1 - 25 of
37
results
for author:"Roberts W."
in Literature Citations
| Copy number variation analysis and sequencing of the X-linked mental retardation gene TSPAN7/TM4SF2 in patients with autism spectrum disorder. Noor A., Gianakopoulos P.J., Fernandez B., Marshall C.R., Szatmari P., Roberts W., Scherer S.W., Vincent J.B. Psychiatr. Genet. 19:154-155(2009) · Mapped (10) |
| Nitric oxide specifically inhibits integrin-mediated platelet adhesion and spreading on collagen. Roberts W., Riba R., Homer-Vanniasinkam S., Farndale R.W., Naseem K.M. J. Thromb. Haemost. 6:2175-2185(2008) · Mapped (10) |
| Trifluoromethylpyrimidine-based inhibitors of proline-rich tyrosine kinase 2 (PYK2): structure-activity relationships and strategies for the elimination of reactive metabolite formation. Walker D.P., Bi F.C., Kalgutkar A.S., Bauman J.N., Zhao S.X., Soglia J.R., Aspnes G.E., Kung D.W., Klug-McLeod J., Zawistoski M.P. et al. Bioorg. Med. Chem. Lett. 18:6071-6077(2008) · Mapped (1) |
| Aftiphilin and gamma-synergin are required for secretagogue sensitivity of Weibel-Palade bodies in endothelial cells. Lui-Roberts W.W., Ferraro F., Nightingale T.D., Cutler D.F. Mol. Biol. Cell 19:5072-5081(2008) · Mapped (7) |
| Contribution of SHANK3 mutations to autism spectrum disorder. Moessner R., Marshall C.R., Sutcliffe J.S., Skaug J., Pinto D., Vincent J., Zwaigenbaum L., Fernandez B., Roberts W., Szatmari P. et al. Am. J. Hum. Genet. 81:1289-1297(2007) · Mapped (4) |
| Proline-rich tyrosine kinase 2 regulates osteoprogenitor cells and bone formation, and offers an anabolic treatment approach for osteoporosis. Buckbinder L., Crawford D.T., Qi H., Ke H.Z., Olson L.M., Long K.R., Bonnette P.C., Baumann A.P., Hambor J.E., Grasser W.A. et al. Proc. Natl. Acad. Sci. U.S.A. 104:10619-10624(2007) · Mapped (11) |
| cGMP-independent inhibition of integrin alphaIIbbeta3-mediated platelet adhesion and outside-in signalling by nitric oxide. Oberprieler N.G., Roberts W., Riba R., Graham A.M., Homer-Vanniasinkam S., Naseem K.M. FEBS Lett. 581:1529-1534(2007) · Mapped (4) |
| Sequence variants within exon 1 of MECP2 occur in females with mental retardation. Harvey C.G., Menon S.D., Stachowiak B., Noor A., Proctor A., Mensah A.K., Mnatzakanian G.N., Alfred S.E., Guo R., Scherer S.W. et al. Am. J. Med. Genet. B Neuropsychiatr. Genet. 144B:355-360(2007) · Mapped (5) |
| Von Willebrand factor activates endothelial nitric oxide synthase in blood platelets by a glycoprotein Ib-dependent mechanism. Riba R., Oberprieler N.G., Roberts W., Naseem K.M. J. Thromb. Haemost. 4:2636-2644(2006) · Mapped (6) |
| Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia. Feuk L., Kalervo A., Lipsanen-Nyman M., Skaug J., Nakabayashi K., Finucane B., Hartung D., Innes M., Kerem B., Nowaczyk M.J. et al. Am. J. Hum. Genet. 79:965-972(2006) · Mapped (12) |
| P-selectin and CD63 use different mechanisms for delivery to Weibel-Palade bodies. Harrison-Lavoie K.J., Michaux G., Hewlett L., Kaur J., Hannah M.J., Lui-Roberts W.W., Norman K.E., Cutler D.F. Traffic 7:647-662(2006) · Mapped (19) |
| Association of the calcyon gene (DRD1IP) with attention deficit/hyperactivity disorder. Laurin N., Misener V.L., Crosbie J., Ickowicz A., Pathare T., Roberts W., Malone M., Tannock R., Schachar R., Kennedy J.L. et al. Mol. Psychiatry 10:1117-1125(2005) · Mapped (1) |
