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Nathalie Ruiz

Showing results (1-10 of 21) with videos related to

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The American Journal of Dermatopathology|February 21, 2025
Dermatofibrosarcoma Protuberans Arising in a Digit: A Case ReportSamantha Sun, Jordan Odom, Nathalie Ruiz, et al.
Food Chemistry|July 6, 2014
Ficus carica L. (Moraceae): an ancient source of food and healthMelisa I Barolo, Nathalie Ruiz Mostacero, Silvia N López
Fungal Biology|February 21, 2016
Ascochyta blight: isolation, characterization, and development of a rapid method to detect inhibitors of the chickpea fungal pathogen Ascochyta rabieiLuciana Bahr, María Victoria Castelli, Melisa Isabel Barolo, et al.
World Journal of Microbiology & Biotechnology|January 4, 2021
Fungal endophytes in Peperomia obtusifolia and their potential as inhibitors of chickpea fungal pathogensNathalie Ruiz Mostacero, María Victoria Castelli, Melisa Isabel Barolo, et al.
Natural Product Research|June 15, 2019
Antibacterial activity of prenylated benzopyrans from <i>Peperomia obtusifolia</i> (Piperaceae)Nathalie Ruiz Mostacero, María Victoria Castelli, Andrea Carmen Cutró, et al.
Diagnostics (Basel, Switzerland)|December 30, 2025
Genetic Heterogeneity Underlying Familial Short StatureMargot Comel, Mouna Barat-Houari, Fanny Alkar, et al.
Clinical Epigenetics|April 29, 2025
Reverse genotyping: unveiling Alu element insertion as a new cause of Kabuki syndrome using DNA methylation signatureQuentin Sabbagh, Nathalie Ruiz-Pallares, Cassandra Rastin, et al.
European Journal of Medical Genetics|February 26, 2023
Association of Meier-Gorlin and microcephalic osteodysplastic primordial dwarfism type II clinical features in an individual with CDK5RAP2 primary microcephalyQuentin Sabbagh, Mylène Tharreau, Camille Cenni, et al.
European Journal of Human Genetics : EJHG|May 16, 2013
Expanding the phenotype of IQSEC2 mutations: truncating mutations in severe intellectual disabilityFrederic Tran Mau-Them, Marjolaine Willems, Beate Albrecht, et al.
European Journal of Medical Genetics|May 19, 2010
De novo 15q21.1q21.2 deletion identified through FBN1 MLPA and refined by 244K array-CGH in a female teenager with incomplete Marfan syndromeLaurence Faivre, Philippe Khau Van Kien, Patrick Callier, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
The American Journal of Dermatopathology|February 21, 2025
Dermatofibrosarcoma Protuberans Arising in a Digit: A Case ReportSamantha Sun, Jordan Odom, Nathalie Ruiz, et al.
Food Chemistry|July 6, 2014
Ficus carica L. (Moraceae): an ancient source of food and healthMelisa I Barolo, Nathalie Ruiz Mostacero, Silvia N López
Fungal Biology|February 21, 2016
Ascochyta blight: isolation, characterization, and development of a rapid method to detect inhibitors of the chickpea fungal pathogen Ascochyta rabieiLuciana Bahr, María Victoria Castelli, Melisa Isabel Barolo, et al.
World Journal of Microbiology & Biotechnology|January 4, 2021
Fungal endophytes in Peperomia obtusifolia and their potential as inhibitors of chickpea fungal pathogensNathalie Ruiz Mostacero, María Victoria Castelli, Melisa Isabel Barolo, et al.
Natural Product Research|June 15, 2019
Antibacterial activity of prenylated benzopyrans from <i>Peperomia obtusifolia</i> (Piperaceae)Nathalie Ruiz Mostacero, María Victoria Castelli, Andrea Carmen Cutró, et al.
Diagnostics (Basel, Switzerland)|December 30, 2025
Genetic Heterogeneity Underlying Familial Short StatureMargot Comel, Mouna Barat-Houari, Fanny Alkar, et al.
Clinical Epigenetics|April 29, 2025
Reverse genotyping: unveiling Alu element insertion as a new cause of Kabuki syndrome using DNA methylation signatureQuentin Sabbagh, Nathalie Ruiz-Pallares, Cassandra Rastin, et al.
European Journal of Medical Genetics|February 26, 2023
Association of Meier-Gorlin and microcephalic osteodysplastic primordial dwarfism type II clinical features in an individual with CDK5RAP2 primary microcephalyQuentin Sabbagh, Mylène Tharreau, Camille Cenni, et al.
European Journal of Human Genetics : EJHG|May 16, 2013
Expanding the phenotype of IQSEC2 mutations: truncating mutations in severe intellectual disabilityFrederic Tran Mau-Them, Marjolaine Willems, Beate Albrecht, et al.
European Journal of Medical Genetics|May 19, 2010
De novo 15q21.1q21.2 deletion identified through FBN1 MLPA and refined by 244K array-CGH in a female teenager with incomplete Marfan syndromeLaurence Faivre, Philippe Khau Van Kien, Patrick Callier, et al.
Pageof 3