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
Gepubliceerd in J Bone Miner Res (2019)

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
Gepubliceerd in Nat Commun (2018)

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.
Gepubliceerd in 2014

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.
Gepubliceerd in Arthritis Rheumatol (2016)

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.
Gepubliceerd in Arthritis Rheumatol (2015)

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.
Gepubliceerd in 2013

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.
Gepubliceerd in PLoS One (2020)

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.
Gepubliceerd in J Bone Miner Res (2020)

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.
Gepubliceerd in 2013

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.
Gepubliceerd in 2014

Lubricin restoration in a mouse model of congenital deficiency

door Hill, Adele, Waller, Kimberly A., Cui, Yajun, Allen, Justin M., Smits, Patrick, Zhang, Ling X., Ayturk, Ugur M., Hann, Steven, Lessard, Samantha G., Zurakowski, David, Warman, Matthew L., Jay, Gregory D.
Gepubliceerd in Arthritis Rheumatol (2015)

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.
Gepubliceerd in Plast Reconstr Surg Glob Open (2017)

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.
Gepubliceerd in Angiogenesis (2017)

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.
Gepubliceerd in 2012

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.
Gepubliceerd in Am J Hum Genet (2016)

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.
Gepubliceerd in Am J Hum Genet (2016)

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.
Gepubliceerd in PLoS Genet (2020)

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
Gepubliceerd in Nat Med (2019)

An osteocalcin-deficient mouse strain without endocrine abnormalities

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, Transgenics Core, VAI Vivarium and, Paracha, Noorulain, Pidhaynyy, Bohdan, Dowd, Terry L., Robling, Alexander G., Warman, Matthew L., Williams, Bart O.
Gepubliceerd in PLoS Genet (2020)