Results 231 to 240 of about 141,474 (306)
[3H]XAC (xanthine amine congener) is a radioligand for A2-adenosine receptors in rabbit striatum [PDF]
Xingchen Ji+2 more
openalex +1 more source
A Longitudinal Study of Multidimensional Prosocial Behavior During Adolescence
ABSTRACT This study examines the distinct developmental trajectories of prosocial and rebellious behaviors in adolescence. Using data from an accelerated three‐wave project (2018–2022) among adolescents aged 9–22 years (N = 142, 63% female, middle‐high SES, white European descent), trajectories of prosocial actions toward friends and peers, prosocial ...
Sophie W. Sweijen+3 more
wiley +1 more source
Trio exome sequencing allowed the identification of two novel compound heterozygous variants in PIK3C2A, defining the fifth family presenting a PIK3C2A‐related syndrome characterized by pulverulent cataracts and deafness. Functional testing revealed impaired PI metabolism and primary dysfunction phenotype.
Adella Karam+9 more
wiley +1 more source
Summary Background and Objective Junctional epidermolysis bullosa (JEB) is a subtype of epidermolysis bullosa caused by mutations in the LAMB3 gene. We treated a patient with JEB using genetically corrected autologous epidermal cultures retrovirally transduced with the functional LAMB3 gene sequence.
Alexander Dermietzel+11 more
wiley +1 more source
In vitro experiments on interactions between dopamine and neurotensin receptors in the rat striatum
Hajime Ishida, Shozo Kito, Rie Miyoshi
openalex +1 more source
Preferential superficial cortical layer activation during seizure propagation
Abstract Objective Focal cortical seizures travel long distances from the onset zone, but the long‐distance propagation pathways are uncertain. In vitro and in vivo imaging techniques have investigated the local spread of seizures but did not elucidate long‐distance spread. Furthermore, classical studies in slices suggested seizure spread locally along
Anastasia Brodovskaya+4 more
wiley +1 more source
Abstract Objective Mutations of the DEP Domain Containing 5 gene (DEPDC5), a mechanistic Target of Rapamycin (mTOR) inhibitor involved in amino acid sensing, are associated with neurological diseases such as epilepsy and/or autism spectrum disorder (ASD). Loss of DEPDC5 impacts early neuronal development via mTOR hyperactivity.
Mattson S. O. Jones+14 more
wiley +1 more source