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Thiol-to-amine cyclization reaction enables screening of large libraries of macrocyclic compounds and the generation of sub-kilodalton ligands

Science advances, 2019-08, Vol.5 (8), p.eaaw2851-eaaw2851

2019

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Silk fibroin regulated mineralization of hydroxyapatite nanocrystals

Journal of crystal growth, 2004-09, Vol.270 (1-2), p.197-202

2004

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Altered heart rate variability during sleep in mild cognitive impairment

Sleep (New York, N.Y.), 2021-04, Vol.44 (4), p.1

2021

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Androgen receptor expression in the skin appendages of patients with acne inversa harboring a mutation in the γ-secretase gene NCSTN

Journal of biological regulators and homeostatic agents, 2021-05, Vol.35 (3), p.1185-1187

2021

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Sleep spindle architecture associated with distinct clinical phenotypes in older adults at risk for dementia

Molecular psychiatry, 2024-02, Vol.29 (2), p.402-411

2024

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Synthesis and biological evaluation of new simple indolic non peptidic HIV Protease inhibitors: The effect of different substitution patterns

Bioorganic & medicinal chemistry, 2014-09, Vol.22 (17), p.4792-4802

2014

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Prenatal diagnosis based on HPRT1 gene mutation in a Lesch-Nyhan family

Journal of obstetrics and gynaecology, 2015-07, Vol.35 (5), p.490-493

2015

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A bi-objective optimization of airport ferry vehicle scheduling based on heuristic algorithm: A real data case study

Advances in production engineering & management, 2022-06, Vol.17 (2), p.183-192

2022

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Effects of Stress and Depolarization on Electrical Behaviors of Ferroelectric Field-Effect Transistor

IEEE electron device letters, 2012-01, Vol.33 (1), p.110-112

2012

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Quantum-state transfer on spin-chain channels with random imperfections

The European physical journal. D, Atomic, molecular, and optical physics, 2009-10, Vol.55 (1), p.211-221

2009

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Room temperature magnetic properties of ZnO nanostructured films

Physica. B, Condensed matter, 2011-03, Vol.406 (6), p.1341-1344

2011

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Bioinformatics analysis of biomarkers and transcriptional factor motifs in Down syndrome

Brazilian journal of medical and biological research, 2014-10, Vol.47 (10), p.834-841

2014

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Different heart rate variability profile during sleep in mid-later life adults with remitted early-onset versus late-onset depression

Journal of affective disorders, 2024-08, Vol.358, p.175-182

2024

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Simulation Modeling of Production System Considering Human Behavior

2020 IEEE International Conference on Industrial Engineering and Engineering Management (IEEM), 2020, p.123-127

2020

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Biocompatible Fibroin Blended Films with Recombinant Human-like Collagen for Hepatic Tissue Engineering

Journal of bioactive and compatible polymers, 2006-01, Vol.21 (1), p.23-37

2006

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Analysis of genetic variation in patients with Waardenburg syndrome type Ⅱ by next generation sequencing

Zhong hua yi xue za zhi, 2020-03, Vol.100 (11), p.853-858

2020

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Validation of the social functioning scale: Comparison and evaluation in early psychosis, autism spectrum disorder and social anxiety disorder

Psychiatry research, 2019-06, Vol.276, p.45-55

2019

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Analysis and application of ATP7B gene mutations in 35 patients with hepatolenticular degeneration

Genetics and molecular research, 2015-01, Vol.14 (4), p.18764-18770

2015

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A novel 3-base pair deletion of the CRYAA gene identified in a large Chinese pedigree featuring autosomal dominant congenital perinuclear cataract

Genetics and molecular research, 2015-01, Vol.14 (1), p.426-432

2015

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Prenatal diagnosis of Chinese families with phenylketonuria

Genetics and molecular research, 2015-01, Vol.14 (4), p.14615-14628

2015

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Mutation screening of 433 families with Duchenne/Becker muscular dystrophy

Zhong hua yi xue za zhi, 2016-04, Vol.96 (16), p.1261-1269

2016

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PAX3 gene mutation analysis for two Waardenburg syndrome type Ⅰ families and their prenatal diagnosis

Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery, 2016-12, Vol.51 (12), p.896

2016

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Mutation analyses and prenatal diagnosis in families of X-linked severe combined immunodeficiency caused by IL2Rγ gene novel mutation

Genetics and molecular research, 2015-01, Vol.14 (2), p.6164-6172

2015

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PTPS gene analysis and prenatal diagnosis in patients with 6-pyruvoyl-tetra hydropterin synthase deficiency

Chung-hua fu chʿan kʿo tsa chih, 2016-12, Vol.51 (12), p.890-894

2016

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Heart rate variability during slow wave sleep is linked to functional connectivity in the central autonomic network

Brain communications, 2023, Vol.5 (3), p.fcad129-fcad129

2023

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Thiol-to-amine cyclization reaction enables screening of large libraries of macrocyclic compounds and the generation of sub-kilodalton ligands

Silk fibroin regulated mineralization of hydroxyapatite nanocrystals

Altered heart rate variability during sleep in mild cognitive impairment

Androgen receptor expression in the skin appendages of patients with acne inversa harboring a mutation in the γ-secretase gene NCSTN

Sleep spindle architecture associated with distinct clinical phenotypes in older adults at risk for dementia

Synthesis and biological evaluation of new simple indolic non peptidic HIV Protease inhibitors: The effect of different substitution patterns

Prenatal diagnosis based on HPRT1 gene mutation in a Lesch-Nyhan family

A bi-objective optimization of airport ferry vehicle scheduling based on heuristic algorithm: A real data case study

Effects of Stress and Depolarization on Electrical Behaviors of Ferroelectric Field-Effect Transistor

Quantum-state transfer on spin-chain channels with random imperfections

Room temperature magnetic properties of ZnO nanostructured films

Bioinformatics analysis of biomarkers and transcriptional factor motifs in Down syndrome

Different heart rate variability profile during sleep in mid-later life adults with remitted early-onset versus late-onset depression

Simulation Modeling of Production System Considering Human Behavior

Biocompatible Fibroin Blended Films with Recombinant Human-like Collagen for Hepatic Tissue Engineering

Analysis of genetic variation in patients with Waardenburg syndrome type Ⅱ by next generation sequencing

Validation of the social functioning scale: Comparison and evaluation in early psychosis, autism spectrum disorder and social anxiety disorder

Analysis and application of ATP7B gene mutations in 35 patients with hepatolenticular degeneration

A novel 3-base pair deletion of the CRYAA gene identified in a large Chinese pedigree featuring autosomal dominant congenital perinuclear cataract

Prenatal diagnosis of Chinese families with phenylketonuria

Mutation screening of 433 families with Duchenne/Becker muscular dystrophy

PAX3 gene mutation analysis for two Waardenburg syndrome type Ⅰ families and their prenatal diagnosis

Mutation analyses and prenatal diagnosis in families of X-linked severe combined immunodeficiency caused by IL2Rγ gene novel mutation

PTPS gene analysis and prenatal diagnosis in patients with 6-pyruvoyl-tetra hydropterin synthase deficiency

Heart rate variability during slow wave sleep is linked to functional connectivity in the central autonomic network

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