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Ecological function transitions of land use in the Beibu Gulf Economic Zone from the perspective of production-living-ecological space
《Journal of Geographical Sciences》2024年第11期2212-2238,共27页ZHOU Guipeng LONG Hualou JIANG Yanfeng TU Shuangshuang 
National Natural Science Foundation of China,No.42301313;Natural Science Foundation of Guangxi Zhuang Autonomous Region,No.2024GXNSFBA010097;National Natural Science Foundation of China,No.41971216。
The ecological function of land use is the basis for developing an ecological civilization and realizing sustainable development.This paper may help guide the coordination of economic development and ecological develo...
关键词：land use transitions ecological function eco-environmental quality production-living-ecological spaces dominant and recessive factors Beibu Gulf 
土地整治助推乡村发展转型的机制与成效识别被引量：3
《Journal of Geographical Sciences》2024年第3期417-438,共22页陈坤秋 陈韵雅 龙花楼 李宁慧 
National Natural Science Foundation of China,No.42201209;Hunan Provincial Natural Science Foundation Project of China,No.2022JJ40053;Research Foundation of the Department of Natural Resources of Hunan Province,No.20230109DC;The Open Research Fund of Hunan Key Laboratory of Sciences of Urban and Rural Human Settlements in Hilly Areas,No.HNU-SAP-KF220205;Youth Humanities and Social Sciences Project of the Ministry of Education of China,No.19YJC840060。
China's rural territory is entering a critical stage of transformation and development.Promoting rural development and transformation is an important path to achieve rural vitalization,and land consolidation is expect...
关键词：land consolidation rural development transformation land system dominant&recessive mechanism rural vitalization 
New recessive compound heterozygous variants of RP1L1 in RP1L1 maculopathy
《International Journal of Ophthalmology(English edition)》2024年第1期107-112,共6页Wen-Chao Cao Qing-Shan Chen Run Gan Tao Huang Xiao-He Yan 
Supported by Shenzhen Science and Technology Program,Shenzhen,China(No.JCYJ20200109145001814,No.SGDX20211123120001001);the National Natural Science Foundation of China(No.81970790);Sanming Project of Medicine in Shenzhen(No.SZSM202011015).
AIM:To identify a maculopathy patient caused by new recessive compound heterozygous variants in RP1L1.METHODS:Comprehensive retinal morphological and functional examinations were evaluated for the patient with RP1L1 m...
关键词：MACULOPATHY RECESSIVE compound heterozygous variants RP1L1 
劳动力变动背景下耕地利用隐性形态影响因素分析——基于农户生产投入意愿与行为视角被引量：2
《Journal of Geographical Sciences》2023年第12期2467-2488,共22页廖柳文 龙花楼 马恩朴 
National Natural Science Foundation of China,No.42101198,No.42101267;Hunan Social Science Review Committee Program,No.XSP22YBZ182。
Land use transition occurs through changes in land use morphologies.The decision-making and land use behavior of farmers is the main factor that causes changes in the land use system and subsequent transitions of land...
关键词：land use transition recessive morphologies willingness and behavior labor change Shandong province 
The R2R3-MYB transcription factor GaPC controls petal coloration in cotton被引量：1
《The Crop Journal》2023年第5期1319-1330,共12页Caiping Cai Fan Zhou Weixi Li Yujia Yu Zhihan Guan Baohong Zhang Wangzhen Guo 
supported by the Fundamental Research Funds for the Central Universities(KYZZ2022003);Jiangsu Collaborative Innovation Center for Modern Crop Production project (No.10)。
Although a few cases of genetic epistasis in plants have been reported, the combined analysis of genetically phenotypic segregation and the related molecular mechanism remains rarely studied. Here, we have identified ...
