Synthesis And Structural Characterization Of Hydroxyapatite Obtained From CaO And CaHP04 By A Hydrothermal Method

2005 ◽  
Vol 9 (1) ◽  
pp. 20-22 ◽  
Author(s):  
V. Rodríguez-Lugo ◽  
C. Angeles-Chavez ◽  
G. Mondragon ◽  
S. Recillas-Gispert ◽  
V.M. Castaño
2014 ◽  
Vol 40 (8) ◽  
pp. 12285-12292 ◽  
Author(s):  
A. Sierra-Fernandez ◽  
L.S. Gomez-Villalba ◽  
O. Milosevic ◽  
R. Fort ◽  
M.E. Rabanal

2011 ◽  
Vol 50 (9R) ◽  
pp. 091501
Author(s):  
Hiroyuki Nii ◽  
Atsuhiro Kunishige ◽  
Hamazo Nakagawa ◽  
Tsuyoshi Koyanagi

2011 ◽  
Vol 50 (9) ◽  
pp. 091501
Author(s):  
Hiroyuki Nii ◽  
Atsuhiro Kunishige ◽  
Hamazo Nakagawa ◽  
Tsuyoshi Koyanagi

2014 ◽  
Vol 40 (7) ◽  
pp. 9997-10004 ◽  
Author(s):  
Ching Yern Chee ◽  
Kalyani Nadarajah ◽  
Mohammad Khalid Siddiqui ◽  
Yhoong Wong

2007 ◽  
Vol 19 (2) ◽  
pp. 797-803 ◽  
Author(s):  
Ming’Ou Li ◽  
Xiufeng Xiao ◽  
Rongfang Liu ◽  
Cuiyu Chen ◽  
Lizhong Huang

2005 ◽  
Vol 59 (29-30) ◽  
pp. 3841-3846 ◽  
Author(s):  
Xiao Lian Tang ◽  
Xiu Feng Xiao ◽  
Rong Fang Liu

Author(s):  
S. F. Hayes ◽  
M. D. Corwin ◽  
T. G. Schwan ◽  
D. W. Dorward ◽  
W. Burgdorfer

Characterization of Borrelia burgdorferi strains by means of negative staining EM has become an integral part of many studies related to the biology of the Lyme disease organism. However, relying solely upon negative staining to compare new isolates with prototype B31 or other borreliae is often unsatisfactory. To obtain more satisfactory results, we have relied upon a correlative approach encompassing a variety EM techniques, i.e., scanning for topographical features and cryotomy, negative staining and thin sectioning to provide a more complete structural characterization of B. burgdorferi.For characterization, isolates of B. burgdorferi were cultured in BSK II media from which they were removed by low speed centrifugation. The sedimented borrelia were carefully resuspended in stabilizing buffer so as to preserve their features for scanning and negative staining. Alternatively, others were prepared for conventional thin sectioning and for cryotomy using modified procedures. For thin sectioning, the fixative described by Ito, et al.


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