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检索条件"作者=Heriberto Diaz Velazquez"
493 条 记 录,以下是1-10 订阅
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温和条件下金属双氮杂环卡宾配合物催化CO_2直接转化为炔酸的高效均相羧化反应
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化学通报 2015年 第3期78卷 220-225页
作者: 吴兆轩 heriberto diaz velazquez 闵梦蝶 原晔 Hussein A. Younus 陈建 Bibimaryam Mousavi Francis Verpoort 武汉理工大学材料复合新技术国家重点实验室 武汉430070 武汉理工大学材料科学与工程学院 武汉430070 根特大学无机与物理化学系金属有机化学与催化实验室 武汉理工大学理学院化学系 武汉430070 武汉理工大学化学工程学院 武汉430070
近年来,催化CO2合成精细化学品的研究备受关注。本研究在温和条件下利用金属双氮杂环卡宾催化剂实现CO2与末端炔烃的直接羧化反应,并提出合理的催化机理。首先,合成制备了铜基、银基两种金属双氮杂环卡宾催化剂,实验证明银双氮杂环卡宾... 详细信息
来源: 维普期刊数据库 维普期刊数据库 同方期刊数据库 同方期刊数据库 评论
Assessment of compressive strength of jet grouting by machine learning
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Journal of Rock Mechanics and Geotechnical Engineering 2024年 第1期16卷 102-111页
作者: Esteban diaz Edgar Leonardo Salamanca-Medina Roberto Tomas Departamento de Ingeniería Civil Escuela Politécnica SuperiorUniversidad de AlicanteP.O.Box 99E-03080AlicanteSpain
Jet grouting is one of the most popular soil improvement techniques,but its design usually involves great uncertainties that can lead to economic cost overruns in construction *** high dispersion in the properties of ... 详细信息
来源: 维普期刊数据库 维普期刊数据库 评论
Polyoxidovanadates a new therapeutic alternative for neurodegenerative and aging diseases
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Neural Regeneration Research 2024年 第3期19卷 571-577页
作者: Sonia Irais Gonzalez-Cano Gonzalo Flores Jorge Guevara Julio Cesar Morales-Medina Samuel Treviño Alfonso diaz Faculty of Chemical Sciences Benemerita Autonomous University of PueblaPueblaMexico Institute of Physiology Benemerita Autonomous University of PueblaPueblaMexico Department of Biochemistry Faculty of MedicineNational Autonomous University of MexicoMexico CityMexico Animal Reproduction Research Center CINVESTAV-Autonomous University of TlaxcalaTlaxcalaMexico
Aging is a natural phenomenon characterized by a progressive decline in physiological integrity,leading to a deterioration of cognitive function and increasing the risk of suffering from chronic-degenerative diseases,... 详细信息
来源: 维普期刊数据库 维普期刊数据库 同方期刊数据库 同方期刊数据库 评论
Emerging and multifaceted potential contributions of polyphenols in the management of type 2 diabetes mellitus
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World Journal of Diabetes 2024年 第2期15卷 154-169页
作者: Ileana González Cristian Lindner Ivan Schneider Erik diaz Miguel Angel Morales Armando Rojas Biomedical Research Laboratories Faculty of MedicineCatholic University of MauleTalca 34600000Chile Department of Radiology Faculty of MedicineUniversity of ConcepciónConcepción 4030000Chile Centre of Primary Attention South Metropolitan Health ServiceSantiago 3830000Chile Faculty of Medicine Catholic University of MauleTalca 3460000Chile Molecular and Clinical Pharmacology Program Institute of Biomedical SciencesUniversity of ChileSantiago 8320000Chile
Type 2 diabetes mellitus(T2DM)is recognized as a serious public health concern with a considerable impact on human life,long-term health expenditures,and substantial health *** this context,the use of dietary polyphen... 详细信息
来源: 维普期刊数据库 维普期刊数据库 评论
Chemically robust superhydrophobic surfaces with a self‐replenishing nanoscale liquid coating
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Droplet 2024年 第1期3卷 136-148页
作者: Xiaoteng Zhou Pranav Sudersan Diego diaz Benjamin Leibauer Chirag Hinduja Fahimeh Darvish Pravash Bista Lukas Hauer Manfred Wagner Werner Steffen Jie Liu Michael Kappl Hans‐Jürgen Butt Max Planck Institute for Polymer Research MainzGermany Key Laboratory of Green Printing Institute of ChemistryChinese Academy of SciencesBeijingChina School of Chemical Sciences University of Chinese Academy of SciencesBeijingChina
Due to poor chemical robustness,superhydrophobic surfaces become susceptible to failure,especially in a highly oxidative *** ensure the longterm efficacy of these surfaces,a more stable and environmentally friendly co... 详细信息
来源: 维普期刊数据库 维普期刊数据库 评论
Evolution of liver transplantation in the metabolic dysfunctionassociated steatotic liver disease era: Tracking impact through time
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World Journal of Transplantation 2024年 第4期14卷 84-94页
