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Journal of Human Genetics|April 5, 2020

The Fabry disease-causing mutation, GLA IVS4+919G>A, originated in Mainland China more than 800 years agoKung-Hao Liang, Yung-Hsiu Lu, Chih-Wei Niu, et al.

Experimental Neurology|March 18, 2015

ENU mutagenesis identifies mice modeling Warburg Micro Syndrome with sensory axon degeneration caused by a deletion in Rab18Chih-Ya Cheng, Jaw-Ching Wu, Jin-Wu Tsai, et al.

Molecular Neurobiology|February 6, 2019

Rab18 Collaborates with Rab7 to Modulate Lysosomal and Autophagy Activities in the Nervous System: an Overlapping Mechanism for Warburg Micro Syndrome and Charcot-Marie-Tooth Neuropathy Type 2BFang-Shin Nian, Lei-Li Li, Chih-Ya Cheng, et al.

Plos One|May 5, 2012

Amyloid-beta (Aβ) D7H mutation increases oligomeric Aβ42 and alters properties of Aβ-zinc/copper assembliesWei-Ting Chen, Chen-Jee Hong, Ya-Tzu Lin, et al.

Plos One|December 15, 2010

ENU mutagenesis identifies mice with morbid obesity and severe hyperinsulinemia caused by a novel mutation in leptinChen-Jee Hong, Pei-Jane Tsai, Chih-Ya Cheng, et al.

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Showing results (21-30 of 25) with videos related to

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You have reached the last page of results.This site can display upto 25 results.

Journal of Human Genetics|April 5, 2020

The Fabry disease-causing mutation, GLA IVS4+919G>A, originated in Mainland China more than 800 years agoKung-Hao Liang, Yung-Hsiu Lu, Chih-Wei Niu, et al.

Experimental Neurology|March 18, 2015

ENU mutagenesis identifies mice modeling Warburg Micro Syndrome with sensory axon degeneration caused by a deletion in Rab18Chih-Ya Cheng, Jaw-Ching Wu, Jin-Wu Tsai, et al.

Molecular Neurobiology|February 6, 2019

Rab18 Collaborates with Rab7 to Modulate Lysosomal and Autophagy Activities in the Nervous System: an Overlapping Mechanism for Warburg Micro Syndrome and Charcot-Marie-Tooth Neuropathy Type 2BFang-Shin Nian, Lei-Li Li, Chih-Ya Cheng, et al.

Plos One|May 5, 2012

Amyloid-beta (Aβ) D7H mutation increases oligomeric Aβ42 and alters properties of Aβ-zinc/copper assembliesWei-Ting Chen, Chen-Jee Hong, Ya-Tzu Lin, et al.

Plos One|December 15, 2010

ENU mutagenesis identifies mice with morbid obesity and severe hyperinsulinemia caused by a novel mutation in leptinChen-Jee Hong, Pei-Jane Tsai, Chih-Ya Cheng, et al.

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