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A mostrar 1 - 20 resultados de 3,325 para a pesquisa '(( j e combs dan non ) OR ((( j new ca e new ) OR ( j e wom dan non ))))*', tempo de pesquisa: 0.95seg Refinar resultados
Genetic mapping of the 21-hydroxylase locus: estimation of small recombination frequencies.
The monoclonal antibody E587 recognizes growing (new and regenerating) retinal axons in the goldfish retinotectal pathway

MINERALOGY, PETROLOGY AND OXYGEN ISOTOPIC COMPOSITION OF NORTHWEST AFRICA (NWA) 12379, A NEW METAL-RICH CHONDRITE WITH AFFINITY TO ORDINARY CHONDRITES
In situ spectroscopic study of the plastic deformation of amorphous silicon under non-hydrostatic conditions induced by indentation

Do nucleic acids moonlight as molecular chaperones?
Current and Emerging Treatments for Postsurgical Cleft Lip Scarring: Effectiveness and Mechanisms

The Combined Performance of ADC, CSF CXC Chemokine Ligand 13, and CSF Interleukin 10 in the Diagnosis of Central Nervous System Lymphoma
Acute Brain MRI Findings in 120 Malawian Children with Cerebral Malaria: New Insights into an Ancient Disease

Novel taxa in the Fusarium fujikuroi species complex from Pinus spp.
Immunotherapy of Malignant Gliomas Using Autologous and Allogeneic Tissue Cells

Magnetic and ferroelectric response of Ca2TiMnO6 manganite-like perovskite
Sensory neuropathy as part of the cerebellar ataxia neuropathy vestibular areflexia syndrome

Topological constraints strongly affect chromatin reconstitution in silico
Source apportionment of fine PM by combining high time resolution organic and inorganic chemical composition datasets

Cytotoxic effects of new bioactive compounds isolated from a Nigerian anticancer plant Melastomastrum capitatum Fern. leaf extract
Tumefactive demyelination following herbal supplement use: Cause or coincidence?

APOE-Mimetic Peptides Reduce Behavioral Deficits, Plaques and Tangles in Alzheimer's Disease Transgenics
A new treatment approach – Eplerenone - in central serous chorioretinopathy - Case report

Multiplex qPCR for reliable detection and differentiation of <it>Burkholderia mallei</it> and <it>Burkholderia pseudomallei</it>
Identification and characterization of novel uroporphyrinogen decarboxylase gene mutations in a large series of porphyria cutanea tarda patients and relatives

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