Adult neural stem/progenitor (B1) cells within the walls of the lateral ventricles generate different types of neurons for the olfactory bulb (OB). The location of B1 cells determines the types of OB neurons they generate. Here we show that the majority of mouse B1 cell precursors are produced between embryonic days (E) 13.5 and 15.5, and remain largely quiescent until they become reactivated postnatally. Using a retroviral library carrying over 100,000 genetic tags, we found that B1 cells share a common progenitor with embryonic cells of the cortex, striatum and septum, but this lineage relationship is lost before E15.5. The regional specification of B1 cells is evident as early as E11.5 and is spatially linked to the production of neurons that populate different areas of the forebrain. This study reveals an early embryonic regional specification of postnatal neural stem cells and the lineage relationship between them and embryonic progenitor cells.
During 2003 and during late September of 2004, more than 1230 cases of gastroenteritis were reported in the south of Sinaloa State, north-western Mexico. All cases were attributed to the consumption of raw or undercooked shrimp collected at the Huizache-Caimanero lagunary system. Vibrio parahaemolyticus was identified by standard biochemical methods, and many strains were positive for PCR amplifications of the tlh and tdh genes and negative for the trh gene. A representative strain belonged to the O3:K6 serogroup. This is the first outbreak of gastroenteritis caused by the pandemic strains of O3:K6 V. parahaemolyticus in México.
A 300 cow Brahman herd kept on improved pasture was subjected to a selection and management programme based on a limited breeding season. Artificial insemination using mainly progeny tested bulls was used in part of the herd and the rest were bred in single sire herds. Of the 200 sires used during the 30 year period, 82% were homebred and selected principally for high estimated breeding value of 18‐month weight. Variance components of birth (BW), weaning (205 W) and 18‐month (548 W) weights of 6130 calves born 1968 through to 1997 were estimated by the Restricted Maximum Likelihood method (REML) using uni‐ and bivariate animal models. For each weight the animal's direct and maternal genetic and the dam's permanent environmental effects were considered random and those of sex, year and month of birth and age of cow were considered fixed, but the models differed as far as the number of significant interactions included. Adjusted least squares means for BW, 205 W and 548 W were 28, 158 and 292 kg. Phenotypic and direct and maternal genetic trends from univariate analysis were for BW: 0.156, 0.061 and −0.001 kg; for 205 W: 0.471, 0.126 and 0.044 kg; for 548 W: 1.973, 0.486 and 0.251 kg per year. Direct and maternal heritabilities from univariate analyses were for BW, 205 W and 548 W, 0.33 and 0.08; 0.07 and 0.14; 0.13 and 0.08, respectively. Genetic direct‐maternal correlations for the three weights were −0.37, −0.13 and 0.49 and permanent environmental variance of the dam as proportion of phenotypic variance (c2) had values of 0.03, 0.16 and 0.01, respectively. Direct and maternal genetic correlations were for BW: 205 W, 0.64 and 0.74; for BW: 548 W, 0.35 and 0.74; and for 205 W: 548 W, 0.64 and 0.96. Future genetic work in the herd should put more emphasis on the improvement of cow efficiency for sustainable beef production on native and improved pasture.
Peripheral primitive neuroectodermal tumours (pPNETs) are a group of soft-tissue tumours of neuroepithelial origin that arise outside the central and sympathetic nervous system. Orbital location is infrequent, and to the best of the authors' knowledge only 16 cases have been reported in the literature. With this article, the authors report the demographics and clinical characteristics, diagnostic features, differential diagnosis, prognosis and therapeutic options of primary orbital peripheral primitive neuroectodermal tumour, based on their patients and on the cases reported in the literature to date. A differential diagnosis should be made with other small round cell tumours; immunohistochemical and ultrastructural techniques are essential for this purpose. Although bone invasion and extraorbital extension are possible, systemic metastases are uncommon in the cases of orbital pPNETs. Surgery has been the initial treatment in most cases; chemotherapy with or without radiotherapy is considered the best additional treatment. The orbital pPNET could be less aggressive than other forms of pPNETs, since most of the patients reported were alive after the follow-up period (at least 6 months).
