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Ana Maia

Showing results (21-30 of 44) with videos related to

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Frontiers in Psychiatry|August 22, 2022
Symptom provocation for treatment of obsessive-compulsive disorder using transcranial magnetic stimulation: A step-by-step guide for professional trainingAna Maia, Sílvia Almeida, Gonçalo Cotovio, et al.
Pediatric Blood & Cancer|June 19, 2008
Genetic diagnosis of alveolar rhabdomyosarcoma in the bone marrow of a patient without evidence of primary tumorSusana Lisboa, Nuno Cerveira, Joana Vieira, et al.
Pediatric Reports|April 3, 2021
Aggressive Neuroblastoma in a Pediatric Patient with Severe Hemophilia ALidia Costa, Maria Eduarda Couto, Juliana Moutinho, et al.
Molecules (Basel, Switzerland)|December 17, 2024
A New Demand for Improved Selectivity and Potency of Cyanine Dyes as Antiproliferative Agents Against Colorectal Cancer CellsAna Maia, Cathy Ventura, Adriana O Santos, et al.
Molecules (Basel, Switzerland)|September 23, 2022
An Insight into Symmetrical Cyanine Dyes as Promising Selective Antiproliferative Agents in Caco-2 Colorectal Cancer CellsJoão L Serrano, Ana Maia, Adriana O Santos, et al.
Journal of Leukocyte Biology|April 19, 2023
Chitin oligomers promote lymphoid innate and adaptive immune cell activationAna Maia, Yamel Cardona Gloria, Katharina Fuchs, et al.
FASEB Bioadvances|March 4, 2020
Can asymmetric post-translational modifications regulate the behavior of STAT3 homodimers?Ricardo Letra-Vilela, Beatriz Cardoso, Catarina Silva-Almeida, et al.
Journal of Visualized Experiments : Jove|December 15, 2025
Protocol for Repetitive Transcranial Magnetic Stimulation with Symptom Provocation to Treat Obsessive-compulsive DisorderNelson Descalco, Gonçalo Cotovio, Ana Maia, et al.
The Journal of Investigative Dermatology|October 10, 2008
Keratitis-ichthyosis-deafness syndrome caused by GJB2 maternal mosaicismMatthias Titeux, Vanessa Mendonça, Audrey Décha, et al.
Frontiers in Cell and Developmental Biology|October 19, 2020
The Endometrial Transcription Landscape of MRKH SyndromeThomas Hentrich, André Koch, Nico Weber, et al.
Pageof 5

Showing results (21-30 of 44) with videos related to

Sort By:
Pageof 5
Frontiers in Psychiatry|August 22, 2022
Symptom provocation for treatment of obsessive-compulsive disorder using transcranial magnetic stimulation: A step-by-step guide for professional trainingAna Maia, Sílvia Almeida, Gonçalo Cotovio, et al.
Pediatric Blood & Cancer|June 19, 2008
Genetic diagnosis of alveolar rhabdomyosarcoma in the bone marrow of a patient without evidence of primary tumorSusana Lisboa, Nuno Cerveira, Joana Vieira, et al.
Pediatric Reports|April 3, 2021
Aggressive Neuroblastoma in a Pediatric Patient with Severe Hemophilia ALidia Costa, Maria Eduarda Couto, Juliana Moutinho, et al.
Molecules (Basel, Switzerland)|December 17, 2024
A New Demand for Improved Selectivity and Potency of Cyanine Dyes as Antiproliferative Agents Against Colorectal Cancer CellsAna Maia, Cathy Ventura, Adriana O Santos, et al.
Molecules (Basel, Switzerland)|September 23, 2022
An Insight into Symmetrical Cyanine Dyes as Promising Selective Antiproliferative Agents in Caco-2 Colorectal Cancer CellsJoão L Serrano, Ana Maia, Adriana O Santos, et al.
Journal of Leukocyte Biology|April 19, 2023
Chitin oligomers promote lymphoid innate and adaptive immune cell activationAna Maia, Yamel Cardona Gloria, Katharina Fuchs, et al.
FASEB Bioadvances|March 4, 2020
Can asymmetric post-translational modifications regulate the behavior of STAT3 homodimers?Ricardo Letra-Vilela, Beatriz Cardoso, Catarina Silva-Almeida, et al.
Journal of Visualized Experiments : Jove|December 15, 2025
Protocol for Repetitive Transcranial Magnetic Stimulation with Symptom Provocation to Treat Obsessive-compulsive DisorderNelson Descalco, Gonçalo Cotovio, Ana Maia, et al.
The Journal of Investigative Dermatology|October 10, 2008
Keratitis-ichthyosis-deafness syndrome caused by GJB2 maternal mosaicismMatthias Titeux, Vanessa Mendonça, Audrey Décha, et al.
Frontiers in Cell and Developmental Biology|October 19, 2020
The Endometrial Transcription Landscape of MRKH SyndromeThomas Hentrich, André Koch, Nico Weber, et al.
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