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Biallelic Mutations in MYORG Cause Autosomal Recessive Primary Familial Brain Calcification

Neuron (Cambridge, Mass.), 2018-06, Vol.98 (6), p.1116-1123.e5

2018

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Clinical spectrum and genetic landscape for hereditary spastic paraplegias in China

Molecular neurodegeneration, 2018-07, Vol.13 (1), p.36-36, Article 36

2018

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Stop-gain mutations in UBAP1 cause pure autosomal-dominant spastic paraplegia

Brain (London, England : 1878), 2019-08, Vol.142 (8), p.2238-2252

2019

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Novel mutations of PDGFRB cause primary familial brain calcification in Chinese families

Journal of human genetics, 2017-07, Vol.62 (7), p.697-701

2017

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Whole Exome Sequencing Identifies Two Novel Mutations in the Reticulon 4–Interacting Protein 1 Gene in a Chinese Family with Autosomal Recessive Optic Neuropathies

Journal of molecular neuroscience, 2019-08, Vol.68 (4), p.640-646

2019

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Analysis of gene expression and functional characterization of XPR1: a pathogenic gene for primary familial brain calcification

Cell and tissue research, 2017-11, Vol.370 (2), p.267-273

2017

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Novel CAPN1 mutations extend the phenotypic heterogeneity in combined spastic paraplegia and ataxia

Annals of clinical and translational neurology, 2020-10, Vol.7 (10), p.1862-1869

2020

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Modeling the phenotype of spinal muscular atrophy by the direct conversion of human fibroblasts to motor neurons

Oncotarget, 2017-02, Vol.8 (7), p.10945-10953

2017

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Novel Compound Missense and Intronic Splicing Mutation in ALDH18A1 Causes Autosomal Recessive Spastic Paraplegia

Frontiers in neurology, 2021-05, Vol.12, p.627531-627531

2021

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Generation of an integration-free induced pluripotent stem cell line, FJMUi001-A, from a hereditary spastic paraplegia patient carrying compound heterozygous p.P498L and p.R618W mutations in CAPN1 (SPG76)

Stem cell research, 2019-01, Vol.34, p.101354-101354, Article 101354

2019

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c.835-5T>G Variant in SMN1 Gene Causes Transcript Exclusion of Exon 7 and Spinal Muscular Atrophy

Journal of molecular neuroscience, 2018-06, Vol.65 (2), p.196-202

2018

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Chinese patients with adrenoleukodystrophy and Zellweger spectrum disorder presenting with hereditary spastic paraplegia

Parkinsonism & related disorders, 2019-08, Vol.65, p.256-260

2019

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Genetic and Clinical Profile of Chinese Patients with Autosomal Dominant Spastic Paraplegia

Molecular diagnosis & therapy, 2019-12, Vol.23 (6), p.781-789

2019

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Correction to: Whole Exome Sequencing Identifies Two Novel Mutations in the Reticulon 4–Interacting Protein 1 Gene in a Chinese Family with Autosomal Recessive Optic Neuropathies

Journal of molecular neuroscience, 2020-04, Vol.70 (4), p.631-631

2020

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Modeling the differential phenotypes of spinal muscular atrophy with high-yield generation of motor neurons from human induced pluripotent stem cells

Oncotarget, 2017-06, Vol.8 (26), p.42030-42042

2017

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Application of urine cells in drug intervention for spinal muscular atrophy

Experimental and therapeutic medicine, 2017-09, Vol.14 (3), p.1993-1998

2017

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大陸「國學熱」現狀的分析與評價

中國文哲研究通訊, 2014-03, Vol.24 (1), p.033-054

董恩林(En-Lin Dong)

2014

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Herbal prescription Chang＇an Ⅱ repairs intestinal mucosal barrier in rats with post-inflammation irritable bowel syndrome

中国药理学报：英文版, 2015 (6), p.708-715

Feng-yun WANG Min SU Yong-qiu ZHENG Xiao-ge WANG Nan KANG Ting CHEN En-lin ZHU Zhao-xiang BIAN Xu-dong TANG

