Mr. G. E. Collins
نویسندگان
چکیده
منابع مشابه
Collins Effect in SIDIS and in e+e− Annihilation
We review the present understanding of the nucleon transversity distribution and Collins fragmentation function, based on Ref.[1], and discuss how Drell-Yan experiments will improve it. 1. Introduction. The chirally odd transversity distribution function h a 1 (x) cannot be extracted from data on semi-inclusive deep inelastic scattering (SIDIS) alone. It enters the expression for the Collins si...
متن کاملMr. R. G. Paul
was a graduate of Edinburgh University in 1927. He became a Fellow of the Royal College of Surgeons in Edinburgh, and was very proud when he was elected Fellow of the Royal College of Surgeons of England (ad eundem) in 1959. In addition, Mr. Paul became a Fellow of the Association of Surgeons of Great Britain, and a member of the council. He was a member and past president of the Moynihan Chiru...
متن کاملCollins asymmetries in inclusive charged KK and Kπ pairs produced in e + e − annihilation
J. P. Lees, V. Poireau, V. Tisserand, E. Grauges, A. Palano, G. Eigen, B. Stugu, D. N. Brown, L. T. Kerth, Yu. G. Kolomensky, M. J. Lee, G. Lynch, H. Koch, T. Schroeder, C. Hearty, T. S. Mattison, J. A. McKenna, R. Y. So, A. Khan, V. E. Blinov, A. R. Buzykaev, V. P. Druzhinin, V. B. Golubev, E. A. Kravchenko, A. P. Onuchin, S. I. Serednyakov, Yu. I. Skovpen, E. P. Solodov, K. Yu. Todyshev, A. J...
متن کاملCatherine Collins
An integrative review of 121 recent studies on collecting and utilising local ecological knowledge (LEK) for fisheries science and management suggests that insufficient attention is given either to conceptualising LEK or to the critical issue of how LEK is defined. Elements from knowledge management guided the analysis. Résumé : Une revue intégrant 121 études récentes traitant de la collecte et...
متن کاملTreacher Collins Syndrome
Treacher Collins syndrome (TCS) is a genetic disease that alters the development of bones and other tissues in the face, and presents variable expressivity. At least three genes TCOF1, POLR1D, and POLR1C were recognized to be at the origin of this syndrome which may be inherited through either an autosomal dominant or autosomal recessive pattern. TCS changes can be divided into otological, opht...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Nature
سال: 1935
ISSN: 0028-0836,1476-4687
DOI: 10.1038/136250a0