作者: Karina Sato-Espinoza Perapa Chotiprasidhi Estefanía Liza Zuly Placido-Damian Javier diaz-Ferrer Division of Gastroenterology and Hepatology Department of MedicineMayo ClinicRochesterMN 55902United States Hepatology Service Department of Digestive DiseasesHospital Nacional Edgardo Rebagliati MartinsLima 15072Peru Medicine Faculty Universidad San Martin de PorresLima 02002Peru Gastroenterology Service Clinica InternacionalLima 02002Peru
Liver transplantation(LT)for metabolic dysfunction-associated steatotic liver disease(MASLD)is increasing globally due to rising rates of obesity and metabolic syndrome,posing significant *** patients typically presen... 详细信息
来源: 维普期刊数据库 维普期刊数据库 评论
Using Linear and Non-Linear Techniques to Characterize Gait Coordination Patterns of Two Individuals with NGLY1 Deficiency
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Case Reports in Clinical Medicine 2024年 第9期13卷 391-409页
作者: Charles S. Layne Dacia Martinez diaz Christopher A. Malaya Brock Futrell Christian Alfaro Hannah E. Gustafson Bernhard Suter Department of Health and Human Performance University of Houston Houston TX USA Center for Neuromotor and Biomechanics Research University of Houston Houston TX USA Center for Neuro Engineering and Cognitive Science University of Houston Houston TX USA Research Center Parker University Dallas TX USA Blue Bird Circle Rett Center Texas Childrens Hospital Houston TX USA Baylor College of Medicine Houston TX USA
Individuals with NGLY1 Deficiency, an inherited autosomal recessive disorder, exhibit hyperkinetic movements including athetoid, myoclonic, dysmetric, and dystonic movements impacting both upper and lower limb motion.... 详细信息
来源: 维普期刊数据库 维普期刊数据库 评论
Quantifying Kinematic Tremor in an NGLY1-Deficient Individual: A Case Study
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Case Reports in Clinical Medicine 2024年 第1期13卷 25-36页
作者: Brock Futrell Christopher Alexander Malaya Dacia Martinez diaz Christian Alfaro Hannah Elizabeth Gustafson Subhalakshmi Chandrasekaran Rhea Mohan Phatak Bernhard Suter Charles Shannon Layne Department of Health and Human Performance University of Houston Houston USA Center for Neuromotor and Biomechanics Research University of Houston Houston USA Department of Computer Science and Engineering Texas A&M University College Station USA Blue Bird Circle Rett Center Texas Children’s Hospital Houston USA Baylor College of Medicine Houston USA Center for NeuroEngineering and Cognitive Science University of Houston Houston USA
NGLY1 Deficiency is an autosomal recessive congenital disorder that has been identified in less than 100 individuals. Most individuals with NGLY1 Deficiency display hyperkinetic movement disorders, including choreifor... 详细信息
来源: 维普期刊数据库 维普期刊数据库 评论
Recent advances in bird sperm morphometric analysis and its role in male gamete characterization and reproduction technologies
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Asian Journal of Andrology 2016年 第6期18卷 882-888页
作者: Julian Santiago-Moreno Milagros Cristina Esteso Silvia Villaverde-Morcillo Adolfo Toledano-diaz Cristina Castafio Rosario velazquez Antonio Lopez-Sebastian Agustin Lopez Goya Javier Gimeno Martinez Department of Animal Reproduction INIA 28040 Madrid Spain Veterinary Clinical and Research Services Fieb Foundation 28760 Tres Cantos Madrid Spain FAUNIA 28032 Madrid Spain
Postcopulatory sexual selection through sperm competition may be an important evolutionary force affecting many reproductive traits, including sperm morphometrics. Environmental factors such as pollutants, pesticides,... 详细信息
来源: 维普期刊数据库 维普期刊数据库 评论
3-Dimensional Kinematic Comparison of Arm Movements between an Individual with NGLY1 Deficiency and a Neurotypical Individual
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Case Reports in Clinical Medicine 2024年 第4期13卷 122-146页
作者: Charles S. Layne Christopher A. Malaya Brock Futrell Dacia Martinez diaz Christian Alfaro Hannah E. Gustafson Subhalakshmi Chandrasekaran Rhea M. Phatak Bernhard Suter Department of Health and Human Performance University of Houston Houston TX USA Center for Neuromotor and Biomechanics Research University of Houston Houston TX USA Center for Neuro Engineering and Cognitive Science University of Houston Houston TX USA Department of Computer Science and Engineering Texas A&M University College Station TX USA Blue Bird Circle Rett Center Texas Children&#8217s Hospital Houston TX USA Baylor College of Medicine Houston TX USA
NGLY1 Deficiency is an ultra-rare autosomal recessively inherited disorder. Characteristic symptoms include among others, developmental delays, movement disorders, liver function abnormalities, seizures, and problems ... 详细信息
来源: 维普期刊数据库 维普期刊数据库 评论