2015

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Cd2Nb2Te4O15: A Novel Pseudo‐Aurivillius‐Type Tellurite with Unprecedented Nonlinear Optical Properties and Excellent Stability

Small (Weinheim an der Bergstrasse, Germany), 2023-09, Vol.19 (39)

2023

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In silico analysis of the immune microenvironment in bladder cancer

BMC cancer, 2020-03, Vol.20 (1), p.265-11, Article 265

2020

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Luminescent Nanomaterials for Energy-Efficient Display and Healthcare

ACS energy letters, 2022-03, Vol.7 (3), p.1001-1020

2022

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A Highly Reliable RRAM Physically Unclonable Function Utilizing Post-Process Randomness Source

IEEE journal of solid-state circuits, 2021-05, Vol.56 (5), p.1641-1650

2021

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Engineering COFs as smart triggers for rapid capture and controlled release of singlet oxygen

Journal of materials chemistry. A, Materials for energy and sustainability, 2021-12, Vol.9 (48), p.27434-27441

2021

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Meta-analysis with zero-event studies: a comparative study with application to COVID-19 data

Military medical research, 2021-07, Vol.8 (1), p.41-41, Article 41

2021

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High Q-factor microring resonator wrapped by the curved waveguide

Scientific reports, 2015-05, Vol.5 (1), p.10078-10078, Article 10078

2015

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Biallelic Mutations in MYORG Cause Autosomal Recessive Primary Familial Brain Calcification

Clinical spectrum and genetic landscape for hereditary spastic paraplegias in China

Stop-gain mutations in UBAP1 cause pure autosomal-dominant spastic paraplegia

Novel mutations of PDGFRB cause primary familial brain calcification in Chinese families

Whole Exome Sequencing Identifies Two Novel Mutations in the Reticulon 4–Interacting Protein 1 Gene in a Chinese Family with Autosomal Recessive Optic Neuropathies

Analysis of gene expression and functional characterization of XPR1: a pathogenic gene for primary familial brain calcification

Novel CAPN1 mutations extend the phenotypic heterogeneity in combined spastic paraplegia and ataxia

Modeling the phenotype of spinal muscular atrophy by the direct conversion of human fibroblasts to motor neurons

Novel Compound Missense and Intronic Splicing Mutation in ALDH18A1 Causes Autosomal Recessive Spastic Paraplegia

Generation of an integration-free induced pluripotent stem cell line, FJMUi001-A, from a hereditary spastic paraplegia patient carrying compound heterozygous p.P498L and p.R618W mutations in CAPN1 (SPG76)

c.835-5T>G Variant in SMN1 Gene Causes Transcript Exclusion of Exon 7 and Spinal Muscular Atrophy

Chinese patients with adrenoleukodystrophy and Zellweger spectrum disorder presenting with hereditary spastic paraplegia

Genetic and Clinical Profile of Chinese Patients with Autosomal Dominant Spastic Paraplegia

Correction to: Whole Exome Sequencing Identifies Two Novel Mutations in the Reticulon 4–Interacting Protein 1 Gene in a Chinese Family with Autosomal Recessive Optic Neuropathies

Modeling the differential phenotypes of spinal muscular atrophy with high-yield generation of motor neurons from human induced pluripotent stem cells

Application of urine cells in drug intervention for spinal muscular atrophy

大陸「國學熱」現狀的分析與評價

Herbal prescription Chang＇an Ⅱ repairs intestinal mucosal barrier in rats with post-inflammation irritable bowel syndrome

Cd2Nb2Te4O15: A Novel Pseudo‐Aurivillius‐Type Tellurite with Unprecedented Nonlinear Optical Properties and Excellent Stability

In silico analysis of the immune microenvironment in bladder cancer

Luminescent Nanomaterials for Energy-Efficient Display and Healthcare

A Highly Reliable RRAM Physically Unclonable Function Utilizing Post-Process Randomness Source

Engineering COFs as smart triggers for rapid capture and controlled release of singlet oxygen

Meta-analysis with zero-event studies: a comparative study with application to COVID-19 data

High Q-factor microring resonator wrapped by the curved waveguide

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