13 research outputs found

    Use of Native Grassland in Small-Scale Dairy Systems in the Highlands of Central Mexico. A Case Study

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    Small-scale dairy systems in Mexico comprise 78% of specialized dairy farms and provide 37% of national production. They are small farms with herds 3-35 cows plus replacements, and rely on family labour (Posadas-DomĂ­nguez et al., 2014). In the highlands, many farms have native grasslands, grazed during the rainy season, and supplemented with other feeds as maize straw, maize grain and maize ears. Native grasslands have not been studied in this context. This is a case study on the use of native grassland in a small-scale dairy farm. The objective was to determine how native grasslands are integrated in feeding milking dairy cows, and the feeding costs involved

    Effect of Supplementation of Dairy Cows under Cut and Carry or Grazing of Irrigated Cultivated Pastures in Small Scale Dairy Systems in the Highlands of Central Mexico

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    Small-scale dairy systems in Mexico represent over 78% of dairy farms and produce 37% of the nation’s milk, and have an important role in reducing rural poverty. Small-scale dairy systems are defined by having herds of 3 to 35 cows plus replacements, and rely mostly on the family for labour. In the central highlands, many small-scale dairy farms base the feeding of herds on irrigated cultivated pastures of ryegrass (Lolium multiflorum, L. perenne) – white clover (Trifolium repens), mostly under cut-and-carry by hand with scythes, straws, and large amounts of commercial compound concentrates that result in high feeding costs and low economic sustainability (Fadul-Pacheco et al., 2013). One option to optimize the use of resources in these systems is to change the use of grasslands to intensive grazing that result in lower feeding costs when compared to cut-and-carry strategies. Also, the high protein content of pasture may meet requirements for moderate yields by dairy cows, so that commercial concentrates may be substituted by lower protein, lower cost supplements like ground maize grain and remove the straws of the diets

    Trasplantes amigdalares embrionarios en ratas adultas con lesiones de la corteza motora: anĂĄlisis molecular y electrofisiolĂłgico

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    Transplants of embryonic nervous tissue ameliorate motor deficits induced by motor cortex lesions in adult animals. Restoration of lost brain functions has been recently shown in grafts of homotopic cortical origin, to be associated with a functional integration of the transplant after development of reciprocal host-graft connections. Nevertheless little is known about physiological properties or gene expression profiles of cortical implants with functional restorative capacity but no cortical origin. In this study, we show molecular and electrophysiological evidence supporting the functional development and integration of heterotopic transplants of embryonic amygdalar tissue placed into pre-lesioned motor cortex of adult rats. Grafts were analyzed 3 months post-transplantation

    Erratum to: 36th International Symposium on Intensive Care and Emergency Medicine

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    [This corrects the article DOI: 10.1186/s13054-016-1208-6.]

    36th International Symposium on Intensive Care and Emergency Medicine : Brussels, Belgium. 15-18 March 2016.

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    Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy

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    We delineate a KMT2E-related neurodevelopmental disorder on the basis of 38 individuals in 36 families. This study includes 31 distinct heterozygous variants in KMT2E (28 ascertained from Matchmaker Exchange and three previously reported), and four individuals with chromosome 7q22.2-22.23 microdeletions encompassing KMT2E (one previously reported). Almost all variants occurred de novo, and most were truncating. Most affected individuals with protein-truncating variants presented with mild intellectual disability. One-quarter of individuals met criteria for autism. Additional common features include macrocephaly, hypotonia, functional gastrointestinal abnormalities, and a subtle facial gestalt. Epilepsy was present in about one-fifth of individuals with truncating variants and was responsive to treatment with anti-epileptic medications in almost all. More than 70% of the individuals were male, and expressivity was variable by sex; epilepsy was more common in females and autism more common in males. The four individuals with microdeletions encompassing KMT2E generally presented similarly to those with truncating variants, but the degree of developmental delay was greater. The group of four individuals with missense variants in KMT2E presented with the most severe developmental delays. Epilepsy was present in all individuals with missense variants, often manifesting as treatment-resistant infantile epileptic encephalopathy. Microcephaly was also common in this group. Haploinsufficiency versus gain-of-function or dominant-negative effects specific to these missense variants in KMT2E might explain this divergence in phenotype, but requires independent validation. Disruptive variants in KMT2E are an under-recognized cause of neurodevelopmental abnormalities
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