Intracorporal injection of hSlo cDNA restores erectile capacity in STZ-diabetic F-344 rats in vivo. (Q45061639)

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1 January 2020

title

Intracorporal injection of hSlo cDNA restores erectile capacity in STZ-diabetic F-344 rats in vivo (English)

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9

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author name string

George J Christ

1

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1 January 2020

Nancy Day

2

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1 January 2020

Cristian Santizo

3

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Yoshi Sato

4

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Weixin Zhao

5

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Theresa Sclafani

6

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Ron Bakal

7

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Masha Salman

8

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Arnold Melman

10

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publication date

1 October 2004

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American Journal of Physiology Heart and Circulatory Physiology

1 January 2020

published in

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volume

287

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issue

4

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page(s)

H1544-53

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Potassium channels and erectile dysfunction

1 January 2020

cites work

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Gene transfer of extracellular SOD to the penis reduces O2-* and improves erectile function in aged rats

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Gene transfer of endothelial nitric oxide synthase partially restores nitric oxide synthesis and erectile function in streptozotocin diabetic rats

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Non-visualization versus normal appearance of cavernous arteries on selective internal pudendal pharmaco-angiograms: comparison with duplex scanning, cavernosal artery systolic occlusion pressure and penile brachial index

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Peripheral channelopathies as targets for potassium channel openers

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Gene therapy of erectile dysfunction in the rat with penile neuronal nitric oxide synthase

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A neuronal beta subunit (KCNMB4) makes the large conductance, voltage- and Ca2+-activated K+ channel resistant to charybdotoxin and iberiotoxin

21 January 2018

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Integrative erectile biology. The effects of age and disease on gap junctions and ion channels and their potential value to the treatment of erectile dysfunction

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The successful long-term treatment of age related erectile dysfunction with hSlo cDNA in rats in vivo.

21 January 2018

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Gene therapy: future therapy for erectile dysfunction

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A comparison of penile brachial index and angiography: evaluation of corpora cavernosa arterial inflow

21 January 2018

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Potassium channel function in vascular disease

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Nitric oxide synthase gene therapy for erectile dysfunction: comparison of plasmid, adenovirus, and adenovirus-transduced myoblast vectors

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