Results 221 to 230 of about 1,209,467 (344)

Hind-Limb Reflexes in the Kitten: Properties of the Two-Neuron Arc [PDF]

, 1960

openalex   +1 more source

Exosome Proteomics of SOD1D90A Mutation Suggest Early Disease Mechanisms, and FN1 as a Biomarker

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Amyotrophic lateral sclerosis (ALS) is a neuromuscular disease. Super oxide dismutase 1 (SOD1) gene mutations cause ALS, and the D90A mutation is associated with primarily upper motor neuron (UMN) loss. Objective Our goal is to reveal the early cellular events in ALS pathology and identify potential pharmacokinetic biomarkers, using well ...
Mukesh Gautam, Ali Laith, Aslihan Gunel, Melda Yilmaz, Nazli Basak, Halil Idrisoglu, P. Hande Ozdinler   +6 more
wiley   +1 more source

Research on the anti-interference characteristics of neural networks with different scales. [PDF]

Sci Rep
Lin J, Lu M.
europepmc   +1 more source

TOPOGRAPHIC RELATIONSHIP BETWEEN THE RECEPTIVE FIELDS OF NEURONS IN THE MOTOR CORTEX AND THE MOVEMENTS ELICITED BY FOCAL STIMULATION IN FREELY MOVING CATS

, 1968
Hideo Sakata, Julio Miyamoto
openalex   +2 more sources

CARDIOVASCULAR NEURONS [PDF]

, 1968
A. C. Przybyla, S. C. Wang
openalex   +1 more source

Growth Differentiation Factor 15 Elevation in the Central Nervous System Is Associated With Failure to Thrive in Alexander Disease

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Alexander disease (AxD) is a severe neurodegenerative disorder caused by gain‐of‐function mutations in the gene for GFAP, which lead to protein aggregation and a primary astrocytopathy. Symptoms vary, but failure to thrive (FTT) and frequent emesis are common and cause significant morbidity. Here we investigate GDF15, a member of the
Tracy L. Hagemann, Michelle M. Sonsalla, Cora Luzinski, Fernando Zacahua, David A. Harris, Dudley W. Lamming, Albee Messing   +6 more
wiley   +1 more source

Genetic basis of maneb-induced dopaminergic neurodegeneration in Drosophila. [PDF]

G3 (Bethesda)
Villalobos-Cantor S, Arreola-Bustos A, Martin I.   +2 more
europepmc   +1 more source

Response Characteristics of Single Neurons in the Rabbit Visual Cortex

, 1968
Tetsuro Ogawa, Keishiro Karita, Yozo Tsuchiya   +2 more
openalex   +2 more sources

Response Characteristics of Kangaroo Rat Cochlear Nucleus Neurons [PDF]

, 1969
George Moushegian, Allen L. Rupert
openalex   +1 more source

SNUPN‐Related Muscular Dystrophy: Novel Phenotypic, Pathological and Functional Protein Insights

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective SNUPN‐related muscular dystrophy or LGMDR29 is a new entity that covers from a congenital or childhood onset pure muscular dystrophy to more complex phenotypes combining neurodevelopmental features, cataracts, or spinocerebellar ataxia. So far, 12 different variants have been described.
Nuria Muelas, Pablo Iruzubieta, Alberto Damborenea, Laura Pérez‐Fernández, Inmaculada Azorín, Juan Carlos Jiménez García, Ana Töpf, Pilar Martí, Lorena Fores‐Toribio, María Manterola, Rosana Blanco‐Mañez, Oihane Pikatza‐Menoio, Sonia Alonso‐Martín, Volker Straub, Aitziber L. Cortajarena, Adolfo López de Munain, David De Sancho, Lorea Blázquez, Juan J. Vilchez   +18 more
wiley   +1 more source