말단비대증 거인증

양병철 대한영상의학회 1975 대한영상의학회지 Vol.11 No.2

A Radiological analysis was made of 13 cases of confirmed acromegaly and gigantism. And observation was made in skeleton and soft tissue of patients at Yonsei University from 1968 to 1973. The results was following as; 1. Main clinical symptoms were headache (8/13) and visual disturbances (5/13) in acromegaly and gigantism. 2. Characteristic radiologic findings were analyzed in 13 cases. a. Plain skull show marked thickenning of skull vault, prominent frontal bossing, thickenning of external occipital protuberance, basal kyphosis increment and decreased facial angle. b. Facial bone show lower positioning of the symphysis of mandible and hyoid bone, curved hard palate, protrusion of tongue and flaring of the teeth. c. Acromegalic measurement of vertebra show increased height of body, interpedicular distance and marginal degenrative changes of vertebra. d. Increased size of hand length, P-M joint spaces of hand, increased tuft width and sesamoid index were shown. e. Marked thick nning of heal pad are also demonstrated. e. Marked thickenning of heel pad are also demonstrated. Details of analysis disclosed overlapping of signs of each indivisualized skeleton and soft tissue.

GFP 및 hFSH Gene을 이용한 형질전환 복제수정란의 생산

양병철,임기순,김동훈,이상기,박수봉,성환후,민관식,이연근,장원경 한국동물번식학회 2003 Reproductive & Developmental Biology(Supplement) Vol.27 No.1s

고능력 한우의 채셰포를 이용한 핵이식 수정란 생산 및 이식

양병철,임기순,성환후,임석기,이상기,이명식,장원경,정일정,김경남 한국동물번식학회 2002 Reproductive & developmental biology Vol.26 No.1

GFP Gene Transfected Cell과 Non Tranfsfected Cell의 핵이식후 발달

양병철,임기순,성환후,임석기,이상기,오현주,이연근,박진기,장원경 한국동물생명공학회(구 한국동물번식학회) 2002 Reproductive & developmental biology Vol.26 No.1

한우 농가의 번식우 관리와 송아지 생산 현황

양병철,강성식,김의형,장선식,양보석,이석동,조상래 한국수정란이식학회 2017 한국동물생명공학회지 Vol.32 No.3

This study was conducted to investigate the breeding status of farms to improve the production efficiency of Hanwoo calf. The study was conducted on 45 farms divided into two groups. This study was conducted to investigate the breeding size and breeding area of Hanwoo cows. The average age at first delivery of Hanwoo was 28.7 months. The number of artificial insemination per pregnancy was 1.45±0.32, and the number of artificial insemination days after birth was 119.8 days. Conception rates were 75.2±16.93% for small farms and 70.6±17.46% for medium sized farms and 71.4±11.03% for large farms. When we looked at farming methods, ‘the farmers using estrus observation aids’ had 10.42% higher calf production rate than the ‘unused farmers’. The farms vaccinated with IBR and BVDV for breeding cattle showed a 4.41% decrease in abortion, stillbirth and mortality. According to farming conditions, conception rate and delivery rate improved by 3.47% and 18.29%, respectively, when grazing and exercising were performed. Observation, immunization and grazing were found to be important indicators for improving calf production efficiency in Hanwoo farm. This study can be used as a research data to improve the reproductive rate of farmhouse sites through the survey on the breeding status of Hanwoo farmers.

GFP 및 hFSH Gene을 이용한 형질전환 복제수정란의 생산

양병철,임기순,김동훈,이상기,박수봉,성환후,민관식,이연근,장원경 한국동물생명공학회(구 한국동물번식학회) 2003 Reproductive & developmental biology Vol.27 No.1

hFSH 유전자가 도입된 소 태아섬유아세포를 이용한 형질 전환 복제 수정란의 발달

양병철,임기순,김동훈,민관식,윤두학,박효숙,김세웅,황인선,서진성,성환후,양보석 韓國受精卵移植學會 2006 한국동물생명공학회지 Vol.21 No.1

