Zobrazeno 1 - 10
of 27
pro vyhledávání: '"D W, Bell"'
Publikováno v:
Biogeosciences, Vol 7, Iss 2, Pp 695-710 (2010)
Inorganic phosphorus (SRP) concentrations in the subtropical North Atlantic are some of the lowest in the global ocean and have been hypothesized to constrain primary production. Based upon data from several transect cruises in this region, it has be
Externí odkaz:
https://doaj.org/article/e8ec79a1bf1e4208ae0e6cb499f2a8d2
Autor:
M. Lawler, A. Locasciulli, A. Bacigalupo, P. Humphries, P. Ljungman, S. R. McCann, N. Nolan, E. W. McDermott, J. R. Reynolds, A. McCann, R. Rafferty, P. Sweeney, D. Carney, N. J. O’Higgins, M. J. Duffy, C. Gardiner, D. J. Reen, M. A. O’Connell, D. Kelleher, N. Hall, L. A. J. O’Neill, A. Long, J. V. McCarthy, R. S. Fernandes, T. G. Cotter, E. Ryan, A. Kitching, P. MacMathuna, E. Mulligan, R. Merriman, P. Dervan, P. Kelly, T. F. Gorey, J. R. Lennon, J. Crowe, M. A. Bennett, E. W. Kay, B. Curran, D. P. O’Donoghue, M. Leader, D. T. Croke, J. M. O’Connor, V. J. McKelvey-Martin, P. G. McKenna, J. M. O’Riordan, A. Tobin, M. O’Mahoney, F. M. Keogh, J. O’Riordan, C. McNamara, P. McEneaney, P. A. Daly, M. Farrell, S. Young, D. Gibbons, P. McCarthy, H. Mulcahy, N. A. Parfrey, K. Sheahan, H. Lambkin, C. Mothersill, D. Chin, K. Sheehan, P. Kelehan, N. Parfrey, M. Morrin, F. Khan, P. Delaney, D. M. Rowan, W. J. Orminston, P. P. Donnellan, A. Khalid, M. Kerin, D. M. O’Hanlon, P. Kent, H. F. Given, S. M. Kennedy, G. McGeoch, N. K. Spurr, J. Barrett, G. O’Sullivan, J. K. Collins, T. Willcocks, S. Kennedy, J. Dolan, W. Gallagher, E. McDermott, N. O’Higgins, R. Hagan, R. McManus, W. Ormiston, P. Daly, O. Sheils, M. McDermott, D. S. O’Briain, D. Maher, P. Costello, F. Flanagan, J. Stack, J. Ennis, H. Grimes, A. Yanni, M. Harrison, W. S. Lowry, S. E. H. Russell, R. J. Atkinson, P. White, I. Hickey, D. W. Bell, D. Biggart, J. Doyle, M. J. Staunton, E. F. Gaffney, P. A. Dervan, M. M. McCabe, J. J. Fennelly, D. N. Carney, M. O’Reilly, J. N. McMahon, M. Moriarty, B. Hurson, A. J. O’Neill, H. Magee, J. O’Loughlin, P. Cremin, W. Orminston, J. McCarthy, P. Redmond, S. Duggan, S. Rea, D. Bouchier-Hayes, J. O’Donnell, C. Duggan, J. Crown, D. Bermingham, A. Nugent, C. Fleming, P. Crosby, S. Wolff, D. McCarthy, C. Barry Walsh, M. Cassidy, S. Husain, E. Kay, M. Thornhilll, D. Whelan, D. Barry, M. Turner, W. Prenderville, F. Murphy, W. Prendiville, G. Gibson, T. O’Grady, M. Carmody, J. Donohoe, J. Walshe, G. M. Murphy, J. O’Donoghue, K. Kerin, S. Ahern, K. Molloy, N. Goulden, D. H. Pamphilon, M. O’Connell, C. Power, A. Leroux, M. Perricaudet, D. Walls, F. Britton, L. Brennan, Y. A. Barnett, B. Madden, L. P. G. Wakelin, H. C. Loughrey, P. Corley, H. P. Redmond, R. W. G. Watson, I. Keogh, D. O’Hanlon, S. Walsh, J. Callaghan, M. McNamara, A. Benedict-Smith, C. Barnes, D. Neylon, M. Fenton, M. Searcey, C. M. Topham, L. G. Wakelin, N. M. Howarth, A. Purohit, M. J. Reed, B. V. L. Potter, W. J. Hatton, G. McKerr, D. Harvey, J. Carson, B. M. Hannigan, P. J. McCarthy, S. McClean, B. T. Hill, C. Costelloe, W. A. Denny, B. Fingleton, S. McDonnell, M. Butler, N. Corbally, J. F. Stephens, G. Martin, A. McGirl, E. Lawlor, N. Gardiner, S. Lynch, M. de Arce, F. O’Brien, A. Duggan, S. O’Herlihy, F. Shanahan, G. O’Keeffe, S. McCann, K. Sweeney, A. O. Neill, D. Pamphilon, M. Sheridan, I. Reid, C. B. Seymour, T. Walshe, T. P. Hennessy, A. O’Mahony, J. O’Connell’, C. Lawlor, S. Nolan, D. Morrisey, P. J. Pedlow, M. Walsh, S. W. Lowry, J. J. A. McAleer, S. R. McKeown, M. Afrasiabi, T. R. J. Lappin, B. Joiner, K. V. Hirst, D. G. Hirst, E. Sweeney, J. VanderSpek, J. Murphy, F. Foss
