Results 41 to 50 of about 1,522,365 (296)

Comparison of the Use of Linkage in Cluster Integration With Path Analysis Approach

open access: yesFrontiers in Applied Mathematics and Statistics, 2022
This study aims to compare integrated clusters on various linkages (Ward, Complete, and Average linkage) with path analysis to classify the behavior of subservient to pay for mortgages.
Adji Achmad Rinaldo Fernandes   +1 more
doaj   +1 more source

Contagious Anxiety: Anxious European Americans Can Transmit Their Physiological Reactivity to African Americans. [PDF]

open access: yes, 2017
During interracial encounters, well-intentioned European Americans sometimes engage in subtle displays of anxiety, which can be interpreted as signs of racial bias by African American partners.
Koslov, Katrina   +4 more
core   +2 more sources

Linking Pathology Datasets – Trials and Triumphs

open access: yesInternational Journal of Population Data Science, 2019
Background with rationale The burden of chronic kidney disease (CKD) has increased rapidly in Australia over recent years. The financial cost of treating people with end-stage kidney failure by conventional models of dialysis or transplantation ...
Brian Stokes   +3 more
doaj   +1 more source

OTU deubiquitinases reveal mechanisms of linkage specificity and enable ubiquitin chain restriction analysis [PDF]

open access: yes, 2013
Sixteen ovarian tumor (OTU) family deubiquitinases (DUBs) exist in humans, and most members regulate cell-signaling cascades. Several OTU DUBs were reported to be ubiquitin (Ub) chain linkage specific, but comprehensive analyses are missing, and the ...
Akutsu, Masato   +12 more
core  

Colorectal cancer linkage on chromosomes 4q21, 8q13, 12q24, and 15q22 [PDF]

open access: yes, 2012
A substantial proportion of familial colorectal cancer (CRC) is not a consequence of known susceptibility loci, such as mismatch repair (MMR) genes, supporting the existence of additional loci.
Allyson S Templeton   +33 more
core   +6 more sources

Sirolimus for Extracranial Arteriovenous Malformations: A Scoping Review of the Evidence in Syndromic and Non‐Syndromic Cases

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Arteriovenous malformations (AVMs) are rare, high‐flow, vascular anomalies that can occur either sporadically or as part of a genetic syndrome. AVMs can progress with serious morbidity and even mortality if left unchecked. Sirolimus is an mTOR inhibitor that is effective in low‐flow vascular malformations; however, its role in AVMs is unclear.
Will Swansson   +3 more
wiley   +1 more source

On the stator flux linkage estimation of an PMSM with extended Kalman filters [PDF]

open access: yes, 2010
The demand for drives with high quality torque control has grown tremendously in a wide variety of applications. Direct torque control (DTC) for permanent magnet synchronous motors can provide this accurate and fast torque control.
Boel, René   +2 more
core   +1 more source

Evaluating the Utility of Paired Tumor and Germline Targeted DNA Sequencing for Pediatric Oncology Patients: A Single Institution Report

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Objective To evaluate the diagnostic yield and utility of universal paired tumor–normal multigene panel sequencing in newly diagnosed pediatric solid and central nervous system (CNS) tumor patients and to compare the detection of germline pathogenic/likely pathogenic variants (PV/LPVs) against established clinical referral criteria for cancer ...
Natalie Waligorski   +9 more
wiley   +1 more source

Outcomes of Live Virus Vaccination in Patients With Vascular Anomalies Being Treated With Sirolimus

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Background Live vaccination in patients with vascular anomalies (VA) receiving sirolimus remains controversial due to immunosuppressive effects and theoretical risks. Procedure This single‐center retrospective study included patients with VA less than 4 years old at the start of sirolimus therapy who were incompletely vaccinated.
Svatava Merkle   +5 more
wiley   +1 more source

Genome-wide search for strabismus susceptibility loci. [PDF]

open access: yes, 2003
The purpose of this study was to search for chromosomal susceptibility loci for comitant strabismus. Genomic DNA was isolated from 10mL blood taken from each member of 30 nuclear families in which 2 or more siblings are affected by either esotropia or ...
Fujiwara, Hirotake   +6 more
core   +1 more source

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