Search Results - (Author, Cooperation:P. C. Phillips)
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1D. W. Parsons ; M. Li ; X. Zhang ; S. Jones ; R. J. Leary ; J. C. Lin ; S. M. Boca ; H. Carter ; J. Samayoa ; C. Bettegowda ; G. L. Gallia ; G. I. Jallo ; Z. A. Binder ; Y. Nikolsky ; J. Hartigan ; D. R. Smith ; D. S. Gerhard ; D. W. Fults ; S. VandenBerg ; M. S. Berger ; S. K. Marie ; S. M. Shinjo ; C. Clara ; P. C. Phillips ; J. E. Minturn ; J. A. Biegel ; A. R. Judkins ; A. C. Resnick ; P. B. Storm ; T. Curran ; Y. He ; B. A. Rasheed ; H. S. Friedman ; S. T. Keir ; R. McLendon ; P. A. Northcott ; M. D. Taylor ; P. C. Burger ; G. J. Riggins ; R. Karchin ; G. Parmigiani ; D. D. Bigner ; H. Yan ; N. Papadopoulos ; B. Vogelstein ; K. W. Kinzler ; V. E. Velculescu
American Association for the Advancement of Science (AAAS)
Published 2010Staff ViewPublication Date: 2010-12-18Publisher: American Association for the Advancement of Science (AAAS)Print ISSN: 0036-8075Electronic ISSN: 1095-9203Topics: BiologyChemistry and PharmacologyComputer ScienceMedicineNatural Sciences in GeneralPhysicsKeywords: Adult ; Cerebellar Neoplasms/*genetics/metabolism ; Child ; DNA Copy Number Variations ; DNA-Binding Proteins/genetics/metabolism ; *Genes, Neoplasm ; Genes, Tumor Suppressor ; Histone-Lysine N-Methyltransferase/genetics/metabolism ; Histones/metabolism ; Humans ; Medulloblastoma/*genetics/metabolism ; Methylation ; MicroRNAs/genetics ; *Mutation ; Neoplasm Proteins/genetics/metabolism ; Oligonucleotide Array Sequence Analysis ; Point Mutation ; Sequence Analysis, DNA ; Signal TransductionPublished by: -
2Staff View
Publication Date: 2018-01-05Publisher: Genetics Society of America (GSA)Electronic ISSN: 2160-1836Topics: BiologyPublished by: -
3Auxin-Mediated Sterility Induction System for Longevity and Mating Studies in Caenorhabditis elegansKasimatis, K. R., Moerdyk-Schauwecker, M. J., Phillips, P. C.
Genetics Society of America (GSA)
Published 2018Staff ViewPublication Date: 2018-08-01Publisher: Genetics Society of America (GSA)Electronic ISSN: 2160-1836Topics: BiologyPublished by: -
4Smith, H. ; Hughes, G. A. ; Douglas, G. H. ; Hartley, D. ; McLoughlin, B. J. ; Siddall, J. B. ; Wendt, G. R. ; Buzby, G. C. ; Herbst, D. R. ; Ledig, K. W. ; McMenamin, J. R. ; Pattison, T. W. ; Suida, J. ; Tokolics, J. ; Edgren, R. A. ; Jansen, A. B. A. ; Gadsby, B. ; Watson, D. H. R. ; Phillips, P. C.
Springer
Published 1963Staff ViewISSN: 1420-9071Source: Springer Online Journal Archives 1860-2000Topics: BiologyMedicineNotes: Zusammenfassung Von mehreren (±) 3-Oxy- und (±) 3-Methoxy-13-alkylgona-1,3,5(10)trien-17-onen und verwandten Verbindungen, einschliesslich von Vertretern der (±) 13-Alkylgon-4-en-3-on-Reihe, werden Totalsynthese und biologische Wirksamkeit beschrieben.Type of Medium: Electronic ResourceURL: -
5Bilaniuk, L. T. ; Molloy, P. T. ; Zimmerman, R. A. ; Phillips, P. C. ; Vaughan, S. N. ; Liu, G. T. ; Sutton, L. N. ; Needle, M.
Springer
Published 1997Staff ViewISSN: 1432-1920Source: Springer Online Journal Archives 1860-2000Topics: MedicineNotes: Abstract We describe the clinical and imaging findings of brain stem tumours in patients with neurofibromatosis type 1 (NF1). The NF1 patients imaged between January 1984 and January 1996 were reviewed and 25 patients were identified with a brain stem tumour. Clinical, radiographical and pathological results were obtained by review of records and images. Brain stem tumour identification occurred much later than the clinical diagnosis of NF1. Medullary enlargement was most frequent (68 %), followed by pontine (52 %) and midbrain enlargement (44 %). Patients were further subdivided into those with diffuse (12 patients) and those with focal (13 patients) tumours. Treatment for hydrocephalus was required in 67 % of the first group and only 15 % of the second group. Surgery was performed in four patients and revealed fibrillary astrocytomas, one of which progressed to an anaplastic astrocytoma. In 40 % of patients both brain stem and optic pathway tumours were present. The biological behaviour of brain stem tumours in NF1 is unknown. Diffuse tumours in the patients with NF1 appear to have a much more favourable prognosis than patients with similar tumours without neurofibromatosis type 1.Type of Medium: Electronic ResourceURL: -
6Girard, N. ; Wang, Z. J. ; Erbetta, A. ; Sutton, L. N. ; Phillips, P. C. ; Rorke, L. B. ; Zimmerman, R. A.
Springer
Published 1998Staff ViewISSN: 1432-1920Keywords: Key words Proton magnetic resonance spectroscopy ; Brain tumor ; pediatric ; Neuro-oncology ; Brain tumors ; prognosisSource: Springer Online Journal Archives 1860-2000Topics: MedicineNotes: Abstract We studied 14 young people with newly diagnosed hemisphere tumors, aged from 3 to 20 years (average 10 years). All underwent surgery following MR imaging (MRI) and spectroscopy (MRS). The tumors studied were three glioblastomas, one each of ganglio-glioblastoma, primitive neuroectodermal tumor (PNET), rhabdoid teratoid tumor, pilocytic astrocytoma, ependymoma, anaplastic ependymoma, and gliomatosis cerebri, and four gangliogliomas. Four patients died; ten patients are alive (five with stable residual tumor, five with no evident tumor). Images and spectra were acquired on a 1.5-T imager. Proton MRS was performed before gadolinium injection in all but one case. Single-voxel techniques were utilized in all cases, using a spin-echo or STEAM sequence with a long echo time (135 or 270 ms). Peak areas of N -acetyl aspartate (NAA), choline (Cho), and creatine and phosphocreatine (Cr) were assessed. The NAA/Cho peak-area ratio was very low in the patients who died (mean ± s. d. 0.20 ± 0.14), and higher in the patients who are alive (0.74 ± 0.47; P = 0.007 by two-tailed t -test). The Cr/Cho peak-area ratio also followed a similar trend for the two groups (mean ± s. d. 0.17 ± 0.07 and 0.49 ± 0.30, respectively; P = 0.01 by two-tailed t -test).Type of Medium: Electronic ResourceURL: