An approximation to the likelihood for a pedigree with loops

This paper presents a new approximation to the likelihood for a pedigree with loops, based on cutting all loops and extending the pedigree at the cuts. An opimum loop-cutting strategy and an iterative extension technique are presented. The likelihood for a pedigree with loops is then approximated by the conditional likelihood for the entire cut-extended pedigree given the extended part. The approximate likelihoods are compared with the exact likelihoods obtained using the program MENDEL for several small pedigrees with loops. The approximation is efficient for large pedigrees with complex loops in terms of computing speed and memory requirements.     

The fine structure and development of calcified skeletal elements in the body wall of holothurian echinoderms

The calcareous ossicles and iron-rich calcified granules in the integument of sea cucumbers (Echinodermata: Holothuroida) have been examined by light and electron microscopy. Most ossicles are perforated, platelike structures that measure 100–500 μm long and consist of magnesium-rich calcite. The formation of ossicles occurs within multinucleated syncytia of sclerocytes that are situated in the dermal layer of the body wall. Sclerocytes possess fairly large numbers of mitochondria and are characteristically enveloped by an external lamina. Each ossicle arises as a minute rodlike spicule that branches and develops into a fenestrated skeletal element. When viewed by SEM, fully developed ossicles appear non-crystalline. Following decoration with synthetically grown calcite seeds, however, each ossicle reveals an ordered array of crystallites that seem to be aligned perpendicular to the ossicle's original plane of growth. Examinations of sectioned ossicles indicate that the mineral phase in each skeletal element lacks a well developed matrix of EDTA-insoluble organic substances. Ossicles first arise in the ciliated, lecithotrophic larvae of Eupentacta quinquesimita at about 1 week postfertilization. Two-week-old specimens adopt an epibenthic existence and subsequently become enveloped by imbricated ossicles that are secreted by sclerocytes resembling those found in adults. In molpadiid holothurians, the adult body wall contains numerous reddish-brown granules that are chiefly composed of iron-rich subunits. The dermal granules differ from calcitic ossicles in developing extracellularly in association with finely filamentous material.     

The L-gulono-gamma-lactone oxidase gene (GULO) which is a candidate for vitamin C deficiency in pigs maps to chromosome 14

Vitamin C deficient pigs, when fed a diet lacking L-ascorbic acid (AscA), manifest deformity of the legs, multiple fractures, osteoporosis, growth retardation and haemorrhagic tendencies. This trait was shown by others to be controlled by a single autosomal recessive allele designated as od (osteogenic disorder). The inability of AscA biosynthesis in primates and guinea pigs that exhibit similar symptoms, when they are not supplemented with AscA in the food, was traced to the lack of L-gulono-gamma-lactone oxidase, which catalyzes the terminal step in the biosynthesis of AscA. The non-functional GULOP was mapped to human chromosome 8p21 that corresponds to an evolutionarily conserved segment on either porcine chromosome 4 (SSC4) or 14 (SSC14). We investigated linkage between OD and SSC4- and 14-specific microsatellite loci in order to map the OD locus. Twenty-seven informative meioses in families from one sire and three dams revealed linkage of od with microsatellites SW857 and S0089, located in the subcentromeric region of SSC14. We isolated part of the GULO gene of the pig by screening a porcine genomic library using a pig GULO cDNA as a probe, and mapped it to SSC14q14 by fluorescence in situ hybridization (FISH). Thus, the porcine GULO gene is both a good physiological and positional candidate gene for vitamin C deficiency in pigs.     

Tumour targeting with antibody-coupled liposomes: Failure to achieve accumulation in xenografts and spontaneous liver metastases

Summary The potential of small unilamellar liposomes coupled to anti-tumour monoclonal antibodies (immunoliposomes) to accumulate in solid tumour tissue was tested in two systems, i.e. a human malignant melanoma xenografted into nude mice and a syngeneic murine lymphoma ESb.Mp exhibiting spontaneous metastasis to the liver. Both monoclonal antibodies tested were partly released from immunoliposomes within a few hours, thus generating a seemingly constant level of circulating antibody. Nevertheless it was possible to follow the biodistribution of intact immunoliposomes by virtue of a radioiodine label incorporated into the lipid moiety. It was found that in both tumor systems, though they differed with respect to the size of lesions and maybe also to the vascular architecture of surrounding tissue, immunoliposome uptake was virtually nil. The blockade of uptake into solid tumour tissue was caused by the limited availability of immunoliposomes due to their moderate stability, but especially by the inability of the particulate carrier to extravasate.