Suchergebnisse - Ayturk, Ugur M.
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Distinct molecular pathways mediate Mycn and Myc-regulated miR-17-92 microRNA action in Feingold syndrome mouse models von Mirzamohammadi, Fatemeh, Kozlova, Anastasia, Papaioannou, Garyfallia, Paltrinieri, Elena, Ayturk, Ugur M., Kobayashi, Tatsuya
Veröffentlicht 2018Text -
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Immediate Administration of Intraarticular Triamcinolone Acetonide after Joint Injury Modulates Molecular Outcomes Associated with Early Synovitis von Sieker, Jakob T., Ayturk, Ugur M., Proffen, Benedikt L., Weissenberger, Manuela H., Kiapour, Ata M., Murray, Martha M.
Veröffentlicht 2016Text -
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An RNA-seq Protocol to Identify mRNA Expression Changes in Mouse Diaphyseal Bone: Applications in Mice with Bone Property Altering Lrp5 Mutations von Ayturk, Ugur M., Jacobsen, Christina M., Christodoulou, Danos C., Gorham, Joshua, Seidman, Jonathan G., Seidman, Christine E., Robling, Alexander G., Warman, Matthew L.
Veröffentlicht 2013Text -
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Proteolysis and cartilage development are activated in the synovium after surgical induction of post traumatic osteoarthritis von Ayturk, Ugur M., Sieker, Jakob T., Haslauer, Carla M., Proffen, Benedikt L., Weissenberger, Manuela H., Warman, Matthew L., Fleming, Braden C., Murray, Martha M.
Veröffentlicht 2020Text -
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Sclerostin Inhibition Reverses Skeletal Fragility in an Lrp5-Deficient Mouse Model of OPPG Syndrome von Kedlaya, Rajendra, Veera, Shreya, Horan, Daniel J., Moss, Rachel E., Ayturk, Ugur M., Jacobsen, Christina M., Bowen, Margot E., Paszty, Chris, Warman, Matthew L., Robling, Alexander G.
Veröffentlicht 2013Text -
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Tmem100- and Acta2-Lineage Cells Contribute to Implant Osseointegration in a Mouse Model von Vesprey, Alexander, Suh, Eun Sung, Aytürk, Didem Göz, Yang, Xu, Rogers, Miracle, Sosa, Branden, Niu, Yingzhen, Kalajzic, Ivo, Ivashkiv, Lionel B, Bostrom, Mathias PG, Ayturk, Ugur M
Veröffentlicht 2021Text -
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Targeting the LRP5 pathway improves bone properties in a mouse model of Osteogenesis Imperfecta von Jacobsen, Christina M., Barber, Lauren A., Ayturk, Ugur M., Roberts, Heather J., Deal, Lauren E., Schwartz, Marissa A., Weis, MaryAnn, Eyre, David, Zurakowski, David, Robling, Alexander G., Warman, Matthew L.
Veröffentlicht 2014Text -
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Abstract 135: A Somatic GNA11 Mutation is Associated with Extremity Capillary Malformation and Overgrowth von Couto, Javier A., Ayturk, Ugur M., Konczyk, Dennis J., Goss, Jeremy A., Huang, August Y., Hann, Steven, Reeve, Jennifer L., Liang, Marilyn G., Bischoff, Joyce, Warman, Matthew L., Greene, Arin K.
Veröffentlicht 2017Text -
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A Somatic GNA11 Mutation is Associated with Extremity Capillary Malformation and Overgrowth von Couto, Javier A., Ayturk, Ugur M., Konczyk, Dennis J., Goss, Jeremy A., Huang, August Y., Hann, Steve, Reeve, Jennifer L., Liang, Marilyn G., Bischoff, Joyce, Warman, Matthew L., Greene, Arin K.
Veröffentlicht 2017Text -
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Somatic Mosaic Activating Mutations in PIK3CA Cause CLOVES Syndrome von Kurek, Kyle C., Luks, Valerie L., Ayturk, Ugur M., Alomari, Ahmad I., Fishman, Steven J., Spencer, Samantha A., Mulliken, John B., Bowen, Margot E., Yamamoto, Guilherme L., Kozakewich, Harry P.W., Warman, Matthew L.
Veröffentlicht 2012Text -
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Somatic Activating Mutations in GNAQ and GNA11 Are Associated with Congenital Hemangioma von Ayturk, Ugur M., Couto, Javier A., Hann, Steven, Mulliken, John B., Williams, Kaitlin L., Huang, August Yue, Fishman, Steven J., Boyd, Theonia K., Kozakewich, Harry P.W., Bischoff, Joyce, Greene, Arin K., Warman, Matthew L.
Veröffentlicht 2016Text -
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Somatic Activating Mutations in GNAQ and GNA11 Are Associated with Congenital Hemangioma von Ayturk, Ugur M., Couto, Javier A., Hann, Steven, Mulliken, John B., Williams, Kaitlin L., Huang, August Yue, Fishman, Steven J., Boyd, Theonia K., Kozakewich, Harry P.W., Bischoff, Joyce, Greene, Arin K., Warman, Matthew L.
Veröffentlicht 2016Text -
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Independent validation of experimental results requires timely and unrestricted access to animal models and reagents von Diegel, Cassandra R., Hann, Steven, Ayturk, Ugur M., Hu, Jennifer C. W., Lim, Kyung-Eun, Droscha, Casey J., Madaj, Zachary B., Foxa, Gabrielle E., Izaguirre, Isaac, Robling, Alexander G., Warman, Matthew L., Williams, Bart O.
Veröffentlicht 2020Text -
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Gain-of-function mutation of microRNA-140 in human skeletal dysplasia von Grigelioniene, Giedre, Suzuki, Hiroshi I., Taylan, Fulya, Mirzamohammadi, Fatemeh, Borochowitz, Zvi U., Ayturk, Ugur M., Tzur, Shay, Horemuzova, Eva, Lindstrand, Anna, Weis, Mary Ann, Grigelionis, Gintautas, Hammarsjö, Anna, Marsk, Elin, Nordgren, Ann, Nordenskjöld, Magnus, Eyre, David R., Warman, Matthew L., Nishimura, Gen, Sharp, Phillip A., Kobayashi, Tatsuya
Veröffentlicht 2019Text