18 research outputs found
Lepton mixing angle with a horizontal symmetry
We discuss a model for the lepton sector based on the seesaw mechanism and on
a family symmetry. The model predicts the mixing angle to
vanish. The solar mixing angle is free--it will in general be
large if one does not invoke finetuning. The model has an enlarged scalar
sector with three Higgs doublets, together with two real scalar gauge singlets
() which have vacuum expectation values _0\theta_{23}\tan
\theta_{23} = _0, and it is maximal if the Lagrangian is
-invariant; but may be broken softly, by a term of dimension two in
the scalar potential, and then < \chi_2_0 becomes different from < \chi_1_0.
Thus, the strength of the soft breaking controls the deviation of
from . The model predicts a normal neutrino mass
spectrum () and allows successful leptogenesis if ; these properties of the model are independent of
the presence and strength of the soft breaking.Comment: 13 pages, one figur
A_4 Symmetry and Lepton Masses and Mixing
Stimulated by Ma's idea which explains the tribimaximal neutrino mixing by
assuming an A_4 flavor symmetry, a lepton mass matrix model is investigated. A
Frogatt-Nielsen type model is assumed, and the flavor structures of the masses
and mixing are caused by the VEVs of SU(2)_L-singlet scalars \phi_i^u and
\phi_i^d (i=1,2,3), which are assigned to {\bf 3} and ({\bf 1}, {\bf 1}',{\bf
1}'') of A_4, respectively.Comment: 13 pages including 1 table, errors in Sec.7 correcte
S_3 Symmetry and Neutrino Masses and Mixings
Based on a universal seesaw mass matrix model with three scalars \phi_i, and
by assuming an S_3 flavor symmetry for the Yukawa interactions, the lepton
masses and mixings are investigated systematically. In order to understand the
observed neutrino mixing, the charged leptons (e, \mu, \tau) are regarded as
the 3 elements (e_1, e_2, e_3) of S_3, while the neutrino mass-eigenstates are
regarded as the irreducible representation (\nu_\eta, \nu_\sigma, \nu_\pi) of
S_3, where (\nu_\pi, \nu_\eta) and \nu_\sigma are a doublet and a singlet,
respectively, which are composed of the 3 elements (\nu_1, \nu_2, \nu_3) of
S_3.Comment: 16 pages, no figure, version to appear in EPJ-
Nematode control failure due to anthelmintic resistance in a sheep farm in Malaysia: First identification of the f200y mutation in the isotype 1 β-tubulin gene
This paper reports total nematode anthelmintic resistance towards albendazole, fenbendazole, levamisole and ivermectin in a commercial sheep farm located in Terengganu, Malaysia. Faecal Egg Count Reduction Test (FECRT) was conducted on 25 sheep, where five sheep in each group were treated with the respective four anthelmintics based on live bodyweight. The balance of five sheep placed in the control group were not treated with any anthelmintics. At day 13 post-treatment, faecal egg count was conducted and nematode worm egg count reduction percentage was calculated to determine the resistance status towards the respective anthelmintics tested. Results showed that nematodes were resistant to all the anthelmintics tested, namely albendazole, fenbendazole, levamisole and ivermectin with reduction percentage of 87%, 46%, 94% and 68%, respectively. Subsequently, the third stage larvae of Haemonchus contortus and Trichostrongylus colubriformis recovered from post-treatment faecal cultures were subjected to allele-specific polymerase chain reaction (AS-PCR) assay to determine the presence of the benzimidazole resistance gene. This study reports the occurrence of the classical F200Y mutation in the isotype 1 β-tubulin gene, for the first time in Malaysia
Prenatal maternal physical activity and stem cells in umbilical cord blood
Purpose: Early life processes, through influence on fetal stem cells, affect postnatal and adult health outcomes. This study examines the effects of physical activity before and during pregnancy on stem cell counts in umbilical cord blood. Methods: We isolated mononuclear cells from umbilical cord blood samples from 373 singleton full-term pregnancies and quantified hematopoietic (CD34+, CD34+ CD38j, and CD34+ c-kit+), endothelial (CD34+CD133+, CD34+CD133+VEGFR2+, CD34+VEGFR2+, and CD133+VEGFR2+), and putative breast (EpCAM+, EpCAM+CD49f +, EpCAM+CD49f +CD117+, CD49f +CD24+, CD24+CD29+, and CD24+CD29+CD49f +) stem/progenitor cell subpopulations by flow cytometry. Information on physical activities before and during pregnancy was obtained from questionnaires. Weekly energy expenditure was estimated based on metabolic equivalent task values. Results: Prepregnancy vigorous exercise was associated positively with levels of endothelial CD34+CD133+, CD34+CD133+VEGFR2+, CD34+VEGFR2+, and CD133+VEGFR2+ progenitor cell populations (P = 0.02, P = 0.01, P = 0.001, and P = 0.003, respectively); positive associations were observed in samples from the first births and those from the second or later births. Prepregnancy moderate and light exercises and light exercise during the first trimester were not significantly associated with any stem/ progenitor cell population. Light exercise during the second trimester was positively associated with CD34+VEGFR2+ endothelial progenitor cells (P = 0.03). In addition, levels of EpCAM+CD49f + and CD49f +CD24+ breast stem cells were significantly lower among pregnant women who engaged in vigorous/moderate exercise during pregnancy (P = 0.05 and P = 0.02, respectively). Conclusions: Vigorous exercise before pregnancy increases the number of endothelial progenitor cells in umbilical cord blood and thus could potentially enhance endothelial function and improve cardiovascular fitness in the offspring. Findings of lower levels of putative breast stem cell subpopulations could have implications on exercise and breast cancer prevention. Prenatal effects of exercise on fetal stem cells warrant further studies. © Copyright 2015 by the American College of Sports Medicine. Unauthorized reproduction of this article is prohibited
A cultural adaptation and validation study of a self-report measure of the extent of and reasons for medication nonadherence among patients with diabetes in Singapore
10.2147/PPA.S208736Patient Preference and Adherence131241-125