To examine the potential of using photodynamic therapy (PDT) in condylomata, we studied the distribution and kinetics of protoporphyrin IX (PpIX) formation in condylomata acuminata and adjacent normal skin after topical application of 5-aminolaevulinic acid (ALA). PpIX fluorescence spectra were measured hourly in vivo after ALA application. After gross fluorescence imaging, the lesions were biopsied, and fluorescence microscopy was performed. All three PpIX fluorescence detection modalities suggested selectivity of PpIX formation in condylomata after topical ALA application. In 17 of 25 condylomata, there was significantly greater fluorescence compared with adjacent normal skin. The greatest lesional to normal skin fluorescence ratios occurred after 2 h. The most likely mechanism for increased lesional PpIX formation in condylomata is enhanced stratum corneum permeability. Based on our results, ALA/PDT is a potential field therapy for condylomata. PpIX fluorescence imaging after ALA application may also be useful for localizing condylomata prior to treatment.
Increase recruitment of BMDCs into the cerebellum, radiation damage to cerebellar cells, or both, increase the formation of fused Purkinje cells. BMDC-Purkinje heterokaryons formation may reflect an endogeneous neuronal repair mechanism, or it could be a by-product of radiation-induced inflammation. In either case, fused Purkinje neurons increase following radiation damage in the developing cerebellum. The above observations reveal a novel consequence of head radiation in neonatal rodents. It will be interesting to determine if similar increase in the number of binucleated Purkinje neurons, occurs in children that receive radiation during early development. Ann Neurol 2009;66:100-109.
To examine the potential of using photodynamic therapy (PDT) in condylomata, we studied the distribution and kinetics of protoporphyrin IX (PpIX) formation in condylomata acuminata and adjacent normal skin after topical application of 5-aminolaevulinic acid (ALA). PpIX fluorescence spectra were measured hourly in vivo after ALA application. After gross fluorescence imaging, the lesions were biopsied, and fluorescence microscopy was performed. All three PpIX fluorescence detection modalities suggested selectivity of PpIX formation in condylomata after topical ALA application. In 17 of 25 condylomata, there was significantly greater fluorescence compared with adjacent normal skin. The greatest lesional to normal skin fluorescence ratios occurred after 2 h. The most likely mechanism for increased lesional PpIX formation in condylomata is enhanced stratum corneum permeability. Based on our results, ALA/PDT is a potential field therapy for condylomata. PpIX fluorescence imaging after ALA application may also be useful for localizing condylomata prior to treatment.
<h4>PURPOSE</h4> <p>To report the demographics and clinical characteristics, therapy logarithm, and prognosis of children with pars planitis.</p> <h4>PATIENTS AND METHODS</h4> <p>The medical records were reviewed of all patients diagnosed with pars planitis between June 1995 and December 2005 in the Department of Pediatric Ophthalmology at Hospital Universitario La Paz, Madrid, Spain. A retrospective, descriptive, and longitudinal study of 30 eyes in 16 children was performed.</p> <h4>RESULTS</h4> <p>Pars planitis was bilateral in 87.5% and more frequent in males (68.8%). Average age at onset was 9.2 years. The main ophthalmologic findings recorded were snowballs (96.7%) and vitritis (93.3%). Cataract formation was the most prevalent complication (36.7%). Mean initial and final best-corrected visual acuities were 0.640 and 0.840, respectively. Periocular corticosteroids were used in 33.3% of cases and cryotherapy or laser photocoagulation in 16.7%. Complications requiring surgical management occurred in 4 eyes (13.3%).</p> <h4>CONCLUSION</h4> <p>Pars planitis treated with adequate medical and surgical procedures has a good prognosis in most cases.</p> <p><cite>J Pediatr Ophthalmol Strabismus</cite> 2007;44:288-293.</p> <h4>AUTHORS</h4> <p>The authors are from the Department of Pediatric Ophthalmology, Hospital Universitario La Paz, Madrid, Spain.</p> <p>Originally submitted July 17, 2006.</p> <p>Accepted for publication October 11, 2006.</p> <p>Address correspondence to Ricardo Romero, MD, Urbanizacion Quinta del Sol 32, Las Rozas, Madrid, 28231, Spain.</p>
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