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- 주제어 : Oramics (검색결과 6 건)
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Cleaning Sounds: Analyzing Oram’s Tumblewash
Eric Delgado(에릭 델가도) 한국전자음악협회 2023 에밀레 Vol.21 No.-
This paper examines the composition Tumblewash by Daphne Oram and how the composer’s ideas about sound are incorporated into the work. Frequency and spectrogram analyses show the relationship between recorded acoustic sounds and synthesized sounds created by the Oramics machine.
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신수환(Suhwan Shin),이호준(Hojoon Lee) 한국정보보호학회 2023 정보보호학회논문지 Vol.33 No.2
ORAM(Oblivious RAM)은 사용자가 믿을 수 없는 서버, 혹은 하드웨어를 이용할 때 해당 기기에서 발생할 수 있는 부채널 공격을 방어할 수 있는 알고리즘이다. ORAM은 데이터 접근 패턴을 감추어 해당 접근 패턴을 통해 정보가 유실되는 것을 방어하게 된다. 그러나, ORAM은 하드웨어의 보안을 강화하나 그로 얻는 이점에 비해 훨씬 큰 처리 속도 감소를 유발하는 단점이 존재하여 현재까지 실용화 되지 못하였다. 본 논문에서는 새롭게 개발되고 있는 하드웨어인 PIM(Process In Memory)를 활용하여 ORAM을 가속화하여 실용적으로 활용할 수 있는 방안을 모색해 보고자 한다. ORAM(Oblivious RAM) is an algorithm that defends side channel attacks when the user uses an untrusted server or hardware. ORAM defends against leaks of information by hiding data access patterns. However, ORAM is not in practical use because as ORAM reinforces hardware security, it also has a severe disadvantage in processing speed. In this paper, we suggest using newly introduced hardware, PIM (Process In Memory), to accelerate ORAM and use it practically.
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정상적인 부모에서 산전초음파로 진단된 Holt-Oram 증후군 1 예
이정건(Jung Gun Lee),최안나(An Na Choi),지은경(Eun Gyung Jee),권태희(Tae Hee Gwon),이용희(Yong Hee Lee),이숙환(Sook Hwan Lee),조주연(Joo Yeon Jo),정창조(Chang Jo Jung),계정웅(Jung Woong Gye),이정노(Jung No Lee) 대한산부인과학회 2000 Obstetrics & Gynecology Science Vol.43 No.11
Holt-Oram Syndrome is an autosomal dominant disorder characterized by the association of upper-limb abnormalities and congenital heart disease. A woman with no family history of genetic disease underwent antenatal sonography at 27 weeks' menstrual age to screen for fetal anomalies. Ultrasonography revealed abnormalities in the upper limbs. The limb abnormalities included abscence of bilateral thumbs and radius: the left humus was short. Pregnancy termination was performed. The postnatal chromosomal analysis revealed a normal 46XX karyotype and the autopsy finding confirmed the Holt-Oram syndrome. We report a case of Holt-Oram Syndrome in fetus with unaffected parents with brief of the literatures.
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이환된 산모에서 산전 초음파로 진단된 Holt-Oram 증후군
서은정 ( Eun Jung Seo ),김광준 ( Gwang Jun Kim ),손문성 ( Mun Seong Son ),이의돈 ( Eui Don Lee ) 대한산부인과학회 2003 Obstetrics & Gynecology Science Vol.46 No.2
The Holt-Oram syndrome or cardiomelic syndrome is characterized by the association of upper limb and heart malformations. Most frequently, abnormalities of the thumb and secundum atrial septal defects are associated with the disease. The mode of inheritan
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A Familial Case with Holt-Oram Syndrome with a Novel TBX5 Mutation
Lee, Beom Hee,Kim, Yoo-Mi,Kim, Gu-Hwan,Kim, Young-Hwue,Yoo, Han-Wook Korean Society of Medical Genetics and Genomics 2012 대한의학유전학회지 Vol.9 No.2
Holt-Oram syndrome (HOS) is the most common heart-hand syndrome, which is inherited in an autosomal dominant manner, but most cases are sporadic. This condition is characterized by upper-extremity malformations involving radial-ray, thenar, and carpal bones, and congenital heart malformations including atrial septal defect and ventricular septal defect. It is caused by mutations in the TBX5 gene. In this report, a Korean case with HOS is described, which is inherited from her father. A novel nonsense mutation, $p.Glu294^*$, was identified. This is the first Korean case with HOS confirmed by genetic testing.
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A Familial Case with Holt-Oram Syndrome with a Novel TBX5 Mutation
Beom Hee Lee,Yoo-Mi Kim,Gu-Hwan Kim,Young-Hwue Kim,Han-Wook Yoo 대한의학유전학회 2012 대한의학유전학회지 Vol.9 No.2
Holt-Oram syndrome (HOS) is the most common heart-hand syndrome, which is inherited in an autosomal dominant manner, but most cases are sporadic. This condition is characterized by upper-extremity malformations involving radial-ray, thenar, and carpal bones, and congenital heart malformations including atrial septal defect and ventricular septal defect. It is caused by mutations in the TBX5 gene. In this report, a Korean case with HOS is described, which is inherited from her father. A novel nonsense mutation, p.Glu294*, was identified. This is the first Korean case with HOS confirmed by genetic testing.
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