Search Results - "Ambrose, C. M"

Melting of hexagonal skyrmion states in chiral magnets by Ambrose, M C, Stamps, R L

“…Skyrmions are spiral structures observed in thin films of certain magnetic materials (Uchida et al 2006 Science 311 359-61). Of the phases allowed by the…”
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Magnetic stripe domain pinning and reduction of in-plane magnet order due to periodic defects in thin magnetic films by Ambrose, M.C., Stamps, R.L.

“…In thin magnetic films with strong perpendicular anisotropy and strong demagnetizing field two ordered phases are possible. At low temperatures,…”
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Monte Carlo simulation of the effects of higher-order anisotropy on the spin reorientation transition in the two-dimensional Heisenberg model with long-range interactions by Ambrose, M. C., Stamps, R. L.

“…The strength of perpendicular anisotropy is known to drive the spin reorientation in thin magnetic films. Here, we consider the effect different order…”
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De novo expansion of a (CAG) n repeat in sporadic Huntington's disease by Myers, R. H, MacDonald, M. E, Koroshetz, W. J, Duyao, M. P, Ambrose, C. M, Taylor, S. A. M, Barnes, G, Srinidhi, J, Lin, C. S, Whaley, W. L, Lazzarini, A. M, Schwarz, M, Wolff, G, Bird, E. D, Vonsattel, J.-P. G, Gusella, J. F

“…Huntington's disease (HD) chromosomes contain an expanded unstable (CAG)n repeat in chromosome 4p16.3. We have examined nine families with potential de novo…”
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Characterization of lymphotoxin-alpha beta complexes on the surface of mouse lymphocytes by Browning, JL, Sizing, ID, Lawton, P, Bourdon, PR, Rennert, PD, Majeau, GR, Ambrose, CM, Hession, C, Miatkowski, K, Griffiths, DA, Ngam-ek, A, Meier, W, Benjamin, CD, Hochman, PS

“…The lymphotoxin-alpha beta complex (LT alpha beta) is found on the surface of activated lymphocytes and binds to a specific receptor called the LT beta…”
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Gametic but not somatic instability of CAG repeat length in Huntington's disease by MacDonald, M E, Barnes, G, Srinidhi, J, Duyao, M P, Ambrose, C M, Myers, R H, Gray, J, Conneally, P M, Young, A, Penney, J

“…Instability of a CAG repeat in 4p16.3 has been found in Huntington's disease (HD) chromosomes. Unlike a similar repeat in the fragile X syndrome, the expanded…”
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Huntington's disease gene: regional and cellular expression in brain of normal and affected individuals by Landwehrmeyer, G B, McNeil, S M, Dure, 4th, L S, Ge, P, Aizawa, H, Huang, Q, Ambrose, C M, Duyao, M P, Bird, E D, Bonilla, E

“…Huntington's disease (HD) is an autosomal dominant disorder characterized by involuntary movements, dementia, and progressive, global, but regionally…”
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BAFF-R by Ambrose, C M

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Identification of a Palmitic Acid-modified Form of Human Sonic hedgehog by Pepinsky, R. Blake, Zeng, Chenhui, Wen, Dingyi, Rayhorn, Paul, Baker, Darren P., Williams, Kevin P., Bixler, Sarah A., Ambrose, Christine M., Garber, Ellen A., Miatkowski, Konrad, Taylor, Frederick R., Wang, Elizabeth A., Galdes, Alphonse

“…During hedgehog biosynthesis, autocatalytic processing produces a lipid-modified amino-terminal fragment (residues 24–197 in the human Sonic hedgehog sequence)…”
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Normal and expanded Huntington's disease gene alleles produce distinguishable proteins due to translation across the CAG repeat by Persichetti, F, Ambrose, C M, Ge, P, McNeil, S M, Srinidhi, J, Anderson, M A, Jenkins, B, Barnes, G T, Duyao, M P, Kanaley, L