The purpose of this study was to develope the transgenic cattle expressing hFSH into the urine using the nuclear transfer. To produce the interest gene in urine, the specific vector was ligated with hFSH gene undo. maUII promoter. The fetal fibroblast cells (KbFF) were isolated from a 45-day male fetus. The hFSH gene was co-transfected with pcDNA3 (neo) vector to KbFF cells by electroporation. The gene-transfected cells were cultured with G-418 selection medium for 2 weeks. Selected colonies were confirmed by PCR. For nuclear transfer, enucleated bovine oocytes were transferred with hFSH transfected or nontransfected fetal fibroblasts. The cleavage and blastocyst formation rates were significantly lower (p<0.05) in cloned embryos transfected with hFSH gene (68.7% and 15.7%) than in those non-transfected (67.6% and 24.5 %), respectively. Apoptosis analysis showed no difference between hFSH transfected and non-transfected blastocysts (p>0.05). The blastocysts were transfected to 77 (control 24, hFSH 53) recipient cows. Two calves were born (1.9%) following transfer with NT embryos transfected with hFSH gene, but they were confirmed not to be transgenic calves. This result shows that the hFSH colonies were mixed with transfected and non transfected cells. Further research will be needed for selection and establishment of gene transfected cells. 본 연구의 목적은 요를 통해 hFSH를 발현하는 형질 전환 소의 생산이다. 요의 분비와 관련 있는 유전자로서 mUII promoter를 사용하여 hFSH유전자를 구성했다. 태아섬유아세포(KbFF)는 임신 45일령의 태아(male)에서 채취하였다. hFSH gene은 pcDNA3(neo) vector와 같이 KbFF 세포에 electroporation 방법으로 transfection하였다. 유전자를 transfection한 세포는 G-418로 2주 동안

동결속도와 평형시간이 소 미성숙 난자의 동결 융해후 생존율에 미치는 영향

양병철,양보석,성환후,임기순,최선호,장원경,진동일,임경순 한국가축번식학회 2001 Reproductive & developmental biology Vol.25 No.1

The present study was undertaken to investigate the effects of cooling rate and equilibration time on the survival, in vitro maturation and development to embryos of frozen-thawed bovine immature oocytes(Germinal Vesicle Stage). The cryoprotectants are used 10% ethylene glycol(EG) as permeating cryoprotectant and 0.05M sucrose(S) or trehalose(T) as low molecular weight nonpermeating cryoprotectants and 5% ficoll(F) or polyvinylpyrrolidone(PVP) as high molecular weight nonpermeating cryoprotectants. Four freezing solution were uysed in this experiment(EFT: 10% EG + 5% F + 0.05M T, EFS: 10% EG + 5% F + 0.05M S, EPT: 10% EG + 5% P + 0.05M T, EPS: 10% EG + 5% P + 0.05M S). The best equilibration time and freezing solution was 15 min in EPT(83% survival rate of frozen-thawed bovine immature oocytes). When frozen-thawed bovine oocytes were cultured following IVM and IVF, there was no significant difference in cleavage and development rates among the EFT, EFS, EPT and EPS solutions. When 9 blastocysts derived from frozen bovine oocytes were transferred to 6 recipients, two recipients were pregnant. And one was aborted at 45 days of pregnancy and the other had a stillbirth.

