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Showing results (31-40 of 43) with videos related to

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Frontiers in Immunology|October 24, 2014
Insights into HLA-G Genetics Provided by Worldwide Haplotype DiversityErick C Castelli, Jaqueline Ramalho, Iane O P Porto, et al.
Molecular Immunology|February 21, 2015
MicroRNAs targeting the immunomodulatory HLA-G gene: a new survey searching for microRNAs with potential to regulate HLA-GIane O P Porto, Celso T Mendes-Junior, Leandro P Felício, et al.
Mutation Research|August 11, 2015
Gene polymorphisms and increased DNA damage in morbidly obese womenB C O Luperini, D C Almeida, M P Porto, et al.
Plant Physiology and Biochemistry : PPB|July 6, 2023
Unveiling the dark side of guard cell metabolismValéria F Lima, Francisco Bruno S Freire, Silvio A Cândido-Sobrinho, et al.
Tissue Antigens|January 10, 2014
Worldwide HLA-E nucleotide and haplotype variability reveals a conserved gene for coding and 3' untranslated regionsL P Felício, I O P Porto, C T Mendes-Junior, et al.
The Plant Journal : for Cell and Molecular Biology|September 6, 2021
Establishment of a GC-MS-based <sup>13</sup> C-positional isotopomer approach suitable for investigating metabolic fluxes in plant primary metabolismValéria F Lima, Alexander Erban, André G Daubermann, et al.
HLA|January 23, 2019
HLA-A promoter, coding, and 3'UTR sequences in a Brazilian cohort, and their evolutionary aspectsThálitta H A Lima, Andreia S Souza, Iane O P Porto, et al.
Molecular Immunology|January 31, 2017
HLA-G variability and haplotypes detected by massively parallel sequencing procedures in the geographicaly distinct population samples of Brazil and CyprusErick C Castelli, Petroula Gerasimou, Michelle A Paz, et al.
Human Immunology|July 19, 2015
HLA-E coding and 3' untranslated region variability determined by next-generation sequencing in two West-African population samplesErick C Castelli, Celso T Mendes-Junior, Audrey Sabbagh, et al.
BMC Medical Genetics|January 16, 2019
Novel ANKRD11 gene mutation in an individual with a mild phenotype of KBG syndrome associated to a GEFS+ phenotypic spectrum: a case reportRita Maria Alves, Paolo Uva, Marielza F Veiga, et al.
Pageof 5

Showing results (31-40 of 43) with videos related to

Sort By:
Pageof 5
Frontiers in Immunology|October 24, 2014
Insights into HLA-G Genetics Provided by Worldwide Haplotype DiversityErick C Castelli, Jaqueline Ramalho, Iane O P Porto, et al.
Molecular Immunology|February 21, 2015
MicroRNAs targeting the immunomodulatory HLA-G gene: a new survey searching for microRNAs with potential to regulate HLA-GIane O P Porto, Celso T Mendes-Junior, Leandro P Felício, et al.
Mutation Research|August 11, 2015
Gene polymorphisms and increased DNA damage in morbidly obese womenB C O Luperini, D C Almeida, M P Porto, et al.
Plant Physiology and Biochemistry : PPB|July 6, 2023
Unveiling the dark side of guard cell metabolismValéria F Lima, Francisco Bruno S Freire, Silvio A Cândido-Sobrinho, et al.
Tissue Antigens|January 10, 2014
Worldwide HLA-E nucleotide and haplotype variability reveals a conserved gene for coding and 3' untranslated regionsL P Felício, I O P Porto, C T Mendes-Junior, et al.
The Plant Journal : for Cell and Molecular Biology|September 6, 2021
Establishment of a GC-MS-based <sup>13</sup> C-positional isotopomer approach suitable for investigating metabolic fluxes in plant primary metabolismValéria F Lima, Alexander Erban, André G Daubermann, et al.
HLA|January 23, 2019
HLA-A promoter, coding, and 3'UTR sequences in a Brazilian cohort, and their evolutionary aspectsThálitta H A Lima, Andreia S Souza, Iane O P Porto, et al.
Molecular Immunology|January 31, 2017
HLA-G variability and haplotypes detected by massively parallel sequencing procedures in the geographicaly distinct population samples of Brazil and CyprusErick C Castelli, Petroula Gerasimou, Michelle A Paz, et al.
Human Immunology|July 19, 2015
HLA-E coding and 3' untranslated region variability determined by next-generation sequencing in two West-African population samplesErick C Castelli, Celso T Mendes-Junior, Audrey Sabbagh, et al.
BMC Medical Genetics|January 16, 2019
Novel ANKRD11 gene mutation in an individual with a mild phenotype of KBG syndrome associated to a GEFS+ phenotypic spectrum: a case reportRita Maria Alves, Paolo Uva, Marielza F Veiga, et al.
Pageof 5