Gene Therapy for Acute Kidney Diseases

Author(s):  
Enyu Imai ◽  
Yoshitaka Isaka
Keyword(s):  
1999 ◽  
Vol 3 (3) ◽  
pp. 147-153
Author(s):  
Y. Isaka
Keyword(s):  

2019 ◽  
Vol 51 (9) ◽  
pp. 449-461
Author(s):  
Lori Davis ◽  
Frank Park

A resurgence in the development of newer gene therapy systems has led to recent successes in the treatment of B cell cancers, retinal degeneration and neuromuscular atrophy. Gene therapy offers the ability to treat the patient at the root cause of their malady by restoring normal gene function and arresting the pathological progression of their genetic disease. The current standard of care for most genetic diseases is based upon the symptomatic treatment with polypharmacy while minimizing any potential adverse effects attributed to the off-target and drug-drug interactions on the target or other organs. In the kidney, however, the development of gene therapy modifications to specific renal cells has lagged far behind those in other organ systems. Some positive strides in the past few years provide continued enthusiasm to invest the time and effort in the development of new gene therapy vectors for medical intervention to treat kidney diseases. This mini-review will systematically describe the pros and cons of the most commonly tested gene therapy vector systems derived from adenovirus, retrovirus, and adeno-associated virus and provide insight about their potential utility as a therapy for various types of genetic diseases in the kidney.


Author(s):  
Yoshitaka Isaka ◽  
Yoshitsugu Takabatake ◽  
Hiromi Rakugi
Keyword(s):  

2006 ◽  
Vol 10 (4) ◽  
pp. 229-235 ◽  
Author(s):  
Yoshitaka Isaka
Keyword(s):  

Author(s):  
Sifeng Chen ◽  
Kirsten M. Madsen ◽  
C. Craig Tisher ◽  
Anupam Agarwal
Keyword(s):  

Author(s):  
Ś Lhoták ◽  
I. Alexopoulou ◽  
G. T. Simon

Various kidney diseases are characterized by the presence of dense deposits in the glomeruli. The type(s) of immunoglobulins (Igs) present in the dense deposits are characteristic of the disease. The accurate Identification of the deposits is therefore of utmost diagnostic and prognostic importance. Immunofluorescence (IF) used routinely at the light microscopical level is unable to detect and characterize small deposits found in early stages of glomerulonephritis. Although conventional TEM is able to localize such deposits, it is not capable of determining their nature. It was therefore attempted to immunolabel at EM level IgG, IgA IgM, C3, fibrinogen and kappa and lambda Ig light chains commonly found in glomerular deposits on routinely fixed ( 2% glutaraldehyde (GA) in 0.1M cacodylate buffer) kidney biopsies.The unosmicated tissue was embedded in LR White resin polymerized by UV light at -10°C. A postembedding immunogold technique was employed


2001 ◽  
Vol 120 (5) ◽  
pp. A349-A349
Author(s):  
J TSENG ◽  
F FARNEBO ◽  
O KISKER ◽  
C BECKER ◽  
C KUO ◽  
...  

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