Disruption of the Serine/Threonine Kinase 9 Gene Causes Severe X-Linked Infantile Spasms and Mental Retardation von Kalscheuer, Vera M., Tao, Jiong, Donnelly, Andrew, Hollway, Georgina, Schwinger, Eberhard, Kübart, Sabine, Menzel, Corinna, Hoeltzenbein, Maria, Tommerup, Niels, Eyre, Helen, Harbord, Michael, Haan, Eric, Sutherland, Grant R., Ropers, Hans-Hilger, Gécz, Jozef

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Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy von Lower, Karen M, Lütcherath, Viggo, Gécz, Jozef, Frints, Suzanna G.M, Partington, Michael, Strømme, Petter, Scheffer, Ingrid E, Gedeon, Ági K, Lewis, Suzanne M.E, Turner, Gillian, Fryns, Jean-Pierre, Sutherland, Grant R, Wallace, Robyn H, Mangelsdorf, Marie E, Shaw, Marie A, Mulley, John C, Bruyere, Helene

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Fcα/μ receptor mediates endocytosis of IgM-coated microbes von Shibuya, Akira, Sakamoto, Norihisa, Shimizu, Yoshio, Shibuya, Kazuko, Osawa, Mitsujiro, Hiroyama, Takashi, Eyre, Helen J, Sutherland, Grant R, Endo, Yuichi, Fujita, Teizo, Miyabayashi, Tomoyuki, Sakano, Seiji, Tsuji, Takao, Nakayama, Eiichi, Phillips, Joseph H, Lanier, Lewis L, Nakauchi, Hiromitsu

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Cutting Edge: Human 2B4, an Activating NK Cell Receptor, Recruits the Protein Tyrosine Phosphatase SHP-2 and the Adaptor Signaling Protein SAP von Tangye, Stuart G, Lazetic, Sasha, Woollatt, Erica, Sutherland, Grant R, Lanier, Lewis L, Phillips, Joseph H

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LAIR-1, a Novel Inhibitory Receptor Expressed on Human Mononuclear Leukocytes von Meyaard, Linde, Adema, Gosse J, Chang, Chiwen, Woollatt, Erica, Sutherland, Grant R, Lanier, Lewis L, Phillips, Joseph H

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Myeloid DAP12-Associating Lectin (MDL)-1 Is a Cell Surface Receptor Involved in the Activation of Myeloid Cells von Alexander B. H. Bakker, Baker, Elizabeth, Sutherland, Grant R., Phillips, Joseph H., Lanier, Lewis L.

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X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment von Jenkinson, Andrew, Varian, Jennifer, Shoubridge, Cheryl, Vandeleur, Lucianne, Shepherd, Rebecca, Hynes, Kim, Shaw, Marie, Gusella, James F, Teague, John, Edkins, Sarah, Dicks, Ed, Dibbens, Leanne M, Haan, Eric, Gécz, Jozef, Halliday, Kelly, Lerman-Sagie, Tally, Sutton, Edwina, Corbett, Mark, Wray, Paul, Bomar, Jamee, Stevens, Claire, Scheffer, Ingrid E, Barthorpe, Syd, Butler, Adam, Tarpey, Patrick S, Jones, David, Bayly, Marta A, Madison, Mark, West, Sofie, Lev, Dorit, Stratton, Michael R, Neufeld, Miriam Y, Korczyn, Amos D, Tofts, Calli, Futreal, P Andrew, Turner, Samantha J, Kim, Hyung-Goo, Berkovic, Samuel F, Buck, Gemma, O'Meara, Sarah, Friend, Kathryn, Kivity, Sara, Afawi, Zaid, Mironenko, Tatiana, McKee, Shane, Cole, Jennifer, Lee, Rebecca, Geschwind, Daniel H, Widaa, Sara, Ryan, Stephen, Smith, Raffaella, Sutherland, Grant R, Menzies, Andrew, Mulley, John C, Mazarib, Aziz, Derry, Christopher P, Thomas, Paul

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The History and Development of the Human Genetics Society of Australasia von Sutherland, Grant R.

