HAPLOGROUP

作品数：15被引量：31H指数：3
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Major depressive disorder is associated with mitochondrial ND6 T14502C mutation in two Han Chinese families
《World Journal of Psychiatry》2024年第11期1746-1754,共9页Pan Jing Hai-Hang Yu Ting-Ting Wu Bi-Hua Yu Ming Liang Ting-Ting Xia Xue-Wen Xu Ting Xu Ling-Jiang Liu Xiao-Bin Zhang 
Supported by the Zhejiang Medical and Health Science and Technology Project,No.2023KY1126;Suzhou Key Technologies Program,No.SKY2021063;Jiangsu Province Social Development Project,No.BE2020764;Suzhou Clinical Medical Center for Mood Disorders,No.Szlcyxzx202109;Suzhou Clinical Key Disciplines for Geriatric Psychiatry,No.SZXK202116;Suzhou Key Laboratory,No.SZS2024016。
BACKGROUND Globally,the World Health Organization ranks major depressive disorder(MDD)as the leading cause of disability.However,MDD molecular etiology is still poorly understood.AIM To explore the possible associatio...
关键词：Major depressive disorder Mitochondrial DNA ND6 T14502C MUTATION HAPLOGROUP CHINESE 
Major depressive disorder is correlated with the mitochondrial ND1 T3394C mutation in two Han Chinese families:Two case reports被引量：1
《World Journal of Psychiatry》2023年第2期75-83,共9页Pan Jing Xi Mei Yuan-Yuan Zhang Fei-Jie Zheng Xiao-Min Luo Ling-Jiang Liu Hai-Hang Yu Xiao-Bin Zhang 
Supported by the Natural Science Foundation of Ningbo,No.2018A610292;the Suzhou Key Technologies Program,No.SKY2021063;the Jiangsu Province Social Development Project,No.BE2020764;the Suzhou Clinical Medical Center for Mood Disorders,No.Szlcyxzx202109;the Zhejiang Medical and Health Science and Technology Project,No.2023KY1126。
BACKGROUND Major depressive disorder(MDD)is the most frequent reason of disabled people in the world,as reported by the World Health Organization.However,the diagnosis of MDD is mainly based on clinical symptoms.CASE ...
关键词：Major depressive disorder Mitochondrial DNA ND1 MUTATION HAPLOGROUP Chinese Case report 
Fine-scale north-to-south genetic admixture profile in Shaanxi Han Chinese revealed by genome-wide demographic history reconstruction被引量：1
《Journal of Systematics and Evolution》2022年第4期955-972,共18页Guang-Lin He Meng-Ge Wang Ying-Xiang Li Xing Zou Hui-Yuan Yeh Ren-Kuan Tang Xiao-Min Yang Zheng Wang Jian-Xin Guo Ting Luo Jing Zhao Jin Sun Rong Hu Lan-Hai Wei Gang Chen Yi-Ping Hou Chuan-Chao Wang 
supported by the National Natural Science Foundation of china(31801040);Nanqiang Outstanding Young Talents Program of Xiamen University(X2123302);and Fundamental Research Funds for the Central Universities(ZK1144).
The Han Chinese are the world's largest ethnic group residing across China.Shaanxi province in northern China was a pastoral-agricultural interlacing region sensitive to climate change since Neolithic times,which make...
关键词：ancestral makeup genetic relationship HAPLOGROUP Northern Han population substructure western Eurasian admixture 
Ancient Y-DNA with reconstructed phylogeny provides insights into the demographic history of paternal haplogroup N1a2-F1360被引量：1
《Journal of Genetics and Genomics》2021年第12期1130-1133,共4页Pengcheng Ma Xuan Yang Shi Yan Chunxiang Li Shizhu Gao Binghua Han Kan Hou Martine Robbeets Lan-Hai Wei Yinqiu Cui 
supported by the Humanities and Social Sciences Key Research Base of the Ministry of Education(16JJD780005);the Science and technology development project of Jilin Province(20190701077GH and 20200201138JC);the Fundamental Research Funds for the Central Universities;the National Natural Science Foundation of China(31900406 and 42072018)。
Northern Eurasia (nEA) has been considered crucial for the dispersal of the anatomically modern human (AMH) in recent studies.After the Last Glacial Maximum (LGM),ancient populations from different locations were redi...
关键词：INSIGHT PHYLOGENY 
Presence of G84E Allelic Heterogeneity of the European Prostate Cancer SNP Mutation of HOX13B-G84E Associated with the European R-Haplogroup of Y-Chromosome and Absence of Gene Flow into Moroccans Patients
《Journal of Biosciences and Medicines》2021年第5期50-61,共12页Ihsan Ali Mahasneh Moulay Mustapha Ennaji Berjas Abumsimir Yassine Kasmi 
SNP mutations in the HOXB13 gene associated with prostate cancer were determined in Moroccans prostate cancer patients (PCa). All PCa SNP mutations were new and belong to the SNP point-mutations located on the stop co...
