نتائج البحث - 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 حسب Mirzamohammadi, Fatemeh, Kozlova, Anastasia, Papaioannou, Garyfallia, Paltrinieri, Elena, Ayturk, Ugur M., Kobayashi, Tatsuya
منشور في 2018نص -
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RNAseq and RNA molecular barcoding reveal differential gene expression in cortical bone following hindlimb unloading in female mice حسب Spatz, Jordan M., Ko, Frank C., Ayturk, Ugur M., Warman, Matthew L., Bouxsein, Mary L.
منشور في 2021نص -
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Immediate Administration of Intraarticular Triamcinolone Acetonide after Joint Injury Modulates Molecular Outcomes Associated with Early Synovitis حسب Sieker, Jakob T., Ayturk, Ugur M., Proffen, Benedikt L., Weissenberger, Manuela H., Kiapour, Ata M., Murray, Martha M.
منشور في 2016نص -
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Identification of a Prg4-positive articular cartilage progenitor cell population حسب Kozhemyakina, Elena, Zhang, Minjie, Ionescu, Andreia, Ayturk, Ugur M., Ono, Noriaki, Kobayashi, Akio, Kronenberg, Henry, Warman, Matthew L., Lassar, Andrew B.
منشور في 2015نص -
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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 حسب Ayturk, Ugur M., Jacobsen, Christina M., Christodoulou, Danos C., Gorham, Joshua, Seidman, Jonathan G., Seidman, Christine E., Robling, Alexander G., Warman, Matthew L.
منشور في 2013نص -
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Proteolysis and cartilage development are activated in the synovium after surgical induction of post traumatic osteoarthritis حسب Ayturk, Ugur M., Sieker, Jakob T., Haslauer, Carla M., Proffen, Benedikt L., Weissenberger, Manuela H., Warman, Matthew L., Fleming, Braden C., Murray, Martha M.
منشور في 2020نص -
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SINGLE CELL RNA SEQUENCING OF CALVARIAL AND LONG BONE ENDOCORTICAL CELLS حسب Ayturk, Ugur M., Scollan, Joseph P., Ayturk, Didem Goz, Suh, Eun Sung, Vesprey, Alexander, Jacobsen, Christina M., Pajevic, Paola Divieti, Warman, Matthew L.
منشور في 2020نص -
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Sclerostin Inhibition Reverses Skeletal Fragility in an Lrp5-Deficient Mouse Model of OPPG Syndrome حسب 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.
منشور في 2013نص -
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Tmem100- and Acta2-Lineage Cells Contribute to Implant Osseointegration in a Mouse Model حسب 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
منشور في 2021نص -
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Targeting the LRP5 pathway improves bone properties in a mouse model of Osteogenesis Imperfecta حسب 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.
منشور في 2014نص -
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Abstract 135: A Somatic GNA11 Mutation is Associated with Extremity Capillary Malformation and Overgrowth حسب 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.
منشور في 2017نص -
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A Somatic GNA11 Mutation is Associated with Extremity Capillary Malformation and Overgrowth حسب 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.
منشور في 2017نص -
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Somatic Mosaic Activating Mutations in PIK3CA Cause CLOVES Syndrome حسب 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.
منشور في 2012نص -
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Somatic Activating Mutations in GNAQ and GNA11 Are Associated with Congenital Hemangioma حسب 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.
منشور في 2016نص -
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Somatic Activating Mutations in GNAQ and GNA11 Are Associated with Congenital Hemangioma حسب 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.
منشور في 2016نص -
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Independent validation of experimental results requires timely and unrestricted access to animal models and reagents حسب 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.
منشور في 2020نص -
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Gain-of-function mutation of microRNA-140 in human skeletal dysplasia حسب 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
منشور في 2019نص