Ezrin is key regulator of Src-induced malignant phenotype in three-dimensional environment
Heiska, L, Melikova, M, Zhao, F, Saotome, I, McClatchey, A I, Carpén, O
Published in Oncogene (15.12.2011)
Published in Oncogene (15.12.2011)
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Mice heterozygous for a mutation at the Nf2 tumor suppressor locus develop a range of highly metastatic tumors
McClatchey, A I, Saotome, I, Mercer, K, Crowley, D, Gusella, J F, Bronson, R T, Jacks, T
Published in Genes & development (15.04.1998)
Published in Genes & development (15.04.1998)
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The Nf2 Tumor Suppressor, Merlin, Functions in Rac-Dependent Signaling
Shaw, Reuben J., Paez, J.Guillermo, Curto, Marcello, Yaktine, Ann, Pruitt, Wendy Morse, Saotome, Ichiko, O'Bryan, John P., Gupta, Vikas, Ratner, Nancy, Der, Channing J., Jacks, Tyler, McClatchey, Andrea I.
Published in Developmental cell (01.07.2001)
Published in Developmental cell (01.07.2001)
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Journal Article
The Nf2 tumor suppressor gene product is essential for extraembryonic development immediately prior to gastrulation
McClatchey, A I, Saotome, I, Ramesh, V, Gusella, J F, Jacks, T
Published in Genes & development (15.05.1997)
Published in Genes & development (15.05.1997)
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Missense variants in the N-terminal domain of the A isoform of FHF2/FGF13 cause an X-linked developmental and epileptic encephalopathy
Fry, Andrew E., Marra, Christopher, Derrick, Anna V., Pickrell, William O., Higgins, Adam T., te Water Naude, Johann, McClatchey, Martin A., Davies, Sally J., Metcalfe, Kay A., Tan, Hui Jeen, Mohanraj, Rajiv, Avula, Shivaram, Williams, Denise, Brady, Lauren I., Mesterman, Ronit, Tarnopolsky, Mark A., Zhang, Yuehua, Yang, Ying, Wang, Xiaodong, Rees, Mark I., Goldfarb, Mitchell, Chung, Seo-Kyung
Published in American journal of human genetics (07.01.2021)
Published in American journal of human genetics (07.01.2021)
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Journal Article
Using data from the 100,000 Genomes Project to resolve conflicting interpretations of a recurrent TUBB2A mutation
Ragoussis, Vassilis, Pagnamenta, Alistair T, Haines, Rebecca L, Giacopuzzi, Edoardo, McClatchey, Martin A, Sampson, Julian R, Suri, Mohnish, Gardham, Alice, Cobben, Jan-Maarten, Osio, Deborah, Fry, Andrew E, Taylor, Jenny C, Ambrose, J C, Arumugam, P, Baple, E L, Bleda, M, Boardman-Pretty, F, Boissiere, J M, Boustred, C R, Brittain, H, Caulfield, M J, Chan, G C, Craig, C E H, Daugherty, L C, de Burca, A, Devereau, A, Elgar, G, Foulger, R E, Fowler, T, Furió-Tarí, P, Hackett, J M, Halai, D, Hamblin, A, Henderson, S, Holman, J E, Hubbard, T J P, Ibáñez, K, Jackson, R, Jones, L J, Kasperaviciute, D, Kayikci, M, Kousathanas, A, Lahnstein, L, Lawson, K, Leigh, S E A, Leong, I U S, Lopez, F J, Maleady-Crowe, F, Mason, J, McDonagh, E M, Moutsianas, L, Mueller, M, Murugaesu, N, Need, A C, Odhams, C A, Patch, C, Pereira, M B, Perez-Gil, D, Polychronopoulos, D, Pullinger, J, Rahim, T, Rendon, A, Riesgo-Ferreiro, P, Rogers, T, Ryten, M, Savage, K, Sawant, K, Scott, R H, Siddiq, A, Sieghart, A, Smedley, D, Smith, K R, Smith, S C, Sosinsky, A, Spooner, W, Stevens, H E, Stuckey, A, Sultana, R, Thomas, E R A, Thompson, S R, Tregidgo, C, Tucci, A, Walsh, E, Watters, S A, Welland, M J, Williams, E, Witkowska, K, Wood, S M, Zarowiecki, M
Published in Journal of medical genetics (01.04.2022)
Published in Journal of medical genetics (01.04.2022)
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Journal Article
Focal segmental glomerulosclerosis and mild intellectual disability in a patient with a novel de novo truncating TRIM8 mutation
McClatchey, Martin A., du Toit, Zachary D., Vaughan, Rhys, Whatley, Sharon D., Martins, Sara, Hegde, Shivaram, Naude, Johann te Water, Thomas, David H., Griffiths, David F., Genomics England Research Consortium, Clarke, Angus J., Fry, Andrew E.
Published in European journal of medical genetics (01.09.2020)
Published in European journal of medical genetics (01.09.2020)
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Journal Article
Analysis of humidity halos around trade wind cumulus clouds
LU, Miao-Ling, JIAN WANG, FREEDMAN, Andrew, JONSSON, Haflidi H, FLAGAN, Richard C, MCCLATCHEY, Robert A, SEINFELD, John H
Published in Journal of the atmospheric sciences (15.04.2003)
Published in Journal of the atmospheric sciences (15.04.2003)
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Journal Article
The genetic defect in familial Alzheimer's disease is not tightly linked to the amyloid beta-protein gene
Tanzi, R E, St George-Hyslop, P H, Haines, J L, Polinsky, R J, Nee, L, Foncin, J F, Neve, R L, McClatchey, A I, Conneally, P M, Gusella, J F
Published in Nature (London) (10.09.1987)
Published in Nature (London) (10.09.1987)
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The genomic structure of the human skeletal muscle sodium channel gene
McClatchey, A I, Lin, C S, Wang, J, Hoffman, E P, Rojas, C, Gusella, J F
Published in Human molecular genetics (01.10.1992)
Published in Human molecular genetics (01.10.1992)
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Journal Article
Retrieving Properties of Thin Clouds from Solar Aureole Measurements
DeVore, J G, Stair, A T, LePage, A, Rall, D, Atkinson, J, Villanucci, D, Rappaport, S A, Joss, P C, McClatchey, R A
Published in Journal of atmospheric and oceanic technology (01.12.2009)
Published in Journal of atmospheric and oceanic technology (01.12.2009)
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Journal Article
Molecular Basis of Ornithine Aminotransferase Deficiency in B-6-Responsive and -Nonresponsive Forms of Gyrate Atrophy
Ramesh, Vijaya, McClatchey, Andrea I., Ramesh, Narayanaswamy, Benoit, Lynne A., Berson, Eliot L., Shih, Vivian E., Gusella, James F.
Published in Proceedings of the National Academy of Sciences - PNAS (01.06.1988)
Published in Proceedings of the National Academy of Sciences - PNAS (01.06.1988)
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