Results 101 to 110 of about 158,397 (231)

Abstracts of the communications presented during the 6th World Rabbit Congress: ETHOLOGIE AND WELFARE. Toulouse, July 9-12, 1996

open access: yes, 1996
World Rabbit Science (1996). Abstracts of the communications presented during the 6th World Rabbit Congress: ETHOLOGIE AND WELFARE. Toulouse, July 9-12, 1996. World Rabbit Science. 04.
World Rabbit Science   +1 more
core   +1 more source

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

Abstracts of the communications presented during the 6th World Rabbit Congress: MANAGEMENT AND PRODUCTION. Toulouse, July 9-12, 1996

open access: yes, 1996
World Rabbit Science (1996). Abstracts of the communications presented during the 6th World Rabbit Congress: MANAGEMENT AND PRODUCTION. Toulouse, July 9-12, 1996. World Rabbit Science. 04.
MANAGEMENT AND PRODUCTION,   +1 more
core   +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

Abstracts of the communications presented during the 7th French Rabbit Days. Lyon, May 13-14th, 1998: CROISSANCE ET VIANDE

open access: yes, 1998
World Rabbit Science (1998). Abstracts of the communications presented during the 7th French Rabbit Days. Lyon, May 13-14th, 1998: CROISSANCE ET VIANDE. World Rabbit Science. 06.
World Rabbit Science   +1 more
core   +1 more source

Characterizing Cutaneous α‐Synuclein Deposition and Seeding Activity in Parkinson's Disease Subtypes

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Cutaneous phosphorylated α‐synuclein (p‐syn) and α‐synuclein seeding activity are promising biomarkers for Parkinson's disease (PD), but their clinical value remains uncertain due to disease heterogeneity. This study evaluates these two biomarkers in PD patients to inform phenotype‐specific diagnosis and disease severity assessment ...
Yuting Jin   +8 more
wiley   +1 more source

Abstracts of the communications presented during the 6th World Rabbit Congress: PATHOLOGY AND PROPHYLAXIS. Toulouse, July 9-12, 1996

open access: yes, 1996
World Rabbit Science (1996). Abstracts of the communications presented during the 6th World Rabbit Congress: PATHOLOGY AND PROPHYLAXIS. Toulouse, July 9-12, 1996. World Rabbit Science. 04.
World Rabbit Science   +1 more
core   +1 more source

Region Specific miRNA–mRNA Networks in Gray and White Matter Lesions of Progressive Multiple Sclerosis

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Multiple sclerosis (MS) is a neurodegenerative demyelinating disease of the central nervous system. This study aimed to identify micro‐RNA (miRNA)–mRNA regulatory networks underlying region‐specific molecular mechanisms in white matter and gray matter lesions in progressive MS.
Adya Sapra   +5 more
wiley   +1 more source

Augmenting and Assaying Nav1.1 Protein Quantity for Dravet Syndrome Therapy

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Dravet Syndrome (DS) is a developmental and epileptic encephalopathy predominantly caused by heterozygous loss‐of‐function variants in SCN1A, which encodes Nav1.1. Conserved upstream open reading frames (uORFs) in SCN1A were validated to regulate translation in reporter assays, demonstrating the therapeutic viability of increasing Nav1.1 from ...
Aiswarya Saravanan   +7 more
wiley   +1 more source

Home - About - Disclaimer - Privacy