Search Results - "Harlin, C"

The magic nature of 132 Sn explored through the single-particle states of 133 Sn by Jones, K. L, Adekola, A. S, Bardayan, D. W, Blackmon, J. C, Chae, K. Y, Chipps, K. A, Cizewski, J. A, Erikson, L, Harlin, C, Hatarik, R, Kapler, R, Kozub, R. L, Liang, J. F, Livesay, R, Ma, Z, Moazen, B. H, Nesaraja, C. D, Nunes, F. M, Pain, S. D, Patterson, N. P, Shapira, D, Shriner, J. F, Smith, M. S, Swan, T. P, Thomas, J. S

“…Atomic nuclei have a shell structure in which nuclei with ‘magic numbers’ of neutrons and protons are analogous to the noble gases in atomic physics. Only ten…”
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Characterization of DCTN1 genetic variability in neurodegeneration by VILARINO-GÜELL, C, WIDER, C, UITTI, R. J, GRAFF-RADFORD, N. R, BOEVE, B. F, JOSEPHS, K. A, MILLER, B, BOYLAN, K. B, GWINN, K, ADLER, C. H, AASLY, J. O, HENTATI, F, SOTO-ORTOLAZA, A. I, DESTEE, A, KRYGOWSKA-WAJS, A, CHARTIER-HARLIN, M.-C, ROSS, O. A, RADEMAKERS, R, FARRER, M. J, COBB, S. A, KACHERGUS, J. M, KEELING, B. H, DACHSEL, J. C, HULIHAN, M. M, DICKSON, D. W, WSZOLEK, Z. K

“…Recently, mutations in DCTN1 were found to cause Perry syndrome, a parkinsonian disorder with TDP-43-positive pathology. Previously, mutations in DCTN1 were…”
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A full Genome Scan for Late Onset Alzheimer's Disease by Kehoe, Patrick, Vrieze, Fabienne Wavrant-De, Crook, Richard, Wu, William S., Holmans, Peter, Fenton, Iain, Spurlock, Gillian, Norton, Nadine, Williams, Hywel, Williams, Nigel, Lovestone, Simon, Perez-Tur, Jordi, Hutton, Mike, Chartier-Harlin, Marie-Christine, Shears, Shantia, Roehl, Kimberly, Booth, Jeremy, Van Voorst, Wendy, Ramic, Dzanan, Williams, Julie, Goate, Alison, Hardy, John, Owen, Michael J.

“…We have genotyped 292 affected sibling pairs (ASPs) with Alzheimer's disease (AD) according to NINCDS-ADRDA diagnostic criteria and with onset ages of ≥65…”
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A New Polymorphism in the Apoe Promoter Associated with Risk of Developing Alzheimer's Disease by Lambert, Jean-Charles, Pasquier, Florence, Cottel, Dominique, Frigard, Bernard, Amouyel, Philippe, Chartier-Harlin, Marie-Christine

“…The ε4 allele of the Apolipoprotein E gene (APOE), one of the main allele of APOE polymorphism, is a major risk factor for the development of Alzheimer's…”
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Contribution of APOE promoter polymorphisms to Alzheimer's disease risk by LAMBERT, J.-C, ARARIA-GOUMIDI, L, FRIGARD, B, PETERSEN, R. C, CUMMING, A. M, PASQUIER, F, SASTRE, I, TIENARI, P. J, FRANK, A, SULKAVA, R, MORRIS, J. C, CLAIR, D. St, MYLLYKANGAS, L, MANN, D. M, WAVRANT-DEVRIEZE, F, EZQUERRA-TRABALON, M, AMOUYEL, P, HARDY, J, HALTIA, M, VALDIVIESO, F, GOATE, A. M, PEREZ-TUR, J, LENDON, C. L, ELLIS, C, CHARTIER-HARLIN, M.-C, WANG, J. C, BULLIDO, M. J, HARRIS, J. M, ARTIGA, M. J, HERNANDEZ, D, KWON, J. M

