Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros











Intervalo de ano de publicação
1.
Zootaxa ; 4379(4): 539-555, 2018 Feb 15.
Artigo em Inglês | MEDLINE | ID: mdl-29689965

RESUMO

We describe a new species of Liolaemus of the L. alticolor-bibronii group of the subgenus Liolaemus sensu stricto. We studied meristic, morphometric and qualitative pattern characters. Statistical tests were performed in order to evaluate morphological differences among the candidate species and the most closely geographically distributed species. Molecular analyses of Cyt-b mitochondrial gene were performed in order to estimate the position of the new species in relation to other taxa. We also recorded natural history data such as habitat, behavior, reproductive state, diet, and body temperature. Liolaemus absconditus sp. nov. differs from other species of Liolaemus in presenting a distinct combination of morphological character states of lepidosis and color pattern, being phylogenetically close to Liolaemus tandiliensis, Liolaemus gracilis and Liolaemus saxatilis. The new species is a saxicolous and endemic lizard of the Tandilia Mountain Range System of Buenos Aires Province.


Assuntos
Lagartos , Animais , Argentina , Ecossistema , Genes Mitocondriais , Filogenia
2.
Invest. clín ; 37(4): 247-53, dic. 1996. ilus
Artigo em Espanhol | LILACS | ID: lil-199243

RESUMO

The allosteric behavior of the p-nitrophenyl-phosphatase (EC.3.1.3.1) from membrane erythrocytes was investigated in the following mulltisystemic diseases: myotonic dystrophy limb-girdle muscular dystrophy, Charcot-Marie-Tooth and juvenile spinal muscular atrophy; in myotonia congenita. which is not a multisystemic disease, and in healthy controls. The Hill coefficient in F-inhibition in controls was different from that in multisystemic diseases patients but not from that in myotonia congenita patients. Changes in the cooperative type kinetics would suggest that the interaction membrane-enzyme in controls and in patients with neuromuscular disorders is only different for multisystemic diseases


Assuntos
Humanos , Masculino , Feminino , Fosfatase Alcalina/uso terapêutico , Doença de Charcot-Marie-Tooth/diagnóstico , Eritrócitos/patologia , Doenças Musculares/genética , Distrofias Musculares/diagnóstico
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA