SwePub
Sök i SwePub databas

  Utökad sökning

Träfflista för sökning "WFRF:(Duggan D) "

Sökning: WFRF:(Duggan D)

  • Resultat 271-280 av 286
Sortera/gruppera träfflistan
   
NumreringReferensOmslagsbildHitta
271.
  • De, K., et al. (författare)
  • A hot and fast ultra-stripped supernova that likely formed a compact neutron star binary
  • 2018
  • Ingår i: Science. - : American Association for the Advancement of Science (AAAS). - 0036-8075 .- 1095-9203. ; 362:6411, s. 201-206
  • Tidskriftsartikel (refereegranskat)abstract
    • Compact neutron star binary systems are produced from binary massive stars through stellar evolution involving up to two supernova explosions. The final stages in the formation of these systems have not been directly observed. We report the discovery of iPTF 14gqr (SN 2014ft), a type Ic supernova with a fast-evolving light curve indicating an extremely low ejecta mass (approximate to 0.2 solar masses) and low kinetic energy (approximate to 2 x 10(50) ergs). Early photometry and spectroscopy reveal evidence of shock cooling of an extended helium-rich envelope, likely ejected in an intense pre-explosion mass-loss episode of the progenitor. Taken together, we interpret iPTF 14gqr as evidence for ultra-stripped supernovae that form neutron stars in compact binary systems.
  •  
272.
  • Hedenfalk, I, et al. (författare)
  • Gene-expression profiles in hereditary breast cancer
  • 2001
  • Ingår i: New England Journal of Medicine. - 0028-4793. ; 344:8, s. 48-539
  • Tidskriftsartikel (refereegranskat)abstract
    • BACKGROUND: Many cases of hereditary breast cancer are due to mutations in either the BRCA1 or the BRCA2 gene. The histopathological changes in these cancers are often characteristic of the mutant gene. We hypothesized that the genes expressed by these two types of tumors are also distinctive, perhaps allowing us to identify cases of hereditary breast cancer on the basis of gene-expression profiles.METHODS: RNA from samples of primary tumor from seven carriers of the BRCA1 mutation, seven carriers of the BRCA2 mutation, and seven patients with sporadic cases of breast cancer was compared with a microarray of 6512 complementary DNA clones of 5361 genes. Statistical analyses were used to identify a set of genes that could distinguish the BRCA1 genotype from the BRCA2 genotype.RESULTS: Permutation analysis of multivariate classification functions established that the gene-expression profiles of tumors with BRCA1 mutations, tumors with BRCA2 mutations, and sporadic tumors differed significantly from each other. An analysis of variance between the levels of gene expression and the genotype of the samples identified 176 genes that were differentially expressed in tumors with BRCA1 mutations and tumors with BRCA2 mutations. Given the known properties of some of the genes in this panel, our findings indicate that there are functional differences between breast tumors with BRCA1 mutations and those with BRCA2 mutations.CONCLUSIONS: Significantly different groups of genes are expressed by breast cancers with BRCA1 mutations and breast cancers with BRCA2 mutations. Our results suggest that a heritable mutation influences the gene-expression profile of the cancer.
  •  
273.
  •  
274.
  • Kauraniemi, P, et al. (författare)
  • MYB oncogene amplification in hereditary BRCA1 breast cancer
  • 2000
  • Ingår i: Cancer Research. - 1538-7445. ; 60:19, s. 5323-5328
  • Tidskriftsartikel (refereegranskat)abstract
