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2016, Di 1 ban., Zhongguo yi shu yan jiu yuan xue shu wen ku, ISBN 7569907361, 231 pages
Book
Journal Article
Heart and Vessels, ISSN 0910-8327, 9/2018, Volume 33, Issue 9, pp. 1094 - 1105
Sinoatrial node fibrosis is involved in the pathogenesis of sinus sick syndrome (SSS). Transient receptor potential (TRP) subfamily M member 7 (TRPM7) is... 
Biomedical Engineering | Smad2 | Medicine & Public Health | Cardiac Surgery | Sinoatrial node | Collagen | Vascular Surgery | TRPM7 | Cardiology | Angiotensin II | Sick sinus syndrome | LOSARTAN | CARDIAC & CARDIOVASCULAR SYSTEMS | INDUCED CARDIAC FIBROSIS | KINASE-C-DELTA | FIBROBLASTS | ATRIAL-FIBRILLATION | CALCIUM | PERIPHERAL VASCULAR DISEASE | SMOOTH-MUSCLE-CELLS | CHANNELS | PACEMAKER | HYPERTENSIVE-RATS | Immunohistochemistry | Cell Proliferation | Male | Sick Sinus Syndrome - diagnosis | Fibrosis - metabolism | Sinoatrial Node - drug effects | RNA - genetics | Smad2 Protein - biosynthesis | TRPM Cation Channels - biosynthesis | Sick Sinus Syndrome - chemically induced | Myocardium - metabolism | Smad2 Protein - genetics | Female | Angiotensin II - toxicity | Real-Time Polymerase Chain Reaction | Sick Sinus Syndrome - genetics | Disease Models, Animal | Enzyme-Linked Immunosorbent Assay | Fibrosis - chemically induced | Signal Transduction | Cells, Cultured | Gene Expression Regulation | Rats | Myocardium - pathology | Rats, Sprague-Dawley | Blotting, Western | Sinoatrial Node - pathology | Animals | Sinoatrial Node - metabolism | TRPM Cation Channels - genetics | Fibrosis - pathology | Heart | Smad protein | Pathogenesis | Collagens | Tissue culture | Sodium hydroxide | Transient receptor potential proteins | Synthesis | Sinus | Smad2 protein | Rodents | Animal tissues | Fibroblasts | Atria | Heart diseases | Enzyme-linked immunosorbent assay | siRNA | Signaling | Sodium | Plasmids | Fibrosis | Angiotensin | Original
Journal Article
Artificial Organs, ISSN 0160-564X, 11/2017, Volume 41, Issue 11, pp. 1004 - 1016
Tissue‐engineered human anterior hemi‐cornea (TE‐aHC) is a promising equivalent for treating anterior lamellar keratopathy to surmount the severe shortage of... 
Canine model | Human corneal stromal cell | Tissue‐engineered anterior hemi‐cornea | Acellular porcine corneal stromata | Human corneal epithelial cell | Lamellar keratoplasty | MATRIX | ENGINEERING, BIOMEDICAL | RECONSTRUCTION | AMNIOTIC MEMBRANE | ESTABLISHMENT | TRANSPLANTATION | Tissue-engineered anterior hemi-cornea | EPITHELIUM | LINE | RABBIT | STROMA | PORCINE CORNEAS | SCAFFOLD | Stromal Cells - transplantation | Cell Proliferation | Epithelial Cells - metabolism | Stromal Cells - pathology | Humans | Male | Epithelium, Corneal - pathology | Regenerative Medicine - methods | Tissue Scaffolds | Corneal Stroma - transplantation | Heterografts | Cell Culture Techniques | Biomarkers - metabolism | Epithelial Cells - transplantation | Tissue Engineering - methods | Corneal Stroma - metabolism | Corneal Transplantation - methods | Stromal Cells - metabolism | Cells, Cultured | Epithelial Cells - pathology | Epithelium, Corneal - transplantation | Regeneration | Phenotype | Animals | Corneal Stroma - pathology | Dogs | Epithelium, Corneal - metabolism | Sus scrofa | Cornea | Animal models | Construction | Transparency | Glycosaminoglycans | Tissue engineering | Stroma | Transplantation | Epithelium | Regeneration (physiology) | Mimicry | Fibers | Proteins | Thickness | Equivalence | Morphology | Collagen | Surgery | Eye (anatomy) | Intraocular pressure
Journal Article
Journal Article
Molecular and Cellular Proteomics, ISSN 1535-9476, 04/2009, Volume 8, Issue 4, pp. 639 - 649
Extensive efforts have been devoted to determining the binding specificity of Src homology 3 (SH3) domains usually in a case-by-case manner. A generic... 
Amino Acid Sequence | Reproducibility of Results | Peptides - metabolism | Peptides - chemistry | Computational Biology | Proto-Oncogene Proteins c-abl - chemistry | Models, Molecular | Molecular Sequence Data | Protein Array Analysis | Protein Binding | Structure-Activity Relationship | src Homology Domains | Research
Journal Article
Journal Article
Journal Article
Oncogene: including Oncogene Reviews, ISSN 0950-9232, 01/2019, Volume 38, Issue 25, pp. 4932 - 4947
Journal Article
Cell death & disease, ISSN 2041-4889, 05/2018, Volume 9, Issue 6, pp. 609 - 10
Limb girdle muscular dystrophy type 2L (LGMD2L) and Miyoshi myopathy type 3 (MMD3) are autosomal recessive muscular dystrophy caused by mutations in the gene... 
CRISPR | Zygotes | Phenotypes | Creatine kinase | Miyoshi myopathy | Fibrosis | Mutation | Dystrophy | Creatine | Kinases | Muscular dystrophy | Myopathy
Journal Article