Results 201 to 210 of about 46,705 (302)

In Memoriam: Dr. Norman Paskin, Founding Director, International DOI Foundation Visionary Pioneer of Reference Linking, Metadata and Persistent Identifier Infrastructure

Data Science Journal, 2017
John S. Erickson, Laurence W. Lannom
doaj   +1 more source

Full-elevational gradient dataset on moth diversity and abundance in a temperate mountain range. [PDF]

Sci Data
Čížek O, Marhoul P, Kadlec T, Kaláb O, Jor T, Hlaváček A.   +5 more
europepmc   +1 more source

European Persistent Identifier Consortium

, 2021
Kálmán, Tibor, Kurzawe, Daniel, Schwardmann, Ulrich, Altenhöner, Reinhard   +3 more
openaire   +1 more source

In‐Depth Profiling Highlights the Effect of Efgartigimod on Peripheral Innate and Adaptive Immune Cells in Myasthenia Gravis

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Myasthenia gravis (MG) is an autoimmune disorder characterized by antibody‐mediated complement activation. Efgartigimod, a neonatal Fc receptor (FcRn) antagonist, is approved for treating generalized MG (gMG). However, its modulatory effects on upstream innate and adaptive immune cells remain largely unexplored.
Lei Jin, Liu Dong, Ying Wang, Dingxian He, Chong Yan, Jianying Xi, Haoqin Jiang, Yu Shi, Ming Guan, Chongbo Zhao, Jie Song, Sushan Luo   +11 more
wiley   +1 more source

Antibody escape drives emergence of diverse spike haplotypes resembling variants of concern in persistent SARS-CoV-2 infections. [PDF]

Cell Rep Med
Snell LB, Pickering S, Alcolea-Medina A, Winstone H, Seow J, Graham C, O'Connell L, Batra R, Malim MH, Doores KJ, Nebbia G, Edgeworth JD, Neil SJD, Galão RP.   +13 more
europepmc   +1 more source

Developmental, Neuroanatomical and Cellular Expression of Genes Causing Dystonia

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Dystonia is one of the most common movement disorders, with variants in multiple genes identified as causative. However, an understanding of which developmental stages, brain regions, and cell types are most relevant is crucial for developing relevant disease models and therapeutics.
Darren Cameron, Nicholas E. Clifton, Daniel Cabezas de la Fuente, Peter Holmans, Nicholas J. Bray, Kathryn J. Peall   +5 more
wiley   +1 more source

The TCXpress lane to T-cell receptor-engineered T cells. [PDF]

Blood Adv
Biernacki MA.
europepmc   +1 more source

Super‐Refractory Status Epilepticus (SRSE) in a Patient With Compound Heterozygous OPA1 Variants: Case Report and Literature Review

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Super‐Refractory Status Epilepticus (SRSE) is a rare, life‐threatening neurological emergency with unclear etiology in many cases. Mitochondrial dysfunction, often due to disease‐causing genetic variants, is increasingly recognized as a cause, with each gene producing distinct pathophysiological mechanisms.
Pouria Mohammadi, Lara Basovic, Christopher Michael McGraw   +2 more
wiley   +1 more source

Selumetinib as an Effective Therapy of Histiocytic Sarcoma Evolving From a B-Cell Acute Lymphoblastic Leukaemia. [PDF]

EJHaem
Largeaud L, Syrykh C, Vial J, Canali A, Luquet I, Vergez F, Dufrechou S, Prade N, Baruchel A, Gerby B, Nolla M, Delabesse E, Pasquet M.   +12 more
europepmc   +1 more source

Abschlussbericht Testbed “Persistent Identifiers”

Archivalia, 2015
openaire   +2 more sources