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The application of interactive speech system based on neural network algorithm in ideological and political network education platform

Soft computing (Berlin, Germany), 2023-06

Lusi, Zhang

2023

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Integrated bioinformatic analysis identified a novel prognostic pan-programmed cell death signature for bladder cancer

Frontiers in immunology, 2022-11, Vol.13, p.1030097-1030097

2022

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Immunogenomic profiles and therapeutic options of the pan-programmed cell death-related lncRNA signature for patients with bladder cancer

Scientific reports, 2024-08, Vol.14 (1), p.18500-15, Article 18500

2024

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A universal synthetic route to carbon nanotube/transition metal oxide nano-composites for lithium ion batteries and electrochemical capacitors

Scientific reports, 2016-11, Vol.6 (1), p.37752, Article 37752

2016

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Phosphorylated S6K1 and 4E-BP1 play different roles in constitutively active Rheb-mediated retinal ganglion cell survival and axon regeneration after optic nerve injury

Neural regeneration research, 2023-11, Vol.18 (11), p.2526-2534

2023

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PRRX1 Is a Novel Prognostic Biomarker and Facilitates Tumor Progression Through Epithelial-Mesenchymal Transition in Uveal Melanoma

Frontiers in immunology, 2022-02, Vol.13, p.754645-754645

2022

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CYP2D6 Genetic Polymorphisms and Risperidone Pharmacokinetics: A Systematic Review and Meta‐analysis

Pharmacotherapy, 2020-07, Vol.40 (7), p.632-647

2020

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Advances in nanoprobes‐based immunoassays

BMEmat (Print), 2024-02, Vol.2 (1), p.n/a

2024

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A Missense Mutation in GJA8 Encoding Connexin 50 in a Chinese Pedigree with Autosomal Dominant Congenital Cataract

The Tohoku Journal of Experimental Medicine, 2018, Vol.244(2), pp.105-111

2018

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Signal Factors Secreted by 2D and Spheroid Mesenchymal Stem Cells and by Cocultures of Mesenchymal Stem Cells Derived Microvesicles and Retinal Photoreceptor Neurons

Stem Cells International, 2017-01, Vol.2017 (2017), p.1-13-54

2017

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Targeted methylation sequencing reveals dysregulated Wnt signaling in Parkinson disease

Journal of genetics and genomics, 2016-10, Vol.43 (10), p.587-592

2016

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A PITX2 splice-site mutation in a family with Axenfeld-Rieger syndrome leads to decreased expression of nuclear PITX2 protein

International ophthalmology, 2021-04, Vol.41 (4), p.1503-1511

2021

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Assessing pharmacogenomic literacy in China through validation of the Chinese version of the Minnesota Assessment of Pharmacogenomic Literacy

Clinical and translational science, 2023-11, Vol.16 (11), p.2356-2368

2023

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Effects of Near-Freezing Temperature Combined with Jujube Polysaccharides Treatment on Proteomic Analysis of 'Diaogan' Apricot ( Prunus armeniaca L.)

Foods, 2023-12, Vol.12 (24), p.4504

2023

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A novel frameshift mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome using targeted exome sequencing

BMC medical genetics, 2019-06, Vol.20 (1), p.105-105, Article 105

2019

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Insertion of a knockout-first cassette in Ampd1 gene leads to neonatal death by disruption of neighboring genes expression

Scientific reports, 2016-10, Vol.6 (1), p.35970-35970, Article 35970

2016

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The MDM2 Single-Nucleotide Polymorphism T309G Is Associated With the Development of Epimacular Membranes

Frontiers in cell and developmental biology, 2022-03, Vol.10, p.841660-841660

2022

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GLA variation p.E66Q identified as the genetic etiology of Fabry disease using exome sequencing

Gene, 2016-01, Vol.575 (2), p.363-367

2016

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Development and Validation of the Minnesota Assessment of Pharmacogenomic Literacy (MAPL)

Journal of personalized medicine, 2022-08, Vol.12 (9), p.1398

2022

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Variations analysis of NLGN3 and NLGN4X gene in Chinese autism patients

