Resultats de la cerca - Ayturk, Ugur M.

The Unmixing Problem: A Guide to Applying Single-Cell RNA Sequencing to Bone: APPLYING SINGLE-CELL RNA SEQUENCING TO BONE per 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 per 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 per 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 per 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 per 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 per 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 per 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 per 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 per 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 per 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 per 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 per 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 per 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 per 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 per 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 per 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 per 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 per 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 per 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 per 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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