The Leishmania antigen-specific pro-inflammatory response in cutaneous leishmaniasis is linked to disease progression but not to the therapeutic failure of pentavalent antimonials
Franca, Mônica, Guimarães, Luiz H., Nascimento, Maurício T., Rocha, Paulo N., Carvalho, Lucas P.
Published in Microbes and infection (01.11.2021)
Published in Microbes and infection (01.11.2021)
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Exome Sequencing Reveals the POLR3H Gene as a Novel Cause of Primary Ovarian Insufficiency
Franca, Monica M, Han, Xingfa, Funari, Mariana F A, Lerario, Antonio M, Nishi, Mirian Y, Fontenele, Eveline G P, Domenice, Sorahia, Jorge, Alexander A L, Garcia-Galiano, David, Elias, Carol F, Mendonca, Berenice B
Published in The journal of clinical endocrinology and metabolism (01.07.2019)
Published in The journal of clinical endocrinology and metabolism (01.07.2019)
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A truncating variant of RAD51B associated with primary ovarian insufficiency provides insights into its meiotic and somatic functions
Franca, Monica M, Condezo, Yazmine B, Elzaiat, Maëva, Felipe-Medina, Natalia, Sánchez-Sáez, Fernando, Muñoz, Sergio, Sainz-Urruela, Raquel, Martín-Hervás, M Rosario, García-Valiente, Rodrigo, Sánchez-Martín, Manuel A, Astudillo, Aurora, Mendez, Juan, Llano, Elena, Veitia, Reiner A, Mendonca, Berenice B, Pendás, Alberto M
Published in Cell death and differentiation (01.12.2022)
Published in Cell death and differentiation (01.12.2022)
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Inhibition of gamma-secretase activity without interfering in Notch signalling decreases inflammatory response in patients with cutaneous leishmaniasis
Nascimento, Maurício T., Franca, Mônica, Carvalho, Augusto M., Amorim, Camila F., Peixoto, Fábio, Beiting, Daniel, Scott, Phillip, Carvalho, Edgar M., Carvalho, Lucas P.
Published in Emerging microbes & infections (01.01.2021)
Published in Emerging microbes & infections (01.01.2021)
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A liquid chromatography–atmospheric pressure photoionization tandem mass spectrometric method for the determination of azaarenes in atmospheric particulate matter
Lintelmann, Jutta, França, Monica Heil, Hübner, Evelyn, Matuschek, Georg
Published in Journal of Chromatography A (05.03.2010)
Published in Journal of Chromatography A (05.03.2010)
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Targeted massively parallel sequencing panel to diagnose genetic endocrine disorders in a tertiary hospital
Narcizo, Amanda M., Cardoso, Lais C., Benedetti, Anna F.F., Jorge, Alexander A.L., Funari, Mariana F.A., Braga, Barbara L., Franca, Monica M., Montenegro, Luciana R., Lerario, Antonio M., Nishi, Mirian Y., Mendonca, Berenice B.
Published in Clinics (São Paulo, Brazil) (01.01.2022)
Published in Clinics (São Paulo, Brazil) (01.01.2022)
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Screening of targeted panel genes in Brazilian patients with primary ovarian insufficiency
França, Monica M, Funari, Mariana F A, Lerario, Antonio M, Santos, Mariza G, Nishi, Mirian Y, Domenice, Sorahia, Moraes, Daniela R, Costalonga, Everlayny F, Maciel, Gustavo A R, Maciel-Guerra, Andrea T, Guerra-Junior, Gil, Mendonca, Berenice B
Published in PloS one (23.10.2020)
Published in PloS one (23.10.2020)
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Human Type 1 Iodothyronine Deiodinase ( DIO1 ) Mutations Cause Abnormal Thyroid Hormone Metabolism
França, Monica M, German, Alina, Fernandes, Gustavo W, Liao, Xiao-Hui, Bianco, Antonio C, Refetoff, Samuel, Dumitrescu, Alexandra M
Published in Thyroid (New York, N.Y.) (01.02.2021)
Published in Thyroid (New York, N.Y.) (01.02.2021)
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Genetics of Primary Ovarian Insufficiency in the Next-Generation Sequencing Era
França, Monica Malheiros, Mendonca, Berenice Bilharinho
Published in Journal of the Endocrine Society (01.02.2020)