Molecular biology reports, 2014-06, Vol.41 (6), p.4133-4140

2014

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Public Attitudes toward Pharmacogenomic Testing and Establishing a Statewide Pharmacogenomics Database in the State of Minnesota

Journal of personalized medicine, 2022-09, Vol.12 (10), p.1615

2022

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One-step synthesis of free-standing α-Ni (OH)2 nanosheets on reduced graphene oxide for high-performance supercapacitors

Nanotechnology, 2014-10, Vol.25 (43), p.435403-435403

2014

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Inflammation Subtypes and Translating Inflammation-Related Genetic Findings in Schizophrenia and Related Psychoses: A Perspective on Pathways for Treatment Stratification and Novel Therapies

Harvard review of psychiatry, 2022-01, Vol.30 (1), p.59-70

2022

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Inflammation subtypes in psychosis and their relationships with genetic risk for psychiatric and cardiometabolic disorders

Brain, behavior, & immunity. Health, 2022-07, Vol.22, p.100459-100459, Article 100459

2022

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Upregulation of HMOX1 associated with M2 macrophage infiltration and ferroptosis in proliferative diabetic retinopathy

International immunopharmacology, 2024-06, Vol.134, p.112231, Article 112231

2024

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The application of interactive speech system based on neural network algorithm in ideological and political network education platform

Integrated bioinformatic analysis identified a novel prognostic pan-programmed cell death signature for bladder cancer

Immunogenomic profiles and therapeutic options of the pan-programmed cell death-related lncRNA signature for patients with bladder cancer

A universal synthetic route to carbon nanotube/transition metal oxide nano-composites for lithium ion batteries and electrochemical capacitors

Phosphorylated S6K1 and 4E-BP1 play different roles in constitutively active Rheb-mediated retinal ganglion cell survival and axon regeneration after optic nerve injury

PRRX1 Is a Novel Prognostic Biomarker and Facilitates Tumor Progression Through Epithelial-Mesenchymal Transition in Uveal Melanoma

CYP2D6 Genetic Polymorphisms and Risperidone Pharmacokinetics: A Systematic Review and Meta‐analysis

Advances in nanoprobes‐based immunoassays

A Missense Mutation in GJA8 Encoding Connexin 50 in a Chinese Pedigree with Autosomal Dominant Congenital Cataract

Signal Factors Secreted by 2D and Spheroid Mesenchymal Stem Cells and by Cocultures of Mesenchymal Stem Cells Derived Microvesicles and Retinal Photoreceptor Neurons

Targeted methylation sequencing reveals dysregulated Wnt signaling in Parkinson disease

A PITX2 splice-site mutation in a family with Axenfeld-Rieger syndrome leads to decreased expression of nuclear PITX2 protein

Assessing pharmacogenomic literacy in China through validation of the Chinese version of the Minnesota Assessment of Pharmacogenomic Literacy

Effects of Near-Freezing Temperature Combined with Jujube Polysaccharides Treatment on Proteomic Analysis of 'Diaogan' Apricot ( Prunus armeniaca L.)

A novel frameshift mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome using targeted exome sequencing

Insertion of a knockout-first cassette in Ampd1 gene leads to neonatal death by disruption of neighboring genes expression

The MDM2 Single-Nucleotide Polymorphism T309G Is Associated With the Development of Epimacular Membranes

GLA variation p.E66Q identified as the genetic etiology of Fabry disease using exome sequencing

Development and Validation of the Minnesota Assessment of Pharmacogenomic Literacy (MAPL)

Variations analysis of NLGN3 and NLGN4X gene in Chinese autism patients

Public Attitudes toward Pharmacogenomic Testing and Establishing a Statewide Pharmacogenomics Database in the State of Minnesota

One-step synthesis of free-standing α-Ni (OH)2 nanosheets on reduced graphene oxide for high-performance supercapacitors

Inflammation Subtypes and Translating Inflammation-Related Genetic Findings in Schizophrenia and Related Psychoses: A Perspective on Pathways for Treatment Stratification and Novel Therapies

Inflammation subtypes in psychosis and their relationships with genetic risk for psychiatric and cardiometabolic disorders

Upregulation of HMOX1 associated with M2 macrophage infiltration and ferroptosis in proliferative diabetic retinopathy

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