“…To determine whether the effects of APOE promoter polymorphisms on AD are independent of the APOE-epsilon4 allele. Recently, the -491 A-->T and -219 G-->T…”
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Early-onset Alzheimer's disease caused by mutations at codon 717 of the β-amyloid precursor protein gene by Chartier-Harlin, Marie-Christine, Crawford, Fiona, Houlden, Henry, Warren, Andrew, Hughes, David, Fidani, Liana, Goate, Alison, Rossor, Martin, Roques, Penelope, Hardy, John, Mullan, Mike

“…A mutation at codon 717 of the beta-amyloid precursor protein gene has been found to cosegregate with familial Alzheimer's disease in a single family. This…”
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Independent association of an APOE gene promoter polymorphism with increased risk of myocardial infarction and decreased APOE plasma concentrations : the ECTIM study by LAMBERT, J.-C, BROUSSEAU, T, CAMBIEN, F, CHARTIER-HARLIN, M.-C, AMOUYEL, P, DEFOSSE, V, EVANS, A, ARVEILER, D, RUIDAVETS, J.-B, HAAS, B, CAMBOU, J.-P, LUC, G, DUCIMETIERE, P

“…Apolipoprotein E (APOE) is a major protein in lipid metabolism existing in three common isoforms: APOE2, -3 and -4. The varepsilon4 allele of the APOE gene (…”
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Are interleukin-1 gene polymorphisms risk factors or disease modifiers in AD? by GREEN, E. K, HARRIS, J. M, LEMMON, H, LAMBERT, J. C, CHARTIER-HARLIN, M. C, CLAIR, D. St, MANN, D. M. A, IWATSUBO, T, LENDON, C. L

“…Polymorphisms in the interleukin-1 genes, IL-1A and IL-1B, have been associated with AD, but not in all studies. The authors genotyped the IL-1A(-889) and…”
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Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease by Goate, Alison, Chartier-Harlin, Marie-Christine, Mullan, Mike, Brown, Jeremy, Crawford, Fiona, Fidani, Liana, Giuffra, Luis, Haynes, Andrew, Irving, Nick, James, Louise, Mant, Rebecca, Newton, Phillippa, Rooke, Karen, Roques, Penelope, Talbot, Chris, Pericak-Vance, Margaret, Roses, Alien, Williamson, Robert, Rossor, Martin, Owen, Mike, Hardy, John

“…A locus segregating with familial Alzheimer's disease (AD) has been mapped to chromosome 21, close to the amyloid precursor protein (APP) gene. Recombinants…”
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The magic nature of 132Sn explored through the single-particle states of 133Sn by Jones, K. L., Adekola, A. S., Bardayan, D. W., Blackmon, J. C., Chae, K. Y., Chipps, K. A., Cizewski, J. A., Erikson, L., Harlin, C., Hatarik, R., Kapler, R., Kozub, R. L., Liang, J. F., Livesay, R., Ma, Z., Moazen, B. H., Nesaraja, C. D., Nunes, F. M., Pain, S. D., Patterson, N. P., Shapira, D., Shriner, J. F., Smith, M. S., Swan, T. P., Thomas, J. S.

“…Nuclear magic Atomic nuclei have a shell structure that allows for 'magic' numbers of neutrons and protons, analogous to the noble gases in atomic physics…”
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Effect of the APOE promoter polymorphisms on cerebral amyloid peptide deposition in Alzheimer's disease by Lambert, J-C, Mann, D, Goumidi, L, Harris, J, Amouyel, P, Iwatsubo, T, Lendon, C, Chartier-Harlin, M-C

“…Polymorphisms in the promoter region of the apolipoprotein E gene (APOE) affect the amount of amyloid peptide (Aβ) in the brains of patients with Alzheimer's…”
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A polymorphic variation in the interleukin 1A gene increases brain microglial cell activity in Alzheimer’s disease by Hayes, A, Green, E K, Pritchard, A, Harris, J M, Zhang, Y, Lambert, J C, Chartier-Harlin, M C, Pickering-Brown, S M, Lendon, C L, Mann, D M A

“…Objective: To investigate the impact of possession of the −889 C/T polymorphism of the interleukin 1A gene (IL-1A) and the −511 C/T polymorphism of the…”
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A high-efficiency compact setup to study evaporation residues formed in reactions induced by low-intensity radioactive ion beams by Shapira, D., Liang, J.F., Gross, C.J., Varner, R.L., Amro, H., Harlin, C., Kolata, J.J., Novotny, S.