Published in Journal of the Endocrine Society (01.02.2020)
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Central Precocious Puberty Caused by a Heterozygous Deletion in the MKRN3 Promoter Region
Macedo, Delanie B, França, Monica M, Montenegro, Luciana R, Cunha-Silva, Marina, Best, Danielle S, Abreu, Ana Paula, Kaiser, Ursula B, Mendonca, Berenice B, Jorge, Alexander A L, Brito, Vinicius N, Latronico, Ana Claudia
Published in Neuroendocrinology (01.01.2018)
Published in Neuroendocrinology (01.01.2018)
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High Frequency of MKRN3 Mutations in Male Central Precocious Puberty Previously Classified as Idiopathic
Bessa, Danielle S, Macedo, Delanie B, Brito, Vinicius N, França, Monica M, Montenegro, Luciana R, Cunha-Silva, Marina, Silveira, Leticia G, Hummel, Tiago, Bergadá, Ignacio, Braslavsky, Debora, Abreu, Ana Paula, Dauber, Andrew, Mendonca, Berenice B, Kaiser, Ursula B, Latronico, Ana Claudia
Published in Neuroendocrinology (01.01.2017)
Published in Neuroendocrinology (01.01.2017)
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Nonautoimmune Hyperthyroidism Caused by a Somatic Mosaic GNAS Mutation Involving Part of the Thyroid Gland
França, Monica M, Levine, Robert L, Pappa, Theodora, Ilaka-Chibuluzo, Sandra, Rothberger, Gary D, Dumitrescu, Alexandra M, Refetoff, Samuel
Published in Thyroid (New York, N.Y.) (01.04.2020)
Published in Thyroid (New York, N.Y.) (01.04.2020)
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STR mutations on chromosome 15q cause thyrotropin resistance by activating a primate-specific enhancer of MIR7-2/MIR1179
Grasberger, Helmut, Dumitrescu, Alexandra M, Liao, Xiao-Hui, Swanson, Elliott G, Weiss, Roy E, Srichomkwun, Panudda, Pappa, Theodora, Chen, Junfeng, Yoshimura, Takashi, Hoffmann, Phillip, França, Monica Malheiros, Tagett, Rebecca, Onigata, Kazumichi, Costagliola, Sabine, Ranchalis, Jane, Vollger, Mitchell R, Stergachis, Andrew B, Chong, Jessica X, Bamshad, Michael J, Smits, Guillaume, Vassart, Gilbert, Refetoff, Samuel
Published in Nature genetics (07.05.2024)
Published in Nature genetics (07.05.2024)
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A Novel Homozygous Missense FSHR Variant Associated with Hypergonadotropic Hypogonadism in Two Siblings from a Brazilian Family
França, Monica M., Lerario, Antonio M., Funari, Mariana F.A., Nishi, Mirian Y., Narcizo, Amanda M., de Mello, Maricilda P., Guerra-Junior, Gil, Maciel-Guerra, Andrea T., Mendonça, Berenice B.
Published in Sexual development (01.01.2017)
Published in Sexual development (01.01.2017)
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Two rare loss-of-function variants in the STAG3 gene leading to primary ovarian insufficiency
França, Monica M., Nishi, Mirian Y., Funari, Mariana F.A., Lerario, Antonio M., Baracat, Edmund C., Hayashida, Sylvia A.Y., Maciel, Gustavo A.R., Jorge, Alexander A.L., Mendonca, Berenice B.
Published in European journal of medical genetics (01.03.2019)
Published in European journal of medical genetics (01.03.2019)
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Journal Article
A novel homozygous 1-bp deletion in the NOBOX gene in two Brazilian sisters with primary ovarian failure
França, Monica M., Funari, Mariana F. A., Lerario, Antonio M., Nishi, Mirian Y., Pita, Carmem C., Fontenele, Eveline G. P., Mendonca, Berenice B.
Published in Endocrine (01.12.2017)
Published in Endocrine (01.12.2017)
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Comprehensive Genetic Analysis of 128 Candidate Genes in a Cohort With Idiopathic, Severe, or Familial Osteoporosis
Rocha-Braz, Manuela G M, França, Monica M, Fernandes, Adriana M, Lerario, Antonio M, Zanardo, Evelin A, de Santana, Lucas S, Kulikowski, Leslie D, Martin, Regina M, Mendonca, Berenice B, Ferraz-de-Souza, Bruno
Published in Journal of the Endocrine Society (01.12.2020)
Published in Journal of the Endocrine Society (01.12.2020)
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