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Showing results (881-890 of 1,277) with videos related to

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Journal of Inherited Metabolic Disease|February 12, 2019
International clinical guidelines for the management of phosphomannomutase 2-congenital disorders of glycosylation: Diagnosis, treatment and follow upRuqaiah Altassan, Romain Péanne, Jaak Jaeken, et al.
Nature Genetics|April 10, 2025
Mutations in the small nuclear RNA gene RNU2-2 cause a severe neurodevelopmental disorder with prominent epilepsyDaniel Greene, Koenraad De Wispelaere, Jon Lees, et al.
Nature|May 6, 2026
Expanding the human proteome with microproteins and peptideinsEric W Deutsch, Leron W Kok, Jonathan M Mudge, et al.
Elife|October 3, 2024
Novel risk loci for COVID-19 hospitalization among admixed American populationsSilvia Diz-de Almeida, Raquel Cruz, Andre D Luchessi, et al.
Research Square|June 21, 2024
GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseasesHellen Lesmann, Alexander Hustinx, Shahida Moosa, et al.
Medrxiv : the Preprint Server for Health Sciences|July 28, 2023
GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseasesHellen Lesmann, Alexander Hustinx, Shahida Moosa, et al.
Human Molecular Genetics|June 16, 2022
Novel genes and sex differences in COVID-19 severityRaquel Cruz, Silvia Diz-de Almeida, Miguel López de Heredia, et al.
Physical Review Letters|December 9, 2017
Measurement of the D^{*}(2010)^{+}-D^{+} Mass DifferenceJ P Lees, V Poireau, V Tisserand, et al.
Physical Review Letters|April 2, 2019
Observation of the Decay D^{0}→K^{-}π^{+}e^{+}e^{-}J P Lees, V Poireau, V Tisserand, et al.
Physical Review Letters|November 16, 2020
Search for a Dark Leptophilic Scalar in e^{+}e^{-} CollisionsJ P Lees, V Poireau, V Tisserand, et al.
Pageof 128

Showing results (881-890 of 1,277) with videos related to

Sort By:
Pageof 128
Journal of Inherited Metabolic Disease|February 12, 2019
International clinical guidelines for the management of phosphomannomutase 2-congenital disorders of glycosylation: Diagnosis, treatment and follow upRuqaiah Altassan, Romain Péanne, Jaak Jaeken, et al.
Nature Genetics|April 10, 2025
Mutations in the small nuclear RNA gene RNU2-2 cause a severe neurodevelopmental disorder with prominent epilepsyDaniel Greene, Koenraad De Wispelaere, Jon Lees, et al.
Nature|May 6, 2026
Expanding the human proteome with microproteins and peptideinsEric W Deutsch, Leron W Kok, Jonathan M Mudge, et al.
Elife|October 3, 2024
Novel risk loci for COVID-19 hospitalization among admixed American populationsSilvia Diz-de Almeida, Raquel Cruz, Andre D Luchessi, et al.
Research Square|June 21, 2024
GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseasesHellen Lesmann, Alexander Hustinx, Shahida Moosa, et al.
Medrxiv : the Preprint Server for Health Sciences|July 28, 2023
GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseasesHellen Lesmann, Alexander Hustinx, Shahida Moosa, et al.
Human Molecular Genetics|June 16, 2022
Novel genes and sex differences in COVID-19 severityRaquel Cruz, Silvia Diz-de Almeida, Miguel López de Heredia, et al.
Physical Review Letters|December 9, 2017
Measurement of the D^{*}(2010)^{+}-D^{+} Mass DifferenceJ P Lees, V Poireau, V Tisserand, et al.
Physical Review Letters|April 2, 2019
Observation of the Decay D^{0}→K^{-}π^{+}e^{+}e^{-}J P Lees, V Poireau, V Tisserand, et al.
Physical Review Letters|November 16, 2020
Search for a Dark Leptophilic Scalar in e^{+}e^{-} CollisionsJ P Lees, V Poireau, V Tisserand, et al.
Pageof 128