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Pedro Cruz

Showing results (111-120 of 126) with videos related to

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Frontiers in Medicine|January 10, 2022
Longitudinal Analysis of Antibody Responses to the mRNA BNT162b2 Vaccine in Patients Undergoing Maintenance Hemodialysis: A 6-Month Follow-UpAndré Weigert, Marie-Louise Bergman, Lígia A Gonçalves, et al.
Ecology and Evolution|February 6, 2025
A Seascape Genomics Perspective on Restrictive Genetic Connectivity Overcoming Signals of Local Adaptations in the Green Abalone (<i>Haliotis fulgens</i>) of the California Current SystemJorge Alberto Mares-Mayagoitia, Paulina Mejía-Ruíz, Fabiola Lafarga-De la Cruz, et al.
Current Pharmaceutical Biotechnology|December 20, 2021
Synthesis, Characterization, Antiproliferative Activity of Galloyl Derivatives and Investigation of Cytotoxic Properties in HepG2/C3A CellsRafael Claudino Dos Santos, Raquel Oliveira Nascimento de Freitas, Mary Ann Foglio, et al.
Current Pharmaceutical Biotechnology|September 6, 2024
<i>Guettarda viburnoides</i> Cham. & Schltdl.: Neuroprotective Activities in Mice, Molecular Docking and Microchemical and Morphoanatomical Characteristics of Leaves and StemsPedro Cruz de Oliveira Junior, Eliana Janet Sanjinez-Argandona, Janaine Alberto Marangoni Faoro, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 6, 2012
Specific inactivation of two immunomodulatory SIGLEC genes during human evolutionXiaoxia Wang, Nivedita Mitra, Ismael Secundino, et al.
Plos One|June 12, 2013
Sequencing of candidate chromosome instability genes in endometrial cancers reveals somatic mutations in ESCO1, CHTF18, and MRE11AJessica C Price, Lana M Pollock, Meghan L Rudd, et al.
BMC Genomics|June 26, 2010
Light whole genome sequence for SNP discovery across domestic cat breedsJames C Mullikin, Nancy F Hansen, Lei Shen, et al.
Neuromuscular Disorders : NMD|March 5, 2013
Novel SNP array analysis and exome sequencing detect a homozygous exon 7 deletion of MEGF10 causing early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)Tyler Mark Pierson, Thomas Markello, John Accardi, et al.
American Journal of Human Genetics|October 6, 2010
Compound heterozygosity for loss-of-function lysyl-tRNA synthetase mutations in a patient with peripheral neuropathyHeather M McLaughlin, Reiko Sakaguchi, Cuiping Liu, et al.
Nature Genetics|July 19, 2011
NBEAL2 is mutated in gray platelet syndrome and is required for biogenesis of platelet α-granulesMeral Gunay-Aygun, Tzipora C Falik-Zaccai, Thierry Vilboux, et al.
Pageof 13

Showing results (111-120 of 126) with videos related to

Sort By:
Pageof 13
Frontiers in Medicine|January 10, 2022
Longitudinal Analysis of Antibody Responses to the mRNA BNT162b2 Vaccine in Patients Undergoing Maintenance Hemodialysis: A 6-Month Follow-UpAndré Weigert, Marie-Louise Bergman, Lígia A Gonçalves, et al.
Ecology and Evolution|February 6, 2025
A Seascape Genomics Perspective on Restrictive Genetic Connectivity Overcoming Signals of Local Adaptations in the Green Abalone (<i>Haliotis fulgens</i>) of the California Current SystemJorge Alberto Mares-Mayagoitia, Paulina Mejía-Ruíz, Fabiola Lafarga-De la Cruz, et al.
Current Pharmaceutical Biotechnology|December 20, 2021
Synthesis, Characterization, Antiproliferative Activity of Galloyl Derivatives and Investigation of Cytotoxic Properties in HepG2/C3A CellsRafael Claudino Dos Santos, Raquel Oliveira Nascimento de Freitas, Mary Ann Foglio, et al.
Current Pharmaceutical Biotechnology|September 6, 2024
<i>Guettarda viburnoides</i> Cham. & Schltdl.: Neuroprotective Activities in Mice, Molecular Docking and Microchemical and Morphoanatomical Characteristics of Leaves and StemsPedro Cruz de Oliveira Junior, Eliana Janet Sanjinez-Argandona, Janaine Alberto Marangoni Faoro, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 6, 2012
Specific inactivation of two immunomodulatory SIGLEC genes during human evolutionXiaoxia Wang, Nivedita Mitra, Ismael Secundino, et al.
Plos One|June 12, 2013
Sequencing of candidate chromosome instability genes in endometrial cancers reveals somatic mutations in ESCO1, CHTF18, and MRE11AJessica C Price, Lana M Pollock, Meghan L Rudd, et al.
BMC Genomics|June 26, 2010
Light whole genome sequence for SNP discovery across domestic cat breedsJames C Mullikin, Nancy F Hansen, Lei Shen, et al.
Neuromuscular Disorders : NMD|March 5, 2013
Novel SNP array analysis and exome sequencing detect a homozygous exon 7 deletion of MEGF10 causing early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)Tyler Mark Pierson, Thomas Markello, John Accardi, et al.
American Journal of Human Genetics|October 6, 2010
Compound heterozygosity for loss-of-function lysyl-tRNA synthetase mutations in a patient with peripheral neuropathyHeather M McLaughlin, Reiko Sakaguchi, Cuiping Liu, et al.
Nature Genetics|July 19, 2011
NBEAL2 is mutated in gray platelet syndrome and is required for biogenesis of platelet α-granulesMeral Gunay-Aygun, Tzipora C Falik-Zaccai, Thierry Vilboux, et al.
Pageof 13