By Hirsch J.G., Page D. (eds.)
What's the Universe made up of? How previous is it? How does a supernova explode? will we notice black holes? And the place do cosmic rays originate? This quantity offers a finished and pedagogical creation to trendy rules and demanding difficulties in nuclear and particle astrophysics. Articles written by means of 8 best specialists conceal a wealth of fascinating themes. jointly, they current the Universe as a laboratory for checking out state of the art physics. This well timed quantity effectively bridges the space among convention complaints and really good monographs. It presents a useful source for graduate scholars and energetic researchers in nuclear and particle physics, astrophysics and cosmology.
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During this quantity, experimentalists and theoreticians talk about which experiments and calculations are had to make major development within the box and in addition how experiments and theoretical descriptions could be in comparison. the subjects handled are the electromagnetic construction of Goldstone bosons, pion--pion and pion--nucleon interactions, hadron polarizability and shape components.
Sino-American nuclear kinfolk are serious given ongoing modernization efforts on either side and an more and more complicated local and international nuclear environment. This quantity pairs chinese language and American authors jointly to supply nationwide views on modern nuclear matters, together with perceptions of strategic context, nationwide safeguard priorities, doctrines, perceptions of local threats, and techniques to handle those risks.
This reprint has been approved by way of Springer-Verlag on the market in Africa, Middle/South the United States, Israel, Jordan, Lebanon, Saudia-Arabia, Syria, South-East-Asia and China simply
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Extra resources for Nuclear and particle astrophysics
However, this is not a universal phenomenon. , 2010). 1, which is implicated in ASD with macrocephaly. , 2010). This is not restricted to neurodevelopmental disorders, as the most common locus affected in CharcotMarie-Tooth (CMT) neuropathy, PMP22, when deleted causes a different neurological phenotype to that associated with gene gain (Chance, 2006). Duplication of PMP22 leads to CMT type 1A, while PMP22 deletion leads to a disease known as hereditary neuropathy with liability to pressure palsies (HNPP).
The xeroderma pigmentosum group D (XPD) gene: one gene, two functions, three diseases. Genes Dev, 15(1):15-23. Lenski C, Kooy RF, Reyniers E, Loessner D, Wanders RJ, et al. (2007). The reduced expression of the HADH2 protein causes X-linked mental retardation, choreoathetosis, and abnormal behavior. Am J Hum Genet, 80(2):372-7. Lesage S, Brice A. (2009). Parkinson's disease: from monogenic forms to genetic susceptibility factors. Hum Mol Genet, 18(R1):R48-59. Lewis DA, Levitt P. (2002). Schizophrenia as a disorder of neurodevelopment.
2004). Dynamics of cancer progression. Nat Rev Cancer, 4(3):197-205. Midic U, Oldfield CJ, Dunker AK, Obradovic Z, Uversky VN. (2009). Protein disorder in the human diseasome: unfoldomics of human genetic diseases. BMC Genomics, 10(Suppl 1):S12. Miller MP, Kumar S. (2001). Understanding human disease mutations through the use of interspecific genetic variation. Hum Mol Genet, 10(21):2319-28. Minshew N, McFadden K. Commentary for special issue of autism research on mouse models in ASD: a clinical perspective.
Nuclear and particle astrophysics by Hirsch J.G., Page D. (eds.)