Normal hematopoiesis and lack of β-catenin activation in osteoblasts of patients and mice harboring Lrp5 gain-of-function mutations

Autor: Galán-Díez, Marta, Isa, Adiba, Ponzetti, Marco, Nielsen, Morten Frost, Kassem, Moustapha, Kousteni, Stavroula

Publikováno v: In BBA - Molecular Cell Research March 2016 1863(3):490-498

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Mitochondrial DNA point mutation is associated with lower bone turnover markers

Autor: Anja Lisbeth Frederiksen, Nielsen Morten Frost, Stinus J. Hansen, Per Heden Andersen, Jakob Høgild Langdahl, John Vissing, Knud Bonnet Yderstræde, Morten Duno

Publikováno v: Bone Abstracts.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0dc1717f24bae8d5c9169f07d7d8a863
https://doi.org/10.1530/boneabs.5.p252

Neonatal High Bone Mass With First Mutation Of The NF-κB Complex: Heterozygous De Novo Missense (p.Asp512Ser) RELA (Rela/p65)

Autor: Frederiksen, Anja Lisbeth, Larsen, Martin Jakob, Brusgaard, Klaus, Norvack, Deborah V, Knudsen, Peter Juel Thiis, Schrøder, Henrik Daa, Qiu, Weimin, Eckhardt, Christina, McAlister, William H, Kassem, Moustapha, Mumm, Steven, Nielsen, Morten Frost Munk, Whyte, Michael P

Publikováno v: Frederiksen, A L, Larsen, M J, Brusgaard, K, Norvack, D V, Knudsen, P J T, Schrøder, H D, Qiu, W, Eckhardt, C, McAlister, W H, Kassem, M, Mumm, S, Nielsen, M F M & Whyte, M P 2016, ' Neonatal High Bone Mass With First Mutation Of The NF-κB Complex : Heterozygous De Novo Missense (p.Asp512Ser) RELA (Rela/p65) ', Journal of Bone and Mineral Research, vol. 31, no. 1, pp. 163–172 . https://doi.org/10.1002/jbmr.2590

Heritable disorders that feature high bone mass (HBM) are rare. The etiology is typically a mutation(s) within a gene that regulates the differentiation and function of osteoblasts (OBs) or osteoclasts (OCs). Nevertheless, the molecular basis is unkn

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::95de496eb3f9090ec8737b096507ba7e
https://europepmc.org/articles/PMC5310715/

Diabetes og hørenedsættelse på grund af mitokondriel punktmutation

Autor: Lauterlein, Jens-Jacob, Olsen, Inger, Yderstræde, Knud Bonnet, Nielsen, Morten Frost Munk

Publikováno v: Lauterlein, J-J, Olsen, I, Yderstræde, K B & Nielsen, M F M 2014, ' Diabetes og hørenedsættelse på grund af mitokondriel punktmutation ', Ugeskrift for Laeger, bind 176, nr. 19, V05130313, s. 1783-1785 .

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3062::961b0b283e51ce71df5577bc42ce3ccd
https://portal.findresearcher.sdu.dk/da/publications/49684dd0-a978-4834-8abb-b132ceef6047