Results 111 to 120 of about 10,314 (209)

ISEV2026 Abstract Book

open access: yes
Journal of Extracellular Vesicles, Volume 15, Issue S1, June 2026.
wiley   +1 more source

Genetic analysis of cis-enhancers associated with bone mineral density and periodontitis in the gene SOST.

open access: yesPLoS ONE
A haplotype block at the sclerostin (SOST) gene correlates with bone mineral density (BMD) and increased periodontitis risk in smokers. Investigating the putative causal variants within this block, our study aimed to elucidate the impact of linked ...
Avneesh Chopra   +4 more
doaj   +1 more source

Simulated Microgravity Induces SOST/Sclerostin Upregulation in Osteocytes [PDF]

open access: yes, 2010
Osteocytes are theorized to be the mechanosensors and transducers of mechanical forces in bone, yet the biological mechanism of this action remains elusive.
Spatz, Jordan   +5 more
core   +1 more source

Relationship of serum calciprotein particles, sclerostin, and dehydroepiandrosterone with coronary artery calcification in maintenance hemodialysis patients

open access: yesLinchuang shenzangbing zazhi
ObjectiveTo investigate the relationships between serum calciprotein particles (CPPs), sclerostin (SOST), and dehydroepiandrosterone (DHEA) and coronary artery calcification (CAC) in maintenance hemodialysis (MHD) patients, and to evaluate the diagnostic
Chai Wen-xiu   +5 more
doaj  

Sosteli, utmark og sosial organisasjon

open access: yes, 2005
Sosteli er en ødegård i det indre av Vest-Agder, datert til folkevandringstiden. Som tittelen på oppgaven antyder er det sammenhengen mellom utnyttelsen av ressursene i utmarka og den sosiale organisasjonen som er fokus for problemstillinga i denne hovedfagsoppgaven. Sosteli er lokalisert ved et heiområdene med et rikt ressursgrunnlag.
openaire   +1 more source

Osteoblastic sclerostin loop3-LRP4 interaction required by sclerostin to inhibit bone formation. [PDF]

open access: yesBone Res
Wang L   +25 more
europepmc   +1 more source

Increased endothelial sclerostin caused by elevated DSCAM mediates multiple trisomy 21 phenotypes

open access: yesThe Journal of Clinical Investigation
Trisomy 21 (T21), a recurrent aneuploidy occurring in 1:800 births, predisposes to congenital heart disease (CHD) and multiple extracardiac phenotypes.
David M. McKean   +23 more
doaj   +1 more source

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