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Nxf and Fbxo33: novel seizure-responsive genes in mice von Flood, Warren D., Moyer, Robert W., Tsykin, Anna, Sutherland, Grant R., Koblar, Simon A.

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Gene structure alternative splicing, and chromosomal localization of pro-apoptotic Bcl-2 relative Bim von Bouillet, P, Zhang, L C, Huang, D C, Webb, G C, Bottema, C D, Shore, P, Eyre, H J, Sutherland, G R, Adams, J M

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Human Chromosomal Fragile Site FRA16B Is an Amplified AT-Rich Minisatellite Repeat von Yu, Sui, Mangelsdorf, Marie, Hewett, Duncan, Hobson, Lynne, Baker, Elizabeth, Eyre, Helen J, Lapsys, Naras, Le Paslier, Denis, Doggett, Norman A, Sutherland, Grant R, Richards, Robert I

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GABRD encoding a protein for extra- or peri-synaptic GABAA receptors is a susceptibility locus for generalized epilepsies von Dibbens, Leanne M., Feng, Hua-Jun, Richards, Michaella C., Harkin, Louise A., Hodgson, Bree L., Scott, Darren, Jenkins, Misty, Petrou, Steven, Sutherland, Grant R., Scheffer, Ingrid E., Berkovic, Samuel F., Macdonald, Robert L., Mulley, John C.

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A novel epithelial-expressed ETS gene, ELF3: human and murine cDNA sequences, murine genomic organization, human mapping to 1q32.2 and expression in tissues and cancer von TYMMS, M. J, NG, A. Y. N, DEBOUCK, C, KOLA, I, THOMAS, R. S, SCHUTTE, B. C, ZHOU, J, EYRE, H. J, SUTHERLAND, G. R, SETH, A, ROSENBERG, M, PAPAS, T

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MUC13, a Novel Human Cell Surface Mucin Expressed by Epithelial and Hemopoietic Cells von Williams, Stephanie J., Wreschner, Daniel H., Tran, Mai, Eyre, Helen J., Sutherland, Grant R., McGuckin, Michael A.

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CHRNB2 Is the Second Acetylcholine Receptor Subunit Associated with Autosomal Dominant Nocturnal Frontal Lobe Epilepsy von Phillips, Hilary A., Favre, Isabelle, Kirkpatrick, Martin, Zuberi, Sameer M., Goudie, David, Heron, Sarah E., Scheffer, Ingrid E., Sutherland, Grant R., Berkovic, Samuel F., Bertrand, Daniel, Mulley, John C.

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HLS5, a Novel RBCC (Ring Finger, B Box, Coiled-coil) Family Member Isolated from a Hemopoietic Lineage Switch, Is a Candidate Tumor Suppressor von Lalonde, Jean-Philippe, Lim, Raelene, Ingley, Evan, Tilbrook, Peta A., Thompson, Martin J., McCulloch, Ross, Beaumont, Jennifer G, Wicking, Carol, Eyre, Helen J., Sutherland, Grant R., Howe, Kathy, Solomon, Ellen, Williams, James H., Klinken, S. Peter

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AMP-activated protein kinase isoenzyme family: subunit structure and chromosomal location von Stapleton, David, Woollatt, Erica, Mitchelhill, Ken I, Nicholl, Jillian K, Fernandez, C.Shamala, Michell, Belinda J, Witters, Lee A, Power, David A, Sutherland, Grant R, Kemp, Bruce E

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A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy von Steinlein, Ortrud K, Mulley, John C, Propping, Peter, Wallace, Robyn H, Phillips, Hilary A, Sutherland, Grant R, Scheffer, Ingrid E, Berkovic, Samuel F

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Two novel mucin genes down-regulated in colorectal cancer identified by differential display von WILLIAMS, S. J, MCGUCKIN, M. A, GOTLEY, D. C, EYRE, H. J, SUTHERLAND, G. R, ANTALIS, T. M

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The molecular basis of fragile sites in human chromosomes von Sutherland, Grant R, Richards, Robert I

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