Results 161 to 170 of about 73,318 (285)
ABSTRACT Speed breeding can shorten breeding cycles and, when combined with genomic selection, can accelerate genetic gain. Yet it remains unclear how different integration strategies affect long‐term response, genetic variance and cost‐efficiency in small public programs.
Jesimiel da Silva Viana +2 more
wiley +1 more source
Predicting longitudinal basal forebrain volume in the Alzheimer's disease spectrum: the role of sex and ApoE epsilon 4 genotype. [PDF]
Grazia A +14 more
europepmc +1 more source
ABCA12 Frameshift Deletion in Domestic Cats With Ichthyosis Fetalis
ABSTRACT Background Ichthyosis fetalis (IF), also known as harlequin ichthyosis, is a rare and often fatal autosomal recessive congenital skin disorder. It is characterized by thickened, hard skin plaques and deep skin fissures that limit mobility and cause malformations of the eyes, lips and ears.
Jeanna M. Blake +2 more
wiley +1 more source
Adeno-associated vector corneal gene therapy reverses corneal clouding in a feline model of mucopolysaccharidosis VI. [PDF]
Gilger BC +11 more
europepmc +1 more source
Abstract figure legend ACE I/D genotype, enzyme activity and integrated physiological adaptations. Upper panel: Conceptual framework linking the ACE I/D polymorphism (left) with circulating/tissue ACE activity (centre; violin plots based on hypothetical data for illustration) and strength/power versus endurance phenotypes (right).
Tórur Sjúrðarson +1 more
wiley +1 more source
Genotype and Haplotype Analysis Between <i>ESR1</i> Variants and Breast Cancer in the Bangladeshi Patients: A PCR-RFLP-Based Genetic Association Study. [PDF]
Hossen MS +6 more
europepmc +1 more source
Caenorhabditis elegans as an in vivo model system for human inherited primary arrhythmia syndromes
Abstract figure legend Most genes involved in inherited primary arrhythmia syndromes (IPAS) are conserved in Caenorhabditis elegans, where genetic manipulation enables functional characterization of variants, identification of regulatory proteins, and in vivo drug testing.
Antoine Delinière +6 more
wiley +1 more source
Host genetic factors modulating dengue virus: a systematic review of TLR polymorphisms. [PDF]
Candrasari DS +4 more
europepmc +1 more source
ABSTRACT TSPEAR (chr. 21q22.3) encodes a protein involved in tooth development and is predominantly expressed in the enamel knot. Biallelic loss of function variants in TSPEAR cause ectodermal dysplasia, tooth agenesis and sensorineural hearing loss. However, the role of TSPEAR in auditory processes is unclear.
Debora Vergani +17 more
wiley +1 more source

