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the Korean Journal of Genetics最新文献

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Delayed discovery of Hsp60 and subsequent characterization of moonlighting functions of multiple Hsp60 genes in Drosophila: a personal historical perspective Hsp60的延迟发现和果蝇中多个Hsp60基因的兼职功能的后续表征:个人历史视角
the Korean Journal of Genetics Pub Date : 2022-10-18 DOI: 10.1007/s12041-022-01389-4
S. C. Lakhotia
{"title":"Delayed discovery of Hsp60 and subsequent characterization of moonlighting functions of multiple Hsp60 genes in Drosophila: a personal historical perspective","authors":"S. C. Lakhotia","doi":"10.1007/s12041-022-01389-4","DOIUrl":"https://doi.org/10.1007/s12041-022-01389-4","url":null,"abstract":"","PeriodicalId":49279,"journal":{"name":"the Korean Journal of Genetics","volume":"49 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82005718","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Molecular characterization of Rhipicephalus microplus in Andaman and Nicobar Islands, India: an insight into genetic assemblages 印度安达曼和尼科巴群岛微型鼻头虫的分子特征:对遗传组合的洞察
the Korean Journal of Genetics Pub Date : 2022-10-13 DOI: 10.1007/s12041-022-01390-x
A. De, D. Bhattacharya, S. Sawhney, P. Bala, J. Sunder, T. Sujatha, Perumal Ponraj, E. Chakurkar
{"title":"Molecular characterization of Rhipicephalus microplus in Andaman and Nicobar Islands, India: an insight into genetic assemblages","authors":"A. De, D. Bhattacharya, S. Sawhney, P. Bala, J. Sunder, T. Sujatha, Perumal Ponraj, E. Chakurkar","doi":"10.1007/s12041-022-01390-x","DOIUrl":"https://doi.org/10.1007/s12041-022-01390-x","url":null,"abstract":"","PeriodicalId":49279,"journal":{"name":"the Korean Journal of Genetics","volume":"106 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89014202","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Long-term changes in the inversion chromosomal polymorphism: Drosophila subobscura population from Rasht (north of Iran) 倒位染色体多态性的长期变化:来自伊朗北部拉什特的亚bobscura果蝇种群
the Korean Journal of Genetics Pub Date : 2022-10-05 DOI: 10.1007/s12041-022-01387-6
Manhaz Khadem, C. Arenas, J. Balanyá, F. Mestres
{"title":"Long-term changes in the inversion chromosomal polymorphism: Drosophila subobscura population from Rasht (north of Iran)","authors":"Manhaz Khadem, C. Arenas, J. Balanyá, F. Mestres","doi":"10.1007/s12041-022-01387-6","DOIUrl":"https://doi.org/10.1007/s12041-022-01387-6","url":null,"abstract":"","PeriodicalId":49279,"journal":{"name":"the Korean Journal of Genetics","volume":"24 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-10-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88514664","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Functional analysis of HADH c.99C>G shows that the variant causes the proliferation of pancreatic islets and leu-sensitive hyperinsulinaemia hadhc . 99c >G的功能分析表明，该变异引起胰岛增生和低敏感性高胰岛素血症
the Korean Journal of Genetics Pub Date : 2022-09-14 DOI: 10.1007/s12041-022-01381-y
Wu Long, Yue-bing Wang, P. Qu, Lin Ma, Si-Jie Wei, Y. Xi, Jin-Liang Du, Xue Tang, Kai Liu, Yu-Hua Li, P. Lei
{"title":"Functional analysis of HADH c.99C>G shows that the variant causes the proliferation of pancreatic islets and leu-sensitive hyperinsulinaemia","authors":"Wu Long, Yue-bing Wang, P. Qu, Lin Ma, Si-Jie Wei, Y. Xi, Jin-Liang Du, Xue Tang, Kai Liu, Yu-Hua Li, P. Lei","doi":"10.1007/s12041-022-01381-y","DOIUrl":"https://doi.org/10.1007/s12041-022-01381-y","url":null,"abstract":"","PeriodicalId":49279,"journal":{"name":"the Korean Journal of Genetics","volume":"14 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-09-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88312088","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Effects of CYP24A1 polymorphisms on premature ejaculation: a case–control study CYP24A1多态性对早泄的影响:一项病例对照研究
the Korean Journal of Genetics Pub Date : 2022-09-14 DOI: 10.1007/s12041-022-01378-7
Fei Wang, Defan Luo, Jianxiang Chen, Cuiqing Pan, Zhongyao Wang, Housheng Fu, Jiangbing Xu, Meng-xuan Yang, Shaowei Mo, Liying Zhuang, Weifu Wang
{"title":"Effects of CYP24A1 polymorphisms on premature ejaculation: a case–control study","authors":"Fei Wang, Defan Luo, Jianxiang Chen, Cuiqing Pan, Zhongyao Wang, Housheng Fu, Jiangbing Xu, Meng-xuan Yang, Shaowei Mo, Liying Zhuang, Weifu Wang","doi":"10.1007/s12041-022-01378-7","DOIUrl":"https://doi.org/10.1007/s12041-022-01378-7","url":null,"abstract":"","PeriodicalId":49279,"journal":{"name":"the Korean Journal of Genetics","volume":"3 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-09-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83747087","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Inheritance and molecular tagging of genes introgressed from Gossypium arboreum to G. hirsutum for leafhopper tolerance 棉对叶蝉耐受性基因渗入的遗传与分子标记
the Korean Journal of Genetics Pub Date : 2022-09-06 DOI: 10.1007/s12041-022-01379-6
Salil Jindal, D. Pathak, Suneet Pandher, P. Rathore, Y. Vikal
{"title":"Inheritance and molecular tagging of genes introgressed from Gossypium arboreum to G. hirsutum for leafhopper tolerance","authors":"Salil Jindal, D. Pathak, Suneet Pandher, P. Rathore, Y. Vikal","doi":"10.1007/s12041-022-01379-6","DOIUrl":"https://doi.org/10.1007/s12041-022-01379-6","url":null,"abstract":"","PeriodicalId":49279,"journal":{"name":"the Korean Journal of Genetics","volume":"123 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-09-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89442433","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Missing apolipoprotein E ɛ4 allele associated with nonamnestic Alzheimer’s disease in a Tunisian population 突尼斯人群中与非遗忘性阿尔茨海默病相关的载脂蛋白e4等位基因缺失
the Korean Journal of Genetics Pub Date : 2022-09-06 DOI: 10.1007/s12041-022-01384-9
S. Fray, Afef Achouri-Rassas, S. Belal, T. Messaoud
{"title":"Missing apolipoprotein E ɛ4 allele associated with nonamnestic Alzheimer’s disease in a Tunisian population","authors":"S. Fray, Afef Achouri-Rassas, S. Belal, T. Messaoud","doi":"10.1007/s12041-022-01384-9","DOIUrl":"https://doi.org/10.1007/s12041-022-01384-9","url":null,"abstract":"","PeriodicalId":49279,"journal":{"name":"the Korean Journal of Genetics","volume":"48 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-09-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88593701","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Spastic paraplegia 51: phenotypic spectrum related to novel homozygous AP4E1 mutation 痉挛性截瘫51:与新型纯合AP4E1突变相关的表型谱
the Korean Journal of Genetics Pub Date : 2022-09-06 DOI: 10.1007/s12041-022-01385-8
Jamal Manoochehri, H. Goodarzi, S. Tabei
{"title":"Spastic paraplegia 51: phenotypic spectrum related to novel homozygous AP4E1 mutation","authors":"Jamal Manoochehri, H. Goodarzi, S. Tabei","doi":"10.1007/s12041-022-01385-8","DOIUrl":"https://doi.org/10.1007/s12041-022-01385-8","url":null,"abstract":"","PeriodicalId":49279,"journal":{"name":"the Korean Journal of Genetics","volume":"70 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-09-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83154100","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Genome survey and development of 13 SSR markers in Eucalyptus cloeziana by NGS 蓝桉13个SSR标记的NGS基因组调查与开发
the Korean Journal of Genetics Pub Date : 2022-09-02 DOI: 10.1007/s12041-022-01382-x
Xinli Liang, Tian-Dao Bai, Jian-zhong Wang, Wei-Xin Jiang
{"title":"Genome survey and development of 13 SSR markers in Eucalyptus cloeziana by NGS","authors":"Xinli Liang, Tian-Dao Bai, Jian-zhong Wang, Wei-Xin Jiang","doi":"10.1007/s12041-022-01382-x","DOIUrl":"https://doi.org/10.1007/s12041-022-01382-x","url":null,"abstract":"","PeriodicalId":49279,"journal":{"name":"the Korean Journal of Genetics","volume":"30 2 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88969320","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
Deletion of 11q24.2-qter in a male child with cleft lip and palate: an atypical feature of Jacobsen syndrome 一个唇腭裂男孩11q24.2四分之一缺失:雅各布森综合征的一个非典型特征
the Korean Journal of Genetics Pub Date : 2022-08-29 DOI: 10.1007/s12041-022-01380-z
Jundao Wang, Tianli Zhao, Zhiping Tan, Xueyang Gong, Yiliya Ahemaiti, Luyao Wei, Shijun Hu
{"title":"Deletion of 11q24.2-qter in a male child with cleft lip and palate: an atypical feature of Jacobsen syndrome","authors":"Jundao Wang, Tianli Zhao, Zhiping Tan, Xueyang Gong, Yiliya Ahemaiti, Luyao Wei, Shijun Hu","doi":"10.1007/s12041-022-01380-z","DOIUrl":"https://doi.org/10.1007/s12041-022-01380-z","url":null,"abstract":"","PeriodicalId":49279,"journal":{"name":"the Korean Journal of Genetics","volume":"23 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-08-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"86948723","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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