Results 31 to 40 of about 106,708 (270)

Intravitreal GD2‐Specific Chimeric Antigen Receptor T‐Cell Therapy for Refractory Retinoblastoma

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Effective treatments for advanced, treatment‐resistant retinoblastoma (RB) remain limited. GD2‐specific chimeric antigen receptor (CAR) T cells show potent antitumor activity with minimal toxicity but have not previously been evaluated in RB.
Subongkoch Subhadhirasakul   +13 more
wiley   +1 more source

[Review of] Jim Zwick. Inuit Entertainers in the United States [PDF]

open access: yes, 2008
The stories documented in this book about Inuit entertainers in the United States reveals important events and circumstances pertaining to the lived experiences of Esther Eneutseak and her daughter Columbia, the only Eskimo born in the United States ...
Baker, Brian
core   +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

Regional features of building museum exhibits on history of the modern Russo-Ukrainian War

open access: yesCхід, 2023
Various aspects of constructing stationary and mobile museum expositions of Ukraine in different regions of the country are analyzed, with the purpose of creating permanent exhibitions on the history of the modern Russo-Ukrainian War.
Юрій Бураков   +1 more
doaj   +1 more source

NRASQ61R Expression in Lymphatic Endothelial Cells Causes Enlarged Vessels, Hemorrhagic Chylous Effusions, and High Mortality in a Mouse Model of Kaposiform Lymphangiomatosis

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Background Kaposiform lymphangiomatosis (KLA) is an aggressive complex lymphatic anomaly. Patients exhibit malformed lymphatic vessels and often develop hemorrhagic effusions and elevated angiopoietin‐2 (Ang‐2) levels. A somatic NRAS p.Q61R (NRASQ61R) mutation has been associated with KLA.
C. Griffin McDaniel   +3 more
wiley   +1 more source

Albert Einstein's 1916 Review Article on General Relativity [PDF]

open access: yes, 2004
The first comprehensive overview of the final version of the general theory of relativity was published by Einstein in 1916 after several expositions of preliminary versions and latest revisions of the theory in November 1915.
Sauer, Tilman
core   +2 more sources

Pulmonary Dysfunction Is Associated With Sleep Study Abnormalities in Children With Sickle Cell Disease: A Multicenter Study

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Introduction Pulmonary dysfunction and sleep abnormalities are common in children with sickle cell disease (SCD) and are associated with worse clinical outcomes. Whether spirometry abnormalities are associated with polysomnography (PSG) findings remains unclear.
Ammar Saadoon Alishlash   +4 more
wiley   +1 more source

Fillers, Mime and Self-Repetitions as Most Frequently Used Communication Strategies in Oral Expositions

open access: yesJPAIR, 2014
Achieving competence in an oral communication situation has always been the ultimate goal of both teacher and students in an ESL classroom. Long years of schooling and prolonged exposure to speech communication had empowered students’ speaking ability ...
Rommel Tabula   +2 more
doaj   +1 more source

Institutions culturelles et réseaux sociaux numériques

open access: yesBalisages, 2021
En 2020, dans un contexte de confinement, les institutions culturelles ont dû faire face à une période inédite de fermeture contrainte. Cet article, en partant du cas de deux institutions françaises parisiennes, le Grand Palais et le musée Jacquemart ...
Camille Rondot
doaj   +1 more source

Germline TP53 Mutations Causing Diamond–Blackfan Anemia: A French Report

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Diamond–Blackfan anemia is a rare congenital erythroblastopenia typically caused by mutations in ribosomal protein genes. Recently, gain‐of‐function mutations in TP53 have been identified as a novel cause of Diamond–Blackfan anemia. We report two French patients who both harbored a heterozygous TP53 deletion (NM_000546.5: c.1077delA; p ...
Rafael Moisan   +6 more
wiley   +1 more source

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