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The Journal of Gene Medicine
|
June 8, 2010
Gene therapy for psoriasis in the K14-VEGF transgenic mouse model by topical transdermal delivery of interleukin-4 using ultradeformable cationic liposome
Jiong Li, Xia Li, Yan Zhang, et al.
The Journal of International Medical Research
|
June 3, 2010
Angiotensin-converting enzyme insertion/deletion polymorphism associated with acute respiratory distress syndrome among caucasians
Z Hu, X Jin, Y Kang, et al.
Clinical Genetics
|
November 1, 2013
Homozygous loss-of-function mutation of the LEPREL1 gene causes severe non-syndromic high myopia with early-onset cataract
H Guo, P Tong, Y Peng, et al.
Zhonghua Xin Xue Guan Bing Za Zhi
|
December 27, 2019
[Cardioversion efficacy of nifekalan in patients with sustained atrial fibrillation after radiofrequency ablation]
F Li, Z Xia, J H Yu, et al.
American Journal of Physiology. Cell Physiology
|
July 21, 2025
Contribution of NLRP3-GSDMD axis to PDGF-BB-induced vascular smooth muscle cell phenotypic transition
Yun-Ting Wang, Alexandra K Moura, Rui Zuo, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
April 15, 2025
Cardiovascular dysfunction and altered lysosomal signaling in a murine model of acid sphingomyelinase deficiency
Yun-Ting Wang, Alexandra K Moura, Rui Zuo, et al.
Research Square
|
April 1, 2025
Cardiovascular Dysfunction and Altered Lysosomal Signaling in a Murine Model of Acid Sphingomyelinase Deficiency
Yun-Ting Wang, Alexandra K Moura, Rui Zuo, et al.
Scientific Reports
|
March 3, 2016
Antiferromagnetic proximity effect in epitaxial CoO/NiO/MgO(001) systems
Q Li, J H Liang, Y M Luo, et al.
FEMS Immunology and Medical Microbiology
|
January 6, 2011
New methods for the detection of orthopedic and other biofilm infections
John William Costerton, James Christopher Post, Garth D Ehrlich, et al.
Zhonghua Xin Xue Guan Bing Za Zhi
|
January 20, 2017
[Recurrent syncope related to catecholaminergic polymorphic ventricular tachycardia due to de novo RyR2-R2401H mutation]
X Liu, J X Li, J Z Hu, et al.
Page
of 125
Search research articles
Search
Showing results (801-810 of 1,250) with videos related to
Sort By:
Page
of 125
The Journal of Gene Medicine
|
June 8, 2010
Gene therapy for psoriasis in the K14-VEGF transgenic mouse model by topical transdermal delivery of interleukin-4 using ultradeformable cationic liposome
Jiong Li, Xia Li, Yan Zhang, et al.
The Journal of International Medical Research
|
June 3, 2010
Angiotensin-converting enzyme insertion/deletion polymorphism associated with acute respiratory distress syndrome among caucasians
Z Hu, X Jin, Y Kang, et al.
Clinical Genetics
|
November 1, 2013
Homozygous loss-of-function mutation of the LEPREL1 gene causes severe non-syndromic high myopia with early-onset cataract
H Guo, P Tong, Y Peng, et al.
Zhonghua Xin Xue Guan Bing Za Zhi
|
December 27, 2019
[Cardioversion efficacy of nifekalan in patients with sustained atrial fibrillation after radiofrequency ablation]
F Li, Z Xia, J H Yu, et al.
American Journal of Physiology. Cell Physiology
|
July 21, 2025
Contribution of NLRP3-GSDMD axis to PDGF-BB-induced vascular smooth muscle cell phenotypic transition
Yun-Ting Wang, Alexandra K Moura, Rui Zuo, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
April 15, 2025
Cardiovascular dysfunction and altered lysosomal signaling in a murine model of acid sphingomyelinase deficiency
Yun-Ting Wang, Alexandra K Moura, Rui Zuo, et al.
Research Square
|
April 1, 2025
Cardiovascular Dysfunction and Altered Lysosomal Signaling in a Murine Model of Acid Sphingomyelinase Deficiency
Yun-Ting Wang, Alexandra K Moura, Rui Zuo, et al.
Scientific Reports
|
March 3, 2016
Antiferromagnetic proximity effect in epitaxial CoO/NiO/MgO(001) systems
Q Li, J H Liang, Y M Luo, et al.
FEMS Immunology and Medical Microbiology
|
January 6, 2011
New methods for the detection of orthopedic and other biofilm infections
John William Costerton, James Christopher Post, Garth D Ehrlich, et al.
Zhonghua Xin Xue Guan Bing Za Zhi
|
January 20, 2017
[Recurrent syncope related to catecholaminergic polymorphic ventricular tachycardia due to de novo RyR2-R2401H mutation]
X Liu, J X Li, J Z Hu, et al.
Page
of 125