99 research outputs found

    Odontography

    Get PDF
    The curious combination of the contrasting hardest and softest tissues in the human body incorporated into teeth requires introspection. The vastly varying modalities of different tissue types, from soft dental pulp and periodontal ligament through cementum into dentine and enamel incorporated in human teeth is astonishing. The durability of human dentitions correlates with their longevity. Moreover, teeth are the longest lasting organs after death, defying postmortem decay, yet contrastingly so susceptible to caries during life. The complex morphology of teeth reveals an historical background of food acquisition from palaeontological evidence.1 The amount of detailed historical information that can be gleaned from a meticulous examination of teeth is incomparable. The molecular mechanisms of dental enamel formation are reveal

    The Complexity of Dental Enamel

    Get PDF
    Dental enamel constitutes the least quantitative and rarest component of all tissues in the human body but is the most enduring and hardest constituent of ecto dermal cellular development. Dental enamel can be a harbinger of history, reflecting the environment during the time it was being formed. Enamel first appeared around 415 million years ago when the suite of genes that encode the proteins required to make enamel appeared in the scales of sarcopterygians.1 The vitreous nature of enamel provides its white lucent, iridescent and gleaming appearance as a physically attractive feature of a human smile, but contrarily, it may provide a snarling repulsive warning of a snee

    Absence of the spleen(s) in conjoined twins: a diagnostic clue of laterality defects? Radiological study of historical specimens

    Get PDF
    Laterality defects are quite common in thoracoileopagus and parapagus dicephalus but rare in other types of conjoined twins. To present the presumed laterality defects in cephalothoracoileopagus and prosopothoracoileopagus conjoined twins, based on the unilateral or bilateral absence or duplication of the spleen. Three human anatomical specimens of craniothoracoileopagus (CTIP) twins and one of prosopothoracoileopagus (PTIP) twins were investigated. The specimens were part of the Museum Vrolik collection of the Department of Anatomy and Embryology of the Academic Medical Centre, University of Amsterdam, The Netherlands. The specimens were taken out of their jars and scanned with multidetector CT and volumetric T2-weighted MRI at 1.5 T. The internal anatomy of the specimens was largely in accordance with previous reports. However, there was no recognisable spleen in the right twin in one CTIP specimen, in the left twin in one other CTIP specimen, and in both twins in the third CTIP specimen and in the PTIP specimen. Asplenia and polysplenia are considered reliable indicators of right and left isomerism, respectively. However, three of our four specimens had laterality patterns that did not correspond with those previously reported. Since no other parameters of laterality defects could be verified in these specimens, we concluded that asplenia was unlikely to be caused by laterality defect

    Canalization and developmental stability in the Brachyrrhine mouse

    Full text link
    The semi-dominant Br mutation affects presphenoid growth, producing the facial retrognathism and globular neurocranial vault that characterize heterozygotes. We analysed the impact of this mutation on skull shape, comparing heterozygotes to wildtype mice, to determine if the effects are skull-wide or confined to the sphenoid region targeted by the mutation. In addition, we examined patterns of variability of shape for the skull as a whole and for three regions (basicranium, face and neurocranium). We found that the Br mice differed significantly from wildtype mice in skull shape in all three regions as well as in the shape of the skull as a whole. However, the significant increases in variance and fluctuating asymmetry were found only in the basicranium of mutant mice. These results suggest that the mutation has a significant effect on the underlying developmental architecture of the skull, which produces an increase in phenotypic variability that is localized to the anatomical region in which the mean phenotype is most dramatically affected. These results suggest that the same developmental mechanisms that produce the change in phenotypic mean also produce the change in variance.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/75710/1/j.1469-7580.2006.00527.x.pd

    Developmental pathways inferred from modularity, morphological integration and fluctuating asymmetry patterns in the human face

    Get PDF
    Facial asymmetries are usually measured and interpreted as proxies to developmental noise. However, analyses focused on its developmental and genetic architecture are scarce. To advance on this topic, studies based on a comprehensive and simultaneous analysis of modularity, morphological integration and facial asymmetries including both phenotypic and genomic information are needed. Here we explore several modularity hypotheses on a sample of Latin American mestizos, in order to test if modularity and integration patterns difer across several genomic ancestry backgrounds. To do so, 4104 individuals were analyzed using 3D photogrammetry reconstructions and a set of 34 facial landmarks placed on each individual. We found a pattern of modularity and integration that is conserved across sub-samples difering in their genomic ancestry background. Specifcally, a signal of modularity based on functional demands and organization of the face is regularly observed across the whole sample. Our results shed more light on previous evidence obtained from Genome Wide Association Studies performed on the same samples, indicating the action of diferent genomic regions contributing to the expression of the nose and mouth facial phenotypes. Our results also indicate that large samples including phenotypic and genomic metadata enable a better understanding of the developmental and genetic architecture of craniofacial phenotypes
    • …
    corecore