Existential Communication and Leadership

The aim of this article is to introduce and explain a number of important existentialist philosophers and concepts that we believe can contribute to a critical approach to leadership theory. Emphasis is placed on understanding the nature of communication from an existentialist perspective and so Jaspers' conceptualization of existential communication is introduced along with important related concepts that may be regarded as important facets of leader communication including Being-in-the-world, the Other, intersubjectivity, dialogue and indirect communication. Particular attention is paid to Buber's ideas on communication as relationship and dialogue. Throughout, reference is made to contemporary, and what is often regarded as orthodox, thinking regarding the centrality of communication to leadership practice as a means by which to highlight the salience of an existentialist analysis

Spatial processing of visual information in the movement-detecting pathway of the fly

1. Spatial processing of visual signals in the fly's movement-detecting pathway was studied by recording the responses of directionally-selective movement-detecting (DSMD) neurons in the lobula plate. The summarized results pertain to a type of neuron which preferentially responds to horizontal movement directed toward the animal's midline. Three kinds of visual stimuli were used: moving gratings, reversing-contrast gratings and reversing-contrast bars.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/47087/1/359_2004_Article_BF00613743.pd

Whole-exome sequencing study identifies four novel gene loci associated with diabetic kidney disease

Diabetic kidney disease (DKD) is recognized as an important public health challenge. However, its genomic mechanisms are poorly understood. To identify rare variants for DKD, we conducted a whole-exome sequencing (WES) study leveraging large cohorts well-phenotyped for chronic kidney disease and diabetes. Our two-stage WES study included 4372 European and African ancestry participants from the Chronic Renal Insufficiency Cohort and Atherosclerosis Risk in Communities studies (stage 1) and 11 487 multi-ancestry Trans-Omics for Precision Medicine participants (stage 2). Generalized linear mixed models, which accounted for genetic relatedness and adjusted for age, sex and ancestry, were used to test associations between single variants and DKD. Gene-based aggregate rare variant analyses were conducted using an optimized sequence kernel association test implemented within our mixed model framework. We identified four novel exome-wide significant DKD-related loci through initiating diabetes. In single-variant analyses, participants carrying a rare, in-frame insertion in the DIS3L2 gene (rs141560952) exhibited a 193-fold increased odds [95% confidence interval (CI): 33.6, 1105] of DKD compared with noncarriers (P = 3.59 × 10-9). Likewise, each copy of a low-frequency KRT6B splice-site variant (rs425827) conferred a 5.31-fold higher odds (95% CI: 3.06, 9.21) of DKD (P = 2.72 × 10-9). Aggregate gene-based analyses further identified ERAP2 (P = 4.03 × 10-8) and NPEPPS (P = 1.51 × 10-7), which are both expressed in the kidney and implicated in renin-angiotensin-aldosterone system modulated immune response. In the largest WES study of DKD, we identified novel rare variant loci attaining exome-wide significance. These findings provide new insights into the molecular mechanisms underlying DKD

Rare genetic variants explain missing heritability in smoking

Common genetic variants explain less variation in complex phenotypes than inferred from family-based studies, and there is a debate on the source of this ‘missing heritability’. We investigated the contribution of rare genetic variants to tobacco use with whole-genome sequences from up to 26,257 unrelated individuals of European ancestries and 11,743 individuals of African ancestries. Across four smoking traits, single-nucleotide-polymorphism-based heritability (hSNP2) was estimated from 0.13 to 0.28 (s.e., 0.10–0.13) in European ancestries, with 35–74% of it attributable to rare variants with minor allele frequencies between 0.01% and 1%. These heritability estimates are 1.5–4 times higher than past estimates based on common variants alone and accounted for 60% to 100% of our pedigree-based estimates of narrow-sense heritability (hped2, 0.18–0.34). In the African ancestry samples, hSNP2 was estimated from 0.03 to 0.33 (s.e., 0.09–0.14) across the four smoking traits. These results suggest that rare variants are important contributors to the heritability of smoking

Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential

Human genetic studies support an inverse causal relationship between leukocyte telomere length (LTL) and coronary artery disease (CAD), but directionally mixed effects for LTL and diverse malignancies. Clonal hematopoiesis of indeterminate potential (CHIP), characterized by expansion of hematopoietic cells bearing leukemogenic mutations, predisposes both hematologic malignancy and CAD. TERT (which encodes telomerase reverse transcriptase) is the most significantly associated germline locus for CHIP in genome-wide association studies. Here, we investigated the relationship between CHIP, LTL, and CAD in the Trans-Omics for Precision Medicine (TOPMed) program (n = 63,302) and UK Biobank (n = 47,080). Bidirectional Mendelian randomization studies were consistent with longer genetically imputed LTL increasing propensity to develop CHIP, but CHIP then, in turn, hastens to shorten measured LTL (mLTL). We also demonstrated evidence of modest mediation between CHIP and CAD by mLTL. Our data promote an understanding of potential causal relationships across CHIP and LTL toward prevention of CAD

Hydrogeologic impact analysis of new water uses in Section 7, T. 10 N. , R. 28 EWM. , of the Hanford Reservation

An evaluation was made of the hydrologic impact upon the Hanford ground water regime of removing 1.7 million gallons per day, MGD (6.4 million liters per day, MLD) from the unconfined aquifer in the north half of Section 7, T. 10 N., R. 28 EWM., and recharging to the aquifer within the same area 1.0 MGD (3.8 MLD). The hydrogeology of the specific area was characterized by examining data obtained from nearby wells. A preliminary well yield analysis was performed which verified that one well could supply 6.4 MLD at the study site. Several reasonable, simplifying assumptions were made which permitted the determination by means of an analytical equation of the water table changes resulting from projected water uses. The results of the analysis show minimal impact upon the water table as a result of either the withdrawal or recharge of water. The estimated size of a pond for recharging the used water would be about three to six acres. If the proposed groundwater use activity is implemented, one step-drawdown and one pump test are recommended to verify the withdrawal well water yield

A molecular probe of dark energy

Many theoretical models of dark energy invoke rolling scaler fields which in turn predict time varying values of the fundamental constants. Establishing the value of the fundamental constants at various times in the universe can probe and test the various dark energy theories. One of the constants that is predicted to vary is the ratio of the electron to proton mass μ. It was established early on that molecular spectra are sensitive to the value of μ and can be used as probes of that value. This article describes the use of the spectrum of molecular hydrogen in high redshift Damped Lyman Alpha systems (DLAs) as a sensitive probe of the time evolution of μ