Publikováno v:
Irish Journal of Medical Science. 164:219-244
Autor:
S B, Lee, S H, Kim, D W, Bell, D C, Wahrer, T A, Schiripo, M M, Jorczak, D C, Sgroi, J E, Garber, F P, Li, K E, Nichols, J M, Varley, A K, Godwin, K M, Shannon, E, Harlow, D A, Haber
Publikováno v:
Cancer research. 61(22)
Li Fraumeni Syndrome (LFS) is a multicancer phenotype, most commonly associated with germ-line mutations in TP53. In a kindred with LFS without an inherited TP53 mutation, we have previously reported a truncating mutation (1100delC) in CHK2, encoding
Autor:
T D, Shafman, S, Levitz, A J, Nixon, L A, Gibans, K E, Nichols, D W, Bell, C, Ishioka, K J, Isselbacher, R, Gelman, J, Garber, J R, Harris, D A, Haber
Publikováno v:
Genes, chromosomescancer. 27(2)
Patients treated with conservative surgery and radiation therapy for early-stage breast cancer develop a contralateral breast cancer at a rate of approximately 0.75% per year. Ataxia-telangiectasia (AT) is an autosomal recessive disease that is chara
Publikováno v:
Cancer research. 59(2)
Comparative genomic hybridization analysis was performed to identify chromosomal imbalances in 24 human malignant mesothelioma (MM) cell lines derived from untreated primary tumors. Chromosomal losses accounted for the majority of genomic imbalances.
Publikováno v:
The New Zealand medical journal. 111(1071)
To measure measles-mumps-rubella (MMR) immunisation status of a birth cohort at 18 months of age.All children born in Christchurch in June, July and August 1995 who were alive at 18 months of age (n = 999), were matched with MMR immunisation benefit
Publikováno v:
Cancer research. 58(13)
Multidrug resistance-associated protein (MRP) and canalicular multispecific organic anion transporter (cMOAT) are closely related mammalian ATP-binding cassette transporters that export organic anions from cells. Transfection studies have established
Publikováno v:
Cancer research. 58(7)
An estramustine-resistant human ovarian carcinoma cell line, SKEM, was generated to explore resistance mechanisms associated with this agent. Cytogenetic analysis revealed that SKEM cells have a homogeneously staining region (hsr) at chromosome 9q34.
Publikováno v:
The New Zealand medical journal. 110(1056)
To ascertain the immunisation status of a birth cohort of infants at 8 months of age.Data on all children born in Christchurch in June, July and August 1995 were matched with immunisation benefit claim information for the 6-week, 3-month and 5-month
Autor:
J Q, Cheng, S C, Jhanwar, W M, Klein, D W, Bell, W C, Lee, D A, Altomare, T, Nobori, O I, Olopade, A J, Buckler, J R, Testa
Publikováno v:
Cancer research. 54(21)
To determine whether p16 is altered in human malignant mesothelioma (MM), molecular analysis of multiple 9p loci was performed on 40 cell lines and 23 primary tumors from 42 MM patients. We identified homozygous deletions of p16 in 34 (85%) cell line