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Anna Perez

Showing results (21-30 of 41) with videos related to

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Skeletal Muscle|September 3, 2016
Failed reinnervation in aging skeletal muscleSudhakar Aare, Sally Spendiff, Madhusudanarao Vuda, et al.
Molecular Genetics and Metabolism Reports|January 28, 2021
Is hematopoietic stem cell transplantation a therapeutic option for mucolipidosis type II?Luise Sophie Ammer, Sandra Pohl, Sandra Rafaela Breyer, et al.
Journal of Clinical Medicine|June 28, 2023
CNS Manifestations in Mucolipidosis Type II-A Retrospective Analysis of Longitudinal Data on Neurocognitive Development and Neuroimaging in Eleven PatientsLuise Sophie Ammer, Karolin Täuber, Anna Perez, et al.
The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|March 12, 2019
Reduced Mitochondrial Content, Elevated Reactive Oxygen Species, and Modulation by Denervation in Skeletal Muscle of Prefrail or Frail Elderly WomenVita Sonjak, Kathryn J Jacob, Sally Spendiff, et al.
Cancer Research|September 7, 2007
ICOVIR-5 shows E2F1 addiction and potent antiglioma effect in vivoMarta M Alonso, Manel Cascallo, Candelaria Gomez-Manzano, et al.
Cancers|July 31, 2019
Pivotal Role of AKT2 during Dynamic Phenotypic Change of Breast Cancer Stem CellsPetra Gener, Diana Rafael, Joaquin Seras-Franzoso, et al.
European Journal of Human Genetics : EJHG|May 30, 2003
An empirical survey on biobanking of human genetic material and data in six EU countriesIsabelle Hirtzlin, Christine Dubreuil, Nathalie Préaubert, et al.
Elife|July 24, 2024
Targeting plasmid-encoded proteins that contain immunoglobulin-like domains to combat antimicrobial resistanceAlejandro Prieto, Luïsa Miró, Yago Margolles, et al.
Frontiers in Immunology|March 10, 2025
Two rare mutations in homozygosity synergize to silence TREX1 in Aicardi-Goutières syndromeTamar Rubin, Stéphane Bernier, Lily Siok Hoon Lim, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 21, 2024
Cognitive function in SMA patients with 2 or 3 SMN2 copies treated with SMN-modifying or gene addition therapy during the first year of lifePaula Steffens, Deike Weiss, Anna Perez, et al.
Pageof 5

Showing results (21-30 of 41) with videos related to

Sort By:
Pageof 5
Skeletal Muscle|September 3, 2016
Failed reinnervation in aging skeletal muscleSudhakar Aare, Sally Spendiff, Madhusudanarao Vuda, et al.
Molecular Genetics and Metabolism Reports|January 28, 2021
Is hematopoietic stem cell transplantation a therapeutic option for mucolipidosis type II?Luise Sophie Ammer, Sandra Pohl, Sandra Rafaela Breyer, et al.
Journal of Clinical Medicine|June 28, 2023
CNS Manifestations in Mucolipidosis Type II-A Retrospective Analysis of Longitudinal Data on Neurocognitive Development and Neuroimaging in Eleven PatientsLuise Sophie Ammer, Karolin Täuber, Anna Perez, et al.
The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|March 12, 2019
Reduced Mitochondrial Content, Elevated Reactive Oxygen Species, and Modulation by Denervation in Skeletal Muscle of Prefrail or Frail Elderly WomenVita Sonjak, Kathryn J Jacob, Sally Spendiff, et al.
Cancer Research|September 7, 2007
ICOVIR-5 shows E2F1 addiction and potent antiglioma effect in vivoMarta M Alonso, Manel Cascallo, Candelaria Gomez-Manzano, et al.
Cancers|July 31, 2019
Pivotal Role of AKT2 during Dynamic Phenotypic Change of Breast Cancer Stem CellsPetra Gener, Diana Rafael, Joaquin Seras-Franzoso, et al.
European Journal of Human Genetics : EJHG|May 30, 2003
An empirical survey on biobanking of human genetic material and data in six EU countriesIsabelle Hirtzlin, Christine Dubreuil, Nathalie Préaubert, et al.
Elife|July 24, 2024
Targeting plasmid-encoded proteins that contain immunoglobulin-like domains to combat antimicrobial resistanceAlejandro Prieto, Luïsa Miró, Yago Margolles, et al.
Frontiers in Immunology|March 10, 2025
Two rare mutations in homozygosity synergize to silence TREX1 in Aicardi-Goutières syndromeTamar Rubin, Stéphane Bernier, Lily Siok Hoon Lim, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 21, 2024
Cognitive function in SMA patients with 2 or 3 SMN2 copies treated with SMN-modifying or gene addition therapy during the first year of lifePaula Steffens, Deike Weiss, Anna Perez, et al.
Pageof 5