“…An expanded CAG trinucleotide repeat is the genetic trigger of neuronal degeneration in Huntington's disease (HD), but its mode of action has yet to be…”
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Structure and expression of the Huntington's disease gene : evidence against simple inactivation due to an expanded CAG repeat by AMBROSE, C. M, DUYAO, M. P, WASMUTH, J, BUCKLER, A, CHURCH, D, HOUSMAN, D, BERKS, M, MICKLEM, G, DURBIN, R, DODGE, A, READ, A, GUSELLA, J, BARNES, G, MACDONALD, M. E, BATES, G. P, LIN, C. S, JAYAKSHIMI SRINIDHI, BAXENDALE, S, HUMMERICH, H, LEBRACH, H, ALTHERR, M

“…Huntington's disease, a neurodegenerative disorder characterized by loss of striatal neurons, is caused by an expanded, unstable trinucleotide repeat in a…”
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A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor by Trofatter, J A, MacCollin, M M, Rutter, J L, Murrell, J R, Duyao, M P, Parry, D M, Eldridge, R, Kley, N, Menon, A G, Pulaski, K

“…Neurofibromatosis 2 (NF2) is a dominantly inherited disorder characterized by the occurrence of bilateral vestibular schwannomas and other central nervous…”
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IT15 gene expression in fetal human brain by Dure, 4th, L S, Landwehrmeyer, G B, Golden, J, McNeil, S M, Ge, P, Aizawa, H, Huang, Q, Ambrose, C M, Duyao, M P, Bird, E D

“…To examine the expression of the gene which causes Huntington's disease (HD), IT15, during development, in situ hybridization of radiolabeled riboprobes was…”
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A gene from chromosome 4p16.3 with similarity to a superfamily of transporter proteins by Duyao, M P, Taylor, S A, Buckler, A J, Ambrose, C M, Lin, C, Groot, N, Church, D, Barnes, G, Wasmuth, J J, Housman, D E

“…We have previously used exon amplification to identify the ADD1 gene in cosmid Y24 from the Huntington's disease (HD) region of 4p16.3. The same technique has…”
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Mouse Huntington's disease gene homolog (Hdh) by BARNES, G. T, DUYAO, M. P, AMBROSE, C. M, MCNEIL, S, PERSICHETTI, F, JAYALAKSHMI SRINIDHI, GUSELLA, J. F, MACDONALD, M. E

“…The incurable neurodegenerative disorder, Huntington's disease (HD), is caused by an expanded, unstable CAG repeat encoding a stretch of polyglutamine in a…”
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Synteny conservation of the Huntington's disease gene and surrounding loci on mouse Chromosome 5 by Grosson, C L, MacDonald, M E, Duyao, M P, Ambrose, C M, Roffler-Tarlov, S, Gusella, J F

“…The mouse homologs of the Huntington's disease (HD) gene and 17 other human Chromosome (Chr) 4 loci (including six previously unmapped) were localized by use…”
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Spin-label study of the mobility of enzyme-bound lipoic acid in the pyruvate dehydrogenase multienzyme complex of Escherichia coli by Ambrose, M C, Perham, R N

“…The lipoic acid residues covalently bound to the transacetylase component of the pyruvate dehydrogenase multienzyme complex of Escherichia coli were…”
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Molecular genetics of Huntington's disease by Gusella, J F, MacDonald, M E, Ambrose, C M, Duyao, M P

“…Huntington's disease is an inherited disorder in which selective neuronal loss in the brain leads to a characteristic choreic movement disorder. The successful…”
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Differential Expression of Normal and Mutant Huntington's Disease Gene Alleles by Persichetti, Francesca, Carlee, Leone, Faber, Peter W., McNeil, Sandra M., Ambrose, Christine M., Srinidhi, Jayalakshmi, Anderson, MaryAnne, Barnes, Glenn T., Gusella, James F., MacDonald, Marcy E.

“…Huntingtin expression was examined by Western blot and immunoprecipitation studies of lymphoblastoid cell lines from Huntington's disease (HD) homozygotes,…”
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Interaction Affinity between Cytokine Receptor Components on the Cell Surface by Whitty, Adrian, Raskin, Natalya, Olson, Dian L., Borysenko, Christopher W., Ambrose, Christine M., Benjamin, Christopher D., Burkly, Linda C.

“…The anti-common gamma chain (γc) mAb CP.B8 is shown to inhibit interleukin 4 (IL-4)-dependent proliferation of phytohemagglutinin (PHA) activated T cells…”
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