journal of Human Genetics, 1997 Hereditary multiple exostoses (HME), the most frequent of all skeletal dysplasias, is an autosomal dominant disorder characterized by the presence of multiple exostoses localized mainly at the end of long bones. HME is genetically heterogeneous, with at least three loci, on 8q24.1 (EXT1), 11p11-p13 (EXT2), and 19p (EXT3).
Philippe, Christophe +6 more
openaire +2 more sources
Cell Reports, 2015 Collective cell migration is a highly regulated morphogenetic movement during embryonic development and cancer invasion that involves the precise orchestration and integration of cell-autonomous mechanisms and environmental signals.
Marina Venero Galanternik +2 more
doaj +1 more source
Zhongshan Daxue xuebao. Yixue kexue ban, 2011 【目的】研究EXT1与EXT2基因在我国南方正常人及致病性突变已明确的遗传性多发性骨软骨瘤病人中的多态性。【方法】 选取50例中国南方健康汉族个体及13例致病突变已明确的遗传性多发性骨软骨瘤病人，提取基因组DNA，对包含5’UTR区、编码区、外显子-内含子交界区及3’UTR区的PCR产物进行直接测序。 鉴定基因内的遗传变异，并将结果和国际数据库中的数据进行对比。【结果】 在所有研究对象中共发现15个不同的EXT1基因的单核苷酸多态性(SNPs)：3个在编码区，为同义突变，11个在内含子区，1个在3 ...
doaj
EXT1 and EXT2 regulate chondrogenesis by modulation of WNT signaling [PDF]
Osteoarthritis and Cartilage, 2018 X. Wang, S. Monteagudo, R. Lories
openaire +1 more source
Identification of a new mutation in an Iranian family with hereditary multiple osteochondromas
Therapeutics and Clinical Risk Management, 2016 Susan Akbaroghli,1,* Maryam Balali,2,* Behnam Kamalidehghan,3,4 Siamak Saber,4 Omid Aryani,5 Goh Yong Meng,6 Massoud Houshmand4 1Mofid Children’s Hospital, Shahid Beheshti University of Medical Sciences, 2ENT and Head & Neck Research Center ...
Akbaroghli S +6 more
doaj