FBXW7 mutations typically found in human cancers are distinct from null alleles and disrupt lung development by Davis, H, Lewis, A, Spencer-Dene, B, Tateossian, H, Stamp, G, Behrens, A, Tomlinson, I

FBXW7 mutations typically found in human cancers are distinct from null alleles and disrupt lung development. by Davis, H, Lewis, A, Spencer-Dene, B, Tateossian, H, Stamp, G, Behrens, A, Tomlinson, I

Multiple endocrine neoplasia type 1 knockout mice develop parathyroid, pancreatic, pituitary and adrenal tumours with hypercalcaemia, hypophosphataemia and hypercorticosteronaemia. by Harding, B, Lemos, M, Reed, A, Walls, G, Jeyabalan, J, Bowl, MR, Tateossian, H, Sullivan, N, Hough, T, Fraser, W, Ansorge, O, Cheeseman, M, Thakker, R

A mutation in Nischarin causes otitis media via LIMK1 and NF-κB pathways by Crompton, M, Purnell, T, Parker, A, Ball, G, Hardisty-Hughes, R, Gale, R, Williams, D, Dean, C, Simon, M, Mallon, A, Wells, S, Bhutta, M, Burton, M, Tateossian, H, Brown, S

Deciphering deafness in Down syndrome: finding the otitis media gene by Southern, A

Other Authors: “…Tateossian, H…”