scholarly journals Development of imaging-based diagnostic procedures for brain protein aging using a mouse model of tauopathy

2018 ◽  
Vol 152 (1) ◽  
pp. 4-9
Author(s):  
Naruhiko Sahara
Keyword(s):  
Mouse Model ◽  
Diagnostic Procedures ◽  
Brain Protein ◽  
Protein Aging

scholarly journals Altered brain protein expression profiles are associated with molecular neurological dysfunction in the PKU mouse model

2014 ◽  
Vol 129 (6) ◽  
pp. 1002-1012 ◽  
Author(s):  
Esther Imperlini ◽  
Stefania Orrù ◽  
Claudia Corbo ◽  
Aurora Daniele ◽  
Francesco Salvatore
Keyword(s):  
Mouse Model ◽  
Protein Expression ◽  
Expression Profiles ◽  
Neurological Dysfunction ◽  
Brain Protein ◽  
Protein Expression Profiles

Tumor Diagnosis

1982 ◽  
Vol 40 ◽  
pp. 262-265
Author(s):  
Bruce Mackay
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Differential Diagnosis ◽  
Light Microscopy ◽  
Clinical Examination ◽  
Ultrastructural Study ◽  
Diagnostic Procedures ◽  
Specific Diagnosis ◽  
Transmission Electron ◽  
Microscopic Diagnosis

The broadest application of transmission electron microscopy (EM) in diagnostic medicine is the identification of tumors that cannot be classified by routine light microscopy. EM is useful in the evaluation of approximately 10% of human neoplasms, but the extent of its contribution varies considerably. It may provide a specific diagnosis that can not be reached by other means, but in contrast, the information obtained from ultrastructural study of some 10% of tumors does not significantly add to that available from light microscopy. Most cases fall somewhere between these two extremes: EM may correct a light microscopic diagnosis, or serve to narrow a differential diagnosis by excluding some of the possibilities considered by light microscopy. It is particularly important to correlate the EM findings with data from light microscopy, clinical examination, and other diagnostic procedures.

Regenerating myofibers in tibialis anterior muscles of young ‘MDX’ mice

1987 ◽  
Vol 45 ◽  
pp. 726-727
Author(s):  
H. D. Geissinge ◽  
L.D. Rhodes
Keyword(s):  
Muscular Dystrophy ◽  
Mouse Model ◽  
Tibialis Anterior ◽  
Physiological Activity ◽  
Mdx Mice ◽  
Mode Of Inheritance

A recently discovered mouse model (‘mdx’) for muscular dystrophy in man may be of considerable interest, since the disease in ‘mdx’ mice is inherited by the same mode of inheritance (X-linked) as the human Duchenne (DMD) muscular dystrophy. Unlike DMD, which results in a situation in which the continual muscle destruction cannot keep up with abortive regenerative attempts of the musculature, and the sufferers of the disease die early, the disease in ‘mdx’ mice appears to be transient, and the mice do not die as a result of it. In fact, it has been reported that the severely damaged Tibialis anterior (TA) muscles of ‘mdx’ mice seem to display exceptionally good regenerative powers at 4-6 weeks, so much so, that these muscles are able to regenerate spontaneously up to their previous levels of physiological activity.

Mouse model of gastric infection with cytotoxin-expressing strain of Helicobacter pylori in studying of pathogenesis of chronic gastric ulcer

1998 ◽  
Vol 13 (11-s4) ◽  
pp. S178-S184 ◽  
Author(s):  
PETER KONTUREK ◽  
TOMASZ BRZOZOWSKI ◽  
STANISLAW KONTUREK ◽  
ELZBIETA KARCZEWSKA ◽  
ROBERT PAJDO ◽  
...  
Keyword(s):  
Helicobacter Pylori ◽  
Gastric Ulcer ◽  
Mouse Model ◽  
Chronic Gastric Ulcer

Melatonin as a sedation substitute for diagnostic procedures

2000 ◽  
Vol 42 (9) ◽  
pp. 646-647 ◽  
Author(s):  
Hilary Espezel ◽  
Carolyn Graves ◽  
James E Jan ◽  
Anton Miller ◽  
Karin Renner ◽  
...  
Keyword(s):  
Diagnostic Procedures
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