Altered mRNA Expression of Basement Membrane Components in Focal Glomerular Sclerosis

2015 ◽  
pp. 102-106
Author(s):  
Isao Ebihara ◽  
Tsukasa Nakamura ◽  
Shigenobu Suzuki ◽  
Yasuhiko Tomino ◽  
Hikaru Koide
Keyword(s):  
Basement Membrane ◽  
Mrna Expression ◽  
Glomerular Sclerosis ◽  
Focal Glomerular Sclerosis ◽  
Membrane Components ◽  
Basement Membrane Components

Comparison of various basement membrane components in benign and malignant peripheral nerve tumours

1992 ◽  
Vol 421 (4) ◽  
pp. 331-338 ◽  
Author(s):  
Sibylle Haraida ◽  
Andreas G. Nerlich ◽  
Karl Bise ◽  
Irmgard Wiest ◽  
Erwin Schleicher
Keyword(s):  
Basement Membrane ◽  
Peripheral Nerve ◽  
Membrane Components ◽  
Peripheral Nerve Tumours ◽  
Basement Membrane Components

Immunohistological Evaluation of Endothelial Markers and Basement Membrane Components in Port-Wine Stains

Dermatology ◽  
1988 ◽  
Vol 176 (5) ◽  
pp. 243-250 ◽  
Author(s):  
Y. Mitsuhashi ◽  
B.F. Odermatt ◽  
B.V. Schneider ◽  
U.W. Schnyder
Keyword(s):  
Basement Membrane ◽  
Port Wine ◽  
Port Wine Stains ◽  
Endothelial Markers ◽  
Membrane Components ◽  
Basement Membrane Components

Differential deposition of basement membrane components during formation of the caudal neural tube in the mouse embryo

Development ◽  
1987 ◽  
Vol 99 (4) ◽  
pp. 509-519
Author(s):  
K.S. O'Shea
Keyword(s):  
Basement Membrane ◽  
Type Iv Collagen ◽  
Heparan Sulphate ◽  
Heparan Sulphate Proteoglycan ◽  
Sulphate Proteoglycan ◽  
Secondary Neurulation ◽  
Type Iv ◽  
Posterior Neuropore ◽  
Membrane Components ◽  
Basement Membrane Components

The distribution of basement membrane and extracellular matrix components laminin, fibronectin, type IV collagen and heparan sulphate proteoglycan was examined during posterior neuropore closure and secondary neurulation in the mouse embryo. During posterior neuropore closure, these components were densely deposited in basement membranes of neuroepithelium, blood vessels, gut and notochord; although deposition was sparse in the midline of the regressing primitive streak. During secondary neurulation, mesenchymal cells formed an initial aggregate near the dorsal surface, which canalized and merged with the anterior neuroepithelium. With aggregation, fibronectin and heparan sulphate proteoglycan were first detected at the base of a 3- to 4-layer zone of radially organized cells. With formation of a lumen within the aggregate, laminin and type IV collagen were also deposited in the forming basement membrane. During both posterior neuropore closure and secondary neurulation, fibronectin and heparan sulphate proteoglycan were associated with the most caudal portion of the neuroepithelium, the region where newly formed epithelium merges with the consolidated neuroepithelium. In regions of neural crest migration, the deposition of basement membrane components was altered, lacking laminin and type IV collagen, with increased deposition of fibronectin and heparan sulphate proteoglycan.

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