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1
Drug transporters: recent advances concerning BCRP and tyrosine kinase inhibitors
Drug transporters: recent advances concerning BCRP and tyrosine kinase inhibitors
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Drug transporters: recent advances concerning BCRP and tyrosine kinase inhibitors

Lemos, C ; Jansen, G ; Peters, G J

British journal of cancer, 2008-03, Vol.98 (5), p.857-862 [Periódico revisado por pares]

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2
CRF1-R activation of the dynorphin/kappa opioid system in the mouse basolateral amygdala mediates anxiety-like behavior
CRF1-R activation of the dynorphin/kappa opioid system in the mouse basolateral amygdala mediates anxiety-like behavior
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CRF1-R activation of the dynorphin/kappa opioid system in the mouse basolateral amygdala mediates anxiety-like behavior

Bruchas, Michael R ; Land, Benjamin B ; Lemos, Julia C ; Chavkin, Charles Tanimoto, Hiromu

PloS one, 2009-12, Vol.4 (12), p.e8528-e8528 [Periódico revisado por pares]

United States: Public Library of Science

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3
Effect of Elderberry (Sambucus nigra L.) Extract Supplementation in STZ-Induced Diabetic Rats Fed with a High-Fat Diet
Effect of Elderberry (Sambucus nigra L.) Extract Supplementation in STZ-Induced Diabetic Rats Fed with a High-Fat Diet
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Effect of Elderberry (Sambucus nigra L.) Extract Supplementation in STZ-Induced Diabetic Rats Fed with a High-Fat Diet

Salvador, Ângelo C ; Król, Ewelina ; Lemos, Virgínia C ; Santos, Sónia A O ; Bento, Fernanda P M S ; Costa, Carina P ; Almeida, Adelaide ; Szczepankiewicz, Dawid ; Kulczyński, Bartosz ; Krejpcio, Zbigniew ; Silvestre, Armando J D ; Rocha, Sílvia M

International journal of molecular sciences, 2017-01, Vol.18 (1), p.13-13 [Periódico revisado por pares]

Switzerland: MDPI AG

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4
Disorder of Sex Development Due to 17-Beta-Hydroxysteroid Dehydrogenase Type 3 Deficiency: A Case Report and Review of 70 Different HSD17B3 Mutations Reported in 239 Patients
Disorder of Sex Development Due to 17-Beta-Hydroxysteroid Dehydrogenase Type 3 Deficiency: A Case Report and Review of 70 Different HSD17B3 Mutations Reported in 239 Patients
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Disorder of Sex Development Due to 17-Beta-Hydroxysteroid Dehydrogenase Type 3 Deficiency: A Case Report and Review of 70 Different HSD17B3 Mutations Reported in 239 Patients

Gonçalves, Catarina I ; Carriço, Josianne ; Bastos, Margarida ; Lemos, Manuel C

International journal of molecular sciences, 2022-09, Vol.23 (17), p.10026 [Periódico revisado por pares]

Switzerland: MDPI AG

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5
Role of HtrA in Growth and Competence of Streptococcus mutans UA159
Role of HtrA in Growth and Competence of Streptococcus mutans UA159
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Role of HtrA in Growth and Competence of Streptococcus mutans UA159

AHN, Sang-Joon ; LEMOS, José A. C ; BURNE, Robert A

Journal of Bacteriology, 2005-05, Vol.187 (9), p.3028-3038 [Periódico revisado por pares]

Washington, DC: American Society for Microbiology

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6
UV-B Filter Octylmethoxycinnamate Induces Vasorelaxation by Ca2+ Channel Inhibition and Guanylyl Cyclase Activation in Human Umbilical Arteries
UV-B Filter Octylmethoxycinnamate Induces Vasorelaxation by Ca2+ Channel Inhibition and Guanylyl Cyclase Activation in Human Umbilical Arteries
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UV-B Filter Octylmethoxycinnamate Induces Vasorelaxation by Ca2+ Channel Inhibition and Guanylyl Cyclase Activation in Human Umbilical Arteries

Lorigo, Margarida ; Quintaneiro, Carla ; Lemos, Manuel ; Martinez-de-Oliveira, José ; Breitenfeld, Luiza ; Cairrao, Elisa

International journal of molecular sciences, 2019-03, Vol.20 (6), p.1376 [Periódico revisado por pares]

Basel: MDPI AG

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7
Hypoparathyroidism, deafness and renal dysplasia syndrome caused by a GATA3 splice site mutation leading to the activation of a cryptic splice site
Hypoparathyroidism, deafness and renal dysplasia syndrome caused by a GATA3 splice site mutation leading to the activation of a cryptic splice site
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Hypoparathyroidism, deafness and renal dysplasia syndrome caused by a GATA3 splice site mutation leading to the activation of a cryptic splice site

Gonçalves, Catarina I. ; Carriço, Josianne N. ; Omar, Omneya M. ; Abdalla, Ebtesam ; Lemos, Manuel C.

Frontiers in endocrinology (Lausanne), 2023-08, Vol.14, p.1207425-1207425 [Periódico revisado por pares]

Frontiers Media S.A

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8
Genetic polymorphisms and protein levels in vocal fold leukoplakia: a systematic review
Genetic polymorphisms and protein levels in vocal fold leukoplakia: a systematic review
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Genetic polymorphisms and protein levels in vocal fold leukoplakia: a systematic review

Campello, C P ; Lima-Silva, M F B ; Lima, E L S de ; Nunes, G R S ; Silva, H A M ; Dellalibera, E ; Britto, L R P B de ; Lemos, C A A ; Muniz, M T C

Brazilian journal of medical and biological research, 2022-01, Vol.55 (1), p.e11920-e11920 [Periódico revisado por pares]

Brazil: Associacao Brasileira de Divulgacao Cientifica (ABDC)

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9
A Novel FGFR1 Missense Mutation in a Portuguese Family with Congenital Hypogonadotropic Hypogonadism
A Novel FGFR1 Missense Mutation in a Portuguese Family with Congenital Hypogonadotropic Hypogonadism
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A Novel FGFR1 Missense Mutation in a Portuguese Family with Congenital Hypogonadotropic Hypogonadism

Fadiga, Lúcia ; Lavrador, Mariana ; Vicente, Nuno ; Barros, Luísa ; Gonçalves, Catarina I ; Al-Naama, Asma ; Saraiva, Luis R ; Lemos, Manuel C

International journal of molecular sciences, 2022-04, Vol.23 (8), p.4423 [Periódico revisado por pares]

Switzerland: MDPI AG

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10
Iodine Supplementation in Pregnancy in an Iodine-Deficient Region: A Cross-Sectional Survey
Iodine Supplementation in Pregnancy in an Iodine-Deficient Region: A Cross-Sectional Survey
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Iodine Supplementation in Pregnancy in an Iodine-Deficient Region: A Cross-Sectional Survey

Lopes, Carla A ; Prazeres, Susana ; Martinez-de-Oliveira, José ; Limbert, Edward ; Lemos, Manuel C

Nutrients, 2022-03, Vol.14 (7), p.1393 [Periódico revisado por pares]

Switzerland: MDPI AG

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