Results 81 to 90 of about 11,099 (162)

Mechanical Properties of Bone Due to SOST Expression: Nanoindentation Assessment of Murine Femurs [PDF]

open access: yes, 2013
In the human genome, the SOST gene codes for a protein sclerostin. Sclerostin is an osteocyte-expressed negative regulator of bone formation. When the SOST gene is not coded, bone formation is reduced in individuals during skeletal maturation. This study
Rafie, Amir
core   +1 more source

Identification of signal peptide domain SOST mutations in autosomal dominant craniodiaphyseal dysplasia

open access: yes, 2011
Sclerosteosis and Van Buchem disease are related recessive sclerosing bone dysplasias caused by alterations in the SOST gene. We tested the hypothesis that craniodiaphyseal dysplasia (CDD) (MIM 122860), an extremely rare sclerosing bone dysplasia ...
Ah-Ra Ko   +33 more
core   +1 more source

BMP Regulation of SOST and Osterix Expression During Embryonic Osteogenesis

open access: yes, 2004
Sclerostin (SOST), a member of the cystine-knot superfamily, is essential for proper skeletogenesis since loss of function mutation in SOST gene results in sclerosteosis featured with massive bone growth in humans.
二藤 彰   +3 more
core  

SOST is a target gene for PTH in bone.

open access: yes, 2005
Intermittent parathyroid hormone (PTH) application is an established pharmacological principle to stimulate bone formation. Yet, the molecular mechanisms underlying this bone anabolic action are not fully understood.
Kneissel, Michaela, Keller, Hansjoerg
core  

Relationship Between Sclerostin (SOST) Expression and Genetic Loci rs851056, rs1230399 Polymorphisms and Bone Mineral Density in Postmenopausal Women with Type 2 Diabetes in Xinjiang

open access: yesDiabetes, Metabolic Syndrome and Obesity, 2021
Jun Li,1,* YanXia Ren,1,* SiYuan Li,2 JiaJia Li3 1Endocrinology and Metabolism Department, First Affiliated Hosptital, School of Medicine, Shihezi University, Shihezi, Xinjiang Uygur Autonomous Region, People’s Republic of China; 2Shihezi ...
Li J, Ren Y, Li S, Li J
doaj  

Prostaglandin E2 signals through PTGER2 to regulate sclerostin expression.

open access: yesPLoS ONE, 2011
The Wnt signaling pathway is a robust regulator of skeletal homeostasis. Gain-of-function mutations promote high bone mass, whereas loss of Lrp5 or Lrp6 co-receptors decrease bone mass.
Damian C Genetos   +2 more
doaj   +1 more source

ESEM Analysis of Mice Femurs with Varying SOST Levels [PDF]

open access: yes, 2012
This project’s goal was to analyze the properties of the cortical femur on 100 mice bones from Lawrence Livermore National Laboratory. Analysis was limited to imaging which determined the ratio of bone volume to total volume (BV/TV) and osteocyte lacunae
McClay, Patrick K.
core  

sost mRNA levels.

open access: yes, 2013
sost mRNA levels normalized actb and rplp in control and L.rhamnosus treated fingerlings sampled 9,16and 23dpf. Error bars indicate mean ± S.D.
Oliana Carnevali (306579)   +6 more
core   +1 more source

Sost down-regulation by mechanical strain in human osteoblastic cells involves PGE2 signaling via EP4 [PDF]

open access: yes, 2011
Sclerostin is a potent inhibitor of bone formation which is down-regulated by mechanical loading. To investigate the mechanisms involved we subjected Saos2 human osteoblastic cells to short periods of dynamic strain and used quantitative reverse ...
Meakin, LB   +25 more
core   +1 more source

血清硬骨素在维生素D缺乏性佝偻病诊断中的检测意义

open access: yesZhongguo shiyan zhenduanxue, 2021
硬骨素(SOST)是一种主要由骨细胞分泌的蛋白质,其主要功能是抑制成骨细胞矿化,进而抑制骨形成[1]。维生素D缺乏性佝偻病患儿早期便会出现骨矿化不足。本研究拟通过分析患维生素D缺乏性佝偻病的婴幼儿血清SOST的水平变化,探讨SOST在佝偻病诊断中的意义。
李嘉, 刘晓燕, 彭慧云, 陈耀武
doaj  

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