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CMT2Q-causing mutation in the Dhtkd1 gene lead to sensory defects, mitochondrial accumulation and altered metabolism in a knock-in mouse model

Acta neuropathologica communications, 2020-03, Vol.8 (1), p.32-32, Article 32

2020

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Geometric distortions in three-dimensional medical electronic endoscopic visualization

Ye jing yu xian shi, 2022, Vol.37 (1), p.29-36

2022

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Deletion of Gpr128 results in weight loss and increased intestinal contraction frequency

World journal of gastroenterology : WJG, 2014-01, Vol.20 (2), p.498-508

2014

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Palladin regulates cell and extracellular matrix interaction through maintaining normal actin cytoskeleton architecture and stabilizing Beta1-integrin

Journal of cellular biochemistry, 2007-04, Vol.100 (5), p.1288-1300

2007

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Event-triggered guaranteed cost control for uncertain networked Markov jump systems

2015 34th Chinese Control Conference (CCC), 2015, p.6759-6764

2015

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Mixed lighting based on the linear dimming of three-primary-color LEDs

Chinese Optics, 2024, Vol.17 (1), p.108-117

2024

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A Nonsense Mutation in DHTKD1 Causes Charcot-Marie-Tooth Disease Type 2 in a Large Chinese Pedigree

American journal of human genetics, 2012-12, Vol.91 (6), p.1088-1094

2012

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Target deletion of the cytoskeleton-associated protein palladin does not impair neurite outgrowth in mice

PloS one, 2009-09, Vol.4 (9), p.e6916-e6916

2009

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Multiple Synostoses Syndrome Is Due to a Missense Mutation in Exon 2 of FGF9 Gene

American journal of human genetics, 2009-07, Vol.85 (1), p.53-63

2009

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Research progress in early diagnosis of Alzheimer's disease

Zhongguo xian dai shen jing ji bing za zhi, 2018-03, Vol.18 (3), p.213-221

2018

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Two nonsense mutations cause protein C deficiency by nonsense-mediated mRNA decay

Thrombosis research, 2015-04, Vol.135 (4), p.733-738

2015

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Dopamine receptor 3 might be an essential molecule in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced neurotoxicity

BMC neuroscience, 2013-07, Vol.14 (1), p.76-76, Article 76

2013

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Design of Wireless Cage Culture Monitoring System Based on Remote Programme Update

Applied Mechanics and Materials, 2014-07, Vol.577 (Applied Decisions in Area of Mechanical Engineering and Industrial Manufacturing), p.655-658

2014

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Disruption of palladin leads to defects in definitive erythropoiesis by interfering with erythroblastic island formation in mouse fetal liver

Blood, 2007-08, Vol.110 (3), p.870-876

2007

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Virtual reality space reconstruction based on visual space orientation theory

Ye jing yu xian shi, 2019-02, Vol.34 (2), p.215-219

2019

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Germinal Cell Aplasia in Kif18a Mutant Male Mice Due to Impaired Chromosome Congression and Dysregulated BubR1 and CENP-E

Genes & cancer, 2010-01, Vol.1 (1), p.26-39

2010

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Nonsense-mediated mRNA decay and human monogenic disease

Yíchuán, 2012-08, Vol.34 (8), p.935

2012

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Exponential stability and stabilization of Markovian jumping singular systems with time-varying delays

Proceedings of the 32nd Chinese Control Conference, 2013, p.1596-1601

2013

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Research progress of myosin heavy chain genes in human genetic diseases

Yíchuán, 2017-10, Vol.39 (10), p.877

2017

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Genome-wide scanning for susceptibility genes in researches on six HLA-associated diseases

Zhonghua yi xue yi chuan xue za zhi, 2003-08, Vol.20 (4), p.336

2003

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Acknowledgment to reviewers of Journal of Translational Genetics and Genomics in 2022

Journal of Translational Genetics and Genomics, 2023, Vol.6 (4), p.443-444

2023

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HUP98-HOXA9 transgenic mice are susceptible to N-ethyl-N-nitrosourea stimulation in leukemogenesis

Zhōnghuá xuèyèxué zázhì, 2004-05, Vol.25 (5), p.257

2004

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Development of human myeloid leukemia-like phenotype in NUP98-PMX1 transgenic mice

Zhōnghuá xuèyèxué zázhì, 2004-05, Vol.25 (5), p.262-265

2004

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The functional mechanisms and clinical application of read-through drugs

Yíchuán, 2016-07, Vol.38 (7), p.623

2016

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The relationship between haplotypes of multilocus markers and ankylosing spondylitis

Zhonghua yi xue yi chuan xue za zhi, 2004-08, Vol.21 (4), p.312

2004

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CMT2Q-causing mutation in the Dhtkd1 gene lead to sensory defects, mitochondrial accumulation and altered metabolism in a knock-in mouse model

Geometric distortions in three-dimensional medical electronic endoscopic visualization

Deletion of Gpr128 results in weight loss and increased intestinal contraction frequency

Palladin regulates cell and extracellular matrix interaction through maintaining normal actin cytoskeleton architecture and stabilizing Beta1-integrin

Event-triggered guaranteed cost control for uncertain networked Markov jump systems

Mixed lighting based on the linear dimming of three-primary-color LEDs

A Nonsense Mutation in DHTKD1 Causes Charcot-Marie-Tooth Disease Type 2 in a Large Chinese Pedigree

Target deletion of the cytoskeleton-associated protein palladin does not impair neurite outgrowth in mice

Multiple Synostoses Syndrome Is Due to a Missense Mutation in Exon 2 of FGF9 Gene

Research progress in early diagnosis of Alzheimer's disease

Two nonsense mutations cause protein C deficiency by nonsense-mediated mRNA decay

Dopamine receptor 3 might be an essential molecule in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced neurotoxicity

Design of Wireless Cage Culture Monitoring System Based on Remote Programme Update

Disruption of palladin leads to defects in definitive erythropoiesis by interfering with erythroblastic island formation in mouse fetal liver

Virtual reality space reconstruction based on visual space orientation theory

Germinal Cell Aplasia in Kif18a Mutant Male Mice Due to Impaired Chromosome Congression and Dysregulated BubR1 and CENP-E

Nonsense-mediated mRNA decay and human monogenic disease

Exponential stability and stabilization of Markovian jumping singular systems with time-varying delays

Research progress of myosin heavy chain genes in human genetic diseases

Genome-wide scanning for susceptibility genes in researches on six HLA-associated diseases

Acknowledgment to reviewers of Journal of Translational Genetics and Genomics in 2022

HUP98-HOXA9 transgenic mice are susceptible to N-ethyl-N-nitrosourea stimulation in leukemogenesis

Development of human myeloid leukemia-like phenotype in NUP98-PMX1 transgenic mice

The functional mechanisms and clinical application of read-through drugs

The relationship between haplotypes of multilocus markers and ankylosing spondylitis

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