    • Comparative genomic hybridization analysis has demonstrated that breast tumors from BRCA1 and BRCA2 germ-line mutation carriers contain a large number of chromosomal copy number gains and losses. A high regional copy number gain at 6q22-q24 was observed in one BRCA1 tumor, and fluorescence in situ hybridization analysis indicated a strong amplification of the MYB oncogene (15 copies of MYB compared with 1 copy of chromosome 6 centromere). Fluorescence in situ hybridization analysis revealed amplification of MYB in 5 (29%) of 17 BRCA1 breast tumors, whereas none of 8 BRCA2 tumors and 13 breast cancer cell lines, and only 2 of 100 sporadic breast tumors exhibited altered MYB copy numbers. Gene amplification resulted in mRNA overexpression as determined by Northern blot and cDNA microarray analysis, and protein overexpression by immunohistochemical staining. We conclude that MYB amplification is infrequent in sporadic breast cancer but common in breast tumors from BRCA1 mutation carriers, suggesting a role of this cell cycle regulator and transcription factor in the progression of some BRCA1 tumors. However, we cannot rule out the significance of other genes in the 6q22-q24 amplicon.
  •  
275.
  •  
276.
  •  
277.
  • Ofek, E. O., et al. (författare)
  • PTF13efv-AN OUTBURST 500 DAYS PRIOR TO THE SNHUNT 275 EXPLOSION AND ITS RADIATIVE EFFICIENCY
  • 2016
  • Ingår i: Astrophysical Journal. - 0004-637X .- 1538-4357. ; 824:1
  • Tidskriftsartikel (refereegranskat)abstract
    • The progenitors of some supernovae (SNe) exhibit outbursts with super-Eddington luminosities prior to their final explosions. This behavior is common among SNe IIn, but the driving mechanisms of these precursors are not yet well-understood. SNHunt 275 was announced as a possible new SN during 2015 May. Here we report on pre-explosion observations of the location of this event by the Palomar Transient Factory (PTF) and report the detection of a precursor about 500 days prior to the 2015 May activity (PTF 13efv). The observed velocities in the 2015 transient and its 2013 precursor absorption spectra are low (1000-2000 km s(-1)), so it is not clear yet if the recent activity indeed marks the final disruption of the progenitor. Regardless of the nature of this event, we use the PTF photometric and spectral observations, as well as Swift-UVOT observations, to constrain the efficiency of the radiated energy relative to the total kinetic energy of the precursor. We find that, using an order-of-magnitude estimate and under the assumption of spherical symmetry, the ratio of the radiated energy to the kinetic energy is in the range of 4 x 10(-2) to 3.4 x 10(3).
  •  
278.
  •  
279.
  •  
280.
  •  
Skapa referenser, mejla, bekava och länka
  • Resultat 271-280 av 286
Typ av publikation
tidskriftsartikel (283)
konferensbidrag (1)
forskningsöversikt (1)
Typ av innehåll
refereegranskat (281)
övrigt vetenskapligt/konstnärligt (4)
Författare/redaktör
Abbott, B. (229)
Brandt, A. (229)
Brock, R. (229)
Burdin, S. (229)
Cooke, M. (229)
Evans, H. (229)
visa fler...
Fox, H. (229)
Hensel, C. (229)
Hubacek, Z. (229)
Khanov, A. (229)
Kupco, A. (229)
Lammers, S. (229)
Meyer, J. (229)
Sawyer, L. (229)
Snyder, S. (229)
Stark, J. (229)
Strauss, M. (229)
Watts, G. (229)
White, A. (229)
Zhou, B. (229)
Zhu, J. (229)
Haley, J. (229)
Savage, G. (229)
Davies, G (229)
Askew, A. (229)
Avila, C. (229)
Barberis, E. (229)
Bean, A. (229)
Borissov, G. (228)
Chakraborty, D. (228)
Pleier, M. -A. (228)
Qian, J. (228)
Quadt, A. (228)
Scanlon, T. (228)
Schwanenberger, C. (228)
Schwienhorst, R. (228)
Severini, H. (228)
Shabalina, E. (228)
Tsybychev, D. (228)
Wicke, D. (228)
Buescher, V. (228)
Nagy, E. (228)
Bernhard, R. (228)
De La Cruz-Burelo, E ... (228)
Duperrin, A. (228)
Xie, Y. (228)
Adams, M. (228)
Alton, A. (228)
Bagby, L. (228)
Baldin, B. (228)
visa färre...
Lärosäte
Uppsala universitet (236)
Stockholms universitet (154)
Kungliga Tekniska Högskolan (120)
Karolinska Institutet (41)
Umeå universitet (19)
Lunds universitet (8)
visa fler...
Göteborgs universitet (6)
Mälardalens universitet (3)
Örebro universitet (3)
Jönköping University (2)
visa färre...
Språk
Engelska (286)
Forskningsämne (UKÄ/SCB)
Naturvetenskap (218)
Medicin och hälsovetenskap (27)

År

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy