Novel molecular cues for dental defects in hypophosphatasia

Melms H, Herrmann M, Förstner K, Bharti R, Schneider D, Mentrup B, Rudert M, Schlagenhauf U, Jakob F, Graser S (2020)

In: ((Bitte Journal prüfen)), 390.

Research article (journal)

Increased resorption activity of osteoclasts observed in Transient Receptor Potential Channel TRPC6 deficient mice and cell lines can be attenuated by inhibition of TRPC3

Birgit Mentrup, Melanie Timmen, Sebastian Klein, Daniel Kronenberg, Richard Stange (2019)

In: 46th European Calcified Tissue Society Congress, Budapest, Ungarn.

Abstract in digital collection (conference)

Direkter Zell-Zell-Kontakt von endothelialen Vorläuferzellen mit mesenchymalen Stammzellen des Knochenmarks steigert die endogene Expression von Klotho

Norbert Schütze, Bettina Hafen, Birgit Mentrup, Susanne Jatzke, Franz Jakob (2019)

In: Osteologie-Tagung, Frankfurt.

Abstract in digital collection (conference)

A Fosmid Pool-Based Next Generation Sequencing Approach to Haplotype-Resolve Whole Genomes.

Suk EK, Schulz S, Mentrup B, Huebsch T, Duitama J, Hoehe MR (2017)

In: ((Bitte Journal prüfen)), 1551.

Research article (journal)

Exome sequencing identifies a nonsense mutation in Fam46a associated with bone abnormalities in a new mouse model for skeletal dysplasia.

Diener S, Bayer S, Sabrautzki S, Wieland T, Mentrup B, Przemeck GK, Rathkolb B, Graf E, Hans W, Fuchs H, Horsch M, Schwarzmayr T, Wolf E, Klopocki E, Jakob F, Strom TM, Hrabě de Angelis M, Lorenz-Depiereux B (2016)

In: ((Bitte Journal prüfen)), 27(3-4).

Research article (journal)

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BMP-2 signaling is enhanced in case of integrin α2β1-dependent collagen upregulation in the musculoskeletal system Brand M, Kronenberg D, Everding J, Timmen M, Mentrup B, Stange (2021) In: The European Calcified Tissue Society, digital. Abstract in digital collection (conference)
Novel molecular cues for dental defects in hypophosphatasia Melms H, Herrmann M, Förstner K, Bharti R, Schneider D, Mentrup B, Rudert M, Schlagenhauf U, Jakob F, Graser S (2020) In: ((Bitte Journal prüfen)), 390. Research article (journal)
Modulation of Transient Receptor Potential Channels 3 and 6 regulates osteoclast function with impact on trabecular bone loss Klein S, Mentrup B, Timmen M, Sherwood J, Lindemann O, Fobker M, Kronenberg D, Pap T, Raschke MJ, Stange R (2020) In: Calcified Tissue International, 106. Research article (journal)
Increased resorption activity of osteoclasts observed in Transient Receptor Potential Channel TRPC6 deficient mice and cell lines can be attenuated by inhibition of TRPC3 Birgit Mentrup, Melanie Timmen, Sebastian Klein, Daniel Kronenberg, Richard Stange (2019) In: 46th European Calcified Tissue Society Congress, Budapest, Ungarn. Abstract in digital collection (conference)
TNAP inhibition in periodontal ligament cells during osteogenic differentiation leads to differential expression of mineralization and inflammation associated genes Hannah Melms, Franz Jakob, Marietta Herrmann, Konrad Förstner, Richa Bhart, Birgit Mentrup, Ullrich Schlagenhauf, Stephanie Graser (2019) In: 46th European Calcified Tissue Society Congress, Budapest, Ungarn. Abstract in digital collection (conference)
Direkter Zell-Zell-Kontakt von endothelialen Vorläuferzellen mit mesenchymalen Stammzellen des Knochenmarks steigert die endogene Expression von Klotho Norbert Schütze, Bettina Hafen, Birgit Mentrup, Susanne Jatzke, Franz Jakob (2019) In: Osteologie-Tagung, Frankfurt. Abstract in digital collection (conference)
A homozygous intronic branch-point deletion in the ALPL gene causes infantile hypophosphatasia. Mentrup B, Girschick H, Jakob F, Hofmann C (2017) In: Bone, 94. Research article (journal)
A Fosmid Pool-Based Next Generation Sequencing Approach to Haplotype-Resolve Whole Genomes. Suk EK, Schulz S, Mentrup B, Huebsch T, Duitama J, Hoehe MR (2017) In: ((Bitte Journal prüfen)), 1551. Research article (journal)
Human Platelet Lysate versus Fetal Calf Serum: These Supplements Do Not Select for Different Mesenchymal Stromal Cells. Fernandez-Rebollo E, Mentrup B, Ebert R, Franzen J, Abagnale G, Sieben T, Ostrowska A, Hoffmann P, Roux PF, Rath B, Goodhardt M, Lemaitre JM, Bischof O, Jakob F, Wagner W (2017) In: ((Bitte Journal prüfen)), 7(1). Research article (journal)
Exome sequencing identifies a nonsense mutation in Fam46a associated with bone abnormalities in a new mouse model for skeletal dysplasia. Diener S, Bayer S, Sabrautzki S, Wieland T, Mentrup B, Przemeck GK, Rathkolb B, Graf E, Hans W, Fuchs H, Horsch M, Schwarzmayr T, Wolf E, Klopocki E, Jakob F, Strom TM, Hrabě de Angelis M, Lorenz-Depiereux B (2016) In: ((Bitte Journal prüfen)), 27(3-4). Research article (journal)