Chemical and forensic analysis of JFK assassination bullet lots: Is a second shooter possible?

The assassination of President John Fitzgerald Kennedy (JFK) traumatized the nation. In this paper we show that evidence used to rule out a second assassin is fundamentally flawed. This paper discusses new compositional analyses of bullets reportedly to have been derived from the same batch as those used in the assassination. The new analyses show that the bullet fragments involved in the assassination are not nearly as rare as previously reported. In particular, the new test results are compared to key bullet composition testimony presented before the House Select Committee on Assassinations (HSCA). Matches of bullets within the same box of bullets are shown to be much more likely than indicated in the House Select Committee on Assassinations' testimony. Additionally, we show that one of the ten test bullets is considered a match to one or more assassination fragments. This finding means that the bullet fragments from the assassination that match could have come from three or more separate bullets. Finally, this paper presents a case for reanalyzing the assassination bullet fragments and conducting the necessary supporting scientific studies. These analyses will shed light on whether the five bullet fragments constitute three or more separate bullets. If the assassination fragments are derived from three or more separate bullets, then a second assassin is likely, as the additional bullet would not easily be attributable to the main suspect, Mr. Oswald, under widely accepted shooting scenarios [see Posner (1993), Case Closed, Bantam, New York].Comment: Published in at http://dx.doi.org/10.1214/07-AOAS119 the Annals of Applied Statistics (http://www.imstat.org/aoas/) by the Institute of Mathematical Statistics (http://www.imstat.org

Response to the Letter to the Editor

This paper has attracted interest around the world from the media (both TV and newspapers). In addition, we have received letters, emails and telephone calls. One of our favorites was a voicemail message asking us to return a call to Australia at which point we would learn who really killed JFK. We welcome the opportunity to respond to the letter to the editor from Mr. Fiorentino. Mr. Fiorentino claims that our ``statement relating to the likelihood of a second assassin based on the premise of three or more separate bullets is demonstrably false.'' In response we would like to simply quote from page 327 of Gerald Posner's book Case Closed, one of the most well known works supporting the single assassin theory: ``If Connally was hit by another bullet, it had to be fired from a second shooter, since the Warren Commission's own reconstructions showed that Oswald could not have operated the bolt and refired in 1.4 seconds.'' Mr. Fiorentino also claims that the ``second fatal flaw is the use of a rather uncomplicated formula based on Bayes Theorem.'' Let $E$ denote the evidence and $T$ denote the theory that there were just two bullets (and hence a single shooter). We used Bayes Theorem to hypothetically calculate $P(T|E)$ from $P(E|T)$ and the prior probability $P(T)$. In order to make $P(T|E)$ ten times more likely than $P(\bar{T}|E)$, the ratio of the prior probabilities [i.e., $P(T) / P(\bar{T})$] would have to be greater than 15. Thus, we again conclude that this casts serious doubt on Dr. Guinn's conclusion that the evidence supported just two bullets. Sadly, this is far from the first time that probability has been misunderstood and/or misapplied in a case of public interest. A notable British example is the Clark case. See Nobles and Schiff (2005) for details. Finally, we welcome and, in fact, encourage members of the scientific community to provide alternative analyses of the data.Comment: Published in at http://dx.doi.org/10.1214/07-AOAS154 the Annals of Applied Statistics (http://www.imstat.org/aoas/) by the Institute of Mathematical Statistics (http://www.imstat.org

The Liquid-Liquid Extraction of Toxic Metals (Cd, Hg and Pb) by Calixarenes

Toxic metals (Cd, Hg and Pb) are mostly present in the environment due to natural phenomenon and human activities as well. Exposure of these non-essential elements in the environment causes severe effects. They are known to cause problems in humans as well as in aquatic life. In this work, we demonstrate various studies regarding liquid-liquid extraction of selected ions with different functionalized calixarenes. This review article briefly discusses several molecular designs of calixarenes for divalent ion (Cd2+, Hg2+ and Pb2+) recognition; as well as the relationship between structure and selectivity of the macrocycles is elaborated. The article does not, however, attempt to cover all of the different approaches to these toxic metal ions extraction

Synthesis, structural studies and photochemistry of cobalt(III) complexes of anthracenylcyclam macrocycles

