Characterization of Pestivirus scrofae infection in the tissues of a persistently infected boar. [PDF]
Dénes L +4 more
europepmc +1 more source
Feeding the newborn: comparative problems in man and animals [PDF]
openaire +2 more sources
Streamlining Diagnosis of Bardet–Biedl Syndrome: New Diagnostic Algorithm With Updated Criteria
ABSTRACT Considerable advances have been made in our understanding of Bardet–Biedl syndrome (BBS), particularly in its core clinical features and molecular genetics, warranting an update to the existing diagnostic criteria framework. Using a rigorous, evidence‐based, and consensus‐driven process, a multidisciplinary group of international experts and ...
Jeremy J. Pomeroy +16 more
wiley +1 more source
Effect of human interference with maternal behaviour on development and blood biochemical parameters in the first 35 d of calves' life. [PDF]
Iwaszkiewicz M +4 more
europepmc +1 more source
ABSTRACT U2 small nuclear RNA auxiliary factor 2 (U2AF2) is an essential pre‐mRNA splicing factor involved in the early stages of pre‐mRNA splicing. To date, multiple individuals have been reported with predominantly heterozygous missense variants presenting intellectual disability, speech and motor delays, seizures, hypotonia, and thin or hypoplastic ...
Amanda Toledo +3 more
wiley +1 more source
Description of a collaborative sperm whale birth and shifts in coda vocal styles during key events. [PDF]
Aluma Y +46 more
europepmc +1 more source
ABSTRACT Smith–Magenis syndrome (SMS) results from either a recurrent 17p11.2 deletion or pathogenic variants in the retinoic acid induced 1 gene (RAI1). While neurodevelopmental impairment and behavioral dysregulation are well recognized, systematic genotype‐stratified analyses across psychiatric domains remain limited.
Albin Blanc +7 more
wiley +1 more source
Bidirectional regulation of gut microbiota and young ruminant host: implications for intestinal development and mucosal immunity. [PDF]
Walelegne M +7 more
europepmc +1 more source
Expanded Phenotype Associated With an Intronic PPP1R12A Variant: A Case Report and Literature Review
ABSTRACT Autosomal dominant PPP1R12A‐related genitourinary and/or brain malformation syndrome is a recently described multisystem disorder caused by loss‐of‐function variants in the protein phosphatase 1 regulatory subunit 12a (PPP1R12A) gene. To date, 22 affected individuals have been reported with variable brain malformations and genitourinary ...
Emily M. Bland +4 more
wiley +1 more source
Prevalence of cryptosporidiosis and other enteric pathogens in calves in France: effects of rotavirus, coronavirus and E. coli vaccination and transmission routes. [PDF]
Costa D +12 more
europepmc +1 more source