“…A setup for measuring cross-sections of evaporation residues produced in the collision of two heavy ions is described. The system, which detects all reaction…”
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Assessment of Nurr1 nucleotide variations in familial Parkinson’s disease by Levecque, C, Destée, A, Mouroux, V, Amouyel, P, Chartier-Harlin, M.-C

“…Parkinson’s disease (PD) is characterised by the death of dopaminergic neurons of the substantia nigra. As Nurr1 seems to regulate the development and…”
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A Novel Presenilin‐2 Splice Variant in Human Alzheimer's Disease Brain Tissue by Sato, Naoya, Hori, Osamu, Yamaguchi, Atsushi, Lambert, Jean‐Charles, Chartier‐Harlin, Marie‐Christine, Robinson, Philip A., Delacourte, Andre, Schmidt, Ann Marie, Furuyama, Tatsuo, Imaizumi, Kazunori, Tohyama, Masaya, Takagi, Tsutomu

“…: Mutations in the presenilin‐1 (PS‐1) and presenilin‐2 (PS‐2) genes account for the majority of cases of early‐onset familial Alzheimer's disease (AD)…”
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A polymorphism in the angiotensin 1-converting enzyme gene is associated with damage to cerebral cortical white matter in Alzheimer's disease by Tian, J, Shi, J, Bailey, K, Harris, J.M, Pritchard, A, Lambert, J.-C, Chartier-Harlin, M.-C, Pickering-Brown, S.M, Lendon, C.L, Mann, D.M.A

“…The impact of the insertion (I)/deletion (D) (I/D) polymorphism in the angiotensin 1-converting enzyme (ACE) gene on the extent of white matter myelin loss…”
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The angiotensin 1-converting enzyme insertion (I)/deletion (D) polymorphism does not influence the extent of amyloid or tau pathology in patients with sporadic Alzheimer's disease by Lendon, C.L, Thaker, U, Harris, J.M, McDonagh, A.M, Lambert, J.-C, Chartier-Harlin, M.-C, Iwatsubo, T, Pickering-Brown, S.M, Mann, D.M.A

“…An insertion (I)/deletion (D) polymorphism in the angiotensin 1-converting enzyme (ACE) gene has, in some studies, been associated with increased risk for…”
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Association of polymorphisms in the Tau and Saitohin genes with Parkinson’s disease by Levecque, C, Elbaz, A, Clavel, J, Vidal, J S, Amouyel, P, Alpérovitch, A, Tzourio, C, Chartier-Harlin, M C

“…Background: The Saitohin gene has recently been identified in intron 9 of the Tau gene. Because an association between Parkinson’s disease and Tau has been…”
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Genetic Studies on Chromosome 12 in Late-Onset Alzheimer Disease by Wu, William S, Holmans, Peter, Wavrant-DeVrièze, Fabienne, Shears, Shantia, Kehoe, Patrick, Crook, Richard, Booth, Jeremy, Williams, Nigel, Pérez-Tur, Jordi, Roehl, Kimberly, Fenton, Iain, Chartier-Harlin, Marie-Christine, Lovestone, Simon, Williams, Julie, Hutton, Mike, Hardy, John, Owen, Michael J, Goate, Alison

“…CONTEXT.— The only genetic locus universally accepted to be important as a risk factor for late-onset Alzheimer disease (AD) is the apolipoprotein E (APOE)…”
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The transcriptional factor LBP-1c/CP2/LSF gene on chromosome 12 is a genetic determinant of Alzheimer's disease by LAMBERT, Jean-Charles, GOUMIDI, Louisa, ST CLAIR, David, MANN, David M. A, HARDY, John, LENDON, Corinne L, AMOUYEL, Philippe, CHARTIER-HARLIN, Marie-Christine, VRIEZE, Fabienne Wavrant-De, FRIGARD, Bernard, HARRIS, Judith M, CUMMINGS, Alistair, COATES, John, PASQUIER, Florence, COTTEL, Dominique, GAILLAC, Marianne

“…Although the varepsilon4 allele of the apolipoprotein E gene appears as an important biological marker for Alzheimer's disease (AD) susceptibility, other…”
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