basic myelin protein
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1995 ◽  
Vol 81 (3) ◽  
pp. 208-212 ◽  
Author(s):  
Cesare Bosman ◽  
Renata Boldrini ◽  
Alessandro Corsi

A 43-year-old man underwent surgical removal of L4-L5 nerve root tumor which bulged to the extra and intradural spaces and extended as a dumbbell through the intervertebral foramen. Histological examination showed pleomorphic tumor cells with heavy melanin pigmentation. Most of the tumor cells were immunohistochemically positive for vimentin, S-100 protein and HMB-45 antigen; basic myelin protein was detectable in single tumor cells. Electron-microscopy revealed melanosomes in different stages of differentiation and some characteristics of Schwann cells, such as redundant basal lamina production. Taken together the tumor showed features of histological malignancy and incomplete schwannian differentiation with considerable overlap between melanoma and malignant melanotic schwannoma.


Author(s):  
G.J. VAN KAMP ◽  
J.C. KOETSIER ◽  
L. LUYENDIJK ◽  
J. O. MISPELBLOM BEIJER ◽  
C.L. VERWEY

1981 ◽  
Vol 34 (2) ◽  
pp. 345-350 ◽  
Author(s):  
G.W. Brady ◽  
N.S. Murthy ◽  
D.B. Fein ◽  
D.D. Wood ◽  
M.A. Moscarello

Biochemistry ◽  
1979 ◽  
Vol 18 (20) ◽  
pp. 4444-4448 ◽  
Author(s):  
Janis Dillaha Young ◽  
Dorinne Tsuchiya ◽  
Diane E. Sandlin ◽  
Michael J. Holroyde

Author(s):  
William Sheremata ◽  
Susan Colby ◽  
Y. Karkhanis ◽  
Edwin H. Eylar

SUMMARY:Lymphocytes of 29 subjects were assayed for MIF production in response to P2 peripheral nerve protein, crude human peripheral nerve and human central nervous system Al basic myelin protein. Seven were performed in normal control subjects, 12 in Guillain-Barré patients (GB), 5 with other polyneuropathies and 5 in patients with multiple sclerosis (MS). Only GB patients with acute illness produced MIF in response to neuritogenic P2 protein and crude human nerve. Two MS patients in the acute phase of an exacerbation and one GB patient produced MIF in Response to Al protein. The results of this study demonstrate cellular hypersensitivity to a neuritogenic constituent in peripheral nervous tissue and support the concept that this may be important in the pathogenesis of GB.


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