Phenotypic variation across mammals is extensive and reflects their ecological diversification into a remarkable range of habitats on every continent and in every ocean …
Combined methylmalonic acidemia and homocystinuria (cblC) is the most common inborn error of intracellular cobalamin metabolism and due to mutations in Methylmalonic Aciduria …
L Loisay, D Komla-Ebri, A Morice, Y Heuzé, C Viaut… - JCI insight, 2023 - ncbi.nlm.nih.gov
Hypochondroplasia (HCH) is a mild dwarfism caused by missense mutations in fibroblast growth factor receptor 3 (FGFR3), with the majority of cases resulting from a heterozygous p …
Simple Summary Landmarks are commonly used to investigate how objects vary in form. However, many objects present few identifiable landmarks. To remedy this, several …
E Lana-Elola, H Cater… - Disease Models & …, 2021 - journals.biologists.com
ABSTRACT Down syndrome (DS), trisomy 21, results in many complex phenotypes including cognitive deficits, heart defects and craniofacial alterations. Phenotypes arise from …
Modern microscopy technologies allow imaging biological objects in 3D over a wide range of spatial and temporal scales, opening the way for a quantitative assessment of …
Adaptive avian radiations associated with the diversification of bird beaks into a multitude of forms enabling different functions are exemplified by Darwin's finches and Hawaiian …
J Devine, M Vidal-García, W Liu, A Neves… - Scientific data, 2022 - nature.com
Complex morphological traits are the product of many genes with transient or lasting developmental effects that interact in anatomical context. Mouse models are a key resource …
We present a novel method for the morphometric analysis of series of 3D shapes, and demonstrate its relevance for the detection and quantification of two craniofacial anomalies …