Nitric oxide and bone

por van'T Hof, Rob J, Ralston, Stuart H
Publicado em 2001

Meniscal and ligament modifications in spontaneous and post-traumatic mouse models of osteoarthritis

por Ramos-Mucci, Lorenzo, Javaheri, Behzad, van ‘t Hof, Rob, Bou-Gharios, George, Pitsillides, Andrew A., Comerford, Eithne, Poulet, Blandine
Publicado no Arthritis Res Ther (2020)

A comparison of the bone and growth phenotype of mdx, mdx:Cmah(−/−) and mdx:Utrn(+/−) murine models with the C57BL/10 wild-type mouse

por Wood, Claire L., Suchacki, Karla J., van ’t Hof, Rob, Cawthorn, Will P., Dillon, Scott, Straub, Volker, Wong, Sze Choong, Ahmed, Syed F., Farquharson, Colin
Publicado no Dis Model Mech (2020)

Altered Bone Development and an Increase in FGF-23 Expression in Enpp1(−/−) Mice

por Mackenzie, Neil Charles Wallace, Zhu, Dongxing, Milne, Elspeth M., van 't Hof, Rob, Martin, Aline, Quarles, Darryl Leigh, Millán, José Luis, Farquharson, Colin, MacRae, Vicky Elisabeth
Publicado em 2012

Correction: Altered Bone Development and an Increase in FGF-23 Expression in Enpp1(−/−) Mice

por Mackenzie, Neil Charles Wallace, Zhu, Dongxing, Milne, Elspeth M., van 't Hof, Rob, Martin, Aline, Quarles, Darryl Leigh, Millán, José Luis, Farquharson, Colin, MacRae, Vicky Elisabeth
Publicado em 2012

Mesenchymal Stromal Cell‐Seeded Biomimetic Scaffolds as a Factory of Soluble RANKL in Rankl‐Deficient Osteopetrosis

por Menale, Ciro, Campodoni, Elisabetta, Palagano, Eleonora, Mantero, Stefano, Erreni, Marco, Inforzato, Antonio, Fontana, Elena, Schena, Francesca, van't Hof, Rob, Sandri, Monica, Tampieri, Anna, Villa, Anna, Sobacchi, Cristina
Publicado no Stem Cells Transl Med (2018)

Deletion of the membrane complement inhibitor CD59a drives age and gender-dependent alterations to bone phenotype in mice

por Bloom, Anja C., Collins, Fraser L., van't Hof, Rob J., Ryan, Elizabeth S., Jones, Emma, Hughes, Timothy R., Morgan, B. Paul, Erlandsson, Malin, Bokarewa, Maria, Aeschlimann, Daniel, Evans, Bronwen A.J., Williams, Anwen S.
Publicado no Bone (2016)

Increase in NF-κB Binding Affinity of the Variant C Allele of the Toll-Like Receptor 9 −1237T/C Polymorphism Is Associated with Helicobacter pylori-Induced Gastric Disease

por Ng, Mike Tsz Hin, van't Hof, Rob, Crockett, Julie C., Hope, Mairi E., Berry, Susan, Thomson, John, McLean, Mairi H., McColl, Kenneth E. L., El-Omar, Emad M., Hold, Georgina L.
Publicado em 2010

A Trans-Acting Protein Effect Causes Severe Eye Malformation in the Mp Mouse

por Rainger, Joe, Keighren, Margaret, Keene, Douglas R., Charbonneau, Noe L., Rainger, Jacqueline K., Fisher, Malcolm, Mella, Sebastien, Huang, Jeffrey T-J., Rose, Lorraine, van't Hof, Rob, Sakai, Lynne Y., Jackson, Ian J., FitzPatrick, David R.
Publicado em 2013

