13 results on '"Pan, Te-Cheng"'
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2. COL6A3 Protein Deficiency in Mice Leads to Muscle and Tendon Defects Similar to Human Collagen VI Congenital Muscular Dystrophy
3. Recessive COL6A2 C-globular Missense Mutations in Ullrich Congenital Muscular Dystrophy: ROLE OF THE C2a SPLICE VARIANT
4. New Molecular Mechanism for Ullrich Congenital Muscular Dystrophy: A Heterozygous In-Frame Deletion in the COL6A1 Gene Causes a Severe Phenotype
5. Effects on Collagen VI mRNA Stability and Microfibrillar Assembly of Three COL6A2Mutations in Two Families with Ullrich Congenital Muscular Dystrophy
6. The exon organization of the triple-helical coding regions of the human α1(VI) and α2(VI) collagen genes is highly similar
7. Fibulin-2 (FBLN2): Human cDNA Sequence, mRNA Expression, and Mapping of the Gene on Human and Mouse Chromosomes
8. There Is Temporal and Spatial Expression of α1 (IV), α2 (IV), α5 (IV), α6 (IV) Collagen Chains and β1 Integrins During the Development of the Basal Lamina in an “In Vitro” Skin Model
9. Skin Fibroblasts Are the Only Source of Nidogen During Early Basal Lamina Formation In Vitro
10. The Role of the α3(VI) Chain in Collagen VI Assembly: EXPRESSION OF AN α3(VI) CHAIN LACKING N-TERMINAL MODULES N10–N7 RESTORES COLLAGEN VI ASSEMBLY, SECRETION, AND MATRIX DEPOSITION IN AN α3(VI)-DEFICIENT CELL LINE
11. Developmental Expression and Molecular Cloning of REMP, a Novel Retinal Epithelial Membrane Protein
12. Extracellular Matrix Protein Fibulin-2 Is Expressed in the Embryonic Endocardial Cushion Tissue and Is a Prominent Component of Valves in Adult Heart
13. The Fibulin-1 Gene (FBLN1) Is Located on Human Chromosome 22 and on Mouse Chromosome 15
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