Results 111 to 120 of about 224,855 (298)

The representation of female characters in Butler’s translation of the “Odyssey”: a corpus-based approach

open access: yesAOQU
In The Authoress of the Odyssey (1897), Samuel Butler developed a notably controversial intuition about the poem’s author. In his analyses, he concluded that the same person could not have created the Iliad and the Odyssey: whilst the former was ...
Daniel Russo
doaj   +1 more source

Synaptic Odyssey [PDF]

open access: yesThe Journal of Neuroscience, 2020
openaire   +2 more sources

Homomorphic Encryption for Speaker Recognition: Protection of Biometric Templates and Vendor Model Parameters

open access: yes, 2018
Data privacy is crucial when dealing with biometric data. Accounting for the latest European data privacy regulation and payment service directive, biometric template protection is essential for any commercial application.
Busch, Christoph   +4 more
core   +1 more source

Atypical Clinical Course of Griscelli Syndrome Type 2 With Primarily Neurologic Presentation and Adult‐Onset in a 46‐Year‐Old Male

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Griscelli Syndrome Type 2 (GS2) is a rare autosomal recessive disorder caused by pathogenic mutations in the RAB27A gene. Typically, it is characterized by cutaneous hypopigmentation, immunodeficiency, with or without neurological abnormalities secondary to hemophagocytic lymphohistiocytosis (HLH). Without treatment, GS2 often results in fatal
Dzhoy Papingi   +6 more
wiley   +1 more source

High energy emission of GRB 130821A: constraining the density profile of the circum-burst medium as well as the initial Lorentz factor of the outflow

open access: yes, 2013
GRB 130821A was detected by Fermi-GBM/LAT, Konus-Wind, SPI-ACS/INTEGRAL, RHESSI and Mars Odyssey-HEND. Although the data of GRB 130821A are very limited, we show in this work that the high energy gamma-ray emission (i.e., above 100 MeV) alone imposes ...
Fan, Yi-Zhong   +5 more
core   +1 more source

The Diagnosis That Arrived Decades Late: Living Without and Then With Myhre Syndrome

open access: yesAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome (MIM #139210) is a rare multisystem disorder first described in 1981, characterized by short stature, neurodevelopmental delay, joint contractures, and cardiopulmonary complications. Its molecular basis, recurrent pathogenic variants in SMAD4, was not discovered until 2011. This narrative is based on a review of medical records,
Abdallah F. Elias
wiley   +1 more source

Superbubble Origin of Cosmic Rays

open access: yes, 2012
After a hundred years of searching for the origin of cosmic rays, where and how they are made has finally become clear. Here we briefly trace that odyssey through both astronomical observations and cosmic ray measurements.Comment: 5 pages, 3 figures ...
Lingenfelter, Richard E.
core   +1 more source

Denial of Inpatient Genetic Testing: A Study on Outpatient Yield and Outcomes

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Genetic conditions suspected in children often require genetic testing for accurate diagnoses, but testing remains costly. Case management teams review genetic test requests to improve access for patients while reducing the financial burden for medical institutions.
Cindy Y. Canales   +6 more
wiley   +1 more source

The present status of the Homeric question [PDF]

open access: yes, 1923
Thesis (M.A.)--Boston ...
Given, Frances Winifred
core   +1 more source

Prenatal Evaluation of RNU4‐2 Variants in Fetuses With Central Nervous System Anomalies

open access: yesAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Fetal central nervous system (CNS) anomalies are among the most common congenital malformations, yet the overall prenatal diagnostic yield of current genetic testing remains below 40%. Variants in RNU4‐2, a non‐coding gene encoding the U4 small nuclear RNA (snRNA), have recently been linked to a novel highly recurrent dominant ...
Yiyao Chen   +13 more
wiley   +1 more source

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