关键词：Prostate Cancer HOXB13 G84E Allelic Heterogeneity Y-Chromosome Haplogroups European Genome Moroccan Genome Gene Flow 
Reconciling the father tongue and mother tongue hypotheses in Indo-European populations
《National Science Review》2019年第2期293-300,共8页Menghan Zhang Hong-Xiang Zheng Shi Yan Li Jin 
supported by projects at the National Natural Science Foundation of China(31501010,31401060,31401062,31521003 and 91731000);the Special Program for Key Basic Research of the Ministry of Science and Technology,China(2015FY111700);the Postdoctoral Science Foundation of China(2015M570316,2015T80394 and 2016M601496);the Science and Technology Committee of Shanghai Municipality(16JC1400500);Shanghai Municipal Science and Technology Major Project(2017SHZDZX01)
In opposition to the mother tongue hypothesis, the father tongue hypothesis states that humans tend to speak their fathers' language, based on a stronger correlation of languages to paternal lineages(Y-chromosome) tha...
关键词：Indo-European populations Y-chromosomal HAPLOGROUP mitochondrial DNA HAPLOGROUP LEXICAL SYSTEM phonemic SYSTEM 
A cryptic mitochondrial DNA link between North European and West African dogs
《Journal of Genetics and Genomics》2017年第3期163-170,共8页Adeniyi C.Adeola Sheila C.Ommeh Jiao-Jiao Song S.Charles Olaogun Oscar J.Sanke Ting-Ting Yin Guo-Dong Wang Shi-Fang Wu Zhong-Yin Zhou Jacqueline K.Lichoti Bernard R.Agwanda Philip M.Dawuda Robert W.Murphy Min-Sheng Peng Ya-Ping Zhang 
supported by Sino-Africa Joint Research Center, Chinese Academy of Sciences (Nos. SAJC201611 and SAJC201306);the National Basic Research program (Nos. 2013CB835200 and 2013CB835202);The Youth Innovation Promotion Association, Chinese Academy of Sciences, provided support to M.S.P. and G.D.W.;supported by the Animal Branch of the Germplasm Bank of Wild Species, Chinese Academy of Sciences (the Large Research Infrastructure Funding);supported, in part, by a Visiting Professorship for Senior International Scientists from the Chinese Academy of Sciences;manuscript preparation by a Natural Sciences and Engineering Research Council of Canada Discovery Grant A3148 to R.W.M
Domestic dogs have an ancient origin and a long history in Africa. Nevertheless, the timing and sources of their introduction into Africa remain enigmatic. Herein, we analyse variation in mitochondrial DNA（mt DNA） D...
关键词：Dog Mitochondrial DNA Africa Haplogroup D Late-glacial dispersal HYBRIDIZATION 
Comprehensive Analysis of Pan-African Mitochondrial DNA Variation Provides New Insights into Continental Variation and Demography
《Journal of Genetics and Genomics》2016年第3期133-143,共11页Maria Cerezo Leonor Gusmao Viktor Cerny Nabeel Uddin Denise Syndercombe-Court Alberto Gdmez-Carballa Tanja Gobel Peter M. Schneider Antonio Salas 
supported by fundings from the People Program (Marie Curie Actions) of the European Union’s Seventh Framework Program FP7/2007-2013/under REA grant agreement (No. 290344);the “Ministerio de Ciencia e Innovación” (No. SAF2011-26983);the Plan Galego IDT (No. EM 2012/045);the Sistema Universitario Gallego e Modalidad REDES (No. 2012-PG226) from the Xunta de Galicia (to A.S.);the Grant Agency of the Czech Republic (No. 13-37998SP505);the grant from “Fundación Barrié” (to M.C.)
Africa is the cradle of all human beings, and although it has been the focus of a number of genetic studies, there are many questions that remain unresolved. We have performed one of the largest and most comprehensive...
关键词：mtDNA HAPLOTYPE HAPLOGROUP SNP MALDI-TOF 
A late Neolithic expansion of Y chromosomal haplogroup O2a1-M95 from east to west被引量：1
《Journal of Systematics and Evolution》2015年第6期546-560,共15页GaneshPrasad Arunkumar Lan-Hai Wei Valampuri John Kavitha Adhikarla Syama Varatharajan Santhakumari Arun Surendra Sathua Raghunath Sahoo R. Balakrishnan Tomo Riba Jharna Chakravarthy Bapukan Chaudhury Premanada Panda Pradipta K. Das Prasanna K. Nayak Hui Li Ramasamy Pitchappan 无 
The origin and dispersal of Y-Chromosomal haplogroup O2a1-M95, distributed across the Austro Asiatic speaking belt of East and South Asia, are yet to be fully understood. Various studies have suggested either an East ...
关键词：Laos migration NEOLITHIC NRY O2a1-M95. 
Mitochondrial haplogroup B increases the risk for hearing loss among the Eastern Asian pedigrees carrying 12S rRNA 1555A〉G mutation被引量：9
《Protein & Cell》2015年第11期844-848,共5页
Dear Editor, Hearing loss is one of the major public health problems. The mitochondrial DNA mutations has been found to be associ- ated with both aminoglycoside-induced and nonsyndromic hearing loss （FischeI-Ghodsian...
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