Comprehensive Expression Analysis of microRNAs and mRNAs in Synovial Tissue from a Mouse Model of Early Post-Traumatic Osteoarthritis

por Kung, Louise H. W., Ravi, Varshini, Rowley, Lynn, Bell, Katrina M., Little, Christopher B., Bateman, John F.
Publicado 2017

Excellent 10-year patient-reported outcomes and survival in a single-radius, cruciate-retaining total knee arthroplasty

por Scott, Chloe E. H., Bell, Katrina R., Ng, Richard T., MacDonald, Deborah J., Patton, James T., Burnett, Richard
Publicado 2018

Familial bilateral cryptorchidism is caused by recessive variants in RXFP2

por Ayers, Katie, Kumar, Rakesh, Robevska, Gorjana, Bruell, Shoni, Bell, Katrina, Malik, Muneer A, Bathgate, Ross A, Sinclair, Andrew
Publicado 2019

ADAMTS-9 in Mouse Cartilage Has Aggrecanase Activity That Is Distinct from ADAMTS-4 and ADAMTS-5

por Rogerson, Fraser M., Last, Karena, Golub, Suzanne B., Gauci, Stephanie J., Stanton, Heather, Bell, Katrina M., Fosang, Amanda J.
Publicado 2019

Fifteen-year prospective longitudinal cohort study of outcomes following single radius total knee arthroplasty: patient-reported outcome measures, response attrition, and survival

por Scott, Chloe E. H., Snowden, Gordon T., Cawley, Will, Bell, Katrina R., MacDonald, Deborah J., Macpherson, Gavin J., Yapp, Liam Z., Clement, Nick D.
Publicado 2023

Transcriptional Profiling of Chondrodysplasia Growth Plate Cartilage Reveals Adaptive ER-Stress Networks That Allow Survival but Disrupt Hypertrophy

por Cameron, Trevor L., Bell, Katrina M., Tatarczuch, Liliana, Mackie, Eleanor J., Rajpar, M. Helen, McDermott, Ben T., Boot-Handford, Raymond P., Bateman, John F.
Publicado 2011

XBP1-Independent UPR Pathways Suppress C/EBP-β Mediated Chondrocyte Differentiation in ER-Stress Related Skeletal Disease

por Cameron, Trevor L., Bell, Katrina M., Gresshoff, Irma L., Sampurno, Lisa, Mullan, Lorna, Ermann, Joerg, Glimcher, Laurie H., Boot-Handford, Raymond P., Bateman, John F.
Publicado 2015

Integral Role of the Mitochondrial Ribosome in Supporting Ovarian Function: MRPS7 Variants in Syndromic Premature Ovarian Insufficiency

por Kline, Brianna L., Jaillard, Sylvie, Bell, Katrina M., Bakhshalizadeh, Shabnam, Robevska, Gorjana, van den Bergen, Jocelyn, Dulon, Jérôme, Ayers, Katie L., Christodoulou, John, Tchan, Michel C., Touraine, Philippe, Sinclair, Andrew H., Tucker, Elena J.
Publicado 2022

Modeling human skeletal development using human pluripotent stem cells

por Lamandé, Shireen R., Ng, Elizabeth S., Cameron, Trevor L., Kung, Louise H. W., Sampurno, Lisa, Rowley, Lynn, Lilianty, Jinia, Patria, Yudha Nur, Stenta, Tayla, Hanssen, Eric, Bell, Katrina M., Saxena, Ritika, Stok, Kathryn S., Stanley, Edouard G., Elefanty, Andrew G., Bateman, John F.
Publicado 2023

The role of cardiac transcription factor NKX2-5 in regulating the human cardiac miRNAome

por Arasaratnam, Deevina, Bell, Katrina M., Sim, Choon Boon, Koutsis, Kathy, Anderson, David J., Qian, Elizabeth L., Stanley, Edouard G., Elefanty, Andrew G., Cheung, Michael M., Oshlack, Alicia, White, Anthony J., Abi Khalil, Charbel, Hudson, James E., Porrello, Enzo R., Elliott, David A.
Publicado 2019

Publisher Correction: The role of cardiac transcription factor NKX2-5 in regulating the human cardiac miRNAome

por Arasaratnam, Deevina, Bell, Katrina M., Sim, Choon Boon, Koutsis, Kathy, Anderson, David J., Qian, Elizabeth L., Stanley, Edouard G., Elefanty, Andrew G., Cheung, Michael M., Oshlack, Alicia, White, Anthony J., Abi Khalil, Charbel, Hudson, James E., Porrello, Enzo R., Elliott, David A.
Publicado 2019

Dominant TP63 missense variants lead to constitutive activation and premature ovarian insufficiency

por Tucker, Elena J., Gutfreund, Niklas, Belaud‐Rotureau, Marc‐Antoine, Gilot, David, Brun, Tiffany, Kline, Brianna L., Bell, Katrina M., Domin‐Bernhard, Mathilde, Théard, Camille, Touraine, Philippe, Robevska, Gorjana, van van den Bergen, Jocelyn, Ayers, Katie L., Sinclair, Andrew H., Dötsch, Volker, Jaillard, Sylvie
Publicado 2022

