http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
루프 분할과 종속함수를 이용한 다중첨자 중첩루프의 종속성 제거 기법
박상일,양황규,윤성대 東西大學校 2001 동서논문집 Vol.7 No.-
In this paper, we propose a new method to parallelize multidimensional subscript loop with non-uniform distance. A loop comprise most of the computation in a program and the most important source of parallelism. Multidimensional subscript within a loop difficult to determine for distance to be required loop dependence elimination. Therefore, we propose new methods that used dependency function to eliminate dependence.
Expression Analysis of the Ligand to Ly-6E.1 Mouse Hematopoietic Stem Cell Antigen
Hwang, Dae-Youn,Min, Dul-Lei,Sonn, Chung-Hee,Chang, Mi-Ra,Lee, Mi-Hyun,Paik, Sang-Gi,Kim, Young-Sang The Korean Society for Integrative Biology 1997 Korean journal of biological sciences Vol.1 No.1
Ly-6E.1 antigen was proposed as a regulatory molecule of T lymphocyte activation, a hematopoietic stem cell marker, a memory cell marker, and an adhesion molecule. Though there were several reports suggesting the presence of Ly-6 ligand, the characterization of the ligand was not yet performed, As an attempt to screen the expression of Ly-6E.1 ligand, we prepared a probe for detecting Ly-6E.1 ligand by producing a fusion protein between Ly-6E.1 and $hlgC_{r1}$, A mammalian cell expression vector with Ly-6E.$1/hlgC_{r1}$ chimeric cDNA was transfected in SP2/0-Ag14 myeloma cells, and stable transfectants were selected. The fusion protein was produced as a dimer and maintained the epitopes for monoclonal antibodies specific for Ly-6E.1 and for anti-human lgG antibody. The purified fusion protein through Gammabind G column was used for FACS analyses for the expression of Ly-6E.1 ligand. The fusion protein interacted with several cell lines originating from B cells, T cells, or monocytes. The fusion Protein also strongly stained bone marrow, lymph node, and spleen cells, but thymic cells weakly, if any. The staining was more obvious in C57BL/6 $(Ly-6^b)$ than Balb/c $(Ly-6^a)$ mice. These results suggest that the interaction of Ly-6E.1 with Ly-6E.1 ligand may function both in the stem cell environment and in the activation of mature lymphocytes. The fusion protein may be a valuable tool in characterization of biochemical properties of the Ly-6E.1 ligand and, further, in isolating its cDNA.
Expression Analysis of the Ligand to Ly-6E.1 Mouse Hematopoietic Stem Cell Antigen
Hwang, Dae Youn,Min, Dullei,Sonn, Chung Hee,Chang, Mi Ra,Lee, Mi Hyun,Paik, Sang-Gi,Kim, Young Sang 충남대학교 생물공학연구소 1998 생물공학연구지 Vol.6 No.-
Ly-6E.1 antigen was proposed as a regulatory molecule of T lymphocyte activation, a hematopoietic stem cell marker, a memory cell marker, and an adhesion molecule. Though there were several reports suggesting the presence of Ly-6 ligand, the characterization of the ligand was not yet performed. As an attempt to screen the expression of Ly-6E.1 ligand, we prepared a probe for detecting Ly-6E.1 ligand by producing a fusion protein between Ly-6E.1 and hlgC_r1. A mammalian cell expression vector with Ly-6E.1/hlgC_r1 chimeric cDNA was transfected in SP2/0-Ag14 myeloma cells, and stable transfectants were selected. The fusion protein was produced as a dimer and maintained the epitopes for monoclonal antibodies specific for Ly-6E.1 and for anti-human lgG antibody. The purified fusion protein through Gammabind G column was used for FACS analyses for the expression of Ly-6E.1 ligand. The fusion protein interacted with several cell lines originating from B cells, T cells, or monocytes. The fusion protein also strongly stained bone marrow, lymph node, and spleen cells, but thymic cells weakly, if any. The staining was more obvious in C57BL/6 (Ly-6^b) than Balb/c (Ly-6^a) mice. These results suggest that the interaction of Ly-6E.1 with Ly-6E.1 ligand may function both in the stem cell environment and in the activation of mature lymphocytes. The fusion protein may be a valuable tool in characterization of biochemical properties of the Ly-6E.1 ligand and, further, in isolating its cDNA.
( Youn Sun Son ),( Bong Yeon Hwang ),( Dae Taek Lee ),( Yoon Jung Bae ) 한국운동영양학회 2014 Physical Activity and Nutrition (Phys Act Nutr) Vol.18 No.2
Youn Sun Son, Bong Yeon Hwang, Dae Taek Lee and Yoon Jung Bae. Effects of active drinking practices on fluid consumptionand sweat rate while exercising in a hot environment. JENB., Vol. 18, No. 2, pp.215-223, 2014 [Purpose]To examine the effectsof active drinking practices on fluid consumption and sweat rate while exercising in a hot environment. [Methods]Nine mencompleted two experiments. Each consisted of 3 phases: pre-testing (pre), training period, and post-testing (post). During testing,the subjects ran on a treadmill at a moderate intensity for 90 min at 39 ± 1℃ followed by a 3-h recovery. They drank ad libitum. During training, they ran for 90 min for 7 days while either drinking actively (AH, 150% of weight loss) or passively (PH,50% of weight loss). [Results]The actual volume consumed in training was three times greater during AH than during PH. Inpost during AH, the volume of drinking was two times greater than pre (1592 ± 953 and 855 ± 551 mL, respectively; p < 0.05). No difference in volume consumption during PH between pre and post was found. The sweat loss during exercise was greaterin post (1377 ± 956 mL) than in pre (558 ± 642 mL) during AH (p < 0.05), but not during PH. Rectal temperature and heartrate decreased after training. Serum osmolality following exercise were not different than the baseline or between the conditions. [Conclusion]Active drinking practices while exercising in a hot environment induced greater voluntary fluid intake and sweatloss. [Keyword]voluntary intake, rehydration, thermoregulation.