Results 51 to 60 of about 2,137 (173)

Adult Otogenic Meningitis in the Pneumococcal Conjugated Vaccines Era

open access: yesInternational Archives of Otorhinolaryngology, 2020
Introduction Streptococcus pneumoniae is a major pathogen of otogenic meningitis (OgM), the most commonly reported intra-cranial complication of otitis media (OM).
Tal Marom   +4 more
doaj   +1 more source

Optical genome mapping to decipher the chromosomal aberrations in families seeking for preconception genetic counseling

open access: yesScientific Reports
Optical genome mapping (OGM) offers high consistency in simultaneously detecting structural and copy number variants. This study aimed to retrospectively evaluate the efficacy and potential applications of OGM in preconception genetic counseling. Herein,
Kaili Yin   +10 more
doaj   +1 more source

GENETIC PERFORMANCE OF SOME VEGETABLE SOYBEAN GENOTYPES UNDER EGYPTION CONDITIONS. [PDF]

open access: yesJournal of Plant Production, 2010
Edamame are large-seeded soybean (Glycine max (L.) Merr) harvested as green pods at the R6 stage when the seed are approximately 80 % matured. The demand for Edamame as fresh or frozen vegetable is increasing world wide.
M. Shokr, H. Ghobary
doaj   +1 more source

Geriatric Medicine Competencies in Postgraduate Training Programs Across Specialties

open access: yesJournal of the American Geriatrics Society, EarlyView.
ABSTRACT Background Aging populations require physicians skilled in competencies essential for the care of older adults. The extent to which such geriatric competencies are included in non‐geriatric postgraduate medical training programs is not known.
Janani Thillainadesan   +5 more
wiley   +1 more source

Follow Me Into Math: Near‐Peer Influencers Take the Stage

open access: yesSchool Science and Mathematics, EarlyView.
ABSTRACT Young people like to be entertained, and to entertain others. What if students were to invest enough of their time and effort into learning topics from our mathematics courses to become experts in the eyes of their peers? In this study we positioned college students and high school students as mathematical performers on the stage in front of ...
Aaron T. Wilson   +3 more
wiley   +1 more source

Cas9-directed long-read sequencing to resolve optical genome mapping findings in leukemia diagnostics

open access: yesScientific Reports
Leukemias are genetically heterogeneous and diagnostics therefore includes various standard-of-care (SOC) techniques, including karyotyping, SNP-array and FISH.
Eddy N. de Boer   +10 more
doaj   +1 more source

Performance différenciée du coton Bt en début de diffusion : cas du Burkina Faso

open access: yesCahiers Agricultures, 2019
L’avantage économique des cultures transgéniques pour les producteurs des pays en développement reste un sujet de préoccupation et de controverse.
Vognan Gaspard, Fok Michel
doaj   +1 more source

Optical Genome Mapping Reveals Frequent Cryptic Structural Aberrations in Normal Karyotype Acute Myeloid Leukemia

open access: yesInternational Journal of Cancer, Volume 159, Issue 5, Page 1218-1227, 1 September 2026.
Acute myeloid leukemia adult cases often appear cytogenetically normal when analyzed with conventional karyotyping. However, acquired structural variants may escape routine detection. Here, optical genome mapping detected diverse genomic alterations in nearly half of the analyzed cytogenetically normal cases.
Tuuni Turtinen   +7 more
wiley   +1 more source

La implantación neoliberal de la sojización transgénica en Argentina. Paquete tecnológico, patentes y consecuencias indeseables previsibles

open access: yesGrafía, 2015
We will journey along some aspects of the implantation of transgenic soy in Argentina and the foreseeable undesirable consequences that were brought about by having approved the use of the technological package without first having carried out ...
Javier Flax
doaj   +1 more source

Optical mapping reveals a higher level of large‐scale structural variants in a family with paternally transmitted myotonic dystrophy and independent Parkinson's disease

open access: yesThe Journal of Pathology, Volume 270, Issue 1, Page 83-97, September 2026.
Abstract Myotonic dystrophy type 1 (DM1) is a clinically challenging multisystem neuromuscular hereditary disorder, with generational increase in severity and earlier age at onset. It is caused by an unstable cytosine‐thymine‐guanine repeat expansion at the DMPK locus, accompanied by associated genetic and epigenetic modifications.
Md Mehedi Hasan   +9 more
wiley   +1 more source

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