전국민 의료보험에 따른 농어촌병원의 실태

양병철,Yang, Byeong-Cheol 대한병원협회 1989 대한병원협회지 Vol.18 No.5

Microdrop과 Straw 방법으로 초자화 동결한 소 난자의 생존율에 관한 연구

양병철,양보석,성환후,임석기,박수봉,장원경,이창규 한국동물자원과학회 2002 한국축산학회지 Vol.44 No.6

본 연구는 소 난자의 초자화 동결 방법을 설정하기 위하여 체외성숙 소 난자에서 난구세포가 부착된 상태 또는 제거한 상태로 microdrop (MD)방법과 straw (Straw) 방법을 이용하여 초자화 동결하여 생존율을 검사하였다. 동결 융해난자는 a) 단위발생을 유도하였고 b) 체외수정 후 전핵 형성을 관찰하였으며 c) 체외수정 후 수정란 발달을 검사하였다. 초자화 동결 난자의 생존율은 MD 방법을 이용하였을 때가 Straw를 이용하였을 때 보다 높았다 (92.50 vs. 74.19%, p<0.05). MD 방법을 이용하였을 때 대부분의 난자가 생존을 하였다. 단위발생을 유도하였을 때 난할율과 배반포 발달율은 MD (45.05%, 10.81%, p<0.05)가 Straw 방법 보다 높았다 (27.17%, 6.52%, p<0.05). 난구세포의 부착 유무에 따라 동결 융해 후 체외수정 하여 자웅 전핵 형성을 각각 검사하였다. 난구세포 제거 난자에서는 MD와 Straw 방법으로 동결 융해하였을 때 차이가 없었다(80.36% vs. 67.31%, p<0.05). 정상 수정율 (2PN)에서는 세 처리간에 차이가 없었다. (Fresh; 54.55% vs. MD; 42.22% vs. Straw; 37.14%, p>0.05). 그러나 미수정란 (<1PN)은 Fresh 난자가 동결융해 난자보다 유의적으로 낮았다 (Fresh; 32.47% vs. MD; 57.78% and Straw 62.86%, p<0.05). 다정자 침입은 (3PN) 신선란 (12,99%)에서 발생하였으나 동결 융해 난자에서는 발생하지 않았다. 난구세포가 제거된 난자에서, 정상 수정율 (2PN)은 Fresh와 동결 융해 난자간에 유의적인 차이를 보였다 (Fresh; 59.38% vs. MD; 17.31% and Straw; 30.43%, p<0.05). 또한 미수정율 (<1PN)에 있어서도 신선란과 동결 융해난은 유의적인 차이를 보였다 (Fresh; 23.44% vs. MD; 73.08% and Straw 58.70%, p<0.05). 다정자 침입 (3PN, >4PN)은 신선란과 동결 융해란 모두에서 나타났다. 체외수정 후, 난구세포가 부착된 난자의 2세포기 발달율은 신선란에 비하여 MD 또는 Straw 처리구에서 유의적으로 낮았다 (Fresh; 81.76% vs. MD; 22.22% and Straw; 11.36%, p<0.05). 동결융해난자는 배반포 발달율에 있어서도 신선란에 비하여 유의적으로 낮았다 (Fresh; 28.38 vs. MD; 1.71% and Straw 0%, p<0.05). 난구세포가 제거된 난자에서 2세포기 발달율은 신선란과 MD에서 차이가 없었다 (27.59% vs. 19.25%, p<0.05), 그러나 배반포 발달율에 있어서는 신선란이 MD 또는 Straw 처리구보다 유의적으로 높았다 (4.31% vs. 0.62% and 0%, respectively; p<0.05). 이상의 결과에서, 초자화 동결융해한 소 난자는 체외수정 후 배반포로 발달이 가능함을 나타내주고 있다. To establish vitrification method for bovine oocytes, mature bovine oocytes were vitrified by microdrop (MD) or straw (Straw) method and the viability of vitrified oocytes with or without cumulus cells (CC) were examined by several methods; a) parthenogenetic activation; b) pronuclear formation after in vitro fertilization (IVF); and c) embryonic development after IVF. The survival rate of vitrified oocytes by MD was significantly higher than by Straw (92.50 vs. 74.19%, p<0.05). Most of the oocytes survived from vitrification using the MD methods. Cleavage and blastocyst development of parthenogenetically activated oocytes were higher in MD (45.05% and 10.81%, respectively; p<0.05)) than those in Straw method (27.17% and 6.52%, respectively; p<0.05). Male and female pronuclear formation of vitrified-thawed oocytes with or without cumulus cells (CC) after IVF were examined, respectively. The survival rate of vitrified oocytes by MD without CC was no difference between MD and Straw (80.368.14% vs. 67.31%). Normal fertilization (2PN) rates were not different among groups (Fresh; 54.55% vs. MD; 42.22% vs. Straw; 37.14%, p>0.05). While no fertilization (<1PN) rates were significantly different between fresh and vitrified-thawed groups (Fresh; 32.47% vs. MD; 57.78% and Straw 62.86%, p<0.05). The polyspermy (3PN) was appeared in the fresh (12.99%), but no appeared in the vitrified-thawed groups. In the without CC, normal fertilization (2PN) rates were significantly different between fresh and vitrified-thawed oocytes (Fresh; 59.38% vs. MD; 17.31% and Straw; 30.43%, p<0.05). Moreover, no fertilization (<1PN) rates were significantly different between fresh and vitrified-thawed groups (Fresh; 23.44% vs. MD; 73.08% and Straw 58.70%, p<0.05). The polyspermy (3PN, >4PN) was appeared not only fresh but vitrified-thawed groups. After IVF, two-cell developmental rates of vitrified oocytes with CC by MD and Straw were significantly low compared to fresh oocytes (Fresh; 81.76% vs. MD; 22.22% and Straw; 11.36%, p<0.05). Blastocyst developmental rates of vitrified oocytes also were significantly low compared to fresh oocytes (Fresh; 28.38 vs. MD; 1.71% and Straw 0%, p<0.05). In the without CC, two-cell developmental rates were no differnce between Fresh and MD (27.59% vs. 19.25%, p<0.05), while blastocyst rates were difference between Fresh and MD or Straw (4.31% vs. 0.62% and 0%, respectively; p<0.05). In conclusion, the results indicate that the vitrified bovine oocytes have the ability to develop to the blastocyst stage after IVF.