Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/1128
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dc.contributor.authorGupta, Sarika-
dc.contributor.authorVijayan, Viji-
dc.date.accessioned2020-10-13T10:01:40Z-
dc.date.available2020-10-13T10:01:40Z-
dc.date.issued2018-
dc.identifier.urihttp://hdl.handle.net/123456789/1128-
dc.description.abstractOver the years, numerous mechanisms have been identified through which homocysteine affects osteoblast functioning. These include alterations in collagen structure, epigenetic modifications and changes in RANKL-OPG production by osteoblasts. These mechanisms are reviewed in this chapter. We have also herein discussed how homocysteine affects osteocyte behavior. With onset of hyperhomocysteinemia induction of osteocyte specific genes particularly the mineralization genes like Dmp1 and Sost is facilitated producing untoward mineralization, osteocyte apoptosis, deviations from regular bone remodeling process and onset of targeted remodeling in bone. These modifications have immense effect on the overall mechanical stability of bone. Homocysteine thus represents an independent risk factor for bone fragility.en_US
dc.language.isoenen_US
dc.publisherIntechOpenen_US
dc.subjecthomocysteine, osteoblast, osteocyte, sclerostin, dentine matrix protein1en_US
dc.titleHow Homocysteine Modulates the Function of Osteoblasts and Osteocytesen_US
dc.journalNon-Proteinogenic Amino Acidsen_US
dc.volumenodoi.org/10.5772/intechopen.76398en_US
Appears in Collections:Molecular Sciences, Publications

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