This work reports the syntheses, structures and some photochemistry in DMF of the cobalt complexes trans-[CoIII( 2)Cl2]Cl·0.5CH3OH and trans-[CoIII( 3)Cl2]Cl·4H2O, where 2 is 6-(anthracen-9-ylmethyl)-1,4,8,11-tetraazacyclotetradecane-5,7-dione and 3 is 6-(anthracen-9-ylmethyl)-1,4,8,11-tetraazacyclotetradecane. In the preparation of the macrocyclic ligand, 3, the formation of a polycyclic bis(aminal) intermediate and its subsequent acid hydrolysis to 3 is a cleaner route than the traditional procedure in which the analogous dioxocyclam 2 is reduced with borane reagents. The crystal structure of trans-[CoIII( 3)Cl2]Cl·4H2O shows that the macrocycle adopts the trans-III conformation, in which the anthracene moiety is extended away from the cobalt ion and the anthracene to Co separation is 7.22 . For the related complex trans-[CoIII( 2)Cl2]Cl·0.5CH3OH, however, the anthracene is bent over the highly conjugated tetracycle and significant interactions between the anthracene and the complex occur. A novel new complex, trans-[Co( 12)Cl2](where 12 is 5,7-hydroxy-6-oxo-1,4,8,11-tetraazacyclotetradecane-4,7-diene) which is a degradation product of the complex trans-[CoIII( 2)Cl2]Cl is also reported

Detection and characterisation of multi-drug resistance protein 1 (MRP-1) in human mitochondria

BACKGROUND: Overexpression of plasma membrane multi-drug resistance protein 1 (MRP-1) can lead to multidrug resistance. In this study, we describe for the first time the expression of mitochondrial MRP-1 in untreated human normal and cancer cells and tissues. METHODS: MRP-1 expression and subcellular localisation in normal and cancer cells and tissues was examined by differential centrifugation and western blotting, and immunofluorescence microscopy. Viable mitochondria were isolated and MRP-1 efflux activity measured using the calcein-AM functional assay. MRP-1 expression was increased using retroviral infection and specific overexpression confirmed by RNA array. Cell viability was determined by trypan blue exclusion and annexin V-propidium iodide labelling of cells. RESULTS: MRP-1 was detected in the mitochondria of cancer and normal cells and tissues. The efflux activity of mitochondrial MRP-1 was more efficient (55-64%) than that of plasma membrane MRP-1 (11-22%; P<0.001). Induced MRP-1 expression resulted in a preferential increase in mitochondrial MRP-1, suggesting selective targeting to this organelle. Treatment with a non-lethal concentration of doxorubicin (0.85 nM, 8 h) increased mitochondrial and plasma membrane MRP-1, increasing resistance to MRP-1 substrates. For the first time, we have identified MRP-1 with efflux activity in human mitochondria. CONCLUSION: Mitochondrial MRP-1 may be an exciting new therapeutic target where historically MRP-1 inhibitor strategies have limited clinical success

Au I Cl-bound N-heterocyclic carbene ligands form MII4(LAuCl) 6 integrally gilded cages

The incorporation of an N-heterocyclic carbene (NHC) moiety into a self-assembled MII4L6 cage framework required the NHC first to be metallated with gold(I). Bimetallic cages could then be constructed using zinc(II) and cadmium(II) templates, showing weak luminescence. The cages were destroyed by the addition of further gold(I) in the form of AuI(2,4,6-trimethoxybenzonitrile)2SbF6, which caused the reversibly-formed cages to disassemble and controllably release the AuI-NHC subcomponent into solution. This release in turn induced the growth of gold nanoparticles. The rate of dianiline release could be tuned by capsule design or through the addition of chemical stimuli, with different release profiles giving rise to different nanoparticle morphologies

Chemotherapy induces Notch1-dependent MRP1 up-regulation, inhibition of which sensitizes breast cancer cells to chemotherapy