Sertoli cells control peritubular myoid cell fate and support adult Leydig cell development in the prepubertal testis

por Rebourcet, Diane, O'Shaughnessy, Peter J., Pitetti, Jean-Luc, Monteiro, Ana, O'Hara, Laura, Milne, Laura, Tsai, Yi Ting, Cruickshanks, Lyndsey, Riethmacher, Dieter, Guillou, Florian, Mitchell, Rod T., van ’t Hof, Rob, Freeman, Tom C., Nef, Serge, Smith, Lee B.
Publicado em 2014

Analysis of Nkx3.1:Cre-driven Erk5 deletion reveals a profound spinal deformity which is linked to increased osteoclast activity

por Loveridge, Carolyn J., van ’t Hof, Rob J., Charlesworth, Gemma, King, Ayala, Tan, Ee Hong, Rose, Lorraine, Daroszewska, Anna, Prior, Amanda, Ahmad, Imran, Welsh, Michelle, Mui, Ernest J., Ford, Catriona, Salji, Mark, Sansom, Owen, Blyth, Karen, Leung, Hing Y.
Publicado no Sci Rep (2017)

Acute Multiple Organ Failure in Adult Mice Deleted for the Developmental Regulator Wt1

por Chau, You-Ying, Brownstein, David, Mjoseng, Heidi, Lee, Wen-Chin, Buza-Vidas, Natalija, Nerlov, Claus, Jacobsen, Sten Eirik, Perry, Paul, Berry, Rachel, Thornburn, Anna, Sexton, David, Morton, Nik, Hohenstein, Peter, Freyer, Elisabeth, Samuel, Kay, van't Hof, Rob, Hastie, Nicholas
Publicado em 2011

Proteinase-activated receptor 2 modulates OA-related pain, cartilage and bone pathology

por Huesa, Carmen, Ortiz, Ana C, Dunning, Lynette, McGavin, Laura, Bennett, Louise, McIntosh, Kathryn, Crilly, Anne, Kurowska-Stolarska, Mariola, Plevin, Robin, van ‘t Hof, Rob J, Rowan, Andrew D, McInnes, Iain B, Goodyear, Carl S, Lockhart, John C, Ferrell, William R
Publicado no Ann Rheum Dis (2016)

Ubiquitin-protein ligase Ubr5 cooperates with hedgehog signalling to promote skeletal tissue homeostasis

por Mellis, David, Staines, Katherine A., Peluso, Silvia, Georgiou, Ioanna Ch., Dora, Natalie, Kubiak, Malgorzata, van’t Hof, Rob, Grillo, Michela, Farquharson, Colin, Kinsella, Elaine, Thornburn, Anna, Ralston, Stuart H., Salter, Donald M., Riobo-Del Galdo, Natalia A., Hill, Robert E., Ditzel, Mark
Publicado no PLoS Genet (2021)

Molecular insights into an ancient form of Paget’s disease of bone

por Shaw, Barry, Burrell, Carla L., Green, Darrell, Navarro-Martinez, Ana, Scott, Daniel, Daroszewska, Anna, van ’t Hof, Rob, Smith, Lynn, Hargrave, Frank, Mistry, Sharad, Bottrill, Andrew, Kessler, Benedikt M., Fischer, Roman, Singh, Archana, Dalmay, Tamas, Fraser, William D., Henneberger, Kirstin, King, Turi, Gonzalez, Silvia, Layfield, Robert
Publicado no Proc Natl Acad Sci U S A (2019)

A Dominant-Negative Mutation of Mouse Lmx1b Causes Glaucoma and Is Semi-lethal via LBD1-Mediated Dimerisation

por Cross, Sally H., Macalinao, Danilo G., McKie, Lisa, Rose, Lorraine, Kearney, Alison L., Rainger, Joe, Thaung, Caroline, Keighren, Margaret, Jadeja, Shalini, West, Katrine, Kneeland, Stephen C., Smith, Richard S., Howell, Gareth R., Young, Fiona, Robertson, Morag, van t' Hof, Rob, John, Simon W. M., Jackson, Ian J.
Publicado em 2014