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Showing results (981-990 of 1,023) with videos related to
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Molecular Cell
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February 7, 2026
Unbalanced chromatin binding of Polycomb complexes drives neurodevelopmental disorders
Rodrigo L Borges, Gretter González-Blanco, Harikumar Arigela, et al.
Human Molecular Genetics
|
May 5, 2018
Functional variants in TBX2 are associated with a syndromic cardiovascular and skeletal developmental disorder
Ning Liu, Kelly Schoch, Xi Luo, et al.
Frontiers in Pharmacology
|
December 20, 2018
<i>Semen cassiae</i> Extract Inhibits Contraction of Airway Smooth Muscle
Yu-Shan She, Li-Qun Ma, Bei-Bei Liu, et al.
Cellular & Molecular Immunology
|
December 31, 2025
MDA5 regulates BCR signaling and B-cell function via NF-κB-mediated DNM1
Li Luo, Yi Wang, Guofeng Fang, et al.
The Journal of Clinical Investigation
|
January 29, 2019
Stress-induced epinephrine enhances lactate dehydrogenase A and promotes breast cancer stem-like cells
Bai Cui, Yuanyuan Luo, Pengfei Tian, et al.
Elife
|
August 27, 2025
Heterozygous variants in <i>PLCG1</i> affect hearing, vision, cardiac, and immune function
Mengqi Ma, Yiming Zheng, Mingxi Deng, et al.
Clinical and Experimental Pharmacology & Physiology
|
January 5, 2019
Azithromycin inhibits muscarinic 2 receptor-activated and voltage-activated Ca<sup>2+</sup> permeant ion channels and Ca<sup>2+</sup> sensitization, relaxing airway smooth muscle contraction
Qian Wang, Meng-Fei Yu, Wen-Jing Zhang, et al.
Clinical Genetics
|
June 23, 2026
Neurodevelopmental Phenotypes and Brain Anomalies in Individuals With Heterozygous SEMA6A Variants
Evan Burchfiel, Xiaonan Zhao, Nichole M Owen, et al.
Biochemistry and Biophysics Reports
|
December 16, 2025
Single nucleotide variants in <i>UNC13C</i> associated with neurodevelopmental disorders affect ethanol sensitivity in <i>Drosophila</i>
Franz Müller, Sonja Neuser, Gaurav Shrestha, et al.
Cell
|
May 30, 2025
A microbial amino-acid-conjugated bile acid, tryptophan-cholic acid, improves glucose homeostasis via the orphan receptor MRGPRE
Jun Lin, Qixing Nie, Jie Cheng, et al.
Page
of 103
Search research articles
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Showing results (981-990 of 1,023) with videos related to
Sort By:
Page
of 103
Molecular Cell
|
February 7, 2026
Unbalanced chromatin binding of Polycomb complexes drives neurodevelopmental disorders
Rodrigo L Borges, Gretter González-Blanco, Harikumar Arigela, et al.
Human Molecular Genetics
|
May 5, 2018
Functional variants in TBX2 are associated with a syndromic cardiovascular and skeletal developmental disorder
Ning Liu, Kelly Schoch, Xi Luo, et al.
Frontiers in Pharmacology
|
December 20, 2018
<i>Semen cassiae</i> Extract Inhibits Contraction of Airway Smooth Muscle
Yu-Shan She, Li-Qun Ma, Bei-Bei Liu, et al.
Cellular & Molecular Immunology
|
December 31, 2025
MDA5 regulates BCR signaling and B-cell function via NF-κB-mediated DNM1
Li Luo, Yi Wang, Guofeng Fang, et al.
The Journal of Clinical Investigation
|
January 29, 2019
Stress-induced epinephrine enhances lactate dehydrogenase A and promotes breast cancer stem-like cells
Bai Cui, Yuanyuan Luo, Pengfei Tian, et al.
Elife
|
August 27, 2025
Heterozygous variants in <i>PLCG1</i> affect hearing, vision, cardiac, and immune function
Mengqi Ma, Yiming Zheng, Mingxi Deng, et al.
Clinical and Experimental Pharmacology & Physiology
|
January 5, 2019
Azithromycin inhibits muscarinic 2 receptor-activated and voltage-activated Ca<sup>2+</sup> permeant ion channels and Ca<sup>2+</sup> sensitization, relaxing airway smooth muscle contraction
Qian Wang, Meng-Fei Yu, Wen-Jing Zhang, et al.
Clinical Genetics
|
June 23, 2026
Neurodevelopmental Phenotypes and Brain Anomalies in Individuals With Heterozygous SEMA6A Variants
Evan Burchfiel, Xiaonan Zhao, Nichole M Owen, et al.
Biochemistry and Biophysics Reports
|
December 16, 2025
Single nucleotide variants in <i>UNC13C</i> associated with neurodevelopmental disorders affect ethanol sensitivity in <i>Drosophila</i>
Franz Müller, Sonja Neuser, Gaurav Shrestha, et al.
Cell
|
May 30, 2025
A microbial amino-acid-conjugated bile acid, tryptophan-cholic acid, improves glucose homeostasis via the orphan receptor MRGPRE
Jun Lin, Qixing Nie, Jie Cheng, et al.
Page
of 103