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Hepatology (Baltimore, Md.)
|
March 30, 2020
The IKKβ-USP30-ACLY Axis Controls Lipogenesis and Tumorigenesis
Li Gu, Yahui Zhu, Xi Lin, et al.
Sensors (Basel, Switzerland)
|
June 24, 2022
A Novel Electrochemical Sensor Modified with a Computer-Simulative Magnetic Ion-Imprinted Membrane for Identification of Uranyl Ion
Li-Qiong He, Zhi-Mei Wang, Yu-Jie Li, et al.
Small (Weinheim an Der Bergstrasse, Germany)
|
May 24, 2022
Exploiting the Synergistic Electronic Interaction between Pt-Skin Wrapped Intermetallic PtCo Nanoparticles and Co-N-C Support for Efficient ORR/EOR Electrocatalysis in a Direct Ethanol Fuel Cell
Jiaojiao Gao, Xuyan Zhou, Yu Wang, et al.
World Journal of Surgery
|
May 7, 2003
Liver trauma: experience in 348 cases
Jing-mou Gao, Ding-yuan Du, Xing-ji Zhao, et al.
European Journal of Human Genetics : EJHG
|
November 29, 2007
Instability of expanded CAG/CAA repeats in spinocerebellar ataxia type 17
Rui Gao, Tohru Matsuura, Mary Coolbaugh, et al.
Journal of Experimental & Clinical Cancer Research : CR
|
February 18, 2010
In-vivo transfection of pcDNA3.1-IGFBP7 inhibits melanoma growth in mice through apoptosis induction and VEGF downexpression
Rong-Yi Chen, Hong-Xiang Chen, Jia-Xi Lin, et al.
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. Acta Academiae Medicinae Sinicae
|
July 19, 2007
[Association between angiotensin-converting enzyme and polymorphisms of N5, N10-methylenetetrahydrofolic acid reductase gene in patients with ischemic stroke]
Cai-ming Li, Cheng Zhang, Xi-lin Lu, et al.
Revista De Biologia Tropical
|
July 16, 2008
Clinical and molecular diagnosis of a Costa Rican family with autosomal recessive myotonia congenita (Becker disease) carrying a new mutation in the CLCN1 gene
Fernando Morales, Patricia Cuenca, Gerardo del Valle, et al.
Angewandte Chemie (International Ed. in English)
|
May 30, 2023
Directional and Ultrafast Charge Transfer in Oxygen-Vacancy-Rich ZnO@Single-Atom Cobalt Core-Shell Junction for Photo-Fenton-Like Reaction
Xi-Lin Wu, Shiang Liu, Yu Li, et al.
Human Genetics
|
April 4, 2008
Gene symbol: CLCN1. Disease: Myotonia congenita
Fernando Morales, Patricia Cuenca, Gerardo del Valle, et al.
Page
of 144
Search research articles
Search
Showing results (721-730 of 1,440) with videos related to
Sort By:
Page
of 144
Hepatology (Baltimore, Md.)
|
March 30, 2020
The IKKβ-USP30-ACLY Axis Controls Lipogenesis and Tumorigenesis
Li Gu, Yahui Zhu, Xi Lin, et al.
Sensors (Basel, Switzerland)
|
June 24, 2022
A Novel Electrochemical Sensor Modified with a Computer-Simulative Magnetic Ion-Imprinted Membrane for Identification of Uranyl Ion
Li-Qiong He, Zhi-Mei Wang, Yu-Jie Li, et al.
Small (Weinheim an Der Bergstrasse, Germany)
|
May 24, 2022
Exploiting the Synergistic Electronic Interaction between Pt-Skin Wrapped Intermetallic PtCo Nanoparticles and Co-N-C Support for Efficient ORR/EOR Electrocatalysis in a Direct Ethanol Fuel Cell
Jiaojiao Gao, Xuyan Zhou, Yu Wang, et al.
World Journal of Surgery
|
May 7, 2003
Liver trauma: experience in 348 cases
Jing-mou Gao, Ding-yuan Du, Xing-ji Zhao, et al.
European Journal of Human Genetics : EJHG
|
November 29, 2007
Instability of expanded CAG/CAA repeats in spinocerebellar ataxia type 17
Rui Gao, Tohru Matsuura, Mary Coolbaugh, et al.
Journal of Experimental & Clinical Cancer Research : CR
|
February 18, 2010
In-vivo transfection of pcDNA3.1-IGFBP7 inhibits melanoma growth in mice through apoptosis induction and VEGF downexpression
Rong-Yi Chen, Hong-Xiang Chen, Jia-Xi Lin, et al.
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. Acta Academiae Medicinae Sinicae
|
July 19, 2007
[Association between angiotensin-converting enzyme and polymorphisms of N5, N10-methylenetetrahydrofolic acid reductase gene in patients with ischemic stroke]
Cai-ming Li, Cheng Zhang, Xi-lin Lu, et al.
Revista De Biologia Tropical
|
July 16, 2008
Clinical and molecular diagnosis of a Costa Rican family with autosomal recessive myotonia congenita (Becker disease) carrying a new mutation in the CLCN1 gene
Fernando Morales, Patricia Cuenca, Gerardo del Valle, et al.
Angewandte Chemie (International Ed. in English)
|
May 30, 2023
Directional and Ultrafast Charge Transfer in Oxygen-Vacancy-Rich ZnO@Single-Atom Cobalt Core-Shell Junction for Photo-Fenton-Like Reaction
Xi-Lin Wu, Shiang Liu, Yu Li, et al.
Human Genetics
|
April 4, 2008
Gene symbol: CLCN1. Disease: Myotonia congenita
Fernando Morales, Patricia Cuenca, Gerardo del Valle, et al.
Page
of 144