Search Results - "Zhang, Bijun"
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Knowledge structure and emerging trends in the application of deep learning in genetics research: A bibliometric analysis [2000–2021]
Published in Frontiers in genetics (23-08-2022)“…Introduction: Deep learning technology has been widely used in genetic research because of its characteristics of computability, statistical analysis, and…”
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An environmentally benign synthesis of isoxazolines and isoxazoles mediated by potassium chloride in water
Published in Tetrahedron letters (02-04-2014)“…An effective and environmentally benign procedure for the synthesis of isoxazolines and isoxazoles has been developed by a cycloaddition of nitrile oxides with…”
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3
Sponges of Carboxymethyl Chitosan Grafted with Collagen Peptides for Wound Healing
Published in International journal of molecular sciences (09-08-2019)“…Burns are physically debilitating and potentially fatal injuries. Two marine biomaterials, carboxymethyl chitosan (CMC) and collagen peptides (COP), have…”
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4
Introduction on IMT-2020 5G Trials in China
Published in IEEE journal on selected areas in communications (01-08-2017)“…Ultrahigh data rate, massive connectivity, ultralow latency, and high reliability, as well as ultraflexible air interface design to support diversified usage…”
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5
Design of chemical space networks using a Tanimoto similarity variant based upon maximum common substructures
Published in Journal of computer-aided molecular design (01-10-2015)“…Chemical space networks (CSNs) have recently been introduced as an alternative to other coordinate-free and coordinate-based chemical space representations. In…”
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6
Renal NKCC2 Is Dual Regulated by the Synergy of 20-HETE and High-Fat Diet in CYP4F2 Transgenic Mice
Published in Kidney & blood pressure research (01-10-2021)“…Introduction: 20-Hydroxyeicosatetraenoic acid (20-HETE) is the metabolite of cytochrome P450, which modulates blood pressure by inhibiting renal sodium…”
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Prenatal diagnosis of auriculocondylar syndrome with a novel missense variant of GNAI3: a case report
Published in BMC pregnancy and childbirth (17-11-2021)“…Auriculocondylar syndrome (ACS) is a rare disorder characterized by micrognathia, mandibular condyle hypoplasia, and auricular abnormalities. Only 6 pathogenic…”
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Nedd4-2 Haploinsufficiency in Mice Impairs the Ubiquitination of Rer1 and Increases the Susceptibility to Endoplasmic Reticulum Stress and Seizures
Published in Frontiers in molecular neuroscience (27-06-2022)“…Neural precursor cell expressed developmentally downregulated gene 4-like (NEDD4-2) is an epilepsy-associated gene encoding an E3 ligase that ubiquitinates…”
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Genetic subtypes and phenotypic characteristics of 110 patients with Prader-Willi syndrome
Published in Italian journal of pediatrics (23-07-2022)“…Prader-Willi syndrome (PWS) is a complex disorder caused by impaired paternally expressed genes on chromosome 15q11-q13. Variable findings have been reported…”
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AnalogExplorer: A New Method for Graphical Analysis of Analog Series and Associated Structure–Activity Relationship Information
Published in Journal of medicinal chemistry (13-11-2014)“…In recent years, several attempts have been made to develop graphical methods for the analysis of structure–activity relationships (SARs) in increasingly large…”
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Molecular and phenotypic characteristics of 15q24 microdeletion in pediatric patients with developmental disorders
Published in Molecular cytogenetics (18-12-2021)“…Chromosome 15q24 microdeletion is a rare genetic disorder characterized by development delay, facial dysmorphism, congenital malformations, and occasional…”
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Autosomal dominant hereditary spastic paraplegia caused by mutation of UBAP1
Published in Neurogenetics (01-07-2020)“…Hereditary spastic paraplegias (HSP) are a group of rare neurodegenerative diseases characterized by progressive spastic paraparesis. UBAP1 was recently found…”
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13
Nonsense suppression induced readthrough of a novel PAX6 mutation in patient‐derived cells of congenital aniridia
Published in Molecular genetics & genomic medicine (01-05-2020)“…Background Congenital aniridia is a severe ocular abnormality characterized by incomplete formation of the iris and many other ocular complications. Most cases…”
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Systematic Assessment of Compound Series with SAR Transfer Potential
Published in Journal of chemical information and modeling (21-12-2012)“…Compound series with different core structures that contain pairs of analogs with corresponding substitution patterns and similar activity represent…”
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15
Hypervalent Iodine Catalyzed Cyclization of Aryl-Substituted Alkanoic Acids
Published in Helvetica chimica acta (01-06-2014)“…A novel and efficient procedure was developed for direct preparation of aryl‐substituted lactones from corresponding aryl‐substituted alkanoic acids, catalyzed…”
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Establishment of an induced pluripotent stem cell line (ZJSHi001-A) from a patient with epileptic encephalopathy carrying KCNB1 Glu330Asp mutation
Published in Stem cell research (01-04-2021)“…Early infantile epileptic encephalopathy 26 (EE26) is a form of epileptic encephalopathy, a heterogeneous group of severe childhood-onset epilepsies…”
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SAR Transfer across Different Targets
Published in Journal of chemical information and modeling (22-07-2013)“…Despite obvious relevance for the practice of medicinal chemistry, SAR transfer events have thus far only been little investigated in a systematic manner. Two…”
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Ammonium Iodide-Promoted Cyclization of Aryl-Substituted Carboxylic Acids
Published in Synthetic communications (03-06-2014)“…An efficient procedure was developed for direct preparation of aryl-substituted lactones from corresponding aryl carboxylic acids, which was promoted by…”
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Hierarchical mining algorithm for high dimensional spatiotemporal big data based on association rules
Published in E3S Web of Conferences (01-01-2021)“…The traditional data mining algorithm focuses too much on a single dimension of data time or space, ignoring the association between time and space, which…”
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Electrophysiological features: The next precise step for SCN2A developmental epileptic encephalopathy
Published in Molecular genetics & genomic medicine (01-07-2020)“…Background To investigate the relationships among phenotypes, genotypes, and funotypes of SCN2A‐related developmental epileptic encephalopathy (DEE). Methods…”
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