Canlyniadau Chwilio - Ayturk, Ugur M.

The Unmixing Problem: A Guide to Applying Single-Cell RNA Sequencing to Bone: APPLYING SINGLE-CELL RNA SEQUENCING TO BONE gan Greenblatt, Matthew B, Ono, Noriaki, Ayturk, Ugur M, Debnath, Shawon, Lalani, Sarfaraz

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Distinct molecular pathways mediate Mycn and Myc-regulated miR-17-92 microRNA action in Feingold syndrome mouse models gan Mirzamohammadi, Fatemeh, Kozlova, Anastasia, Papaioannou, Garyfallia, Paltrinieri, Elena, Ayturk, Ugur M., Kobayashi, Tatsuya

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SHP2 Regulates Chondrocyte Terminal Differentiation, Growth Plate Architecture and Skeletal Cell Fates gan Bowen, Margot E., Ayturk, Ugur M., Kurek, Kyle C., Yang, Wentian, Warman, Matthew L.

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RNAseq and RNA molecular barcoding reveal differential gene expression in cortical bone following hindlimb unloading in female mice gan Spatz, Jordan M., Ko, Frank C., Ayturk, Ugur M., Warman, Matthew L., Bouxsein, Mary L.

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Immediate Administration of Intraarticular Triamcinolone Acetonide after Joint Injury Modulates Molecular Outcomes Associated with Early Synovitis gan Sieker, Jakob T., Ayturk, Ugur M., Proffen, Benedikt L., Weissenberger, Manuela H., Kiapour, Ata M., Murray, Martha M.

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The role of Meteorin‐like in skeletal development and bone fracture healing gan Huang, Rong, Balu, Abhinav R., Molitoris, Kristin H., White, James P., Robling, Alexander G., Ayturk, Ugur M., Baht, Gurpreet S.

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Identification of a Prg4-positive articular cartilage progenitor cell population gan Kozhemyakina, Elena, Zhang, Minjie, Ionescu, Andreia, Ayturk, Ugur M., Ono, Noriaki, Kobayashi, Akio, Kronenberg, Henry, Warman, Matthew L., Lassar, Andrew B.

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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 gan Ayturk, Ugur M., Jacobsen, Christina M., Christodoulou, Danos C., Gorham, Joshua, Seidman, Jonathan G., Seidman, Christine E., Robling, Alexander G., Warman, Matthew L.

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Proteolysis and cartilage development are activated in the synovium after surgical induction of post traumatic osteoarthritis gan Ayturk, Ugur M., Sieker, Jakob T., Haslauer, Carla M., Proffen, Benedikt L., Weissenberger, Manuela H., Warman, Matthew L., Fleming, Braden C., Murray, Martha M.

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SINGLE CELL RNA SEQUENCING OF CALVARIAL AND LONG BONE ENDOCORTICAL CELLS gan Ayturk, Ugur M., Scollan, Joseph P., Ayturk, Didem Goz, Suh, Eun Sung, Vesprey, Alexander, Jacobsen, Christina M., Pajevic, Paola Divieti, Warman, Matthew L.

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Sclerostin Inhibition Reverses Skeletal Fragility in an Lrp5-Deficient Mouse Model of OPPG Syndrome gan 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.

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Tmem100- and Acta2-Lineage Cells Contribute to Implant Osseointegration in a Mouse Model gan 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

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Targeting the LRP5 pathway improves bone properties in a mouse model of Osteogenesis Imperfecta gan 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.

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Abstract 135: A Somatic GNA11 Mutation is Associated with Extremity Capillary Malformation and Overgrowth gan 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.

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A Somatic GNA11 Mutation is Associated with Extremity Capillary Malformation and Overgrowth gan 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.

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Somatic Mosaic Activating Mutations in PIK3CA Cause CLOVES Syndrome gan 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.

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Somatic Activating Mutations in GNAQ and GNA11 Are Associated with Congenital Hemangioma gan 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.

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Somatic Activating Mutations in GNAQ and GNA11 Are Associated with Congenital Hemangioma gan 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.

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Independent validation of experimental results requires timely and unrestricted access to animal models and reagents gan 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.

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Gain-of-function mutation of microRNA-140 in human skeletal dysplasia gan 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

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