Zoekresultaten - Ayturk, Ugur M.

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

Volledige tekst Volledige tekst Volledige tekst

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

Volledige tekst Volledige tekst Volledige tekst

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

Volledige tekst Volledige tekst Volledige tekst

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

Volledige tekst Volledige tekst Volledige tekst

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

Volledige tekst Volledige tekst Volledige tekst

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

Volledige tekst Volledige tekst Volledige tekst

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

Volledige tekst Volledige tekst Volledige tekst

An RNA-seq Protocol to Identify mRNA Expression Changes in Mouse Diaphyseal Bone: Applications in Mice with Bone Property Altering Lrp5 Mutations door Ayturk, Ugur M., Jacobsen, Christina M., Christodoulou, Danos C., Gorham, Joshua, Seidman, Jonathan G., Seidman, Christine E., Robling, Alexander G., Warman, Matthew L.

Volledige tekst Volledige tekst Volledige tekst

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

Volledige tekst Volledige tekst Volledige tekst

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

Volledige tekst Volledige tekst Volledige tekst

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

Volledige tekst Volledige tekst Volledige tekst

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

Volledige tekst Volledige tekst Volledige tekst

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

Volledige tekst Volledige tekst Volledige tekst

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

Volledige tekst Volledige tekst

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

Volledige tekst Volledige tekst Volledige tekst

Somatic Mosaic Activating Mutations in PIK3CA Cause CLOVES Syndrome door 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.

Volledige tekst Volledige tekst Volledige tekst

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

Volledige tekst Volledige tekst Volledige tekst

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

Volledige tekst Volledige tekst Volledige tekst

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

Volledige tekst Volledige tekst Volledige tekst

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

Volledige tekst Volledige tekst Volledige tekst