Results 21 to 30 of about 1,292,475 (265)

The susceptible patient [PDF]

open access: yesNephrology Dialysis Transplantation, 1996
Acute hypotension is a common complication of haemodialysis, occurring in 20-33% of patients in different series. Although the immediate cause is increasing intravascular hypovolaemia related to the dialysis procedure, no constant relationship exists between volume status or degree of volume loss and development of hypotension, emphasizing the ...
openaire   +2 more sources

Genetic Susceptibility

open access: yesClinics in Chest Medicine, 2014
Why only 20% of smokers develop clinically relevant chronic obstructive pulmonary disease (COPD) was a puzzle for many years. Now, epidemiologic studies point clearly toward a large heritable component. The combination of genome-wide association studies and candidate gene analysis is helping to identify those genetic variants responsible for an ...
Marciniak, Stefan J, Lomas, David A
openaire   +3 more sources

Systematic Approximations to Susceptible-Infectious-Susceptible Dynamics on Networks [PDF]

open access: yesPLOS Computational Biology, 2016
Network-based infectious disease models have been highly effective in elucidating the role of contact structure in the spread of infection. As such, pair- and neighbourhood-based approximation models have played a key role in linking findings from network simulations to standard (random-mixing) results.
Matt J. Keeling   +3 more
openaire   +6 more sources

Introduction to Quantitative Susceptibility Mapping and Susceptibility Weighted Imaging [PDF]

open access: yesThe British Journal of Radiology, 2019
Quantitative Susceptibility Mapping (QSM) and Susceptibility Weighted Imaging (SWI) are MRI techniques that measure and display differences in the magnetization that is induced in tissues, i.e. their magnetic susceptibility, when placed in the strong external magnetic field of an MRI system. SWI produces images in which the contrast is heavily weighted
Pascal P. R. Ruetten   +2 more
openaire   +2 more sources

Minigene Splicing Assays Identify 12 Spliceogenic Variants of BRCA2 Exons 14 and 15

open access: yesFrontiers in Genetics, 2019
A relevant fraction of BRCA2 variants is associated with splicing alterations and with an increased risk of hereditary breast and ovarian cancer (HBOC). In this work, we have carried out a thorough study of variants from BRCA2 exons 14 and 15 reported at
Eugenia Fraile-Bethencourt   +5 more
doaj   +1 more source

A ferroptosis-targeting ceria anchored halloysite as orally drug delivery system for radiation colitis therapy

open access: yesNature Communications, 2023
Radiation colitis is the leading cause of diarrhea and hematochezia in pelvic radiotherapy patients. This work advances the pathogenesis of radiation colitis from the perspective of ferroptosis.
Yue Feng   +6 more
doaj   +1 more source

Personal susceptibility to pitch [PDF]

open access: yesOccupational and Environmental Medicine, 1970
Hodgson, G. A., and Whiteley, H. J. (1970).Brit. J. industr. Med.,27, 160-166. Personal susceptibility to pitch. During the years 1957 to 1963, 59 cases of hyperplastic squamous lesions were referred to us from a local patent fuel works where ovoids were made by fusing coal dust and pitch together by steam heat.
G A, Hodgson, H J, Whiteley
openaire   +2 more sources

Identification of Eight Spliceogenic Variants in BRCA2 Exon 16 by Minigene Assays

open access: yesFrontiers in Genetics, 2018
Genetic testing of BRCA1 and BRCA2 identifies a large number of variants of uncertain clinical significance whose functional and clinical interpretations pose a challenge for genetic counseling.
Eugenia Fraile-Bethencourt   +5 more
doaj   +1 more source

UGT1A1 Variants c.864+5G>T and c.996+2_996+5del of a Crigler-Najjar Patient Induce Aberrant Splicing in Minigene Assays

open access: yesFrontiers in Genetics, 2020
A large fraction of DNA variants impairs pre-mRNA splicing in human hereditary disorders. Crigler-Najjar syndrome (CNS) is characterized by a severe unconjugated hyperbilirubinemia caused by variants in the UGT1A1 gene.
Linda Gailite   +5 more
doaj   +1 more source

Home - About - Disclaimer - Privacy