Stem Cell Therapy in Bladder Dysfunction: Where Are We? And Where Do We Have to Go?
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kim, Jae Heon | - |
dc.contributor.author | Lee, Sang-Rae | - |
dc.contributor.author | Song, Yun Seob | - |
dc.contributor.author | Lee, Hong Jun | - |
dc.date.accessioned | 2021-08-12T02:25:21Z | - |
dc.date.available | 2021-08-12T02:25:21Z | - |
dc.date.issued | 2013 | - |
dc.identifier.issn | 2314-6133 | - |
dc.identifier.issn | 2314-6141 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/14580 | - |
dc.description.abstract | To date, stem cell therapy for the bladder has been conducted mainly on an experimental basis in the areas of bladder dysfunction. The therapeutic efficacy of stem cells was originally thought to be derived from their ability to differentiate into various cell types. Studies about stem cell therapy for bladder dysfunction have been limited to an experimental basis and have been less focused than bladder regeneration. Bladder dysfunction was listed in MESH as "urinary bladder neck obstruction", "urinary bladder, overactive", and "urinary bladder, neurogenic". Using those keywords, several articles were searched and studied. The bladder dysfunction model includes bladder outlet obstruction, cryoinjured, diabetes, ischemia, and spinal cord injury. Adipose derived stem cells (ADSCs), bone marrow stem cells (BMSCs), and skeletal muscle derived stem cells (SkMSCs) are used for transplantation to treat bladder dysfunction. The main mechanisms of stem cells to reconstitute or restore bladder dysfunction are migration, differentiation, and paracrine effects. The aim of this study is to review the stem cell therapy for bladder dysfunction and to provide the status of stem cell therapy for bladder dysfunction. | - |
dc.language | 영어 | - |
dc.language.iso | ENG | - |
dc.publisher | Hindawi Publishing Corporation | - |
dc.title | Stem Cell Therapy in Bladder Dysfunction: Where Are We? And Where Do We Have to Go? | - |
dc.type | Article | - |
dc.publisher.location | 영국 | - |
dc.identifier.doi | 10.1155/2013/930713 | - |
dc.identifier.scopusid | 2-s2.0-84885660838 | - |
dc.identifier.wosid | 000324939200001 | - |
dc.identifier.bibliographicCitation | BioMed Research International, v.2013 | - |
dc.citation.title | BioMed Research International | - |
dc.citation.volume | 2013 | - |
dc.type.docType | Review | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Biotechnology & Applied Microbiology | - |
dc.relation.journalResearchArea | Research & Experimental Medicine | - |
dc.relation.journalWebOfScienceCategory | Biotechnology & Applied Microbiology | - |
dc.relation.journalWebOfScienceCategory | Medicine, Research & Experimental | - |
dc.subject.keywordPlus | SMALL-INTESTINAL SUBMUCOSA | - |
dc.subject.keywordPlus | MARROW STROMAL CELLS | - |
dc.subject.keywordPlus | GROWTH-FACTOR HGF | - |
dc.subject.keywordPlus | 1-YEAR FOLLOW-UP | - |
dc.subject.keywordPlus | ADIPOSE-TISSUE | - |
dc.subject.keywordPlus | PROMOTE RECOVERY | - |
dc.subject.keywordPlus | RAT MODEL | - |
dc.subject.keywordPlus | COLLAGEN DEPOSIT | - |
dc.subject.keywordPlus | CHRONIC ISCHEMIA | - |
dc.subject.keywordPlus | SKELETAL-MUSCLE | - |
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