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

Por Gorvin, Caroline M, Cranston, Treena, Hannan, Fadil M, Rust, Nigel, Qureshi, Asjid, Nesbit, M Andrew, Thakker, Rajesh V
Publicado no J Bone Miner Res (2016)

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

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

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

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

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

Por 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.
Publicado em 2013

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

Por 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.
Publicado no J Biol Chem (2016)

Cinacalcet for Symptomatic Hypercalcemia Caused by AP2S1 Mutations

Por 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.
Publicado no 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)

Por 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
Publicado no J Bone Miner Res (2016)

Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3

Por 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.
Publicado em 2012

Threat to Hospital Privileges

Por 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
Publicado em 1968