| The SNAP25 gene as a susceptibility gene contributing to attention-deficit hyperactivity disorder. Feng Y., Crosbie J., Wigg K., Pathare T., Ickowicz A., Schachar R., Tannock R., Roberts W., Malone M., Swanson J. et al. Mol. Psychiatry 10:998-1005, 2005:973-973(2005) · Mapped (1) |
| Sequence variation in the 3'-untranslated region of the dopamine transporter gene and attention-deficit hyperactivity disorder (ADHD). Feng Y., Wigg K.G., Makkar R., Ickowicz A., Pathare T., Tannock R., Roberts W., Malone M., Kennedy J.L., Schachar R. et al. Am. J. Med. Genet. B Neuropsychiatr. Genet. 139B:1-6(2005) · Mapped (4) |
| Characterization of a novel cation transporter ATPase gene (ATP13A4) interrupted by 3q25-q29 inversion in an individual with language delay. Kwasnicka-Crawford D.A., Carson A.R., Roberts W., Summers A.M., Rehnstrom K., Jarvela I., Scherer S.W. |
| Root resorption associated with orthodontic force in IL-1Beta knockout mouse. Al-Qawasmi R.A., Hartsfield J.K., Hartsfield J.K. Jr., Everett E.T., Weaver M.R., Foroud T.M., Roberts W.E. J Musculoskelet Neuronal Interact 4:383-385(2004) · Mapped (2) |
| Mutation screening of X-chromosomal neuroligin genes: no mutations in 196 autism probands. Vincent J.B., Kolozsvari D., Roberts W.S., Bolton P.F., Gurling H.M., Scherer S.W. Am. J. Med. Genet. B Neuropsychiatr. Genet. 129B:82-84(2004) · Mapped (12) |
| Association and transmission analysis of the FMR1 IVS10 + 14C-T variant in autism. Vincent J.B., Thevarkunnel S., Kolozsvari D., Paterson A.D., Roberts W., Scherer S.W. Am. J. Med. Genet. B Neuropsychiatr. Genet. 125B:54-56(2004) · Mapped (6) |
| Glutamate receptor, ionotropic, N-methyl D-aspartate 2A (GRIN2A) gene as a positional candidate for attention-deficit/hyperactivity disorder in the 16p13 region. Adams J., Crosbie J., Wigg K., Ickowicz A., Pathare T., Roberts W., Malone M., Schachar R., Tannock R., Kennedy J.L. et al. Mol. Psychiatry 9:494-499(2004) · Mapped (5) |
| Linkage of the dopamine receptor D1 gene to attention-deficit/hyperactivity disorder. Misener V.L., Luca P., Azeke O., Crosbie J., Waldman I., Tannock R., Roberts W., Malone M., Schachar R., Ickowicz A. et al. Mol. Psychiatry 9:500-509(2004) · Mapped (2) |
| Genetic predisposition to external apical root resorption in orthodontic patients: linkage of chromosome-18 marker. Al-Qawasmi R.A., Hartsfield J.K. Jr., Everett E.T., Flury L., Liu L., Foroud T.M., Macri J.V., Roberts W.E. J. Dent. Res. 82:356-360(2003) · Mapped (2) |
| Human chromosome 7: DNA sequence and biology. Scherer S.W., Cheung J., MacDonald J.R., Osborne L.R., Nakabayashi K., Herbrick J.-A., Carson A.R., Parker-Katiraee L., Skaug J., Khaja R. et al. Science 300:767-772(2003) · UniProtKB (658) |
| Genetic predisposition to external apical root resorption. Al-Qawasmi R.A., Hartsfield J.K. Jr., Everett E.T., Flury L., Liu L., Foroud T.M., Macri J.V., Roberts W.E. Am J Orthod Dentofacial Orthop 123:242-252(2003) · Mapped (3) |
| Cysteine-rich LIM-only proteins CRP1 and CRP2 are potent smooth muscle differentiation cofactors. Chang D.F., Belaguli N.S., Iyer D., Roberts W.B., Wu S.P., Dong X.R., Marx J.G., Moore M.S., Beckerle M.C., Majesky M.W. et al. Dev. Cell 4:107-118(2003) · Mapped (3) |
| The norepinephrine transporter gene and attention-deficit hyperactivity disorder. Barr C.L., Kroft J., Feng Y., Wigg K., Roberts W., Malone M., Ickowicz A., Schachar R., Tannock R., Kennedy J.L. Am. J. Med. Genet. 114:255-259(2002) · Mapped (7) |