Background Multi-drug Resistance associated Protein-1 (MRP1) can export chemotherapeutics from cancer cells and is implicated in chemoresistance, particularly as is it known to be up-regulated by chemotherapeutics. Our aims in this study were to determine whether activation of Notch signalling is responsible for chemotherapy-induced MRP1 expression Notch in breast cancers, and whether this pathway can be manipulated with an inhibitor of Notch activity. Methods MRP1 and Notch1 were investigated in 29 patients treated with neoadjuvant chemotherapy (NAC) for breast cancer, using immunohistochemistry on matched biopsy (pre-NAC) and surgical samples (post-NAC). Breast epithelial cell cultures (T47D, HB2) were treated with doxorubicin in the presence and absence of functional Notch1, and qPCR, siRNA, Western blots, ELISAs and flow-cytometry were used to establish interactions. Results In clinical samples, Notch1 was activated by neoadjuvant chemotherapy (Wilcoxon signed-rank p < 0.0001) and this correlated with induction of MRP1 expression (rho = 0.6 p = 0.0008). In breast cell lines, doxorubicin induced MRP1 expression and function (non-linear regression p < 0.004). In the breast cancer line T47D, doxorubicin activated Notch1 and, critically, inhibition of Notch1 activation with the γ-secretase inhibitor DAPT abolished the doxorubicin-induced increase in MRP1 expression and function (t-test p < 0.05), resulting in enhanced cellular retention of doxorubicin and increased doxorubicin-induced apoptosis (t-test p = 0.0002). In HB2 cells, an immortal but non-cancer derived breast cell line, Notch1-independent MRP1 induction was noted and DAPT did not enhance doxorubicin-induced apoptosis. Conclusions Notch inhibitors may have potential in sensitizing breast cancer cells to chemotherapeutics and therefore in tackling chemoresistance

REDUCING CHILD POVERTY AMONGST CHILDREN 0 TO 5 YEARS OF AGE THROUGH ECONOMIC AND NUTRITIONAL STABILITY IN CLEVELAND COUNTY, NORTH CAROLINA

Economic stability, as a social determinant of health, creates hardships for many low-income families and can contribute to people living in poverty. Children growing up in low socioeconomic settings fall behind early on, with gaps evident as early as infancy. Children between the ages of 0 and 5 in Cleveland County, North Carolina, have a higher prevalence of experiencing poverty compared to the state and United States. To reduce child poverty in ages 0 to 5, implementing an evidence-based program and policy is necessary. “Ways to WIC” leverages existing resources, the West End REACH Transit, Special Supplemental Nutrition Program for Women, Infants, and Children (WIC), and Walmart to increase access to nutritious foods, decrease transportation barriers, and maximize WIC benefit usage through online ordering platforms and curbside pick-up. Doing so, will act as a buffer against the impacts of economic hardship and lift these children above the federal poverty line.Master of Public Healt

REDUCING CHILD POVERTY AMONGST CHILDREN 0 TO 5 YEARS OF AGE THROUGH ECONOMIC AND NUTRITIONAL STABILITY IN CLEVELAND COUNTY, NORTH CAROLINA

Economic stability, as a social determinant of health, creates hardships for many low-income families and can contribute to people living in poverty. Children growing up in low socioeconomic settings fall behind early on, with gaps evident as early as infancy. Children between the ages of 0 and 5 in Cleveland County, North Carolina, have a higher prevalence of experiencing poverty compared to the state and United States. To reduce child poverty in ages 0 to 5, implementing an evidence-based program and policy is necessary. “Ways to WIC” leverages existing resources, the West End REACH Transit, Special Supplemental Nutrition Program for Women, Infants, and Children (WIC), and Walmart to increase access to nutritious foods, decrease transportation barriers, and maximize WIC benefit usage through online ordering platforms and curbside pick-up. Doing so, will act as a buffer against the impacts of economic hardship and lifts these children above the federal poverty line. Keywords: social determinants of health, economic stability, food insecurity, public transportation, WIC, children, child povertyMaster of Public Healt

Reducing Child Poverty Amongst Children 0 to 5 Years of Age Through Economic and Nutritional Stability in Cleveland County, North Carolina

Economic stability, as a social determinant of health, creates hardships for many low-income families and can contribute to people living in poverty. Children growing up in low socioeconomic settings fall behind early on, with gaps evident as early as infancy. Children between the ages of 0 and 5 in Cleveland County, North Carolina, have a higher prevalence of experiencing poverty compared to the state and United States. To reduce child poverty in ages 0 to 5, implementing an evidence-based program and policy is necessary. “Ways to WIC” leverages existing resources, the West End REACH Transit, Special Supplemental Nutrition Program for Women, Infants, and Children (WIC), and Walmart to increase access to nutritious foods, decrease transportation barriers, and maximize WIC benefit usage through online ordering platforms and curbside pick-up. Doing so, will act as a buffer against the impacts of economic hardship and lifts these children above the federal poverty line.Master of Public Healt