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A mostrar 1 - 20 resultados de 1,273 para a pesquisa '(( j nair comer viana niero ) OR ( ((j ac) OR (j a)) ((camp da) OR (camp a)) new ))*', tempo de pesquisa: 1.38seg Refinar resultados
A New Minimal Replicon of Bacillus anthracis Plasmid pXO1
Absence of sporidesmin production by twelve Texas isolates of Pithomyces spp.

INFLAMMATORY REACTIONS IN RABBITS WITH A SEVERE LEUCOPENIA
A Workstation for Interactive Display and Quantitative Analysis of 3-D and 4-D Biomedical Images

Parents’ Preferences for Enhanced Access to the Pediatric Medical Home: A Qualitative Study
A New Addition to the Cell Plan of Anammox Bacteria: “Candidatus Kuenenia stuttgartiensis” Has a Protein Surface Layer as the Outermost Layer of the Cell

Visual motion integration by neurons in the middle temporal area of a New World monkey, the marmoset
New Agents for Prevention of Ultraviolet-Induced Nonmelanoma Skin Cancer

Non-smoke spontaneous contrast in left atrium intensified by respiratory manoeuvres: a new transoesophageal echocardiographic observation.
Autotrophic Methanotrophy in Verrucomicrobia: Methylacidiphilum fumariolicumSolV Uses the Calvin-Benson-Bassham Cycle for Carbon Dioxide Fixation

Outcomes of neonatal retinoblastoma in pre-chemotherapy and chemotherapy eras
Preliminary Characterization of Voltage-Activated Whole-Cell Currents in Developing Human Vestibular Hair Cells and Calyx Afferent Terminals

FALSE-POSITIVE TANGIBLE OUTCOMES OF FUNCTIONAL ANALYSES
Pairwise shared genomic segment analysis in three Utah high-risk breast cancer pedigrees

Adaptable Mechanisms That Regulate the Contrast Response of Neurons in the Primate Lateral Geniculate Nucleus
Replication of the 10q11 and Xp11 Prostate Cancer Risk Variants: Results from a Utah pedigree-based Study

A New Minimal Replicon of Bacillus anthracis Plasmid pXO1
Pairwise shared genomic segment analysis in high-risk pedigrees: application to Genetic Analysis Workshop 17 exome-sequencing SNP data

Haplotype association analyses in resources of mixed structure using Monte Carlo testing
Forty-six genes causing nonsyndromic hearing impairment: which ones should be analyzed in DNA diagnostics?

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