A G‐protein Subunit‐α11 Loss‐of‐Function Mutation, Thr54Met, Causes Familial Hypocalciuric Hypercalcemia Type 2 (FHH2)

od Gorvin, Caroline M, Cranston, Treena, Hannan, Fadil M, Rust, Nigel, Qureshi, Asjid, Nesbit, M Andrew, Thakker, Rajesh V
izdano v J Bone Miner Res (2016)

IL-23–responsive innate lymphoid cells are increased in inflammatory bowel disease

od Geremia, Alessandra, Arancibia-Cárcamo, Carolina V., Fleming, Myles P.P., Rust, Nigel, Singh, Baljit, Mortensen, Neil J., Travis, Simon P.L., Powrie, Fiona
Izdano 2011

Analysis of C. elegans intestinal gene expression and polyadenylation by fluorescence-activated nuclei sorting and 3′-end-seq

od Haenni, Simon, Ji, Zhe, Hoque, Mainul, Rust, Nigel, Sharpe, Helen, Eberhard, Ralf, Browne, Cathy, Hengartner, Michael O., Mellor, Jane, Tian, Bin, Furger, André
Izdano 2012

Mutations Affecting G-Protein Subunit α(11) in Hypercalcemia and Hypocalcemia

od Nesbit, M. Andrew, Hannan, Fadil M., Howles, Sarah A., Babinsky, Valerie N., Head, Rosie A., Cranston, Treena, Rust, Nigel, Hobbs, Maurine R., Heath, Hunter, Thakker, Rajesh V.
Izdano 2013

Allosteric Modulation of the Calcium-sensing Receptor Rectifies Signaling Abnormalities Associated with G-protein α-11 Mutations Causing Hypercalcemic and Hypocalcemic Disorders

od Babinsky, Valerie N., Hannan, Fadil M., Gorvin, Caroline M., Howles, Sarah A., Nesbit, M. Andrew, Rust, Nigel, Hanyaloglu, Aylin C., Hu, Jianxin, Spiegel, Allen M., Thakker, Rajesh V.
izdano v J Biol Chem (2016)

Cinacalcet for Symptomatic Hypercalcemia Caused by AP2S1 Mutations

od Howles, Sarah A., Hannan, Fadil M., Babinsky, Valerie N., Rogers, Angela, Gorvin, Caroline M., Rust, Nigel, Richardson, Tristan, McKenna, Malachi J., Nesbit, M. Andrew, Thakker, Rajesh V.
izdano v N Engl J Med (2016)

Identification of a G‐Protein Subunit‐α11 Gain‐of‐Function Mutation, Val340Met, in a Family With Autosomal Dominant Hypocalcemia Type 2 (ADH2)

od Piret, Sian E, Gorvin, Caroline M, Pagnamenta, Alistair T, Howles, Sarah A, Cranston, Treena, Rust, Nigel, Nesbit, M Andrew, Glaser, Ben, Taylor, Jenny C, Buchs, Andreas E, Hannan, Fadil M, Thakker, Rajesh V
izdano v J Bone Miner Res (2016)

Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3

od Nesbit, M. Andrew, Hannan, Fadil M., Howles, Sarah A., Reed, Anita A.C., Cranston, Treena, Thakker, Clare E., Gregory, Lorna, Rimmer, Andrew J., Rust, Nigel, Graham, Una, Morrison, Patrick J., Hunter, Steven J., Whyte, Michael P., McVean, Gil, Buck, David, Thakker, Rajesh V.
Izdano 2012

Threat to Hospital Privileges

od Attenborough, John, Aubrey, D. Roland, Auger, H., Austin, A. J., Bartlett, Calum I. S., Bellamy, R. C. T., Bergel, Richard C., Bryant, David, Carpenter, Michael E., Cates, Richard, Christmas, A. R., Clyne, G. Elsa, Collings-Wells, John A., Crawshaw, P. F. A., Cule, John H., Dobbin, L. W. B., Donovan, Brian, Edwards, John, Evans, Keith M., Faber, Vernon C., France, Richard, Gent, N. S. C., Hadfield, George W., Haskins, T. D., Henley, Brian, Henry, D. O., Holden, J. J., James, John P., Kayll, J. N., Kent, S. G., Key, Ian A., Kieft, B. T., Wright, M. F. Lind, Lister, C. O., MacAdam, A. D., McNutt, Joe, Mason, J. Y. J. M., Mason, D. Paul, Mathewson, Jack, May, William, Morrison, Robert W. M., Narula, Y. P., Price, J. C. Newell, Norman, J. M., Page, H. J. Clifford, Perry, J. R., Poole, P. B., Porter, Alan M. W., Powell, John K., Poyntz-Wright, R. C., Price, D. J., Price, John, Pritchard, J. N. A., Robinson, Ian H., Rust, Nigel E., Scriven, Jeanne M., Singer, Geoffrey E., Smart, Peter C., Smith, Paul S., Summerhayes, John L. V., Tilly, Clifford R., Tipler, H. Bolton, Trust, Desmond G. L., Turner, A. G., Urquhart, D. R. H., Walker, Colin D., Wallace, Ian W., Watson, M., Whitehouse, Michael S., Whittingham, M. Anne, Whittingham, W., Williams, Eileen M., Winchurch, Brian
Izdano 1968