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E Calvo

Showing results (391-400 of 628) with videos related to

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Cell Metabolism|September 13, 2011
Mutations in MTFMT underlie a human disorder of formylation causing impaired mitochondrial translationElena J Tucker, Steven G Hershman, Caroline Köhrer, et al.
Nature Genetics|September 7, 2010
High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiencySarah E Calvo, Elena J Tucker, Alison G Compton, et al.
Cell Death & Disease|January 16, 2015
Stromal SLIT2 impacts on pancreatic cancer-associated neural remodelingV Secq, J Leca, C Bressy, et al.
Human Molecular Genetics|May 3, 2023
Multi-omics identifies large mitoribosomal subunit instability caused by pathogenic MRPL39 variants as a cause of pediatric onset mitochondrial diseaseSumudu S C Amarasekera, Daniella H Hock, Nicole J Lake, et al.
Cell Metabolism|December 15, 2023
ChREBP is activated by reductive stress and mediates GCKR-associated metabolic traitsCharandeep Singh, Byungchang Jin, Nirajan Shrestha, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|October 1, 2022
Oncology phase I trial design and conduct: time for a change - MDICT Guidelines 2022D Araujo, A Greystoke, S Bates, et al.
Cancer Discovery|June 1, 2023
Effectors Enabling Adaptation to Mitochondrial Complex I Loss in Hürthle Cell CarcinomaRaj K Gopal, Venkata R Vantaku, Apekshya Panda, et al.
Plos One|December 2, 2021
Characteristics and clinical outcomes of patients hospitalized with laboratory-confirmed COVID-19-Puerto Rico, March-August 2020Hannah R Volkman, Janice Pérez-Padilla, Joshua M Wong, et al.
Nature Genetics|January 15, 2013
Loss-of-function mutations in MGME1 impair mtDNA replication and cause multisystemic mitochondrial diseaseCornelia Kornblum, Thomas J Nicholls, Tobias B Haack, et al.
ESMO Open|August 20, 2022
Isatuximab plus atezolizumab in patients with advanced solid tumors: results from a phase I/II, open-label, multicenter studyM Simonelli, E Garralda, F Eskens, et al.
Pageof 63

Showing results (391-400 of 628) with videos related to

Sort By:
Pageof 63
Cell Metabolism|September 13, 2011
Mutations in MTFMT underlie a human disorder of formylation causing impaired mitochondrial translationElena J Tucker, Steven G Hershman, Caroline Köhrer, et al.
Nature Genetics|September 7, 2010
High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiencySarah E Calvo, Elena J Tucker, Alison G Compton, et al.
Cell Death & Disease|January 16, 2015
Stromal SLIT2 impacts on pancreatic cancer-associated neural remodelingV Secq, J Leca, C Bressy, et al.
Human Molecular Genetics|May 3, 2023
Multi-omics identifies large mitoribosomal subunit instability caused by pathogenic MRPL39 variants as a cause of pediatric onset mitochondrial diseaseSumudu S C Amarasekera, Daniella H Hock, Nicole J Lake, et al.
Cell Metabolism|December 15, 2023
ChREBP is activated by reductive stress and mediates GCKR-associated metabolic traitsCharandeep Singh, Byungchang Jin, Nirajan Shrestha, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|October 1, 2022
Oncology phase I trial design and conduct: time for a change - MDICT Guidelines 2022D Araujo, A Greystoke, S Bates, et al.
Cancer Discovery|June 1, 2023
Effectors Enabling Adaptation to Mitochondrial Complex I Loss in Hürthle Cell CarcinomaRaj K Gopal, Venkata R Vantaku, Apekshya Panda, et al.
Plos One|December 2, 2021
Characteristics and clinical outcomes of patients hospitalized with laboratory-confirmed COVID-19-Puerto Rico, March-August 2020Hannah R Volkman, Janice Pérez-Padilla, Joshua M Wong, et al.
Nature Genetics|January 15, 2013
Loss-of-function mutations in MGME1 impair mtDNA replication and cause multisystemic mitochondrial diseaseCornelia Kornblum, Thomas J Nicholls, Tobias B Haack, et al.
ESMO Open|August 20, 2022
Isatuximab plus atezolizumab in patients with advanced solid tumors: results from a phase I/II, open-label, multicenter studyM Simonelli, E Garralda, F Eskens, et al.
Pageof 63