Results 51 to 60 of about 14,985 (294)

Guiding AlphaFold to predict how Munc13‐1 opens Syntaxin‐1

open access: yesFEBS Open Bio, EarlyView.
The syntaxin‐1 Habc‐domain (orange), linker (pink) and SNARE motif (yellow) form a closed conformation that binds to Munc18‐1 (violet) and is opened by the Munc13‐1 MUN domain (cyan) to form the SNARE complex that triggers neurotransmitter release.
Madhurima Chattopadhyay   +2 more
wiley   +1 more source

Medalii și decorații din colecția Institutului de Arheologie din Iași (II)

open access: yesArheologia Moldovei, 2022
The authors continue the exhaustive presentation of the medals and decorations stored in the Institute’s Numismatic collection with a small group of five awards.
Sever-Petru Boțan, Lucian Munteanu
doaj   +1 more source

Diffusion Spectrum Imaging Maps Early Axonal Loss and a Unique Progressive Signal in Neuronal Intranuclear Inclusion Disease

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To delineate specific in vivo white matter pathology in neuronal intranuclear inclusion disease (NIID) using diffusion spectrum imaging (DSI) and define its clinical relevance. Methods DSI was performed on 42 NIID patients and 38 matched controls.
Kaiyan Jiang   +10 more
wiley   +1 more source

(a)) and the guidance in DoD Instruction 1348.33 (Reference (b)), this Manual reissues DoD [PDF]

open access: yes, 2013
procedures. b. Volume. This Volume: (1) Provides procedures and guidance regarding creation, activation, and award of DoD service awards – campaign, expeditionary, and service (CE&S) medals.
Service Medals
core  

UMP wins 14 gold, 10 silver medals for innovative research tools [PDF]

open access: yes, 2022
KUANTAN: An innovation to boost the extraction of agarwood oil was among the outstanding products that saw Universiti Malaysia Pahang (UMP) walk away with 14 gold medals at the International Invention, Innovation and Technology Exhibition (ITEX) 2022 at ...
Siti Nur Azwin, Zulkapri
core  

Onasemnogene Abeparvovec in Type I Spinal Muscular Atrophy: 24‐Month Follow‐Up From the Italian Registry

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Onasemnogene abeparvovec (OA) is an AAV9‐based gene therapy for spinal muscular atrophy type I (SMA I). Real‐world outcomes show increased response variability compared to clinical trials, and follow‐up data beyond 12–18 months are limited.
Marika Pane   +43 more
wiley   +1 more source

Franjo von Miskić (1828–1900): Habsburg officer, poet and collector

open access: yesStudia Lexicographica
The paper examines the life and activities of Franjo von Miskić (1828–1900), a Habsburg army officer, poet, and numismatist, a figure until recently relatively unknown outside of specific numismatic circles, where he was recognised for his impressive ...
Filip Šimunjak, Sven Matović
doaj   +1 more source

British historical medals of the 17th century medallists, books, authors, collectors, book-sellers & antiquaries [PDF]

open access: yes, 2017
As attractive as historical or commemorative medals are in their own right and as telling as they are by their designs and inscriptions of the persons or events they honour (or, in some cases, vilify or deride), they tell us much more: by means of ...
Platt, Arleen Kay   +1 more
core  

Comprehensive Characterization of 98 Chinese Cases of Genetic Creutzfeldt‐Jakob Disease With T188K Mutation

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To characterize the demographic, clinical, and laboratory features of the Chinese patients of genetic Creutzfeldt‐Jakob disease with T188K variant (T188K‐gCJD), the most common subtype of genetic prion diseases (gPrDs) in China. Methods In this nationwide retrospective study, data from 98 genetically confirmed T188K‐gCJD patients ...
Chun‐Jie Li   +11 more
wiley   +1 more source

Plasma EV Proteomics Identifies ECM Remodeling and Inflammatory Proteins LUM and C7 as Candidate Biomarkers in FSHD

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Facioscapulohumeral muscular dystrophy (FSHD) is one of the most debilitating and common muscular dystrophies. Despite its severity, no approved therapy exists for FSHD patients. However, several therapeutic candidates are currently under development, and some have recently entered clinical trials, marking the need for reliable ...
Mustafa Bilal Bayazit   +11 more
wiley   +1 more source

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