Copy Number Variation in Patients with Disorders of Sex Development Due to 46,XY Gonadal Dysgenesis

por White, Stefan, Ohnesorg, Thomas, Notini, Amanda, Roeszler, Kelly, Hewitt, Jacqueline, Daggag, Hinda, Smith, Craig, Turbitt, Erin, Gustin, Sonja, van den Bergen, Jocelyn, Miles, Denise, Western, Patrick, Arboleda, Valerie, Schumacher, Valerie, Gordon, Lavinia, Bell, Katrina, Bengtsson, Henrik, Speed, Terry, Hutson, John, Warne, Garry, Harley, Vincent, Koopman, Peter, Vilain, Eric, Sinclair, Andrew
Publicado 2011

Diagnostic and cost utility of whole exome sequencing in peripheral neuropathy

por Walsh, Maie, Bell, Katrina M., Chong, Belinda, Creed, Emma, Brett, Gemma R., Pope, Kate, Thorne, Natalie P., Sadedin, Simon, Georgeson, Peter, Phelan, Dean G., Day, Timothy, Taylor, Jessica A., Sexton, Adrienne, Lockhart, Paul J., Kiers, Lynette, Fahey, Michael, Macciocca, Ivan, Gaff, Clara L., Oshlack, Alicia, Yiu, Eppie M., James, Paul A., Stark, Zornitza, Ryan, Monique M.
Publicado 2017

Deficiency of the mitochondrial ribosomal subunit, MRPL50, causes autosomal recessive syndromic premature ovarian insufficiency

por Bakhshalizadeh, Shabnam, Hock, Daniella H., Siddall, Nicole A., Kline, Brianna L., Sreenivasan, Rajini, Bell, Katrina M., Casagranda, Franca, Kamalanathan, Sadishkumar, Sahoo, Jayaprakash, Narayanan, Niya, Naik, Dukhabandhu, Suryadevara, Varun, Compton, Alison G., Amarasekera, Sumudu S. C., Kapoor, Ridam, Jaillard, Sylvie, Simpson, Andrea, Robevska, Gorjana, van den Bergen, Jocelyn, Pachernegg, Svenja, Ayers, Katie L., Thorburn, David R., Stroud, David A., Hime, Gary R., Sinclair, Andrew H., Tucker, Elena J.
Publicado 2023

Premature Ovarian Insufficiency in CLPB Deficiency: Transcriptomic, Proteomic and Phenotypic Insights

por Tucker, Elena J, Baker, Megan J, Hock, Daniella H, Warren, Julia T, Jaillard, Sylvie, Bell, Katrina M, Sreenivasan, Rajini, Bakhshalizadeh, Shabnam, Hanna, Chloe A, Caruana, Nikeisha J, Wortmann, Saskia B, Rahman, Shamima, Pitceathly, Robert D S, Donadieu, Jean, Alimi, Aurelia, Launay, Vincent, Coppo, Paul, Christin-Maitre, Sophie, Robevska, Gorjana, van den Bergen, Jocelyn, Kline, Brianna L, Ayers, Katie L, Stewart, Phoebe N, Stroud, David A, Stojanovski, Diana, Sinclair, Andrew H
Publicado 2022

NKX2-5 regulates human cardiomyogenesis via a HEY2 dependent transcriptional network

por Anderson, David J., Kaplan, David I., Bell, Katrina M., Koutsis, Katerina, Haynes, John M., Mills, Richard J., Phelan, Dean G., Qian, Elizabeth L., Leitoguinho, Ana Rita, Arasaratnam, Deevina, Labonne, Tanya, Ng, Elizabeth S., Davis, Richard P., Casini, Simona, Passier, Robert, Hudson, James E., Porrello, Enzo R., Costa, Mauro W., Rafii, Arash, Curl, Clare L., Delbridge, Lea M., Harvey, Richard P., Oshlack, Alicia, Cheung, Michael M., Mummery, Christine L., Petrou, Stephen, Elefanty, Andrew G., Stanley, Edouard G., Elliott, David A.
Publicado 2018

Integrated multi-omics for rapid rare disease diagnosis on a national scale

por Lunke, Sebastian, Bouffler, Sophie E., Patel, Chirag V., Sandaradura, Sarah A., Wilson, Meredith, Pinner, Jason, Hunter, Matthew F., Barnett, Christopher P., Wallis, Mathew, Kamien, Benjamin, Tan, Tiong Y., Freckmann, Mary-Louise, Chong, Belinda, Phelan, Dean, Francis, David, Kassahn, Karin S., Ha, Thuong, Gao, Song, Arts, Peer, Jackson, Matilda R., Scott, Hamish S., Eggers, Stefanie, Rowley, Simone, Boggs, Kirsten, Rakonjac, Ana, Brett, Gemma R., de Silva, Michelle G., Springer, Amanda, Ward, Michelle, Stallard, Kirsty, Simons, Cas, Conway, Thomas, Halman, Andreas, Van Bergen, Nicole J., Sikora, Tim, Semcesen, Liana N., Stroud, David A., Compton, Alison G., Thorburn, David R., Bell, Katrina M., Sadedin, Simon, North, Kathryn N., Christodoulou, John, Stark, Zornitza
Publicado 2023