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Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|May 1, 2017
Heterozygous Nonsense Mutation in the Androgen Receptor Gene Associated with Partial Androgen Insensitivity Syndrome in an Individual with 47,XXY KaryotypeRafael L Batista, Andresa S Rodrigues, Mirian Y Nishi, et al.
Scandinavian Journal of Immunology|March 25, 2015
Protective Profile Involving CD23/IgE-mediated NO Release is a Hallmark of Cutaneous Leishmaniasis Patients from the Xakriabá Indigenous Community in Minas Gerais, BrazilR Carvalho-Gontijo, V Peruhype-Magalhães, M F Costa-Silva, et al.
The Journal of Clinical Endocrinology and Metabolism|May 14, 2010
Nonsense mutations in FGF8 gene causing different degrees of human gonadotropin-releasing deficiencyEricka B Trarbach, Ana Paula Abreu, Leticia Ferreira Gontijo Silveira, et al.
Environmental Toxicology and Pharmacology|July 26, 2011
Colour vision and contrast sensitivity losses of mercury intoxicated industry workers in BrazilD F Ventura, A L Simões, S Tomaz, et al.
Letters in Applied Microbiology|August 2, 2021
Lactobacillus plantarum Lp62 exerts probiotic effects against Gardnerella vaginalis ATCC 49154 in bacterial vaginosisN N Selis, H B M Oliveira, C L S Souza, et al.
Brazilian Journal of Biology = Revista Brasleira De Biologia|December 10, 2025
Genetic diversity and population structure of lima bean (Phaseolus lunatus L.) based on cpSSR markersJ S Penha, G C X Oliveira, A C A Lopes, et al.
Beneficial Microbes|April 11, 2018
Oral administration of Simbioflora® (synbiotic) attenuates intestinal damage in a mouse model of 5-fluorouracil-induced mucositisL M Trindade, V D Martins, N M Rodrigues, et al.
Visual Neuroscience|July 5, 2008
Psychophysical analysis of contrast processing segregated into magnocellular and parvocellular systems in asymptomatic carriers of 11778 Leber's hereditary optic neuropathyM Gualtieri, M Bandeira, R D Hamer, et al.
Clinical Endocrinology|July 31, 2014
Quality of life in a large cohort of adult Brazilian patients with 46,XX and 46,XY disorders of sex development from a single tertiary centreRita Cassia Amaral, Marlene Inacio, Vinicius N Brito, et al.
Human Molecular Genetics|January 5, 2019
Mutations in MAP3K1 that cause 46,XY disorders of sex development disrupt distinct structural domains in the proteinAdam Chamberlin, Robert Huether, Aline Z Machado, et al.
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