关键词：COTTON Petal color R2R3-MYB transcription factor LTR-RT insertion Flavonoid/anthocyanin biosynthesis Recessive epistasis 
Compound heterozygous mutations in tripeptidyl peptidase 1 cause rare autosomal recessive spinocerebellar ataxia type 7:A case report
《World Journal of Clinical Cases》2023年第27期6618-6623,共6页Rui-Han Liu Xin-Yu Wang Yuan-Yuan Jia Xing-Chen Wang Min Xia Qiong Nie Jia Guo Qing-Xia Kong 
Supported by Postdoctoral program of the Affiliated Hospital of Jining Medical University,No.JYFY303573;Health Commission of Shandong Province,No.202006010928;Academician Lin He New Medicine in Jining Medical University,No.JYHL2018FMS05;Affiliated Hospital of Jining Medical University,No.2018-BS-004.
BACKGROUND Spinocerebellar ataxia recessive type 7(SCAR7)is a rare clinical manifestation beginning in childhood or adolescence.SCAR7 is caused by tripeptidyl peptidase 1(TPP1)gene mutations,and presents with cerebell...
关键词：Spinocerebellar ataxia recessive type 7 Tripeptidyl peptidase 1 Compound heterozygous variant Case report 
Analysis of clinical audiological characteristics of noise-induced silent hearing loss
《Discussion of Clinical Cases》2023年第1期22-27,共6页Chunmin Li Xiaoxu Du Dandan Zhang Tuya Bai Xiuli Xu 
supported by the Science and Technology Bureau of Baotou City(project number jkws202057).
Objective:To explore the characteristics of audiology examination of Noise-Induced Hidden Hearing Loss(NIHHL),and then explore its valuable diagnostic methods.Methods:A total of 80 young men aged between 19 and 35 wer...
关键词：Noise-induced recessive hearing loss Extended high frequency threshold test Speech audiometry under noise Otoacoustic emission 
X-linked recessive Kallmann syndrome:A case report
《World Journal of Clinical Cases》2022年第25期8990-8997,共8页Ping Zhang Jing-Yun Fu 
Supported by the National Natural Science Foundation of China,No.81860265;the Special Foundation for Discipline Leaders of High-level Health Technical Talents in Yunnan Province,No.D-2018035。
BACKGROUND Kallmann syndrome(KS),also known as hypogonadotropic hypogonadism(HH)or olfactory-gonadal dysplasia,is a genetic condition in which the primary symptom is a failure to begin puberty or a failure to fully co...
关键词：X-linked recessive Kallmann syndrome Gonadotropin-releasing hormone Hormone replacement therapy DIAGNOSIS TREATMENT Case report 
Autosomal recessive spinocerebellar ataxia type 4 with a VPS13D mutation:A case report
《World Journal of Clinical Cases》2022年第2期703-708,共6页Xin Huang Dong-Sheng Fan 
BACKGROUND Autosomal recessive spinocerebellar ataxia type 4(SCAR4)is a type of SCA that is a group of hereditary diseases characterized by gait ataxia.The main clinical features of SCAR4 are progressive cerebellar at...
关键词：Spinocerebellar ataxia RECESSIVE VPS13D gene Compound heterozygous mutation Case report 
A Recessive Mutant of argonaute 1b/gsnl4 Leads to Narrow Leaf, Small Grain Size and Low Seed Setting in Rice
《Rice science》2021年第6期521-524,I0002-I0026,共29页SONG Mengqiu RUAN Shuang PENG Youlin WANG Zhongwei Jahan NOUSHIN ZHANG Yu CUI Yongtao HU Haitao JIANG Hongzhen DING Shilin SHEN Lan GAO Zhenyu HU Xingming QIAN Qian GUO Longbiao 
supported by the National Natural Science Foundation of China(Grant Nos.31771887,31671761 and 32001491);supported by the National Natural Science Foundation of China(Grant Nos.31771887,31671761 and 32001491).
A gsnl4 mutant characterized by small grain size,narrow leaf and low seed-setting rate was obtained by ethyl methane sulfonate(EMS)mutagenesis of a japonica rice variety Wuyunjing 21.Genetic analysis showed that gsnl4...
关键词：CRISPR/Cas9 NARROW SMALL 
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