• 한국가금학회지
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• 제17권4호
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• pp.269-274
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• 1990

일본산메추리(Coturnix coturnix japonica)의 핵형연구를 위하여 정소조직 및 백혈구, 초기태아조직들로서 염색체 분석을 수행하였다. 이들 염색체의 수는 정상 이배체(2n)가 78개로 나타나고, 계2 감수분열 중기상태의 정모세포의 관찰에서 반수체(n)가 39개로 나타났다. 한편 8개의 대형염색체 및 성 염상체에 대한 형태적 분석은 동원체지수 및 상대적 길이비로서 측정하였다. 이용된 여러 조직간의 염색체의 형태적 차이는 거의 없는 것으로 나타났으나 4번 염색체템서 p-alm의 존재유무에 따라 상당한 변이를 나타내었다.

• 생명과학회지
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• 제9권6호
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• pp.704-708
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• 1999

This research was carried out for evaluating diagnostic value of antibody test in Fragile X syndrome. In antibody test of control individuals and carriers with a premutation, FMRP were detected in the lymphocytes, whereas the lymphocytes of male Fragile X syndrome patients were devoid of FMRP. Five Fragile X syndrome male patient, two Fragile X syndrome female patients, three carriers were diagnosed by southern blot. Five boys who were diagnosed as the patients by antibody test were turned out full mutation and having multiple smear beside normal single band. However, fragile site of X chromosome was not expressed in Fragile X syndrome patients by chromosome analysis. These results showed that antibody test was a fast and simple method, but the diagnostic power was "perpect" for males, whereas the results were less specific for females.r females.

• Journal of Plant Biology
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• 제38권4호
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• pp.321-328
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• 1995

Calli obtained from basal disc explants of Allium victorialis var.platyphyllum wre grown in three kinds of nutrient media (MS, BDS, and B5), and the frequencies of mitotic index and the chromosomal aberrations were analysed. The mitotic index varied from 0.55% to 1.01% with respect to culture media and ages. The mitotic irregularities like micro-, bi- and multi-nuclei, chromosome bridge and laggards were noted in each types of calli. The chromosome number variations observed in metaphase stage were identified aneuploid and tetraploid. Structural variations such as dicentric chromosomes, centromere breakage and small chromosomes were observed. Relationship between basal medium and chromosomal variability was not observed in this study. But, in BDS medium, NAA and BA had a more effect on number variation than kinetin.

• 한국어류학회지
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• 제20권1호
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• pp.61-65
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• 2008

멸종위기에 처한 한국 고유종인 미꾸리과(Cobitidae) 소형어류 좀수수치, Kichulchoia brevifasciata의 핵형을 분석하였다. 전라남도 고흥군 금산면에서 6개체를 채집하여 핵형분석 결과 염색체 수는 2n=48 으로서 16 meta-submetacentric, 32 subtelo-telocentric chromosomes로 구성되어 있었으며 FN=64 이었고 유연관계에 있는 수수미꾸리, Niwaella multifasciata와 핵형과 구성에 있어 큰 차이를 나타냈다.

• 한국동물위생학회지
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• 제33권2호
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• pp.207-211
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• 2010

None of the numerous published canis idiogram and karyotypes has yet been generally accepted as a standard one because the dog has 76 acrocentric autosomes of similar size and shape. The karyotypes of DongGyeongi dog were analysed by conventional trypsin/Giemsa staining (GTG-banding techniques), and were compared with one another. There were no variations in karyotypes which were analysed by conventional GTG-banding techniques, but differences were observed in G-banding patterns with sapsaree (or canis familiaris strains). It is not clear that these disagreements in G-banding patterns between strains of dog were caused by chromosome polymorphism or a difference in interpretation.

• 한국동물학회지
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• 제16권4호
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• pp.211-217
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• 1973

Streptomyces caespitosus에서 分離된 抗生物質인 Mitomycin C를 Chinese hamster, Cricetulus griseus (2n=22) euploid 細胞朱인 22Emb. (♀, 20일된 embryo에서 培養한 것)과 5PSP (♂, polyoma transformed subclone)에 分量과 時間을 달리해서 處理했을 경우 일어나게 되는 特異한 染色體 異常을 觀察하였다. Mitomycin C의 分量과 處理時間 그리고 細胞朱에 따라서 染色體에 미치는 影響이 한결같지 않지만 第1, 第2 染色體의 region 5와 7, 그리고 X 染色體의 第2 收縮環(secondary constriction)에 보다 甚한 染色體 切斷을 보여 주었다. 이것은 Mitomycin C가 特히 染色體의 人形成體(nucleolar-organizar)에 關聯되어 일어나는 現象이 아닌가 생각된다.

• Animal Systematics, Evolution and Diversity
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• 제2권1호
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• pp.1-10
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• 1986

문경산 흰 넓적다리 붉은 쥐, Apodemus peninsulae peninsulae, 의 염색체 핵형 분석과 단변량 및 다변량분석방법들을 사용한 등줄쥐, Apodemus agrarius coreae, 와의 형태적 형질의 비교를 하였다. 흰 넓적다리 붉은 쥐의 염색체수는 2n=50-54R지 수적 변이를 보였다. 차단부 염색체의 수는 48개로 개체간에 일정하였으나 , 중부 염색체의 수는 2-6개의 변이가 나타났다. 형태적 형질의 분석결과는 등줄쥐보다 흰 넓적다리 붉은 쥐가 크다고 판정되었으며 가장 구별이 잘 되는 경구개의 길이였다.

• Journal of Genetic Medicine
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• 제9권1호
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• pp.35-37
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• 2012

Emanuel syndrome is a rare genomic syndrome which is characterized by multiple congenital anomalies and developmental disability. This syndrome is related to the presence of the supernumerary derivative chromosome originating from both chromosome 11 and 22. In most cases, one of the parents is a balanced carrier of a translocation. Our case results from 3:1 meiotic segregation of the maternal translocation carrier and is a rare case in Korea confirmed by genetic analysis.

• Animal Bioscience
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• 제34권4호
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• pp.482-488
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• 2021

Objective: This study was conducted to estimate effect of single nucleotide polymorphisms (SNP) on the estimated breeding value of Hungarian Grey (HG) bulls and to find markers associated with horn colour. Methods: Genotypes 136 HG animals were determined on Geneseek high-density Bovine SNP 150K BeadChip. A multi-locus mixed-model was applied for statistical analyses. Results: Six SNPs were identified to be associated (-log10P>10) with green and white horn. These loci are located on chromosome 1, 3, 9, 18, and 25. Seven loci (on chromosome 1, 3, 6, 9, 10, 28) showed considerable association (-log10P>10) with the estimated breeding value. Conclusion: Analysis provides markers for further research of horn colour and supplies markers to achieve more effective selection work regarding estimated breeding value of HG.

• 대한생식의학회:학술대회논문집
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• 대한불임학회 2005년도 제49차 추계학술대회
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• pp.104-104
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• 2005