Results 161 to 170 of about 76,266 (294)

The oscillatory response of the electroretinogram and neuronal adaptation

open access: yesActa Ophthalmologica, EarlyView.
Abstract After more than 50 years, there still remains a challenge and an interest to know more as well as extend and deepen our understanding of the small rapid wavelets, the oscillatory potentials (OPs), of the electroretinogram (ERG) and the neuronal adaptation of the retina.
Lillemor Wachtmeister, Anders Eklund
wiley   +1 more source

A muscular dystrophy associated with bi‐allelic LEMD2 variants: Expanding the genotype of nuclear envelopathies

open access: yesBrain Pathology, EarlyView.
Proteomics‐guided exome re‐analysis identifies bi‐allelic variants in the nuclear envelope LEMD2 gene, expanding its phenotypic spectrum. Created in BioRender. Pauper, M. (2026) https://BioRender.com/xamvo92.
Marc Pauper   +17 more
wiley   +1 more source

Genetic architecture of cowpea domestication: QTL mapping and comparison shed new light on the dual domestication events. [PDF]

open access: yesG3 (Bethesda)
Dramé D   +10 more
europepmc   +1 more source

Views and Experiences of Children and Social Workers About Communication in Social Work Exchanges: A Mixed Methods Systematic Review

open access: yesChild &Family Social Work, EarlyView.
ABSTRACT Communication is critical to effective social work. Successful communication supports relationship‐based practices and higher quality assessments of children's needs and safety. The aim of this systematic review is to examine the existing evidence about the views and experiences of children and social workers about communication in social work
Charlotte Friel   +2 more
wiley   +1 more source

Biallelic MYH3 Variants Cause Distal Arthrogryposis in Compound Heterozygosity and a Subclinical Phenotype in Simple Heterozygosity. Codominance or Recessive Inheritance?

open access: yesClinical Genetics, EarlyView.
A nuclear family affected by distal arthrogryposis with novel biallelic MYH3 variants, which at the heterozygous state yield a subclinical phenotype, highlighting the complexity of MYH3‐related disorders and their inheritance modes. ABSTRACT Distal arthrogryposis constitutes a highly heterogeneous group of disorders with a critical need for clear ...
Omar Zgheib   +6 more
wiley   +1 more source

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